Benzene Derivatives
Benzene
Anaerobic oxidation of o-xylene, m-xylene, and homologous alkylbenzenes by new types of sulfate-reducing bacteria. (1/635)
Various alkylbenzenes were depleted during growth of an anaerobic, sulfate-reducing enrichment culture with crude oil as the only source of organic substrates. From this culture, two new types of mesophilic, rod-shaped sulfate-reducing bacteria, strains oXyS1 and mXyS1, were isolated with o-xylene and m-xylene, respectively, as organic substrates. Sequence analyses of 16S rRNA genes revealed that the isolates affiliated with known completely oxidizing sulfate-reducing bacteria of the delta subclass of the class Proteobacteria. Strain oXyS1 showed the highest similarities to Desulfobacterium cetonicum and Desulfosarcina variabilis (similarity values, 98.4 and 98.7%, respectively). Strain mXyS1 was less closely related to known species, the closest relative being Desulfococcus multivorans (similarity value, 86.9%). Complete mineralization of o-xylene and m-xylene was demonstrated in quantitative growth experiments. Strain oXyS1 was able to utilize toluene, o-ethyltoluene, benzoate, and o-methylbenzoate in addition to o-xylene. Strain mXyS1 oxidized toluene, m-ethyltoluene, m-isoproyltoluene, benzoate, and m-methylbenzoate in addition to m-xylene. Strain oXyS1 did not utilize m-alkyltoluenes, whereas strain mXyS1 did not utilize o-alkyltoluenes. Like the enrichment culture, both isolates grew anaerobically on crude oil with concomitant reduction of sulfate to sulfide. (+info)Properties of 5-aminolaevulinate synthetase and its relationship to microsomal mixed-function oxidation in the southern armyworm (Spodoptera eridania). (2/635)
1. Activity of 5-aminolaevulinate synthetase was measured in the midgut and other tissues of the last larval instar of the southern armyworm (Spodoptera eridania Cramer, formerly Prodenia eridania Cramer). 2. Optimum conditions for measuring the activity were established with respect to all variables involved and considerable differences from those reported for mammalian enzyme preparations were found. 3. Maximum activity (20 nmol/h per mg of protein) occurs 18-24 h after the fifth moult and thereafter decreases to trace amounts as the larvae age and approach pupation. 4. Synthetase activity was rapidly induced by oral administration (in the diet) of pentamethylbenzene, phenobarbital, diethyl 1,4-dihydro-2,4,6-trimethylpyridine-3, 5-dicarboxylate, and 2-allyl-2-isopropylacetamide. 5. Puromycin inhibited the induction of synthetase by pentamethylbenzene. 6. Induction of 5-aminolaevulinate synthetase correlated well with the induction of microsomal N-demethylation of p-chloro-N-methylaniline, except for phenobarbital, which induced the microsomal oxidase relatively more than the synthetase. (+info)Localization and comparative toxicity of methylsulfonyl-2,5- and 2,6-dichlorobenzene in the olfactory mucosa of mice. (3/635)
Several methylsulfonyl (MeSO2) metabolites formed from chlorinated aromatic hydrocarbons have been identified in human milk, lung, and body fat, as well as in the tissues of Baltic grey seals and arctic polar bears. The tissue localization and nasal toxicity of two methylsulfonyl-substituted dichlorobenzenes (diCl-MeSO2-B), with the chlorine atoms in the 2,5-, and 2,6- positions, were investigated in female NMRI and C57B1 mice. Using tape-section autoradiography, animals dosed i.v. with 14C-labeled 2,5-, or 2,6-(diCl-MeSO2-B) showed a preferential uptake of radioactivity in the olfactory mucosa and the tracheobronchial epithelium. Histopathology showed that 2,6-(diCl-MeSO2-B) is a potent toxicant that induces necrosis in the olfactory mucosa following a single dose as low as 4 mg/kg (i.p. injection), whereas 2,5-(diCl-MeSO2-B) induced no signs of toxicity in the olfactory mucosa at doses as high as 130 mg/kg (i.p. injection). Necrosis of the Bowman's glands was the first sign of 2,6-(diCl-MeSO2-B)-induced toxicity followed by degeneration of the neuroepithelium, which implies