Worldwide shipping · 120+ destinationsCOA & GHS SDS with every lotMon–Sat, 09:30–18:30 IST
VAQORACHEMICALS
Impurity reference standards

Gilteritinib impurities & reference standards

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

12reference materials
2isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Gilteritinib
1254053-43-4 · C29H44N8O3
View API
Reference Standard
Gilteritinib chemical structure
Gilteritinib
CAS
1254053-43-4
Formula
C29H44N8O3
MW
552.7 g/mol
In stock
Reference Standard
Gilteritinib-D3 chemical structure
Gilteritinib-D3
CAS
2377109-67-4
Formula
C29H44N8O3
MW
555.7 g/mol
VQ-037515
Reference Standard
Gilteritinib-D8 chemical structure
Gilteritinib-D8
CAS
2377109-74-3
Formula
C29H44N8O3
MW
560.8 g/mol
VQ-048528

FAQs — Gilteritinib impurities

Which Gilteritinib impurities do you supply?

We list 12 Gilteritinib-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 Gilteritinib 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 Gilteritinib 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 Gilteritinib impurity standards

We reply within one business day with price, pack options, lead time and documentation.

By submitting you agree to our privacy policy. We never share your details.