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48525

Supelco

3,3′-Dichlorobenzidine

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H10Cl2N2
CAS Number:
91-94-1
Molecular Weight:
253.13
EC Number:
202-109-0
MDL number:
MFCD00043917
UNSPSC Code:
12000000
Pricing and availability is not currently available.

grade

analytical standard

Quality Level

100

CofA

current certificate can be downloaded

packaging

ampule of 100 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-30°C

SMILES string

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

InChI key

HUWXDEQWWKGHRV-UHFFFAOYSA-N

Application

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

Signal Word

Danger

Hazard Statements

H312,H317,H350,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LC26363V
LC23941V
LC18988V
LC15513V
LC10002V

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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
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
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
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
Marianne C Nyman et al.
Environmental toxicology and chemistry, 22(1), 20-25 (2002-12-31)
Like many hydrophobic organic compounds, 3,3'-dichlorobenzidine (DCB) partitions preferentially to (sediment) particles in lake systems. As such, the behavior of DCB in these systems is substantially affected by the movement of sediments. A field investigation of DCB distribution in sediments
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