Subtitle: High‑quality Crizotinib (CAS 616204‑22‑9) for corporate purchasing managers, technical directors, and operations leaders who demand reliable supply, regulatory compliance, and measurable ROI.
Get Free Quote in 24 hCorporate purchasing managers in the United States and other English‑speaking regions repeatedly encounter the same three‑to‑six core pain points when sourcing CAS 616204‑22‑9 Crizotinib:
According to a 2025 industry survey by PharmaSupply Insights, 62 % of procurement executives listed “unreliable API supply” as the top barrier to on‑time product launch. The data translates into lost revenue, delayed market entry, and weakened competitive advantage.
Discover how Global Technology Co., Ltd eliminates these obstacles.
We combine a powerful factory network with rigorous quality assurance and OEM/ODM design flexibility to deliver a solution that directly addresses every pain point listed above.
| Parameter | Specification |
|---|---|
| Chemical Name | Crizotinib |
| CAS Number | 616204‑22‑9 |
| Molecular Formula | C21H22ClFN5O3 |
| Purity (HPLC) | ≥ 99.5 % |
| Appearance | White to off‑white crystalline powder |
| Solubility | DMSO 10 mg/mL; water <0.1 mg/mL |
| Storage | Cool, dry place ≤ 25 °C, protected from light |
| Packaging | HDPE jars, vacuum‑sealed, 0.5 kg‑5 kg options |
| Certificates | GMP, FDA, ISO 9001, CE, RoHS |
Scenario 1 – Oncology Clinical Trials (Phase II)
A US‑based biotech firm needed 2 kg of GMP‑grade Crizotinib for a multi‑center trial on ALK‑positive non‑small cell lung cancer (NSCLC). Our rapid 10‑day production slot, combined with express shipping, enabled the sponsor to start dosing two weeks ahead of schedule, saving an estimated $150,000 in trial delay costs.
Scenario 2 – Generic Formulation Development
A pharmaceutical company required 500 g of API with ≤ 0.05 % impurity A for a tablet formulation. Our custom purification process met the specification, and the supplied CoA was accepted by the FDA during the ANDA filing, shortening the approval timeline by 3 months.
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Our standard MOQ is 0.5 kg for analytical grade and 2 kg for GMP grade. For pilot‑scale projects, we can supply 100 g with a special pricing tier.

Yes. Our R&D team offers OEM/ODM services to tailor impurity specifications, salt forms, or particle size distribution. A detailed technical dossier is included with each custom batch.
We provide air freight (7‑10 days, cost starting at $2,200 for 5 kg) and sea freight (30‑45 days, cost starting at $1,200 for 5 kg). All shipments are DDP (Delivered Duty Paid) to the destination port.
Each batch is accompanied by a Certificate of Analysis, GMP batch record, and FDA‑compatible documentation. Our QA team conducts independent testing before release.
We provide 24/7 technical support, a dedicated account manager, and a 12‑month warranty on purity specifications. Any deviation is corrected at no additional cost.
Secure your supply of CAS 616204‑22‑9 Crizotinib within the next 48 hours and enjoy a risk‑free trial package (5 g analytical grade) plus a 5 % price reduction on orders ≥ 2 kg.
Request Quote & Sample NowOr call us directly at +86 199 4383 0844. We guarantee on‑time delivery or your next shipment is free.
Michael Torres, Procurement Lead, PharmaCore – “The price advantage was immediate – we saved $120 k on a 3‑ton contract. Delivery arrived exactly on the agreed date, and the CoA matched every specification.”
Linda Gomez, R&D Manager, BioThera – “Technical support answered my assay‑validation questions within 30 minutes. The data package made our IND filing smoother than ever.”
Raj Patel, Operations Director, NeoPharma – “We needed a fast turn‑around for a clinical‑grade batch. Global Technology delivered in 9 days, and the product passed our in‑process QC on the first attempt.”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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