A group of compounds that contain the general formula R-OCH3.
'Ethers' in a medical context are a class of organic compounds used as medication, particularly as an inhalational agent to induce and maintain general anesthesia, characterized by their ability to produce a state of unconsciousness while providing muscle relaxation and analgesia.
Steroids which are substituted with one or more bromine atoms in any position.
Enzymes that catalyze the oxidation of estradiol at the 17-hydroxyl group in the presence of NAD+ or NADP+ to yield estrone and NADH or NADPH. The 17-hydroxyl group can be in the alpha- or beta-configuration. EC 1.1.1.62
A mobile, very volatile, highly flammable liquid used as an inhalation anesthetic and as a solvent for waxes, fats, oils, perfumes, alkaloids, and gums. It is mildly irritating to skin and mucous membranes.
"Ethyl ethers, also known as diethyl ether, is a colorless, highly volatile, and flammable liquid that belongs to the class of organic compounds called ethers, used as an anesthetic in medicine."
Acetals are chemical compounds formed when a carbonyl group (aldehyde or ketone) reacts with two equivalents of alcohol in the presence of a strong acid, resulting in the formation of a stable carbon-carbon bond and producing water as a byproduct.
3-Acetyl-5-sec-butyl-4-hydroxy-3-pyrrolin-2-one. A metabolite found in a strain of the fungus Alternaria tenuis Auct. which functions as an antibiotic with antiviral and antineoplastic properties, and may also act as a mycotoxin.
Arginine derivative which is a substrate for many proteolytic enzymes. As a substrate for the esterase from the first component of complement, it inhibits the action of C(l) on C(4).
A group of compounds that are derivatives of methoxybenzene and contain the general formula R-C7H7O.
Drug metabolizing enzymes which oxidize methyl ethers. Usually found in liver microsomes.
Four fused benzyl rings with three linear and one angular, that can be viewed as a benzyl-phenanthrenes. Compare with NAPHTHACENES which are four linear rings.
CELL CYCLE regulatory signaling systems that are triggered by DNA DAMAGE or lack of nutrients during G2 PHASE. When triggered they restrain cells transitioning from G2 phase to M PHASE.
Compounds that contain two halogenated benzene rings linked via an OXYGEN atom. Many polybrominated diphenyl ethers are used as FLAME RETARDANTS.
Changing an open-chain hydrocarbon to a closed ring. (McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
Ethers that are linked to a benzene ring structure.
The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
A system of traditional medicine which is based on the beliefs and practices of the Chinese culture.
The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds.
Macrocyclic polyethers with the repeating unit of (-CH2-CH2-O)n where n is greater than 2 and some oxygens may be replaced by nitrogen, sulfur or phosphorus. These compounds are useful for coordinating CATIONS. The nomenclature uses a prefix to indicate the size of the ring and a suffix for the number of heteroatoms.
Phospholipids which have an alcohol moiety in ethereal linkage with a saturated or unsaturated aliphatic alcohol. They are usually derivatives of phosphoglycerols or phosphatidates. The other two alcohol groups of the glycerol backbone are usually in ester linkage. These compounds are widely distributed in animal tissues.
Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING).
Compounds in which one or more of the three hydroxyl groups of glycerol are in ethereal linkage with a saturated or unsaturated aliphatic alcohol; one or two of the hydroxyl groups of glycerol may be esterified. These compounds have been found in various animal tissue.
The 17-beta-isomer of estradiol, an aromatized C18 steroid with hydroxyl group at 3-beta- and 17-beta-position. Estradiol-17-beta is the most potent form of mammalian estrogenic steroids.
A non-selective inhibitor of nitric oxide synthase. It has been used experimentally to induce hypertension.
An ethylene compound with two hydroxy groups (-OH) located on adjacent carbons. They are viscous and colorless liquids. Some are used as anesthetics or hypnotics. However, the class is best known for their use as a coolant or antifreeze.
Biphenyl compounds which are extensively brominated. Many of these compounds are toxic environmental pollutants.
The methyl homolog of parathion. An effective, but highly toxic, organothiophosphate insecticide and cholinesterase inhibitor.
Materials applied to fabrics, bedding, furniture, plastics, etc. to retard their burning; many may leach out and cause allergies or other harm.
Brominated hydrocarbons are organic compounds containing carbon (C), hydrogen (H) atoms, and bromine (Br) atoms, where bromine atoms replace some or all of the hydrogen atoms in the hydrocarbon structure.
A substance that is an irritant to the eyes and respiratory tract and may be carcinogenic.
An alkylating agent in cancer therapy that may also act as a mutagen by interfering with and causing damage to DNA.
A hydrocarbon used as an industrial solvent. It has been used as an aerosal propellent, as a refrigerant and as a local anesthetic. (From Martindale, The Extra Pharmacopoeia, 31st ed, p1403)
Compounds of the general formula R-O-R arranged in a ring or crown formation.
'Tert-butyl alcohol' is a type of alcohol, specifically a secondary alcohol, with the chemical formula (CH3)3COH, used as a solvent and synthetic intermediate in organic chemistry and as an antifreeze in industrial applications.
GLYCEROPHOSPHOLIPIDS in which one of the two acyl chains is attached to glycerol with an ether alkenyl linkage instead of an ester as with the other glycerophospholipids.
"Esters are organic compounds that result from the reaction between an alcohol and a carboxylic acid, playing significant roles in various biological processes and often used in pharmaceutical synthesis."
Vinyl compounds, in the context of medical materials, refer to synthetic polymers made from vinyl chloride or vinyl acetate monomers, which are used in the production of various medical devices and supplies such as blood bags, intravenous (IV) bags, tubing, and gloves due to their flexibility, transparency, and resistance to chemicals and heat.
Fractionation of a vaporized sample as a consequence of partition between a mobile gaseous phase and a stationary phase held in a column. Two types are gas-solid chromatography, where the fixed phase is a solid, and gas-liquid, in which the stationary phase is a nonvolatile liquid supported on an inert solid matrix.
Addition of methyl groups. In histo-chemistry methylation is used to esterify carboxyl groups and remove sulfate groups by treating tissue sections with hot methanol in the presence of hydrochloric acid. (From Stedman, 25th ed)
A microanalytical technique combining mass spectrometry and gas chromatography for the qualitative as well as quantitative determinations of compounds.
Derivatives of ACETIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that contain the carboxymethane structure.
An industrial solvent which causes nervous system degeneration. MBK is an acronym often used to refer to it.
Chromatography on thin layers of adsorbents rather than in columns. The adsorbent can be alumina, silica gel, silicates, charcoals, or cellulose. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Physiologic methyl radical donor involved in enzymatic transmethylation reactions and present in all living organisms. It possesses anti-inflammatory activity and has been used in treatment of chronic liver disease. (From Merck, 11th ed)
A subclass of enzymes of the transferase class that catalyze the transfer of a methyl group from one compound to another. (Dorland, 28th ed) EC 2.1.1.
The rate dynamics in chemical or physical systems.
Iodinated hydrocarbons are organic compounds containing carbon and hydrogen atoms, with iodine atoms covalently bonded to them, which are used in medical imaging as radiocontrast agents.
'Ketones' are organic compounds with a specific structure, characterized by a carbonyl group (a carbon double-bonded to an oxygen atom) and two carbon atoms, formed as byproducts when the body breaks down fats for energy due to lack of glucose, often seen in diabetes and starvation states.
Volative flammable fuel (liquid hydrocarbons) derived from crude petroleum by processes such as distillation reforming, polymerization, etc.
Unsaturated hydrocarbons of the type Cn-H2n, indicated by the suffix -ene. (Grant & Hackh's Chemical Dictionary, 5th ed, p408)
The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups.
Liquids that dissolve other substances (solutes), generally solids, without any change in chemical composition, as, water containing sugar. (Grant & Hackh's Chemical Dictionary, 5th ed)
A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
A colorless, flammable liquid used in the manufacture of FORMALDEHYDE and ACETIC ACID, in chemical synthesis, antifreeze, and as a solvent. Ingestion of methanol is toxic and may cause blindness.
Organic compounds that include a cyclic ether with three ring atoms in their structure. They are commonly used as precursors for POLYMERS such as EPOXY RESINS.

Speed of onset and offset and mechanisms of ventilatory depression from sevoflurane: an experimental study in the cat. (1/1149)

BACKGROUND: Inhalational anesthetics depress breathing dose dependently. The authors studied the dynamics of ventilation on changes in end-tidal sevoflurane partial pressure. To learn more about the mechanisms of sevoflurane-induced respiratory depression, the authors also studied its influence on the dynamic ventilatory response to carbon dioxide. METHODS: Experiments were performed in cats anesthetized with alpha chloralose-urethane. For protocol 1, step changes in end-tidal sevoflurane partial pressure were applied and inspired ventilation was measured. Breath-to-breath inspired ventilation was related to the sevoflurane concentration in a hypothetical effect compartment based on an inhibitory sigmoid Emax model. For protocol 2, step changes in the end-tidal partial pressure of carbon dioxide were applied at 0, 0.5, and 1% end-tidal sevoflurane. The inspired ventilation-end-tidal partial pressure of carbon dioxide data were analyzed using a two-compartment model of the respiratory controller, which consisted of a fast peripheral and slow central compartment. Values are the mean +/- SD. RESULTS: In protocol 1, the effect-site half-life of respiratory changes caused by alterations in end-tidal sevoflurane partial pressure was 3.6+/-1.0 min. In protocol 2, at 0.50% sevoflurane, the central and peripheral carbon dioxide sensitivities decreased to 43+/-20% and 36+/-18% of control. At 1% sevoflurane, the peripheral carbon dioxide sensitivity decreased further, to 12+/-13% of control, whereas the central carbon dioxide sensitivity showed no further decrease. CONCLUSIONS: Steady state inspired ventilation is reached after 18 min (i.e., 5 half-lives) on stepwise changes in end-tidal sevoflurane. Anesthetic concentrations of sevoflurane have, in addition to an effect on pathways common to the peripheral and central chemoreflex loops, a selective effect on the peripheral chemoreflex loop. Sevoflurane has similar effects on ventilatory control in humans and cats.  (+info)

Comparison of the effects of sevoflurane and isoflurane on arterial oxygenation during one lung ventilation. (2/1149)

We have compared the effects of sevoflurane and isoflurane on arterial oxygenation, heart rate and mean arterial pressure during one lung anaesthesia in a prospective, crossover study. We studied 28 patients undergoing oesophagogastrectomy, allocated alternatively to one of two groups. Patients in group I/S (n = 14) received 1 MAC (1.1%) of isoflurane in oxygen from induction until the end of 30 min of open chest one lung ventilation (OLV) in the lateral position. This was followed by 1 MAC (2.1%) of sevoflurane in oxygen for the next 30 min of OLV. Patients in group S/I (n = 14) received the two anaesthetic agents in the reverse order. We found no significant difference in arterial oxygenation, heart rate or mean arterial pressure between the two potent inhalation agents. In the subgroup of patients with pulmonary artery catheters (n = 12), we found a significant increase (P < 0.05) in derived shunt during sevoflurane anaesthesia. There was no significant difference in mixed venous saturation and cardiac output. We conclude that during one lung ventilation, the choice between sevoflurane and isoflurane did not significantly influence arterial oxygenation.  (+info)

