(R,R)-(-)-2,3-Butanediol is a chiral compound widely used in asymmetric synthesis to produce molecules with specific biological activities. This material plays a crucial role in laboratories where precise control over stereochemistry is required. It is a key component in the synthesis of various organic compounds, pharmaceuticals, and chemical intermediates. Its chiral nature allows it to act as a chiral building block, enabling the creation of enantiomerically pure products. This makes it indispensable in research settings where stereochemical specificity is essential.
The compound is known for its chemical stability and compatibility with a range of reaction conditions. Its unique asymmetric structure enables the formation of products with defined stereochemistry, which is vital in drug development and chemical synthesis. The ability to selectively influence the stereochemical outcome of reactions makes it a preferred choice for chemists working in both academic and industrial environments. Its reliability and consistency in performance further enhance its appeal in laboratory applications.
In Indonesian laboratories, (R,R)-(-)-2,3-Butanediol is commonly used in pharmaceutical and chemical research. It is particularly valuable in educational institutions and research centers that focus on organic chemistry and pharmacology. Its application in the development of new compounds with controlled stereochemistry supports advancements in medicinal chemistry and synthetic methodologies. The compound is an essential tool for researchers aiming to achieve high stereochemical efficiency in their experiments.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 16
- Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds due to its chiral structure, which allows for precise stereochemical control in complex reactions.
- Pharmaceutical Research: It is widely used in drug development to produce molecules with specific biological activities, enhancing the efficiency of synthetic pathways.
- Organic Chemistry Studies: Its role as a chiral building block makes it essential in the synthesis of various organic compounds, supporting both teaching and research activities.
- Academic Research: It is frequently employed in university laboratories for teaching and research in stereochemistry and synthetic organic chemistry.
- Industrial Chemical Production: Its stability and reactivity make it suitable for large-scale chemical synthesis processes requiring controlled stereochemistry.
| Brand | TCI |
|---|---|
| CAS number | 24347-58-8 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per standard laboratory supply |
| Physical form | Liquid |
| Storage | Store in a cool, dry place away from direct sunlight |
This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its chemical stability, it does not require refrigeration but should be protected from environmental fluctuations. In laboratory settings, it is important to handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper labeling and storage in designated chemical cabinets are essential to ensure safety and prevent accidental exposure. Always follow standard laboratory safety protocols when working with chiral compounds to maintain a secure and efficient research environment.
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