CAS 17199-29-0
:(S)-(+)-Mandelic acid
Description:
(S)-(+)-Mandelic acid is an aromatic alpha-hydroxy acid characterized by its chiral nature, existing as a single enantiomer. It is a white crystalline solid that is soluble in water and organic solvents, making it versatile in various applications. The compound features a hydroxyl group (-OH) and a carboxylic acid group (-COOH) attached to a benzene ring, contributing to its acidity and reactivity. Its molecular formula is C8H8O3, and it has a relatively low melting point. (S)-(+)-Mandelic acid is known for its use in pharmaceuticals, particularly in the treatment of urinary tract infections, and as a chiral building block in organic synthesis. Additionally, it exhibits antibacterial properties and is utilized in cosmetic formulations for its exfoliating effects. The compound's stereochemistry plays a crucial role in its biological activity, with the (S)-enantiomer being more therapeutically relevant than its counterpart. Overall, (S)-(+)-Mandelic acid is a significant compound in both medicinal chemistry and industrial applications.
Formula:C8H8O3
InChI:InChI=1/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)/p-1/t7-/m0/s1
InChI key:InChIKey=IWYDHOAUDWTVEP-ZETCQYMHSA-N
SMILES:[C@H](C(O)=O)(O)C1=CC=CC=C1
Synonyms:- (+)-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)-
- (S)-(+)-Mandelic Acid
- a-Hydroxy-benzeneacetic acid
- Hydroxy(phenyl)acetic acid
- L-PHENYLGLYCOLIC ACID
- (S)-(+)-ALPHA-HYDROXYPHENYLACETIC ACID
- L-A-HYDROXYPHENYLACETIC ACID
- (S)-ALPHA-HYDROPHENYLACETIC ACID
- amygdalic acid
- L-AMYGDALIC ACID
- L-ALPHA-HYDROXYPHENYLACETIC ACID
- (S)-ALPHA-HYDROXYPHENYLACETIC ACID
- 2-phenylglycolic acid
- alpha-Hydroxy-benzeneacetic acid
- See more synonyms
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Found 13 products.
L-(+)-Mandelic Acid
CAS:Formula:C8H8O3Purity:>99.0%(GC)(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:152.15(S)-(+)-Mandelic acid, 99+%
CAS:<p>(S)-(+)-Mandelic acid is a versatile reagent used in the resolution of racemates and the preparation of amides, Pharmaceutical Intermediates. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to </p>Formula:C8H8O3Purity:99+%Color and Shape:White, Crystals or powder or crystalline powderMolecular weight:152.15(S)-(+)-Mandelic acid, 98% e.e.
CAS:Formula:C8H8O3Purity:98%Color and Shape:SolidMolecular weight:152.1473L-(+)-Mandelic acid
CAS:Formula:C8H8O3Purity:98.0 - 102.0 %Color and Shape:White to almost white crystalline powder or colourless crystalsMolecular weight:152.15(S)-(+)-Mandelic acid
CAS:Formula:C8H8O3Purity:98.0%Color and Shape:Crystalline PowderMolecular weight:152.149L-(+)-Mandelic acid
CAS:<p>L-(+)-Mandelic acid</p>Purity:99%Color and Shape:White SolidMolecular weight:152.15g/mol(S)-(+)-Mandelic Acid
CAS:Controlled Product<p>Impurity Atomoxetine EP Impurity E<br>Applications (S)-(+)-Mandelic Acid (Atomoxetine EP Impurity E) is an antiseptic (urinary).<br>References Pessela, B., et al.: Enzyme Microb. Technol., 40, 310 (2007), Carrasco-Lopez, C., et al.: J. Biol. Chem., 284, 4365 (2009),<br></p>Formula:C8H8O3Color and Shape:NeatMolecular weight:152.15(S)-(+)-Mandelic acid
CAS:Controlled Product<p>(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.</p>Formula:C8H8O3Purity:Min. 99 Area-%Color and Shape:White PowderMolecular weight:152.15 g/molS-(+)-Mandelic Acid extrapure, 99%
CAS:Formula:C8H8O3Purity:min. 99%Color and Shape:White, Crystalline compoundMolecular weight:152.15











