Veterinary Medicine Ciprofloxacin Hydrochloride Powder CAS 86483-48-9 Raw Materials

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Ciprofloxacin Hydrochloride Powder Usage and Synthesis.

Ciprofloxacin Hydrochloride is indicated for urinary tract infections, moderate and severe respiratory tract infections, intestinal infections, soft tissue skin infections, sepsis and intra-abdominal infections caused by sensitive organisms.

Ciprofloxacin Hydrochloride PowderWhite or slightly yellow crystalline powder. Melting point 255-257 ℃ (decomposition).

Ciprofloxacin Hydrochloride Raw MaterialsBroad-spectrum antimicrobial drugs for heavy mixed infections,Ciprofloxacin Hydrochloride Powder,mainly used for chronic respiratory tract,E. coli drugs,infectious rhinitis,avian cholera,avian avian cholera, avian typhoid, etc.

Uses and functions of Ciprofloxacin Hydrochloride Powder.

It is one of the excellent representatives of quinolone antimicrobials, which was successfully developed by Bayer Pharmaceuticals, Germany in 1983. The first generation of quinolone antimicrobials is represented by nalidixic acid, the second generation is represented by piperic acid, and the third generation is represented by haloperidol.

Cyclopropyl haloperidol has a wide antibacterial spectrum, strong antibacterial activity, and is effective against both Gram-positive and Gram-negative bacteria, as well as Pseudomonas aeruginosa, with few adverse reactions. It is a variety of drugs with large sales in the international market, and the domestic production is developing rapidly.

Broad-spectrum antimicrobials, suitable for heavy mixed infections, mainly used for chronic respiratory tract, E. coli, infectious rhinitis, avian cholera, avian typhoid, etc.

Pharmacological Effects of Ciprofloxacin Hydrochloride Powder.

Pefloxacin is a synthetic chemotherapeutic agent used to treat severe and life-threatening bacterial infections. Pefloxacin is commonly referred to Pefloxacin is commonly referred to as a fluoroquinolone (or quinolone) drug and is a member of the fluoroquinolone class of antibacterials. It is an analog of norfloxacin. It is a synthetic fluoroquinolone, belonging to the 3rd generation of quinolones.

Production method of Ciprofloxacin Hydrochloride Powder.

3-Chloro-4-fluoroaniline was diazotized and replaced to produce 2,4-dichlorofluorobenzene, then acetylated to obtain 2,4-dichloro-5-fluoroacetophenone, which was condensed with diethyl carbonate to prepare ethyl 2,4-dichloro-5-fluorobenzoylacetate, and then reacted with diethyl orthoformate, acetic anhydride,

and cyclopropylamine to make 2-(3,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminopropanoic acid in one step. ethyl ester, the latter reacted with NaH in anhydrous dioxane and refluxed for 2h to produce 1-cyclopropyl-7-chloro-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, and finally reacted with aqueous piperazine to obtain cyclopropylpiperazine.

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