Empagliflozin Synthesis Intermediate: (3S)-3-[4-[(2-Chloro-5-iodophenyl)methyl]phenoxy]tetrahydrofuran

A critical building block for diabetes treatment, enabling efficient Empagliflozin production.

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Key Advantages

High Purity & Quality Assurance

With a purity of ≥99.0%, this intermediate ensures the integrity of the Empagliflozin synthesis, supporting stringent quality control for drug synthesis.

Critical Role in Diabetes Therapy

As a vital component in pharmaceutical intermediates for diabetes treatment, it directly impacts the availability of effective medications for type 2 diabetes.

Streamlined Supply Chain

Partnering with a reliable supplier of Empagliflozin intermediates like NINGBO INNO PHARMCHEM CO.,LTD. secures a consistent supply for manufacturing needs.

Key Applications

Empagliflozin Manufacturing

The primary application is as a direct precursor in the large-scale synthesis of Empagliflozin, an essential drug for managing type 2 diabetes. This involves intricate steps in pharmaceutical chemical suppliers networks.

Drug Development & Research

Used in R&D settings to explore new synthetic routes, optimize existing processes, and develop novel diabetes therapies, contributing to advancements in diabetes drug development.

Reference Standards

Can serve as a reference compound for analytical testing and quality assurance during the production of Empagliflozin, ensuring product consistency and adherence to regulatory standards.

Process Optimization

Its availability facilitates research into improving yields and reducing costs in the chemical synthesis of Empagliflozin, making treatments more accessible.

Why Choose Us?

Leverage our expertise and state-of-the-art infrastructure to accelerate your journey from discovery to commercial success.

Global Experience

With 20 years of R&D, manufacturing, and sales experience, we proudly serve clients across 60 countries and regions worldwide.

Advanced Facilities

Our in-house R&D laboratory, pilot platform, and large-scale production workshop are equipped to meet the audit requirements of global customers.

Seamless Scalability

We facilitate a perfect transition from small-scale lab requirements (grams) to full commercialization (hundreds of tons).