Impurity reference standards
Carvedilol impurities & reference standards
Characterised Carvedilol impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
51reference materials
2nitrosamine impurities
4isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Carvedilol
72956-09-3 · C24H26N2O4
2-(2-Methoxyphenoxy)ethylamine hydrochloride monohydrate
- CAS
- 2057412-43-6
- Formula
- C9H16ClNO3
- MW
- 221.68 g/mol
VQ-022035
4-(Oxiran-2-ylmethoxy)-9-(oxiran-2-ylmethyl)-9H-carbazole
- CAS
- 1198090-71-9
- Formula
- C18H17NO3
- MW
- 295.3 g/mol
VQ-024820
![N-[2-(2-Methoxyphenoxy)ethyl]acetamide chemical structure](/media/structures/LYUSMRCJQLYGGS-UHFFFAOYSA-N.svg)
![N-[2-(2-Methoxyphenoxy)ethyl]benzylamine chemical structure](/media/structures/SZDYRZVWNVIYGO-UHFFFAOYSA-N.svg)
FAQs — Carvedilol impurities
Which Carvedilol impurities do you supply?
We list 51 Carvedilol-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 Carvedilol 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 Carvedilol 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 Carvedilol impurity standards
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