that the Bowman's gland may be the primary site of toxicity and degeneration of the neuroepithelium may be a secondary effect. Administration of the parent compounds, 1,3-dichlorobenzene and 1,4-dichlorobenzene, or the chlorinated analog 1,2,3-trichlorobenzene (85, 85, and 105 mg/kg, respectively; i.p. injection), induced no signs of toxicity in the olfactory mucosa. These and previous results suggest that 2,6-positioned chlorine atoms and an electron withdrawing substituent in the primary position is an arrangement that predisposes for toxicity in the olfactory mucosa. (+info)Ratio-fluorescence microscopy of lipid oxidation in living cells using C11-BODIPY(581/591). (4/635)
A ratio-fluorescence assay was developed for on-line localization and quantification of lipid oxidation in living cells. The assay explores the oxidative sensitivity of C11-BODIPY(581/591). Upon oxidation, the fluorescence of this fluorophore shifts from red to green. The probe incorporates readily into cellular membranes and is about twice as sensitive to oxidation as arachidonic acid. Using confocal microscopy, the cumene hydroperoxide-induced oxidation of C11-BODIPY(581/591) was visualized at the sub-cellular level in rat-1 fibroblasts. Preloading of the cells with tocopherol retarded this oxidation. The data demonstrate that C11-BODIPY(581/591) is a valuable tool to quantify lipid oxidation and anti-oxidant efficacy in single cells. (+info)Protective effect of dehydroepiandrosterone against lipid peroxidation in a human liver cell line. (5/635)
OBJECTIVE: Dehydroepiandrosterone (DHEA) is a widely studied steroid hormone with multi-functional properties. Reports suggest that some of the many activities of DHEA are due to its protective effect against lipid peroxidation. Nevertheless, the antioxidant properties of DHEA are still the subject of debate. The aim was to evaluate whether its two opposed effects on lipid peroxidation reported in the literature may be dependent on schedule and doses used. METHODS: Chang liver cells, a line derived from normal human liver, were grown in media containing either no steroids (control) or DHEA at concentrations ranging from 0.1 micromol/l to 50 micromol/l. At specific times, cultures were halted and cells received a pro-oxidant stimulus (cumene (CuOOH) 0.5 mmol/l), at which time cell viability (by trypan blue staining and lactate dehydrogenase (LDH) release) and thiobarbituric acid reactive substances (TBARS) concentration (spectrophotometrical assay) were evaluated. RESULTS: At concentrations ranging from 0.1 micromol/l to 1 micromol/l, DHEA protects Chang liver cells against lipid peroxidation and/or death induced by cumene. This effect disappears if the concentration is increased to 10 micromol/l; at higher concentrations (50 micromol/l) a pro-oxidant/cytotoxic effect of DHEA appears. CONCLUSIONS: DHEA exhibits two opposed effects on lipid peroxidation; depending on its concentration it acts either to limit or to induce oxidative stress. The threshold concentration at which the pro-oxidant activity of DHEA prevails is not far in excess of that having an antioxidant effect. Either effect of DHEA on lipid peroxidation is only evident after a 'lag-phase'. (+info)The branched-chain dodecylbenzene sulfonate degradation pathway of Pseudomonas aeruginosa W51D involves a novel route for degradation of the surfactant lateral alkyl chain. (6/635)
Pseudomonas aeruginosa W51D is able to grow by using branched-chain dodecylbenzene sulfonates (B-DBS) or the terpenic alcohol citronellol as a sole source of carbon. A mutant derived from this strain (W51M1) is unable to degrade citronellol but still grows on B-DBS, showing that the citronellol degradation route is not the main pathway involved in the degradation of the surfactant alkyl moiety. The structures of the main B-DBS isomers and of some intermediates were identified by gas chromatography-mass spectrometric analysis, and a possible catabolic route is proposed. (+info)Randomized phase II study of the neurokinin 1 receptor antagonist CJ-11,974 in the control of cisplatin-induced emesis. (7/635)
