Phenolsulfonphthalein
Phenolphthaleins
Arylsulfotransferase
A sulfotransferase that catalyzes the sulfation of a phenol in the presence of 3'-phosphoadenylylsulfate as sulfate donor to yield an aryl sulfate and adenosine 3',5'-bisphosphate. A number of aromatic compounds can act as acceptors; however, organic hydroxylamines are not substrates. Sulfate conjugation by this enzyme is a major pathway for the biotransformation of phenolic and catechol drugs as well as neurotransmitters. EC 2.8.2.1.
Biodegradation, Environmental
Parabens
Benzene
Toxic, volatile, flammable liquid hydrocarbon byproduct of coal distillation. It is used as an industrial solvent in paints, varnishes, lacquer thinners, gasoline, etc. Benzene causes central nervous system damage acutely and bone marrow damage chronically and is carcinogenic. It was formerly used as parasiticide.
Mixed Function Oxygenases
Widely distributed enzymes that carry out oxidation-reduction reactions in which one atom of the oxygen molecule is incorporated into the organic substrate; the other oxygen atom is reduced and combined with hydrogen ions to form water. They are also known as monooxygenases or hydroxylases. These reactions require two substrates as reductants for each of the two oxygen atoms. There are different classes of monooxygenases depending on the type of hydrogen-providing cosubstrate (COENZYMES) required in the mixed-function oxidation.
Catechol 1,2-Dioxygenase
Thauera
Catechol 2,3-Dioxygenase
Catalyzes the oxidation of catechol to 2-hydroxymuconate semialdehyde in the carbazole and BENZOATE degradation via HYDROXYLATION pathways. It also catalyzes the conversion of 3-methylcatechol to cis, cis-2-hydroxy-6-oxohept-2,4-dienoate in the TOLUENE and XYLENE degradation pathway. This enzyme was formerly characterized as EC 1.13.1.2.
Oxygenases
Pentachlorophenol
An insecticide and herbicide that has also been used as a wood preservative. Pentachlorphenol is a widespread environmental pollutant. Both chronic and acute pentachlorophenol poisoning are medical concerns. The range of its biological actions is still being actively explored, but it is clearly a potent enzyme inhibitor and has been used as such as an experimental tool.
Tyrosine Phenol-Lyase
Anisoles
Pseudomonas
Trichosporon
Benzopyrenes
Guaiacol
Benzoic Acid
Monophenol Monooxygenase
Nails, Ingrown
Humic Substances
Organic matter in a state of advanced decay, after passing through the stages of COMPOST and PEAT and before becoming lignite (COAL). It is composed of a heterogenous mixture of compounds including phenolic radicals and acids that polymerize and are not easily separated nor analyzed. (E.A. Ghabbour & G. Davies, eds. Humic Substances, 2001).
Encyclopedias as Topic
Galaxies
Ice Cream
Stars, Celestial
Copyright
It is a form of protection provided by law. In the United States this protection is granted to authors of original works of authorship, including literary, dramatic, musical, artistic, and certain other intellectual works. This protection is available to both published and unpublished works. (from Circular of the United States Copyright Office, 6/30/2008)
Computer Security
Protective measures against unauthorized access to or interference with computer operating systems, telecommunications, or data structures, especially the modification, deletion, destruction, or release of data in computers. It includes methods of forestalling interference by computer viruses or so-called computer hackers aiming to compromise stored data.
Privacy
Licensure
Coal Tar
A by-product of the destructive distillation of coal used as a topical antieczematic. It is an antipruritic and keratoplastic agent used also in the treatment of psoriasis and other skin conditions. Occupational exposure to soots, tars, and certain mineral oils is known to be carcinogenic according to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985) (Merck Index, 11th ed).
Dictionaries as Topic
Disinfectants
Substances used on inanimate objects that destroy harmful microorganisms or inhibit their activity. Disinfectants are classed as complete, destroying SPORES as well as vegetative forms of microorganisms, or incomplete, destroying only vegetative forms of the organisms. They are distinguished from ANTISEPTICS, which are local anti-infective agents used on humans and other animals. (From Hawley's Condensed Chemical Dictionary, 11th ed)
Television
The transmission and reproduction of transient images of fixed or moving objects. An electronic system of transmitting such images together with sound over a wire or through space by apparatus that converts light and sound into electrical waves and reconverts them into visible light rays and audible sound. (From Webster, 3rd ed)
Circadian Rhythm
Fellowships and Scholarships
Biofuels
United States Public Health Service
The direct spectrophotometric observation of benzo(a)pyrene phenol formation by liver microsomes. (1/4452)
Optical spectral repetitive scan analysis during the oxidative metabolism of benzo(a)pyrene by liver microsomal suspensions reveals the time-dependent formation of an intermediate(s) of which the visible spectra resemble those of several benzo(a)pyrene phenols. Liver microsomes from 3-methylcholanthrene-treated rats showed a greater rate of formation of the phenols than did microsomes from control animals; the rate of formation catalyzed by liver microsomes from phenobarbital-pretreated rats was intermediate. When 3-hydroxybenzo(a)pyrene was used as a standard for comparison of activity, the rates of formation of phenols were compared when measured by fluorometric, spectrophotometric, or high-pressure liquid chromatographic analytical techniques. An epoxide hydrase inhibitor, 1,1,1-trichloropropene-2,3-oxide, enhanced phenol formation regardless of the source of liver microsomes, and 7,8-benzoflavone inhibited control and 3-methylcholanthrene-induced microsomal metabolism of benzo(a)pyrene, 7,8-Benzoflavone did not effect benzo(a)pyrene metabolism by liver microsomes from phenobarbital-pretreated rats. The effect of inhibitors on the spectrophotometric assay correlates well with the results obtained from benzo(a)pyrene metabolite analysis using high-pressure liquid chromatography. (+info)Hierarchical cluster analysis applied to workers' exposures in fiberglass insulation manufacturing. (2/4452)
The objectives of this study were to explore the application of cluster analysis to the characterization of multiple exposures in industrial hygiene practice and to compare exposure groupings based on the result from cluster analysis with that based on non-measurement-based approaches commonly used in epidemiology. Cluster analysis was performed for 37 workers simultaneously exposed to three agents (endotoxin, phenolic compounds and formaldehyde) in fiberglass insulation manufacturing. Different clustering algorithms, including complete-linkage (or farthest-neighbor), single-linkage (or nearest-neighbor), group-average and model-based clustering approaches, were used to construct the tree structures from which clusters can be formed. Differences were observed between the exposure clusters constructed by these different clustering algorithms. When contrasting the exposure classification based on tree structures with that based on non-measurement-based information, the results indicate that the exposure clusters identified from the tree structures had little in common with the classification results from either the traditional exposure zone or the work group classification approach. In terms of the defining homogeneous exposure groups or from the standpoint of health risk, some toxicological normalization in the components of the exposure vector appears to be required in order to form meaningful exposure groupings from cluster analysis. Finally, it remains important to see if the lack of correspondence between exposure groups based on epidemiological classification and measurement data is a peculiarity of the data or a more general problem in multivariate exposure analysis. (+info)Complete sequence of a 184-kilobase catabolic plasmid from Sphingomonas aromaticivorans F199. (3/4452)
The complete 184,457-bp sequence of the aromatic catabolic plasmid, pNL1, from Sphingomonas aromaticivorans F199 has been determined. A total of 186 open reading frames (ORFs) are predicted to encode proteins, of which 79 are likely directly associated with catabolism or transport of aromatic compounds. Genes that encode enzymes associated with the degradation of biphenyl, naphthalene, m-xylene, and p-cresol are predicted to be distributed among 15 gene clusters. The unusual coclustering of genes associated with different pathways appears to have evolved in response to similarities in biochemical mechanisms required for the degradation of intermediates in different pathways. A putative efflux pump and several hypothetical membrane-associated proteins were identified and predicted to be involved in the transport of aromatic compounds and/or intermediates in catabolism across the cell wall. Several genes associated with integration and recombination, including two group II intron-associated maturases, were identified in the replication region, suggesting that pNL1 is able to undergo integration and excision events with the chromosome and/or other portions of the plasmid. Conjugative transfer of pNL1 to another Sphingomonas sp. was demonstrated, and genes associated with this function were found in two large clusters. Approximately one-third of the ORFs (59 of them) have no obvious homology to known genes. (+info)Isolation from estuarine sediments of a Desulfovibrio strain which can grow on lactate coupled to the reductive dehalogenation of 2,4, 6-tribromophenol. (4/4452)
