(S)-Mandelic Acid丨CAS 17199-29-0

(S)-Mandelic Acid丨CAS 17199-29-0
Product Introduction:
Catalog No.: SS145810
CAS No.: 17199-29-0
Assay (on dry basis): 99% min
Product Name: (S)-Mandelic acid
Molecular Formula: C8H8O3
Molecular Weight: 152.15
Synonym(s): (S)-(+)-Mandelic acid; (S)-2-Hydroxy-2-phenylacetic acid; L-mandelic acid
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Technical Parameters
Description

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(S)-Mandelic acid (CAS 17199-29-0) is an optically active alpha-hydroxy carboxylic acid featuring a chiral center and aromatic structure. It is an important chiral building block widely used in pharmaceutical synthesis, asymmetric chemistry, and specialty chemical applications due to its excellent stereochemical properties.

 

Capability: 600+MT/year

 

Specifications

 

Appearance White or off-white crystalline powder
Assay (On Dry Basis) ≥99%
Specific Optical Rotation (D20) +153° to +157.5°
Melting Point 130℃–135℃
Moisture ≤0.5%

 

Chemical Identifiers

 

InChI InChI=1S/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)/t7-/m0/s1
InChI Key IWYDHOAUDWTVEP-ZETCQYMHSA-N
Smiles C1=CC=C(C=C1)[C@@H](C(=O)O)O
EC No. 241-240-8
MDL No. MFCD00004495
PubChem CID 439616

 

 

 

 

Applications

 

Pharmaceutical Industry

Used as a chiral intermediate for the synthesis of active pharmaceutical ingredients (APIs), drug candidates, and enantiomerically pure compounds.

Chemical Synthesis & Fine Chemicals

Applied as a resolving agent and versatile building block in asymmetric synthesis, chiral separation, and the preparation of specialty organic compounds.

Cosmetic Industry

Used as a research ingredient in skincare formulations due to its alpha-hydroxy acid (AHA) properties and applications in skin exfoliation studies.

Laboratory Applications

Serves as a reference compound in stereochemistry, analytical chemistry, and chiral molecule research.

 

 

 

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