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Phenyl glycidyl ether, is a liquid aromatic organic chemical in the glycidyl ether class of compounds. [2] It has the formula C 9 H 10 O 2.It has the CAS Registry Number 122-60-1 and the IUPAC name of 2-(phenoxymethyl)oxirane.
The product of this reaction is 2-(1-methylpropyl)phenol. The second step in the synthesis of dinoseb is the nitration of 2-(1-methylpropyl)phenol. First, the nitronium ion is formed from nitric acid and sulfuric acid. [21] 2-(1-methylpropyl)phenol takes up the nitronium ion to form the arenium ion, which has three resonance structures. Water ...
An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.
e-SDS, otherwise known as an extended SDS.An extended SDS is a document of chemical safety. It is much longer and detailed than the standard SDS. It consists of a standard SDS which has more subsections than the general one, and an additional annex containing one or more exposure scenario(s).
The nonyl group can be attached to the phenol ring at various locations, usually the 4- and, to lesser extent, the 2-positions, and can be either branched or linear. A branched nonylphenol, 4-nonylphenol, is the most widely produced and marketed nonylphenol. [ 12 ]
2,4,6-Tris(dimethylaminomethyl)phenol is an aromatic organic chemical that has tertiary amine and phenolic hydroxyl functionality in the same molecule. [1] The formula is C 15 H 27 N 3 O and the CAS Registry Number is 90-72-2. It is REACH registered and the European Community Number is 202-013-9. [2] [3] [4]
Phenol is also a versatile precursor to a large collection of drugs, most notably aspirin but also many herbicides and pharmaceutical drugs. Phenol is a component in liquid–liquid phenol–chloroform extraction technique used in molecular biology for obtaining nucleic acids from tissues or cell culture samples.
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