(+)-O-Acetyl-L-mandelic acid is a chiral compound widely used in asymmetric synthesis and the creation of chiral molecules. It plays a critical role in laboratory settings where the development of complex molecular structures with specific biological activities is required. This compound serves as a fundamental building block in the synthesis of various pharmaceuticals, organic chemicals, and industrial products. Its unique stereochemistry allows for the controlled formation of enantiomers, making it essential in the field of chiral chemistry.
The compound's stable molecular structure and appropriate reactivity make it a preferred choice for asymmetric reactions. Its ability to participate in a range of chemical transformations without compromising stereochemical integrity is a key factor in its popularity. Additionally, its availability in crystalline form simplifies handling and processing in laboratory environments. These properties ensure that it remains a reliable and versatile reagent for chemists working on complex synthetic routes.
In Indonesian laboratories, (+)-O-Acetyl-L-mandelic acid is commonly used in organic chemistry research, pharmacology studies, and molecular synthesis projects. It is a key component in the development of new compounds with potential medical or industrial applications. Many research institutions and universities rely on this compound to advance their work in drug discovery and chemical innovation.
TCI brochures (PDF)
- Reagents for the Determination of Optical Purity by NMR 2025-01-17 · p. 1
- Chiral Building Blocks 2025-04-14 · p. 13
- Asymmetric synthesis of pharmaceutical compounds due to its chiral structure and reactivity.
- Development of chiral molecules for drug discovery and biological activity studies.
- Organic chemistry research requiring precise stereochemical control in synthetic pathways.
- Pharmaceutical formulation processes that rely on chiral building blocks for enantiomer specificity.
- Industrial chemical production where chiral intermediates are essential for final product quality.
| Brand | TCI |
|---|---|
| CAS number | 7322-88-5 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Crystalline solid |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation when working with this material. Avoid contact with incompatible substances and follow standard chemical safety protocols to maintain a safe working environment.
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