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VAQORACHEMICALS
Impurity reference standards

Valsartan impurities & reference standards

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

69reference materials
11nitrosamine impurities
6isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Valsartan
137862-53-4 · C24H29N5O3
View API
Reference Standard
4-Hydroxy Valsartan chemical structure
4-Hydroxy Valsartan
CAS
188259-69-0
Formula
C24H29N5O4
MW
451.5 g/mol
VQ-028618
Reference Standard
4-Phenyltoluene chemical structure
4-Phenyltoluene
CAS
644-08-6
Formula
C13H12
MW
168.23 g/mol
VQ-043931
Reference Standard
5-Hydroxy Valsartan
5-Hydroxy Valsartan
CAS
1186103-57-0
Formula
C24H29N5O4
MW
451.52 g/mol
VQ-042809
Reference Standard
N1-Trityl Valsartan
N1-Trityl Valsartan
CAS
783369-52-8
Formula
C43H43N5O3
MW
677.83 g/mol
VQ-034529
IP/BP/USP
Valsartan chemical structure
Valsartan
CAS
137862-53-4
Formula
C24H29N5O3
MW
435.5 g/mol
VQ-004113
Reference Standard
Valsartan Disodium chemical structure
Valsartan Disodium
CAS
391230-93-6
Formula
C24H27N5Na2O3
MW
479.5 g/mol
In stock
Reference Standard
Valsartan L-Luceine
Valsartan L-Luceine
CAS
137863-55-9
Formula
C25H31N5O3
MW
449.6 g/mol
VQ-044623

FAQs — Valsartan impurities

Which Valsartan impurities do you supply?

We list 69 Valsartan-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 Valsartan 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 Valsartan 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 Valsartan impurity standards

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