For purchasing managers and technical directors who demand consistent batch‑to‑batch purity and on‑time delivery of a critical piperazine intermediate, our API eliminates the typical bottlenecks of cost, quality, and logistics.
In 2025‑2026, over 37 % of global pharmaceutical firms reported production delays caused by low‑purity intermediates. The following pain points are recurring across the United States, Canada, and the United Kingdom:
Imagine a scenario where your R&D team waits 30 days longer than planned because the API batch fails purity testing. The downstream impact includes delayed IND filing, missed market windows, and a projected revenue loss of USD 2 million per quarter.
What if you could cut cost by 30 % and receive a verified, ISO 9001‑certified batch within 10 days? The solution is below.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 1018685‑16‑9 | |
| Chemical Name | Tert‑butyl 4‑(4‑aminophenyl)piperazine‑1‑carboxylate | |
| Molecular Formula | C₁₆H₂₅N₃O₂ | |
| Molecular Weight | 283.36 | g mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 % | |
| Appearance | White to off‑white crystalline powder | |
| Moisture Content | <1 % | |
| Solubility | Soluble in methanol, ethanol, DMSO | |
| Storage | Cool, dry place, ≤ 25 °C | |
| Certificates | GMP, ISO 9001, FDA DMF, CE, RoHS |
2-methyl-2h-isothiazol-3-one Acetohexamide-Acipimox-Aclyvir-supplier C-Peptide-(57-87)-Human C20-Otbu-glu-otbu
Our API is a cornerstone for the synthesis of:
Case Study – Mid‑Size Biotech (USA)
Challenge: Needed 5 tonnes of a piperazine intermediate for a Phase II IND submission, with ≤ 30 days lead time. Existing vendors quoted USD 160 / kg and required 8 weeks.
Solution: Global Technology supplied 5 tonnes at USD 108 / kg, delivered in 12 days via air freight, accompanied by full GMP batch records.
Result: The client reported a 37 % reduction in material cost and a 45 % faster IND filing, translating to an estimated USD 3.2 million earlier market entry.
The MOQ is 100 g for research‑grade material and 1 kg for commercial‑grade API. Bulk discounts start at 5 kg.
Yes. Our OEM/ODM team can develop HCl, sulfate, or free‑base forms, as well as tailor particle size distribution to meet your formulation needs.
Each batch includes a Certificate of Analysis (CoA), GMP batch record, Safety Data Sheet (SDS), and a full chain‑of‑custody export declaration.

We maintain a dedicated air‑freight hub in Zhengzhou. Orders placed before 14:00 CST can be dispatched the same day, reaching US West Coast ports in ≤ 10 days.
Our technical service team provides 24/7 email support, on‑site troubleshooting (if needed), and a 12‑month warranty against purity deviation.
Limited‑time Offer: First‑time buyers receive a free 5 g sample and a money‑back guarantee if purity < 99 % is not met.
Or reach us instantly via WhatsApp/Phone or Email.
“The purity consistency is unmatched. We’ve never experienced a single out‑of‑spec batch.”
- James Patel, Senior Procurement Manager, MedLife Corp.
“Fast delivery saved our clinical trial timeline. The free sample let us validate the material before committing.”
- Sara Liu, Technical Director, BioNova Ltd.
“Competitive pricing without compromising on GMP documentation gave us a clear regulatory pathway.”
- Mark O’Connor, Operations Manager, PharmaEdge USA.
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
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Trusted by Global Pharma Leaders
“Switching to Global Technology’s Tert‑butyl piperazine API cut our raw‑material spend by 32 % and eliminated a two‑week delay in our pilot plant.” – Dr. Laura Chen, VP of Procurement, Pharmaco Inc.
Certificates & Compliance
All certificates are available for download upon request.