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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Diroximel, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Diroximel impurity reference standards are invaluable for pharmaceutical research, supporting product development, ANDA and DMF submissions, quality control (QC), method validation, and stability studies. They also aid in identifying unknown impurities and assessing genotoxic potential.
Our Diroximel-related products undergo thorough characterization and are supplied with detailed Certificates of Analysis (COA) and analytical data that meet regulatory requirements. All supplied products are re-tested at regular intervals to ensure ongoing quality and compliance.

Diroximel Related Compounds

Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(2E)-4-[2-(2,5-dioxopyrrolidin-1-yl)ethoxy]- 4-oxobut-2-eno... Impurities CS-EO-00855 2101811-41-8 Enquire
2-(2,5-dioxopyrrolidin-1-yl)ethyl methyl (2Z)-but-2-enedioat... Impurities CS-EO-00856 Not Available Enquire
2-{4-[2-(2,5-dioxopyrrolidin-1-yl)ethoxy]-4-oxobutanamido}et... Impurities CS-O-37516 Not Available Enquire
Diroximel Fumarate-d4 Impurities CS-O-45473 Not Available Enquire
Diroximel Impurity 2 Impurities CS-EO-00678 Not Available Enquire