S7007

Sulfadimethoxin

98.0-102.0%

• Synonym(e): 4-Amino-N-(2,6-dimethoxy-4-pyrimidinyl)-benzolsulfonamid
• Empirische Formel (Hill-System): C₁₂H₁₄N₄O₄S
• CAS-Nummer: 122-11-2
• Molekulargewicht: 310.33
• UNSPSC Code: 41116107
• NACRES: NA.24
• PubChem Substance ID: 329824574
• EC Number: 204-523-7
• Beilstein/REAXYS Number: 306856
• MDL number: MFCD00057345

Eigenschaften

• Quality Segment: 200
• assay: 98.0-102.0%
• form: powder
• technique(s): HPLC: suitable, gas chromatography (GC): suitable
• antibiotic activity spectrum: Gram-negative bacteria, Gram-positive bacteria
• application(s): forensics and toxicology; pharmaceutical (small molecule)
• mode of action: DNA synthesis | interferes, enzyme | inhibits
• storage temp.: 2-8°C
• SMILES string: 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)
• InChI key: ZZORFUFYDOWNEF-UHFFFAOYSA-N

Beschreibung

General description

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.

Biochem/physiol Actions

Sulfonamid Antibiotikum, blockiert die Synthese von Dihydrofolsäure durch Inhibierung des Enzyms Dihydropteroatsynthase.
Wirkungsweise: Inhibiert Folsäuresynthese in Prokaryoten.
Antimikrobielles Spektrum: Gram positive, Gram negative, Chlamydia
Mode of Resistance: Abänderung der Dihydropteroatsynthase oder alternativer Weg für Folsäuresynthese.

Sicherheitshinweise

• pictograms: GHS07
• signalword: Warning
• hcodes: H302
• pcodes: P264 - P270 - P301 + P312 - P501
• Hazard Classifications: Acute Tox. 4 Oral
• Lagerklasse: 11 - Combustible Solids
• wgk: WGK 3
• ppe: dust mask type N95 (US), Eyeshields, Faceshields, Gloves