(S)-(+)-Mandelic acid

CAS: 17199-29-0

Ref. 3D-FM25008

Product Information

• Name: (S)-(+)-Mandelic acid
• Synonyms: (S)-2-Hydroxy-2-phenylacetic acidD-2-Hydroxy-2-phenylacetic acid(S)-(+)-a-Hydroxyphenylacetic acid, (+)-Mandelic acid, (+)-α-Hydroxyphenylacetic acid, (2S)-2-Hydroxy-2-(phenyl)ethanoic acid, (2S)-2-Hydroxy-2-phenylacetic acid, (S)-(+)-Hydroxyphenylacetic acid, (S)-2-Hydroxy-2-(phenyl)ethanoic acid, (S)-2-Hydroxy-2-phenylacetic acid, (S)-Amygdalic acid, (S)-α-Hydroxybenzeneacetic acid, (S)-α-Hydroxyphenylacetic acid, (αS)-α-Hydroxybenzeneacetic acid, <span class="text-smallcaps">L</span>-(+)-Mandelic acid, Acide D-2-hydroxy-2-phenylacetique, Benzeneacetic acid, α-hydroxy-, (S)-, Benzeneacetic acid, α-hydroxy-, (αS)-, D-2-Hydroxy-2-phenylessigsaure, D-2-hydroxy-2-phenylacetic acid, L-mandelic acid, Mandelic acid, <span class="text-smallcaps">L</span>-(+)-, Mandelic acid, L-(+)-, Mandelic acid, S-(+)-, acido D-2-hidroxi-2-fenilacetico, α-Hydroxybenzeneacetic acid, (S)-
• CAS: 17199-29-0

Description

(S)-(+)-Mandelic acid is a crystalline polymorph that belongs to the amide class of chemicals. It is an amphoteric substance, meaning it can act as either an acid or a base depending on the pH of its surroundings. (S)-(+)-Mandelic acid has been shown to inhibit enzyme activity in vitro, with the exception of hydrogen bonding interactions and hydroxyl group reactions. This chemical also inhibits the synthesis of proteins and DNA, which may be due to its ability to react with water molecules in aqueous solution. (S)-(+)-Mandelic acid has been found to have anti-inflammatory properties, which may be due to its ability to decrease prostaglandin synthesis by inhibiting cyclooxygenase enzymes.

• Brand: Biosynth

Chemical properties

• Molecular weight: 152.15 g/mol
• Formula: C₈H₈O₃
• Purity: Min. 99 Area-%
• Color/Form: White Powder