Chloramine B supplier | CasNO.127-52-6

Name
Chloramine B
EINECS 204-847-9
CAS No. 127-52-6
Article Data11
CAS DataBase
Density 0.8
Solubility water: 0.1 g/mL, clear
Melting Point 170oC
Formula C₆H₅ClNNaO₂S
Boiling Point 303.8 °C at 760 mmHg
Molecular Weight 213.62
Flash Point 137.6 °C
Transport Information UN 3263 8/PG 2
Appearance White crystalline powder
Safety 7-22-26-36/37/39-45
Risk Codes 22-31-34-42-2
Molecular Structure
Hazard Symbols C
Synonyms N-Chloro Benzenesulfonamide sodium salt
PSA 45.76000
LogP 2.37620

Synthetic route

: 98-10-2
benzenesulfonamide

: 127-52-6
chloramine-B

Conditions

Conditions	Yield
Stage #1: benzenesulfonamide With sodium hydroxide In water at 24.84℃; Stage #2: With chlorine at 64.84 - 69.84℃;	99%
With sodium hydroxide; chlorine at 70℃; for 1h;
With sodium hydroxide; chlorine at 70℃; for 1h;

: 98-10-2
benzenesulfonamide

: 473-29-0
N,N-Dichlorobenzenesulfonamide

: 127-52-6
chloramine-B

Conditions

Conditions	Yield
With sodium hydroxide; chlorine

: 105896-90-0
N-Phenylsulfonyl-p-toluolsulfenamid

: 127-52-6
chloramine-B

: N,N'-bis(phenylsulfonyl)-p-toluenesulfinimidamide

Conditions

Conditions	Yield
Stage #1: N-Phenylsulfonyl-p-toluolsulfenamid With sodium methylate In methanol Stage #2: chloramine-B In acetone for 0.25h;	100%

: 43136-32-9
N-phenylsulfonylbenzenesulfenamide

: 127-52-6
chloramine-B

: N,N'-bis(phenylsulfonyl)benzenesulfinimidamide

Conditions

Conditions	Yield
Stage #1: N-phenylsulfonylbenzenesulfenamide With sodium methylate In methanol Stage #2: chloramine-B In acetone for 0.25h;	100%

: 1202-36-4
diphenyl telluride

: 127-52-6
chloramine-B

: 71150-48-6
N-phenylsulfonyl-Te,Te-diphenyltellurimide

Conditions

Conditions	Yield
With 18-crown-6 ether In chloroform for 0.166667h; Heating;	96%

: 4456-34-2
bis(4-methoxyphenyl)telluride

: 127-52-6
chloramine-B

: 62486-36-6
N-(phenylsulfonyl)di(p-methoxyphenyl)tellurimide

Conditions

Conditions	Yield
With 18-crown-6 ether In chloroform for 0.166667h;	95%

: 281-15-2
9-thia-bicyclo[3.3.1]nonane

: 127-52-6
chloramine-B

: 9-thiabicyclo[3.3.1]nonane-N-phenylsulfonylsulfilimine

Conditions

Conditions	Yield
In acetonitrile at 20℃; for 16h;	95%

: 127-52-6
chloramine-B

: N-chloro-N-fluoro-benzenesulfonamide

Conditions

Conditions	Yield
With Selectfluor In water at 20℃; Reagent/catalyst;	95%
With Selectfluor In water at 30℃; for 12h;

: 875-30-9
1,3-dimethylindole

: 127-52-6
chloramine-B

: (E)-N-(3-chloro-1,3-dimethylindolin-2-ylidene)benzenesulfonamide

Conditions

Conditions	Yield
With acetic acid In acetonitrile at 0℃; for 0.5h;	94%
With iodine; potassium carbonate In acetonitrile at 20℃; for 12h;	71%

