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B3383

Sigma-Aldrich

Benzidine dihydrochloride

≥99% (titration)

Sinonimo/i:

4,4′-Diaminobiphenyl dihydrochloride

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About This Item

Formula empirica (notazione di Hill):
C12H12N2 · 2HCl
Numero CAS:
531-85-1
Peso molecolare:
257.16
Beilstein:
3914846
Numero CE:
208-519-6
Numero MDL:
MFCD00040389
Codice UNSPSC:
12352116
ID PubChem:
24891713
NACRES:
NA.25

Livello qualitativo

200

Saggio

≥99% (titration)

Stato

powder

Stringa SMILE

Cl[H].Cl[H].Nc1ccc(cc1)-c2ccc(N)cc2

InChI

1S/C12H12N2.2ClH/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10;;/h1-8H,13-14H2;2*1H
RUAXWVDEYJEWRY-UHFFFAOYSA-N

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Applicazioni

Benzidine (4,4′-Diaminobiphenyl) is an environmental genotoxin that posses increased risks of cancer to exposed people. Benzidine may be used as a reference material in procedures that analyze for benzidine. Benzidine can be used in studies on its mechanisms of genotoxicity.

Azioni biochim/fisiol

Tumor initiator in mammary glands of experimental animal.

Attenzione

Cancer suspect agent.

Avvertenze

Danger

Indicazioni di pericolo

H302,H350,H410

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
E314499/1V
078K1153
083K2521
026K2509
314499/1

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Nuclear Fast Red

Sigma-Aldrich

N8002

Nuclear Fast Red

o-Dianisidine peroxidase substrate

Sigma-Aldrich

D9143

o-Dianisidine

p-Phenylenediamine 98% (GC)

Sigma-Aldrich

P6001

p-Phenylenediamine

Copper(II) acetate powder, 99.99% trace metals basis

Sigma-Aldrich

517453

Copper(II) acetate

K C Morton et al.
Carcinogenesis, 2(8), 747-752 (1981-01-01)
To evaluate the role of metabolism in benzidine (BZ) carcinogenesis, BZ and 2 or its metabolites, N,N'-diacetylbenzidine and N-hydroxy-N,N'-diacetylbenzidine (NOHDABZ), were given by i.p. injection to female CD rats twice weekly for 4 weeks beginning at 30 days of age.
Yan Cao et al.
Stem cells and development, 24(22), 2660-2673 (2015-07-17)
Autophagy is required for hematopoietic stem cell multilineage differentiation, but the underlying mechanism is unknown. Using a conditional mouse model and human leukemia cells, we uncovered a mechanistic link between autophagy and hematopoietic stem cell differentiation. Loss of autophagy in
Yan-Li Zhao et al.
Journal of the American Chemical Society, 132(37), 13016-13025 (2010-08-31)
The development of drug delivery systems for the targeted and on-demand release of pharmaceutical products has risen rapidly to become a contemporary challenge in the field of nanobiotechnology. Biocompatible mechanized phosphonate-clothed silica nanoparticles have been designed and fabricated in which
Lu Zhu et al.
Optics letters, 36(10), 1821-1823 (2011-05-20)
We have fabricated an organic deep ultraviolet photodetector (PD) using PEDOT:PSS (PH 1000) as a transparent anode. NPB and PBD were employed as electron donor and acceptor, respectively. The PD exhibits a dark current of 0.0829 μA/cm(2) and a photocurrent
Jungsun Park et al.
American journal of industrial medicine, 52(8), 625-632 (2009-06-30)
Many corporations move their manufacturing facilities or technologies from developed to developing countries. Stringent regulations have made it costly for industries to operate in developed, industrialized countries. In addition, labor costs are high in these countries, and there is increasing
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