(S)-(+)-Glycidyl Butyrate: Synthesis Routes and Manufacturer Insights
The synthesis of enantiomerically pure chiral compounds is a cornerstone of modern organic chemistry, particularly in the pharmaceutical sector. (S)-(+)-Glycidyl Butyrate (CAS 65031-96-1) is a prime example of a valuable chiral intermediate whose efficient synthesis is critical. As a leading manufacturer, we focus on optimizing these routes to deliver high-quality products consistently. Understanding these synthesis methods provides insight into the value and complexity behind this essential chemical building block.
Key Synthesis Methodologies
Several pathways exist for synthesizing (S)-(+)-Glycidyl Butyrate, each with its own advantages and challenges:
- Asymmetric Synthesis using Chiral Precursors: This often involves starting with an already chiral precursor, such as (S)-epichlorohydrin or a related chiral alcohol, and reacting it with butyric acid or its derivatives. For example, reacting (S)-glycidol with butyric anhydride under controlled conditions can yield the desired product. These methods aim to preserve or transfer the stereochemistry from the starting material to the final product.
- Enzymatic Resolution: A highly effective approach involves the kinetic resolution of a racemic mixture of glycidyl butyrate using enzymes, typically lipases. These enzymes selectively catalyze the reaction (e.g., hydrolysis or transesterification) of one enantiomer, leaving the other enriched. For instance, certain lipases can selectively hydrolyze the (R)-enantiomer, allowing for the isolation of the desired (S)-enantiomer. This method is favored for its high enantioselectivity.
- Chemoenzymatic Approaches: These strategies combine chemical synthesis steps with enzymatic transformations. For example, a chemical synthesis might produce a racemic intermediate, which is then subjected to enzymatic resolution to obtain the pure (S)-enantiomer.
Our manufacturing process often leverages optimized versions of these methods, ensuring high yields and exceptional enantiomeric purity (typically >95% for (S)-(+)-Glycidyl Butyrate). We continuously refine our techniques to improve efficiency and sustainability.
Manufacturer's Perspective on Quality and Supply
For procurement managers and R&D scientists, purchasing (S)-(+)-Glycidyl Butyrate (CAS 65031-96-1) means relying on a supplier that understands the nuances of its synthesis and quality control. Our commitment as a manufacturer is to:
- Deliver Consistent Purity: We ensure that our product consistently meets the 95%min purity standard required for critical applications.
- Maintain Supply Chain Robustness: Our production capacity and logistical network in China guarantee a stable and reliable supply for our clients, whether for R&D or large-scale manufacturing.
- Offer Competitive Pricing: By managing the synthesis process directly, we can offer cost-effective solutions for bulk purchases.
- Provide Technical Expertise: Our team is available to discuss synthesis details, specifications, and handling of the product.
If you are looking to buy (S)-(+)-Glycidyl Butyrate, partnering with a dedicated manufacturer like us provides the assurance of quality and reliability. We invite you to contact us to learn more about our synthesis capabilities and to discuss your specific needs for this essential chiral intermediate.
Perspectives & Insights
Silicon Analyst 88
“For instance, certain lipases can selectively hydrolyze the (R)-enantiomer, allowing for the isolation of the desired (S)-enantiomer.”
Quantum Seeker Pro
“Chemoenzymatic Approaches: These strategies combine chemical synthesis steps with enzymatic transformations.”
Bio Reader 7
“For example, a chemical synthesis might produce a racemic intermediate, which is then subjected to enzymatic resolution to obtain the pure (S)-enantiomer.”