Impurity reference standards
Fluvastatin impurities & reference standards
Characterised Fluvastatin impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
23reference materials
COAHPLC · NMR · MS on request
(E)-3-(1-Ethyl-3-(4-fluorophenyl)-1H-indol-2-yl)acrylaldehyde
- CAS
- 93937-37-2
- Formula
- C19H16FNO
- MW
- 293.3 g/mol
VQ-037387
![6-[3-(4-Fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl]-4-hydroxyhex-5-en-2-one chemical structure](/media/structures/UMQYSJUFQJPZRH-UHFFFAOYSA-N.svg)
6-[3-(4-Fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl]-4-hydroxyhex-5-en-2-one
- CAS
- 920275-09-8
- Formula
- C23H24FNO2
- MW
- 365.4 g/mol
VQ-044278
FAQs — Fluvastatin impurities
Which Fluvastatin impurities do you supply?
We list 23 Fluvastatin-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 Fluvastatin 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 Fluvastatin 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 Fluvastatin impurity standards
We reply within one business day with price, pack options, lead time and documentation.