Sulfamethoxazole

Name: Sulfamethoxazole
SKU: 02156711-CF

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SKU: 02156711-CF

Key features and details

Sulfamethoxazole

Synonyms

4-Amino-N-(5-methyl-3-isoxazolyl)benzenesulfonamide; N1-(5-Methylisoxazol-3-yl)sulfanilamide; 5-Methyl-3-sulfanilamidoisoxazole; 3-Sulfanilamido-5-methylisoxazole; 3-(p-Aminophenylsulfonamido)-5-methylisoxazole; Sulfisomezole; Sulfamethylisoxazole; Sulfamethoxizole

CAS Number:

723-46-6

Molecular Formula:

C10H11N3O3S

Molecular Weight:

253.276 g/mol

Beilstein Registry Number:

6732984

EC Number:

211-963-3

MDL Number:

MFCD00010546

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Product Description

Sulfamethoxazole

Application Notes

Sulfamethoxazole is used for treating various types of bacterial infections, including urinary tract infections, acute worsening of chronic bronchitis, and ear infections. In addition it can be used as an alternative to amoxicillin-based antibiotics to treat sinusitis.

Usage Statement

Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.

Key Applications

Antibiotic

Specifications

SKU	02156711-CF
Alternate Names	4-Amino-N-(5-methyl-3-isoxazolyl)benzenesulfonamide; N1-(5-Methylisoxazol-3-yl)sulfanilamide; 5-Methyl-3-sulfanilamidoisoxazole; 3-Sulfanilamido-5-methylisoxazole; 3-(p-Aminophenylsulfonamido)-5-methylisoxazole; Sulfisomezole; Sulfamethylisoxazole; Sulfamethoxizole
Applications	Antibiotic
Application Notes	Sulfamethoxazole is used for treating various types of bacterial infections, including urinary tract infections, acute worsening of chronic bronchitis, and ear infections. In addition it can be used as an alternative to amoxicillin-based antibiotics to treat sinusitis.
Base Catalog Number	156711
Beilstein Registry Number	6732984
Biochemical Physiological Actions	Sulfonamide antibiotic that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Mode of Action: Inhibits folic acid synthesis in prokaryotes. Anti-microbial Spectrum: Gram positive, Gram negative, Chlamydia. Mode of Resistance: Alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis.
CAS #	723-46-6
EC Number	211-963-3
Format	Powder
Hazard Statements	H315-H317-H319-H335
Melting Point	333° F (NTP, 1992)
Molecular Formula	C10H11N3O3S
Molecular Weight	253.276 g/mol
Personal Protective Equipment	Dust mask, Eyeshields, Faceshields, Gloves
RTECS Number	WP0700000
Safety Symbol	GHS07
Solubility	>38 [ug/mL]
Usage Statement	Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.
Vapor Pressure	6.93X10-8 mm Hg at 25 deg c (est)