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VAQORACHEMICALS
Impurity reference standards

Tenofovir impurities & reference standards

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

76reference materials
1nitrosamine impurities
1isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Tenofovir
147127-20-6 · C9H14N5O4P
View API
Reference Standard
(S)-Tenofovir chemical structure
(S)-Tenofovir
CAS
147127-19-3
Formula
C9H14N5O4P
MW
287.21 g/mol
VQ-034108
Reference Standard
Isopropyl Tenofovir chemical structure
Isopropyl Tenofovir
CAS
1346597-36-1
Formula
C12H20N5O4P
MW
329.29 g/mol
VQ-028263
Reference Standard
MOC-POC Tenofovir chemical structure
MOC-POC Tenofovir
CAS
1246812-43-0
Formula
C17H26N5O10P
MW
491.4 g/mol
VQ-043317
Reference Standard
N-Nitroso Adenine chemical structure
N-Nitroso Adenine
CAS
2615274-45-6
Formula
C5H4N6O
MW
164.13 g/mol
VQ-024142
Reference Standard
rac Tenofovir-d6 chemical structure
rac Tenofovir-d6
CAS
1020719-94-1
Formula
C9H14N5O4P
MW
293.25 g/mol
VQ-042429
Reference Standard
rac-Tenofovir chemical structure
rac-Tenofovir
CAS
107021-12-5
Formula
C9H14N5O4P
MW
287.21 g/mol
VQ-034116
IP/BP/USP
Tenofovir chemical structure
Tenofovir
CAS
147127-20-6
Formula
C9H14N5O4P
MW
287.21 g/mol
VQ-003986

FAQs — Tenofovir impurities

Which Tenofovir impurities do you supply?

We list 76 Tenofovir-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 Tenofovir 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 Tenofovir 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 Tenofovir impurity standards

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