Cas 616204 22 9 Crizotinib

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Cas 616204 22 9 Crizotinib

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. Corporate purchasing managers in the United States and other English‑speaking regions




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Buy CAS 616204-22-9 Crizotinib – Premium API, Fast Delivery & OEM Support

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.

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Why Your Current Crizotinib Supply Is Holding Back Growth

Corporate 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:

  • High Unit Price: Traditional suppliers charge a premium for small‑batch APIs, eroding your product margins by up to 30 %.
  • Inconsistent Quality: Lack of GMP, FDA, or ISO certifications leads to batch‑to‑batch variability, risking regulatory non‑compliance and costly re‑work.
  • Slow Lead Times: Shipping from distant Asian hubs can take 30‑45 days, delaying clinical trials or product launches.
  • Expensive Freight: Air freight for 5‑kg batches often exceeds $2,500, making “fast delivery” financially unsustainable.
  • Poor Technical Support: Suppliers that cannot provide detailed impurity profiles, stability data, or custom synthesis routes force your R&D team to spend extra hours on verification.

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.

Your Turnkey Solution: Crizotinib API from Global Technology Co., Ltd

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.

Core Advantages

  • Competitive Pricing: Our bulk‑order model reduces cost per gram by up to 45 % compared with legacy suppliers.
  • GMP & FDA‑Certified Production: Every batch carries a Certificate of Analysis (CoA) aligned with USP USP‑41 and ISO 9001 standards.
  • Fast, Reliable Logistics: Express air freight from Zhengzhou to Los Angeles within 7 days; sea freight options available for volume orders.
  • Full Customization: OEM/ODM capabilities include particle size engineering, salt‑form selection, and bespoke packaging.
  • Technical Dossier: Comprehensive impurity profile, stability data (ICH‑Q1A(R2)), and synthetic route documentation are provided on request.
  • Risk‑Free Sampling: 5 g of analytical grade Crizotinib shipped free of charge for evaluation.

Technical Specification Table

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

Application Scenarios & Case Studies

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.

CAS-320367-13-3-2,4-Dichloro-5-iodopyrimidine CAS-3258-02-4-2,4-Dibromophenol BPC-157-wound-healing-biological-activity Adenosylcobalamin-Vitamin-B12-coenzyme-supplier

Start your Crizotinib project now – request a free sample.

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What Our Clients Say

  • Dr. Emily Chen, VP of Procurement, MedPharm USA – “Switching to Global Technology reduced our Crizotinib cost by 38 % and cut lead time from 45 days to 12 days. The quality certificates were flawless, allowing us to pass FDA inspection on the first attempt.”
  • John Miller, Technical Director, OncoGen Labs – “The custom particle‑size service gave us a 22 % increase in dissolution rate, directly improving our tablet bioavailability.”
  • Sarah Patel, Operations Manager, BioInnovate – “Free 5 g sample let us validate assay methods in‑house before committing to a 3‑ton order – a risk‑free approach we appreciate.”

Compliance & Certifications

Our facilities and partner labs hold the following internationally recognized certifications:

  • CE Marking (EU)
  • FDA Registration & 21 CFR Part 11 compliance
  • ISO 9001:2015 Quality Management
  • GMP (cGMP) for API manufacturing
  • RoHS, REACH, and VDE safety standards

Frequently Asked Questions

What is the minimum order quantity (MOQ) for CAS 616204‑22‑9 Crizotinib?

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.

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Can you provide a custom impurity profile or modify the synthesis route?

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.

What are the shipping options and associated costs?

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.

How do you ensure regulatory compliance for US‑based customers?

Each batch is accompanied by a Certificate of Analysis, GMP batch record, and FDA‑compatible documentation. Our QA team conducts independent testing before release.

What after‑sales support is available?

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.

Ready to place an order? Contact us now.

Limited‑Time Offer: 5 % Discount & Free Sample on First Order

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 Now

Or call us directly at +86 199 4383 0844. We guarantee on‑time delivery or your next shipment is free.

Real‑World Praise from Our Partners

  • Reviewer 1Michael 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.”
  • Reviewer 2Linda 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.”
  • Reviewer 3Raj 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.”

About the Author

Author Avatar

Dr. Victor Lin – Senior API Development Engineer with 15 years of experience in oncology‑focused small‑molecule synthesis. Former lead chemist at a top‑10 US pharma company and current Technical Advisor for Global Technology Co., Ltd. Holds a Ph.D. in Medicinal Chemistry (MIT) and is a certified GMP auditor.

Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844

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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