: 36062-30-3
N-p-tolylsulfonyl-1,4-naphthoquinone-4-imine

: 127-52-6
chloramine-B

: 85229-37-4
2-benzenesulfonamido-N-p-tolylsulfonyl-1,4-naphthoquinonemonoimine

Conditions

Conditions	Yield
In acetone for 1h;	92.8%

: 127-52-6
chloramine-B

: 41601-47-2
benzenesulfenamide

: 80960-55-0
C12H12N2O2S2

Conditions

Conditions	Yield
In acetone	92.8%

: 834-15-1
bis(p-tolyl)telluride

: 127-52-6
chloramine-B

: 107590-65-8
N-(phenylsulfonyl)di(p-methylphenyl)tellurimide

Conditions

Conditions	Yield
With 18-crown-6 ether In chloroform for 0.166667h;	92%

: 127-52-6
chloramine-B

: 41601-47-2
benzenesulfenamide

: N-phenylsulfonylbenzenesulfinimidamide

Conditions

Conditions	Yield
In acetone	92%

: 603-76-9
1-methylindole

: 127-52-6
chloramine-B

: (E)-N-(3,3-dichloro-1-methylindolin-2-ylidene)benzenesulfonamide

Conditions

Conditions	Yield
With acetic acid In acetonitrile at 0℃; for 0.5h; Solvent; Reagent/catalyst;	92%

: 6887-59-8
1-methylpyridine-4(1H)-thione

: 127-52-6
chloramine-B

: 126957-64-0
S-(1-Methyl-4-pyridyliden)-N-phenylsulfonylsulfimid

Conditions

Conditions	Yield
In ethanol; chloroform at 0℃; for 1.5h;	91%

: 3-isobutyl-1,2-dimethyl-1H-indole

: 127-52-6
chloramine-B

: (E)-N-((3-isobutyl-1-methyl-1H-indol-2-yl)methylene)benzenesulfonamide

Conditions

Conditions	Yield
With iodine In 1,4-dioxane at 20℃; for 11h; Green chemistry; regioselective reaction;	91%

: 9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole

: 127-52-6
chloramine-B

: N-(9-(4-methoxybenzyl)-2,3,4,9-tetrahydro-1H-carbazol-1-yl)benzenesulfonamide

Conditions

Conditions	Yield
With iodine In 1,4-dioxane at 20℃; for 9h; Green chemistry; regioselective reaction;	90%

: 71032-76-3
N-Acetylbenzenesulfenamide

: 127-52-6
chloramine-B

: 74448-83-2
N-Acetyl-N'-phenylsulfonylsulfinamidine

Conditions

Conditions	Yield
In acetone for 2h; Heating;	89%

: 127-52-6
chloramine-B

: 78972-22-2
methyl piperidinosulfenate

: 132151-51-0
S-Methoxy-S-piperidino-N-benzenesulfonyl sulfimide

Conditions

Conditions	Yield
In acetone for 2h; Heating;	89%

: 127-52-6
chloramine-B

: 158632-45-2
N-cyano-2-nitrobenzenesulfenamide

: 158632-37-2
N-cyano-N'-phenylsulfonyl-2-nitrobenzenesulfinamidine

Conditions

Conditions	Yield
In acetone	89%

: 51281-98-2
N-allyl-1,2,3,4-tetrahydrocarbazole

: 127-52-6
chloramine-B

: N-(9-allyl-2,3,4,9-tetrahydro-1H-carbazol-1-yl)benzenesulfonamide

Conditions

Conditions	Yield
With iodine In 1,4-dioxane at 20℃; for 9h; Green chemistry; regioselective reaction;	89%

: 83102-63-0
benzenesulfonyl-bis-(4-nitro-benzenesulfenyl)-amine

: 127-52-6
chloramine-B

: 83102-67-4
C24H18N4O8S4

Conditions

Conditions	Yield
In benzene for 2h; Ambient temperature;	88%

: 127-52-6
chloramine-B

: 54748-03-7
4-methyl-N,N'-bis(phenylsulfonyl)-1,2-benzoquinone diimine

: 93343-39-6
2-Methyl-5-benzenesulfonamido-N,N'-bis(phenylsulfonyl)-1,4-benzoquinone diimine

