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

Neohesperidin Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Neohesperidin API CS-E-00294 13241-33-3 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Neohesperidin Dihydrochalcone Impurity A Impurity CS-ED-42320 23643-71-2 Enquire
Neohesperidin Dihydrochalcone Impurity B Impurity CS-ED-42321 38665-01-9 Enquire
Neohesperidin Dihydrochalcone Impurity E Impurity CS-ED-42322 35573-79-6 Enquire
Neohesperidin Dihydrochalcone Impurity F Impurity CS-ED-42323 21940-36-3 Enquire
Neohesperidin Dihydrochalcone Impurity G Impurity CS-ED-42324 35400-60-3 Enquire