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Ciprofloxacin Hydrochloride

Base Information Edit
  • Chemical Name:Ciprofloxacin Hydrochloride
  • CAS No.:93107-08-5
  • Molecular Formula:C17H18FN3O3.HCl
  • Molecular Weight:367.808
  • Hs Code.:29339900
  • European Community (EC) Number:642-985-5,658-041-0,849-041-3
  • NSC Number:620634
  • UNII:0MP32MFP6C
  • DSSTox Substance ID:DTXSID1047788
  • Wikidata:Q27105154
  • NCI Thesaurus Code:C47976
  • RXCUI:81981
  • ChEMBL ID:CHEMBL1202
  • Mol file:93107-08-5.mol
Ciprofloxacin Hydrochloride

Synonyms:Anhydrous, Ciprofloxacin Hydrochloride;Bay 09867;Bay-09867;Bay09867;Ciprinol;Cipro;Ciprofloxacin;Ciprofloxacin Hydrochloride;Ciprofloxacin Hydrochloride Anhydrous;Ciprofloxacin Monohydrochloride Monohydrate;Hydrochloride Anhydrous, Ciprofloxacin;Hydrochloride, Ciprofloxacin;Monohydrate, Ciprofloxacin Monohydrochloride;Monohydrochloride Monohydrate, Ciprofloxacin

Suppliers and Price of Ciprofloxacin Hydrochloride
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • Ciprofloxacin HCl Pharmaceutical Secondary Standard; Certified Reference Material
  • 1 g
  • $ 80.10
  • Sigma-Aldrich
  • Ciprofloxacin hydrochloride European Pharmacopoeia (EP) Reference Standard
  • $ 190.00
  • Sigma-Aldrich
  • Ciprofloxacin hydrochloride United States Pharmacopeia (USP) Reference Standard
  • 400 mg
  • $ 366.00
  • Crysdot
  • 1-Cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylicacidhydrochloride 95+%
  • 500g
  • $ 190.00
  • Crysdot
  • 1-Cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylicacidhydrochloride 95+%
  • 100g
  • $ 60.00
  • ChemScene
  • Ciprofloxacin(monohydrochloride) 99.73%
  • 1g
  • $ 72.00
  • ChemScene
  • Ciprofloxacin(monohydrochloride) 99.73%
  • 500mg
  • $ 50.00
  • ChemScene
  • Ciprofloxacin(monohydrochloride) 99.73%
  • 5g
  • $ 108.00
  • Cayman Chemical
  • Ciprofloxacin (hydrochloride) ≥95%
  • 50g
  • $ 125.00
  • Cayman Chemical
  • Ciprofloxacin (hydrochloride) ≥95%
  • 10g
  • $ 48.00
Total 130 raw suppliers
Chemical Property of Ciprofloxacin Hydrochloride Edit
Chemical Property:
  • Appearance/Colour:white or light yellow crystalline powder 
  • Melting Point:>300 °C 
  • Boiling Point:581.8 °C at 760 mmHg 
  • Flash Point:305.6 °C 
  • PSA:74.57000 
  • LogP:2.77910 
  • 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 
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:3
  • Exact Mass:367.1098973
  • Heavy Atom Count:25
  • Complexity:571
Purity/Quality:

99% *data from raw suppliers

Ciprofloxacin HCl Pharmaceutical Secondary Standard; Certified Reference Material *data from reagent suppliers

Safty Information:
  • Pictogram(s): R36/37/38:; 
  • Hazard Codes: Xi:Irritant;
     
  • Statements: R36/37/38:; 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)O.Cl
  • Recent ClinicalTrials:Bioequivalence Study of Ciprofloxacin in Healthy Adult Subjects Under Fasting Condition
  • Recent EU Clinical Trials:ABSORB 2:An exploratie study determining the oral antibiotic drug absorption in patients with short bowel syndrome.
  • 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.
  • Uses Anti-bacterial 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]
Technology Process of Ciprofloxacin Hydrochloride

There total 26 articles about Ciprofloxacin Hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogenchloride; In water; Heating;
Guidance literature:
With hydrogenchloride; In water; at 0 ℃; for 4h; pH=< 1;
Guidance literature:
In ethanol; for 24 - 72h; Product distribution / selectivity;
Refernces Edit
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