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Catalog Number:
12130
CAS Number:
17199-29-0
L (+)-Mandelic acid
Purity:
≥ 99% (Assay)
Synonym(s):
L-2-Hydroxyphenylacetic acid, (S)-(+)-α-Hydroxyphenylacetic acid, L-phenylglycolic acid
Documents
$20.00 /25G
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Product Information

L (+)-Mandelic acid is a versatile organic compound renowned for its applications in pharmaceuticals, cosmetics, and analytical chemistry. This chiral molecule, characterized by its unique hydroxyl and carboxylic acid functional groups, serves as a key intermediate in the synthesis of various therapeutic agents. Its ability to act as a racemization inhibitor makes it particularly valuable in the production of optically pure compounds, enhancing the efficacy and safety of medications. Additionally, L (+)-Mandelic acid is utilized in skincare formulations due to its gentle exfoliating properties, promoting cell turnover and improving skin texture.

In the realm of analytical chemistry, L (+)-Mandelic acid is employed as a chiral resolving agent, aiding in the separation of enantiomers in complex mixtures. Its low toxicity and biocompatibility further bolster its appeal for use in research and industrial applications. With its multifaceted uses and benefits, L (+)-Mandelic acid stands out as a crucial compound for professionals seeking reliable solutions in their respective fields.

Synonyms
L-2-Hydroxyphenylacetic acid, (S)-(+)-α-Hydroxyphenylacetic acid, L-phenylglycolic acid
CAS Number
17199-29-0
Purity
≥ 99% (Assay)
Molecular Formula
C8H8O3
Molecular Weight
152.2
MDL Number
MFCD00004495
PubChem ID
1292
Melting Point
131 - 134 °C
Appearance
White crystalline powder
Optical Rotation
[a]D30 = 148.5 ± 2 º
Conditions
Store at 0 - 8 °C
General Information
Synonyms
L-2-Hydroxyphenylacetic acid, (S)-(+)-α-Hydroxyphenylacetic acid, L-phenylglycolic acid
CAS Number
17199-29-0
Purity
≥ 99% (Assay)
Molecular Formula
C8H8O3
Molecular Weight
152.2
MDL Number
MFCD00004495
PubChem ID
1292
Melting Point
131 - 134 °C
Appearance
White crystalline powder
Optical Rotation
[a]D30 = 148.5 ± 2 º
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

L (+)-Mandelic acid is widely utilized in research focused on:

  • Pharmaceuticals: It serves as an intermediate in the synthesis of various drugs, particularly in the production of antibiotics and anti-infective agents.
  • Cosmetics: This compound is incorporated into skincare products for its exfoliating properties, helping to improve skin texture and clarity.
  • Food Industry: Used as a flavoring agent and preservative, it enhances the taste of certain food products while providing antimicrobial benefits.
  • Analytical Chemistry: It acts as a chiral resolving agent in chromatography, aiding in the separation of enantiomers for more precise analytical results.
  • Biotechnology: Employed in the production of biodegradable plastics, it contributes to sustainable practices in material science.

Citations