2,4-Dimethyl-1H-pyrrole-3-carboxylic Acid Ethyl Ester
- CAS
- 2199-51-1
- Formula
- C9H13NO2
- MW
- 167.2 g/mol
VQ-039276
Impurity reference standards
Sunitinib impurities & reference standards
Characterised Sunitinib impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
39reference materials
5nitrosamine impurities
1isotope-labelled
COAHPLC · NMR · MS on request
3,5-Dimethyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester
- CAS
- 86770-31-2
- Formula
- C14H21NO4
- MW
- 267.32 g/mol
VQ-033994
4-(Ethoxycarbonyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid
- CAS
- 5442-91-1
- Formula
- C10H13NO4
- MW
- 211.21 g/mol
VQ-044113
Ethyl Ethylene diamine nitroso Impurity (Mixture of Rotamers)
- CAS
- 2680539-26-6
- Formula
- C4H11N3O
- MW
- 117.15 g/mol
In stock
Sunitinib Dimethyl Pyrrole Nitroso Impurity (Mixture of Rotamers)
- Formula
- C11H18N4O2
- MW
- 238.29 g/mol
In stock
Sunitinib Formyl Dimethyl Pyrrole Nitroso Impurity (Mixture of Rotamers)
- Formula
- C12H18N4O3
- MW
- 266.3 g/mol
In stock
![Sunitinib Impurity-A (Mixture of E & Z isomers)[ 557795-19-4(Z Isomer) + 1691223-83-2 (E Isomer)]](/media/pack/sunitinib-impurity-a-mixture-of-e-and-z-isomers-557795-19-4z-isomer-plus-1691223-83-2-e.svg?v=3)
Sunitinib Impurity-A (Mixture of E & Z isomers)[ 557795-19-4(Z Isomer) + 1691223-83-2 (E Isomer)]
- Formula
- C22H27FN4O2
- MW
- 398.47 g/mol
In stock
Sunitinib N,N-Didesethyl Hydrochloride Impurity
- CAS
- 1217216-61-9
- Formula
- C18H20ClFN4O2
- MW
- 378.8 g/mol
In stock
Sunitinib Tert Butyl Dimethyl Pyrrole Nitroso Impurity (Mixture of Rotamers)
- Formula
- C16H26N4O4
- MW
- 338.4 g/mol
In stock
FAQs — Sunitinib impurities
Which Sunitinib impurities do you supply?
We list 39 Sunitinib-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 Sunitinib 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 Sunitinib 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 Sunitinib impurity standards
We reply within one business day with price, pack options, lead time and documentation.