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Merck

317802

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

97%

Synonym(s):

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

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About This Item

Linear Formula:
SCNC6H4N=NC6H4N(CH3)2
CAS Number:
7612-98-8
Molecular Weight:
282.36
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
24859100
EC Number:
231-521-3
Beilstein/REAXYS Number:
752568
MDL number:
MFCD00004812

Key Documents

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InChI key

OSWZKAVBSQAVFI-ISLYRVAYSA-N

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+

SMILES string

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

assay

97%

form

crystals

mp

167-171 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Related Categories

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H317,H334

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificates of Analysis (COA)

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

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R Aebersold et al.
Analytical biochemistry, 136(2), 465-469 (1984-02-01)
Proteins and polypeptides are derivatized with dimethylaminoazobenzene isothiocyanate (DABITC) before their separation on sodium dodecyl sulfate-polyacrylamide gels. DABITC-derivatized proteins are detected visually in the picomole range without further staining and destaining procedures. The recovered colored protein can also be used
A S Babu et al.
Toxicon : official journal of the International Society on Toxinology, 29(10), 1251-1262 (1991-01-01)
The effects of chemical modification with 4-NN-dimethyl amino azo benzene-4'-isothiocyanate on various biological activities of phospholipases A2, NN-XIII-PLA2 from Naja naja naja and VRV-PL-VIIIa from Vipera russelli snake venoms were investigated. Modification of the enzymes resulted in significant reduction of
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
P Mellet et al.
Biochemistry, 34(8), 2645-2652 (1995-02-28)
Heparin accelerates the inhibition of neutrophil elastase by mucus proteinase inhibitor (MPI), the physiological antielastase of airways as a result of its binding with the inhibitor [Faller, B., Mély, Y., Gérard, D., & Bieth, J. G. (1992) Biochemistry 31, 8285-8290].
F J Colilla et al.
Journal of chromatography, 548(1-2), 303-310 (1991-07-12)
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 digests were derivatized with phenyl isothiocyanate to form the phenylthiocarbamyl peptides followed by reversed-phase high-performance liquid chromatographic
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