109665
1,3-Diphenyltriazene
95%
Sinonimo/i:
Diazoaminobenzene
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About This Item
Formula condensata:
C6H5NHN=NC6H5
Numero CAS:
Peso molecolare:
197.24
Numero CE:
Numero MDL:
Codice UNSPSC:
12171500
ID PubChem:
Densità del vapore
6.8 (vs air)
Saggio
95%
P. ebollizione
146 °C (lit.)
Stringa SMILE
N(\N=N\c1ccccc1)c2ccccc2
Applicazioni
Diazoaminobenzene is an azo compound used as an intermediate, complexing agent, and polymer additive. DAAB is a manufacturing intermediate that metabolizes primarily to known carcinogens, benzene and aniline. DAAB has been identified as an impurity in a number of dyes and coloring agents.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Feng Li et al.
Biosensors & bioelectronics, 25(9), 2084-2088 (2010-03-09)
A novel protocol for the gold nanoparticles (AuNPs) modification on the electrode surface was proposed, which was based on the self-assembly of AuNPs on the mercapto-diazoaminobenzene monolayer modified electrode. The mercapto-diazoaminobenzene monolayer was obtained by covalent immobilization of 4-aminothiophenol (4-ATP)
Chhanda Mukhopadhyay et al.
Organic & biomolecular chemistry, 8(20), 4720-4729 (2010-09-08)
An efficient and highly versatile method for the synthesis of diverse regiospecific 1-arylbenzotriazoles being important medicinal scaffolds, by the copper (1) catalysed intramolecular N-arylation of diazoaminobenzenes of 2-haloaryldiazonium salts in PEG-water has been developed. A very simple reaction protocol, large
Diazoaminobenzene.
Report on carcinogens : carcinogen profiles, 12, 132-134 (2011-08-19)
J E Bailey
Journal of chromatography, 321(1), 185-197 (1985-03-08)
Data are presented for the determination of trace levels of 1,3-diphenyltriazene (DPT) and azobenzene (AB) in D&C Red No. 33. The contaminants are extracted with chloroform from an aqueous solution of the color, and the chloroform is removed under vacuum.
Nancy B Ress et al.
Mutation research, 521(1-2), 201-208 (2002-11-20)
Diazoaminobenzene (DAAB), a manufacturing intermediate metabolized primarily to the known carcinogens benzene and aniline, has been identified as an impurity in a number of dyes and coloring agents that are components of cosmetics, food products, and pharmaceuticals. Several structural analogs
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