| Weight | 152.149 g/mol |
|---|---|
| Formula | C8H8O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
dl-Mandelic acid (611-72-3, 90-64-2)
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- Sigma-Aldrich - dl-Mandelic acid47.90 - 294.00 USD
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- The Mechanism of the Photoreduction of Azo Dyes in the Presence of DL-Mandelic Acid and in the Absence of Oxygen (The Journal of Physical Chemistry, 1966)
- Direct enantiomeric TLC resolution of dl-penicillamine using (R)-mandelic acid and l-tartaric acid as chiral impregnating reagents and as chiral mobile phase additive. (Biomedical Chromatography, 2008)
- Choice of a suitable hetero-aromatic nitrogen base as promoter for chromic acid oxidation of dl-mandelic acid in aqueous media at room temperature (Research on Chemical Intermediates, 2013)
- Growth, spectral, thermal, laser damage threshold, microhardness, dielectric, linear and nonlinear optical properties of an organic single crystal: L-phenylalanine DL-mandelic acid (Physica B-condensed Matter, 2016)
- Growth, spectral and optical characterization of a novel nonlinear optical organic material: d -Alanine dl -Mandelic acid single crystal (Journal of Molecular Structure, 2017)
- Crystallographic Data. 61. dl-Mandelic Acid (Analytical Chemistry, 1952)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(C(=O)O)O
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InChIKeyIWYDHOAUDWTVEP-UHFFFAOYSA-N
- Pubchem - dl-Mandelic acid
- Wikipedia - mandelic acid
Mandelic acid is an aromatic alpha hydroxy acid with the molecular formula C6H5CH(OH)CO2H. It is a white crystalline solid that is soluble in water and polar organic solvents. It is a useful precursor to various drugs.
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