Regorafenib
I have found results from30+products and10+suppliers aboutRegorafenib
99% Raw Material Regorafenib CAS 755037-03-7 Pharmaceutical Powder Regorafenib
1019206-88-2 Regorafenib Monohydrate Manufacturer From Hangzhou Royal
Anticancer Inhibitor Raw Material Powder CAS 755037-03-7 Regorafenib
CAS 1019206-88-2 Regorafenib Monohydrate Pharmaceutical Raw Materials
Chemical Intermediate Regorafenib Hydrate Powder CAS 1019206-88-2 Regorafenib Hydrate
Anticancer Inhibitor Raw Material Powder CAS 755037-03-7 Regorafenib Research
Reasonable Price Good Quality Regorafenib CAS 755037-03-7
China Synthetic Raw Materials Regorafenib Hydrate 1019206-88-2 C21h17clf4n4o4 1308068-626-2 White Crystalline Powder
China Factory Direct Industrial Use Sales Regorafenib Hydrate 1019206-88-2 C21h17clf4n4o4
Superior Regorafenib Monohydrate with CAS 1019206-88-2 for Apis Raw Materials
High Quality Regorafenib Monohydrate Medicine Grade Regorafenib Monohydrate Powder
Sonwu Supply Pharmaceutical Powder Regorafenib API CAS 835621-07-3 Regorafenib
Sonwu Supply CAS 755037-03-7 Pharmaceutical Powder Regorafenib
Sowu Supply Pharmaceutical Grade Regorafenib CAS 755037-03-7 Regorafenib
Sourcing guidance for Regorafenib
What are the key technical specifications and quality standards for sourcing Regorafenib API?
When sourcing Regorafenib as an Active Pharmaceutical Ingredient (API), buyers must prioritize purity levels of ≥99% as determined by HPLC analysis. It is essential to verify the molecular formula (C21H15ClF4N4O3) and ensure the product meets USP or EP compendial standards. Suppliers should provide a detailed Certificate of Analysis (CoA) covering heavy metals, residual solvents, and related substances to ensure clinical or research efficacy.
What regulatory compliance documents are mandatory for international procurement of Regorafenib?
Due to its nature as a potent multi-kinase inhibitor, procurement requires strict documentation. Buyers must ensure the manufacturer holds a GMP (Good Manufacturing Practice) certification. For entry into regulated markets, a DMF (Drug Master File) or CEP (Certificate of Suitability) is highly preferred. Additionally, a valid MSDS (Material Safety Data Sheet) is required to manage handling risks and environmental safety.
How should the stability and storage conditions of Regorafenib be validated?
Regorafenib is sensitive to environmental factors. Suppliers must demonstrate that the product is stored at 2°C to 8°C (refrigerated) or as specified by stability testing data to prevent degradation. Ensure the packaging uses amber glass vials or high-density polyethylene (HDPE) containers with moisture-proof sealing to maintain chemical integrity during long-term storage and transit.
What are the primary usage scenarios for Regorafenib in a B2B context?
Regorafenib is primarily sourced for pharmaceutical manufacturing of finished dosage forms (tablets) or for oncology research and development. It is widely utilized in the treatment of metastatic colorectal cancer (mCRC), gastrointestinal stromal tumors (GIST), and hepatocellular carcinoma (HCC). B2B buyers must ensure the grade (Research Grade vs. Pharma Grade) aligns with their specific end-use application.
Cross-Border Procurement Risks and Strategic Advice for Regorafenib
What are the common risks in cross-border purchasing of pharmaceutical chemicals?
The primary risks include customs seizure due to lack of proper medical import licenses and quality inconsistency between sample and bulk batches. To mitigate this, use third-party testing services (like SGS or Intertek) to verify the chemical composition before final payment. Always confirm the Harmonized System (HS) Code (typically 2933.39) to ensure correct tariff application and avoid legal delays.
How can buyers ensure transaction security when dealing with new suppliers?
Utilize secure payment terms such as Letters of Credit (L/C) or platforms that offer Trade Assurance to protect your funds until delivery is confirmed. On Made-in-China.com, prioritize Audited Suppliers who have undergone on-site verification of their production facilities and business licenses to reduce the risk of fraud.
What logistics strategies should be employed for shipping Regorafenib internationally?
Given its high value and sensitivity, use cold-chain logistics with temperature data loggers included in the shipment. Select reputable couriers experienced in handling dangerous goods (DG) if the concentration requires it. Ensure all export permits from the country of origin and import permits for the destination country are synchronized to prevent port storage fees.
What are the best practices for negotiating with pharmaceutical suppliers?
Focus on long-term supply stability rather than just the lowest price. Negotiate for tiered pricing based on annual volume commitments, which can yield 10-20% discounts. Request a Quality Agreement that defines liability in case of batch failure, and ensure the supplier can provide stability data updates throughout the contract period.





























