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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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Ines Sherifi et al.
Scientific reports, 10(1), 14030-14030 (2020-08-21)
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)
Kantam, M. L. et al
Tetrahedron Letters, 44, 9029-9029 (2003)
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.
Pal, A. et al
Tetrahedron, 55, 4123-4123 (1999)
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