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Benzenesulfonamide, 4-(aminomethyl)-, hydrochloride (1:1)

Benzenesulfonamide, 4-(aminomethyl)-, hydrochloride (1:1) structure

Benzenesulfonamide, 4-(aminomethyl)-, hydrochloride (1:1) 

structure
  • CAS No:

    138-37-4

  • Formula:

    C7H10N2O2S.ClH

  • Chemical Name:

    Benzenesulfonamide, 4-(aminomethyl)-, hydrochloride (1:1)

  • Synonyms:

    Benzenesulfonamide,4-(aminomethyl)-,hydrochloride (1:1);p-Toluenesulfonamide,α-amino-,monohydrochloride;Benzenesulfonamide,4-(aminomethyl)-,monohydrochloride;p-Toluenesulfonamide,α-amino-,hydrochloride;p-(Aminomethyl)benzenesulfonamide hydrochloride;p-Aminomethylphenylsulfonamide hydrochloride;α-Amino-p-toluenesulfonamide hydrochloride;4-Homosulfanilamide hydrochloride;Mafenide hydrochloride;Sulfamylon hydrochloride;Homosulfamine;Marfanil;Homosulfanilamide hydrochloride;Homosulfamine hydrochloride;p-(Aminomethyl)benzenesulfonamide monohydrochloride;4-(Aminomethyl)benzene sulfonamide monohydrochloride;4-Aminosulfonylbenzylamine hydrochloride;(4-Sulfamoylphenyl)methanaminium chloride

  • Categories:

    Cosmetic Ingredient  >  Antimicrobials

Description

Mafenide hydrochloride is a sulfonamide-type medication used as an antibiotic.Target: AntibacterialMafenide is a sulfonamide-type medication. Mafenide works by reducing the bacterial population present in the avascular tissues of burns and permits spontaneous healing of deep partial-thickness burns. It is used to treat severe burns. It is used topically as an adjunctive therapy for second- and third-degree burns. It is bacteriostatic against many gram-positive and gram-negative organisms

Benzenesulfonamide, 4-(aminomethyl)-, hydrochloride (1:1) Basic Attributes

222.69

222.022980

205-325-3

2935009090

Characteristics

94.6

256 °C

184.8ºC

Safety Information

NONH for all modes of transport

2

42/43

22-36/37-45

XT5425000

Xn

P280

H317

Benzenesulfonamide, 4-(aminomethyl)-, hydrochloride (1:1) Use and Manufacturing

Methods of Manufacturing

General procedure: A 1.0 M solution of 4-aminobenzenesulfanilamide (17.2 g, 0.1 mol, 1.0 equiv) in acetone (100 ml) was added dropwise to a vigorously stirred suspension of cyanuric chloride (18.4 g, 1.0 equiv) in the same solvent (100 ml) at 0 C. The white slurry was stirred at the same temperature for 30 min. and then a 1.7 M aqueous solution of NaOH (4.0 g, 1.0 equiv) was added over a period of 20 min. Stirring was continued for 1 h, the reaction was quenched by addition of slush (100 ml) and the solid filtered off.

Uses

Antibacterial;Inhibitor of folic acid biosynthesis

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