6-Bromo-4-((dimethylamino)methyl)-5-hydroxy-1-methyl-2-((phenylthio)methyl)-1H-indole-3-carboxylic acid
- CAS
- 3026921-16-1
- Formula
- C20H21BrN2O3S
- MW
- 449.4 g/mol
VQ-044135
Impurity reference standards
Umifenovir impurities & reference standards
Characterised Umifenovir impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
7reference materials
COAHPLC · NMR · MS on request
![6,7-Dibromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-[(phenylthio)methyl]-1H-Indole-3-carboxylic Acid Ethyl Ester chemical structure](/media/structures/YISQEJGSCYLMGZ-UHFFFAOYSA-N.svg)
6,7-Dibromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-[(phenylthio)methyl]-1H-Indole-3-carboxylic Acid Ethyl Ester
- CAS
- 153633-10-4
- Formula
- C22H24Br2N2O3S
- MW
- 556.3 g/mol
VQ-021357
![Ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1,2-dimethyl-1H-indole-3-carboxylate chemical structure](/media/structures/ORLWKKITHVJZOV-UHFFFAOYSA-N.svg)
Ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1,2-dimethyl-1H-indole-3-carboxylate
- CAS
- 153633-07-9
- Formula
- C16H21BrN2O3
- MW
- 369.25 g/mol
VQ-034488
![Ethyl 6-bromo-5-hydroxy-1-methyl-2-[(phenylsulfanyl)methyl]-1H-indole-3-carboxylate chemical structure](/media/structures/DAFNNZWQTJQQAP-UHFFFAOYSA-N.svg)
Ethyl 6-bromo-5-hydroxy-1-methyl-2-[(phenylsulfanyl)methyl]-1H-indole-3-carboxylate
- CAS
- 131707-24-9
- Formula
- C19H18BrNO3S
- MW
- 420.3 g/mol
VQ-023950
Ethyl 6-bromo-5-hydroxy-1-methyl-4-((methylamino)methyl)-2-((phenylthio)methyl)-1H-indole-3-carboxylate
- CAS
- 1130901-04-0
- Formula
- C21H23BrN2O3S
- MW
- 463.4 g/mol
VQ-028923
Methyl 6-bromo-4-((dimethylamino)methyl)-5-hydroxy-1-methyl-2-((phenylthio)methyl)-1H-indole-3-carboxylate
- CAS
- 1332614-17-1
- Formula
- C21H23BrN2O3S
- MW
- 463.4 g/mol
VQ-035195
FAQs — Umifenovir impurities
Which Umifenovir impurities do you supply?
We list 7 Umifenovir-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 Umifenovir 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 Umifenovir 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 Umifenovir impurity standards
We reply within one business day with price, pack options, lead time and documentation.