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VAQORACHEMICALS
Impurity reference standards

Rilpivirine impurities & reference standards

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

21reference materials
1isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Rilpivirine
500287-72-9 · C22H18N6
View API
Reference Standard
Rilpivirine chemical structure
Rilpivirine
CAS
500287-72-9
Formula
C22H18N6
MW
366.4 g/mol
VQ-007715
Reference Standard
Rilpivirine N-oxide chemical structure
Rilpivirine N-oxide
CAS
2734549-19-8
Formula
C22H18N6O
MW
382.4 g/mol
VQ-027821
Reference Standard
Rilpivirine-d6 chemical structure
Rilpivirine-d6
CAS
1312424-26-2
Formula
C22H18N6
MW
372.5 g/mol
VQ-033545

FAQs — Rilpivirine impurities

Which Rilpivirine impurities do you supply?

We list 21 Rilpivirine-related reference materials, including process impurities, degradation products, 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 Rilpivirine 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 Rilpivirine 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 Rilpivirine impurity standards

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