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Merck
CN

12115

Sigma-Aldrich

联苯胺

purum p.a., ≥98.0% (N)

别名:

4,4'-二氨基联苯

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About This Item

经验公式(希尔记法):
C12H12N2
CAS号:
分子量:
184.24
Beilstein:
742770
EC 号:
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.25

等级

purum p.a.

质量水平

方案

≥98.0% (N)

SMILES字符串

Nc1ccc(cc1)-c2ccc(N)cc2

InChI

1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2

InChI key

HFACYLZERDEVSX-UHFFFAOYSA-N

基因信息

human ... UGT1A4(54657)

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应用

Benzidine can be used to study bioactive small molecules and cell biology. Benzidine has been used to determine pollen viability and stigma receptivity of Angelica dahurica. Benzidine has also been used to study cross-linking of horseradish peroxidase adsorbed on polycationic films.
for spectrophotometric determination of CN-, NO2-, ClO3-, SO42-

其他说明

Reagent for the det. of blood; Reagent for the det. of peroxidases.; Reagent for the spectrophotometric det. of CN-, NO2-, ClO3-, etc.
Sales restrictions may apply

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1A

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

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

法规信息

监管及禁止进口产品

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分析证书(COA)

Lot/Batch Number

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THE BENZIDINE TEST: A CRITICAL REVIEW.
B J CULLIFORD et al.
Journal of forensic sciences, 9(1), 175-191 (1964-01-01)
J.L. Royer et al.
Analytical Letters, 6, 619-619 (1973)
E.A. Burns
Analytical Chemistry, 32, 1800-1800 (1960)
Brian J Pak et al.
PLoS neglected tropical diseases, 8(8), e3002-e3002 (2014-08-08)
Strongyloidiasis is a persistent human parasitic infection caused by the intestinal nematode, Strongyloides stercoralis. The parasite has a world-wide distribution, particularly in tropical and subtropical regions with poor sanitary conditions. Since individuals with strongyloidiasis are typically asymptomatic, the infection can
P D Josephy
Federation proceedings, 45(10), 2465-2470 (1986-09-01)
Benzidine oxidative activation may proceed by peroxidase-catalyzed one-electron oxidation via free radical intermediates, or by N-acetylation followed by monooxygenase-catalyzed N-hydroxylation. The peroxidase route has been examined by using horseradish peroxidase or prostaglandin H synthase in vitro. In the presence of

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