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VAQORACHEMICALS
Impurity reference standards

Levofloxacin impurities & reference standards

Characterised Levofloxacin impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.

37reference materials
1nitrosamine impurities
1isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Levofloxacin
100986-85-4 · C18H20FN3O4
View API
Reference Standard
(R)-Ofloxacin chemical structure
(R)-Ofloxacin
CAS
100986-86-5
Formula
C18H20FN3O4
MW
361.4 g/mol
VQ-022969
Reference Standard
Ethyl chemical structure
Ethyl
CAS
110548-02-2
Formula
C15H15F4NO4
MW
349.28 g/mol
VQ-031527
IP/BP/USP
Levofloxacin chemical structure
Levofloxacin
CAS
100986-85-4
Formula
C18H20FN3O4
MW
361.4 g/mol
VQ-003930
Reference Standard
Levofloxacin-d8 chemical structure
Levofloxacin-d8
CAS
1217716-71-6
Formula
C18H20FN3O4
MW
369.4 g/mol
VQ-038013

FAQs — Levofloxacin impurities

Which Levofloxacin impurities do you supply?

We list 37 Levofloxacin-related reference materials, including process impurities, degradation products, nitrosamine impurities, stable-isotope-labelled standards and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.

What are Levofloxacin 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 Levofloxacin 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 Levofloxacin impurity standards

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