Effects of enflurane, isoflurane, sevoflurane and desflurane on reperfusion injury after regional myocardial ischaemia in the rabbit heart in vivo. (3/1149)

It is known that volatile anaesthetics protect myocardial tissue against ischaemic and reperfusion injury in vitro. In this investigation, we have determined the effects of the inhalation anaesthetics, enflurane, isoflurane, sevoflurane and desflurane, administered only during early reperfusion, on myocardial reperfusion injury in vivo. Fifty chloralose-anaesthetized rabbits were subjected to 30 min of occlusion of a major coronary artery followed by 120 min of reperfusion. Left ventricular pressure (LVP, tip-manometer), cardiac output (CO, ultrasonic flow probe) and infarct size (triphenyltetrazolium staining) were determined. During the first 15 min of reperfusion, five groups of 10 rabbits each received 1 MAC of enflurane (enflurane group), isoflurane (isoflurane group), sevoflurane (sevoflurane group) or desflurane (desflurane group), and 10 rabbits served as untreated controls (control group). Haemodynamic baseline values were similar between groups (mean LVP 106 (SEM 2) mm Hg; CO 281(7) ml min-1). During coronary occlusion, LVP and CO were reduced to the same extent in all groups (LVP 89% of baseline; CO 89%). Administration of inhalation anaesthetics during early reperfusion further reduced both variables, but they recovered after discontinuation of the anaesthetics to values not different from control animals. Infarct size was reduced from 49 (5)% of the area at risk in the control group to 32 (3)% in the desflurane group (P = 0.021), and to 36 (2)% in the sevoflurane group (P = 0.097). In the enflurane group, infarct size was 39 (5)% (P = 0.272). Isoflurane had no effect on infarct size (48 (5)%, P = 1.000). The results show that desflurane and sevoflurane markedly reduced infarct size and therefore can protect myocardium against reperfusion injury in vivo. Enflurane had only a marginal effect and isoflurane offered no protection against reperfusion injury in vivo. These different effects suggest different protective mechanisms at the cellular level.  (+info)

Sevoflurane-induced reduction of hypoxic drive is sex-independent. (4/1149)

BACKGROUND: Although the mu-opioid agonist morphine affects ventilatory control in men and women in different ways, no data exist regarding the influence of sex on the ventilatory effects of inhalational anesthetics. The authors compared the effect of sevoflurane on the ventilatory response to isocapnic hypoxia in healthy young men and women. METHODS: Breath-to-breath ventilatory responses to hypoxic steps (number of hypoxic steps, four-six; duration, 3 min; end-tidal oxygen tension, approximately 50 mmHg; end-tidal carbon dioxide tension clamped at approximately 4 mmHg above resting values) were assessed in nine men and nine women without and with low-dose sevoflurane (end-tidal concentration, 0.25%). The bispectral index of the electroencephalogram was measured concomitantly. RESULTS: Sevoflurane reduced the hypoxic ventilatory sensitivity significantly in both sexes (men: control, 0.62 +/- 0.17 vs. sevoflurane, 0.38 +/- 0.19 l x min(-1) x %(-1); women: control, 0.52 +/- 0.30 vs. sevoflurane, 0.34 +/- 0.15 l x min(-1) x %(-1)). Sevoflurane-induced reductions of the hypoxic responses were not different in the men and women. During sevoflurane inhalation, the bispectral index values decreased equally in men and women. CONCLUSION: In contrast to morphine, the influence of a low dose of the inhalational anesthetic sevoflurane on the ventilatory response to hypoxia is independent of sex.  (+info)

The dynamic relationship between end-tidal sevoflurane and isoflurane concentrations and bispectral index and spectral edge frequency of the electroencephalogram. (5/1149)

BACKGROUND: Inhalational anesthetics produce dose-dependent effects on electroencephalogram-derived parameters, such as 95% spectral edge frequency (SEF) and bispectral index (BIS). The authors analyzed the relationship between end-tidal sevoflurane and isoflurane concentrations (FET) and BIS and SEF and determined the speed of onset and offset of effect (t1/2k(e0)). METHODS: Twenty-four patients with American Society of Anesthesiologists physical status I or II were randomly assigned to receive anesthesia with sevoflurane or isoflurane. Several transitions between 0.5 and 1.5 minimum alveolar concentration were performed. BIS and SEF data were analyzed with a combination of an effect compartment and an inhibitory sigmoid Emax model, characterized by t1/2k(e0), the concentration at which 50% depression of the electroencephalogram parameters occurred (IC50), and shape parameters. Parameter values estimated are mean +/- SD. RESULTS: The model adequately described the FET-BIS relationship. Values for t1/2k(e0), derived from the BIS data, were 3.5 +/- 2.0 and 3.2 +/- 0.7 min for sevoflurane and isoflurane, respectively (NS). Equivalent values derived from SEF were 3.1 +/- 2.4 min (sevoflurane) and 2.3 +/- 1.2 min (isoflurane; NS). Values of t1/2k(e0) derived from the SEF were smaller than those from BIS (P < 0.05). IC50 values derived from the BIS were 1.14 +/- 0.31% (sevoflurane) and 0.60 +/- 0.11% (isoflurane; P < 0.05). CONCLUSIONS: The speed of onset and offset of anesthetic effect did not differ between isoflurane and sevoflurane; isoflurane was approximately twice as potent as sevoflurane. The greater values of t1/2k(e0) derived from the BIS data compared with those derived from the SEF data may be related to computational and physiologic delays.  (+info)

Effect of sevoflurane and desflurane on the myogenic constriction and flow-induced dilation in rat coronary arterioles. (6/1149)

BACKGROUND: Determinants of myocardial blood flow distribution include metabolic, myogenic, endothelial, and neurohumoral control mechanisms. The authors studied the effect of sevoflurane and desflurane on the myogenic and endothelial mechanisms. METHODS: Wistar rat subepicardial microvessels, approximately 100 microm in diameter, were monitored for diameter changes in vitro using a video detection system. Myogenic vasomotion was studied by varying the intraluminal pressure from 10 mmHg to 120 mmHg. Flow-induced, endothelium-dependent dilation was evaluated in U46619-preconstricted vessels by varying the pressure gradient across the isolated vessel from 10 mmHg to 80 mmHg, while maintaining the midpoint luminal pressure constant at 40 mmHg to avoid myogenic effects. Myogenic and flow-induced vasomotion both were studied in the presence of sevoflurane, 1 or 2 minimum alveolar concentration (MAC) (MAC is a unit of inhalational anesthetic potency), desflurane, 1 or 2 MAC, or no anesthetic (control). RESULTS: Myogenic constriction was shown above intraluminal pressures of 70 mmHg. Myogenic constriction was unchanged by sevoflurane, 1 MAC (P = 0.24), but was mildly enhanced by sevoflurane, 2 MAC (P < 0.05), or desflurane, 1 (P < 0.05) or 2 MAC (P < 0.01). Flow-induced dilation was shown over the pressure gradient range of 10-80 mmHg. Flow-induced dilation was not altered significantly by sevoflurane, 1 or 2 MAC (P > 0.3 each), but was significantly attenuated by desflurane, 1 or 2 MAC (P < 0.001 each). CONCLUSIONS: Sevoflurane maintains myogenic and endothelial determinants of myocardial blood flow distribution. Conversely, desflurane attenuates endothelium-dependent flow-induced dilation while mildly enhancing myogenic constriction.  (+info)

Effects of sevoflurane on regional myocardial blood flow distribution: quantification with myocardial contrast echocardiography. (7/1149)

BACKGROUND: Using myocardial contrast echocardiography, the authors tried to determine whether sevoflurane causes myocardial blood maldistribution in humans and dogs. METHODS: In animal experiments, 15 mongrel dogs were organized into dipyridamole (n = 6) and sevoflurane (n = 9) groups. Sonicated albumin was infused into the left main coronary artery. The peak gray level corrected for background was analyzed at the following intervals: (1) at baseline, (2) after stenosis of the left circumflex coronary artery (blood flow reduced by 40%), (3) after administration of dipyridamole (1 mg/kg given intravenously) or sevoflurane (1 minimum alveolar concentration) during stenosis, and (4) after phenylephrine during stenosis and administration of dipyridamole or sevoflurane. In human studies, nine patients undergoing coronary artery bypass grafting were studied. During partial extracorporeal circulation, the peak gray level was analyzed before and 20 min after sevoflurane (1 minimum alveolar concentration). RESULTS: In animal experiments, dipyridamole decreased significantly the inner:outer ratio of the peak gray level in the ischemic area and the ischemic:normal ratio of the peak gray level. After arterial pressure was restored with phenylephrine, neither the inner:outer ratio nor the ischemic:normal ratio improved. In contrast, after sevoflurane administration, the inner:outer ratio and the ischemic:normal ratio remained unchanged, but these increased with phenylephrine. In human studies, sevoflurane did not change the inner:outer ratio in the area supplied by the most stenotic coronary artery. CONCLUSION: These results suggest that dipyridamole, a potent coronary vasodilator, produces maldistribution of coronary blood flow in our dog models, whereas sevoflurane does not do this in animal or human studies.  (+info)

Effect of sevoflurane concentration on inhalation induction of anaesthesia in the elderly. (8/1149)

We have conducted a randomized, double-blind comparison of 4% and 8% sevoflurane for induction of anaesthesia in unpremedicated patients aged more than 60 yr. Sevoflurane was inhaled in 50% nitrous oxide using a vital capacity breath technique, and mean, systolic and diastolic arterial pressures and heart rate were monitored continuously using a Finapres cuff. In the 8% sevoflurane group, time to successful laryngeal mask insertion was significantly shorter (mean 168 (SD 34) s vs 226 (62) s; P < 0.01) and achieved more often at the first attempt than in the 4% sevoflurane group. Arterial pressures were lower in the 8% group, but this was not significant. No patient had apnoea lasting longer than 1 min. A total of 69% of patients described induction as pleasant and 85% would choose to have it again. We conclude that compared with 8% sevoflurane, the use of 4% sevoflurane in the elderly resulted in greater cardiovascular stability but at the cost of prolonged and occasionally unsuccessful induction.  (+info)

Methyl ethers are a type of organic compound where a methyl group (CH3-) is attached to an oxygen atom, which in turn is connected to another carbon atom. They are formed by the process of methylation, where a methyl group replaces a hydrogen atom in another molecule.

Methyl ethers can be found in various natural and synthetic substances. For example, dimethyl ether (CH3-O-CH3) is a common fuel used in refrigeration systems and as a propellant in aerosol sprays. Anisole (CH3-O-C6H5), another methyl ether, is found in anise oil and is used as a flavoring agent and solvent.

It's worth noting that some methyl ethers have been associated with potential health risks, particularly when they are volatile and can be inhaled or ingested. For example, exposure to high levels of dimethyl ether can cause respiratory irritation, headaches, and dizziness. Therefore, it's important to handle these substances with care and follow appropriate safety guidelines.

In medical or clinical terms, "ethers" do not have a specific relevance as a single medical condition or diagnosis. However, in a broader chemical context, ethers are a class of organic compounds characterized by an oxygen atom connected to two alkyl or aryl groups. Ethers are not typically used as therapeutic agents but can be found in certain medications as solvents or as part of the drug's chemical structure.

