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Postion:Product Catalog >Tranilast Impurity 14
Tranilast Impurity 14
  • Tranilast Impurity 14
  • Tranilast Impurity 14
  • Tranilast Impurity 14

Tranilast Impurity 14 NEW

Price Get Latest Price
Package 30mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 100000
Update Time: 2025-02-22

Product Details

Product Name: Tranilast Impurity 14 CAS No.: 41270-80-8
Min. Order: 10mg Purity: 98
Supply Ability: 100000 Release date: 2025/02/22
Tranilast Impurity 41270-80-8
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I. Product Name

Tranilast Impurity Reference Standard



II. Product Description

The Tranilast Impurity Reference Standard is a crucial substance used in drug quality control and research and development processes, specifically for detecting and identifying potential impurities in Tranilast drugs. These impurities may originate from various factors such as raw materials, production processes, or storage conditions. By comparing with the impurity reference standard, the types and quantities of impurities in Tranilast drugs can be accurately determined, ensuring the safety and effectiveness of the drugs.

III. Product Characteristics

  1. High Purity: The impurity reference standard itself has high purity to ensure the accuracy of test results.

  2. Structural Stability: Under specified storage conditions, the impurity reference standard remains stable and is not prone to structural changes.

  3. Wide Applicability: It is suitable for multiple analytical techniques, such as High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC), meeting different testing needs.

IV. Application Fields

The Tranilast Impurity Reference Standard is widely used in drug research and development, production, quality control, and drug regulation fields. It is an important tool for ensuring the quality and safety of Tranilast drugs.

V. Storage Conditions

It should be stored in a dry, cool, and light-protected environment, avoiding high temperatures, humidity, and direct sunlight.

VI. Precautions

  1. Before use, please read the product instruction manual carefully to understand the product characteristics and usage methods.

  2. Avoid contamination or cross-contamination of the impurity reference standard.

  3. Use within the validity period; do not use expired products.

  4. During storage and use, strictly comply with relevant safety regulations and operating procedures.

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Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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