BACAMPICILLIN HYDROCHLORIDE

PRODUCT IDENTIFICATION

CAS NO. 50972-17-3 (Base)
37661-08-8 (Hydrochloride)

BACAMPICILLIN

EINECS NO. 253-580-4
FORMULA C21H27N3O7S·HCl
MOL WT. 501.98

H.S. CODE

 

TOXICITY

 
SYNONYMS  
1-Ethoxycarbonyloxyethyl (2S,5R,6R)-6((R)-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo- 4-thia-1-azabicyclo(3.2.0)heptan-2-carboxylatate monohydrochloride;
DERIVATION

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE white to yellowish crystalline powder
MELTING POINT  
BOILING POINT  
SPECIFIC GRAVITY

 

SOLUBILITY IN WATER  

SOLVENT SOLUBILITY

 
pH  
VAPOR PRESSURE  

REFRACTIVE INDEX

 
AUTOIGNITION

 

NFPA RATINGS  
FLASH POINT  
STABILITY

Stable under ordinary conditions

APPLICATIONS

AMPICILLIN is a semisynthetic antibiotic, a member of the penicillin family of antibiotics. To extend the usefulness of the penicillins to the treatment of infections caused by gram-negative rods, the broad-spectrum penicillins (ampicillin, amoxicillin, carbenicillin, and ticarcillin) were developed.  It is created by attaching acid radicals to the central structure of 6-aminopenicillanic acid. Chemically, it is D-(-)-6-(2-amino-2-phenylacetamido) -3,3-dimethyl-7 -oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylic acid trihydrate.  Similar in action to penicillin G--the most widely used natural penicillin--ampicillin (or alpha-aminobenzylpenicillin) is more stable in stomach acids and therefore may be given orally; it is also more active against certain strains of bacteria. It is used regularly to treat common urinary-tract infections, some respiratory infections, and bacterial meningitis in children, although many strains of Hemophilus influenzae (the most common cause of bacterial meningitis) are now resistant to ampicillin, and it commonly is used along with other drugs.The potential side effects of ampicillin are similar to those of other penicillins--i.e., chiefly allergic reactions ranging from skin rashes and hives to life-threatening anaphylactic shock (very rare). People who are allergic to other drugs in this family are also likely to react to ampicillin. The incidence of skin rashes is higher with ampicillin than with other penicillins, a factor that suggests a possible toxic reaction, as well as a truly allergic response. Bacampicillin is a modified ampicillin class semisynthetic penicillin for oral administration. It has the same actions and uses as ampicillin as it is hydrolyzed to ampicillin during absorption.

Members of ampicillin derivatives

Product

CAS RN

Ampicillin sodium 69-52-3
Ampicillin 69-53-4
Penicillin G benzathine 1538-09-6
Metampicillin 6489-97-0
Ampicillin trihydrate 7177-48-2
Broadcillin 8067-85-4
Pivampicillin hydrochloride 26309-95-5
Epicillin 26774-90-3
Amoxicillin trihydrate 26787-78-0
Ampicillin benzathine 33276-75-4
Pivampicillin 33817-20-8
Amoxicillin sodium 34642-77-8
Bacampicillin hydrochloride 37661-08-8
Pivampicillin pamoate 39030-72-3
Talampicillin hydrochloride 39878-70-1
Pivampicillin probenate 42190-91-0
Talampicillin 47747-56-8
Bacampicillin 50972-17-3
Combipenix 51004-51-4
Ampicillinoic acid 57457-66-6
Amoxicillin anhydrous 61336-70-7
N-(N'-Methylasparaginyl)amoxicillin 63329-59-9
Aspoxicillin 63358-49-6
N-Propionylampicillin 74226-27-0
Amoxicillin-potassium clavulanate combination 74469-00-4
Amoxicillin-clavulanic acid mixture 79198-29-1
Lenampicillin hydrochloride 80734-02-7
Lenampicillin 86273-18-9
Sulacillin 94935-63-4
SALES SPECIFICATION

APPEARANCE

white to yellowish crystalline powder

ASSAY

623 ug/mg - 727 ug/mg (as ampicillin)

WATER

1.0% max

TRANSPORTATION
PACKING

 

HAZARD CLASS  
UN NO.  
OTHER INFORMATION

Hazard Symbols: XN, Risk Phrases: 36/37/38-42/43, Safety Phrases: 22-26-36/37