4-(4-Isothiocyanatophenylazo)-N,N-dimethylaniline
Names
[ CAS No. ]:
7612-98-8
[ Name ]:
4-(4-Isothiocyanatophenylazo)-N,N-dimethylaniline
[Synonym ]:
4-((4-Isothiocyanatophenyl)azo)-N,N-dimethylaniline
4-[(4-isothiocyanatophenyl)diazenyl]-N,N-dimethylaniline
Benzenamine, 4-[(E)-2-(4-isothiocyanatophenyl)diazenyl]-N,N-dimethyl-
EINECS 231-521-3
MFCD00004812
4-[(E)-(4-Isothiocyanatophenyl)diazenyl]-N,N-dimethylaniline
Biological Activity
[Description]:
[Related Catalog]:
[References]
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
466.2±30.0 °C at 760 mmHg
[ Melting Point ]:
167-171 °C(lit.)
[ Molecular Formula ]:
C15H14N4S
[ Molecular Weight ]:
282.363
[ Flash Point ]:
235.7±24.6 °C
[ Exact Mass ]:
282.093903
[ PSA ]:
72.41000
[ LogP ]:
5.95
[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C
[ Index of Refraction ]:
1.613
[ Water Solubility ]:
dioxane: 20 mg/mL, clear, red
MSDS
Safety Information
[ Symbol ]:
GHS08
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H317-H334
[ Precautionary Statements ]:
P261-P280-P342 + P311
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Faceshields;Gloves
[ Hazard Codes ]:
Xn
[ Risk Phrases ]:
42
[ Safety Phrases ]:
S22-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ RTECS ]:
NX9125000
[ HS Code ]:
2930909090
Customs
[ HS Code ]: 2930909090
[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
Biochem. J. 211(1) , 173-80, (1983)
The first complete sequence of the variable region of a kappa-light chain (V kappa) from a mouse anti-(streptococcal group A polysaccharide) antibody (immunoglobulin 7S34.1) is reported. Immunoglobuli...
Peptide maps at picomolar levels obtained by reversed-phase high-performance liquid chromatography and pre-column derivatization with phenyl isothiocyanate. Microsequencing of Phenylthiocarbamyl Peptides.J. Chromatogr. A. 548(1-2) , 303-10, (1991)
A new reversed-phase high-performance liquid chromatography approach to the production of analytical peptide maps by pre-column derivatization using phenylisothiocyanate is described. Tryptic peptide ...
Evidence for the formation of a novel glutathione conjugate in the metabolism of an aromatic amine derivative.Drug Metab. Dispos. 12(4) , 523-4, (1984)