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Jiangsu Jingye Pharmaceutical Co., Ltd. has been delivering high-purity chemical synthesis intermediates since 1994. With decades of innovation and a global footprint across the USA, Europe, and Japan, we ensure quality-first solutions backed by DMF registration and Dun & Bradstreet certification.
Founded as Jintan Depei Research Institute, our journey began over 28 years ago with a commitment to innovation and quality. On May 16, 2016, we officially became Jiangsu Jingye Pharmaceutical Co., Ltd., obtaining the Drug Manufacturing License for key APIs including Loratadine, Crotamiton, and Amitriptyline Hydrochloride.
Today, we are a trusted partner for pharmaceutical companies worldwide, exporting premium-grade intermediates and active pharmaceutical ingredients (APIs) to the United States, European Union, and Japan. Our products are recognized for their consistency, purity, and compliance with international standards.
50,000 m²
Total Site Area
36
R&D Technicians
20,000
m² Plant Area
40
km to Changzhou
28+
Years of Experience
Discover our comprehensive portfolio of pharmaceutical intermediates, APIs, and customized impurities. All products are manufactured under strict quality control with competitive pricing and fast delivery.
CAS No.: Not listed | Application: Pharmaceuticals, intermediates, APIs, custom synthesis
Superior spot product with customizable delivery options.
CAS No.: Not listed | Key intermediate in benzophenone-based drug synthesis
Outer Packing: 25 kg Fiber Drum | Inner: Double PE Bags
CAS No.: 1137-42-4 | MW: 313.86 | EINECS: 208-964-6
Used in synthesis of Amitriptyline Hydrochloride and other tricyclic compounds.
View Details
CAS No.: 6836-19-7 | MW: 313.86 | EINECS: 208-964-6
Key building block for CNS-active pharmaceuticals and antihistamines.
View DetailsCAS No.: 969-33-5 | MW: 313.86 | EINECS: 208-964-6
Antihistamine and antiserotonergic agent used in allergy and appetite stimulation therapies.
View DetailsImportant fluorinated intermediate for modern API development.
From R&D to global delivery, we offer end-to-end capabilities to support your pharmaceutical supply chain needs.
36 R&D technicians including 4 experts, 16 engineers, and 5 external professors driving innovation and custom synthesis.
50,000 m² site with 20,000 m² dedicated plant area and QC equipped with hundreds of analytical instruments.
DMF registration, Dun & Bradstreet certification, and adherence to international quality standards.
Established long-term cooperation with U.S. clients. Our high-quality products have earned unanimous praise across the American pharmaceutical industry.
Supplied to EU markets with full compliance. Trusted partner for European manufacturers seeking reliable API intermediates.
Long-standing relationships with Japanese pharmaceutical companies. Recognized for consistency, purity, and on-time delivery.
We specialize in pharmaceutical intermediates, APIs (Active Pharmaceutical Ingredients), benzophenone series compounds, and customized impurities for drug development and quality control.
Yes, we provide custom synthesis and process development services tailored to client specifications, supported by our experienced R&D team.
Yes, many of our products are DMF registered with the U.S. FDA, ensuring compliance with regulatory requirements for pharmaceutical manufacturing.
We hold the Dun & Bradstreet Certificate and comply with international quality standards. Our facility is licensed for drug manufacturing in China.
Please visit jingyepharma.com to submit an inquiry for pricing, samples, or technical data sheets.
For inquiries about products, pricing, or partnerships, please visit our official website to connect with our team.
📧 Email: guml@depeichem.com
📞 Phone: 0086 18001493616
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