L-(-)-3-Phenyllactic Acid 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 chiral compounds. Its unique structure enables it to serve as a key intermediate in the synthesis of various pharmaceutical and industrial chemicals. In the laboratory, it is essential for creating molecules with defined stereochemistry, which is vital for drug development and other advanced chemical applications.
The compound’s optical activity and reactive functional groups make it a preferred choice for chemists working on chiral synthesis. Its ability to rotate polarized light indicates its chiral nature, ensuring precise control over the stereochemistry of the final product. This property is critical in applications where enantiomeric purity is required. Additionally, its chemical structure, featuring a phenyl group and a lactic acid moiety, contributes to its reactivity and versatility in synthetic pathways.
In Indonesian laboratories, L-(-)-3-Phenyllactic Acid is commonly used in organic chemistry research, especially in pharmaceutical and food chemistry fields. Local researchers rely on this compound to develop bioactive substances, such as antifungal agents, by leveraging its chiral properties. Its application supports the creation of compounds with specific biological functions, making it a valuable tool in both academic and industrial research settings.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 13
- Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, essential in pharmaceutical development.
- Chiral Compound Development: Its chiral structure allows for the synthesis of molecules with specific stereochemistry, crucial for drug design.
- Organic Chemistry Research: Widely used in academic and industrial labs for constructing complex molecular frameworks.
- Pharmaceutical Applications: Supports the synthesis of bioactive compounds, including antifungal agents and other therapeutic agents.
- Food Chemistry Studies: Utilized in the development of chiral compounds relevant to food science and flavor chemistry.
| Brand | TCI |
|---|---|
| CAS number | 20312-36-1 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid, crystalline |
| Storage | Store in a cool, dry place away from light |
L-(-)-3-Phenyllactic Acid should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. Due to its chiral nature, it is important to ensure that the storage conditions do not lead to any degradation or loss of optical activity. The compound should be handled with care to avoid exposure to air and light, which can affect its stability. In laboratory settings, it should be stored in a designated chemical storage area that is accessible only to authorized personnel. Proper labeling and documentation are essential to ensure safe handling and usage.
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