Amoxicillin Trihydrate structure
Human APIs

Amoxicillin Trihydrate

CAS Registry Number: 26787-78-0

Amoxicillin Trihydrate — active pharmaceutical ingredient (API) manufactured to pharmacopoeial specification. Purity ≥99.0% (HPLC). Physical form: White crystalline powder. CAS Registry Number: 26787-78-0. Supplied in 50g, 200g, 1000g quant

Product information

Amoxicillin Trihydrate — active pharmaceutical ingredient (API) manufactured to pharmacopoeial specification. Purity ≥99.0% (HPLC). Physical form: White crystalline powder. CAS Registry Number: 26787-78-0. Supplied in 50g, 200g, 1000g quantities from $32.00/g entry for laboratory research, analytical method development, and reference-standard applications.

Product specifications

CAS Registry Number
26787-78-0
Therapeutic Category
Human APIs
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 Amoxicillin Trihydrate-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 Amoxicillin Trihydrate

What is Amoxicillin Trihydrate used for?

Amoxicillin Trihydrate is supplied as a pharmaceutical-grade human apis for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using Amoxicillin Trihydrate typically reference it under CAS Registry Number 26787-78-0.

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

Our Amoxicillin Trihydrate 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 Amoxicillin Trihydrate?

Quote requests for Amoxicillin Trihydrate 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 Amoxicillin Trihydrate to?

We export Amoxicillin Trihydrate 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 Human APIs catalogue or the full 560+ product directory. Reference documents: certifications portfolio · quality system · FDA DMF buyer guide · EU CEP supplier guide.