(S)-6-(2-Fluorobenzyl)-1-(1-hydroxy-3-methylbutan-2-yl)-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
- CAS
- 2055025-82-4
- Formula
- C23H24FNO5
- MW
- 413.4 g/mol
VQ-025519
Impurity reference standards
Elvitegravir impurities & reference standards
Characterised Elvitegravir impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
10reference materials
COAHPLC · NMR · MS on request
(S)-6-(3-Chloro-2-fluorobenzyl)-1-(1-hydroxy-4-methylpentan-2-yl)-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
- CAS
- 1534364-53-8
- Formula
- C24H25ClFNO5
- MW
- 461.9 g/mol
VQ-025518
(S)-6-(3-Chloro-2-fluorobenzyl)-1-(1-hydroxypropan-2-yl)-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
- CAS
- 697761-63-0
- Formula
- C21H19ClFNO5
- MW
- 419.8 g/mol
VQ-035433
1-(5-(3-Chloro-2-fluorobenzyl)-2,4-dimethoxyphenyl)ethan-1-one
- CAS
- 1551444-36-0
- Formula
- C17H16ClFO3
- MW
- 322.8 g/mol
VQ-048189
![7-Fluoro-1,4-dihydro-1-[(1S)-1-(hydroxymethyl)-2-methylpropyl]-6-iodo-4-oxo-3-Quinolinecarboxylic acid ethyl ester chemical structure](/media/structures/VCHTVAKQQUGTTA-OAHLLOKOSA-N.svg)
7-Fluoro-1,4-dihydro-1-[(1S)-1-(hydroxymethyl)-2-methylpropyl]-6-iodo-4-oxo-3-Quinolinecarboxylic acid ethyl ester
- CAS
- 697762-60-0
- Formula
- C17H19FINO4
- MW
- 447.24 g/mol
VQ-048188
Ethyl 3-(5-(3-chloro-2-fluorobenzyl)-2,4-dimethoxyphenyl)-3-oxopropanoate
- CAS
- 949465-81-0
- Formula
- C20H20ClFO5
- MW
- 394.8 g/mol
VQ-036963
FAQs — Elvitegravir impurities
Which Elvitegravir impurities do you supply?
We list 10 Elvitegravir-related reference materials, including process impurities, degradation products and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Elvitegravir 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 Elvitegravir 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 Elvitegravir impurity standards
We reply within one business day with price, pack options, lead time and documentation.