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Sigma-Aldrich

N-Chlorobenzenesulfonamide sodium salt

~28% active chlorine basis

Synonym(s):

Benzene chloramine, Chloramine B, Sodium (phenylsulfonyl)chloramide

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About This Item

Linear Formula:
C6H5SO2NClNa · aq
CAS Number:
Molecular Weight:
213.62 (anhydrous basis)
Beilstein:
3599287
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22

form

solid

reaction suitability

reagent type: oxidant

concentration

~28% (active chlorine)

SMILES string

O.[Na]N(Cl)S(=O)(=O)c1ccccc1

InChI

1S/C6H5ClNO2S.Na.H2O/c7-8-11(9,10)6-4-2-1-3-5-6;;/h1-5H;;1H2/q-1;+1;

InChI key

YVICIJMKLANTNN-UHFFFAOYSA-N

Application

Used in investigations of the toxicity response of electroactive microbial biofilms

Catalyst for rearrangement of aziridinofullerenes to azafulleroids

Oxidizing agent for polymerization of thiophenol, synthesis of o-aminobenzenesulfonic acids and ciproflaxin

Decontaminant for mustard

Other Notes

Review

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Resp. Sens. 1 - Skin Corr. 1B

Supplementary Hazards

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

Certificates of Analysis (COA)

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E George et al.
Acta crystallographica. Section C, Crystal structure communications, 56 ( Pt 10), 1208-1209 (2000-10-12)
In the title compound, sodium N-chlorobenzenesulfonamide sesquihydrate, Na(+).C(6)H(5)ClNO(2)S(-).1.5H(2)O, the sodium ion exhibits octahedral coordination by O atoms from three water molecules and by three sulfonyl O atoms of three different N-chlorobenzenesulfonamide anions. A two-dimensional polymeric layer consists of units, each
[Chemical method of sterilizing plastic bacteriological dishes].
B E Bilich et al.
Laboratornoe delo, (3)(3), 176-178 (1984-01-01)
G V Lobacheva et al.
Kosmicheskaia biologiia i aviakosmicheskaia meditsina, 19(1), 70-72 (1985-01-01)
The comparative toxicity of halogen-containing oxidizing agents was investigated with the purpose of their utilization as urine preservatives in water reclamation systems. It was found that the high toxicity of the agents (LD50 of agent 1 was 15.7 +/- 1.1
O Hlavácek et al.
Epidemiologie, mikrobiologie, imunologie : casopis Spolecnosti pro epidemiologii a mikrobiologii Ceske lekarske spolecnosti J.E. Purkyne, 47(4), 150-153 (1999-01-27)
The sporicidal effect of Presept was compared with Chloramine B on the spores of Bacillus cereus. Either compound was calibrated to the same concentration of active chlorine. While a portion of spore population after 4 hrs of treatment by Chloramine
[Comparative sensitivity of microorganisms to monochloramine B].
T B Krucheniuk
Gigiena i sanitariia, (6)(6), 75-77 (1985-06-01)

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