Strain TBP-1, an anaerobic bacterium capable of reductively dehalogenating 2,4,6-tribromophenol to phenol, was isolated from estuarine sediments of the Arthur Kill in the New York/New Jersey harbor. It is a gram-negative, motile, vibrio-shaped, obligate anaerobe which grows on lactate, pyruvate, hydrogen, and fumarate when provided sulfate as an electron acceptor. The organism accumulates acetate when grown on lactate and sulfate, contains desulfoviridin, and will not grow in the absence of NaCl. It will not utilize acetate, succinate, propionate, or butyrate for growth via sulfate reduction. When supplied with lactate as an electron donor, strain TBP-1 will utilize sulfate, sulfite, sulfur, and thiosulfate for growth but not nitrate, fumarate, or acrylate. This organism debrominates 2-, 4-, 2,4-, 2,6-, and 2,4,6-bromophenol but not 3- or 2,3-bromophenol or monobrominated benzoates. It will not dehalogenate monochlorinated, fluorinated, or iodinated phenols or chlorinated benzoates. Together with its physiological characteristics, its 16S rRNA gene sequence places it in the genus Desulfovibrio. The average growth yield of strain TBP-1 grown on a defined medium supplemented with lactate and 2,4,6-bromophenol is 3.71 mg of protein/mmol of phenol produced, and the yield was 1.42 mg of protein/mmol of phenol produced when 4-bromophenol was the electron acceptor. Average growth yields (milligrams of protein per millimole of electrons utilized) for Desulfovibrio sp. strain TBP-1 grown with 2,4,6-bromophenol, 4-bromophenol, or sulfate are 0.62, 0.71, and 1.07, respectively. Growth did not occur when either lactate or 2,4,6-bromophenol was omitted from the growth medium. These results indicate that Desulfovibrio sp. strain TBP-1 is capable of growth via halorespiration. (+info)In vivo demonstration of H3-histaminergic inhibition of cardiac sympathetic stimulation by R-alpha-methyl-histamine and its prodrug BP 2.94 in the dog. (5/4452)
1. The aim of this study was to investigate whether histamine H3-receptor agonists could inhibit the effects of cardiac sympathetic nerve stimulation in the dog. 2. Catecholamine release by the heart and the associated variation of haemodynamic parameters were measured after electrical stimulation of the right cardiac sympathetic nerves (1-4 Hz, 10 V, 10 ms) in the anaesthetized dog treated with R-alpha-methyl-histamine (R-HA) and its prodrug BP 2.94 (BP). 3. Cardiac sympathetic stimulation induced a noradrenaline release into the coronary sinus along with a tachycardia and an increase in left ventricular pressure and contractility without changes in mean arterial pressure. Intravenous administration of H3-receptor agonists significantly decreased noradrenaline release by the heart (R-HA at 2 micromol kg(-1) h(-1): +77 +/- 25 vs +405 +/- 82; BP 2.94 at 1 mg kg(-1): +12 +/- 11 vs +330 +/- 100 pg ml(-1) in control conditions, P < or = 0.05), and increases in heart rate (R-HA at 2 micromol kg(-1) h(-1): +26 +/- 8 vs +65 +/- 10 and BP 2.94 at 1 mg kg(-1): +30 +/- 8 vs 75 +/- 6 beats min(-1), in control conditions P < or = 0.05), left ventricular pressure, and contractility. Treatment with SC 359 (1 mg kg(-1)) a selective H3-antagonist, reversed the effects of H3-receptor agonists. Treatment with R-HA at 2 micromol kg(-1) h(-1) and BP 2.94 at 1 mg kg(-1) tended to decrease, while that with SC 359 significantly increased basal heart rate (from 111 +/- 3 to 130 +/- 5 beats min(-1), P < or = 0.001). 4. Functional H3-receptors are present on sympathetic nerve endings in the dog heart. Their stimulation by R-alpha-methyl-histamine or BP 2.94 can inhibit noradrenaline release by the heart and its associated haemodynamic effects. (+info)Antioxidative and chelating activities of phenylpropanoid glycosides from Pedicularis striata. (6/4452)
AIM: To study the antioxidative and iron chelating activities of phenylpropanoid glycosides (PPG) isolated from a Chinese herb Pedicularis striata. METHODS: Antioxidative effects of PPG on lipid peroxidation induced by FeSO4-edetic acid in linoleic acid were measured by thiobarbituric acid method. Chelating activities of PPG for Fe2+ were tested by differential spectrum method. RESULTS: The reaction rates (A532.min-1) of lipid peroxidation were 0.0046 in the control, 0.0021 in verbascoside group, and 0.0008 in isoverbascoside group. The chelating activity of isoverbascoside was 2-fold stronger than that of verbascoside. Permethyl verbascoside showed neither antioxidative nor chelating activities. CONCLUSION: The inhibitory effects of PPG with phenolic hydroxy groups on lipid peroxidation are owing to their chelating properties. Under physiological condition PPG-Fe2+ chelates are sufficiently stable. Thus PPG are able to inhibit the Fe(2+)-dependent lipid peroxidation in vivo through chelating Fe2+ and exhibit their therapeutic potential by the same mechanism in vitro. (+info)Developing hypothalamic dopaminergic neurones as potential targets for environmental estrogens. (7/4452)
Environmental chemicals which mimic the actions of estrogen have the potential to affect any estrogen responsive tissue. The aim of the present study was to investigate their potential to mimic the effects of 17beta-estradiol (E2) on developing primary rat hypothalamic dopaminergic (DA) neurones maintained in a chemically defined medium. We now show that both E2 and octylphenol (OP), but not the non-aromatizable androgen, dihydrotestosterone, enhanced the uptake of [3H]DA by the cultured cells, whereas they had no effect on the uptake of [14C]GABA. Although the sensitivity of responses may change with the age of the developing cultures, the dose response curves for E2 and OP were typically 'bell-shaped', with a rise in response followed by a decline to control levels with increasing concentrations. Effects were seen as low as 10(-14) M for E2 and 10(-11) M for OP. Responses to E2 (10(-12) M) and OP (10(-9) M) were reversed in the presence of the antiestrogen, ZM 182780 (10(-5) M). This study thus provides direct evidence, using a mechanistic rather than toxicological end-point, in support of the hypothesis that inappropriate exposure to environmental estrogens at critically sensitive stages of development, could potentially perturb the organisational activities of estrogen on selected neuronal populations in the CNS. (+info)Characterization of the pyoluteorin biosynthetic gene cluster of Pseudomonas fluorescens Pf-5. (8/4452)
Ten genes (plt) required for the biosynthesis of pyoluteorin, an antifungal compound composed of a bichlorinated pyrrole linked to a resorcinol moiety, were identified within a 24-kb genomic region of Pseudomonas fluorescens Pf-5. The deduced amino acid sequences of eight plt genes were similar to the amino acid sequences of genes with known biosynthetic functions, including type I polyketide synthases (pltB, pltC), an acyl coenzyme A (acyl-CoA) dehydrogenase (pltE), an acyl-CoA synthetase (pltF), a thioesterase (pltG), and three halogenases (pltA, pltD, and pltM). Insertions of the transposon Tn5 or Tn3-nice or a kanamycin resistance gene in each of these genes abolished pyoluteorin production by Pf-5. The presumed functions of the eight plt products are consistent with biochemical transformations involved in pyoluteorin biosynthesis from proline and acetate precursors. Isotope labeling studies demonstrated that proline is the primary precursor to the dichloropyrrole moiety of pyoluteorin. The deduced amino acid sequence of the product of another plt gene, pltR, is similar to those of members of the LysR family of transcriptional activators. pltR and pltM are transcribed divergently from the pltLABCDEFG gene cluster, and a sequence with the characteristics of a LysR binding site was identified within the 486-bp intergenic region separating pltRM from pltLABCDEFG. Transcription of the pyoluteorin biosynthesis genes pltB, pltE, and pltF, assessed with transcriptional fusions to an ice nucleation reporter gene, was significantly greater in Pf-5 than in a pltR mutant of Pf-5. Therefore, PltR is proposed to be a transcriptional activator of linked pyoluteorin biosynthesis genes. (+info)
The antioxidant neuroprotective effects of estrogens and phenolic compounds are independent from their estrogenic properties. :...
The effects of dietary phenolic compounds on cytokine and antioxidant production by a549 cells - Enlighten: Publications
Sorption of phenol and phenol derivatives in hydrotalcite; Sorcion de fenol y derivados de fenol en hidrotalcita (Thesis...
Effects of octylphenol and bisphenol A on the expressions of calcium transport genes during pregnancy in mice
Combinations of physiologic estrogens with xenoestrogens alter calcium and kinase responses, prolactin release, and membrane...
United States 2-Fluorophenol Market Report 2017 : ReportsnReports
Androgen and Progesterone Receptors Are Targets for Bisphenol A (BPA), 4-Methyl-2,4-bis-(P-Hydroxyphenyl)Pent-1-Ene-A Potent...
Surveying the Effect of the Phenol Compounds on Antibacterial Activity of Herbal Extracts: In vitro Assessment of Herbal...
Alternatives to toxic phenol compounds are being developed | EurekAlert! Science News
Estrogenic activity and contributing compounds in stagnant water bodies with massive occurrence of phytoplankton | Masarykova...
The role of phenolic compounds in plant resistance
Boots Ingredients Bakuchiol Serum Review - Beautiful With Brains
Bakuchiol Is the Natural Retinol Alternative Thats Gentle on Skin - Visha Skincare
NEW! AgeWell Firming Neck Cream with 0.5% Bakuchiol AU #8381 - Arbonne
Chemical Database: 2,4-Dimethyl-3-(Chloromethyl)-6-Tert-Butylphenol (EnvironmentalChemistry.com)
Environmental Health Perspectives - Systematic Review and Meta-Analysis of Early-Life Exposure to Bisphenol A and Obesity...
EWG || Human Toxome Project
tri styrenated phenol ethoxylate
Glossary - Wacker Chemie AG Sustainability Report 2011/2012
Side Effects of Tapentadol ER
Could Bakuchiol Be Retinols Match?
Phenol Compound Information and Applications for GC (Gas Chromatography) and LC (Liquid Chromatography) Analysis / Benvenuto
/...
Plant Phenolics and Human Health : Biochemistry, Nutrition and Pharmacology / Edition 1 by Cesar G. Fraga, IUBMB | |...
RI UFLA: Simultaneous analysis of 25 phenolic compounds in grape juice for HPLC: method validation and characterization of São...
Search
What is Bisphenol A (BPA)? - Definition from FertilitySmarts
Bisphenol A | GreenMedInfo | Toxic Ingredient | Natural Medicine
Bisphenol A | GreenMedInfo | Toxic Ingredient | Natural Medicine
Bisphenol A Triggers Changes in Rats That May Lead to Breast Cancer - ONA
Why Worry? | Tantrum
What Does Bisphenol A have To Do With PMS?
ACQUITY Bisphenol A Method Kit : Waters
Eco Tip: Dont Recycle Thermal Paper Receipts | Weavers Way Co-op
Exposure to Bisphenol A hard to avoid in everyday life
Bisphenol A type Compounds | Reagent for High-Performance Polymer Research | Spectrum Chemical
TriRNA Pure Kit (TRPD050/TRPD100/TRPD200) with DNase | Geneaid
TriRNA Pure Kit (TRP050/TRP100/TRP200) | Geneaid
Bisphenol A linked to chemo resistance | Scientist Live
10192-62-8 | MFCD00026194 | Bisphenol a diacetate
PQR | 4,4-(2,3-diisocyano-1,3-butadiene-1,4-diyl)bisphenol
2017-2022 Global Top Countries Hydrogenated Bisphenol A Market Report : ReportsnReports
Dietary phenolic compound with the presence of C2=C3 double bond take the pre-emptive opportunities to enhance its biological...
