Impurity reference standards
Risdiplam impurities & reference standards
Characterised Risdiplam impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
5reference materials
1nitrosamine impurities
COAHPLC · NMR · MS on request
![tert-Butyl 7-(2-(2,8-dimethylimidazo[1,2-b]pyridazin-6-yl)-4-oxo-4H-pyrido[1,2-a]pyrimidin-7-yl)-4,7-diazaspiro[2.5]octane-4-carboxylate chemical structure](/media/structures/IMUOFNBINVQDLO-UHFFFAOYSA-N.svg)
tert-Butyl 7-(2-(2,8-dimethylimidazo[1,2-b]pyridazin-6-yl)-4-oxo-4H-pyrido[1,2-a]pyrimidin-7-yl)-4,7-diazaspiro[2.5]octane-4-carboxylate
- CAS
- 2133298-74-3
- Formula
- C27H31N7O3
- MW
- 501.6 g/mol
VQ-044418
FAQs — Risdiplam impurities
Which Risdiplam impurities do you supply?
We list 5 Risdiplam-related reference materials, including process impurities, degradation products, nitrosamine impurities and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Risdiplam 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 Risdiplam 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 Risdiplam impurity standards
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