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Merck

48525

Supelco

3,3′-二氯联苯胺

analytical standard

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About This Item

经验公式(希尔记法):
C12H10Cl2N2
CAS号:
分子量:
253.13
EC 号:
MDL编号:
UNSPSC代码:
12000000

等级

analytical standard

CofA

current certificate can be downloaded

包装

ampule of 100 mg

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

neat

储存温度

2-30°C

SMILES字符串

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

应用

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

警示用语:

Danger

危险分类

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

储存分类代码

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

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
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

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