Ciprofloxacin HCl Powder CAS 93107-08-5 Raw Material

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Ciprofloxacin HCl Powder Usage and Synthesis.

Ciprofloxacin HCl Powder is an off-white or yellowish crystalline powder; odorless, bitter; hygroscopic.Ciprofloxacin Hydrochloride Powder is the hydrochloride of ciprofloxacin, which is a synthetic second-generation quinolone antibacterial drug. Ciprofloxacin HCl Raw Material has broad-spectrum antibacterial activity, good bactericidal effect, almost all bacteria antibacterial activity is stronger than norfloxacin and enrofloxacin 2 to 4 times, to enterobacteria, Pseudomonas aeruginosa, Haemophilus influenzae, gonococcus, streptococcus, Legionella, Staphylococcus aureus has antibacterial effect.

Application/Function of Ciprofloxacin HCl Powder.

Ciprofloxacin is an anti-infective drug used for the treatment or prevention of confirmed or highly suspected infections with sensitive bacteria, and is also the most active and safest quinolone against Pseudomonas aeruginosa in clinical practice, mainly for respiratory tract infections, genitourinary infections and intestinal infections.

Ciprofloxacin hydrochloride can be used for sensitive bacteria caused by

• (1) Genitourinary infections, including simple and complicated urinary tract infections, bacterial prostatitis, Neisseria gonorrhoeae urethritis or cervicitis (including those caused by enzyme-producing strains).
• (2) Respiratory tract infections, including acute attacks of bronchial infections and pulmonary infections due to sensitive gram-negative bacilli.
• (3) Gastrointestinal infections, caused by Shigella spp., Salmonella spp., enterotoxin-producing Escherichia coli, Aeromonas hydrophila, Vibrio parahaemolyticus, etc.
• (4) Typhoid fever.
• (5) Bone and joint infections.
• (6) Skin and soft tissue infections.
• (7) Septicemia and other systemic infections.

Pharmacological Effects of Ciprofloxacin HCl Powder

This product is a new type of quinolone antibacterial drug. The mechanism of action is that it can bind to bacterial DNA gyrase subunit A, which inhibits the cleavage and linkage function of the enzyme and prevents the replication of bacterial DAN, and presents antibacterial effect. It has good water solubility, broad spectrum and high efficiency. It has significant antibacterial effect on Escherichia coli,
Salmonella, Pseudomonas aeruginosa, Haemophilus influenzae, gonococcus, streptococcus, Legionella, Staphylococcus aureus, Bacteroides fragilis and Mycoplasma, better than other similar drugs and cephalosporins, aminoglycoside antibacterial agents, and also has obvious effect on β-lactam and gentamicin-resistant pathogens.

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