The pharmaceutical industry constantly seeks innovative solutions and efficient pathways for drug development. Central to this endeavor is the availability of high-quality chemical intermediates that serve as foundational building blocks for therapeutic agents. 3-Phenylbutyric Acid, identified by CAS number 4593-90-2, plays a critical role in this landscape as a versatile pharmaceutical intermediate. Its chemical structure and properties make it invaluable for synthesizing a wide array of drug candidates and active pharmaceutical ingredients (APIs).
The journey from drug discovery to market launch is complex and demanding, requiring stringent quality control at every stage. 3-Phenylbutyric Acid, with its molecular formula C10H12O2, is often employed in the early stages of pharmaceutical synthesis. Researchers and process chemists rely on its predictable reactivity and the availability of high-purity grades, typically exceeding 99%, to ensure the efficacy and safety of the final pharmaceutical product. The compound's physical characteristics, such as its solid form and melting point (35-38°C), also contribute to its ease of handling in laboratory and manufacturing settings.
For pharmaceutical companies, securing a reliable supply chain for essential intermediates like 3-Phenylbutyric Acid is a strategic priority. Partnering with experienced manufacturers, especially those with a strong track record in producing pharmaceutical-grade chemicals, is paramount. Sourcing from reputable Chinese manufacturers can offer significant advantages, including competitive pricing for bulk orders and a consistent supply of material that meets rigorous quality standards. When evaluating suppliers, it's essential to request detailed Certificates of Analysis (COA) and inquire about their manufacturing processes and quality assurance protocols.
Ultimately, the successful development of new pharmaceuticals hinges on the quality and availability of key intermediates. By understanding the properties and applications of 3-Phenylbutyric Acid and by choosing to buy from trusted, high-quality manufacturers, pharmaceutical developers can accelerate their research and development timelines, bringing vital new treatments to patients more efficiently.
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.