(Z)-7-((1R,2R,3R,5S)-3,5-Dihydroxy-2-((S,E)-3-hydroxyoct-1-en-1-yl)cyclopentyl)hept-5-enoate sodium
- CAS
- 58581-22-9
- Formula
- C20H33NaO5
- MW
- 376.47 g/mol
VQ-037032
Impurity reference standards
Epoprostenol impurities & reference standards
Characterised Epoprostenol impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
6reference materials
COAHPLC · NMR · MS on request
![5-((3AS,4R,5R,6aS)-5-Hydroxy-4-((S,E)-3-hydroxyoct-1-en-1-yl)-3a,5,6,6a-tetrahydro-4H-cyclopenta[b]furan-2-yl)pentanoic acid, sodium Salt](/media/pack/5-3as4r5r6as-5-hydroxy-4-se-3-hydroxyoct-1-en-1-yl-3a566a-tetrahydro-4h-cyclopentabfuran.svg?v=3)
5-((3AS,4R,5R,6aS)-5-Hydroxy-4-((S,E)-3-hydroxyoct-1-en-1-yl)-3a,5,6,6a-tetrahydro-4H-cyclopenta[b]furan-2-yl)pentanoic acid, sodium Salt
- CAS
- 68979-98-6
- Formula
- C20H31NaO5
- MW
- 374.45 g/mol
VQ-030517
FAQs — Epoprostenol impurities
Which Epoprostenol impurities do you supply?
We list 6 Epoprostenol-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 Epoprostenol 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 Epoprostenol 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 Epoprostenol impurity standards
We reply within one business day with price, pack options, lead time and documentation.