Bisphenol A is everywhere - is it safe? | New Scientist
Search Results for phenolics | ASHS
Does Antibacterial Hand Gel Do More Harm Than Good? | HuffPost UK Life
Potential Sources of Bisphenol A in the Neonatal Intensive Care Unit | Articles | Pediatrics
Impact of Early-Life Bisphenol A Exposure on Behavior and Executive Function in Children | Articles | Pediatrics
BPA Exposure in the NICU
Influence of phenolic compounds on the growth and arginine deiminase system in a wine lactic acid bacterium
Childhood Wheezing Caused By Prenatal BPA Exposure? - Redorbit
Phenol Derivatives Market worth 19.78 Billion USD by 2026
Oxygen radical absorbance capacity (ORAC) of cyclodextrin-solubilized flavonoids, resveratrol and astaxanthin as measured with...
Effects of Extra Virgin Olive Oil (EVOO) Oleocanthal and Oleacein Content on Platelet Reactivity in Healthy Adults - Goutis...
Plant Polyphenols as Dietary Antioxidants in Human Health and Disease
Prenatal BPA Exposure Linked with Higher Levels of Oxidative Damage
April 28, 2012: Prenatal BPA Exposure and Child Behavior - ccceh.org
A Simplified Analytical Procedure for Simultaneous Determination of Alkylphenol Ethoxylates and Brominated Flame Retardants in...
Butyl Phenol - Laboratory Chemicals
Study Finds Highest Reported BPA Level In Pregnant Woman And Associated Abnormalities In Infant - Redorbit
First peer-reviewed study finds BPA levels in US foods 1,000 times less than limits
Harvard Study Finds BPA Exposure Lowers IVF Success Rates | Inhabitots
2,4-Di-tert-butyl-6-({4-[(3,5-di-tert-butyl-2-hydroxyphenyl)methyl]piperazin-1-yl}methyl)phenol | C34H54N2O2 - PubChem
Apitherapy News: March 2016
BPA Levels Soar After Eating Canned Soup | Food Court
antibodies fading - Chemicals Cas Numbers
biology cells notes - Chemicals Cas Numbers
The Neighborhood Toxicologist: Polycarbonate plastics: if only toxicology could be that clear
Computational study of the adsorption and dissociation of phenol on Pt and Rh surfaces
Activated carbons as green and effective catalysts for generation of reactive radicals in degradation of aqueous phenol
octadecyl 3- 3 5-di-tert-butyl-4-hydroxyphenyl propionate antioxidant 1076 cas no 2082-79-3
Give an account of the properties and uses of phenol - GCSE Science - Marked by Teachers.com
Unscramble phenols | Words unscrambled from letters phenols | Scrabble Word phenols | Words Made with the Letters phenols
urinary bisphenol a and plasma hormone concentrations in male workers exposed to bisphenol a diglycidyl ether and mixed organic...
Common phenolic metabolites of flavonoids, but not their unmetabolized precursors, reduce the secretion of vascular cellular...
TIPS CHANNEL: Canned soup ups BPA levels 1200% in urine
BPA Exposure Linked To Asthma In Kids | TIME.com
BPA Exposure Linked To Asthma In Kids | TIME.com
Figure 6 | Antioxidant, Cytotoxic, and Antiproliferative Activities and Total Polyphenol Contents of the Extracts of...
Water Science & Technology
NTP Finalizes Report on Bisphenol A, September 3, 2008 News Release - National Institutes of Health (NIH)
Bisphenol India | Zanran
Oleocanthal - the Natural Healer
Study Finds How BPA Affects Gene Expression, Anxiety; Soy Mitigates Effects | NC State News | NC State University
Levels of selected alkylphenol ethoxylates (APEs) in water and sediment samples from the Jukskei River catchment area in...
Plant Polyphenols Dont Help Heart Health - AnabolicMinds.com
Effect of perinatal and postnatal bisphenol A exposure to the regulatory circuits at the hypothalamus-pituitary-gonadal axis of...
Polyphenols: Biological Activities, Molecular Targets, and the Effect of Methylation | Bentham Science
BPA exposure during pregnancy causes oxidative stress in child, mother | EurekAlert! Science News
Total phenolics, flavonoids content and antioxidant activities of some Eulophia species
Epoxy
Phenols[edit]. Polyphenols, such as bisphenol A or novolacs can react with epoxy resins at elevated temperatures (130-180 °C ... Reaction of phenols with formaldehyde and subsequent glycidylation with epichlorohydrin produces epoxidised novolacs, such as ... Common classes of hardeners for epoxy resins include amines, acids, acid anhydrides, phenols, alcohols and thiols. Relative ... Tertiary amines, carboxylic acids and alcohols (especially phenols) are effective accelerators. Bisphenol A is a highly ...
Phenolic content in wine
Red wines will also have the phenols found in white wines. Wine simple phenols are further transformed during wine aging into ... Natural phenols and polyphenols from cork stoppers[edit]. Extracted cork closure inscribed with "Bottled at origin" in Spanish ... 4 Natural phenols and polyphenols from cork stoppers. *5 Phenolic content in relation with wine making techniques *5.1 ... The phenolic content in wine refers to the phenolic compounds-natural phenol and polyphenols-in wine, which include a large ...
Mass spectral interpretation
Phenol[edit]. Phenol exhibit a strong molecular ion peak. Loss of H· is observed (M - 1), CO (M - 28) and formyl radical (HCO ...
Nakdong River
... phenol contamination incident[edit]. Main article: 1991 Nakdong river phenol contamination incident ... The phenol ended up at a water processing facility used for drinking water in Daegu and began to smell after becoming ... In 1991, there were two incidents where phenol was leaked into the river from Doosan Electronics. There were two leaks, the ...
Plant defense against herbivory
... sometimes called phenols, consist of an aromatic 6-carbon ring bonded to a hydroxy group. Some phenols have antiseptic ... "Phenols". Plant Defense Systems & Medicinal Botany. Retrieved 2007-05-21. Van Soest, Peter J. (1982). Nutritional ecology of ...
Palladium on carbon
Musliner, Walter J.; Gates, Jr, John W. (1971). "Dehydroxylation of Phenols; Hydrogenolysis of Phenolic Ethers: Biphenyl". ...
Phenol
PhenolsEdit. Main article: Phenols. The word phenol is also used to refer to any compound that contains a six-membered aromatic ... Phenol is also used as a preservative in some vaccines.[25]. Phenol spray is used medically to help sore throat.[26] It is the ... Phenol is reduced to benzene when it is distilled with zinc dust, or when phenol vapour is passed over granules of zinc at 400 ... "Phenol_msds".. *^ a b c d e NIOSH Pocket Guide to Chemical Hazards. "#0493". National Institute for Occupational Safety and ...
Donald E. Pearson
V. Breder (1967). "Ortho bromination of phenols". Journal of Organic Chemistry. 32 (7): 2358-2360. doi:10.1021/jo01282a063. D. ...
Ben Feringa
Asymmetric oxidation of phenols. Atropisomerism and optical activity. Archived from the original on 2015-01-06. Retrieved 2015- ... He subsequently obtained a PhD degree at the same university in 1978, with the thesis titled "Asymmetric oxidation of phenols. ...
RAVEN (Respecting Aboriginal Values & Environmental Needs)
... phenols, hydrocarbons • and polycyclic aromatic hydrocarbons • other acute and chronic toxicants In many cases, huge ponds sit ...
Raschig-Hooker process
Tyman, J.H.P. (1996-08-21). Synthetic and Natural Phenols. p. 7. ISBN 9780080542195. Losch, P; Kolb, J.F.; Astafan, A; Daou, T. ... The Raschig-Hooker process is a chemical process for the production of phenol. The main steps in this process are the ... Due to the two step nature, the Raschig-Hooker process can be used to produce either chlorobenzene or phenol.[citation needed] ... Kropf, H. (1964). "Moderne technische Phenol-Synthesen I". Chemie Ingenieur Technik. 36 (7): 759-768. doi:10.1002/cite. ...
Allura Red AC
2004). The Chemistry of Phenols. Chichester: John Wiley & Sons. ISBN 9780470869451. Sharma, Vinita; McKone, Harold T.; Markow, ...
Streptomyces resistomycificus
Tyman, J.H.P. (1996). Synthetic and Natural Phenols. Burlington: Elsevier. ISBN 0-08-054219-0. ed.-in-chief, George M. Garrity ...
Penicillium citrinum
Curtis, R. F.; Hassall, C. H.; Nazar, M. (1968). "The biosynthesis of phenols. Part XV. Some metabolites of Penicillium ...
Galvinoxyl
Kharasch, M. S.; Joshi, B. S. (1957). "Reactions of Hindered Phenols. II. Base-Catalyzed Oxidations of Hindered Phenols". J. Am ... It may be synthesized by oxidation of the parent phenol with lead dioxide or potassium hexacyanoferrate(III). Its radical ...
Pine tar
Due to the high presence of phenol in the early manufacturing of pine tar, it was deemed carcinogenic. However, now much of the ... "Phenols and Related Compounds". The Merck Veterinary Manual. Merck Manuals. Retrieved 16 April 2015. Laura Bryant. Chickens: A ... phenol has been removed. Pine tar was banned by the FDA along with many other ingredients categorized as over the counter drugs ...
