1,3-Diphenyltriazene

Quality products?make an important contribution to long-term revenue and profitability. China cas 136-35-6 manufacturer wholesale 1,3-Diphenyltriazene at affordable price

1.What is the 1,3-Diphenyltriazene ?

Diazoaminobenzene is used as a chemical intermediate, complexing agent, and polymer additive (Mathews and De Costa 1999). It has uses associated with organic synthesis and dye and insecticide manufacture (Lewis 1997), and it is an effective dopant for laser ablation (micro-machining) of polymethylmethacrylate (Bolle et al. 1990). Diazoaminobenzene has been identified as a low-level contaminant in the dyes D&C red no. 33, FD&C yellow no. 5 (tartrazine), and FD&C yellow no. 6; all three are permitted for use in drugs and cosmetics, and the latter two are permitted in food (FDA 2010).

2.What is the CAS number for 1,3-Diphenyltriazene ?

The CAS number of 1,3-Diphenyltriazene is 136-35-6.

More information of 1,3-Diphenyltriazene 136-35-6 are:

3.What are another words for 1,3-Diphenyltriazene ?

Synonyms?for?1,3-Diphenyltriazene 136-35-6:Triazene,1,3-diphenyl- (6CI,7CI,8CI); 1,3-Diphenyltriazene; Aniline, N-(phenylazo)-;Diazoaminobenzene; NSC 2077

4.What is the molecular formula of 1,3-Diphenyltriazene?

The chemical formula of ?1,3-Diphenyltriazene is?C12H11 N3 which containing 12 Carbon atoms,11 Hydrogen atoms and 3 Nitrogen atoms,and the molecular weight of??1,3-Diphenyltriazene?is 197.239.

5.What is 1,3-Diphenyltriazene (136-35-6) used for?

Diazoaminobenzene (DAAB) is an aromatic amine that is a suspected carcinogen. It is harmful if inhaled, ingested, or absorbed through the skin. It causes skin irritation and severe irritation to eyes. DAAB can be made by diazotizing aniline dissolved in hydrochloric acid with sodium nitrite and then adding a concentrated solution of sodium acetate. DAAB is listed in the US Environmental Protection Agency’s Toxic Substances Control Act Inventory. DAAB has three major use areas: intermediate, complexing agent, and polymer additive. Use as an intermediate is reported in several industry sectors, including organic synthesis, dye manufacture, and agrochemical manufacture (insecticides). DAAB is also a versatile metal complexing agent. A series of metabolism studies in rodents and human liver slices, electron spin resonance spectroscopy studies, short-term dermal toxicity studies in rodents, and acute bone marrow micronucleus studies in mice demonstrated that DAAB is metabolized and shares similar genotoxic and toxicological properties to the known human carcinogen, benzene, and the known rodent carcinogen, aniline.

InChI:InChI=1/C15H15N3/c1-3-8-14(9-4-1)17-12-7-13-18(16-17)15-10-5-2-6-11-15/h1-12,16H,13H2

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