28221

Oxacillin sodium salt

815-950 μg/mg (Oxacillin)

• Synonyme(s) : Sodium 5-methyl-3-phenyl-4-isoxazolyl penicillin
• Formule empirique (notation de Hill) : C₁₉H₁₈N₃NaO₅S
• Numéro CAS: 1173-88-2
• Poids moléculaire : 423.42
• UNSPSC Code: 51283505
• NACRES: NA.85
• PubChem Substance ID: 57648295
• EC Number: 214-636-3
• Beilstein/REAXYS Number: 4098179
• MDL number: MFCD00082382

Propriétés

• biological source: synthetic
• Quality Segment: 200
• form: powder
• concentration: 815-950 μg/mg (Oxacillin)
• color: white to off-white
• antibiotic activity spectrum: Gram-negative bacteria, Gram-positive bacteria
• mode of action: cell wall synthesis | interferes
• storage temp.: 2-8°C
• SMILES string: [Na+].Cc1onc(-c2ccccc2)c1C(=O)N[C@H]3C4SC(C)(C)[C@@H](N4C3=O)C([O-])=O
• InChI: 1S/C19H19N3O5S.Na/c1-9-11(12(21-27-9)10-7-5-4-6-8-10)15(23)20-13-16(24)22-14(18(25)26)19(2,3)28-17(13)22;/h4-8,13-14,17H,1-3H3,(H,20,23)(H,25,26);/q;+1/p-1/t13-,14+,17?;/m1./s1
• InChI key: VDUVBBMAXXHEQP-ZTRPPZFVSA-M

Description

General description

Chemical structure: β-lactam

Application

Oxacillin is used to study mechanisms of penicillinase resistance and antimicrobial susceptibility . It has been used to study autolysins

Biochem/physiol Actions

Oxacillin inhibits bacterial cell wall biosynthesis at the level of transpeptidation (PBP) of peptidoglycan. Used to study mechanisms of penicillinase resistance.

Packaging

1g, 5g

Other Notes

Keep container tightly closed in a dry and well-ventilated place.

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)
• pictograms: GHS08
• signalword: Danger
• hcodes: H317,H334
• pcodes: P261 - P272 - P280 - P284 - P302 + P352 - P333 + P313
• Hazard Classifications: Resp. Sens. 1 - Skin Sens. 1