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Postion:Product Catalog >Chemical Reagents>Organic reagents>Aromatic acids>Terbutaline Impurity
Terbutaline Impurity
  • Terbutaline Impurity
  • Terbutaline Impurity
  • Terbutaline Impurity

Terbutaline Impurity NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 1000000000000
Update Time: 2024-12-23
Related documents: MSDS NMR COA IR

Product Details

Product Name: Terbutaline Impurity CAS No.: 99-10-5
Min. Order: 10mg Purity: 98
Supply Ability: 1000000000000 Release date: 2024/12/23
Terbutaline EP Impurity A
Article illustration
Product ID:T017012
Synonyms:3,5-dihydroxybenzoic acid 
CAS No.:99-10-5
Molecular Formula:C7H6O4 
Molecular Weight:
154.12 

Our products are mainly drug impurity reference products, drug standards, analytical chemistry, standard substances, organic chemical synthesis, chemical custom synthesis. For impurity localization, quantification, and quality control in drug development processes. Our laboratory area is more than 5000 square meters, we have more than 20 analytical instruments such as HPLC and MS/LC-MS/GC-MS, we also have TGA, IR and other testing instruments. We have the most advanced SFC preparation separation equipment.

Article illustration


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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  • Address: Room 005-01, 15th Floor, Building D2, Phase III, Software New Town, No. 8 Huacheng Avenue, East Lake
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