2,3-Butanediol (mixture of stereoisomers) is a versatile chemical compound widely used in laboratory settings as a building block for various synthetic reactions. This compound plays a crucial role in organic chemistry by serving as a foundational element for the synthesis of more complex molecules. Its molecular structure allows it to participate in multiple reaction types, including substitution and reduction reactions, making it an essential tool for chemists. In Indonesian laboratories, it is frequently utilized in both academic and industrial research due to its reliability and broad applicability.
The compound is known for its polar nature, which enables it to dissolve in common organic solvents such as ethyl acetate and acetone. This solubility characteristic enhances its utility in chemical reactions and purification processes. Additionally, 2,3-Butanediol is chemically stable under normal conditions, which simplifies its storage and long-term use. These properties make it a preferred choice for researchers seeking a reliable and efficient reagent.
In Indonesian laboratories, 2,3-Butanediol is commonly used in pharmaceutical research, cosmetic formulation, and molecular structure studies. Its ability to participate in diverse chemical transformations makes it a valuable resource for scientists working on drug development and material synthesis. Its widespread use in both academic and industrial contexts highlights its importance in the chemical research landscape of Indonesia.
TCI brochures (PDF)
- Biomaterials Research Reagents 2025-02-19 · p. 19
- Monomers 2025-05-28 · p. 23
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- In the synthesis of heterocyclic compounds, 2,3-Butanediol serves as a key intermediate due to its ability to undergo various functional group transformations.
- For the preparation of non-heterocyclic compounds, this reagent provides a stable and versatile platform for chemical modifications and derivatization.
- In substitution reactions, its polar nature allows it to act as both a nucleophile and a solvent, enhancing reaction efficiency and yield.
- During reduction processes, its chemical stability ensures consistent results and minimal by-product formation.
- In molecular structure studies, its availability in multiple stereoisomeric forms aids in understanding stereochemical behavior and reaction mechanisms.
| Brand | TCI |
|---|---|
| CAS number | 513-85-9 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | Available in various sizes as per standard laboratory requirements |
| Physical form | Liquid |
| Storage | Store in a cool, dry place away from direct sunlight |
2,3-Butanediol should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a tightly sealed container to minimize exposure to air and moisture. Due to its polar nature, it is advisable to use glass or plastic containers that are resistant to chemical corrosion. In laboratory settings, it is important to handle the compound with appropriate safety measures, such as using gloves and working in a well-ventilated area. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in chemical reactions and research applications.
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