Conditions

Conditions	Yield
In acetone at 25℃; for 0.25h;	87%

: 127-52-6
chloramine-B

: 4-sulfono-1-phenyldiazonium tetrafluoroborate

: C12H10ClNO5S2

Conditions

Conditions	Yield
With copper(II) ion In water; acetone at 20 - 25℃; Substitution;	87%

: 17017-63-9
9-benzyl-2,3,4,9-tetrahydro-1H-carbazole

: 127-52-6
chloramine-B

: N-(9-benzyl-2,3,4,9-tetrahydro-1H-carbazol-1-yl)benzenesulfonamide

Conditions

Conditions	Yield
With iodine In 1,4-dioxane at 20℃; for 9h; Green chemistry; regioselective reaction;	87%
With iodine In 1,4-dioxane at 20℃; for 9h; Schlenk technique;	87%

: C15H19N

: 127-52-6
chloramine-B

: N-(6-ethyl-9-methyl-2,3,4,9-tetrahydro-1H-carbazol-1-yl)benzenesulfonamide

Conditions

Conditions	Yield
With iodine In 1,4-dioxane at 20℃; for 9h; Green chemistry; regioselective reaction;	87%

: C15H19N

: 127-52-6
chloramine-B

: N-(5,8,9-trimethyl-2,3,4,9-tetrahydro-1H-carbazol-1-yl)benzenesulfonamide

Conditions

Conditions	Yield
With iodine In 1,4-dioxane at 20℃; for 9h; Green chemistry; regioselective reaction;	87%

: 28195-12-2
1,3-Diphenyl-2-phenylthio-1,3-propandion

: 127-52-6
chloramine-B

: 82725-04-0
N-(1-Benzoyl-2-oxo-2-phenyl-1-phenylsulfanyl-ethyl)-benzenesulfonamide

Conditions

Conditions	Yield
In acetone for 4h; Ambient temperature;	86.2%

: 2044-27-1
1-methyl-2-pyridinethione

: 127-52-6
chloramine-B

: 126957-58-2
S-(1-Methyl-2-pyridyliden)-N-phenylsulfonylsulfimid

Conditions

Conditions	Yield
In ethanol; chloroform at -20℃; for 4h;	86%

: 127-52-6
chloramine-B

: 6522-21-0, 10502-30-4, 14965-28-7
endo,endo-2,6-Dichlor-9-thiabicyclo<3.3.1>nonan

: 2,6-dichloro-9-thiabicyclo[3.3.1]nonane-N-phenylsulfonylsulfilimine

Conditions

Conditions	Yield
In acetonitrile at 20℃; for 16h;	86%

: 127-52-6
chloramine-B

: 128742-76-7
methyl 1-methyl-1H-indole-5-carboxylate

: (E)-methyl 3,3-dichloro-1-methyl-2-((phenylsulfonyl)imino)indoline-5-carboxylate

Conditions

Conditions	Yield
With acetic acid In acetonitrile at 0℃; for 0.5h;	86%

Chloramine B Chemical Properties

CAS NO, 127-52-6.
EINECS NO. 204-847-9.
FORMULA:C₆H₅ClNO₂SNa.
MOL WT. 213.61

Chloramine B Uses

Sodium N-chlorobenzenesulfonamide(chloramine B),it can be used in wound irrigation as a substitute for chloramine B T.

Chloramine B Toxicity Data With Reference

SODIUM N-CHLOROBENZENESULFONAMIDE is a nontoxic antiseptic substance.

Chloramine B Safety Profile

Explodes when heated to 185°C. When heated to decomposition it emits toxic fumes of Cl⁻, SO_x, NO_x, and Na₂O.

Product Name

Chloramine B

Synthetic route

Chloramine B Chemical Properties

Chloramine B Uses

Chloramine B Toxicity Data With Reference

Chloramine B Safety Profile

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