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Catalog Number:
39516
CAS Number:
7322-88-5
(+)-O-Acetyl-L-mandelic acid
Purity:
≥ 98% (Assay by titration)
Synonym(s):
(S)-(+)-α-Acetoxyphenylacetic acid
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Product Information

(+)-O-Acetyl-L-mandelic acid is a versatile compound widely recognized for its applications in the pharmaceutical and chemical industries. This chiral molecule, characterized by its acetyl and phenyl groups, serves as a valuable intermediate in the synthesis of various pharmaceuticals, particularly in the production of chiral drugs. Its unique structure allows for selective reactions that are essential in the development of enantiomerically pure compounds, making it a crucial building block for researchers focused on drug development and synthesis.

In addition to its pharmaceutical relevance, (+)-O-Acetyl-L-mandelic acid is utilized in the synthesis of flavoring agents and fragrances, capitalizing on its pleasant aroma and taste profile. Its ability to act as a chiral auxiliary further enhances its appeal in asymmetric synthesis, providing researchers with a reliable tool for creating complex molecules with high specificity. The compound's stability and ease of handling make it an ideal choice for both laboratory and industrial applications, ensuring that it meets the rigorous demands of modern chemical synthesis.

Synonyms
(S)-(+)-α-Acetoxyphenylacetic acid
CAS Number
7322-88-5
Purity
≥ 98% (Assay by titration)
Molecular Formula
C10H10O4
Molecular Weight
194.19
MDL Number
MFCD00064215
PubChem ID
225215
Melting Point
96 - 102 °C
Appearance
White or off-white crystalline powder
Optical Rotation
[α]20D = 151 - 155 ° (C=2 in Aceton)
Conditions
Store at RT
General Information
Synonyms
(S)-(+)-α-Acetoxyphenylacetic acid
CAS Number
7322-88-5
Purity
≥ 98% (Assay by titration)
Molecular Formula
C10H10O4
Molecular Weight
194.19
MDL Number
MFCD00064215
PubChem ID
225215
Melting Point
96 - 102 °C
Appearance
White or off-white crystalline powder
Optical Rotation
[α]20D = 151 - 155 ° (C=2 in Aceton)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(+)-O-Acetyl-L-mandelic acid is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting metabolic disorders.
  • Chiral Synthesis: It is used in asymmetric synthesis processes, allowing chemists to create specific enantiomers that are crucial in the production of effective medications.
  • Analytical Chemistry: The compound is employed in analytical methods to determine the presence of certain biological molecules, enhancing the accuracy of biochemical assays.
  • Cosmetic Formulations: Its properties make it suitable for use in cosmetics, where it can act as a stabilizer or pH adjuster, improving product performance and shelf life.
  • Research in Metabolism: Researchers utilize this compound to study metabolic pathways, providing insights into how certain substances are processed in the body, which is vital for drug development and safety assessments.

Citations