Triptorelin Acetate is a synthetic decapeptide analogue of gonadotropin-releasing hormone (GnRH), used in the palliative treatment of advanced prostate cancer, endometriosis, uterine fibroids, and precocious puberty. Manufactured via solid-phase peptide synthesis (SPPS) to Ph. Eur. specifications with full amino acid analysis, HRMS characterisation, and counter-ion documentation.
We maintain regulatory dossiers in the following jurisdictions for Triptorelin Acetate-relevant molecules. Letter of Authorization (LoA) and CEP / DMF / ASMF references are issued at no charge to qualified buyers.
Triptorelin Acetate is supplied as a pharmaceutical-grade peptides for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using Triptorelin Acetate typically reference it under CAS Registry Number 57773-63-4.
Our Triptorelin Acetate is manufactured under WHO-GMP and ISO 9001:2015 conditions in Pune, India. Per-batch Certificate of Analysis (CoA) is released against USP / Ph. Eur. / IP / JP specifications depending on destination market. We hold US FDA Drug Master File and EDQM Certificate of Suitability dossiers for the molecules where regulatory recognition is required; Letter of Authorization (LoA) is issued at no charge to qualified buyers.
Quote requests for Triptorelin Acetate are turned around within 24 business hours (IST, Pune). Bulk APIs typically ship within 7-10 business days of confirmed PO; air freight to North America and Europe runs 4-5 days door-to-door. Sample agreements are signed before shipping QC-grade material to your formulation laboratory.
We export Triptorelin Acetate to 50+ countries including the United States, Canada, Mexico, Brazil, the European Union, the United Kingdom, Japan, Australia, South Korea, the GCC and across South-East Asia. All regulatory documents (DMF / CEP / LoA) and shipping incoterms (EXW, FCA, CIP, DAP, DDP) are negotiated per buyer.
Other peptides molecules from Longshine Boi-Tech's WHO-GMP catalogue — each with active regulatory filings, audit-ready CoA, and samples available under CDA.
Browse the full Peptides catalogue or all 560+ products. Reference documents: certifications portfolio · quality system · FDA DMF buyer guide · EU CEP supplier guide · complete product index.