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Documentos

317802

Sigma-Aldrich

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

97%

Sinônimo(s):

4-(Dimethylamino)azobenzene-4′-isothiocyanate, DABITC

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About This Item

Fórmula linear:
SCNC6H4N=NC6H4N(CH3)2
Número CAS:
7612-98-8
Peso molecular:
282.36
Beilstein:
752568
Número CE:
231-521-3
Número MDL:
MFCD00004812
Código UNSPSC:
12171500
ID de substância PubChem:
24859100
NACRES:
NA.47

Ensaio

97%

forma

crystals

pf

167-171 °C (lit.)

aplicação(ões)

diagnostic assay manufacturing
hematology
histology

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

CN(C)c1ccc(cc1)\N=N\c2ccc(cc2)N=C=S

InChI

1S/C15H14N4S/c1-19(2)15-9-7-14(8-10-15)18-17-13-5-3-12(4-6-13)16-11-20/h3-10H,1-2H3/b18-17+

chave InChI

OSWZKAVBSQAVFI-ISLYRVAYSA-N

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Categorias relacionadas

Pictogramas

Health hazard
GHS08

Palavra indicadora

Danger

Frases de perigo

H317,H334

Classificações de perigo

Resp. Sens. 1 - Skin Sens. 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
MKBC7832
14127JI
12029JC
09630CC
06912HO

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Dabcyl-OSu Novabiochem®

Sigma-Aldrich

8.51022

Dabcyl-OSu

4-Aminoazobenzene analytical standard

Supelco

46130

4-Aminoazobenzene

4-(Dimethylamino)azobenzene-4′-sulfonyl chloride ≥97.5% (AT)

Sigma-Aldrich

39068

4-(Dimethylamino)azobenzene-4′-sulfonyl chloride

J Hempel et al.
FEBS letters, 194(2), 333-337 (1986-01-06)
A synthetic peptide analog, with one peptide carbonyl group replaced by a methylene bridge, was submitted to structural analysis by Edman degradation. Multiple cleavages were obtained in the first cycle, due to phenylthiocarbamylation of the internal secondary amine as well
Evidence for the formation of a novel glutathione conjugate in the metabolism of an aromatic amine derivative.
D H Hutson et al.
Drug metabolism and disposition: the biological fate of chemicals, 12(4), 523-524 (1984-07-01)
E Kinoshita et al.
Bioscience, biotechnology, and biochemistry, 62(8), 1488-1491 (1998-10-03)
An easy and highly sensitive method for measuring histamine by HPLC analysis coupled with precolumn derivatization was established. The amino group of histamine was completely colorimetrically labelled with 4-N,N-dimethylamino-azobenzene-4'-isothiocyanate (DABITC) in the presence of sodium bicarbonate at 90 degrees C
P P Nair et al.
Steroids, 59(3), 212-216 (1994-03-01)
N-epsilon-lithocholyl lysine (NELL) is a component of tissue-bound lithocholic acid (TBL). The isolation of NELL from native protein sources was simulated by hydrolysis of lithocholyl-bovine serum albumin (BSA) (synthesized by coupling lithocholyl-N-hydroxysuccinimide to fatty acid-free BSA) by digestion with a
P M Fischer et al.
Analytical biochemistry, 177(1), 46-49 (1989-02-15)
A single-column high-performance liquid chromatographic separation of 4-N,N-dimethylaminoazobenzene 4'-thiohydantoin amino acid derivatives, generated during polypeptide sequence analysis by the 4-N,N-dimethylaminoazobenzene 4'-isothiocyanate/phenylisothiocyanate double coupling technique, is described. Recovery of the serine and threonine derivatives was improved by substituting boron trifluoride-diethyl etherate
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