Ad
related to: phenol ez swabs sds
Search results
Results from the WOW.Com Content Network
The method of sample acquisition can be refined to avoid unnecessary collection of inhibitors. For example, in forensics, swab-transfer of blood on fabric or saliva on food, may prevent or reduce contamination with inhibitors present in the fabric or food. [3]
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 ]
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.
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]
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).
2,6-Di-tert-butylphenol is an organic compound with the structural formula 2,6-((CH 3) 3 C) 2 C 6 H 3 OH.This colorless solid alkylated phenol and its derivatives are used industrially as UV stabilizers and antioxidants for hydrocarbon-based products ranging from petrochemicals to plastics. [1]
Bis(phenol) substrates undergo oxidative coupling under these conditions. Iodonium ylides are relatively stable, versatile compounds that undergo substitution and cycloaddition reactions. They are represented using two resonance forms, one zwitterionic (the "betaine" form) and the other neutral (the "ylide" form).
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.
Ad
related to: phenol ez swabs sds