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N-Acetylsulfanilyl chloride

N-Acetylsulfanilyl chloride Structure
CAS No.
121-60-8
Chemical Name:
N-Acetylsulfanilyl chloride
Synonyms
ASC;4-ACETAMIDOBENZENESULFONYL CHLORIDE;NASC;Acetylsulfanilyl chloride;CARD5;NSC 127860;dagenanchloride;acetylsulfanilyl;Dagenan chloride;N-Acetylsulfanilyl
CBNumber:
CB4452614
Molecular Formula:
C8H8ClNO3S
Molecular Weight:
233.67
MOL File:
121-60-8.mol
MSDS File:
SDS
Modify Date:
2024/6/4 19:18:49

N-Acetylsulfanilyl chloride Properties

Melting point 142-145 °C (dec.)(lit.)
Boiling point 426.8±28.0 °C(Predicted)
Density 1.2977 (rough estimate)
vapor pressure 0Pa at 25℃
refractive index 1.6300 (estimate)
storage temp. Sealed in dry,2-8°C
solubility Acetonitrile (Slightly), Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pka 13.75±0.70(Predicted)
form Granular Crystalline Powder or Crystals
color White to cream-beige
Water Solubility SLIGHTLY SOLUBLE
Sensitive Moisture Sensitive
Merck 14,103
BRN 746676
LogP 2.05 at 25℃
CAS DataBase Reference 121-60-8(CAS DataBase Reference)
NIST Chemistry Reference P-acetamidobenzene sulfonyl chloride(121-60-8)
EPA Substance Registry System Benzenesulfonyl chloride, 4-(acetylamino)- (121-60-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05,GHS07
Signal word  Danger
Hazard statements  H314-H335
Precautionary statements  P260-P271-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  C
Risk Statements  22-34-37
Safety Statements  26-36/37/39-45-28B
RIDADR  UN 3261 8/PG 2
WGK Germany  3
RTECS  DB8837500
9-21
TSCA  Yes
HazardClass  8
PackingGroup  II
HS Code  29242995
Toxicity LD50 oral in rat: > 3200mg/kg
NFPA 704
0
3 0

N-Acetylsulfanilyl chloride price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 112747 N-Acetylsulfanilyl chloride 98% 121-60-8 100G ₹1894.38 2022-06-14 Buy
Sigma-Aldrich(India) 112747 N-Acetylsulfanilyl chloride 98% 121-60-8 1KG ₹10825 2022-06-14 Buy
TCI Chemicals (India) A0074 4-Acetamidobenzenesulfonyl Chloride 121-60-8 25G ₹8600 2022-05-26 Buy
Product number Packaging Price Buy
112747 100G ₹1894.38 Buy
112747 1KG ₹10825 Buy
A0074 25G ₹8600 Buy

N-Acetylsulfanilyl chloride Chemical Properties,Uses,Production

Chemical Properties

OFF-WHITE TO SLIGHTLY GREY GRANULAR CRYST. POWDER

Uses

N-Acetylsulfanilyl chloride is used?in the preparation of sulfanilamide and its derivatives which are intermediates to produce sulfa drugs. They are used in the prevention and treatment of bacterial infections, diabetes mellitus, edema, hypertension, and gout. It is also used as a Pharma raw material. N-Acetylsulfanilyl chloride widely used in the fields of dye, medicine, mainly used for preparation of Sulfanilamide, Sulfanilylureal, Sulfatolamide, Sulphathiourea , Sulfaguanidine and Sulfacetamide and etc.

Production Methods

Acetanilide is introduced into stirred chlorosulfuric acid solution at 20 ℃. The solution is then heated to 55 ℃ and kept at this temperature for 1.5 h. The solution is cooled to 20 ℃ and introduced as a thin jet into water, the temperature of which is kept at 0 – 5 ℃ by external cooling. The precipitated sulfochloride is filtered and washed with cold water until neutral to Congo Red. Yield is 80 – 82%. The crude product contains about 60% water; the dried product melts at 144 – 147 ℃. About 1 – 2% of bis(acetylaminophenyl) sulfone is obtained as a byproduct. If thionyl chloride is added, less chlorosulfuric acid is needed because it can be replaced partly byoleum. The product is stable for several days if kept in a cool place. It is generally used directly in the moist state. 4-(Acetylamino)benzenesulfonyl chloride is an important intermediate in the manufacture of sulfonamides and in the synthesis of parabase ester.

