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Ciprofloxacin HCl

CAS No.
93107-08-5
Chemical Name:
Ciprofloxacin HCl
Synonyms
CIPROFLOXACIN HYDROCHLORIDE;1-Cyclopropyl-6-fluoro;1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid hydrochloride;3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, hydrochloride;Cyproxan;BAY-o-9867;CIPROFLOXACIN HCL;Bay-09867 (hydrochloride);Clprofloxacin hydrochloride;Ciprofloxacin hydrochloride CAS 93107-08-5
CBNumber:
CB02130396
Molecular Formula:
C17H18FN3O3.HCl
Molecular Weight:
367.8
MDL Number:
MOL File:
93107-08-5.mol
MSDS File:
SDS
Last updated:2024-04-25 13:42:50

Ciprofloxacin HCl Properties

Melting point >300 ºC
storage temp. Sealed in dry,Room Temperature
solubility insoluble in EtOH; ≥33.87 mg/mL in H2O; ≥9.34 mg/mL in DMSO with ultrasonic
form crystalline solid
BCS Class 3
InChI InChI=1S/C17H18FN3O3.ClH/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24;/h7-10,19H,1-6H2,(H,23,24);1H
InChIKey DIOIOSKKIYDRIQ-UHFFFAOYSA-N
SMILES O=C(O)C1C(=O)C2=CC(=C(C=C2N(C2CC2)C=1)N1CCNCC1)F.[H]Cl
CAS DataBase Reference 93107-08-5
FDA UNII 0MP32MFP6C

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Safety Statements  24/25
HS Code  29339900

Ciprofloxacin HCl price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 14286 Ciprofloxacin (hydrochloride) ≥95% 93107-08-5 5g $28 2022-04-27 Buy
Cayman Chemical 14286 Ciprofloxacin (hydrochloride) ≥95% 93107-08-5 10g $53 2022-04-27 Buy
Cayman Chemical 14286 Ciprofloxacin (hydrochloride) ≥95% 93107-08-5 25g $82 2022-04-27 Buy
Cayman Chemical 14286 Ciprofloxacin (hydrochloride) ≥95% 93107-08-5 50g $136 2022-04-27 Buy
ChemScene CS-8134 Ciprofloxacin(monohydrochloride) 99.73% 93107-08-5 5g $108 2021-12-16 Buy
Product number Packaging Price Buy
14286 5g $28 Buy
14286 10g $53 Buy
14286 25g $82 Buy
14286 50g $136 Buy
CS-8134 5g $108 Buy

Ciprofloxacin HCl Chemical Properties,Uses,Production

Description

Ciprofloxacin hydrochloride is the hydrochloride of ciprofloxacin, which is a synthetic second-generation quinolone antibacterial drug with broad-spectrum antibacterial activity and good bactericidal effect. It is 2 to 4 times stronger than enoxacin, and has antibacterial effects on Enterobacter, Pseudomonas aeruginosa, Haemophilus influenzae, Neisseria gonorrhoeae, Streptococcus, Legionella, and Staphylococcus aureus.

Mechanism of action

Ciprofloxacin hydrochloride is a new type of quinolone antibacterial drug. Its mechanism of action is that it can combine with bacterial DNA gyrase subunit A, thereby inhibiting the cleavage and linking functions of the enzyme, preventing the replication of bacterial DNA, and showing antibacterial effect.

Uses

Ciprofloxacin hydrochloride, C17H18FN3O3 •HCl•H2O, is a synthetic broad-spectrum antibacterial agent. Ciprofloxacin differs from other quinolones in that it has a fluorine atom at the 6-position, a piperazine moiety at the 7-position, and a cyclopropyl ring at the 1-position. it was the drug of choice forcombating anthrax.
Ciprofloxacin hydrochloride (Cipro, 500-mg tablets) is highly active against the important bacterial causes of enteritis, including diarrheogenic Escherichia coli, Vibrio cholerae, Salmonella species, Shigella species, Campylobacter jejuni, Aeromonas species, and Yersinia enterocolitica.

Uses

Ciprofloxacin hydrochloride is a fluoroquinolone antibiotic that is widely used as an antimicrobial and immunomodulatory agent. Its range of activity includes most strains of bacterial pathogens capable of inducing respiratory, urinary tract, gastrointestinal, and abdominal infections. It functions by inhibiting DNA gyrase (a type II topoisomerase) and topoisomerase IV, the enzymes responsible for negative supercoiling of chromosomes and DNA strand separation, thus blocking initiation of bacterial replication. Most recently Ciprofloxacin hydrochloride has been used in the management of postexposure inhalational anthrax and radiation combined injury resulting from nuclear disasters.[Cayman Chemical]

Uses

Anti-bacterial

Definition

ChEBI: Ciprofloxacin hydrochloride (anhydrous) is the anhydrous form of the monohydrochloride salt of ciprofloxacin. It has a role as an EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor, an antibacterial drug, a topoisomerase IV inhibitor and an antiinfective agent. It contains a ciprofloxacin.

brand name

Ciloxan (Alcon); Cipro (Bayer); Proquin (Esprit).

