6 Chloro 1 cyclopropyl 7 fluoro 4 oxo 1 4 dihydroquinoline 3 carboxylic acid
- CAS
- 160312-26-5
- Formula
- C13H9ClFNO3
- MW
- 281.66 g/mol
VQ-048216
Impurity reference standards
Enrofloxacin impurities & reference standards
Characterised Enrofloxacin impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
12reference materials
COAHPLC · NMR · MS on request
7-Chloro-1-cyclopropyl-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid
- CAS
- 93110-13-5
- Formula
- C13H10ClNO3
- MW
- 263.67 g/mol
VQ-035066
FAQs — Enrofloxacin impurities
Which Enrofloxacin impurities do you supply?
We list 12 Enrofloxacin-related reference materials, including process impurities, degradation products and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Enrofloxacin impurity standards used for?
They are used for analytical method development and validation, impurity identification and quantification, forced-degradation and stability studies, and to support ANDA, DMF and other regulatory submissions under ICH Q3A/Q3B (and ICH M7 for mutagenic impurities).
Can you synthesise a Enrofloxacin impurity that is not listed?
Yes. Our custom synthesis service can prepare and characterise unlisted impurities, metabolites and labelled analogues from milligram to gram scale. Share the structure or name and required quantity for a quotation.
Request Enrofloxacin impurity standards
We reply within one business day with price, pack options, lead time and documentation.