General Description

L-hydroxyproline has been derivatized with N-acetylsulfanilyl chloride and 5-chlorovaleric acid during the synthesis of the haptens HP1 and HP2.

Safety Profile

A poison by intraperitoneal route.Moderately toxic by ingestion. When heated todecomposition it emits toxic vapors of NOx, SOx, and Cl.

Purification Methods

Crystallise the chloride from toluene, CHCl3, or ethylene dichloride. [Beilstein 14 IV 2703.]

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4-ACETYLAMINO BENZENESULFONYL CHLORIDE 4-ACETAMIDOPHENYLSULFONYL CHLORIDE 4-ACETAMIDOBENZENESULPHONYL CHLORIDE -(acetylamino)benzenesulfonylchloride 4-(acetylamino)-benzenesulfonylchlorid 4'-(Chlorosulfonyl)acetanilide 4’-(chlorosulfonyl)acetanilide 4-acetamido-benzenesulfonicacichloride 4-Acetamido-benzoylsulfochloride 4-acetaminobenzenesulfochloride 4-Acetylamino-benzensulfonylchlorid 4-chlorosulfonylacetanilide P-ACETAMINOBENZENESULFONYL CHLORIDE P-ACETYL AMINOBENZENE SULFONYL CHLORIDE P-ACETAMIDOBENZENESULFONYLCHLORIDE N-ACETYLSULFANILIC ACID CHLORIDE N-ACETYLSULFANILYL CHLORIDE N-ACETYLSULPHANILYL CHLORIDE Acetanilide-p-sulfonyl chloride acetanilide-p-sulfonylchloride n-acetyl-sulfanilylchlorid 4-AcetamidobenzenesulphonylChloride98% 4-Acetamidobenzenesulfonyl chloride, 98+% p-(chlorosulfonyl)acetanilide p-Acetamidophenylsulfonyl chloride p-acetamidophenylsulfonylchloride p-Acetaminobenzenesulfonechloride p-Acetylaminobenzenesulfochloride Sulfanilyl chloride, N-acetyl- 4-Acetamidobenzenesulfonyl chloride for synthesis acetylsulfanilyl acetylsulfanilylchloride Benzenesulfonyl chloride, 4-(acetylamino)- Benzenesulfonylchloride,4-(acetylamino-)- Dagenan chloride dagenanchloride n(4)-acetylsulfanilylchloride n(sup4)-acetylsulfanilylchloride N4-Acetylsulfanilyl chloride 4-Acetamidobenzenesulphonyl Chloride 98% 4-ACETYLSULFANILYL CHLORIDE P-ACETAMIDOBENZENE SULFONYL CHLORIDE ASC 4-(ACETYLAMINO)-BENZENESULPHONYLCHLORIDE ACETYLSULPHANILYLCHLORIDE PARA-ACETYLAMINOBENZENESULPHONYLCHLORIDE Anti-ASC, N-Terminal antibody produced in rabbit apoptosis-associated speck-like protein containing a CARD CARD5 caspase recruitment domain protein 5 N-Acetylsulfanilyl chloride, 98+% N-Acetylsulfanilyl 4-Acetaminobenzenesulfonyl chloride N-Acetylsulfanilyl chloride,99% N-Acetylsulfanilyl c 4-Acetylaminobenzenesulfonic acid chloride N-Acetylsulfanilyl chloride, 99% 100GR 4-(AcetylaMino)benzene-2,3,5,6-sulfonyl Chloride 4-(AcetylaMino)phenylsulfonyl Chloride