Salicylaldehyde
... is prepared from phenol and chloroform by heating with sodium hydroxide or potassium hydroxide in a Reimer- ... Salicylaldehydes in general may be prepared by other ortho-selective formylation reactions from the corresponding phenol, for ... "Ortho-Formylation of Phenols; Preparation of 3-Bromosalicylaldehyde". Organic Syntheses. 82: 64. doi:10.15227/orgsyn.089.0220. ... Tiemann reaction: Alternatively, it is produced by condensation of phenol or its derivatives with formaldehyde to give ...
Rubbing alcohol
"Alcohols, phenols, and ethers". University of Nebraska-Lincoln. Britannica.com. Retrieved 22 January 2016. "12 Ways to Use ...
Groningen
ISBN 978-81-7648-743-6. Asymmetric oxidation of phenols. Atropisomerism and optical activity. Archived from the original on 6 ...
Chlorobenzene
At one time, chlorobenzene was the main precursor for the manufacture of phenol: C6H5Cl + NaOH → C6H5OH + NaCl The reaction ... nov., a novel bioprocessor isolated actinomycete with the ability to degrade chlorobenzene, dichlorobenzene and phenol as sole ... nov., a novel bioprocessor isolated actinomycete with the ability to degrade chlorobenzene, dichlorobenzene and phenol as sole ... Weber, Manfred; Weber, Markus; Kleine-Boymann, Michael (2004). "Phenol". Ullmann's Encyclopedia of Industrial Chemistry. doi: ...
Niaprazine
... (INN) (brand name Nopron) is a sedative-hypnotic drug of the phenylpiperazine group.[1][2] It has been used in the treatment of sleep disturbances since the early 1970s in several European countries including France, Italy, and Luxembourg.[3][4] It is commonly used with children and adolescents on account of its favorable safety and tolerability profile and lack of abuse potential.[5][6][7][8][9][10] Originally believed to act as an antihistamine and anticholinergic,[11] niaprazine was later discovered to have low or no binding affinity for the H1 and mACh receptors (Ki = , 1 μM), and was instead found to act as a potent and selective 5-HT2A and α1-adrenergic receptor antagonist (Ki = 75 nM and 86 nM, respectively).[12] It possesses low or no affinity for the 5-HT1A, 5-HT2B, D2, and β-adrenergic, as well as at SERT and VMAT (Ki = all , 1 μM), but it does have some affinity for the α2-adrenergic receptor (Ki = 730 nM),[12] likely acting as an antagonist there as well. Niaprazine ...
Captodiame
... (INN), also known as captodiamine, is an antihistamine sold under the trade names Covatine, Covatix, and Suvren which is used as a sedative and anxiolytic. The structure is related to diphenhydramine.[1] A 2004 study suggested captodiame may be helpful in preventing benzodiazepine withdrawal syndrome in people discontinuing benzodiazepine treatment.[1] In addition to its actions as an antihistamine, captodiamine has been found to act as a 5-HT2C receptor antagonist and σ1 receptor and D3 receptor agonist.[2] It produces antidepressant-like effects in rats.[2] However, captodiamine is unique among antidepressant-like drugs in that it increases brain-derived neurotrophic factor (BDNF) levels in the hypothalamus but not in the frontal cortex or hippocampus.[2] This unique action may be related to its ability to attenuate stress-induced anhedonia and corticotropin-releasing factor (CRF) signaling in the hypothalamus.[2] ...
Paraldehyde
... is the cyclic trimer of acetaldehyde molecules.[2] Formally, it is a derivative of 1,3,5-trioxane. The corresponding tetramer is metaldehyde. A colourless liquid, it is sparingly soluble in water and highly soluble in ethanol. Paraldehyde slowly oxidizes in air, turning brown and producing an odour of acetic acid. It quickly reacts with most plastics and rubber. Paraldehyde was first observed in 1835 by the German chemist Justus Liebig; its empirical formula was determined in 1838 by Liebig's student Hermann Fehling.[3][4] Paraldehyde was first synthesized in 1848 by the German chemist Valentin Hermann Weidenbusch (1821-1893), another student of Liebig; he obtained paraldehyde by treating acetaldehyde with acid (either sulfuric or nitric acid).[5][6] It has uses in industry and medicine. ...
1,1,1-Trichloroethane
... is generally considered a non-polar solvent. Owing to the good polarizability of the chlorine atoms, it is a superior solvent for organic compounds that do not dissolve well in hydrocarbons such as hexane. It is an excellent solvent for many organic materials and also one of the least toxic of the chlorinated hydrocarbons. Prior to the Montreal Protocol, it was widely used for cleaning metal parts and circuit boards, as a photoresist solvent in the electronics industry, as an aerosol propellant, as a cutting fluid additive, and as a solvent for inks, paints, adhesives, and other coatings. 1,1,1-Trichloroethane is also used as an insecticidal fumigant. It was also the standard cleaner for photographic film (movie/slide/negatives, etc.). Other commonly available solvents damage emulsion, and thus are not suitable for this application. The standard replacement, Forane 141 is much less effective, and tends to leave a residue. 1,1,1-Trichloroethane was used as a thinner in ...
Menthyl isovalerate
... , also known as validolum, is the menthyl ester of isovaleric acid. It is a transparent oily, colorless liquid with a smell of menthol. It is very slightly soluble in ethanol, while practically insoluble in water. It is used as a food additive for flavor and fragrance.[1] ...
Phenibut
Phenols (e.g., propofol). *Phenytoin. *Piperidinediones (e.g., glutethimide). *Propanidid. *Pyrazolopyridines (e.g., etazolate) ...
Cyclobarbital
... , also known as cyclobarbitol or cyclobarbitone, is a drug that is a barbiturate derivative.[1] It is primarily available in fixed-dose combination with diazepam under the brand name Reladorm (100 mg cyclobarbital + 10 mg diazepam) and is used to treat insomnia in Russia.[2] ...
Amobarbital
When given slowly by an intravenous route, sodium amobarbital has a reputation for acting as a so-called truth serum. Under the influence, a person will divulge information that under normal circumstances they would block. This was most likely due to loss of inhibition. As such, the drug was first employed clinically by Dr. William Bleckwenn at the University of Wisconsin to circumvent inhibitions in psychiatric patients.[7] The use of amobarbital as a truth serum has lost credibility due to the discovery that a subject can be coerced into having a "false memory" of the event.[8](subscription required)[citation needed] The drug may be used intravenously to interview patients with catatonic mutism, sometimes combined with caffeine to prevent sleep.[9] It was used by the United States armed forces during World War II in an attempt to treat shell shock and return soldiers to the front-line duties.[10] This use has since been discontinued as the powerful sedation, cognitive impairment, and ...
Zolpidem
... has potential for either medical misuse when the drug is continued long term without or against medical advice, or for recreational use when the drug is taken to achieve a "high".[53][54] The transition from medical use of zolpidem to high-dose addiction or drug dependence can occur with use, but some believe it may be more likely when used without a doctor's recommendation to continue using it, when physiological drug tolerance leads to higher doses than the usual 5 mg or 10 mg, when consumed through inhalation or injection, or when taken for purposes other than as a sleep aid.[53] Recreational use is more prevalent in those having been dependent on other drugs in the past, but tolerance and drug dependence can still sometimes occur in those without a history of drug dependence. Chronic users of high doses are more likely to develop physical dependence on the drug, which may cause severe withdrawal symptoms, including seizures, if abrupt withdrawal from zolpidem occurs.[55] Other ...
Clonazolam
... (also known as clonitrazolam) is a benzodiazepine that has had very little research done about its effects and metabolism, and has been sold online as a designer drug.[1][2][3][4][5] The synthesis of clonazolam was first reported in 1971 and the drug was described as the most active compound in the series tested.[6][7] Clonazolam is reported to be highly potent, and concerns have been raised that clonazolam and flubromazolam in particular may pose comparatively higher risks than other designer benzodiazepines, due to their ability to produce strong sedation and amnesia at oral doses of as little as 0.5 mg.[8] ...
Naturally occurring phenols - Wikipedia
Natural sources of phenols on www.britannica.com. Databases[edit]. *Phenol-Explorer (phenol-explorer.eu), a database dedicated ... Phenol extraction[edit]. Phenol extraction is a processing technology used to prepare phenols as raw materials, compounds or ... For the molecule alone, see Phenol.. In biochemistry, naturally occurring phenols refers to phenol functional group that is ... Unfiltered olive oil has the higher levels of phenols, or polar phenols that form a complex phenol-protein complex. ...
Phenol | NIOSH | CDC
Exposure to phenol may cause irritation to the skin, eyes, nose, throat, and nervous system. Some symptoms of exposure to ... Phenol (C6H6O or C6H5OH) is a colorless to light-pink, crystalline solid with a sweet, acrid odor. ... phenol are weight loss, weakness, exhaustion, muscle aches, and pain ... Phenol (C6H6O or C6H5OH) is a colorless to light-pink, crystalline solid with a sweet, acrid odor. Exposure to phenol may cause ...
Phenol - Wiktionary
Phenols
Chemical compound - Alcohols and phenols | Britannica
When the hydroxyl group is joined to an aryl ring, a phenol results (shown above). Both alcohols and phenols are widespread in ... The hydroxyl group of alcohols and phenols is responsible for an interesting variety of physical and ... Alcohols and phenols: An oxygen atom normally forms two σ bonds with other atoms; the water molecule, H2O, is the simplest and ... When the hydroxyl group is joined to an aryl ring, a phenol results (shown above). Both alcohols and phenols are widespread in ...
phenol (CHEBI:15882)
... has role mouse metabolite (CHEBI:75771) phenol (CHEBI:15882) is a phenols (CHEBI:33853) phenol (CHEBI: ... phenol (CHEBI:15882) has role antiseptic drug (CHEBI:48218) phenol (CHEBI:15882) has role disinfectant (CHEBI:48219) phenol ( ... phenol O-(β-D-glucuronide) (CHEBI:64681) has functional parent phenol (CHEBI:15882). phenoxenium (CHEBI:52245) has functional ... tert-butyl 4-hydroxy-3-methoxybenzoate (CHEBI:142523) is a phenol (CHEBI:15882). piperlactam S (CHEBI:132657) is a phenol ( ...