PURPOSE: To determine the efficacy and safety of the neurokinin type 1 receptor antagonist CJ-11,974 for the control of high-dose cisplatin-induced emesis. PATIENTS AND METHODS: A double-blind, randomized, phase II design with a group sequential stopping rule was used in this study. Sixty-one patients with cancer who were receiving cisplatin at a dose of at least 100 mg/m2 for the first time were enrolled. All patients received granisetron 10 microg/kg and dexamethasone 20 mg intravenously 30 minutes before they were given cisplatin. Patients were randomly assigned to two groups: group 1 received CJ-11,974 100 mg, and group 2 received placebo orally 30 minutes before and 12 hours after cisplatin and then twice daily on days 2 through 5 after cisplatin. The primary end point was the percentage of patients who developed delayed emesis (emesis on the second to fifth days after cisplatin). RESULTS: Thirty patients were enrolled in group 1, and 31 patients were enrolled in group 2. Fifty-eight patients were assessable for efficacy. Complete control of emesis (expressed as the percentage of patients who had no emesis) was as follows: day 1, 85.7% (group 1) and 66.7% (group 2) (P = .090); days 2 through 5, 67.8% (group 1) and 36.6% (group 2) (P = .0425, adjusted); days 1 through 5, 64.3% (group 1) and 30% (group 2) (P = .009). Patients in group 1 experienced significantly less nausea than patients in group 2 on day 1 (P = .024). Treatment was well tolerated in both groups. CONCLUSION: We conclude from this exploratory phase II trial that CJ-11,974 is superior to placebo in controlling cisplatin-induced delayed emesis and may provide additive benefit in acute emesis and nausea control when combined with a 5-hydroxytryptamine-3 receptor antagonist and dexamethasone. Additional larger trials are indicated to confirm the clinical value of CJ-11,974. (+info)In vitro studies on the initial reactions of anaerobic ethylbenzene mineralization. (8/635)
Anaerobic mineralization of ethylbenzene by the denitrifying bacterium Azoarcus sp. strain EB1 was recently shown to be initiated by dehydrogenation of ethylbenzene to 1-phenylethanol. 1-Phenylethanol is converted to benzoate (benzoyl coenzyme A) via acetophenone as transient intermediate. We developed in vitro assays to examine ethylbenzene dehydrogenase and 1-phenylethanol dehydrogenase activities in cell extracts of this strain. With p-benzoquinone as the electron acceptor, cell extracts of Azoarcus sp. strain EB1 catalyzed ethylbenzene oxidation at a specific rate of 10 nmol min(-1) [mg of protein](-1) and an apparent K(m) for ethylbenzene of approximately 60 microM. The membrane-associated ethylbenzene dehydrogenase activity was found to oxidize 4-fluoroethylbenzene and propylbenzene but was unable to transform 4-chloro-ethylbenzene, the ethyltoluenes, and styrene. Enzymatic ethylbenzene oxidation was stereospecific, with (S)-(-)-1-phenylethanol being the only enantiomer detected by chiral high-pressure liquid chromatography analysis. Moreover, cell extracts catalyzed the oxidation of (S)-(-)-1-phenylethanol but not of (R)-(+)-1-phenylethanol to acetophenone. When cell extracts were dialyzed, (S)-(-)-1-phenylethanol oxidation occurred only in the presence of NAD(+), suggesting that NAD(+) is the physiological electron acceptor of 1-phenylethanol dehydrogenase. Both ethylbenzene dehydrogenase and 1-phenylethanol dehydrogenase activities were present in Azoarcus sp. strain EB1 cells that were grown anaerobically on ethylbenzene, 1-phenylethanol, and acetophenone, but these activities were absent in benzoate-grown cells. (+info)Benzene derivatives are chemical compounds that are derived from benzene, which is a simple aromatic hydrocarbon with the molecular formula C6H6. Benzene has a planar, hexagonal ring structure, and its derivatives are formed by replacing one or more of the hydrogen atoms in the benzene molecule with other functional groups.
