99% up Ciprofloxacin Hydrochloride Ciprofloxacin HCL CAS NO.86393-32-0

Category:Active Pharmaceutical Ingredients > Other Active Pharmaceutical Ingredients
Product Name:99% up Ciprofloxacin Hydrochloride Ciprofloxacin HCL CAS NO.86393-32-0
CAS No.:86393-32-0
Standard:USP, BP, EP, JP, In-house Standards
Price(USD):Negotiable
Company:Sinoway Industrial Co.Ltd.

Basic Info
  • Grade: Pharmaceutical Grade

    Factory Location: Xiamen, Fujian

    Main Sales Markets: North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East

  • Monthly Production Capacity: 1000kg

    Packaging Information: 25kg/drum 1kg/bottle

  • Delivery Lead Time: 7 days after payment

    Sample Provided: yes

    Payment Terms: L/L

    name:

    ciprofloxacin hydrochloride/ ciprofloxacin hcl

    cas no.:

    86393-32-0

    molecular formula:

    c17h18fn3o3hcl

    molecular weight :

    385.81

    chemical name :

    1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic

     

     

    Function:

    use: pharmaceutical raw material

    ciprofloxacin hcl drug is used for the treatment of bacterial infection of respiratory tract, uti, uncomplicated cystitis in females, gi, chronic bacterial prostatitis, cns, immuno compromised patients, skin, bone and joint infections, uncomplicated cervical and urethral gonorrhea.

    ciprofloxacin hcl drug has in vitro activity against a wide range of gram-negative and gram-positive organisms.

    ciprofloxacin hcl drug inhibits bacterial dna gyrase, an enzyme responsible for counteracting excessive supercoiling of dna during replication or transcription. the mechanism of action of quinolones, including

    ciprofloxacin hcl drug, is different from that of other antimicrobial agents such as beta-lactams, macrolides, tetracyclines, or aminoglycosides; therefore, organisms resistant to these drugs may be susceptible to ciprofloxacin hcl drug. there is no known cross-resistance between ciprofloxacin hcl drug and other classes of antimicrobials.

     

    COA:

    item

    standard(usp35)

    test result

    description

    white or off-white crystalline powder

    conform

    solubility

    meets the requirement

    conform

    colour of solution

    meets the requirement

    conform

    fluoroquinoloic acid

    ≤0.2%

    <0.2%

    sulfate

    ≤0.04%

    <0.04%

    ph

    3.0~4.5

    3.7

    water

    4.7~6.7%

    6.20%

    residue on ignition

    ≤0.1%

    0.02%

    heavy metals

    ≤0.002%

    <0.002%

    chromatographic purity

    meets the requirement

    conform

    single impurity

    ≤0.2%

    0.11%

    any other individual impurities

    ≤0.2%

    <0.2%

    total impurities

    ≤0.5%

    0.38%

    assay

    98.0~102.0%

    99.40%

     

     

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