Sodium cloxacillin monohydrate
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Grundinformationen
- CAS
7081-44-9- Standard-SMILES
Cc1onc(-c2ccccc2Cl)c1C(=O)N[C@@H]1C(=O)N2[C@@H]1SC(C)(C)[C@@H]2C(=O)[O-].O.[Na+]- InChIKey
KCUWTKOTPIUBRI-VICXVTCVSA-M- Summenformel
- C19H19ClN3NaO6S
- Durchschnittliche Molmasse
- 475,886 g/mol
- Monoisotopische Masse
- 475,05807829
Namen und Bezeichner
- Bevorzugter Name
- Sodium cloxacillin monohydrate
- IUPAC
- Sodium (2S,5R,6R)-6-{[3-(2-chlorophenyl)-5-methyl-1,2-oxazole-4-carbonyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate--water (1/1/1)
- Englischer Name
- Sodium cloxacillin monohydrate
- Summenformel
- C19H19ClN3NaO6S
- Molmasse
- 475.88
Namen und Synonyme
Cloxacillin sodiumbactopenCloxacillin sstaphobristol-250orbeninsodiumhydrateα-Amino-p-toluic acidCloxacillin sodium RSCloxacillin sodium CRSOxacillin EP Impurity Eprostaphlin-amonohydrate
Datenbank-Bezeichner
- CAS
7081-44-9- PubChem CID
- 23675743
- DTXSID
DTXSID60110018- ChEBI
CHEBI:34978- UNII
- 65LCB00B4Y
- EC Number
- 629-588-2、918-626-6
Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 170 ℃ · 170℃
- Siedepunkt
- 689 ℃ · 689℃
- Flammpunkt
- 110 ° · >110°(230°F)
- storage temp.
- 2 · Keep in dark place,Inert atmosphere,2-8°C
- Löslichkeit
- 2 O: · H2O: soluble50mg/mL
- Aggregatzustand
- solid
- Farbe
- White to Orange to Green
- Wasserlöslichkeit
- Soluble in water
- Merck
- 13 · 13,2444
- BRN
- 5403885 · 5403885
- Major Application
- clinical testing
- InChIKey
- MUYUWQFVGNJMPH-UHFFFAOYSA-M
- SMILES
- [Na+].N12C(C(NC(C3=C(C)OCN3C3=CC=CC=C3Cl)=O)C1=O)SC(C)(C)C2C([O-])=O.[H]O[H]
- CAS Datenbank
- 7081 · 7081-44-9(CAS DataBase Reference)
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Sicherheitsdaten
- wgk
- 2
- hs_code
- 29411099
- RTECS-Nr.
- XH8920000
- risk_code
- 36/37/38-42/43
- hazard_code
- Xn
- safety_code
- 26-36
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Eye Irrit. 2Resp. Sens. 1Skin Irrit. 2Skin Sens. 1STOT SE 3
Chemie und Industrie
Anwendungen
BeschreibungCloxacillin was synthesized by Beecham Research Laboratories in 1962 starting with 6- aminopenicillanic acid. It was the first semisynthetic penicillin with a halogen atom in the side chain to be used clinically. It shows 5- to 20-fold stronger activity than methicillin and is twice as active as oxacillin against Staphylococcus aureus, including benzylpenicillin-resistant strains. Cloxacillin is highly stable against penicillinase and well absorbed by oral administration. It has been widely used, by oral and intramuscular administration, to treat internal, surgical, gynecological, and other infections caused by both benzylpenicillin-sensitive and benzylpenicillin-resistant bacteria.
VerwendenPenicillin antibacterial.
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