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VAQORACHEMICALS
Impurity reference standards

Emtricitabine impurities & reference standards

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

38reference materials
1isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Emtricitabine WS
143491-57-0 · C8H10FN3O3S
View API
Reference Standard
(-)-Neoisomenthol chemical structure
(-)-Neoisomenthol
CAS
64282-88-8
Formula
C10H20O
MW
156.26 g/mol
VQ-022515
Reference Standard
(-)-Neomenthol chemical structure
(-)-Neomenthol
CAS
20747-49-3
Formula
C10H20O
MW
156.26 g/mol
VQ-030465
Reference Standard
(+)-Isomenthol chemical structure
(+)-Isomenthol
CAS
23283-97-8
Formula
C10H20O
MW
156.26 g/mol
VQ-022513
Reference Standard
(+)-Menthol chemical structure
(+)-Menthol
CAS
15356-60-2
Formula
C10H20O
MW
156.26 g/mol
VQ-030463
Reference Standard
(+)-Neomenthol chemical structure
(+)-Neomenthol
CAS
2216-52-6
Formula
C10H20O
MW
156.26 g/mol
VQ-025532
Reference Standard
2-epi-Emtricitabine chemical structure
2-epi-Emtricitabine
CAS
145416-34-8
Formula
C8H10FN3O3S
MW
247.25 g/mol
VQ-022514
Reference Standard
5-epi Emtricitabine chemical structure
5-epi Emtricitabine
CAS
145986-26-1
Formula
C8H10FN3O3S
MW
247.25 g/mol
VQ-022517
Reference Standard
Emtricitabine WS chemical structure
Emtricitabine WS
CAS
143491-57-0
Formula
C8H10FN3O3S
MW
247.25 g/mol
In stock
Reference Standard
Ent-Emtricitabine chemical structure
Ent-Emtricitabine
CAS
137530-41-7
Formula
C8H10FN3O3S
MW
247.25 g/mol
VQ-022512
Reference Standard
Flucytosine chemical structure
Flucytosine
CAS
2022-85-7
Formula
C4H4FN3O
MW
129.09 g/mol
In stock

FAQs — Emtricitabine impurities

Which Emtricitabine impurities do you supply?

We list 38 Emtricitabine-related reference materials, including process impurities, degradation products, 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 Emtricitabine 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 Emtricitabine 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 Emtricitabine impurity standards

We reply within one business day with price, pack options, lead time and documentation.

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