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The Chemical Profile of Bimatoprost Ophthalmic Solution: A Manufacturer's Perspective

As a leading manufacturer and supplier of pharmaceutical intermediates, understanding the intricate chemical profile of Bimatoprost Ophthalmic Solution is at the core of our operations. This compound, vital for both ophthalmic treatments and cosmetic applications, demands precision in synthesis, rigorous quality control, and a deep understanding of its chemical characteristics. This article provides an overview from a manufacturer's perspective, focusing on the chemical properties, synthesis, and quality assurance measures involved in producing high-purity Bimatoprost.

Chemical Identity and Properties

Bimatoprost is chemically known as 7-O-deacetyl-17-phenyl-15-methyl prostaglandin F2α amide. Its molecular formula is C₂₅H₃₇NO₄, and it has a molecular weight of 415.57 g/mol. The CAS number for Bimatoprost is 155206-00-1. In its pure form, Bimatoprost is typically a white to off-white powder or a clear, colorless liquid when dissolved in appropriate solvents for ophthalmic use. Its chemical structure, a prostamide analog, dictates its biological activity.

Synthesis and Manufacturing Process

The synthesis of Bimatoprost is a complex, multi-step process that requires specialized expertise and state-of-the-art facilities. As a manufacturer, we employ advanced synthetic routes to achieve high yields and exceptional purity. The process typically involves:

  • Starting Material Selection: Careful selection of high-quality starting materials is crucial for the success of the synthesis.
  • Chiral Synthesis: Bimatoprost has specific stereochemistry, requiring precise chiral synthesis techniques to ensure the correct enantiomer is produced.
  • Intermediate Purification: Each intermediate product is thoroughly purified to remove by-products and impurities.
  • Final Product Synthesis and Purification: The final steps involve forming the amide linkage and subsequent purification to achieve pharmaceutical-grade purity. Techniques like chromatography and crystallization are employed.
  • Formulation: For ophthalmic solutions, the pure Bimatoprost API is formulated with excipients such as preservatives, buffering agents, and tonicity adjusters, ensuring stability and compatibility with ocular tissues.

Quality Control and Assurance

At our manufacturing facility, quality assurance is paramount. Every batch of Bimatoprost Ophthalmic Solution undergoes stringent testing:

  • Purity Analysis: High-performance liquid chromatography (HPLC) is routinely used to determine the purity of the Bimatoprost, ensuring it meets or exceeds pharmacopoeial standards.
  • Identification Tests: Spectroscopic methods like NMR and Mass Spectrometry are employed to confirm the identity of the compound.
  • Impurity Profiling: We meticulously analyze for any related substances or process impurities, ensuring they are within acceptable limits.
  • Physical and Chemical Properties: Tests are conducted to verify physical attributes like appearance, pH, and osmolality, critical for ophthalmic formulations.
  • Stability Studies: Comprehensive stability studies are performed to determine the shelf-life and recommended storage conditions.

Sourcing Bimatoprost Ophthalmic Solution from a Trusted Manufacturer

When you choose to buy Bimatoprost Ophthalmic Solution from us, you are partnering with a manufacturer committed to excellence. We offer:

  • High-Purity API: Our Bimatoprost API is synthesized and purified to meet rigorous pharmaceutical standards.
  • Consistent Quality: Batch-to-batch consistency is guaranteed through our robust quality management system.
  • Competitive Pricing: Leveraging our efficient manufacturing processes, we offer competitive prices for bulk orders.
  • Reliable Supply: Our large production capacity ensures a stable and dependable supply for your ongoing needs.
  • Technical Support: We provide comprehensive technical documentation and support to assist our clients.

For businesses looking to secure a dependable supply of Bimatoprost Ophthalmic Solution, understanding its chemical intricacies and the manufacturing process is crucial. Partnering with an experienced and quality-focused manufacturer like ourselves ensures you receive a product that meets the highest standards, enabling the development of effective and safe pharmaceutical and cosmetic products. Contact us today to get a quote and discuss your specific requirements.

Manufacturing Facilities

NINGBO INNO PHARMCHEM CO.,LTD. was established in 2007. It is committed to the R&D, production and sales of raw materials, pharmaceutical intermediates and fine chemicals. We striving to create a high-efficiency and high-quality integrated chemical service platform to better serve domestic and foreign customers.

Professional Export Experience

to Global Customers

WHY CHOSE US?

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).

FAQ

  • 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.

CONTACT US
Should you need to contact us; you may call during regular business hours, Monday through Friday, 8am – 6 pm.
NINGBO INNO PHARMCHEM CO.,LTD.
Address: No.163 Ruiqing Rd.,Ningbo 315000 China
Phone: 86-574-87319282
Fax: 86-574-27912196
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