An example of a medication with an ether group is the antihistamine diphenhydramine (Benadryl), which has a phenyl ether moiety in its chemical structure. Another example is the anesthetic sevoflurane, which is a fluorinated methyl isopropyl ether used for inducing and maintaining general anesthesia during surgeries.

It's important to note that 'ethers' as a term primarily belongs to the field of chemistry rather than medicine.

Brominated steroids are a class of compounds that are derived from natural or synthetic steroid hormones and have been chemically modified to contain bromine atoms. Steroids are a type of organic compound with a specific structure that includes four fused rings, typically composed of carbon and hydrogen atoms. In the case of brominated steroids, bromine atoms replace some of the hydrogen atoms in the steroid molecule.

Bromination of steroids is a process that can alter their biological activity and pharmacological properties. These compounds have been studied for various medical applications, including as anti-inflammatory agents, anticancer drugs, and contraceptives. However, it's important to note that brominated steroids may also have potential risks and side effects, and their use in clinical settings is subject to regulatory approval and medical supervision.

Estradiol dehydrogenases are a group of enzymes that are involved in the metabolism of estradiols, which are steroid hormones that play important roles in the development and maintenance of female reproductive system and secondary sexual characteristics. These enzymes catalyze the oxidation or reduction reactions of estradiols, converting them to other forms of steroid hormones.

There are two main types of estradiol dehydrogenases: 1) 3-alpha-hydroxysteroid dehydrogenase (3-alpha HSD), which catalyzes the conversion of estradi-17-beta to estrone, and 2) 17-beta-hydroxysteroid dehydrogenase (17-beta HSD), which catalyzes the reverse reaction, converting estrone back to estradiol.

These enzymes are widely distributed in various tissues, including the ovaries, placenta, liver, and adipose tissue, and play important roles in regulating the levels of estradiols in the body. Abnormalities in the activity of these enzymes have been associated with several medical conditions, such as hormone-dependent cancers, polycystic ovary syndrome, and hirsutism.

In medical terms, "ether" is an outdated term that was used to refer to a group of compounds known as diethyl ethers. The most common member of this group, and the one most frequently referred to as "ether," is diethyl ether, also known as sulfuric ether or simply ether.

Diethyl ether is a highly volatile, flammable liquid that was once widely used as an anesthetic agent in surgical procedures. It has a characteristic odor and produces a state of unconsciousness when inhaled, allowing patients to undergo surgery without experiencing pain. However, due to its numerous side effects, such as nausea, vomiting, and respiratory depression, as well as the risk of explosion or fire during use, it has largely been replaced by safer and more effective anesthetic agents.

It's worth noting that "ether" also has other meanings in different contexts, including a term used to describe a substance that produces a feeling of detachment from reality or a sense of unreality, as well as a class of organic compounds characterized by the presence of an ether group (-O-, a functional group consisting of an oxygen atom bonded to two alkyl or aryl groups).

Ethyl ether, also known as diethyl ether or simply ether, is a type of organic compound that is classified as a simple ether. It is a colorless and highly volatile liquid with a characteristic odor that is often described as sweet or fruity. In medical contexts, ethyl ether has been historically used as an anesthetic agent due to its ability to produce unconsciousness and insensitivity to pain when inhaled. However, its use as an anesthetic has largely been replaced by safer and more effective alternatives due to its flammability, explosiveness, and potential for causing serious adverse effects such as heart problems and liver damage.

Ethyl ether is a simple ether consisting of two ethyl groups (-C2H5) linked to an oxygen atom (O), with the molecular formula C4H10O. It is produced by the reaction of ethanol with sulfuric acid, followed by distillation to separate the resulting ethyl ether from other products.

In addition to its historical use as an anesthetic, ethyl ether has been used in various industrial and laboratory applications, such as a solvent for fats, oils, resins, and waxes, and as a starting material for the synthesis of other chemicals. However, due to its flammability and potential for causing harm, it is important to handle ethyl ether with care and follow appropriate safety precautions when using it.

An acetal is a chemical compound that contains two ether functional groups (-O-) bonded to two carbon atoms, which in turn are bonded to two other carbon atoms forming a six-membered ring. Acetals are formed by the reaction of an aldehyde with two equivalents of an alcohol under acid catalysis, followed by removal of water. They are stable compounds that do not easily hydrolyze back to their starting materials, making them useful in various chemical and industrial applications. In the context of organic chemistry, acetals are a subclass of hemiacetals, which contain only one ether functional group bonded to a carbon atom that is also bonded to another oxygen-containing group.

Tenuazonic acid is a mycotoxin, which is a toxic compound produced by certain types of fungi. It is primarily produced by the fungus Alternaria spp., and can be found in various food sources such as grains, vegetables, and fruits that have been contaminated with this fungus.

Tenuazonic acid has been reported to have several toxic effects, including neurotoxicity, immunotoxicity, and genotoxicity. It has also been shown to inhibit protein synthesis in both prokaryotic and eukaryotic cells, which can lead to cell death. Exposure to tenuazonic acid can occur through the ingestion of contaminated food or inhalation of contaminated air.

It is important to note that exposure to high levels of tenuazonic acid can be harmful to human health, and regulatory bodies have set limits on the allowable levels of this mycotoxin in food and feed. However, further research is needed to fully understand the potential health risks associated with exposure to tenuazonic acid.

Tosylarginine Methyl Ester (TAME) is not a medication or a therapeutic agent, but it is a research compound used in scientific studies. It is a synthetic molecule that is often used as a control or a reference standard in enzyme inhibition assays. TAME is an esterified form of the amino acid arginine, with a tosyl group (p-toluenesulfonyl) attached to the nitrogen atom.

TAME is specifically used as a selective and reversible inhibitor of the enzyme called butyrylcholinesterase (BChE), which is involved in the breakdown of certain neurotransmitters in the body. By inhibiting BChE, TAME can help to increase the levels of these neurotransmitters in the brain, making it a useful tool for studying the mechanisms of this enzyme and its role in various physiological processes.

It's important to note that while TAME is used in research settings, it is not approved for use as a drug or therapeutic agent in humans or animals.

Anisoles are organic compounds that consist of a phenyl ring (a benzene ring with a hydroxyl group replaced by a hydrogen atom) attached to a methoxy group (-O-CH3). The molecular formula for anisole is C6H5OCH3. Anisoles are aromatic ethers and can be found in various natural sources, including anise plants and some essential oils. They have a wide range of applications, including as solvents, flavoring agents, and intermediates in the synthesis of other chemicals.

Oxidoreductases, O-demethylating are enzymes that belong to the larger family of oxidoreductases. Specifically, they are involved in catalyzing the removal of methyl groups (-CH3) from various substrates through oxidation reactions. This process is known as O-demethylation.

These enzymes play a crucial role in the metabolism of xenobiotics (foreign substances) such as drugs, toxins, and carcinogens. They help convert these substances into more water-soluble forms, which can then be easily excreted from the body. O-demethylating oxidoreductases are often found in the liver, where they contribute to the detoxification of xenobiotics.

The reaction catalyzed by these enzymes involves the transfer of a hydrogen atom and the addition of an oxygen atom to the methyl group, resulting in the formation of formaldehyde (-CH2O) and a demethylated product. The cytochrome P450 family of enzymes is one example of O-demethylating oxidoreductases.

The G2 phase cell cycle checkpoint is a point in the cell cycle, specifically in the G2 phase, where the cell checks for any DNA damage or other issues that may have occurred during the DNA synthesis phase (S phase) before proceeding to mitosis. This checkpoint serves as a quality control mechanism to ensure that the genetic material is accurately and completely replicated and that the cell is ready to divide. If DNA damage or other problems are detected, the cell cycle is halted at the G2 checkpoint until the issues can be resolved. If the damage is too severe or cannot be repaired, the cell may undergo programmed cell death (apoptosis) to prevent the propagation of potentially harmful mutations.

Halogenated diphenyl ethers are a group of chemical compounds that consist of two phenyl rings (aromatic hydrocarbon rings) linked by an ether group, with one or more halogens attached to the rings. The halogens can include chlorine, bromine, fluorine, or iodine atoms.

One of the most well-known halogenated diphenyl ethers is polychlorinated biphenyl (PCB), which was widely used in electrical equipment and industrial applications until it was banned due to its toxicity and environmental persistence. PCBs are known to have various adverse health effects, including cancer, reproductive disorders, and endocrine disruption.

Other halogenated diphenyl ethers, such as polybrominated diphenyl ethers (PBDEs), have also been used as flame retardants in consumer products, but their use has been restricted or phased out due to health and environmental concerns. Exposure to these compounds can occur through contaminated food, air, dust, and water, and may lead to similar health effects as PCB exposure.

Cyclization is a chemical process that involves forming a cyclic structure or ring-shaped molecule from a linear or open-chain compound. In the context of medicinal chemistry and drug design, cyclization reactions are often used to synthesize complex molecules, including drugs, by creating rings or fused ring systems within the molecule's structure.

Cyclization can occur through various mechanisms, such as intramolecular nucleophilic substitution, electrophilic addition, or radical reactions. The resulting cyclized compounds may exhibit different chemical and biological properties compared to their linear precursors, making them valuable targets for drug discovery and development.

In some cases, the cyclization process can lead to the formation of stereocenters within the molecule, which can impact its three-dimensional shape and how it interacts with biological targets. Therefore, controlling the stereochemistry during cyclization reactions is crucial in medicinal chemistry to optimize the desired biological activity.

Overall, cyclization plays a significant role in the design and synthesis of many pharmaceutical compounds, enabling the creation of complex structures that can interact specifically with biological targets for therapeutic purposes.

I'm sorry for any confusion, but "Phenyl Ethers" is not a recognized medical term. Phenyl ethers are a class of organic compounds consisting of an ether with a phenyl group as one of the components. They are widely used in industry and research, including as solvents, intermediates in chemical synthesis, and pharmaceuticals.

However, if you have any concerns about exposure to certain chemicals or their effects on health, it would be best to consult with a medical professional who can provide advice based on your specific situation and symptoms.

Stereoisomerism is a type of isomerism (structural arrangement of atoms) in which molecules have the same molecular formula and sequence of bonded atoms, but differ in the three-dimensional orientation of their atoms in space. This occurs when the molecule contains asymmetric carbon atoms or other rigid structures that prevent free rotation, leading to distinct spatial arrangements of groups of atoms around a central point. Stereoisomers can have different chemical and physical properties, such as optical activity, boiling points, and reactivities, due to differences in their shape and the way they interact with other molecules.

There are two main types of stereoisomerism: enantiomers (mirror-image isomers) and diastereomers (non-mirror-image isomers). Enantiomers are pairs of stereoisomers that are mirror images of each other, but cannot be superimposed on one another. Diastereomers, on the other hand, are non-mirror-image stereoisomers that have different physical and chemical properties.

Stereoisomerism is an important concept in chemistry and biology, as it can affect the biological activity of molecules, such as drugs and natural products. For example, some enantiomers of a drug may be active, while others are inactive or even toxic. Therefore, understanding stereoisomerism is crucial for designing and synthesizing effective and safe drugs.

Traditional Chinese Medicine (TCM) is a system of medicine that has been developed in China over thousands of years. It is based on the philosophy that the body's vital energy (Qi) circulates through a network of channels called meridians, and that disease results from an imbalance or blockage in this flow of Qi.

