3,5-Dimethyl-1-adamantanol: Your Essential Pharmaceutical Intermediate
Discover the critical role of this adamantane derivative in pharmaceutical synthesis and quality control.
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3,5-Dimethyl-1-adamantanol
This compound is a vital pharmaceutical intermediate, primarily recognized as an impurity in the synthesis of Memantine (Memantine USP Related Compound B). Its precise characterization and availability are crucial for ensuring the quality and safety of pharmaceutical products.
- As a key component in pharmaceutical intermediate synthesis, understanding the 3,5-dimethyl-1-adamantanol synthesis is paramount for drug development.
- Ensuring the quality of pharmaceutical products relies heavily on the purity of intermediates like Memantine impurity B.
- Researchers leverage chemicals with CAS 707-37-9 for various organic synthesis pathways.
- The availability of 1-hydroxy-3,5-dimethyladamantane as a reference standard aids in analytical method validation.
Key Advantages
High Purity Standards
Achieve reliable results in your research and development with our 97% pure 3,5-dimethyl-1-adamantanol, a critical factor when dealing with pharmaceutical intermediates.
Crucial for Quality Control
Utilize this compound as a standard for identifying and quantifying impurities, thereby enhancing the safety of your final pharmaceutical products, especially when focusing on memantine impurity B.
Versatile in Organic Synthesis
Explore the potential of CAS 707-37-9 in various custom synthesis projects and advanced organic chemistry research.
Key Applications
Pharmaceutical Quality Control
Essential for the accurate detection and quantification of Memantine USP Related Compound B, ensuring compliance and product safety.
Advanced Organic Synthesis
A valuable building block for complex molecule construction in academic and industrial research settings, exploring diverse 3,5-dimethyl-1-adamantanol synthesis routes.
Drug Development Research
Supports the investigation of adamantane derivatives in new therapeutic applications, contributing to the discovery of novel pharmaceutical intermediates.
Reference Standards
Serves as a reliable reference standard for analytical testing and method validation in the pharmaceutical industry.