Topotecan HCl pharmaceutical API powder — CAS 119413-54-6 — WHO-GMP manufacturer Longshine Boi-Tech, Pune, India
Human APIs

Topotecan HCl

CAS Registry Number: 119413-54-6

Topotecan HCl — active pharmaceutical ingredient (API) manufactured to pharmacopoeial specification. Purity ≥99.0%. CAS Registry Number: 119413-54-6. Supplied in bulk quantities from $55000.00/g entry for laboratory research, analytical met

Product information

Topotecan HCl — active pharmaceutical ingredient (API) manufactured to pharmacopoeial specification. Purity ≥99.0%. CAS Registry Number: 119413-54-6. Supplied in bulk quantities from $55000.00/g entry for laboratory research, analytical method development, and reference-standard applications.

Product specifications

CAS Registry Number
119413-54-6
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 Topotecan HCl-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.
View interactive page & request quote Email sales Order a sample

Frequently asked questions about Topotecan HCl

What is Topotecan HCl used for?

Topotecan HCl 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 Topotecan HCl typically reference it under CAS Registry Number 119413-54-6.

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

Our Topotecan HCl 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 Topotecan HCl?

Quote requests for Topotecan HCl 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 Topotecan HCl to?

We export Topotecan HCl 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 Human APIs APIs

Other human apis molecules from Longshine Boi-Tech's WHO-GMP catalogue — each with active regulatory filings, audit-ready CoA, and samples available under CDA.

Trametinib
CAS 871700-17-3
Capecitabine
CAS 154361-50-9
Abiraterone Acetate
CAS 154229-18-2
Emtricitabine
CAS 143491-57-0
Valacyclovir HCl
CAS 124832-27-5
Quetiapine Fumarate
CAS 111974-72-2
Tamsulosin HCl
CAS 106463-17-6
Vildagliptin
CAS 274901-16-5

Related categories & resources

Browse the full Human APIs catalogue or all 560+ products. Reference documents: certifications portfolio · quality system · FDA DMF buyer guide · EU CEP supplier guide · complete product index.