TCM uses a variety of treatments to restore balance and promote health, including acupuncture, herbal medicine, moxibustion (the burning of herbs near the skin), cupping, dietary therapy, and tuina (Chinese massage). The use of Chinese herbal medicines is a major component of TCM, with formulas often consisting of combinations of several different herbs tailored to the individual patient's needs.

In addition to these treatments, TCM practitioners may also use diagnostic techniques such as pulse diagnosis and tongue examination to assess a person's overall health and determine the underlying cause of their symptoms. The goal of TCM is not only to treat specific symptoms or diseases but to address the root causes of illness and promote overall wellness.

Molecular structure, in the context of biochemistry and molecular biology, refers to the arrangement and organization of atoms and chemical bonds within a molecule. It describes the three-dimensional layout of the constituent elements, including their spatial relationships, bond lengths, and angles. Understanding molecular structure is crucial for elucidating the functions and reactivities of biological macromolecules such as proteins, nucleic acids, lipids, and carbohydrates. Various experimental techniques, like X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and cryo-electron microscopy (cryo-EM), are employed to determine molecular structures at atomic resolution, providing valuable insights into their biological roles and potential therapeutic targets.

Crown ethers are a type of organic compound that contain a ring of atoms, typically oxygen and carbon, with alternating single and double bonds. The name "crown ether" comes from the crown-like shape of these molecules, which have a central cavity that can bind to metal ions or other positively charged species through a process called coordination.

The size of the cavity in a crown ether determines which ions it can bind to. For example, smaller crown ethers with cavities that are just a few angstroms across may be able to bind to small metal ions like lithium or sodium, while larger crown ethers with cavities up to about 10 angstroms across may be able to bind to larger ions like potassium or ammonium.

Crown ethers have a variety of uses in chemistry and biology. For example, they can be used as catalysts to speed up chemical reactions, or as tools for studying the properties of metal ions and other charged species. They also have potential applications in medicine, as drugs that can selectively bind to and inhibit the activity of certain proteins or enzymes.

Phospholipid ethers are a type of phospholipid in which the traditional fatty acid chains are replaced by alkyl or alkenyl groups linked to the glycerol backbone via an ether bond. They are a significant component of lipoproteins and cell membranes, particularly in archaea, where they contribute to the stability and rigidity of the membrane at extreme temperatures and pressures.

The two main types of phospholipid ethers are plasmalogens and diether lipids. Plasmalogens contain a vinyl ether bond at the sn-1 position, while diether lipids have an ether bond at both the sn-1 and sn-2 positions. These unique structures give phospholipid ethers distinct chemical and biological properties compared to conventional phospholipids with ester-linked fatty acids.

Magnetic Resonance Spectroscopy (MRS) is a non-invasive diagnostic technique that provides information about the biochemical composition of tissues, including their metabolic state. It is often used in conjunction with Magnetic Resonance Imaging (MRI) to analyze various metabolites within body tissues, such as the brain, heart, liver, and muscles.

During MRS, a strong magnetic field, radio waves, and a computer are used to produce detailed images and data about the concentration of specific metabolites in the targeted tissue or organ. This technique can help detect abnormalities related to energy metabolism, neurotransmitter levels, pH balance, and other biochemical processes, which can be useful for diagnosing and monitoring various medical conditions, including cancer, neurological disorders, and metabolic diseases.

There are different types of MRS, such as Proton (^1^H) MRS, Phosphorus-31 (^31^P) MRS, and Carbon-13 (^13^C) MRS, each focusing on specific elements or metabolites within the body. The choice of MRS technique depends on the clinical question being addressed and the type of information needed for diagnosis or monitoring purposes.

Glyceryl ethers, also known as glycerol ethers or alkyl glycosides, are a class of compounds formed by the reaction between glycerol and alcohols. In the context of medical definitions, glyceryl ethers may refer to a group of naturally occurring compounds found in some organisms, including humans.

These compounds are characterized by an ether linkage between the glycerol molecule and one or more alkyl chains, which can vary in length. Glyceryl ethers have been identified as components of various biological tissues, such as lipid fractions of human blood and lung surfactant.

In some cases, glyceryl ethers may also be used as pharmaceutical excipients or drug delivery systems due to their unique physicochemical properties. For example, they can enhance the solubility and bioavailability of certain drugs, making them useful in formulation development. However, it is important to note that specific medical applications and uses of glyceryl ethers may vary depending on the particular compound and its properties.

Estradiol is a type of estrogen, which is a female sex hormone. It is the most potent and dominant form of estrogen in humans. Estradiol plays a crucial role in the development and maintenance of secondary sexual characteristics in women, such as breast development and regulation of the menstrual cycle. It also helps maintain bone density, protect the lining of the uterus, and is involved in cognition and mood regulation.

Estradiol is produced primarily by the ovaries, but it can also be synthesized in smaller amounts by the adrenal glands and fat cells. In men, estradiol is produced from testosterone through a process called aromatization. Abnormal levels of estradiol can contribute to various health issues, such as hormonal imbalances, infertility, osteoporosis, and certain types of cancer.

NG-Nitroarginine Methyl Ester (L-NAME) is not a medication, but rather a research chemical used in scientific studies. It is an inhibitor of nitric oxide synthase, an enzyme that synthesizes nitric oxide, a molecule involved in the relaxation of blood vessels.

Therefore, L-NAME is often used in experiments to investigate the role of nitric oxide in various physiological and pathophysiological processes. It is important to note that the use of L-NAME in humans is not approved for therapeutic purposes due to its potential side effects, which can include hypertension, decreased renal function, and decreased cerebral blood flow.

Ethylene glycols are a class of synthetic chemical compounds that are commonly used as automotive antifreeze, de-icing agents, and as raw materials in the manufacture of polyester fibers and resins. The two most common types of ethylene glycol are ethylene glycol monoethyl ether (also known as ethylene glycol monomethyl ether or EGME) and diethylene glycol (DEG).

Ethylene glycols are colorless, odorless liquids with a sweet taste. They are highly toxic to humans and animals if ingested, inhaled, or absorbed through the skin. Exposure can cause a range of symptoms, including nausea, vomiting, abdominal pain, dizziness, confusion, seizures, coma, and even death.

In medical terms, ethylene glycols are often referred to as "toxic alcohols" or "antifreeze poisoning" when they cause toxicity in humans. Treatment typically involves supportive care, such as fluid replacement and kidney dialysis, as well as the use of specific antidotes, such as fomepizole or ethanol, to prevent further absorption and metabolism of the toxic alcohol.

Polybrominated Biphenyls (PBBs) are a group of chemically related compounds that were widely used as flame retardants in various consumer products, such as electronics, appliances, and textiles. Structurally, they consist of two benzene rings with bromine atoms attached to them in different positions. PBBs have been banned or restricted in many countries due to their environmental persistence, bioaccumulation, and potential adverse health effects.

Here is a medical definition for Polybrominated Biphenyls (PBBs):

A class of brominated aromatic compounds that were historically used as flame retardants in various industrial and consumer applications. Due to their environmental persistence, bioaccumulation potential, and toxicity concerns, their production and use have been significantly restricted or banned in many countries. Exposure to PBBs can occur through ingestion, inhalation, or dermal contact and may lead to a variety of health issues, including endocrine disruption, reproductive and developmental effects, neurodevelopmental toxicity, and immune system alterations. Long-term exposure to high levels of PBBs can result in skin irritation, liver damage, and thyroid hormone disruption.

Methyl parathion is an organophosphate insecticide and acaricide. It functions by inhibiting the enzyme cholinesterase, which leads to an accumulation of the neurotransmitter acetylcholine, causing nervous system excitation and ultimately damage or death in insects. However, it can also have toxic effects on mammals, including humans, if ingested, inhaled, or absorbed through the skin. It is classified as a highly hazardous pesticide by the World Health Organization (WHO) and its use is restricted or banned in many countries due to its high toxicity and environmental persistence.

Flame retardants are chemical compounds that are added to materials, such as textiles, plastics, and foam furnishings, to reduce their flammability and prevent or slow down the spread of fire. They work by releasing non-flammable gases when exposed to heat, which helps to suppress the flames and prevent ignition. Flame retardants can be applied during the manufacturing process or added as a coating or treatment to existing materials. While flame retardants have been shown to save lives and property by preventing fires or reducing their severity, some types of flame retardants have been linked to health concerns, including endocrine disruption, neurodevelopmental toxicity, and cancer. Therefore, it is important to use flame retardants that are safe for human health and the environment.

Brominated hydrocarbons are organic compounds that contain carbon (C), hydrogen (H), and bromine (Br) atoms. These chemicals are formed by replacing one or more hydrogen atoms in a hydrocarbon molecule with bromine atoms. Depending on the number and arrangement of bromine atoms, these compounds can have different properties and uses.

Some brominated hydrocarbons occur naturally, while others are synthesized for various applications. They can be found in consumer products like flame retardants, fumigants, refrigerants, and solvents. However, some brominated hydrocarbons have been linked to health and environmental concerns, leading to regulations on their production and use.

Examples of brominated hydrocarbons include:

1. Methyl bromide (CH3Br): A colorless gas used as a pesticide and fumigant. It is also a naturally occurring compound in the atmosphere, contributing to ozone depletion.
2. Polybrominated diphenyl ethers (PBDEs): A group of chemicals used as flame retardants in various consumer products, such as electronics, furniture, and textiles. They have been linked to neurodevelopmental issues, endocrine disruption, and cancer.
3. Bromoform (CHBr3) and dibromomethane (CH2Br2): These compounds are used in chemical synthesis, as solvents, and in water treatment. They can also be found in some natural sources like seaweed or marine organisms.
4. Hexabromocyclododecane (HBCD): A flame retardant used in expanded polystyrene foam for building insulation and in high-impact polystyrene products. HBCD has been linked to reproductive and developmental toxicity, as well as endocrine disruption.

It is essential to handle brominated hydrocarbons with care due to their potential health and environmental risks. Proper storage, use, and disposal of these chemicals are crucial to minimize exposure and reduce negative impacts.

Methyl methanesulfonate (MMS) is not a medication, but rather a chemical compound with the formula CH3SO3CH3. It's an alkylating agent that is used in laboratory settings for various research purposes, including as a methylating agent in biochemical and genetic studies.

MMS works by transferring its methyl group (CH3) to other molecules, which can result in the modification of DNA and other biological macromolecules. This property makes it useful in laboratory research, but it also means that MMS is highly reactive and toxic. Therefore, it must be handled with care and appropriate safety precautions.

It's important to note that MMS is not used as a therapeutic agent in medicine due to its high toxicity and potential to cause serious harm if mishandled or misused.

Methyl chloride, also known as methyl chloride or chloromethane, is not typically considered a medical term. However, it is a chemical compound with the formula CH3Cl. It is a colorless and extremely volatile liquid that easily evaporates at room temperature.

In terms of potential health impacts, methyl chloride can be harmful if inhaled, swallowed, or comes into contact with the skin. Exposure to high levels can cause symptoms such as headache, dizziness, irritation of the eyes, nose, and throat, nausea, vomiting, and difficulty breathing. Prolonged exposure or significant inhalation can lead to more severe health effects, including damage to the nervous system, liver, and kidneys.

It is essential to handle methyl chloride with care, following appropriate safety measures and guidelines, to minimize potential health risks.

