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857319

Sigma-Aldrich

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:
149358-73-6
Molecular Weight:
227.64 (anhydrous basis)
EC Number:
204-854-7
MDL number:
MFCD00149065
UNSPSC Code:
12352002
PubChem Substance ID:
24888439
NACRES:
NA.22

Quality Level

100

Assay

95%

form

solid

reaction suitability

reagent type: oxidant

mp

167-170 °C (dec.) (lit.)

SMILES string

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

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

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Application

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

Signal Word

Danger

Hazard Statements

H302,H314,H334,H411

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Jong Deok Na et al.
Food & function, 10(2), 1225-1234 (2019-02-13)
Betaine is a methyl donor utilized in regeneration of methionine from homocysteine in a metabolic reaction catalyzed by betaine-homocysteine methyltransferase (BHMT), an enzyme mostly localized in the liver. However, we recently showed that the metabolism of sulfur-containing amino acids in
Silica-water reaction media: its application to the formation and ring opening of aziridines.
Satoshi Minakata et al.
Angewandte Chemie (International ed. in English), 43(1), 79-81 (2003-12-25)
Kano, D. et al
Journal of the Chemical Society. Perkin Transactions 1, 3186-3186 (2001)
J. Sci. Ind. Res., 49, 13-13 (1990)
G D Kishore Kumar et al.
Chemical communications (Cambridge, England), (8), 1026-1027 (2004-04-08)
Environmentally benign HPA is found to be an efficient catalyst for aziridination of olefins in the presence of inexpensive Chloramine-T as a nitrogen source: instantaneous at room temperature, requires only stoichiometric amount of olefin and no allyl amine side product.
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