Sodium cloxacillin monohydrate Chemical Properties

Melting point:

170℃

Boiling point:

689℃

Flash point:

>110°(230°F)

storage temp. 

Keep in dark place,Inert atmosphere,2-8°C

solubility 

H2O: soluble50mg/mL

form 

solid

color 

White to Orange to Green

Water Solubility 

Soluble in water

Merck 

13,2444

BRN 

5403885

CAS DataBase Reference

7081-44-9(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xn

Risk Statements 

36/37/38-42/43

Safety Statements 

26-36

WGK Germany 

2

RTECS 

XH8920000

HS Code 

29411099

MSDS

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Sodium cloxacillin monohydrate Usage And Synthesis

Brand Name(s) in US

Cloxapen, Orbenin, Tegopen

Description

Cloxacillin 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.

Chemical Properties

White or almost white, hygroscopic, crystalline powder.

Uses

Penicillin antibacterial.

Uses

Targets primarily Gram-positive bacteria, especially -lactamase producing Staphylococci

Definition

ChEBI: Cloxacillin sodium monohydrate is an organic sodium salt and a hydrate. It contains a cloxacillin sodium.

brand name

Cloxapen (GlaxoSmithKline); Tegopen (Apothecon).

Contact allergens

Cloxacillin is a semisynthetic penicillin close to oxacillin. It induced contact dermatitis in a pharmaceutical factory worker with positive reactions to ampicillin, but not to penicillin. In cutaneous drug reactions such as acute generalized exanthematous pustulosis due to amoxicillin, cross-reactivity is frequent to cloxacillin (personal observations).

Clinical Use

The chlorine atom ortho to the position of attachment of thephenyl ring to the isoxazole ring enhances the activity ofcloxacillin sodium, [3-(o-chlorophenyl)-5-methyl-4-isoxazolyl]penicillin sodium monohydrate (Tegopen), over that ofoxacillin, not by increasing its intrinsic antibacterial activitybut by enhancing its oral absorption, leading to higher plasmalevels. In almost all other respects, it resembles oxacillin.

Safety Profile

Moderately toxic by intraperitoneal, intramuscular, subcutaneous, and intravenous routes. Mildly toxic by ingestion. When heated to decomposition it emits very toxic fumes of Cl-, NOx, Na2O, and SOx.

Veterinary Drugs and Treatments

Cloxacillin is used via intramammary infusion in dry and lactating dairy cattle.

Sodium cloxacillin monohydrate(7081-44-9)Related Product Information

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• 3,4'-DIAMINODIPHENYLMETHANE
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• Sodium hydroxide
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