Benzene derivatives have a wide range of applications in various industries, including pharmaceuticals, dyes, plastics, and explosives. Some common examples of benzene derivatives include toluene, xylene, phenol, aniline, and nitrobenzene. These compounds can have different physical and chemical properties depending on the nature and position of the substituents attached to the benzene ring.
It is important to note that some benzene derivatives are known to be toxic or carcinogenic, and their production, use, and disposal must be carefully regulated to ensure safety and protect public health.
Benzene is a colorless, flammable liquid with a sweet odor. It has the molecular formula C6H6 and is composed of six carbon atoms arranged in a ring, bonded to six hydrogen atoms. Benzene is an important industrial solvent and is used as a starting material in the production of various chemicals, including plastics, rubber, resins, and dyes. It is also a natural component of crude oil and gasoline.
In terms of medical relevance, benzene is classified as a human carcinogen by the International Agency for Research on Cancer (IARC) and the Environmental Protection Agency (EPA). Long-term exposure to high levels of benzene can cause various health effects, including anemia, leukemia, and other blood disorders. Occupational exposure to benzene is regulated by the Occupational Safety and Health Administration (OSHA) to protect workers from potential health hazards.
It's important to note that while benzene has legitimate uses in industry, it should be handled with care due to its known health risks. Exposure to benzene can occur through inhalation, skin contact, or accidental ingestion, so appropriate safety measures must be taken when handling this chemical.
Sorbic acid is a chemical compound that is commonly used as a preservative in various food and cosmetic products. Medically, it's not typically used as a treatment for any specific condition. However, its preservative properties help prevent the growth of bacteria, yeast, and mold, which can improve the safety and shelf life of certain medical supplies such as ointments and eye drops.
The chemical structure of sorbic acid is that of a carboxylic acid with two double bonds, making it a unsaturated fatty acid. It's naturally found in some fruits like rowanberries and serviceberries, but most commercial sorbic acid is synthetically produced.
Food-grade sorbic acid is generally recognized as safe (GRAS) by the U.S. Food and Drug Administration (FDA), and it has a wide range of applications in food preservation, including baked goods, cheeses, wines, and fruit juices. In cosmetics, it's often used to prevent microbial growth in products like creams, lotions, and makeup.
It is important to note that some people may have allergic reactions to sorbic acid or its salts (sorbates), so caution should be exercised when introducing new products containing these substances into personal care routines or diets.
Taft equation
Acid dissociation constant
Alkyne trimerisation
Benzene
Carbon nanothread
C. V. Raman
Parent structure
Structural isomer
Dow process
1,3,5-Trinitrobenzene
Bismabenzene
Topological index
Carbon-hydrogen bond activation
Edward Bartow
Bergman cyclization
Organogold chemistry
1,2,3-Trinitrobenzene
Catechol
Niveen Khashab
Alexander Borodin
1,2,4-Trichlorobenzene
Quinonoid zwitterion
1,2-Dibromobenzene
Hafnium trifluoromethanesulfonate
Eilhard Mitscherlich
Dibenzothiazepine
Metallosphaera hakonensis
Cyclohexylbenzene
Cyclophane
Phthalonitrile
Sydney Young (chemist)
Aromatic compound
Benzenedicarboxylic acid
Benzene Derivatives: The Dudley Synthesis of Coprinol
Herbicidal benzene- and pyridine-sulfonamide derivatives - Patent EP-0035893-B1 - PubChem
BJOC - Friedel-Crafts acylation of benzene derivatives in tunable aryl alkyl ionic liquids (TAAILs)
An Improved Free Energy Perturbation FEP+ Sampling Protocol for Flexible Ligand-Binding Domains | Scientific Reports
benzene derivative - L-OPTIMA ELEMENT
nomenclature of benzene derivatives
Bromobenzenes - Halobenzenes - Benzene and substituted derivatives - Benzenoids - Organic Compounds - Chemicals
Beyond Jablonski diagrams in organic systems: ab initio studies of substituted benzene derivatives
Taft equation - Wikipedia
DYNA-DIGGR - An Automatic Spade-Shovel
ISO 11423-2:1997 - Water quality - Determination of benzene and some derivatives - Part 2: Method using extraction and gas...