Cyclic ethers are a type of organic compound that contain an ether functional group (-O-) within a cyclic (ring-shaped) structure. In a cyclic ether, one or more oxygen atoms are part of the ring, which can consist of various numbers of carbon atoms. The simplest example of a cyclic ether is oxirane, also known as ethylene oxide, which contains a three-membered ring with two carbon atoms and one oxygen atom.

Cyclic ethers have diverse applications in the chemical industry, including their use as building blocks for the synthesis of other chemicals, pharmaceuticals, and materials. Some cyclic ethers, like tetrahydrofuran (THF), are common solvents due to their ability to dissolve a wide range of organic compounds. However, some cyclic ethers can be hazardous or toxic, so they must be handled with care during laboratory work and industrial processes.

Tert-butyl alcohol, also known as t-butanol or 2-methylpropan-2-ol, is not a medication or a substance used in medical treatments. Therefore, it does not have a specific medical definition. However, I can provide you with a general chemical definition:

Tert-butyl alcohol is a primary alcohol with the molecular formula (CH3)3COH. It is a colorless and flammable liquid with a characteristic camphor-like odor. Tert-butyl alcohol is used as a solvent, denaturant for alcohols, and an intermediate in chemical synthesis. It is less toxic than other common alcohols like ethanol or methanol, but it can still cause irritation to the eyes, skin, and respiratory tract.

Plasmalogens are a type of complex lipid called glycerophospholipids, which are essential components of cell membranes. They are characterized by having a unique chemical structure that includes a vinyl ether bond at the sn-1 position of the glycerol backbone and an ester bond at the sn-2 position, with the majority of them containing polyunsaturated fatty acids. The headgroup attached to the sn-3 position is typically choline or ethanolamine.

Plasmalogens are abundant in certain tissues, such as the brain, heart, and skeletal muscle. They have been suggested to play important roles in cellular functions, including membrane fluidity, signal transduction, and protection against oxidative stress. Reduced levels of plasmalogens have been associated with various diseases, including neurological disorders, cardiovascular diseases, and aging-related conditions.

Esters are organic compounds that are formed by the reaction between an alcohol and a carboxylic acid. They are widely found in nature and are used in various industries, including the production of perfumes, flavors, and pharmaceuticals. In the context of medical definitions, esters may be mentioned in relation to their use as excipients in medications or in discussions of organic chemistry and biochemistry. Esters can also be found in various natural substances such as fats and oils, which are triesters of glycerol and fatty acids.

"Vinyl compounds" is not a term used in medical definitions. It is a term used in chemistry and materials science to refer to a group of chemicals that contain carbon-based molecules with a vinyl group, which is a functional group consisting of a double bond between two carbon atoms, with one of the carbons also being bonded to a hydrogen atom (-CH2=CH-).

Vinyl compounds are used in various industrial and consumer products, including plastics, resins, adhesives, and coatings. Some vinyl compounds, such as polyvinyl chloride (PVC), have been used in medical devices and supplies, such as intravenous (IV) bags, tubing, and blood vessel catheters. However, the use of PVC and other vinyl compounds in medical applications has raised concerns about potential health risks due to the release of toxic chemicals, such as phthalates and dioxins, during manufacturing, use, and disposal. Therefore, alternative materials are being developed and used in medical devices and supplies.

Chromatography, gas (GC) is a type of chromatographic technique used to separate, identify, and analyze volatile compounds or vapors. In this method, the sample mixture is vaporized and carried through a column packed with a stationary phase by an inert gas (carrier gas). The components of the mixture get separated based on their partitioning between the mobile and stationary phases due to differences in their adsorption/desorption rates or solubility.

The separated components elute at different times, depending on their interaction with the stationary phase, which can be detected and quantified by various detection systems like flame ionization detector (FID), thermal conductivity detector (TCD), electron capture detector (ECD), or mass spectrometer (MS). Gas chromatography is widely used in fields such as chemistry, biochemistry, environmental science, forensics, and food analysis.

Methylation, in the context of genetics and epigenetics, refers to the addition of a methyl group (CH3) to a molecule, usually to the nitrogenous base of DNA or to the side chain of amino acids in proteins. In DNA methylation, this process typically occurs at the 5-carbon position of cytosine residues that precede guanine residues (CpG sites) and is catalyzed by enzymes called DNA methyltransferases (DNMTs).

DNA methylation plays a crucial role in regulating gene expression, genomic imprinting, X-chromosome inactivation, and suppression of repetitive elements. Hypermethylation or hypomethylation of specific genes can lead to altered gene expression patterns, which have been associated with various human diseases, including cancer.

In summary, methylation is a fundamental epigenetic modification that influences genomic stability, gene regulation, and cellular function by introducing methyl groups to DNA or proteins.

Gas Chromatography-Mass Spectrometry (GC-MS) is a powerful analytical technique that combines the separating power of gas chromatography with the identification capabilities of mass spectrometry. This method is used to separate, identify, and quantify different components in complex mixtures.

In GC-MS, the mixture is first vaporized and carried through a long, narrow column by an inert gas (carrier gas). The various components in the mixture interact differently with the stationary phase inside the column, leading to their separation based on their partition coefficients between the mobile and stationary phases. As each component elutes from the column, it is then introduced into the mass spectrometer for analysis.

The mass spectrometer ionizes the sample, breaks it down into smaller fragments, and measures the mass-to-charge ratio of these fragments. This information is used to generate a mass spectrum, which serves as a unique "fingerprint" for each compound. By comparing the generated mass spectra with reference libraries or known standards, analysts can identify and quantify the components present in the original mixture.

GC-MS has wide applications in various fields such as forensics, environmental analysis, drug testing, and research laboratories due to its high sensitivity, specificity, and ability to analyze volatile and semi-volatile compounds.

Acetates, in a medical context, most commonly refer to compounds that contain the acetate group, which is an functional group consisting of a carbon atom bonded to two hydrogen atoms and an oxygen atom (-COO-). An example of an acetate is sodium acetate (CH3COONa), which is a salt formed from acetic acid (CH3COOH) and is often used as a buffering agent in medical solutions.

Acetates can also refer to a group of medications that contain acetate as an active ingredient, such as magnesium acetate, which is used as a laxative, or calcium acetate, which is used to treat high levels of phosphate in the blood.

In addition, acetates can also refer to a process called acetylation, which is the addition of an acetyl group (-COCH3) to a molecule. This process can be important in the metabolism and regulation of various substances within the body.

Methyl n-Butyl Ketone, also known as Methyl Amyl Ketone or 2-Hexanone, is an organic compound with the molecular formula C6H12O. It is a colorless liquid with a pungent, fruity odor. It is used as a solvent in various industrial applications, including coatings, cleaning agents, and adhesives.

In a medical context, Methyl n-Butyl Ketone is primarily relevant as a potential occupational hazard. Exposure to this chemical can occur through inhalation, skin contact, or accidental ingestion during its use in industrial settings. Acute exposure to high levels of Methyl n-Butyl Ketone can lead to symptoms such as headache, dizziness, nausea, and respiratory irritation. Chronic exposure has been associated with neurological issues, including memory loss, confusion, and peripheral neuropathy.

It is essential for medical professionals to be aware of the potential health effects of Methyl n-Butyl Ketone, particularly in occupational settings, to ensure appropriate prevention measures are in place and to diagnose and manage potential exposures effectively.

Thin-layer chromatography (TLC) is a type of chromatography used to separate, identify, and quantify the components of a mixture. In TLC, the sample is applied as a small spot onto a thin layer of adsorbent material, such as silica gel or alumina, which is coated on a flat, rigid support like a glass plate. The plate is then placed in a developing chamber containing a mobile phase, typically a mixture of solvents.

As the mobile phase moves up the plate by capillary action, it interacts with the stationary phase and the components of the sample. Different components of the mixture travel at different rates due to their varying interactions with the stationary and mobile phases, resulting in distinct spots on the plate. The distance each component travels can be measured and compared to known standards to identify and quantify the components of the mixture.

TLC is a simple, rapid, and cost-effective technique that is widely used in various fields, including forensics, pharmaceuticals, and research laboratories. It allows for the separation and analysis of complex mixtures with high resolution and sensitivity, making it an essential tool in many analytical applications.

S-Adenosylmethionine (SAMe) is a physiological compound involved in methylation reactions, transulfuration pathways, and aminopropylation processes in the body. It is formed from the coupling of methionine, an essential sulfur-containing amino acid, and adenosine triphosphate (ATP) through the action of methionine adenosyltransferase enzymes.

SAMe serves as a major methyl donor in various biochemical reactions, contributing to the synthesis of numerous compounds such as neurotransmitters, proteins, phospholipids, nucleic acids, and other methylated metabolites. Additionally, SAMe plays a crucial role in the detoxification process within the liver by participating in glutathione production, which is an important antioxidant and detoxifying agent.

In clinical settings, SAMe supplementation has been explored as a potential therapeutic intervention for various conditions, including depression, osteoarthritis, liver diseases, and fibromyalgia, among others. However, its efficacy remains a subject of ongoing research and debate within the medical community.

Methyltransferases are a class of enzymes that catalyze the transfer of a methyl group (-CH3) from a donor molecule to an acceptor molecule, which is often a protein, DNA, or RNA. This transfer of a methyl group can modify the chemical and physical properties of the acceptor molecule, playing a crucial role in various cellular processes such as gene expression, signal transduction, and DNA repair.

In biochemistry, methyltransferases are classified based on the type of donor molecule they use for the transfer of the methyl group. The most common methyl donor is S-adenosylmethionine (SAM), a universal methyl group donor found in many organisms. Methyltransferases that utilize SAM as a cofactor are called SAM-dependent methyltransferases.

Abnormal regulation or function of methyltransferases has been implicated in several diseases, including cancer and neurological disorders. Therefore, understanding the structure, function, and regulation of these enzymes is essential for developing targeted therapies to treat these conditions.

In the context of medicine and pharmacology, "kinetics" refers to the study of how a drug moves throughout the body, including its absorption, distribution, metabolism, and excretion (often abbreviated as ADME). This field is called "pharmacokinetics."

1. Absorption: This is the process of a drug moving from its site of administration into the bloodstream. Factors such as the route of administration (e.g., oral, intravenous, etc.), formulation, and individual physiological differences can affect absorption.

2. Distribution: Once a drug is in the bloodstream, it gets distributed throughout the body to various tissues and organs. This process is influenced by factors like blood flow, protein binding, and lipid solubility of the drug.

3. Metabolism: Drugs are often chemically modified in the body, typically in the liver, through processes known as metabolism. These changes can lead to the formation of active or inactive metabolites, which may then be further distributed, excreted, or undergo additional metabolic transformations.

4. Excretion: This is the process by which drugs and their metabolites are eliminated from the body, primarily through the kidneys (urine) and the liver (bile).

Understanding the kinetics of a drug is crucial for determining its optimal dosing regimen, potential interactions with other medications or foods, and any necessary adjustments for special populations like pediatric or geriatric patients, or those with impaired renal or hepatic function.

I'd be happy to help! However, it seems there might be a slight confusion in your question. Hydrocarbons and iodinated compounds are two different types of chemical substances.

