Description
Benzyl (2S)-2-hydroxypropanoate (CAS: 56777-24-3) is a high-purity chiral ester widely used in pharmaceutical synthesis, flavor and fragrance formulation, and advanced chemical research. This compound, with the molecular formula C10H12O3, is a versatile intermediate known for its enantiomeric purity and compatibility with sensitive organic reactions. As a derivative of (S)-lactic acid, it serves as a key building block for asymmetric synthesis, chiral auxiliaries, and specialty polymers. Available in technical grade (90%) or higher purity upon request, this product is rigorously tested for consistency, stability, and low trace impurities. Ideal for GMP-compliant applications, it is supplied with full analytical documentation including HPLC, GC-MS, and NMR spectra upon request. Store under inert atmosphere at 2-8°C to maintain optimal stability.
Properties
- CAS Number: 56777-24-3
- Complexity: 162
- IUPAC Name: benzyl (2S)-2-hydroxypropanoate
- InChI: InChI=1S/C10H12O3/c1-8(11)10(12)13-7-9-5-3-2-4-6-9/h2-6,8,11H,7H2,1H3/t8-/m0/s1
- InChI Key: ZYTLPUIDJRKAAM-QMMMGPOBSA-N
- Exact Mass: 180.078644241
- Molecular Formula: C10H12O3
- Molecular Weight: 180.20
- SMILES: C[C@@H](C(=O)OCC1=CC=CC=C1)O
- Topological: 46.5
- Monoisotopic Mass: 180.078644241
- Synonyms: 56777-24-3, BENZYL (2S)-2-HYDROXYPROPANOATE, 962-379-7, Benzyl (S)-(-)-lactate, benzyl l-lactate, Benzyl (S)-Lactate, (S)-(-)-Lactic Acid Benzyl Ester, (S)-Benzyl 2-hydroxypropanoate, benzyl-l-lactate, MFCD00209546, (s)-benzyllactate, (S)-benzyl lactate, (s)-lactic acid benzyl ester, SCHEMBL320610, (S)-benzyl-2-hydroxypropanoate, Propanoic acid, 2-hydroxy-, phenylmethyl ester, (2S)-, ZYTLPUIDJRKAAM-QMMMGPOBSA-N, AKOS015836390, FB60140, AS-56743, (S)-2-Hydroxy-propionic acid benzyl ester, CS-0045408, L0161, EN300-332138, F17734, Benzyl (S)-(-)-lactate, technical grade, 90%
Benzyl (2S)-2-hydroxypropanoate is primarily employed as a chiral synthon in asymmetric pharmaceutical synthesis, particularly for prostaglandins and β-lactam antibiotics. It serves as a flavor precursor in food-grade applications due to its mild fruity-lactonic notes. Researchers utilize it to develop biodegradable polymers with controlled stereochemistry. The compound also functions as a protecting group reagent in peptide chemistry and carbohydrate chemistry.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statements
- P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2A (100%)
- STOT SE 3 (100%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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