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48525

Supelco

3,3′-Diclorobencidina

analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C12H10Cl2N2
Número de CAS:
91-94-1
Peso molecular:
253.13
Número CE:
202-109-0
Número MDL:
MFCD00043917
Código UNSPSC:
12000000

grado

analytical standard

Nivel de calidad

100

CofA

current certificate can be downloaded

envase

ampule of 100 mg

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

temp. de almacenamiento

2-30°C

cadena SMILES

Clc1c(ccc(c1)c2cc(c(cc2)N)Cl)N

InChI

1S/C12H10Cl2N2/c13-9-5-7(1-3-11(9)15)8-2-4-12(16)10(14)6-8/h1-6H,15-16H2

Clave InChI

HUWXDEQWWKGHRV-UHFFFAOYSA-N

Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Palabra de señalización

Danger

Frases de peligro

H312,H317,H350,H410

Clasificaciones de peligro

Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Skin Sens. 1

Código de clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
LC26363V
LC23941V
LC18988V
LC15513V
LC10002V

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I Zwirner-Baier et al.
Archives of toxicology, 68(1), 8-14 (1994-01-01)
The release and availability of the carcinogenic component of the soluble azo dye Direct Red 46 and the insoluble azo pigment Pigment Yellow 17 were analyzed in Wistar rats using hemoglobin adducts as a dosimeter. The levels of hemoglobin adducts
M C Nyman et al.
Journal of the American Society for Mass Spectrometry, 10(11), 1152-1156 (1999-10-28)
3,3'-Dichlorobenzidine (DCB) and its degradation products, 3-chlorobenzidine (MCB) and benzidine, are of environmental concern because of their carcinogenic nature. The suitability of a small Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer for the analysis of these environmental contaminants in
R Joppich-Kuhn et al.
International archives of occupational and environmental health, 69(4), 240-246 (1997-01-01)
A method based on gas chromatography/mass spectrometry-negative ion chemical ionization detection (GC/MS-NCI) was developed for the determination of 3,3'-dichlorobenzidine (DCB)-hemoglobin adducts. Adducts were released from hemoglobin by mild alkaline hydrolysis and determined by GC/MS-NCI after extraction and derivatization with heptafluorobutyric
Kristian F Knoell et al.
Journal of toxicology and environmental health. Part A, 75(8-10), 551-556 (2012-06-13)
In a chemical plant in Germany producing 3,3'-dichlorobenzidine dihydrochloride for the manufacture of colorants, blood and urine samples were taken for biological monitoring. 3,3'-Dichlorobenzidine (DBZ) was analyzed in urine by thin-layer chromatography and subsequently further combined with analysis of adducts
Jin-Heon Lee et al.
Industrial health, 41(3), 242-248 (2003-08-15)
3,3'-dichlorobenzidine (DCB) is suspected to be arcinogenic in experimental animal and human. Several studies have investigated excretion of metabolites in urine, hemoglobin adduction and cancer incidence among workers exposed occupationally to DCB. In these researches, metabolites of DCB had a
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