CAS 63-74-1
:Sulfanilamide
Description:
Sulfanilamide, with the CAS number 63-74-1, is an organic compound that belongs to the sulfonamide class of antibiotics. It is characterized by its sulfonamide functional group, which consists of a sulfonyl group (–SO2) attached to an amine (–NH2). This compound is typically a white crystalline solid that is soluble in water and exhibits a melting point that varies based on purity. Sulfanilamide was historically significant as one of the first synthetic antibacterial agents, effectively inhibiting bacterial growth by interfering with folic acid synthesis. Its mechanism of action involves mimicking para-aminobenzoic acid (PABA), a substrate necessary for bacterial metabolism. While sulfanilamide has been largely replaced by more effective antibiotics, it laid the groundwork for the development of sulfa drugs and remains important in the study of medicinal chemistry. Additionally, it has applications in various fields, including biochemistry and pharmacology, and is used in research settings to explore antibiotic resistance and microbial metabolism.
Formula:C6H8N2O2S
InChI:InChI=1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)
InChI key:InChIKey=FDDDEECHVMSUSB-UHFFFAOYSA-N
SMILES:S(N)(=O)(=O)C1=CC=C(N)C=C1
Synonyms:- (4-(Aminosulfonyl)phenyl)amine
- 1162F
- 4-(Aminosulfonyl)aniline
- 4-Aminobenzene-1-sulfonamide
- 4-Aminobenzenesulfonamide
- 4-Aminophenylsulfonamide
- 4-Aminosulfoneamide
- 4-Sulfamoylaniline
- A-349
- AVC
- Albexan
- Albosal
- Ambeside
- Aminobenzenesulfonamide
- Antistrept
- Astreptine
- Astrocid
- Bacteramid
- Bactesid
- Collomide
- Colsulanyde
- Copticide
- Deseptyl
- Dipron
- Ergaseptine
- Erysipan
- Estreptocida
- Exoseptoplix
- Gerison
- Gombardol
- Infepan
- Lusil
- Lysococcine
- Neococcyl
- Orgaseptine
- P-Aminophenylsulfonamide
- Pabs
- Prontalbin
- Prontylin
- Proseptal
- Proseptine
- Proseptol
- Pysococcine
- Sanamid
- Septanilam
- Septinal
- Septolix
- Septoplex
- Septoplix
- Stramid
- Strepamide
- Strepsan
- Streptagol
- Streptamid
- Streptasol
- Streptocid
- Streptocide
- Streptoclase
- Streptocom
- Streptol
- Strepton
- Streptopan
- Streptosil
- Streptozol
- Streptozone
- Streptrocide
- Sulfamidyl
- Sulfamine
- Sulfana
- Sulfanalone
- Sulfanidyl
- Sulfanil
- Sulfanilamid
- Sulfanilamida
- Sulfanilimide
- Sulfocidine
- Sulfonamid
- Sulfonamide
- Sulfonylamide
- Sulphanilamide
- Sulphonamide
- Therapol
- Tolder
- Vagitrol
- p-Aminobenzenesulfonamide
- p-Anilinesulfonamide
- p-Sulfamidoaniline
- p-Sulfamoylaniline
- sulfonamide p
- prontosil albom
- aniline-p-sulfonic amide
- pronzin album
- rubiazol a
- septamide album
- fourneau 1162
- Industrial Sulfanilamide
- Sulphanilamide crystals
- prontosil white
- stopton album
- Streptocid album
- Prontosil album
- Sulfanilamide
- prontosil i
- 1162 F
- F 1162
- F 1162
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4-Aminobenzenesulfonamide
CAS:Formula:C6H8N2O2SPurity:99.0%Color and Shape:Crystalline PowderMolecular weight:172.2Ministry of Agriculture Veterinary Drug Mixture 348 10 µg/mL in Acetonitrile:Water
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Color and Shape:MixtureSulfanilamide
CAS:SulfanilamideFormula:C6H8N2O2SPurity:99%Color and Shape: white to off white crystalline solidMolecular weight:172.20g/molSulphanilamide
CAS:Impurity Sulfamethoxazole EP Impurity E
Applications The active metabolite of the antibacterial dye, Sulfamidochrysoidine. Inhibits folic acid synthesis in prokaryotes. Antibacterial.
References Colebrook, L., et al.: Lancet, 233, 1291 (1937), Dye, C., et al.: Nat. Rev. Microbiol., 7, 81 (2009), Isik, S., et al.: Bioorg. Med. Chem., 17, 1158 (2009),Formula:C6H8N2O2SColor and Shape:WhiteMolecular weight:172.20Sulphanilamide
CAS:Sulphanilamide is an antimicrobial agent that inhibits the growth of bacteria by binding to their enzymes and blocking protein synthesis. In addition, sulphanilamide has been shown to inhibit the production of sulfanilamide, a potent inhibitor of tetracycline. Sulphanilamide is soluble in water and alcohol but not in organic solvents. The solubility of sulphanilamide can be increased by adding sodium salts or pH adjustment. Sulphanilamide is also used for wastewater treatment as it has inhibitory properties against sulfate-reducing bacteria. X-ray crystal structures have revealed that sulphanilamide binds to the active site of bacterial beta-lactamases through hydrogen bonds with both the NH group and the COOH group on its sulfur atom, resulting in inhibition of these enzymes. Sulphanilamide also interferes with bacterial DNA replication by inhibiting dna gyrase and topoisomerase IV. Sulphanilamide alsoFormula:C6H8N2O2SColor and Shape:PowderMolecular weight:172.21 g/molSulphanilamide extrapure AR, ExiPlus, Multi-Compendial, 99%
CAS:Formula:C6H8N2O2SPurity:min. 99%Color and Shape:White to off white, Crystalline powder, Clear to slight opalascent, Colourless to almost colourless, Clear, Colourless to almost colourlessMolecular weight:172.20Sulphanilamide extrapure AR, 99%
CAS:Formula:C6H8N2O2SPurity:min. 99%Color and Shape:White to off white, Crystalline powder, Clear to slight opalascent, Colourless to almost colourless, Clear, Colourless to almost colourlessMolecular weight:172.20Sulphanilamide pure, 99%
CAS:Formula:C6H8N2O2SPurity:min. 99%Color and Shape:White to Off white, Crystalline powder, Clear to slight opalascent, Colourless to pale yellow, Clear, Colourless to pale yellowMolecular weight:172.20









