Impurity reference standards
Valganciclovir impurities & reference standards
Characterised Valganciclovir impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
23reference materials
COAHPLC · NMR · MS on request
Parent API: Valganciclovir
175865-60-8 · C14H22N6O5
2-(((2-Amino-6-oxo-3,6-dihydro-9H-purin-9-yl)methoxy)methoxy)-3-hydroxypropyl D-valinate
- CAS
- 1356353-76-8
- Formula
- C15H24N6O6
- MW
- 384.39 g/mol
VQ-023963
Valganciclovir EP Impurity N (Hydrochloride)
- CAS
- 1401562-16-0
- Formula
- C15H25ClN6O5
- MW
- 404.85 g/mol
In stock
Valganciclovir O-Acetyl N-Benzyloxycarbonyl Impurity
- CAS
- 194159-22-3
- Formula
- C24H30N6O8
- MW
- 530.5 g/mol
VQ-028612
FAQs — Valganciclovir impurities
Which Valganciclovir impurities do you supply?
We list 23 Valganciclovir-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 Valganciclovir 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 Valganciclovir 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 Valganciclovir impurity standards
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