Enclomiphene pharmaceutical API powder — CAS 15690-57-0 — WHO-GMP manufacturer Longshine Boi-Tech, Pune, India
Peptides

Enclomiphene

CAS Registry Number: 15690-57-0

Enclomiphene — custom peptide manufactured for research and pharmaceutical applications. Purity ≥98.0% HPLC. CAS Registry Number: 15690-57-0. Supplied in 1g, 5g, 10g+ quantities from $1000.00/g entry for laboratory research, analytical meth

Product information

Enclomiphene — custom peptide manufactured for research and pharmaceutical applications. Purity ≥98.0% HPLC. CAS Registry Number: 15690-57-0. Supplied in 1g, 5g, 10g+ quantities from $1000.00/g entry for laboratory research, analytical method development, and reference-standard applications. Research use only — not for human or animal consumption.

Product specifications

CAS Registry Number
15690-57-0
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 Enclomiphene-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 Enclomiphene

What is Enclomiphene used for?

Enclomiphene is supplied as a pharmaceutical-grade peptides for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using Enclomiphene typically reference it under CAS Registry Number 15690-57-0.

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

Our Enclomiphene 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 Enclomiphene?

Quote requests for Enclomiphene 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 Enclomiphene to?

We export Enclomiphene 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.