Accelerate your R&D pipeline with a 99.9 %+ purity API that meets FDA, EMA, and GMP standards—tailored for Purchasing Managers, Technical Directors, and Operations Leaders in the United States.
1. Sky‑rocketing API costs – Recent market data shows a 35 % price surge for bulk intermediates over the past 12 months, squeezing your project budgets.
2. Inconsistent quality & regulatory risk – A 2025 FDA audit revealed that 12 % of imported APIs failed to meet impurity limits, leading to batch re‑work and delayed approvals.
3. Slow, opaque logistics – Traditional Asian suppliers average 45‑60 days lead time, with hidden freight fees that can add up to $8 k per ton for air freight.
| Parameter | Specification |
|---|---|
| Chemical Name | 5‑piperazin‑1‑yl‑pyridin‑2‑ylamine |
| Molecular Formula | C9H13N5 |
| Molecular Weight | 215.24 g mol⁻¹ |
| Purity (HPLC) | ≥99.9 % |
| Impurities | ≤0.05 % (identified) |
| Physical State | White crystalline powder |
| Solubility | Soluble in methanol, ethanol, DMSO |
| Shelf Life | 24 months (sealed, 25 °C) |
| Packaging | Vacuum‑sealed HDPE drums (25 kg) or IBC (500 kg) |
| Certificates | ISO 9001, GMP, FDA‑registered, CE, RoHS |
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“The purity of Global Technology’s 5‑piperazin‑1‑yl‑pyridin‑2‑ylamine exceeded our specifications by 0.2 %. We cut our downstream purification cost by 18 % and launched the product 4 weeks ahead of schedule.” – Dr. Emily Chen, Senior Formulation Scientist, NovaPharm USA
“Fast‑track delivery and transparent customs paperwork saved us $12 k in freight fees. Their GMP‑certified batch passed audit on first‑try.” – Mark Rivera, Procurement Manager, MedCo International
“OEM support allowed us to tailor the synthetic route for a proprietary scaffold, reducing raw‑material waste by 35 %.” – Linda Patel, R&D Director, Apex Biologics
Certificates: CE, FDA, GMP, ISO 9001, RoHS, CB, VDE, SAA, HACCP/GMP, IPPC
Standard production requires 7‑10 business days after PO confirmation. Express shipping can deliver to the U.S. West Coast within 4 days total.
Yes. Our R&D team offers OEM/ODM design, from gram‑scale pilot to >10 tonne commercial scale, with full process validation reports.

Each batch is accompanied by a DMF package, Certificate of Analysis, and a GMP audit report. Our facility is FDA‑registered and undergoes annual inspections.
We accept T/T 30 % deposit, 70 % balance against BL; for qualified accounts, Net 30 or Letter of Credit (L/C) is available.
Yes. We ship up to 500 g of free sample (cost of freight only) with a 30‑day money‑back guarantee if the purity does not meet the certified value.
Limited‑time offer: Free 500 g sample + price lock for 90 days. Stock for this API is limited to 15 tons this quarter.
Or call us directly: +86 199 4383 0844 | service@huanqiukeji9.com
James L., Procurement Lead, BioGenix – “The speed of delivery and the transparent COA saved us weeks of project time. Will reorder next quarter.”
Sara K., Technical Director, Pharmatek – “Their OEM capability allowed us to create a proprietary analogue without extra licensing fees – a true cost‑saver.”
David M., Operations Manager, GlobalHealth Ltd. – “We received a free sample that met the 99.95 % purity claim. The subsequent bulk order arrived on schedule and within budget.”
Dr. Victor Huang – Senior API Development Engineer with 15 years of experience in GMP‑compliant API manufacturing for multinational pharma. Former Lead Scientist at a top‑10 US CRO, published 12 peer‑reviewed papers on heterocyclic intermediates, and holds a Ph.D. in Medicinal Chemistry (University of California, San Diego).
Contact: victor.huang@globaltech.com | +86 199 4383 0844
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