In the intricate and highly regulated field of pharmaceutical manufacturing, the sourcing of high-quality chemical intermediates is of paramount importance. 2,2-Dichloro-1,1,1-trifluoroethane, identified by its CAS number 306-83-2, stands out as a crucial building block in the synthesis of various Active Pharmaceutical Ingredients (APIs). Its unique chemical structure and properties make it an indispensable component for creating complex drug molecules. For pharmaceutical companies, understanding its role and how to effectively buy it from reliable Chinese manufacturers is key to successful drug development and production.
Understanding 2,2-Dichloro-1,1,1-trifluoroethane in Synthesis
The value of 2,2-Dichloro,1,1,1-trifluoroethane (often abbreviated as HCFC-123) in pharmaceutical synthesis lies in its trifluoromethyl (-CF3) and dichloro (-CHCl2) groups. These functional groups can be incorporated into larger organic molecules, imparting specific characteristics that are often desired in drug candidates. For instance, the trifluoromethyl group can enhance metabolic stability, lipophilicity, and binding affinity of a drug molecule, thereby improving its efficacy and pharmacokinetic profile.
As a pharmaceutical intermediate, it serves as a starting material or a key reagent in multi-step synthetic pathways. The precise control over its purity, typically above 98%, is non-negotiable in this sector, as impurities can compromise the safety and effectiveness of the final drug product. When looking to purchase this compound, pharmaceutical scientists and procurement managers must prioritize suppliers who can guarantee exceptional purity and provide comprehensive documentation.
Why Source from Chinese Manufacturers?
China has become a global leader in the production of fine chemicals and pharmaceutical intermediates. For 2,2-Dichloro,1,1,1-trifluoroethane, Chinese manufacturers offer several advantages:
When searching for a supplier, it is crucial to vet potential partners thoroughly. Look for manufacturers with ISO certifications, a strong track record in supplying the pharmaceutical industry, and transparent communication regarding their quality assurance processes. Requesting samples for internal testing is also a standard practice before committing to bulk orders.
The Procurement Process for Pharmaceutical Intermediates
For companies requiring 2,2-Dichloro,1,1,1-trifluoroethane for their synthesis needs, the procurement process involves:
By partnering with a trusted Chinese manufacturer, pharmaceutical companies can ensure a reliable and cost-effective supply of 2,2-Dichloro,1,1,1-trifluoroethane, a compound critical for advancing modern medicine.
Manufacturing Facilities
Professional Export Experience
to Global Customers
1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.