Impurity reference standards
Sumatriptan impurities & reference standards
Characterised Sumatriptan impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
38reference materials
1nitrosamine impurities
1isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Sumatriptan Succinate
103628-46-2 · C14H21N3O2S
1-(4-Hydrazinylphenyl)-N-methylmethanesulfonamide
- CAS
- 139272-29-0
- Formula
- C8H13N3O2S
- MW
- 215.28 g/mol
VQ-042317
4-Chloro-1-hydroxy Butane Sulphonic Acid Sodium Salt
- CAS
- 54322-20-2
- Formula
- C4H8ClNaO4S
- MW
- 210.61 g/mol
In stock
O-(2,3,4,5,6-Pentafluorobenzyl)hydroxylaminehydrochloride
- CAS
- 57981-02-9
- Formula
- C7H5ClF5NO
- MW
- 249.56 g/mol
VQ-033989
FAQs — Sumatriptan impurities
Which Sumatriptan impurities do you supply?
We list 38 Sumatriptan-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 Sumatriptan 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 Sumatriptan 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 Sumatriptan impurity standards
We reply within one business day with price, pack options, lead time and documentation.