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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Suzetrigine, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Suzetrigine 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 Suzetrigine-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.

Suzetrigine Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Suzetrigine-d3 Stable Isotopes CS-O-59185 2649467-62-7 Enquire
Suzetrigine-d6 Stable Isotopes CS-O-59184 3078074-72-0 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Suzetrigine 4-Desfluoro Impurity Impurity CS-O-60914 2879214-09-0 Enquire
Suzetrigine Desfluoro Impurity Impurity CS-O-60910 ---- Enquire
Suzetrigine Enantiomer Impurity Impurity CS-O-60913 2649467-65-0 Enquire
Suzetrigine Methyl Acetate Impurity Impurity CS-O-60912 2879218-02-5 Enquire