Biological Activity

ciprofloxacin (hydrochloride) is a fluoroquinolone antibiotic that has antimicrobial and immunomodulatory activities [1].ciprofloxacin functions by inhibiting dna gyrase and topoisomerase iv, the enzymes responsible for negative supercoiling of chromosomes and dna strand separation, thus blocking initiation of bacterial replication. topoisomerase iv is the primary target of ciprofloxacin in s. aureus [2].ciprofloxacin (hydrochloride) is a fluoroquinolone antibiotic that acts as an antimicrobial and immunomodulatory agent. in b6d2f1/j mice received radiation combined injury (ci), ciprofloxacin significantly reduced pro-inflammatory cytokine and chemokine concentrations (il-6 and kc), and enhanced il-3 production. cip also inhibited ci-induced apoptosis and autophagy in ileal villi, systemic bacterial infection, and iga production [1]. ciprofloxacin (hydrochloride) had been approved by fda for management of postexposure inhalational anthrax. in animals after exposure to aerosolized b. anthracis, ciprofloxacin significantly improved survival rate. ciprofloxacin inhibited the growth of b. anthracis with mic90 of 0.06 μg/ml. in the usamriid rhesus monkey model of inhalational anthrax, the maximum concentration (cmax) of ciprofloxacin was 1.74 μg/ml and the minimum concentration (cmin) was 0.17 μg/ml [3].

Synthesis

The preparation method of ciprofloxacin HCl, its step is as follows:
a) cyclopropyl carboxylic acid is added in the organic solvent, and the adding piperazine, reacted 3~8 hours down as acid binding agent with alkali at 60~120 ℃, the monitoring cyclopropyl carboxylic acid is residual less than 2% o'clock termination reaction, stirring is cooled to 0~30 ℃, leaves standstill suction filtration;
b) add water and hydrochloric acid in the products therefrom toward a) step, under agitation be warming up to molten clearly, add activated carbon decolorizing, filtered while hot, and transfer filtrate pH to 2~4 with hydrochloric acid, and the cooling crystallization filters, rinsing, and drying makes ciprofloxacin HCl.

References

[1]. fukumoto r, cary lh, gorbunov nv, et al. ciprofloxacin modulates cytokine/chemokine profile in serum, improves bone marrow repopulation, and limits apoptosis and autophagy in ileum after whole body ionizing irradiation combined with skin-wound trauma. plos one. 2013;8(3):e58389.
[2]. drlica k, zhao x. dna gyrase, topoisomerase iv, and the 4-quinolones. microbiol mol biol rev. 1997 sep;61(3):377-92.
[3]. meyerhoff a, albrecht r, meyer jm, et al. us food and drug administration approval of ciprofloxacin hydrochloride for management of postexposure inhalational anthrax. clin infect dis. 2004 aug 1;39(3):303-8.

85721-33-1
93107-08-5
Synthesis of Ciprofloxacin HCl from Ciprofloxacin

Ciprofloxacin HCl Preparation Products And Raw materials

Global( 262)Suppliers
Supplier Tel Email Country ProdList Advantage
XINGTAI XINGJIU NEW MATERIAL TECHNOLOGY CO., LTD
+8617731987558 xingjiu@xingjiubiotech.com China 990 58
Hebei ZB Gamay Biological Technology Co.,Ltd
+86-031189171450 +86-15632359451 chem@zbvet.net China 222 58
Guangzhou Tosun Pharmaceutical Limited
+8618922120635 sales@toref-standards.com China 1000 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618740459177 sarah@tnjone.com China 1141 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 6011 58
XI'AN TIANGUANGYUAN BIOTECH CO., LTD.
+86-029-86333380 18829239519 sales06@tgybio.com China 943 58
Hebei Guanlang Biotechnology Co,.LTD
+8619930503252 daisy@crovellbio.com China 5961 58
shandong perfect biotechnology co.ltd
+86-53169958659; +8618596095638 sales@sdperfect.com China 294 58
Henan Suikang Pharmaceutical Co.,Ltd.
+86-18239973690 +86-18239973690 sales@suikangpharm.com China 186 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21689 55

View Lastest Price from Ciprofloxacin HCl manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ciprofloxacin HCl pictures 2024-05-21 Ciprofloxacin HCl
93107-08-5
US $0.00 / kg 25kg 98.0%~102.0% 10tons Henan Suikang Pharmaceutical Co.,Ltd.
Ciprofloxacin Hydrochloride pictures 2024-04-16 Ciprofloxacin Hydrochloride
93107-08-5
US $0.00-0.00 / kg 1kg 88.5% 1000kg Hebei ZB Gamay Biological Technology Co.,Ltd
Clprofloxacin Hydrochloride pictures 2024-04-11 Clprofloxacin Hydrochloride
93107-08-5
US $0.00-0.00 / mg 10mg 98% 10g/month Guangzhou Tosun Pharmaceutical Limited
  • Ciprofloxacin HCl pictures
  • Ciprofloxacin HCl
    93107-08-5
  • US $0.00 / kg
  • 98.0%~102.0%
  • Henan Suikang Pharmaceutical Co.,Ltd.

Ciprofloxacin HCl Spectrum

3-Quinolinecarboxylicacid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-,hydrochloride (1:1) BAY-o-9867 Cyproxan 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid monohydrochloride 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, monohydrochloride Clprofloxacin hydrochloride 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid hydrochloride CIPROFLOXACIN HCL Ciprofloxacin hydrochloride CAS 93107-08-5 Bay-09867 (hydrochloride) Enrofloxacin EP Impurity BQ: What is Enrofloxacin EP Impurity B Q: What is the CAS Number of Enrofloxacin EP Impurity B 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, hydrochloride 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid hydrochloride CIPROFLOXACIN HYDROCHLORIDE 1-Cyclopropyl-6-fluoro 93107-08-5 C17H19ClFN3O3xHCl Pharmaceutical intermediate 93107-08-5