Diethyl L-(-)-Malate is a chiral building block widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in organic chemistry research, particularly in the development of pharmaceuticals and bioactive compounds. Its chiral nature allows for precise control over stereocenter formation, making it essential in the synthesis of enantiomerically pure compounds. As a key reagent in asymmetric catalysis, it supports the creation of complex molecular structures with defined stereochemistry, which is vital in drug discovery and development.
The compound is valued for its stability, solubility in organic solvents, and reactivity, which facilitate efficient synthetic processes. Its ability to participate in various chemical transformations enhances its utility in laboratory settings. The chiral configuration of Diethyl L-(-)-Malate ensures that it is an ideal choice for stereoselective reactions, contributing to the synthesis of compounds with desired optical properties. These characteristics make it a reliable and versatile material for advanced chemical research.
In Indonesian laboratories, Diethyl L-(-)-Malate is commonly used in pharmaceutical, organic, and biochemical research. It is a preferred material for researchers aiming to develop new therapeutic agents or understand complex biochemical pathways. Its availability in the local market supports ongoing scientific investigations, making it a practical choice for both academic and industrial applications.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 11
- Asymmetric synthesis is a key application where Diethyl L-(-)-Malate enables the creation of enantiomerically pure compounds, essential for drug development.
- Organic chemistry research benefits from its stability and reactivity, allowing for the synthesis of complex molecular structures with controlled stereochemistry.
- Biochemical studies utilize this compound to investigate the effects of chiral molecules on biological systems and enzyme interactions.
- Pharmaceutical development relies on its ability to produce optically active compounds, crucial for the design of effective and selective drugs.
- Academic research in Indonesian universities uses it to explore new synthetic methods and understand the role of chirality in molecular behavior.
| Brand | TCI |
|---|---|
| CAS number | 691-84-9 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and light |
Diethyl L-(-)-Malate should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture and air, which can affect its purity and reactivity. The compound should be stored away from direct sunlight and sources of heat to ensure long-term integrity. In laboratory settings, it is important to handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper labeling of containers is essential to prevent cross-contamination and ensure safe handling. Regular inspection of storage conditions is advised to maintain optimal preservation of the compound.
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