Tesamorelin Acetate pharmaceutical API powder — CAS 218949-48-5 — WHO-GMP manufacturer Longshine Boi-Tech, Pune, India
Peptides

Tesamorelin Acetate

CAS Registry Number: 218949-48-5

Tesamorelin Acetate is a synthetic 44-amino-acid analogue of human growth hormone-releasing hormone (GHRH), FDA-approved for the treatment of HIV-associated lipodystrophy (excess abdominal fat accumulation in patients on antiretroviral ther

Product information

Tesamorelin Acetate is a synthetic 44-amino-acid analogue of human growth hormone-releasing hormone (GHRH), FDA-approved for the treatment of HIV-associated lipodystrophy (excess abdominal fat accumulation in patients on antiretroviral therapy). Manufactured via SPPS with convergent fragment condensation for the 44-residue chain, characterised per Ph. Eur. peptide monograph requirements.

Product specifications

CAS Registry Number
218949-48-5
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 Tesamorelin 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 Tesamorelin Acetate

What is Tesamorelin Acetate used for?

Tesamorelin 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 Tesamorelin Acetate typically reference it under CAS Registry Number 218949-48-5.

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

Our Tesamorelin 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 Tesamorelin Acetate?

Quote requests for Tesamorelin 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 Tesamorelin Acetate to?

We export Tesamorelin 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

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