Hydrocarbons refer to organic compounds consisting entirely of hydrogen and carbon atoms. They can be categorized into several types, such as alkanes, alkenes, alkynes, and aromatic hydrocarbons, based on their structure and properties.

On the other hand, iodinated compounds are organic or inorganic molecules containing iodine atoms. These compounds have various applications, especially in medical imaging and therapy, such as radioactive iodine therapy for thyroid cancer and the use of iodinated contrast agents in X-ray and CT scans.

There isn't a specific category called "iodinated hydrocarbons" since hydrocarbons don't inherently contain iodine. However, it is possible to create molecules that combine both hydrocarbon structures and iodine atoms. An example of such a compound would be iodinated alkanes, where iodine atoms replace some hydrogen atoms in an alkane molecule.

So, if you're looking for a medical definition related to iodinated compounds, I can provide that. If you meant something else, please let me know!

Ketones are organic compounds that contain a carbon atom bound to two oxygen atoms and a central carbon atom bonded to two additional carbon groups through single bonds. In the context of human physiology, ketones are primarily produced as byproducts when the body breaks down fat for energy in a process called ketosis.

Specifically, under conditions of low carbohydrate availability or prolonged fasting, the liver converts fatty acids into ketone bodies, which can then be used as an alternative fuel source for the brain and other organs. The three main types of ketones produced in the human body are acetoacetate, beta-hydroxybutyrate, and acetone.

Elevated levels of ketones in the blood, known as ketonemia, can occur in various medical conditions such as diabetes, starvation, alcoholism, and high-fat/low-carbohydrate diets. While moderate levels of ketosis are generally considered safe, severe ketosis can lead to a life-threatening condition called diabetic ketoacidosis (DKA) in people with diabetes.

I'm sorry for any confusion, but "gasoline" is not a medical term. It is a petroleum-derived liquid used as fuel in internal combustion engines. If you have any questions about medical terms or concepts, I would be happy to help with those!

Alkenes are unsaturated hydrocarbons that contain at least one carbon-carbon double bond in their molecular structure. The general chemical formula for alkenes is CnH2n, where n represents the number of carbon atoms in the molecule.

The double bond in alkenes can undergo various reactions, such as addition reactions, where different types of molecules can add across the double bond to form new compounds. The relative position of the double bond in the carbon chain and the presence of substituents on the carbon atoms can affect the physical and chemical properties of alkenes.

Alkenes are important industrial chemicals and are used as starting materials for the synthesis of a wide range of products, including plastics, resins, fibers, and other chemicals. They are also found in nature, occurring in some plants and animals, and can be produced by certain types of bacteria through fermentation processes.

A Structure-Activity Relationship (SAR) in the context of medicinal chemistry and pharmacology refers to the relationship between the chemical structure of a drug or molecule and its biological activity or effect on a target protein, cell, or organism. SAR studies aim to identify patterns and correlations between structural features of a compound and its ability to interact with a specific biological target, leading to a desired therapeutic response or undesired side effects.

By analyzing the SAR, researchers can optimize the chemical structure of lead compounds to enhance their potency, selectivity, safety, and pharmacokinetic properties, ultimately guiding the design and development of novel drugs with improved efficacy and reduced toxicity.

Solvents, in a medical context, are substances that are capable of dissolving or dispersing other materials, often used in the preparation of medications and solutions. They are commonly organic chemicals that can liquefy various substances, making it possible to administer them in different forms, such as oral solutions, topical creams, or injectable drugs.

However, it is essential to recognize that solvents may pose health risks if mishandled or misused, particularly when they contain volatile organic compounds (VOCs). Prolonged exposure to these VOCs can lead to adverse health effects, including respiratory issues, neurological damage, and even cancer. Therefore, it is crucial to handle solvents with care and follow safety guidelines to minimize potential health hazards.

In the context of medicine, "chemistry" often refers to the field of study concerned with the properties, composition, and structure of elements and compounds, as well as their reactions with one another. It is a fundamental science that underlies much of modern medicine, including pharmacology (the study of drugs), toxicology (the study of poisons), and biochemistry (the study of the chemical processes that occur within living organisms).

In addition to its role as a basic science, chemistry is also used in medical testing and diagnosis. For example, clinical chemistry involves the analysis of bodily fluids such as blood and urine to detect and measure various substances, such as glucose, cholesterol, and electrolytes, that can provide important information about a person's health status.

Overall, chemistry plays a critical role in understanding the mechanisms of diseases, developing new treatments, and improving diagnostic tests and techniques.

Methanol, also known as methyl alcohol or wood alcohol, is a volatile, colorless, flammable liquid with a distinctive odor similar to that of ethanol (drinking alcohol). It is used in various industrial applications such as the production of formaldehyde, acetic acid, and other chemicals. In the medical field, methanol is considered a toxic alcohol that can cause severe intoxication and metabolic disturbances when ingested or improperly consumed. Methanol poisoning can lead to neurological symptoms, blindness, and even death if not treated promptly and effectively.

Epoxy compounds, also known as epoxy resins, are a type of thermosetting polymer characterized by the presence of epoxide groups in their molecular structure. An epoxide group is a chemical functional group consisting of an oxygen atom double-bonded to a carbon atom, which is itself bonded to another carbon atom.

Epoxy compounds are typically produced by reacting a mixture of epichlorohydrin and bisphenol-A or other similar chemicals under specific conditions. The resulting product is a two-part system consisting of a resin and a hardener, which must be mixed together before use.

Once the two parts are combined, a chemical reaction takes place that causes the mixture to cure or harden into a solid material. This curing process can be accelerated by heat, and once fully cured, epoxy compounds form a strong, durable, and chemically resistant material that is widely used in various industrial and commercial applications.

In the medical field, epoxy compounds are sometimes used as dental restorative materials or as adhesives for bonding medical devices or prosthetics. However, it's important to note that some people may have allergic reactions to certain components of epoxy compounds, so their use must be carefully evaluated and monitored in a medical context.

