Synonym: (2S,5R,6R)-6-[[[3-(2-Chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid sodium; BRL 2039 sodium; FK 900 sodium; Floxacillin sodium
CAS Number: 1847-24-1
Empirical Formula (Hill Notation): C19H16ClFN3O5S · Na
Molecular Weight: 475.85
EC Number: 217-428-0
Linear Formula: C19H16ClFN3O5S · Na
Product Type: Chemical
assay |
≥95% (HPLC) |
color |
white to beige |
form |
powder |
InChI |
1S/C19H17ClFN3O5S.Na/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24;/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28);/q;+1/p-1/t13-,14+,17-;/m1./s1 |
InChI key |
OTEANHMVDHZOPB-SLINCCQESA-M |
Quality Level |
100 |
solubility |
H2O: 20 mg/mL, clear |
storage condition |
protect from light |
storage temp. |
−20°C |
Application: |
Flucloxacillin sodium has been used as a β-lactam antibiotic to study its effects on methicillin-resistant Staphylococcus aureus (MRSA) ΔfloA mutant. |
Biochem/physiol Actions: |
Flucloxacillin exhibits antimicrobial property. |
Biochem/physiol Actions: |
Flucloxacillin is a narrow-spectrum β-lactam antibiotic used to treat Gram-positive bacterial infections. Flucloxacillin induces cholestatic liver damage. |
General description: |
Flucloxacillin sodium, a sodium salt of flucloxacillin, is a member of the penicillin class. |
Other Notes: |
Light sensitive |
Packaging: |
10, 50 mg in glass bottle |
RIDADR |
NONH for all modes of transport |
WGK Germany |
WGK 3 |
Flash Point(F) |
Not applicable |
Flash Point(C) |
Not applicable |
Purity |
≥95% (HPLC) |
Storage Temp. |
−20°C |
UNSPSC |
12352200 |