The Influence and Mechanism of Benzodihydropyran Benzene and Dihydro Pyran Derivatives xy2004 Effect on Breast Cancer Cell...
Synthesis, In Vitro Anti-Microbial Analysis and Molecular Docking Study of Aliphatic Hydrazide-Based Benzene Sulphonamide...
Publications | Computational Biology and Drug Design Group
Intracluster cyclization reaction producing a benzene derivative: Photoionization mass spectrometric study of alkali metal...
The Novel Zinc (II) Phthalocyanine Substituted With Benzene Sulfonamide Derivative Compound Containing Pyridine And Nitro...
Jiangsu Liansheng Pharmaceutical Co., Ltd.--Benzene ring derivative|Pyridine derivative|Other fine chemicals|IM-antiviral drug...
Functional group - New World Encyclopedia
Publications | Computational Biology and Drug Design Group
IUCr) Facing the phase problem
Erowid.org: References Database
13446-18-9|Magnesium nitrate hexahydrate|lookchem
You searched for UOP - Page 2 of 4 - Market Research Reports & Consulting | GlobalData UK Ltd.
WTS database | WHO FCTC
WTS database | WHO FCTC
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Styrene | Harvard Catalyst Profiles | Harvard Catalyst
Advanced Search Results - Public Health Image Library(PHIL)
Synthesis and electroluminescence property of new hexaphenylbenzene derivatives including amine group for blue emitters |...
Toluene5
- 1993. A comparative study of the kinetic and bioavailability of pure and soil-adsorbed benzene, toluene, and m -xylene after dermal exposure. (cdc.gov)
- The pollutants released include benzene, toluene, ethylbenzene and xylenes (BTEX), which are significant due to their high level of toxicity. (who.int)
- Additionally, there were incidences where individuals were at potential hazard risk of benzene and toluene that may pose non-carcinogenic effects to employees. (who.int)
- OBJECTIVE: To set up a method for the low concentration of benzene and its homologues (toluene, ethylbenzene and xylene, BTEX) in indoor air monitored simultaneously by portable gas chromatography (GC). (who.int)
- Toluene is a benzene derivative (CH3) and is less volatile than acetone and has been known to make people stupid. (woodweb.com)
Synthesis1
- Furthermore, this method provides a direct approach for the synthesis of fluorinated drug derivatives, which has important application for drug discovery and development. (nature.com)
Alkyl2
- An iron(III) chloride hexahydrate-catalyzed Friedel-Crafts acylation of benzene derivatives in tunable aryl alkyl ionic liquids (TAAILs) has been developed. (beilstein-journals.org)
- Benzene, mono-C11-13-branched alkyl derivs. (europa.eu)
Aromatic2
Phenol1
- 10.1002/anie.201410375 ) that the phenol derivative 12 could be ortho carboxylated, leading to 13 . (organic-chemistry.org)
Formaldehyde2
- First, the arylimidazole is obtained through a ring closing reaction using an aniline derivative, glyoxal, formaldehyde and ammonium chloride. (beilstein-journals.org)
- The bromomethylation (or chloromethylation, with HCl) of a benzene derivative is straightforward with formaldehyde and HBr. (organic-chemistry.org)
Organic2
Methyl1
- 2005. Effect of methyl substitution of benzene in the percutaneous absorption and skin irritation in hairless rats. (cdc.gov)
Aniline1
- Ionic liquids 1 - 6 were synthesized via a three-step procedure starting from commercially available aniline derivatives (see Scheme 1 ). (beilstein-journals.org)
Exposure3
- Due to poor ventilation and high exposure duration, the average benzene concentration over the sampling campaign exceeded the US Environmental Protection Agency's chronic inhalation exposure reference concentration. (who.int)
- Lifetime cancer risk estimation showed that on average there is a 3.78 x 10-4 cancer risk, corresponding to an average chronic daily intake of 1.38 x 10-3 mg/kg/day of benzene exposure. (who.int)
- The authors point out that further studies are needed to describe exposure pathways of petroleum and its closest derivatives (e.g. benzene), in order to identify the drivers of the observed modifiers of cancer risk. (who.int)
