Triptorelin Acetate structure
Peptides

Triptorelin Acetate

CAS Registry Number: 57773-63-4

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-

Product information

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.

Product specifications

CAS Registry Number
57773-63-4
Therapeutic Category
Peptides
API Technology
Synthetic / Semi-synthetic (per molecule)
Development Status
Commercial — stocked
Manufacturer
Longshine Boi-Tech Pvt. Ltd.
Facility
Pune, Maharashtra, India 411001

Regulatory filings & 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.

US FDA DMF (Type II)
EDQM CEP (where applicable)
Brazil ANVISA
Canada Health Canada
Japan PMDA
Korea MFDS
GCC SFDA
EU CEP
WHO-GMP & ISO 9001:2015 certified. US FDA Drug Master File available. EDQM CEP supplied for EU procurement. Pharmacopoeial release against USP, Ph. Eur., IP, JP. CoA on every batch. First-shipment lead time 7-10 business days for stocked APIs.
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Frequently asked questions about Triptorelin Acetate

What is Triptorelin Acetate used for?

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.

What quality and regulatory standards does Longshine Boi-Tech's Triptorelin Acetate meet?

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.

How do I request a quote, sample, or proforma invoice for Triptorelin Acetate?

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.

Which countries does Longshine Boi-Tech supply Triptorelin Acetate to?

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.

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Related categories & resources

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.