ICSC 0070 - PHENOL
The substance and the vapour are corrosive to the eyes, skin and respiratory tract. Corrosive on ingestion. Inhalation of the vapour may cause lung oedema, but only after initial corrosive effects on eyes and/or airways have become manifest. See Notes. The substance may cause effects on the central nervous system, heart and kidneys. This may result in convulsions, coma, cardiac disorders, respiratory failure and collapse. The effects may be delayed. Medical observation is indicated. Exposure could cause death ...
Phenol | ToxFAQs™ | ATSDR
Skin exposure to high levels of phenol has resulted in liver damage, diarrhea, dark urine, and hemolytic anemia. Phenol has ... Phenol is a manufactured substance found in a number of consumer products. ... normal concentration of phenol in the urine may suggest recent exposure to phenol or to substances that are converted to phenol ... Phenol can remain in water for a week or more.. *Larger or repeated releases of phenol can remain in the air, water, and soil ...
Phenol | Toxicological Profile | ATSDR
Phenols - Wikipedia
Phenols undergo esterification. Phenol esters are active esters, being prone to hydrolysis. Phenols are reactive species toward ... Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. Phenols ... Phenols are more acidic than typical alcohols. The acidity of the hydroxyl group in phenols is commonly intermediate between ... Phenol is readily alkylated at the ortho positions using alkenes in the presence of a Lewis acid such as aluminium phenoxide: ...
Phenols - definition of Phenols by The Free Dictionary
Phenols synonyms, Phenols pronunciation, Phenols translation, English dictionary definition of Phenols. n. 1. A caustic, ... phenol. (redirected from Phenols). Also found in: Thesaurus, Medical, Encyclopedia, Wikipedia. phe·nol. (fē′nôl′, -nōl′, -nŏl′) ... phenol index).. Delivery of the cfa flow analyzer for determination of free cyanide / general and phenols (phenol index) ... inhibition of estrogen sulfotransferase by phenols and chlorinated phenols.. Characterization of Phenol Degrading Bacteria ...
Category:Phenol red - Wikimedia Commons
Rouge de phenol, Vert brillant et Rouge de Phénol, Rouge phenol, Phénolsulfonephtaléine (fr) ... Media in category "Phenol red". The following 24 files are in this category, out of 24 total. ... Phenol red, 4,4-(3H-2,1-benzoxathiol-3-ylidene)bisphenol S,S-dioxide, PSP, 3,3-bis(p-hydroxyphenyl)-3H-2,1-benzoxathiole 1,1- ... phenol red (fa); Fenol crveno (sh); феноловый красный (ru); Fenol kırmızısı (tr); Phenolrot (de); vermelho de fenol (pt); ...
Oily phenol injection
... is used in sclerotherapy to treat piles (haemorrhoids). It is injected into the base of the piles, in ... Oily phenol injection. Oily phenol injection is used in sclerotherapy to treat piles (haemorrhoids). It is injected into the ... Oily phenol injection is used in sclerotherapy to treat piles (haemorrhoids). It is injected into the base of the piles, in ...
NIOSH Skin Notation Profiles: Phenol | NIOSH | CDC
Phenol is potentially capable of causing both systemic toxicity and direct adverse effects on the skin following dermal ... phenol are capable of causing skin corrosion, whereas diluted solutions (1 to 3% phenol) are irritating to the skin [European ... Phenol is potentially capable of causing both systemic toxicity and direct adverse effects on the skin following dermal ... The following section provides additional detail about the potential health hazards of skin contact with phenol and the ...
Phenol
Phenol
Evans J.C., The vibrational spectra phenol and phenol-OD, Spectrochim. Acta, 1960, 16, 1382-1392. [all data] ... Phenol alcohol; Phenol, molten; Rcra waste number U188; UN 1671; UN 2312; UN 2821; Phenic alcohol; NSC 36808; Campho-Phenique ... Bartmess, J.E.; Scott, J.A.; McIver, R.T., Jr., The gas phase acidity scale from methanol to phenol, J. Am. Chem. Soc., 1979, ... Capponi, M.; Gut, I.G.; Hellrung, B.; Persy, G.; Wirz, J., Ketonization equilibria of phenol in aqueous solution, Can. J. Chem. ...
Phenols - Wikipedia
Natural sources of phenols on www.britannica.com. DatabasesEdit. *Phenol-Explorer (phenol-explorer.eu), a database dedicated to ... Phenol extractionEdit. Phenol extraction is a processing technology used to prepare phenols as raw materials, compounds or ... Unfiltered olive oil has the higher levels of phenols, or polar phenols that form a complex phenol-protein complex. ... Synthesis of phenolsEdit. Several laboratory methods for the synthesis of phenols:. *by an ester rearrangement in the Fries ...
Phenol | Define Phenol at Dictionary.com
Phenol definition, Also called carbolic acid, hydroxybenzene, oxybenzene, phenylic acid. a white, crystalline, water-soluble, ... phenol phe·nol (fēnôl, -nōl). n. *. A caustic, poisonous, white crystalline compound derived from benzene and used in ... Some phenols occur naturally in the essential oils of plants. Phenols are used in industry to make plastics and detergents. ... Word Origin and History for phenol Expand. n. "carbolic acid," 1844, from pheno- + -ol. Discovered in coal tar in 1834; used as ...
PHENOL || Skin Deep® Cosmetics Database | EWG
About PHENOL: Phenol is an aromatic compound. In the United States, Phenol may be used as an active ingredient in OTC drug ... Synonym(s): BENZENOL; CARBOLIC ACID; HYDROXYBENZENE; LIQUID PHENOL; OXYBENZENE; PHENOL,; PHENYL ALCOHOL; ACIDE CARBOLIQUE ( ... When used as an active drug ingredient, the established name is Phenol.. Function(s): Antimicrobial Agent; Cosmetic Biocide; ...
Naturally occurring phenols - Wikipedia
Unfiltered olive oil has the higher levels of phenols, or polar phenols that form a complex phenol-protein complex. Phenolic ... Natural sources of phenols on www.britannica.com Phenol-Explorer (phenol-explorer.eu), a database dedicated to phenolics found ... Some phenols are sold as dietary supplements. Phenols have been investigated as drugs. For instance, Crofelemer (USAN, trade ... Phenol extraction is a processing technology used to prepare phenols as raw materials, compounds or additives for industrial ...
Phenol source
Phenols - Alfa Aesar
Phenols are employed in medicinal products such as ear and nose drops, throat lozenges and mouthwashes. The substituted phenols ... Phenols are also wide-spread in nature. Phenols substituted with bulky groups at ortho- positions, like butylated ... Depending on the number of phenolic units in the molecule, they are classified as simple phenols and polyphenols. Phenols are ... Phenols are employed in the preparation of resins, dyes, explosives, lubricants, and plastics. Phenol and its derivatives are ...
Scientists Identify New Way To Regulate Production Of Phenols - Redorbit
While the goal of this work was to learn how to improve plant biofuel feedstocks, knowing how to manipulate plant phenols may ... For example, the set of molecular tools identified in this study might be used to increase the synthesis of certain phenols ... The conventional approach takes aim at the regulation of genes that instruct plant cells to make enzymes involved in phenol ... These enzymes are proteins that serve as catalysts to speed up the chemical reactions that synthesize phenols. Instead of ...
Major industrial polymers - Phenol formaldehyde | Britannica.com
Also known as phenolic resins, phenol-formaldehyde polymers were the first completely synthetic polymers to be commercialized. ... In 1872 the German chemist Adolf von Baeyer condensed trifunctional phenol and ... applied for a patent on a phenol-formaldehyde thermoset that eventually became known by the trademarked name Bakelite. ... Phenol formaldehyde: Many people date the beginning of the modern plastics industry to 1907, when Leo Hendrik Baekeland, a ...
Phenol Topical Comparison - Drugs.com
Phenol-soluble modulins. - PubMed - NCBI
ICSC 0070 - PHENOL
Acid Phenol/chloroform
I have a brand new bottle of phenol ph 6.7. What do I need to add to ,, make acid phenol/chloroform? Thanks. ,, -Ed ,, ,, ... I suppose it means to melt phenol , (Sigma) and add the same volume of chloroform - you will get acid , phenol/chloroform. The ... Ed Jasenka Pigac wrote: , Phenol is acid as such when melted. If you add either water or , chloroform it will remain acid. ... Acid Phenol/chloroform. Ed Siefker via methods%40net.bio.net (by ebs15242 from creighton.edu). Wed Nov 7 12:05:49 EST 2007 * ...
Phenol Red Results
Principle: Phenol Red Fermentation medium contains peptone, phenol red (a pH indicator) and the carbohydrate to be tested. ... Phenol red is yellow at a pH , 6.8 and red at a pH of > 7.4, therefore if a bacterium ferments a sugar to acid a yellow color ... Phenol Red Fermentation Tubes. Purpose: To determine if a bacterium can ferment a particular carbohydrate and determine the end ... Possible phenol red tube results include: (A) Formation of acid and gas (bubble is indicated by arrow), (B) Formation of acid ...
AdvanSix Issues Statement on Phenol Customer Force Majeure
... today informed its phenol customers that it is declaring force majeure as a result of shortages and delivery delays of its key ... AdvanSix (ASIX) today informed its phenol customers that it is declaring force majeure as a result of shortages and delivery ... The force majeure has been declared only for phenol and will not impact shipments of other products produced at the Companys ... As a result of this force majeure event, phenol production at the Companys Frankford, Pennsylvania facility and caprolactam ...