Acid2
Study1
- A unique series of sulphonamide derivatives was attempted to be synthesized in this study using a new and effective method. (nottingham.edu.cn)
Include1
- In this chapter, electrophilic agents nogenicity from studies of exposed (benzene, 1,3-butadiene, and eth- include direct-acting electrophilic humans. (who.int)
Risk1
- For example, polymorphisms of NAD(P)H:quinone oxidoreductase (NQO1), an enzyme that metabolizes benzene derivatives, are associated with an increased risk of AML. (medscape.com)
Systems1
- The following table gives an overview about the physicochemical properties considered for the rating of strategic bonds linked to benzene ring systems. (uni-erlangen.de)
Chapter1
- Benzene is discussed in a separate chapter. (cdc.gov)
Difference1
- The variation of functionalities in the benzene moiety was well-tolerated, and only a moderate difference in yield and degree of purity was noticed. (lu.se)
Main1
- The main products of chlorobenzene degradation were O-3, CON, benzene derivatives, and nitrogenous organics. (cheric.org)
Aromatic3
- Benzene is an aromatic organic molecule composed of six carbon atoms and six hydrogen atoms that form a ring. (fishersci.com)
- An aromatic hydrocarbon, benzene is produced by refining crude oil . (marketresearchcommunity.com)
- Advanced oxidation processes (APOs) of aromatic compounds, particularly of phenol, yield several benzene derivatives, such as hydroquinone, catechol, and resorcinol, as intermediate metabolites of its transformation. (hindawi.com)
Toluene3
- 1993. A comparative study of the kinetic and bioavailability of pure and soil-adsorbed benzene, toluene, and m -xylene after dermal exposure. (cdc.gov)
- Linear Relationships Between Total Hydrocarbons and Benzene, Toluene, Ethylbenzene, Xylene, and n-Hexane during the Deepwater Horizon Response and Clean-up. (nih.gov)
- By using Bio-TCat technology, Anellotech and its partners are accelerating the development of biobased paraxylene and other widely-used chemicals including benzene, toluene and other xylenes (commonly known as BTX) from non-food sources. (plasticstoday.com)
Compounds7
- For the biological evaluation of the N-(ferrocenylmethylamino acid) fluorinated benzene carboxamide series of compounds, were tested on the estrogen positive (ER+) breast cancer cell line, MCF-7. (dcu.ie)
- Includes substituted derivative compounds. (fishersci.com)
- Benzene is utilised by some companies to create other compounds that go into the creation of nylon, plastics, synthetic fibres, and resins. (marketresearchcommunity.com)
- Researchers have successfully synthesized and structurally characterized boron-nitrogen compounds that are isoelectronic and isostructural to the fundamentally important benzene molecule. (sciencedaily.com)
- Researchers in the lab of University of Oregon chemist Shih-Yuan Liu have successfully synthesized and structurally characterized boron-nitrogen compounds that are isoelectronic and isostructural to the fundamentally important benzene molecule. (sciencedaily.com)
- phenolic compounds" shall mean any hydroxy derivative of benzene, or its condensed nuclei. (london.ca)
- Organic compounds derived from BENZENE . (nih.gov)
Substituents1
- The concept includes derivatives with any substituents on the benzene ring. (umassmed.edu)
Hepatic1
- This is based on the observation that hepatic metabolism of this agent results in the production of benzene derivatives during hepatic metabolism. (medscape.com)
Amino2
- Synthesis, characterization and biological evaluation of N-ferrocenylmethyl amino acid benzene carboxamide derivatives and N-ferrocenyl benzoyl amino alkane derivatives as anti-cancer agents. (dcu.ie)
- The synthesis of N-(ferrocenylmethylamino acid) fluorinated benzene carboxamide derivatives was achieved by coupling the free N-terminus of the ferrocenylmethylamine with the carboxylic acid group of the N-(fluorobenzoyl)-amino acid using N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC) and 1-hydroxybenzotriazole (HOBt) coupling protocol. (dcu.ie)
