Adrafinil structure
Nootropics

Adrafinil

CAS Registry Number: 63547-13-7

Cognitive-enhancement research compound Adrafinil — high-purity analytical reference standard. Purity ≥99.0%. CAS Registry Number: 63547-13-7. Supplied in bulk quantities from $550.00/g entry for laboratory research, analytical method devel

Product information

Cognitive-enhancement research compound Adrafinil — high-purity analytical reference standard. Purity ≥99.0%. CAS Registry Number: 63547-13-7. Supplied in bulk quantities from $550.00/g entry for laboratory research, analytical method development, and reference-standard applications.

Product specifications

CAS Registry Number
63547-13-7
Therapeutic Category
Nootropics
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 Adrafinil-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 Adrafinil

What is Adrafinil used for?

Adrafinil is supplied as a pharmaceutical-grade nootropics for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using Adrafinil typically reference it under CAS Registry Number 63547-13-7.

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

Our Adrafinil 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 Adrafinil?

Quote requests for Adrafinil 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 Adrafinil to?

We export Adrafinil 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.

Related categories

Browse our Nootropics catalogue or the full 560+ product directory. Reference documents: certifications portfolio · quality system · FDA DMF buyer guide · EU CEP supplier guide.