4-(4-Isothiocyanatophenylazo)-N,N-dimethylaniline

Modify Date: 2024-01-02 00:17:01

4-(4-Isothiocyanatophenylazo)-N,N-dimethylaniline structure	Common Name	4-(4-Isothiocyanatophenylazo)-N,N-dimethylaniline
	CAS Number	7612-98-8	Molecular Weight	282.363
	Density	1.1±0.1 g/cm3	Boiling Point	466.2±30.0 °C at 760 mmHg
	Molecular Formula	C₁₅H₁₄N₄S	Melting Point	167-171 °C(lit.)
	MSDS	Chinese USA	Flash Point	235.7±24.6 °C
	Symbol	GHS08	Signal Word	Danger

Use of 4-(4-Isothiocyanatophenylazo)-N,N-dimethylaniline

4-(N,N-Dimethylamino)azobenzene-4'-isothiocyanate is a chromophoric, hydrophobic reagent for probing membrane-buried segments of intrinsic proteins[1].

Name	4-(n,n-dimethylamino)azobenzene-4'-isothiocyanate
Synonym	More Synonyms

Description	4-(N,N-Dimethylamino)azobenzene-4'-isothiocyanate is a chromophoric, hydrophobic reagent for probing membrane-buried segments of intrinsic proteins[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Kempf C, et al. 4-N-N-dimethylamino-azobenzene-4'-isothiocyanate: a chromophoric, hydrophobic reagent for probing membrane-buried segments of intrinsic proteins. FEBS Lett. 1981 Feb 23;124(2):225-8.

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(Chinese)

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

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%

A new isotype sequence (V kappa 27) of the variable region of kappa-light chains from a mouse hybridoma-derived anti-(streptococcal group A polysaccharide) antibody containing an additional cysteine residue. Application of the dimethylaminoazobenzene isothiocyanate technique for the isolation of peptides.

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)