20211
- The Benzene and Its Derivatives Market was valued at USD 34.52 Bn in 2021, at CAGR of 6.34% during the forecast period (2022-2030), and the Market is projected to be worth USD 60.03 Bn by 2030. (marketresearchcommunity.com)
Benzoyl3
- A series of N-(ferrocenylmethylamino acid)-fluorinated-benzene carboxamide derivatives and a series of N-(ferrocenyl)-benzoyl-aminoalkane derivatives have been synthesised, structurally characterised and biologically evaluated for their anti-proliferative activity on various cancer cell lines, principally, the (estrogen receptor positive) MCF-7 breast cancer cell line. (dcu.ie)
- The synthesis of the N-{(ferrocenyl)-benzoyl}-aminoalkanes derivatives involved the coupling of the free N-terminus of the amine group of the aminoalkanes to the carboxylic acid group of the ferrocenyl-benzoic acid (ortho-, meta- and para-) using N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS) coupling protocol. (dcu.ie)
- 1,3-Dipolar cycloaddition of C-benzoyl-N-phenylnitrone with dihydrofuran derivatives. (cas.cz)
Synthesis1
- Tückmantel, W. Synthesis and Reactions of Oligomethylene-Clamped 1 H-Azepines and Benzene Imines. (nih.gov)
Chemicals1
- Cancer patients have been shown to have traces of chemicals â€" like alkanes and benzene derivatives â€" in their breath, and other studies have shown dogs can detect chemicals in concentrations as small as a few parts per trillion. (blather.net)
Parameters1
- The report provides comprehensive coverage of all parameters of the Benzene industry. (researchandmarkets.com)
Demand4
- The increased adoption of Benzene and Its Derivatives in the Petrochemicals industry is due to high workability, Stability of structure, good quality, and Demand for making things better. (marketresearchcommunity.com)
- The demand for Benzene and Its Derivatives also has other significant aspects, such as analysis, purchasing volume, costs, pricing analysis, and regulatory framework. (marketresearchcommunity.com)
- Additionally, the increased demand of Benzene and Its Derivatives in many sectors also boosts the market growth during the forecast period. (marketresearchcommunity.com)
- The report offers historical and forecast market size, demand and production forecasts, end-use demand details, price trends, trade balance data, and company shares of the country's leading Benzene producers. (researchandmarkets.com)
Series2
Market Size1
- The publisher's report, 'Benzene Industry Outlook in Canada to 2026 - Market Size, Company Share, Price Trends, Capacity Forecasts of All Active and Planned Plants', provides up to date in-depth information on Canada's Benzene industry. (researchandmarkets.com)
Agents1
- These agents are derivatives of vitamin A and lead to increased keratinocyte turnover and decreased melanocyte activity. (medscape.com)
Report2
- Benzene and Its Derivatives Market Research Report" was just released by Market Research Community. (marketresearchcommunity.com)
- The report covers Canada's Benzene plants and presents installed capacity by process and technology. (researchandmarkets.com)
COMPANY1
- Company capacity shares for key Benzene producers in Canada. (researchandmarkets.com)
Major1
- Hydroquinone, the major benzene metabolite, is a ubiquitous chemical in the environment due to its widespread application in human and industrial activities. (hindawi.com)
Technology1
- Anellotech's proprietary thermal catalytic biomass conversion technology (Bio-TCat) produces "drop in" green aromatics, including paraxylene and benzene, from non-food biomass. (plasticstoday.com)
World1
- The COVID-19 pandemic has had a substantial negative influence on the Benzene and Its Derivatives market in many different regions of the world. (marketresearchcommunity.com)
Issue1
- The contribution of benzene and its metabolites to this issue is well recognized, making them a public health problem. (hindawi.com)