(R)-(-)-3-(Carbamoylmethyl)-5-methylhexanoic Acid: A Critical Pharmaceutical Intermediate
Essential building block for anticonvulsant drugs, ensuring quality and efficacy in pharmaceutical manufacturing.
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(R)-(-)-3-(Carbamoylmethyl)-5-methylhexanoic acid
This high-purity chemical intermediate plays a vital role in the synthesis of Pregabalin, a widely used medication for conditions such as epilepsy, neuropathic pain, and anxiety disorders. Its precise chiral structure is critical for the drug's therapeutic activity.
- Explore the synthesis of Pregabalin intermediates to ensure your production pipeline is robust and efficient.
- Discover high purity pharmaceutical intermediates that meet stringent quality control standards for API manufacturing.
- Understand the significance of Pregabalin impurity standards in maintaining drug safety and compliance.
- Learn about the chemical synthesis of anticonvulsant drugs and the role of key building blocks.
Key Advantages
Exceptional Purity
Achieve superior drug quality with this intermediate boasting purity levels of ≥99%, crucial for effective pharmaceutical synthesis.
Pregabalin Synthesis Efficiency
Optimize your production processes by utilizing a precisely manufactured intermediate specifically designed for Pregabalin manufacturing.
Reliable Supply Chain
Ensure uninterrupted production by sourcing from reputable suppliers, vital for maintaining the pharmaceutical manufacturing supply chain.
Key Applications
Pregabalin Manufacturing
This compound is a foundational element in the complex chemical synthesis of anticonvulsant drugs like Pregabalin, directly impacting treatments for neurological conditions.
Pharmaceutical R&D
Its availability as a high-quality intermediate supports ongoing research and development in novel drug discovery and synthesis optimization.
Impurity Profiling
Serves as a reference standard for identifying and quantifying impurities during Pregabalin production, ensuring drug safety and regulatory compliance.
Chiral Synthesis
Essential for stereoselective synthesis, guaranteeing the correct enantiomer is produced, which is critical for pharmacological activity.