Methyl ether may refer to: Any chemical compound of the ether class that includes a methyl group Dimethyl ether, often simply ... called methyl ether Methoxy group, -OCH3 This set index article lists chemical compounds articles associated with the same name ...
Methyl tert-butyl ether (MTBE) is a flammable liquid which is used as an additive in unleaded gasoline. Drinking or breathing ... ToxFAQsTM for Methyl tert-Butyl Ether (MTBE). Spanish: Éter metil tert-butílico (MTBE) ... Methyl tert-butyl ether (MTBE) is a flammable, colorless liquid with a disagreeable odor. ...
The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database ...
... methyl trityl; Triphenylmethyl methyl ether; Trityl methyl ether; Methyl triphenylmethyl ether; Triphenylmethanol, methyl ether ... Methoxy(diphenyl)methyl]benzene * Permanent link for this species. Use this link for bookmarking this species for future ...
Methyl tert-butyl ether (MTBE) is a flammable liquid that has been used as an additive for unleaded gasoline since the 1980s. ...
58 FR 35195, June 30, 1993; 61 FR 5507, Feb. 13, 1996; 61 FR 9227, March 7, 1996; 61 FR 31427, June 20, 1996]. ...
An ether having methyl and ,ital,tert,/ital,-butyl as the two alkyl components. ChEBI CHEBI:27642. ... An ether having methyl and tert-butyl as the two alkyl components. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI: ... Methyl Silicone; Data type: Kovats RI; Authors: Boneva, S.; Toromanova-Petrova, P., Capillary gas chromatography of C1-C4 alkyl ... Methyl Silicone; Data type: Kovats RI; Authors: Boneva, S.; Toromanova-Petrova, P., Capillary gas chromatography of C1-C4 alkyl ...
CDC/ATSDRs Response to Reviewers Comments: Response to Methyl tert-Butyl Ether (MTBE) pdf icon[PDF - 480 KB] ... Title: Toxicological Profile for Methyl tert-Butyl Ether (MTBE). Subject of planned Report: The ATSDR toxicological profile ... Toxicological Profile for Methyl tert-Butyl Ether (MTBE). ... Toxicological Profile for Methyl tert-Butyl Ether (MTBE). * ...
... methyl tert-butyl ether, MTBE; ethyl tert-butyl ether, ETBE; and tert-amyl methyl ether, TAME) and their most characteristic ... methyl acetate, and acetone. When the method was applied to effluent from a column microcosm prepared with core material from ... An analytical method is described that can detect the major alkyl ether compounds that are used as gasoline oxygenates ( ... methyl tert-butyl ether, MTBE; ethyl tert-butyl ether, ETBE; and tert-amyl methyl ether, TAME) and their most characteristic ...
... methyl ether thiol average Mn 2,000; Synonyms: Methoxy PEG thiol,Methoxypolyethylene glycol thiol,PEG thiol,mPEG thiol; Linear ...
... 800261. ... "Evaporative and Exhaust Emissions from Cars Fueled with Gasoline Containing Ethanol or Methyl tert-Butyl Ether," SAE Technical ...
... germanicol methyl ether (miliacin), 3-methoxyfern-9(11)-ene (arundoin), ,svg style=vertical-align:-3.56265pt;width:10px; id= ... amyrin methyl ether (,i ,iso,/i,-sawamilletin), and 3-methoxytaraxer-14-ene (sawamilletin or crusgallin) were characterized in ... Pentacyclic triterpenol methyl ethers (PTMEs), germanicol methyl ether (miliacin), 3-methoxyfern-9(11)-ene (arundoin), -amyrin ... Pentacyclic triterpenol methyl ethers (PTMEs) in the bottom sediments were monitored with the m/z 440 key ion (M.+) in the MS ...
Dipropylene glycol methyl ether , C7H16O3 , CID 25485 - structure, chemical names, physical and chemical properties, ...
... a methyl phenyl ether group and an aliphatic ether chain. For subsequent reactions, I would like to cleave the aryl methyl ... Re: Chemoselective cleavage of aryl methyl ethers « Reply #1 on: June 09, 2021, 06:17:00 AM » ... Re: Chemoselective cleavage of aryl methyl ethers « Reply #2 on: June 10, 2021, 01:15:04 PM » ... Re: Chemoselective cleavage of aryl methyl ethers « Reply #3 on: June 10, 2021, 02:19:02 PM » ...
MTBE (methyl tertiary-butyl ether) is an additive to gasoline. It is added to increase the octane in gas. It is also considered ... Its methyl tertiary-butyl ether (or MTBE as an abbreviation) and is used as an additive to gasoline to increase octane for ... The chemical compound is an ether or alcohol.. Where does MTBE originate?. Its a flammable mixture of isobutylene and methanol ... MTBE manufacturers switched over to making a more environmentally friendly additive called ETBE - ethyl tertiary butyl ether, ...
Methyl Tertiary-Butyl Ether (MTBE) Market Insights & Future Development till 2026. Methyl Tertiary-Butyl Ether (MTBE) Market ... Methyl tertiary-butyl ether (MTBE) seeks widespread adoption as a fuel additive in gasoline engines on the coattails of its ... Processing of methyl tertiary-butyl ether for extracting isobutylene is a major trend observed in the market. Isobutylene is ... Europe and North America will also prevail as major markets for methyl tertiary-butyl ether, in terms of value. There has been ...
... [107 Pages Report] Methyl Tertiary Butyl Ether Market ... Browse 70 market data Tables and 37 Figures spread through 107 Pages and in-depth TOC on "Methyl Tertiary Butyl Ether Market by ... EMAILWIRE.COM, July 31, 2018 ) The report "Methyl Tertiary Butyl Ether Market by Manufacturing Process, (Steam Cracker, Fluid ... The Methyl Tertiary Butyl Ether (MTBE) market is projected to reach USD 18.99 Billion by 2022 from an estimated USD 14.99 ...
In re Methyl Tertiary Butyl Ether Products Liability Litigation ELR Citation: 44 ELR 20033 No(s). 1:00-1898 (S.D.N.Y. Feb 6, ... an oil company for groundwater contamination stemming from the companys use and handling of methyl tertiary butyl ether (MTBE ...
Methyl Tertiary Butyl Ether (MTBE) Products Liability Litigation Filing 2552 Attachment 3 In Re: Methyl Tertiary Butyl Ether ... See, e.g., In re Methyl Tertiary Butyl Ether (MTBE) Products Liability Litigation Slip Copy, 2008 WL 5188193 (S.D.N.Y., Dec. 09 ... See, e.g., In re Methyl Tertiary Butyl Ether (MTBE) Products Liability Litigation Slip Copy, 2008 WL 5188193 (S.D.N.Y., Dec. 09 ... See, e.g., In re Methyl Tertiary Butyl Ether (MTBE) Products Liability Litigation Slip Copy, 2008 WL 5188193 (S.D.N.Y. Dec. 09 ...
Methyl Ether Badge, Lab Analysis Included quantity. Add to cart. SKU: OV-197 Categories: Advanced Chemical Sensors Inc, Store ...
Qi Y, Ding Z, Yao Y, Ma D, Ren F, Yang H and Chen A: Novel triazole analogs of apigenin‑7‑methyl ether exhibit potent antitumor ... Qi, Y., Ding, Z., Yao, Y., Ma, D., Ren, F., Yang, H., Chen, A.Novel triazole analogs of apigenin‑7‑methyl ether exhibit potent ... Qi, Y., Ding, Z., Yao, Y., Ma, D., Ren, F., Yang, H., Chen, A.Novel triazole analogs of apigenin‑7‑methyl ether exhibit potent ... Qi, Y., Ding, Z., Yao, Y., Ma, D., Ren, F., Yang, H., & Chen, A. (2019). Novel triazole analogs of apigenin‑7‑methyl ether ...
Bis(chloromethyl) ether and chloromethyl methyl ether / Government of Canada, Environment Canada, Health and Welfare Canada. : ... Bis(chloromethyl) ether and chloromethyl methyl ether / Government of Canada, Environment Canada, Health and Welfare Canada.. ...
http://clu-in.org/contaminantfocus/default.focus/sec/methyl_tertiary_butyl_ether_(mtbe)/cat/additional_resources/ Last updated ...
Propylene Glycol Methyl Ether Acetate Market By End-Use (Direct Solvent, Chemical Intermediate, Surface Adherent, Pesticides), ... Propylene Glycol Methyl Ether Acetate Market. Propylene Glycol Methyl Ether Acetate Market By End-Use (Direct Solvent, Chemical ...
Dipropylene Glycol Methyl Ether Acetate Market: Introduction Dipropylene glycol methyl ether acetate is a clear, colorless to a ... Dipropylene Glycol Methyl Ether Acetate Market: Dynamics Dipropylene glycol methyl ether acetateMarket Drivers:. *Demand from ... Dipropylene Glycol Methyl Ether Acetate Market. Dipropylene Glycol Methyl Ether Acetate Market - Global Industry Analysis 2014 ... Dipropylene glycol methyl ether acetate Supply & Demand. *Dipropylene glycol methyl ether acetate Current Trends/Issues/ ...
Widespread contamination of groundwater by methyl tertiary butyl ether (MTBE) has triggered the exploration of different ... Widespread contamination of groundwater by methyl tertiary butyl ether (MTBE) has triggered the exploration of different ... versus bioaugmentation with bacterial strain PM1 for treatment of groundwater contaminated with methyl tertiary butyl ether ( ...
... Home :: Tables for Chemistry :: Compound classes 1-methoxyhexane; methyl hexyl ether; methyl n-hexyl ether ...
Lisätietoa aiheesta Benzyl methyl ether. Me mahdollistamme tieteen tekemisen tarjoamalla käyttöösi kattavan tuotevalikoiman, ...
Borkovec, A. B. ; Chang, S. C. ; Horwitz, S. B. / Chemosterilization of house flies with anthramycin methyl ether. In: Journal ... Chemosterilization of house flies with anthramycin methyl ether. / Borkovec, A. B.; Chang, S. C.; Horwitz, S. B. In: Journal of ... Borkovec, A. B., Chang, S. C., & Horwitz, S. B. (1971). Chemosterilization of house flies with anthramycin methyl ether. ... Borkovec, AB, Chang, SC & Horwitz, SB 1971, Chemosterilization of house flies with anthramycin methyl ether., Journal of ...
Double-Layered Polyvinylpyrrolidone-Poly(Methyl Vinyl Ether-Alt-Maleic Acid) based Microneedles to Deliver Meloxicam: An In ... Double-Layered Polyvinylpyrrolidone-Poly(Methyl Vinyl Ether-Alt-Maleic Acid) based Microneedles to Deliver Meloxicam: An In ... Specifically, we develop a double-layered MN formulation using polyvinylpyrrolidone and cross-linked poly(methyl vinyl ether- ... Double-Layered Polyvinylpyrrolidone-Poly(methyl vinyl ether-alt-maleic acid)-Based Microneedles to Deliver MeloxicamFinal ...
  • Methyl tert -butyl ether (MTBE) is a flammable, colorless liquid with a disagreeable odor. (cdc.gov)
  • Methyl tert -butyl ether (MTBE) is a flammable liquid that has been used as an additive for unleaded gasoline since the 1980s. (cdc.gov)
  • MTBE (methyl tertiary-butyl ether) is an additive to gasoline. (burke-eisner.com)
  • It's methyl tertiary-butyl ether (or MTBE as an abbreviation) and is used as an additive to gasoline to increase octane for fuel. (burke-eisner.com)
  • The intelligent report also anticipates that Methyl Tertiary-Butyl Ether (MTBE) Market would grow at a constructive CAGR until 2026. (clickpress.com)
  • In order to study the various trends and patterns prevailing in the concerned market, FactMR has included a new report titled 'Global Methyl Tertiary-Butyl Ether (MTBE) Market Insights, Trends & Future Development Status Recorded during 2018-2026' to its wide online database including upcoming trends and growth factors. (clickpress.com)
  • Methyl tertiary-butyl ether (MTBE) seeks widespread adoption as a fuel additive in gasoline engines on the coattails of its property of high oxygen content raising. (clickpress.com)
  • According to a recent analytical research report developed by FactMR, the global methyl tertiary-butyl ether (MTBE) market will exhibit a value CAGR of 4.7% between the forecast period, 2017 and 2026. (clickpress.com)
  • A district court dismissed New Jersey's claims against an oil company for groundwater contamination stemming from the company's use and handling of methyl tertiary butyl ether (MTBE). (elr.info)
  • UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF NEW YORK -------------------------------------------------------------------- x In Re: Methyl Tertiary Butyl Ether ( MTBE ) Products Liability Litigation -------------------------------------------------------------------- x This document relates to the following case: City of New York v. Amerada Hess Corp., et al. (justia.com)
  • Comparison of biostimulation versus bioaugmentation with bacterial strain PM1 for treatment of groundwater contaminated with methyl tertiary butyl ether (MTBE). (escholarship.org)
  • Widespread contamination of groundwater by methyl tertiary butyl ether (MTBE) has triggered the exploration of different technologies for in situ removal of the pollutant, including biostimulation of naturally occurring microbial communities or bioaugmentation with specific microbial strains known to biodegrade the oxygenate. (escholarship.org)
  • 1. Methyl tert-butyl ether MTBE is an organic compound with molecular formula (CH3)3COCH3. (sinochemi.com)
  • MTBE, commonly known as methyl tert-butyl ether, is a colorless liquid with a strong anesthetic-like odor. (outfitclothingsuite.com)
  • Methyl tertiary butyl ether (MTBE) has been used as a gasoline additive since the 1970s. (vexof.com)
  • The toxicity effects of the individual and combined exposure of methyl tert-butyl ether (MTBE) and tire rubber powder (RP) on Nile tilapia fish (Oreochromis niloticus). (bvsalud.org)
  • Methyl tert-butyl ether (MTBE) is soluble in water and can contaminate water sources when it spills during transportation or leaks from underground storage tanks . (bvsalud.org)
  • 2,4-di-tert-butyl phenol and methyl tert-butyl ether (MTBE) were two of the major individual components detected. (who.int)
  • Dermal permeability was estimated from 11 adult subjects following immersion of their hand and forearm into a sealed 4.8-L Plexiglas cylinder containing 100 microg/L each of chloroform , 1,1,1-trichloroethane (111-TCA), and toluene and 400 microg/L of methyl tertiary butyl ether (MTBE) in water. (cdc.gov)
  • In response to a request from the National Centers for Environmental Health (NCEH), NIOSH investigated occupational exposures to methyl- tert-butyl-ether (1634044) (MtBE), benzene (71432), xylene (1330207), toluene (108883), and carbon-monoxide (630080) (CO) at worksites where workers were exposed to gasoline (8006619) and exhaust emissions. (cdc.gov)
  • Furey, R. and King, J., "Evaporative and Exhaust Emissions from Cars Fueled with Gasoline Containing Ethanol or Methyl tert-Butyl Ether," SAE Technical Paper 800261, 1980, https://doi.org/10.4271/800261 . (sae.org)
