Home > Compound List > Product Information
Oxacillin sodium salt_Molecular_structure_CAS_1173-88-2)
Click picture or here to close

Oxacillin sodium salt

Catalog No. 28221 Name Sigma Aldrich
CAS Number 1173-88-2 Website http://www.sigmaaldrich.com
M. F. C19H18N3NaO5S Telephone 1-800-521-8956
M. W. 423.41809 Fax
Purity ~95% (TLC) Email
Storage Chembase ID: 155978

SYNONYMS

Title
苯唑西林 钠盐
IUPAC name
sodium (2S,6R)-3,3-dimethyl-6-(5-methyl-3-phenyl-1,2-oxazole-4-amido)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
IUPAC Traditional name
sodium (2S,6R)-3,3-dimethyl-6-(5-methyl-3-phenyl-1,2-oxazole-4-amido)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate

DATABASE IDS

PubChem SID 24857028
EC Number 214-636-3
MDL Number MFCD00082382
Beilstein Number 4098179
CAS Number 1173-88-2

PROPERTIES

Empirical Formula (Hill Notation) C19H18N3NaO5S
Impurities ≤10% water
Purity ~95% (TLC)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RTECS XH9100000
Storage Temperature 2-8°C
German water hazard class 2

DETAILS

Description (English)
Application
Oxacillin is used to study mechanisms of penicillinase resistance and antimicrobial susceptibility 1. It has been used to study autolysins2
Biochem/physiol Actions
Oxacillin inhibits bacterial cell wall biosynthesis at the level of transpeptidation (PBP) of peptidoglycan. Used to study mechanisms of penicillinase resistance.
Description (简体中文)
Application
Oxacillin is used to study mechanisms of penicillinase resistance and antimicrobial susceptibility 1. It has been used to study autolysins2
Biochem/physiol Actions
Oxacillin inhibits bacterial cell wall biosynthesis at the level of transpeptidation (PBP) of peptidoglycan. Used to study mechanisms of penicillinase resistance.

REFERENCES