FormaldehydeCarbolicResinsAromaticHydroxylMoleculeContaining a phenol groupExposure to phenolOxidationSimple phenolsCompoundsBenzeneAcetoneHydroxybenzeneAqueousChemicalDetergentsWeight of the phenolAcidicEthersAlcohols and phenolsReactionClass of phenolsAmounts of phenolMethylolation of phenolConcentrations of phenolAcidityAntisepticSynthesisSimplestINEOS PhenolContain phenolNatural phenolsSearchReactionsDerivativesCamphorCumeneAntioxidantSore throatCrystallineIrritationMixturesDisinfectantOdorColorlessToxicSodiumUndergoDegradationWastewaterSolubleToxicity
Formaldehyde24
- Many people date the beginning of the modern plastics industry to 1907, when Leo Hendrik Baekeland , a Belgian-born American chemist, applied for a patent on a phenol-formaldehyde thermoset that eventually became known by the trademarked name Bakelite . (britannica.com)
- Also known as phenolic resins , phenol-formaldehyde polymers were the first completely synthetic polymers to be commercialized. (britannica.com)
- In 1872 the German chemist Adolf von Baeyer condensed trifunctional phenol and difunctional formaldehyde, and in subsequent decades Baeyer's student Werner Kleeberg and other chemists investigated the products, but they failed to pursue the reaction because they were unable to crystallize and characterize the amorphous resinous products. (britannica.com)
- Two methods are used to make phenol-formaldehyde polymers. (britannica.com)
- In one, an excess of formaldehyde is reacted with phenol in the presence of a base catalyst in water solution to yield the resole, which is a low-molecular-weight prepolymer with CH 2 OH groups attached to the phenol rings. (britannica.com)
- The other method involves reacting formaldehyde with an excess of phenol using an acid catalyst to produce prepolymers called novolacs. (britannica.com)
- Phenol-formaldehyde polymers make excellent wood adhesives for plywood and particleboard because they form chemical bonds with the phenollike lignin component of wood. (britannica.com)
- It is also used in the production of drugs (it is the starting material in the industrial production of aspirin ), weedkiller, and synthetic resins ( Bakelite , one of the first synthetic resins to be manufactured, is a polymer of phenol with formaldehyde ). (newworldencyclopedia.org)
- Reaction of formaldehyde with phenols: a computational chemistry study. (usda.gov)
- A method of manufacturing a lignosulfonate-phenol-formaldehyde resin includes heating a mixture of phenol, formaldehyde, lignosulfonate and alkali at a temperature of 60 C. to 100 C. and a pH of 8-13. (google.com)
- The lignosulfonate comprises about 5 to about 80 percent of the total weight of phenol, formaldehyde. (google.com)
- The lignosulfonate comprises about 5 to about 80 percent of the total weight of phenol, formaldehyde and lignosulfonate and the lignosulfonate is mixed with said phenol and formaldehyde before substantial reaction between said phenol and said formaldehyde. (google.com)
- heating a mixture of phenol, formaldehyde, lignosulfonate and alkali wherein said lignosulfonate comprises about 5 to about 80 percent of the total weight of phenol, formaldehyde and lignosulfonate.Iadd. (google.com)
- heating said mixture to form a lignosulfonate-phenol-formaldehyde polymer. (google.com)
- 3. The method of claim 1 wherein said phenol, formaldehyde and lignosulfonate are mixed prior to heating. (google.com)
- 4. The method of claim 1 wherein said lignosulfonate comprises abouit 30% to about 60% by total weight of lignosulfonate, phenol and formaldehyde. (google.com)
- The rates ( k) of hydroxymethylation of phenol, resorcinol, phloroglucinol, and several methylphenols in diluted 10% dimethylformamide aqueous alkaline solution were calculated based on the consumption of phenols and formaldehyde. (springer.com)
- Dijkstra R, DeJonge J, Lammers MF (1962) The kinetics of the reaction of phenol and formaldehyde. (springer.com)
- 1. Mechanisms and kinetics of phenol and of the first polycondensates towards formaldehyde in solution. (springer.com)
- Zavitsas AA, Beaulieu RD, Leblanc JR (1968) Base-catalyzed hydroxymethylation of phenol by aqueous formaldehyde: kinetics and mechanism. (springer.com)
- The soy-based resin is considered to be a copolymer of soy and phenol formaldehyde. (usda.gov)
- Thermosetting water-immiscible phenol-formaldehyde resins in which a large proportion of the linkages between the benzene rings are benzyl ether linkages located ortho to the phenolic hydroxyl groups are produced by reaction of at least one mole of formaldehyde with 1 mole of phenol in an aqueous reaction. (google.es)
- Methods of control of the exothermic addition of formaldehyde to phenol are described. (google.es)
- 2. The process of claim 1 wherein said mole ratio of formaldehyde to phenol is about 1.5:1 to about 2.5:1. (google.es)
Carbolic6
- Joseph Lister (1827-1912), an English surgeon at the Glasgow Royal Infirmary, used solutions of phenol dissolved in water, known as carbolic acid , to kill germs in wounds and to sterilize medical equipment, drastically cutting down the number of deaths caused by infections. (angelo.edu)
- phenol , better known as carbolic acid, finds a use as a developer. (dictionary.com)
- Phenol , also known under an older name of carbolic acid , is a toxic, colorless crystalline solid with a distinctive sweet tarry odor. (newworldencyclopedia.org)
- Phenol was also the main ingredient of the Carbolic Smoke Ball, a device sold in London designed to protect the user against influenza and other ailments. (newworldencyclopedia.org)
- The simplest of the class is phenol, which is also called carbolic acid C6H5OH. (homedistiller.org)
- phenol (carbolic acid), molecular model. (pond5.com)
Resins3
- Phenol is used primarily in the production of phenolic resins and in the manufacture of nylon and other synthetic fibers. (cdc.gov)
- Phenol is an important commodity chemical, and is a starting material for the production of numerous industrial chemicals and polymers, including bisphenol A and phenolic resins, and others. (innovations-report.com)
- However, they have huge market potential, since phenol-based glue resins have a global market of around 4 million tonnes per year and a value of EUR 10 billion. (eurekalert.org)
Aromatic13
- In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of one or more hydroxyl groups (-OH) bonded directly to an aromatic hydrocarbon group. (wikipedia.org)
- Phenols are susceptible to Electrophilic aromatic substitutions. (wikipedia.org)
- Aromatic compounds such as phenols vastly occur in wastewater, being generated in petroleum refining, petrochemical, plastics, coal conversion industries and steel industries [1]. (thefreedictionary.com)
- Phenols can have two or more hydroxy groups bonded to the aromatic ring(s) in the same molecule. (wikipedia.org)
- Among these aromatic substances are indol, phenol , and skatol. (dictionary.com)
- Phenol is an aromatic compound. (ewg.org)
- Organic compounds with a hydroxyl group directly attached to an aromatic carbon atom are called phenols. (alfa.com)
- Phenols are efficient partners in a variety of reactions such as electrophilic aromatic substitutions, Bucherer carbazole synthesis and oxidative de-aromatization to quinones in the Teuber reaction. (alfa.com)
- The aromatic amino acid phenylalanine, synthesized in the shikimic acid pathway, is the common precursor of phenol containing amino acids and phenolic compounds. (wikipedia.org)
- The word phenol is also used to refer to any compound which contains a six-membered aromatic ring, bonded directly to a hydroxyl group (-OH). (newworldencyclopedia.org)
- Phenol is an aromatic organic compound with the molecular formula C 6 H 5 OH. (wikipedia.org)
- One explanation for why phenol is more acidic than aliphatic compounds containing an -OH group is resonance stabilization of the phenoxide anion by the aromatic ring. (wikipedia.org)
- Several kinds of atomic charge of the carbons on the aromatic ring of phenols were calculated using the semiempirical or ab initio method. (springer.com)
Hydroxyl10
- When the hydroxyl group is joined to an aryl ring, a phenol results (shown above). (britannica.com)
- The hydroxyl group of alcohols and phenols is responsible for an interesting variety of physical and chemical properties. (britannica.com)
- The polar bonds of the hydroxyl group are responsible for the major reaction characteristics of alcohols and phenols. (britannica.com)
- Phenols are organic compounds which contain a hydroxyl (-OH) group attached to a carbon atom in a benzene ring. (angelo.edu)
- The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pKa is usually between 10 and 12). (wikipedia.org)
- Phenols are a class of compounds consisting of a hydroxyl group (-OH) bonded directly to a benzene ring. (thefreedictionary.com)
- Although similar to alcohols , phenols have unique properties and are not classified as alcohols (since the hydroxyl group is not bonded to a saturated carbon atom). (wikipedia.org)
- Loss of a hydrogen cation (H + ) from the hydroxyl group of a phenol forms a corresponding negative phenolate ion or phenoxide ion , and the corresponding salts are called phenolates or phenoxides , although the term aryloxides is preferred according to the IUPAC Gold Book . (wikipedia.org)
- The simplest phenol, consisting of a benzene ring attached to a hydroxyl group (OH). (dictionary.com)
- The phenols that have methyl or hydroxyl groups at the C-3 or C-5 position (or both) have larger rate constants than phenols with substituents at other positions. (springer.com)
Molecule2
- For the molecule alone, see Phenol . (wikipedia.org)
- Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. (wikipedia.org)
Containing a phenol group2
- This article is about the class of chemicals containing a phenol group. (wikipedia.org)
- For the group of chemicals containing a phenol group, see Phenols . (wikipedia.org)
Exposure to phenol6
- Workers may be harmed from exposure to phenol.The level of harm depends upon the dose, duration, and work being done. (cdc.gov)
- The following resources provide information about occupational exposure to phenol. (cdc.gov)
- Presents a standard to prevent the adverse effects of exposure to phenol over a working lifetime. (cdc.gov)
- Short-term exposure to phenol in the air can cause respiratory irritation, headaches, and burning eyes. (cdc.gov)
- Phenol has antiseptic properties and was used by Sir Joseph Lister (1827-1912) in his pioneering technique of antiseptic surgery, though the skin irritation caused by continual exposure to phenol eventually led to the substitution of aseptic (germ-free) techniques in surgery. (newworldencyclopedia.org)
