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N-Isopropylbenzenesulfonamide

CAS No.
5339-69-5
Chemical Name:
N-Isopropylbenzenesulfonamide
Synonyms
N-Isopropylbenzenesulfonamide;N-propan-2-ylbenzenesulfonamide;N-(1-Methylethyl)benzenesulfonamide;Benzenesulfonamide, N-(1-methylethyl)-
CBNumber:
CB02415453
Molecular Formula:
C9H13NO2S
Molecular Weight:
199.27
MDL Number:
MOL File:
5339-69-5.mol
MSDS File:
SDS
Last updated:2026-05-27 17:23:42

N-Isopropylbenzenesulfonamide Properties

storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Oil
color Colourless

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P501-P270-P264-P301+P312+P330
HS Code  2935909099

N-Isopropylbenzenesulfonamide price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC TRC-I874673-50MG N-Isopropylbenzenesulfonamide 5339-69-5 50mg $59 2026-06-03 Buy
TRC TRC-I874673-500MG N-Isopropylbenzenesulfonamide 5339-69-5 500mg $256 2026-06-03 Buy
TRC TRC-I874673-100MG N-Isopropylbenzenesulfonamide 5339-69-5 100mg $78 2026-06-03 Buy
Apolloscientific OR958001 N-Isopropylbenzenesulfonamide 98% 5339-69-5 250mg $47 2026-06-04 Buy
Apolloscientific OR958001 N-Isopropylbenzenesulfonamide 98% 5339-69-5 1g $56 2026-06-04 Buy
Product number Packaging Price Buy
TRC-I874673-50MG 50mg $59 Buy
TRC-I874673-500MG 500mg $256 Buy
TRC-I874673-100MG 100mg $78 Buy
OR958001 250mg $47 Buy
OR958001 1g $56 Buy

N-Isopropylbenzenesulfonamide Chemical Properties, Uses, Production

Uses

N-Isopropylbenzenesulfonamide can be used to treat hypertension.

Synthesis

Benzenesulfonamide

98-10-2

Isopropyl alcohol

67-63-0

N-Isopropylbenzenesulfonamide

5339-69-5

GENERAL METHOD: Benzenesulfonamide (2 mmol) was dissolved with isopropanol (10 mmol) in 1,4-dioxane (3 mL), followed by the addition of trifluoromethanesulfonic anhydride (Tf2O, 2 mmol). The reaction mixture was sealed and the reaction was stirred at 120 °C until thin layer chromatography (TLC) monitoring showed that the reaction was complete. After completion of the reaction, the reaction was quenched with saturated aqueous sodium bicarbonate (NaHCO3). The reaction mixture was extracted three times with ethyl acetate (EtOAc) and the organic phases were combined and dried with anhydrous sodium sulfate (Na2SO4). After concentration under reduced pressure to remove the solvent, the residue was purified by fast column chromatography using petroleum ether (PE) and ethyl acetate (EtOAc) (3:1, v/v/v) as eluents to give pure N-isopropylbenzenesulfonamide (IBSA).

References

[1] Bulletin of the Chemical Society of Japan, 2015, vol. 88, # 4, p. 610 - 612

N-Isopropylbenzenesulfonamide Preparation Products And Raw materials

N-Isopropylbenzenesulfonamide Suppliers

Global Suppliers ( 37)
Supplier Tel Email Country ProdList Advantage
HBCChem, Inc. +1-510-219-6317 sales@hbcchem.com United States 10628 60
Zhengzhou kangnuochenrui Chemical Technology Co.,Ltd 18210788515; 18210788515 zhuzixin999@163.c0m China 4999 55
Zhengzhou Alfachem Co., Ltd. 0371-53765687 18937137882 3969243885@qq.com China 7734 55
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
Amadis Chemical Company Limited 571-89925085 sales@amadischem.com China 131885 58
Yantai ShengKailun Chemical Technology Co., Ltd. 13356901049 3119594100@qq.com China 7964 55
Dalian lichuang Chemical Co., Ltd 0411-0411-00000000 13644282108 3500508746@qq.com China 2942 55
Aikon International Limited 025-66061636 19370895928 qqyang@aikonchem.com China 15810 58
Tianjin heowns Biochemical Technology Co., Ltd. 400-6387771-6039 18920764717 sales@heowns.com China 24636 60
Shanghai Jizhi Biochemical Technology Co. Ltd. 021-4009004166/18616739031 18616739031 3007523370@qq.com China 40000 58

N-Isopropylbenzenesulfonamide Spectrum

N-Isopropylbenzenesulfonamide Benzenesulfonamide, N-(1-methylethyl)- N-propan-2-ylbenzenesulfonamide N-(1-Methylethyl)benzenesulfonamide 5339-69-5