Ciprofloxacin Impurities

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Parent Drug Name Name of Impurity Catalogue No.
Ciprofloxacin Chloro ciprofloxacin VL204008View CAS 93106-58-2
Ciprofloxacin Ciprofloxacin EP Impurity A VL204004View CAS 86393-33-1
Ciprofloxacin Ciprofloxacin EP Impurity B VL204005View
Ciprofloxacin Ciprofloxacin EP Impurity C VL204002View CAS 528851-31-2
Ciprofloxacin Ciprofloxacin EP Impurity C (Free Base) VE007082View CAS 103222-12-4
Ciprofloxacin Ciprofloxacin EP Impurity D VL204006View CAS 526204-10-4
Ciprofloxacin Ciprofloxacin EP Impurity D (Free Base) VE007083View CAS 133210-96-5
Ciprofloxacin Ciprofloxacin EP Impurity E VL204003View CAS 105394-83-0
Ciprofloxacin Ciprofloxacin EP Impurity E (HCl Salt) VE0010231View
Ciprofloxacin Ciprofloxacin EP Impurity F VL204001View CAS 226903-07-7
Ciprofloxacin Ciprofloxacin N-Formyl Impurity VL204011View CAS 93594-39-9
Ciprofloxacin Desfluoro Ciprofloxacin (Free Base) VE007084View CAS 93107-11-0
Ciprofloxacin N-ethoxy Carbonyl Ciprofloxacin Impurity VL204010View CAS 93594-29-7

Ciprofloxacin Related Compound

        Ciprofloxacin is used to treat or prevent certain bacterial diseases, including pneumonia, gonorrhea (a sexually transmitted disease), typhoid fever (a dangerous infection frequent in poor countries), and infectious diarrhea.

References

FAQ’s

 

What therapeutic category does ciprofloxacin fall under?

Ciprofloxacin belongs to the quinolone antibiotic group of medicines.

Does ciprofloxacin treat UTI?

Ciprofloxacin extended-release tablets are specifically prescribed for the treatment of urinary tract infections, such as acute uncomplicated pyelonephritis.

What is the mechanism of action of ciprofloxacin?

Ciprofloxacin’s bactericidal activity is caused by suppression of the enzymes topoisomerase

II (DNA gyrase) and topoisomerase IV (both Type II topoisomerases), which are necessary

for bacterial DNA replication, transcription, repair, and recombination.

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103222-12-4: Ciprofloxacin EP Impurity C (Free Base)

103222-12-4: Ciprofloxacin EP Impurity C (Free Base)
Catalogue No.

VE007082

CAS No.

103222-12-4

Molecular Formula

C15H16FN3O3

Molecular Weight

305.3 g/mol

Parent drug

Ciprofloxacin

IUPAC Name

7-[(2-Aminoethyl)amino]-1-cyclopropyl-6-fluoro-4-oxo-1, 4-dihydroquinoline-3-carboxylic acid

Synonyms

Enrofloxacin EP Impurity G/ Desethylene Ciprofloxacin

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References

Mack, Gladys. “Improved High-Performance Liquid Chromatographic Determination of Ciprofloxacin and Its Metabolites in Human Specimens.” Journal of Chromatography B: Biomedical Sciences and Applications, vol. 582, no. 1-2, Nov. 1992, pp. 263–67, https://doi.org/10.1016/0378-4347(92)80331-j. Campoli-Richards, Deborah M., et al. “Ciprofloxacin.” Drugs, vol. 35, no. 4, Apr. 1988, pp. 373–447, https://doi.org/10.2165/00003495-198835040-00003. ‌

Status

In-stock

ListName

Ciprofloxacin EP Impurity C (Free Base)

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