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VAQORACHEMICALS
Impurity reference standards

Metoprolol impurities & reference standards

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

51reference materials
1nitrosamine impurities
3isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Metoprolol
51384-51-1 · C15H25NO3
View API
Reference Standard
(R)-Metoprolol chemical structure
(R)-Metoprolol
CAS
81024-43-3
Formula
C15H25NO3
MW
267.36 g/mol
VQ-038381
Reference Standard
(S)-Metoprolol chemical structure
(S)-Metoprolol
CAS
81024-42-2
Formula
C15H25NO3
MW
267.36 g/mol
VQ-031855
Reference Standard
Metoprolol chemical structure
Metoprolol
CAS
51384-51-1
Formula
C15H25NO3
MW
267.36 g/mol
VQ-007578
Reference Standard
Metoprolol Acid D5 chemical structure
Metoprolol Acid D5
CAS
1215404-47-9
Formula
C14H21NO4
MW
272.35 g/mol
VQ-049097
Reference Standard
Metoprolol Fumarate chemical structure
Metoprolol Fumarate
CAS
80274-67-5
Formula
C34H54N2O10
MW
650.8 g/mol
VQ-007579
Reference Standard
Metoprolol Fumarate chemical structure
Metoprolol Fumarate
CAS
119637-66-0
Formula
C34H54N2O10
MW
650.8 g/mol
VQ-049096
Reference Standard
Metoprolol Tartrate chemical structure
Metoprolol Tartrate
CAS
56392-17-7
Formula
C34H56N2O12
MW
684.8 g/mol
VQ-007581
Reference Standard
Metoprolol-d5 chemical structure
Metoprolol-d5
CAS
959786-79-9
Formula
C15H25NO3
MW
272.39 g/mol
VQ-031859
Reference Standard
Metoprolol-d7 chemical structure
Metoprolol-d7
CAS
959787-96-3
Formula
C15H25NO3
MW
274.41 g/mol
VQ-043368

FAQs — Metoprolol impurities

Which Metoprolol impurities do you supply?

We list 51 Metoprolol-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 Metoprolol 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 Metoprolol 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 Metoprolol impurity standards

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