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121568

Sigma-Aldrich

Fast Garnet GBC base

97%

Synonym(s):

o-Aminoazotoluene, 4′-Amino-2,3′-dimethylazobenzene, Solvent Yellow 3

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About This Item

Linear Formula:
CH3C6H4N=NC6H3(CH3)NH2
CAS Number:
Molecular Weight:
225.29
Colour Index Number:
11160
Beilstein/REAXYS Number:
6506005
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

Quality Level

assay

97%

form

powder

mp

101-102 °C (lit.)

solubility

ethanol: 10 mg/mL, clear

λmax

491 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

Cc1ccccc1\N=N\c2ccc(N)c(C)c2

InChI

1S/C14H15N3/c1-10-5-3-4-6-14(10)17-16-12-7-8-13(15)11(2)9-12/h3-9H,15H2,1-2H3/b17-16+

InChI key

PFRYFZZSECNQOL-WUKNDPDISA-N

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Application

Fast Garnet GBC base has been used:
  • as a stain in papain activity inhibition assay.
  • to stain for tryptase-activity and chymase-like activity.
  • to gel stain for esterolytic activity.

pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

6.1D - Non-combustible, acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Histochemical and morphological characteristics of canine cardiac mast cells.
Frangogiannis NG
The Histochemical Journal, 31(4), 221-229 (1999)
Proteinase C (Carboxypeptidase Y) Mutant of Yeast
Wolf D H and Fink G R
Journal of Bacteriology, 123, 1150-1156 (1975)
Characterization of Active Components in Food-Grade Proteinase Inhibitors for Surimi Manufacture
Weerasinghe V C
Journal of Agricultural and Food Chemistry, 44(9), 2584-2590 (1996)
M Yu Pakharukova et al.
Bulletin of experimental biology and medicine, 152(1), 101-104 (2012-07-18)
Transcription factors of the FoxA family (forkhead box A) regulate cell metabolism and differentiation and maintain specificity of liver cell proteome and phenotype of mature hepatocytes. The relationship between hepatocarcinogenicity of azo compounds o-aminoazotoluene (OAT) and 3'-methyl-4-dimethylaminobenzene (3'MeDAB) for GR
A V Eremeev et al.
Tsitologiia, 46(4), 301-311 (2004-09-07)
A most convenient model to study mechanisms of live organism response to chemical carcinogens is tumor induction in murine liver by aminoazodyes, in particular by ortho-aminoazotoluene (OAT). We studied both early and late stages of hepatocarcinogenesis on several lines of

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