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

Name: 99% up Ciprofloxacin Hydrochloride Ciprofloxacin HCL CAS NO.86393-32-0
Availability: 99-up-ciprofloxacin-hydrochloride-ciprof-276392.html

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

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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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NICOTINAMIDE MONONUCLEOTIDE (NMN) 1094-61-7

STEVIA LEAF EXTRACT 57817-89-7

L-GLUTATHIONE REDUCED (GSH) 70-18-8

NICOTINAMIDE ADENINE DINUCLEOTIDE 58-84-9

ALPHA GPC 28319-77-9

PALMITOYLETHANOLAMIDE (PEA) 544-31-0

PTEROSTILBENE 537-42-8

VONOPRAZAN FUMARATE 1260141-27-2

AZILSARTAN 147403-03-0

LOSARTAN POTASSIUM 124750-99-8

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

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

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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