S7007

Sulfadimethoxine

98.0-102.0%

• Synonyme(s) : 4-Amino-N-(2,6-dimethoxy-4-pyrimidinyl)benzenesulfonamide
• Formule empirique (notation de Hill) : C₁₂H₁₄N₄O₄S
• CAS Number: 122-11-2
• Poids moléculaire : 310.33
• Beilstein: 306856
• Numéro CE : 204-523-7
• Numéro MDL: MFCD00057345
• Code UNSPSC : 41116107
• ID de substance PubChem : 329824574
• Nomenclature NACRES : NA.24

Propriétés

• Niveau de qualité: 200
• Essai: 98.0-102.0%
• Forme: powder
• Technique(s): HPLC: suitable; gas chromatography (GC): suitable
• Spectre d'activité de l'antibiotique: Gram-negative bacteria; Gram-positive bacteria
• Application(s): forensics and toxicology; pharmaceutical (small molecule)
• Mode d’action: DNA synthesis | interferes; enzyme | inhibits
• Température de stockage: 2-8°C
• Chaîne SMILES: COc1cc(NS(=O)(=O)c2ccc(N)cc2)nc(OC)n1
• InChI: 1S/C12H14N4O4S/c1-19-11-7-10(14-12(15-11)20-2)16-21(17,18)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H,14,15,16)
• Clé InChI: ZZORFUFYDOWNEF-UHFFFAOYSA-N

Description

Description générale

Chemical structure: sulfonamide

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Actions biochimiques/physiologiques

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.

Informations sur la sécurité

• Pictogrammes: GHS07
• Mention d'avertissement: Warning
• Mentions de danger: H302
• Conseils de prudence: P264 - P270 - P301 + P312 - P501
• Classification des risques: Acute Tox. 4 Oral
• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Équipement de protection individuelle: dust mask type N95 (US), Eyeshields, Faceshields, Gloves