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Specifications
| Appearance | Colorless to yellow liquid |
| Specific Rotation | +17 to +18° |
| Water | 0.5% max |
| Assay | 99% min |
| Total Impurities | 1.0% max |
| Any Single Impurity | 0.5% max |
| D-Isomer | 0.3% max |
Transport Information
|
Parameter |
Specification |
|
UN Number |
2735 |
|
Class |
8 |
|
Packing Group |
II |
|
H.S. Code |
2905199090305 |
|
Stability & Reactivity |
The product is chemically stable under standard ambient conditions. |
|
Storage |
Keep container tightly closed in a dry and well-ventilated place. |
|
Condition to Avoid |
|
|
Package |
Applications
L-Alaninol is primarily used as a chiral building block in organic synthesis and pharmaceutical development. It serves as a precursor for the preparation of optically active amino alcohols, peptide derivatives, and various bioactive molecules. The compound is employed in asymmetric synthesis to introduce chirality into target molecules and is used in the development of enzyme inhibitors, drug intermediates, and specialty chemicals requiring stereochemically pure components.
Benefits
L-Alaninol provides high enantiomeric purity, which is essential for synthesizing biologically active compounds with desired optical activity. Its amino and hydroxyl functional groups enable versatile chemical transformations, including protection, oxidation, and coupling reactions. The compound's stability and reactivity allow efficient multi-step synthesis with predictable outcomes, supporting high yields and reproducibility.
Conclusion
L-Alaninol is a valuable chiral intermediate in pharmaceutical and fine chemical synthesis. Its stereochemical purity and multifunctional structure make it indispensable for producing optically active compounds, supporting drug development, asymmetric synthesis, and advanced chemical research.

