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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:
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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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)
o-Aminoazotoluene.
Report on carcinogens : carcinogen profiles, 10, 12-13 (2004-08-20)
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 Y Pakharukova et al.
Bulletin of experimental biology and medicine, 144(3), 338-341 (2008-05-07)
Selective increase of DNA-binding activity of constitutive androstane receptor was detected in rat and mouse liver in response to aminoazo dyes exhibiting hepatocarcinogenic activity for these species (ortho-aminoazotoluene for mice and 3'-methyl-4-dimethylaminobenzene for rats). Competition of azo dyes with 3H-5alpha-androst-16-ene-3alpha-ol

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