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Key Documents

153591

Sigma-Aldrich

Diphenylcarbamoyl chloride

98%

Synonym(s):

Chloroformic acid diphenylamide, Diphenylcarbamic chloride, NSC 6788

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About This Item

Linear Formula:
(C6H5)2NCOCl
CAS Number:
Molecular Weight:
231.68
Beilstein:
515312
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

powder

solubility

organic solvents: soluble

functional group

amine

SMILES string

ClC(=O)N(c1ccccc1)c2ccccc2

InChI

1S/C13H10ClNO/c14-13(16)15(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H

InChI key

XNBKKRFABABBPM-UHFFFAOYSA-N

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Application

Diphenylcarbamoyl chloride was used to isolate peptido-keratan sulphate fragments from bovine intervertebral discs.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

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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J M Dickenson et al.
The Biochemical journal, 282 ( Pt 1), 267-271 (1992-02-15)
Peptido-keratan sulphate fragments were isolated from the nucleus pulposus of bovine intervertebral discs (2-year-old animals) after digestion with chondroitin ABC lyase followed by digestion with diphenylcarbamoyl chloride-treated trypsin of A1D1 proteoglycans and gel-permeation chromatography on Sepharose CL-6B. The peptido-keratan sulphate

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