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    1,4-Benzoquinone

    1,4-Benzoquinone, commonly known as para-quinone, is a chemical compound with the formula C 6 H 4 O 2.In a pure state, it forms bright-yellow crystals with a characteristic irritating odor, resembling that of chlorine, bleach, and hot plastic or formaldehyde.This six-membered ring compound is the oxidized derivative of 1,4-hydroquinone.The molecule is multifunctional: it exhibits properties of

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    Get supplier listing of p-Benzoquinone and equal product . CM Fine Chemicals, being a privately owned Swiss company, has been manufacturing and providing fine chemicals, intermediates and reagents to all kind of industries and research organizations all over the world.

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    1,4-Benzoquinone C6H4O2

    1,4-benzoquinone is the simplest member of the class of 1,4-benzoquinones, obtained by the formal oxidation of hydroquinone to the corresponding diketone. It is a metabolite of benzene.It has a role as a cofactor, a human xenobiotic metabolite and a mouse metabolite.

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    Chemical Database: p-Benzoquinone

    This page contains information on the chemical p-Benzoquinone including: 88 synonyms/identifiers; U.S. Code of Federal Regulations Title 49 Section 172 shipping regulations and proper shipping name; USDOT 2008 Emergency Response Guidebook initial response information.

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    Benzene (CAS Registry Number 71-43-2; C6H6; molecular weight 78.1 g/mol) is an aromatic compound with a single six-member unsaturated carbon ring. It is a clear, colourless, volatile, highly flammable liquid with a characteristic odour and a density of 874 kg/m3 at 25 °C (1).

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    18.03.2004· Rubber composition comprising plastisol formed flow properties . United States Patent Application 20040052951 . Kind Code: A1 . Abstract: Hot-curing reactive compositions based on natural and/or synthetic elastomers which contain olefinic double bonds and vulcanization agents which contain, apart from conventional liquid polyenes, at least one liquid cis-1,4-polyisophere with a molecular

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    However, it is still used as a solvent in scientific laboratories, industrial paints, rubber cements, adhesives, paint removers, degreasing agents, production of artificial leather and of rubber goods, and in the shoe industry (Mara & Lee, 1978; Windholz et al., 1983; Gilman et al., 1985). For many solvent uses, benzene has been replaced by other less toxic organic solvents. However, in the

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    Phenol has been found to react with nitrous acid in waste water to form cyanide (Adachi et al., 1987), and to form chlorophenols in chlorinated drinking-water (Jarvis et al., 1985) and p-benzoquinone in the presence of chlorine dioxide (Wajon et al., 1982).

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    THE TROUBLING BENZENE RING Its impact on health, crops, drug development, environmental policy-making and the therapeutic challenge. Beldeu Singh. Key words : occupational hea

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    Howard CA,Sheldon T.,Richardson CR Chromosomal analysis of human lymphocytes exposed in vitro to five chemicals . In Ashby J,deSerres FJ,Draper M eds. Evaluation of short-term tests for carcinogens. Report of the international program on chemical safety collaborative study on in-vitro assays . Elsevier, 1985: 457 — 67. Google Scholar

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    SUBSTANCE: invention provides a water-based coating system which can be used to form durable, wear-resistant and corrosion-resistant protective barriers on a wide range of substrates. The coating system is particularly effective for protecting metal-containing substrates, such as intermodal containers, from corrosion. The invention provides water-based primer compositions used to form priming

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    40 CFR Ch. I (7-1-19 Edition) Environmental Protection

    February 22, 2019 Title 40 Protection of Environment Parts 260 to 265 Revised as of July 1, 2019 Containing a codification of documents of general applicability and future effect As of July 1, 2019. Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register

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