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Repaglinide Powder CAS 135062-02-1: High-Purity Pharmaceutical Intermediate for Diabetes Medication

Repaglinide Powder, identified by the CAS number 135062-02-1, stands as a crucial pharmaceutical intermediate and raw material within the healthcare industry. As a key component in the synthesis of medications, its purity and quality are paramount for producing effective and safe drug products. This compound was first developed in 1983, marking its significance in the history of antidiabetic treatments. It is classified within the meglitinide class of oral antidiabetic drugs.

The physical form of this essential material is a solid powder. Ensuring a high level of purity, typically exceeding 99%, is non-negotiable for its application in pharmaceutical manufacturing. This stringent purity standard is verified through rigorous testing methods, including High-Performance Liquid Chromatography (HPLC), which confirms the chemical integrity and concentration of the compound. The molecular formula of Repaglinide is C27H36N2O4, representing its specific chemical structure that enables its therapeutic action.

The primary application of Repaglinide Powder is in the production of oral medication used for managing Type 2 Diabetes Mellitus. This medication serves as an adjunct to diet and exercise, helping patients control their blood sugar levels effectively. By stimulating insulin release from the pancreas in a glucose-dependent manner, it addresses a core issue in Type 2 diabetes management. The role of Repaglinide in this widely prevalent condition underscores its importance as a pharmaceutical raw material, contributing to global health efforts in combating diabetes.

For pharmaceutical manufacturers, sourcing a reliable supply of high-quality Repaglinide Powder is critical. Consistency in the raw material directly impacts the consistency and efficacy of the final drug product. Therefore, partnering with a supplier that adheres to strict quality control standards and possesses robust manufacturing capabilities is essential. The material requires specific storage conditions, namely keeping it in a cool, dry, and dark location, to maintain its stability and ensure a shelf life typically extending up to 24 months when stored properly. This attention to storage and handling is part of the overall quality assurance process.

The packaging of Repaglinide Powder is designed to protect its integrity during transit and storage. Common packaging options include aluminum foil bags and paper drums, which safeguard the powder from moisture and light. Minimum order quantities, often starting from 1kg, make the material accessible for various scales of manufacturing, from research and development batches to larger production runs. Understanding the technical specifications, such as assay purity and test methods like HPLC, allows manufacturers to confirm they are receiving a product that meets the necessary standards for pharmaceutical use.

Securing a consistent and high-quality supply of pharmaceutical intermediates like Repaglinide Powder is a key factor in the efficiency and success of drug manufacturing operations. Manufacturers need to ensure that their raw materials are sourced from entities that can provide detailed documentation, including specifications and test reports, guaranteeing compliance with regulatory requirements. The process of procurement involves evaluating potential partners based on their quality systems, reliability, and ability to meet demand.

For companies looking to expand their portfolio of diabetes medications or ensure a stable supply for existing production lines, finding a reputable manufacturer or supplier of Repaglinide Powder is a priority. Information regarding the price of this intermediate is typically provided upon inquiry, reflecting factors such as order volume, purity, and market conditions. Pharmaceutical businesses seeking to buy or purchase Repaglinide Powder should engage directly with potential suppliers to discuss their specific needs and secure competitive terms. The purchase process involves verifying quality credentials, negotiating price, and arranging logistics for secure and timely delivery. Obtaining a transparent and favorable price for high-purity Repaglinide Powder is crucial for cost-effective drug production.

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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.

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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.

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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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