- And if exposure to PHENOL inspires something in you to go head first into modular synths, your initial investment can be incorporated into your more ambitious modular systems. (musiciansfriend.com)
Oxidation11
- Phenols are reactive species toward oxidation. (wikipedia.org)
- Phenols are oxidized to hydroquinones in the Elbs persulfate oxidation. (wikipedia.org)
- Natural phenols are reactive species toward oxidation, notably the complex mixture of phenolics, found in food for example, can undergo autoxidation during the ageing process. (wikipedia.org)
- Phenol can be made from the partial oxidation of benzene or benzoic acid , by the cumene process, or by the Raschig process. (newworldencyclopedia.org)
- You can prepare phenols in large quantities by the pyrolysis of the sodium salt of benzene sulfonic acid, by the Dow process, and by the air oxidation of cumene. (cliffsnotes.com)
- You can also prepare small amounts of phenol by the peroxide oxidation of phenylboronic acid and the hydrolysis of diazonium salts. (cliffsnotes.com)
- The air oxidation of cumene (isopropyl benzene) leads to the production of both phenol and acetone, as shown in the following figure. (cliffsnotes.com)
- Blanchard rmqn L. Hume/g7 b ,ym/ff United States Patent This invention relates to a method of utilization new compounds as catalysts in the oxidation of phenols. (google.es)
- More specifically, this invention relates to the use of a cupric complex having the empirical formula CH=C11 z 2 n where X is selected from the group consisting of chlorine and bromine and n is an integer and is at least 1, as catalysts for the oxidation of phenols, and more particularly to the oxidation of phenols to either phenylene oxide polymers or to diphenoquinones. (google.es)
- We have now found that the brown crystalline cupric complexes having the empirical formula i \CH=CH 2 2 n where X is selected from the group consisting of chlorine and bromine, and n is an integrer and is at least 1, are extremely active catalysts for the oxidation of phenols, either to phenylene ether polymers, also known as polyphenylene ethers and polyphenylene om'des, or to diphenoquinones. (google.es)
- The antioxidant properties of phenols, tyrosol and hydoxytyrosol, may increase bone formation, act as free radical scavengers and prevent oxidation-induced damage to bone cells. (oliveoiltimes.com)
Simple phenols1
- They can therefore be called simple phenols or monophenols , with only one phenolic group, or di- ( bi- ), tri- and oligophenols , with two, three or several phenolic groups respectively. (wikipedia.org)
Compounds9
- A diverse family natural phenols are the flavonoids , which include several thousand compounds, among them the flavonols , flavones , flavan-3ol ( catechins ), flavanones , anthocyanidins , and isoflavonoids . (wikipedia.org)
- In effect, phenols are a class of organic compounds of which the phenol discussed in this article is the simplest member. (newworldencyclopedia.org)
- Finnish softwood bark contains large amounts of water-soluble tannin-polyphenols, which can be used as renewable alternatives to the fossil and toxic phenol compounds widely used in glues. (eurekalert.org)
- The phenolic compounds, in particular phenol and cresol along with eugenol and guaiacol are the source of particularly strong, smoky and bitter flavours and aromas found within whisky. (homedistiller.org)
- Phenol, cresols, xylenol and guaiacol are amongst the most important phenolic compounds in whisky, in terms of contribution to flavor. (homedistiller.org)
- They observed that the phenolic compounds in the extracts altered the cells' development, reducing the adipocytes' fat content from 8%-56%, depending on the differing phenols used. (scienceblog.com)
- S. Thomas, S. Sarfaraz, L. C. Mishra and L. Iyengar "Degradation of Phenol and Phenolic Compounds by a Defined Denitrifying Bacterial Culture," World Journal of Microbiology, Vol. 18, No. 1, 2002, pp. 57-63. (scirp.org)
- Many common disinfectants out there contain phenols-caustic, poisonous and dangerous compounds that are used to cover smells. (sixwise.com)
- Many common household disinfectants co-ntain phenols-caustic and dangerous compounds that could be harming your family's health. (sixwise.com)
Benzene5
- Natural phenols show optical properties characteristic of benzene, e.g. absorption near 270 nm. (wikipedia.org)
- Phenol , or hydroxybenzene, is the parent compound of the phenols, consisting of an OH group directly connected to a benzene ring. (angelo.edu)
- They are typically produced by the alkylation of benzene/toluene with propylene to form cumene then O 2 is added with H 2SO 4 to form phenol (Hock process). (wikipedia.org)
- phenol is obtained from coal-tar, or made synthetically from benzene. (dictionary.com)
- At present, the production of phenol entirely depends on the chemical synthesis from benzene, and its annual production exceeds 8 million tons worldwide. (innovations-report.com)
Acetone8
- The force majeure has been declared only for phenol and will not impact shipments of other products produced at the Company's Frankford facility, including acetone and alpha-methylstyrene due to adequate inventory levels. (yahoo.com)
- In making this conclusion, we cite the pK a of acetone enol, which is 10.9 (in comparison to phenol with a pK a of 10.0). (newworldencyclopedia.org)
- In support of the second explanation, the p K a of the enol of acetone in water is 10.9, making it only slightly less acidic than phenol (p K a 10.0). (wikipedia.org)
- Phenol tar is a heavy, viscous byproduct produced in the industrial synthesis of phenol and acetone from cumene. (freepatentsonline.com)
- INEOS Phenol is the largest producer of Phenol and Acetone in the world. (ineos.com)
- We produce just under 1.9 million tonnes of Phenol and around 1.2 million tonnes of Acetone annually. (ineos.com)
- INEOS Phenol's products (Phenol, Acetone, Alphamethylstyrene, Cumene) are all registered with the European Chemicals Agency (ECHA). (ineos.com)
- In making this conclusion, one can examine the pK a of the enol of acetone , which is 10.9 in comparison to phenol with a pK a of 10.0. (wikidoc.org)
Hydroxybenzene1
- Phenols are named after the parent compound, phenol (hydroxybenzene). (angelo.edu)
Aqueous4
- Dejong JI, Dejong J (1953) Kinetics of the hydroxymethylation of phenols in dilute aqueous solution. (springer.com)
- The product of this reaction is sodium phenoxide, which is acidified with aqueous acid to yield phenol. (cliffsnotes.com)
- Effectiveness of photocatalytic degradation of phenol in aqueous solution using semiconductor oxides (SO) prepared by a sol-gel method was examined. (hindawi.com)
- Equal volumes of a phenol:chloroform mixture and the aqueous DNA sample are mixed, forming a biphasic mixture. (bionity.com)
Chemical9
- If you work in an industry that uses phenol, please read chemical labels and the accompanying Safety Data Sheet for hazard information. (cdc.gov)
- Phenol is both a manufactured chemical and a natural substance. (cdc.gov)
- You may be exposed to phenol if you undergo "chemical peels" to remove skin lesions with phenol-containing products or are treated for chronic pain or spasticity with injections of phenol. (cdc.gov)
- These enzymes are proteins that serve as catalysts to speed up the chemical reactions that synthesize phenols. (redorbit.com)
- But the phenol - a deadly chemical used in Aristech's processes that is known to cause internal burns, muscle spasms and organ failure - indicated that something might have gone wrong. (propublica.org)
- Phenol and its chemical derivatives are essential for production of polycarbonates , epoxies , Bakelite , nylon , detergents , herbicides such as phenoxy herbicides , and numerous pharmaceutical drugs . (wikipedia.org)
- Dow Chemical U.S.A. is increasing the selling price for phenol by 8 cents a pound less a 2 cent/lb. (joc.com)
- In the paper published online in Biotechnology Journal, a Korean research team led by Distinguished Professor Sang Yup Lee at the Department of Chemical and Biomolecular Engineering from the Korea Advanced Institute of Science and Technology (KAIST) reported the successful development of an engineered Escherichia coli (E. coli) strain which can produce phenol from glucose. (innovations-report.com)
- Para Bromo Phenol provided by our company, is a type of chemical which is insoluble in water as well as soluble in 5% ethanol. (tradeindia.com)
Detergents2
- Phenols are used in industry to make plastics and detergents. (dictionary.com)
- Friends of the Earth (FoE) has called for a ban on alkyl phenol ethoxylate (APE) detergents and alkyl phenols. (endsreport.com)
Weight of the phenol4
- 7. The tar processing method according to claim 1, wherein the amount of steam added to the tar is 1% to 15% by weight of the phenol tar introduced into the reactor. (freepatentsonline.com)
- 13. The process according to claim 10, wherein the amount of steam added to the tar is 1% to 15% by weight of the phenol tar. (freepatentsonline.com)
- In a specific aspect, the phenol resin composition of the present invention is characterized in that it contains boehmite having an aspect ratio within a range from 1 to 100 and also contains an alumina-based compound as a filler, an amount of the boehmite being from 1 to 150 parts by weight based on 100 parts by weight of the phenol resin. (google.com.au)
- 5 . A phenol resin composition comprising a phenol resin and acicular or cylindrical boehmite having an average particle diameter (minor diameter) of 100 nm or less, the amount of the boehmite being from 1 to 150 parts based on 100 parts by weight of the phenol resin. (google.com.au)
Acidic1
- Phenols are more acidic than typical alcohols. (wikipedia.org)
Ethers3
- Although ethers contain two polar carbon-oxygen bonds, they are much less reactive than alcohols or phenols. (britannica.com)
- This invention relates to novel reactive diluents for use with bismaleimide formulatioss, and more particularly to ethylenically-unsaturated ethers of alkenyl phenols as novel reactive liquid diluents, and to thermosetting bismaleimide formulations comprising bismaleimides and the novel reactive diluents of this invention. (freepatentsonline.com)
- Electrocatalytic hydrogenation and catalytic thermal hydrogenation of substituted phenols and diaryl ethers were studied on carbon-supported Rh. (osti.gov)
Alcohols and phenols2
- Both alcohols and phenols are widespread in nature, with alcohols being especially ubiquitous . (britannica.com)
- The chemists show the reaction works with a broad scope of allylic alcohols and phenols, and even successfully swaps the phenol for cumene hydroperoxide in several examples. (acs.org)
