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Merck
CN

857319

Chloramine-T hydrate

95%

Synonym(s):

N-Chloro-p-toluenesulfonamide sodium salt hydrate

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About This Item

Linear Formula:
CH3C6H4SO2N(Cl)Na · xH2O
CAS Number:
Molecular Weight:
227.64 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352002
EC Number:
204-854-7
MDL number:
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Product Name

Chloramine-T hydrate, 95%

InChI

1S/C7H7ClNO2S.Na.H2O/c1-6-2-4-7(5-3-6)12(10,11)9-8;;/h2-5H,1H3;;1H2/q-1;+1;

InChI key

BXSDMMPOQRECKB-UHFFFAOYSA-N

SMILES string

O.Cc1ccc(cc1)S(=O)(=O)N([Na])Cl

assay

95%

form

solid

reaction suitability

reagent type: oxidant

mp

167-170 °C (dec.) (lit.)

Quality Level

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Application

A review.
Capable of oxidative cyclization to produce various heterocycles.
Nitrene source for aziridinations and aminohydroxylations.
Reactant for:
  • Preparation of factor Xa inhibitors as novel anticoagulants

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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Ines Sherifi et al.
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Tissue-engineered grafts may be useful in Anterior Cruciate Ligament (ACL) repair and provide a novel, alternative treatment to clinical complications of rupture, harvest site morbidity and biocompatibility associated with autografts, allografts and synthetic grafts. We successfully used supercritical carbon dioxide
J. Sci. Ind. Res., 49, 13-13 (1990)
Li, G. et al
Angewandte Chemie (International Edition in English), 35, 451-451 (1996)
Jeong, J. U. et al
Journal of the American Chemical Society, 120, 6844-6844 (1998)
Brandt, P. et al
Journal of the American Chemical Society, 122, 8013-8020 (2000)

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