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VAQORACHEMICALS
Impurity reference standards

Imatinib impurities & reference standards

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

44reference materials
1nitrosamine impurities
5isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Imatinib
220127-57-1 · C30H35N7O4S
View API
Reference Standard
2-Toluidine-d7 chemical structure
2-Toluidine-d7
CAS
68408-22-0
Formula
C7H9N
MW
114.2 g/mol
VQ-048658
IP/BP/USP
Imatinib chemical structure
Imatinib
CAS
220127-57-1
Formula
C30H35N7O4S
MW
589.7 g/mol
VQ-004215
Reference Standard
Imatinib chemical structure
Imatinib
CAS
152459-95-5
Formula
C29H31N7O
MW
493.6 g/mol
VQ-031168
Reference Standard
Imatinib Impurity 1 chemical structure
Imatinib Impurity 1
CAS
106261-48-7
Formula
C13H18N2O2
MW
234.29 g/mol
In stock
Reference Standard
Imatinib Impurity 2 chemical structure
Imatinib Impurity 2
CAS
1356565-46-2
Formula
C42H47N9O2
MW
709.9 g/mol
In stock
Reference Standard
Imatinib-D3 chemical structure
Imatinib-D3
CAS
1134803-18-1
Formula
C29H31N7O
MW
496.6 g/mol
VQ-048657
Reference Standard
Imatinib-d4 chemical structure
Imatinib-d4
CAS
1134803-16-9
Formula
C29H31N7O
MW
497.6 g/mol
VQ-037673
Reference Standard
Imatinib-d8 chemical structure
Imatinib-d8
CAS
1092942-82-9
Formula
C29H31N7O
MW
501.7 g/mol
VQ-037672
Reference Standard
Isomaltitol chemical structure
Isomaltitol
CAS
534-73-6
Formula
C12H24O11
MW
344.31 g/mol
VQ-032721

FAQs — Imatinib impurities

Which Imatinib impurities do you supply?

We list 44 Imatinib-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 Imatinib 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 Imatinib 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 Imatinib impurity standards

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

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