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VAQORACHEMICALS
Impurity reference standards

Ezetimibe impurities & reference standards

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

93reference materials
2nitrosamine impurities
3isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Ezetimibe
163222-33-1 · C24H21F2NO3
View API
Reference Standard
Entanercept
Entanercept
CAS
185243-69-0
Formula
C2224H3475N621O6
MW
51235.07 g/mol
VQ-048283
IP/BP/USP
Ezetimibe chemical structure
Ezetimibe
CAS
163222-33-1
Formula
C24H21F2NO3
MW
409.4 g/mol
VQ-004090
Reference Standard
Ezetimibe chemical structure
Ezetimibe
CAS
163222-33-1
Formula
C24H21F2NO3
MW
409.4 g/mol
In stock
Reference Standard
Ezetimibe Diacetate chemical structure
Ezetimibe Diacetate
CAS
163380-20-9
Formula
C28H25F2NO5
MW
493.5 g/mol
VQ-025708

FAQs — Ezetimibe impurities

Which Ezetimibe impurities do you supply?

We list 93 Ezetimibe-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 Ezetimibe 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 Ezetimibe 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 Ezetimibe impurity standards

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