  • Processing of methyl tertiary-butyl ether for extracting isobutylene is a major trend observed in the market. (clickpress.com)
  • Isobutylene is widely utilized for manufacturing butyl rubber, methyl methacrylate, and poly-isobutylene, which seek tremendous applications in various end-use industries such as electronics, manufacturing, industrial and automotive. (clickpress.com)
  • Refining companies have been considering employment of methyl tertiary-butyl ether as a fuel additive in light of its excellent blending characteristics and economic viability. (clickpress.com)
  • In terms of value, Asia-Pacific excluding Japan (APEJ) will continue to lead the global methyl tertiary-butyl market. (clickpress.com)
  • Europe and North America will also prevail as major markets for methyl tertiary-butyl ether, in terms of value. (clickpress.com)
  • Occupancy of numerous key suppliers is a major factor responsible for the fragmented nature of the global methyl tertiary-butyl ether market. (clickpress.com)
  • The boiling point of methyl tert-butyl ether is approximately 131°F, while its flash point is 18°F. Methyl tert-butyl ether is less thicker than water and quite soluble in water. (outfitclothingsuite.com)
  • Gasoline contains methyl tert-butyl ether as an octane booster. (outfitclothingsuite.com)
  • The majority of methyl tert-butyl ester is produced in China. (outfitclothingsuite.com)
  • Procurement Resource does an in-depth analysis of the price trend to bring forth the monthly, quarterly, half-yearly, and yearly information on the methyl tert-butyl ether price, cellulose price and ethylene price etc. in its latest pricing dashboard. (outfitclothingsuite.com)
  • The methyl tert-butyl ether price trend , pricing database, and analysis can prove valuable for procurement managers, directors, and decision-makers to build up their strongly backed-up strategic insights to attain progress and profitability in the business. (outfitclothingsuite.com)
  • Methyl tert-butyl ether is used in a range of industrial applications, including the acyclic hydrocarbonisation of ether, gasoline and fuel additives. (outfitclothingsuite.com)
  • Methyl tert-butyl ether is also utilised in solvents, anti-knocking chemicals, and automotive applications. (outfitclothingsuite.com)
  • Methyl Alcohol or Butyl Alcohol Polyalkylene Ether Epoxy Group End Capped Description: These end capped polyethers have a functional group epoxy group, for most applications, the epoxy group of the polyether is reacted with the azyl(-NH2). (tjskl.org.cn)
  • Look no further than Hengli 's methyl tertiary butyl ether ! (vexof.com)
  • Methyl tertiary butyl ether is also used in other industries, such as the production of plastics and adhesives. (vexof.com)
  • The use of methyl tertiary butyl ether has come under scrutiny in recent years due to its potential environmental impacts. (vexof.com)
  • Methyl tertiary butyl ether can leach into groundwater and contaminate drinking water supplies. (vexof.com)
  • Despite these concerns, methyl tertiary butyl ether has some surprising benefits for the environment. (vexof.com)
  • Methyl tertiary butyl ether can actually help to reduce emissions of other pollutants, such as carbon monoxide and volatile organic compounds (VOCs). (vexof.com)
  • The benefits of methyl tertiary butyl ether outweigh its potential risks. (vexof.com)
  • Hengli's methyl tertiary butyl ether has been gaining popularity as an effective alternative to gasoline. (vexof.com)
  • For these reasons, it is clear that methyl tertiary butyl ether can be an invaluable addition to any fuel supply chain! (vexof.com)
  • We describe a rapid and efficient method for selective deprotection of methoxymethyl (MOM) ethers using ZnBr2 and n-PrSH, which completely removed MOM from diverse MOM ethers of primary, secondary, and tertiary alcohols or phenol derivatives. (headshotsmarathon.org)
  • Methyl chloromethyl ether. (osha.gov)
  • Bis(chloromethyl) ether and chloromethyl methyl ether / Government of Canada, Environment Canada, Health and Welfare Canada. (gc.ca)
  • Dipropylene glycol methyl ether acetate is a clear, colorless to a yellow liquid organic chemical compound with moderate evaporation rate and sweet odor. (persistencemarketresearch.com)
  • Dipropylene glycol methyl ether acetate is used in an industrial solvent and coalescing agent. (persistencemarketresearch.com)
  • As a solvent, dipropylene glycol methyl ether acetate is dissolved in the resins to various typed of surface coatings such as paints, inks, lacquers, among others. (persistencemarketresearch.com)
  • Moreover, the common uses of dipropylene glycol methyl ether acetate as household and industrial cleaners, Inks, automotive and industrial coatings, among others. (persistencemarketresearch.com)
  • The dipropylene glycol methyl ether acetate consumption is primarily attributing by the growing p-series glycol consumption across the globe. (persistencemarketresearch.com)
  • Several factors such as low toxic and safe for health as compared to other propylene glycol ether remains to contribute in the market growth of dipropylene glycol methyl ether acetate across the globe. (persistencemarketresearch.com)
  • Dipropylene glycol methyl ether acetate is widely used as a solvent in the paints and coatings formulation. (persistencemarketresearch.com)
  • Such aspects are expected to pave the way for dipropylene glycol methyl ether acetate market growth in the upcoming years. (persistencemarketresearch.com)
  • Nowadays, intensifying demand for cleaners across the industrial and residential sector is expected to lay a strong path for robust dipropylene glycol methyl ether acetate market growth during the forecast period. (persistencemarketresearch.com)
  • Some other applications of dipropylene glycol methyl ether acetate such as silkscreen inks, metal finishes are also anticipated to contributing to the dipropylene glycol methyl ether acetate market growth in the near future. (persistencemarketresearch.com)
  • Such factor is expected to act as challenge for dipropylene glycol methyl ether acetate market growth during the forecast period. (persistencemarketresearch.com)
  • From the regional perspective, Europe is estimated to account for dominating share in the global dipropylene glycol methyl ether acetate market in the coming years, owing to the growing demand for glycol ether together with coatings application across various end-use industries. (persistencemarketresearch.com)
  • The Asia Pacific followed by North America is projected to hold second-highest share in the global dipropylene glycol methyl ether acetate market during the forecast period. (persistencemarketresearch.com)
  • All ethylene glycol methyl ether wholesalers & ethylene glycol methyl ether manufacturers come from members. (tjskl.org.cn)
  • We doesn't provide ethylene glycol methyl ether products or service, please contact them directly and verify their companies info carefully. (tjskl.org.cn)
  • Methyl Perfluorobutyl Ether (163702-08-7) is a colorless, low odor, low-toxicity, non-flammable liquid, with a boiling point of 190°C. It is a perfluorinated ether with a structure of Rn-C4F9O-Rn, where each Rn is either methyl or ethyl. (codchem.com)
  • Hydroxyethyl Methyl Cellulose manufacturers-Hydroxypropyl methylcellulose has many effects on cement hydration Hydroxypropyl methyl cellulose has a delay in the hydration of cement-based mortar, and the delay effect increases with the increase of the cellulose content. (998766.com)
  • Hydroxyethyl Methyl Cellulose (MHEC) is also named as Methyl Hydroxyethyl Cellulose (HEMC),used as high efficient water retention agent, stabilizer, adhesives and film-forming agent in kinds of building materials.is widely used in industrial applications ,such as construction, detergent ,paint and coating ,we also can provide HEMC according to customers requirements. (kimachemical.com)
  • MikaZone™ Hydroxypropyl Methyl Cellulose (HPMC) is a non-ionic cellulose ether made from natural polymer material cellulose through a series of etherification. (mikacelluloseether.com)
  • MikaZone™ Hydroxypropyl Methyl Cellulose (HPMC) is used very often as a thickener in building applications as it prevents segregation and improves the cohesion of the formulation components. (mikacelluloseether.com)
  • MikaZone™ Hydroxypropyl Methyl Cellulose (HPMC) can effectively prevent too fast and low penetration of water into the base surface in cement-based products, allowing more water to stay in the mortar and participate in the cement hydration reaction. (mikacelluloseether.com)
  • MikaZone™ Hydroxypropyl Methyl Cellulose (HPMC) can significantly increase the thixotropic properties of the mortar system, which allows the mortar with excellent anti-sagging ability, thereby improving construction efficiency, especially when building on walls. (mikacelluloseether.com)
  • In gypsum-based and ash-calcium-based products, MikaZone™ cellulose ethers also play an important role in ensuring their open time and strength development. (mikacelluloseether.com)
  • In addition, there types of cellulose ethers exhibit properties of thermal gelation, metabolic inertness, enzyme resistance, low odor and taste, and PH stability. (bestchemhpmc.com)
  • Methyl Perfluorobutyl Ether is an excellent solvent for polar and non-polar compounds alike. (codchem.com)
  • The new method can also give simultaneous identification of polar compounds that might occur as degradation products of gasoline oxygenates, such as TBA, TBF, TAA, methyl acetate, and acetone. (usgs.gov)
  • Methyl ether may refer to: Any chemical compound of the ether class that includes a methyl group Dimethyl ether, often simply called methyl ether Methoxy group, -OCH3 This set index article lists chemical compounds articles associated with the same name. (wikipedia.org)
  • ETHYLENE GLYCOL BIS(PROPYLENE GLYCOL -B- ETHYLENE GLYCOL) ETHER ;1,2-Propyleneglycol,ethoxylatedandpropoxylated;ethyleneglycolbis(propyleneglycol-b-ethyleneg;Oxirane, methyl . (tjskl.org.cn)
  • hydroxypropyl methylcellulose manufacturer-Preparation of cotton for hydroxypropyl methylcellulose The term hydroxypropyl methyl cellulose is not only a bit awkward to pronounce, but it is hard to understand its composition and use as mortar. (998766.com)
  • How do you remove a methyl group from an ester? (headshotsmarathon.org)
  • The packaging is based on the quantity of Acohol Ether Sulfonate and Compound Fatty Acid methyl Ester. (evchargingsolutions.be)
  • Compound Fatty Alcohol Methyl Ester, Acohol Ethersulfonate and Compound Fatty Ester packing 1kg/bottle. (evchargingsolutions.be)
  • You can find this in Greens protective groups in organic synthesis under protection of phenols, methyl ether. (chemicalforums.com)
  • A new reagent for the deprotection of various aromatic methyl ethers, 2-(diethylamino)ethanethiol, affords the corresponding phenols in good to excellent yields. (headshotsmarathon.org)
  • Some polymeric photoinitiators based on alpha-hydroxymethylbenzoin and its methyl ether are used to initiate the polymerization of methyl methacrylate in solution and the crosslinking of an epoxyacrylate formulation in thin films. (kent.ac.uk)
  • Alkoxymethyl ethers are widely used to protect hydroxyl groups in organic synthesis. (headshotsmarathon.org)
  • Methyl Perfluorobutyl Ether is widely used in applications such as the production of catalysts, surfactants, dispersants, and corrosion inhibitors. (codchem.com)
  • I have a molecule which contains both, a methyl phenyl ether group and an aliphatic ether chain. (chemicalforums.com)
  • Taken together, these results showed that the apigenein‑7‑methyl ether novel derivative 3d may prove an important lead molecule for the treatment of ovarian cancer. (spandidos-publications.com)
  • Demethylation is the chemical process resulting in the removal of a methyl group (CH3) from a molecule. (headshotsmarathon.org)
  • 3. It has a minty odor vaguely reminiscent of diethyl ether, leading to unpleasant taste and odor in water. (sinochemi.com)
  • Both the reagent and the byproduct 2-(diethylamino)ethyl methyl sulfide are soluble in dilute acid, which allows an essentially odorless workup. (headshotsmarathon.org)
  • A common way of demethylation is the replacement of a methyl group by a hydrogen atom, resulting in a net loss of one carbon and two hydrogen atoms. (headshotsmarathon.org)
  • Do you have experience/suggestions with selective ether cleavage reactions? (chemicalforums.com)
  • We're going to dedicate ourselves to offering our esteemed shoppers with the most enthusiastically considerate solutions for Cheapest Price Mhec Methyl Hydroxyethyl Cellulose Powder for Construction, Never-ending improvement and striving for 0% deficiency are our two main quality policies. (kimachemical.com)
  • FMES is formed through the compound sulfonation fatty acid methyl esters and fatty alcohol esters. (evchargingsolutions.be)
  • Methyl Perfluorobutyl Ether is a stable, low-toxicity liquid with a wide range of applications in the industrial, consumer, and medical fields. (codchem.com)
  • MikaZone™ cellulose ether products are suitable for a variety of construction mortars. (mikacelluloseether.com)
  • For subsequent reactions, I would like to cleave the aryl methyl ether group to obtain a phenol. (chemicalforums.com)
  • Why methyl group is ortho and para directing and activating? (headshotsmarathon.org)
  • Methyl group shows +I effect i.e it is electron donating group soo it increases the electron density at o - p position.So it is o and p directing for electrophilic addition reaction. (headshotsmarathon.org)
  • A methyl group is an electron donor. (headshotsmarathon.org)

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