PE 22-28 pharmaceutical API powder — CAS LB-PE22-28 — WHO-GMP manufacturer Longshine Boi-Tech, Pune, India
Peptides

PE 22-28

CAS Registry Number: LB-PE22-28

PE 22-28 is a humanin-derived heptapeptide research reference standard studied in mitochondrial protection research. Supplied as lyophilised powder in glass vial, ≥98% HPLC purity, MS-verified. Per-lot CoA. Research use only.

Product information

PE 22-28 is a humanin-derived heptapeptide research reference standard studied in mitochondrial protection research. Supplied as lyophilised powder in glass vial, ≥98% HPLC purity, MS-verified. Per-lot CoA. Research use only.

Product specifications

CAS Registry Number
LB-PE22-28
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 PE 22-28-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 PE 22-28

What is PE 22-28 used for?

PE 22-28 is supplied as a pharmaceutical-grade peptides for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using PE 22-28 typically reference it under CAS Registry Number LB-PE22-28.

What quality and regulatory standards does Longshine Boi-Tech's PE 22-28 meet?

Our PE 22-28 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 PE 22-28?

Quote requests for PE 22-28 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 PE 22-28 to?

We export PE 22-28 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.