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

Ganirelix Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Ganirelix Acetate API CS-T-55218 129311-55-3 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Ganirelix Acetate Impurity B Impurity CS-T-93825 2135326-92-8 Enquire
Ganirelix Impurity A Impurity CS-P-01379 ---- In Stock
Ganirelix Impurity B Impurity CS-P-01380 Not Available In Stock
Ganirelix Impurity C Impurity CS-P-01381 Not Available In Stock
Ganirelix Impurity F Impurity CS-T-00968 ---- In Stock
Ganirelix Impurity F (RRR)Impurity Impurity CS-T-64473 129225-22-5 Enquire
Ganirelix Impurity D (Mono-Acetyl- Ganilelix) Impurity CS-P-01382 Not Available Enquire
Ganirelix Impurity E Impurity CS-P-04717 Not Available Enquire


Peptide

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
D-Ser(4)-Ganirelix Peptide CS-O-44481 Not Available Enquire
L-Ala(10)-Ganirelix Peptide CS-O-44482 Not Available Enquire