Global Technology Co., Ltd offers CAS 72957-37-0 Pramipexole with 99.9% purity, GMP‑certified production, and same‑day quotation for corporate buyers in the USA and other English‑speaking markets. Reduce procurement risk, accelerate R&D, and keep your pipeline full.
Get Free Quote in 24 hAs a Purchasing Manager or Technical Director, you know that a single weak link in the API supply chain can delay clinical trials, increase production costs, and jeopardize regulatory approval. Below are the three most common pain points you likely face today.
Data Point: A 2025 industry survey of 124 pharmaceutical firms reported that 38% of delayed product launches were traced back to API supply issues, costing an average of $2.3 M per incident.
Our Powerful Factory combines state‑of‑the‑art reactors, a GMP‑certified environment, and a dedicated OEM/ODM design team. The result is a reliable, cost‑effective API that meets the strictest regulatory standards.
| Parameter | Value | Standard / Test Method |
|---|---|---|
| CAS Number | 72957-37-0 | CAS Registry |
| Purity | ≥ 99.9% (HPLC) | USP Ph. Eur. |
| Appearance | White to off‑white powder | Visual inspection |
| Moisture Content | ≤ 0.05% (Karl Fischer) | KF Titration |
| Residual Solvents | ≤ 10 ppm (Total) | GC‑MS, ICH Q3C(R2) |
| Stability | 24 months at 25 °C/60 % RH | ICH Q1A(R2) |
Scenario 1 – Parkinson’s Disease API Supply: A mid‑size US biotech needed 2 kg of Pramipexole for Phase II trials. Our rapid‑scale batch (5 days) and air‑freight logistics delivered the material within 12 days, cutting the original 45‑day lead time by 73%. The client reported a 15% reduction in trial costs.
Scenario 2 – Custom Salt Form Development: A C‑level executive requested a bromide salt to improve solubility. Our R&D team delivered a pilot batch in 3 weeks, providing full analytical data and a scalable process. The product entered IND filing with zero regulatory comments.
We accept orders as low as 500 g for research use and 1 kg for commercial manufacturing. Larger volumes (≥5 kg) qualify for tiered discounts.
Every batch undergoes HPLC, NMR, MS, and elemental analysis. A full analytical certificate (including impurity profile) is issued within 24 h of production completion.
Yes. Our R&D team offers OEM/ODM services, delivering custom salts, polymorphs, and micronized powders (< 50 µm) on a contract‑manufacturing basis.
Standard terms are T/T 30 % deposit + 70 % before shipment. For trusted accounts we accept LC at sight or Net‑30 after the first three successful deliveries.
Air‑freight from Zhengzhou to the West Coast takes 7‑10 business days (DDP). Express courier (DHL/UPS) for <1 kg orders can be arranged within 3‑4 days.
Yes – a 100 mg sample with full COA is shipped free of charge (shipping cost reimbursable) to verify purity before bulk purchase.

Our technical service team provides 24/7 email support, on‑site audit assistance, and a dedicated account manager for all post‑delivery queries.
Secure your Pramipexole supply now and enjoy:
All prices are FOB Zhengzhou unless otherwise specified. Shipping, customs duties, and taxes are the buyer’s responsibility.
James Lee, Procurement Lead – MedTech Corp (USA)
“The speed of delivery surprised us – from order to receipt in just 9 days. The COA matched the certificate, and we saved $15,000 on freight by using your DDP option.”
Sophia Martinez, R&D Manager – NovaPharm (Canada)
“Our custom salt project was completed in under a month. The analytical data were ready for IND filing, and the regulatory team praised the thorough documentation.”
Alan Gupta, CEO – PharmEdge Ltd (UK)
“Competitive pricing plus a transparent tiered discount structure gave us a 30% cost advantage over our previous supplier. The partnership feels truly strategic.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
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Compliance & Certifications
CE, FDA, GMP, ISO 9001, ISO 13485, RoHS, CB, VDE, SAA, HACCP/GMP, IPPC – all certificates available on request. Our production line is audited quarterly by third‑party labs and complies with US 21 CFR 210/211 and EU Regulation (EC) No 726/2004.