Reaction2
- Reaction of naphtols and hydrazines and sodium bisulfite in the Bucherer carbazole synthesis Many phenols of commercial interest are prepared by elaboration of phenol or cresols. (wikipedia.org)
- The activity of semiconductor oxides prepared by the sol-gel methods was investigated under the same conditions for searching of the most effective system in the reaction of the phenol photodegradation. (hindawi.com)
Class of phenols2
- The parent of the class of phenols. (ebi.ac.uk)
- Anthocyanins are one class of phenols, and studies have associated the consumption of anthocyanin-rich foods with reduced risks of cardiovascular disease, Type 2 diabetes and certain types of cancer. (scienceblog.com)
Amounts of phenol1
- People who had skin exposure to high amounts of phenol had skin burns, liver damage, dark urine, irregular heart beat, and some died. (cdc.gov)
Methylolation of phenol1
- Aldersley JW, Hope P (1972) A study of the methylolation of phenol using gel permeation chromatography. (springer.com)
Concentrations of phenol4
- Ingestion of high concentrations of phenol has resulted in internal burns and death. (cdc.gov)
- Exposure to high concentrations of phenol in the air for several weeks caused paralysis and severe injury to the heart, liver, kidneys, and lungs, and in some cases, death. (cdc.gov)
- Some animals that drank water with very high concentrations of phenol suffered muscle tremors and loss of coordination. (cdc.gov)
- A critical review of available data indicates that contact of a significant area of skin with subjectively low concentrations of phenol (5-6%) may be extremely hazardous and life-threatening [ATSDR 2008]. (cdc.gov)
Acidity1
- A recent in silico comparison of the gas phase acidities of the vinylogues of phenol and cyclohexanol in conformations that allow for or exclude resonance stabilization leads to the inference that about 1 ⁄ 3 of the increased acidity of phenol is attributable to inductive effects, with resonance accounting for the remaining difference. (wikipedia.org)
Antiseptic2
- Phenol can have beneficial effects when used medically as an antiseptic or anesthetic. (cdc.gov)
- Phenol was also the first compound to be used in antiseptic surgery. (angelo.edu)
Synthesis4
- Finding ways to effectively tailor phenol synthesis toward these different purposes could have a large impact on society," said Chang-Jun Liu, who led the team conducting this research. (redorbit.com)
- The scientists' main finding was the discovery of three such components (called F-box proteins) that specifically recognize the first key enzyme in the series of phenol synthesis reactions. (redorbit.com)
- For example, the set of molecular tools identified in this study might be used to increase the synthesis of certain phenols that have been shown to exhibit antioxidant properties, which could potentially enhance the health benefits of so-called functional foods. (redorbit.com)
- Modular synthesis was the root inspiration for the PHENOL, and a cosdt and sizxe that is a fraction of the original modular systems as well as modular systems that are available today, PHENOL offers the creative potential, sound and hands-on experience of a modular synth in a sleek, compact and affordable package. (musiciansfriend.com)
Simplest2
- Phenol - the simplest of the phenols. (wikipedia.org)
- The simplest is phenol, C 6H 5OH. (wikipedia.org)
INEOS Phenol1
- The registration includes all INEOS Phenol sites worldwide to ensure unrestricted trade of our products. (ineos.com)
Contain phenol2
Natural phenols4
- Two natural phenols from two different categories, for instance a flavonoid and a lignan, can combine to form a hybrid class like the flavonolignans . (wikipedia.org)
- Many natural phenols are chiral . (wikipedia.org)
- Simple natural phenols can lead to the formation of B-type procyanidins in wines or in model solutions. (wikipedia.org)
- In plants, the phenolic units are esterified or methylated and are submitted to conjugation, which means that the natural phenols are mostly found in the glycoside form instead of the aglycone form. (wikipedia.org)
Search2
- NIOSHTIC-2 search results on phenol - A searchable database of worker safety and health publications, documents, grant reports, and journal articles supported in whole or in part by NIOSH. (cdc.gov)
- This review will discuss the most recent advances in the search of naturally occurring phenols and their synthetic derivatives that inhibit the CAs and their mechanisms of action at molecular level. (mdpi.com)
Reactions1
- Phenols substituted with bulky groups at ortho- positions, like butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), are endowed with antioxidant property and are used as antioxidants in many formulations such as pharmaceuticals, cosmetics, electrical transformer oil, solvents, and organic reactions. (alfa.com)
Derivatives2
- Phenol derivatives find use in the preparation of cosmetics comprising sunscreens, hair colourings and skin lightening preparations. (alfa.com)
- V. Coman and Z. Moldovan, "RP-HPLC Method for the Separation of Some Phenol Derivatives Using Gradient Elution and UV Detection," Journal of High Resolution Chromatography, Vol. 23, No. 12, 2000, pp. 699-701. (scirp.org)
Camphor7
- Iocamfen is a liquid composed of iodine, camphor and phenol . (dictionary.com)
- What is the most important information I should know about allantoin, camphor, and phenol topical? (cigna.com)
- Camphor and phenol are mild topical (for the skin) pain relievers. (cigna.com)
- Allantoin, camphor, and phenol topical is a combination medicine used to treat pain, itching, or severe lip dryness caused by chapped lips or cold sores (fever blisters). (cigna.com)
- Allantoin, camphor, and phenol topical may also be used for purposes not listed in this medication guide. (cigna.com)
- What should I discuss with my health care provider before using allantoin, camphor, and phenol topical? (cigna.com)
- How should I use allantoin, camphor, and phenol topical? (cigna.com)
Cumene1
- AdvanSix ( ASIX ) today informed its phenol customers that it is declaring force majeure as a result of shortages and delivery delays of its key raw material, cumene. (yahoo.com)
Antioxidant1
- Most solutions also have an antioxidant, as oxidized phenol will damage the DNA. (bionity.com)
Sore throat1
- If you are using glycerin/phenol spray for relief of sore throat irritation or pain, apply to the affected area as directed by your doctor or the package labeling. (drugs.com)
Crystalline1
- Phenol (C 6 H 6 O or C 6 H 5 OH) is a colorless to light-pink, crystalline solid with a sweet, acrid odor. (cdc.gov)
Irritation1
- In animals, breathing air with high levels of phenol resulted in irritation of the lungs. (cdc.gov)
Mixtures3
- Phenol is an organic compound appreciably soluble in water, with about 84.2 g dissolving in 1000 mL (0.895 M ). Homogeneous mixtures of phenol and water at phenol to water mass ratios of ~2.6 and higher are possible. (wikipedia.org)
- The present invention is particularly useful for separating valuable products from phenol tar and/or mixtures of phenol tar with bisphenol-A tar. (freepatentsonline.com)
- For phenol:chloroform mixtures or for chloroform, glass pipettes should be used, or micropipettors exclusively, as the chloroform is usually able to attack plastic pipettes. (bionity.com)
Disinfectant1
- Phenol is used as a disinfectant and is found in a number of consumer products. (cdc.gov)
Odor1
- Phenol has a distinct odor that is sickeningly sweet and tarry. (cdc.gov)
Colorless1
- Phenols are similar to alcohols but are more soluble in water, and occur as colorless solids or liquids at room temperature. (dictionary.com)
Toxic3
- Phenol has caused minor birth defects and low birth weight in animals generally at exposure levels that also were toxic to the pregnant mothers. (cdc.gov)
- According to the National Institutes of Health, phenol is toxic and people who are hypersensitive to it could experience death or serious side effects at very low exposures. (sixwise.com)
- Even the Environmental Protection Agency lists disinfectants that contain phenols as "corrosive and toxic. (sixwise.com)
Sodium3
- The sodium salt of phenol, sodium phenoxide , is far more water-soluble. (wikipedia.org)
- This notice announces the availability of EPA's preliminary risk assessment, and related documents for the antimicrobial pesticide Phenol/Sodium phenate, and opens a 12-day public comment period on these documents. (federalregister.gov)
- EPA is developing a Reregistration Eligibility Decision (RED) for Phenol/Sodium Phenate using a modified, 4-phase public participation process. (federalregister.gov)
Undergo1
- Phenols undergo esterification. (wikipedia.org)
Degradation4
- The optimal conditions of the photocatalytic degradation of phenol using prepared titanium dioxide sample were defined. (hindawi.com)
- Dinda and Icli found that ZnO was as reactive as TiO 2 for the photocatalytic degradation of phenol under concentrated sunlight [ 11 ]. (hindawi.com)
- Experiments consisting of suspended cultures demonstrated the native ability of this organism to utilize phenol for its metabolic pathways enabling degradation, at levels of nearly 100 ppm within 24 hours. (scirp.org)
- University of Minnesota Biocatalysis/Biodegradation Data- base, Phenol Family Degradation Pathway Map. (scirp.org)
Wastewater1
- We developed a model system for the biodegradation of phenol-contaminated wastewater by the bacterium Corynebacterium glutamicum . (scirp.org)
Soluble4
- Phenol-soluble modulins. (nih.gov)
- Phenol-soluble modulins and staphylococcal infection. (nih.gov)
- Phenol-soluble modulins (PSMs) have recently emerged as a novel toxin family defining the virulence potential of highly aggressive S. aureus isolates. (nih.gov)
- Phenol is naturally somewhat water-soluble, and gives a 'fuzzy' interface that is sharpened by the presence of chloroform. (bionity.com)
Toxicity5
- Vomiting and lethargy were the most frequent signs of toxicity observed in children who accidentally ingested phenol and were treated at a poison control center. (cdc.gov)
- Phenol is potentially capable of causing both systemic toxicity and direct adverse effects on the skin following dermal exposure. (cdc.gov)
- Microbial production of phenol seems to be a non-viable process considering the high toxicity of phenol to the cell. (innovations-report.com)
- Furthermore, the team developed a biphasic extractive fermentation process to minimize the toxicity of phenol to E. coli cells. (innovations-report.com)
- Glycerol tributyrate was found to have low toxicity to E. coli and allowed efficient extraction of phenol from the culture broth. (innovations-report.com)