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Merck
CN

40026

Supelco

3,3′-二氯联苯胺 溶液

new

certified reference material, 5000 μg/mL in methanol

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关于此项目

经验公式(希尔记法):
C12H10Cl2N2
化学文摘社编号:
分子量:
253.13
UNSPSC代码:
41116105
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等级

certified reference material
TraceCERT®

产品线

TraceCERT®

CofA

current certificate can be downloaded

包装

ampule of 1 mL

浓度

5000 μg/mL in methanol

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

single component solution

储存温度

2-8°C

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

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应用

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

法律信息

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Carc. 1B - Flam. Liq. 2 - STOT SE 1

靶器官

Eyes

WGK

WGK 3

闪点(°F)

50.0 °F

闪点(°C)

10 °C

法规信息

危险化学品
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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
Francis P Donaldson et al.
Environmental toxicology and chemistry, 24(5), 1022-1028 (2005-08-23)
Aromatic amines, such as benzidine and 3,3'-dichlorobenzidine (DCB), are part of the dyes and pigments manufacturing process. The prolonged use of these carcinogenic chemicals in the past generation has introduced a significant amount of contamination to the environment. Their persistency
Lei Wang et al.
Toxicology, 207(3), 411-418 (2005-01-25)
DCB, 3,3'-dichlorobenzidine, is used primarily as an intermediate in the manufacture of diarylide yellow or azo red pigments for printing ink, textile, paint, and plastics. It is also used in tattoo inks. In this article, we investigate light-induced toxicity of
Marianne C Nyman et al.
Environmental toxicology and chemistry, 21(3), 500-506 (2002-03-07)
Laboratory experiments have been conducted to elucidate the photochemical behavior of 3,3'-dichlorobenzidine (DCB) and its congeners in aquatic systems. Photodechlorination of DCB was observed in aqueous samples that were irradiated with monochromatic radiation from a variable-wavelength laser at several wavelengths
Jin Heon Lee et al.
Toxicology and industrial health, 18(4), 191-199 (2003-09-17)
3,3'-dichlorobenzidine (DCB) can be metabolically N-acetylated and/or N-oxidized, and can form hemoglobin adducts. Gas chromatography/mass spectrometry-selected ion monitoring detection mode (GC/MS-SIM) could be a good analytical method to detect them. 4-Aminobiphenyl and phenanthrene-d10 were used as internal standards, and standard

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