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(±)-Mandelic Acid, 99%
CAS: 90-64-2 | C8H8O3 | 152.149 g/mol
$52.07 - $617.42
Chemical Identifiers
| CAS | 90-64-2 |
|---|---|
| Molecular Formula | C8H8O3 |
| Molecular Weight (g/mol) | 152.149 |
| MDL Number | MFCD00064250 |
| InChI Key | IWYDHOAUDWTVEP-UHFFFAOYSA-N |
| Synonym | mandelic acid, dl-mandelic acid, phenylglycolic acid, amygdalic acid, almond acid, uromaline, p-mandelic acid, racemic mandelic acid, paramandelic acid, rs-mandelic acid |
| PubChem CID | 1292 |
| ChEBI | CHEBI:35825 |
| IUPAC Name | 2-hydroxy-2-phenylacetic acid |
| SMILES | C1=CC=C(C=C1)C(C(=O)O)O |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1422322
|
Thermo Scientific Chemicals
A1422322 |
100 g |
Each for $52.07
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|
AAA1422336
|
Thermo Scientific Chemicals
A1422336 |
500 g |
Each for $141.74
|
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|
AAA142230E
|
Thermo Scientific Chemicals
A142230E |
2500 g |
Each for $617.42
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Description
Mandelic acid is used in the pharmaceutical industry as an antibacterial to treat urinary tract infections. It acts as a precursor for making various drugs. It is also used as an oral antibiotic. Mandelic acid peels are widely used for treating damaged skin due to its less penetrating and irritating property. Enantiomeric resolution of (±)-Mandelic acid is performed by using the chiral amine (1R,2S)-(-)-ephedrine followed by acidification to prepare (R)-( -)-Mandelic acid.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsMandelic acid is used in the pharmaceutical industry as an antibacterial to treat urinary tract infections. It acts as a precursor for making various drugs. It is also used as an oral antibiotic. Mandelic acid peels are widely used for treating damaged skin due to its less penetrating and irritating property. Enantiomeric resolution of (±)-Mandelic acid is performed by using the chiral amine (1R,2S)-(-)-ephedrine followed by acidification to prepare (R)-( -)-Mandelic acid.
Solubility
Soluble in water, diethyl ether, ethanol and isopropanol.
Notes
Hydrophobic and light sensitive. Incompatible with strong oxidizing agents and reducing agents.
Chemical Identifiers
| 90-64-2 | |
| 152.149 | |
| IWYDHOAUDWTVEP-UHFFFAOYSA-N | |
| 1292 | |
| 2-hydroxy-2-phenylacetic acid |
| C8H8O3 | |
| MFCD00064250 | |
| mandelic acid, dl-mandelic acid, phenylglycolic acid, amygdalic acid, almond acid, uromaline, p-mandelic acid, racemic mandelic acid, paramandelic acid, rs-mandelic acid | |
| CHEBI:35825 | |
| C1=CC=C(C=C1)C(C(=O)O)O |
Specifications
| 118°C to 121°C | |
| 99% | |
| MFCD00064250 | |
| 14,5717 | |
| Soluble in water,diethyl ether,ethanol and isopropanol. | |
| C1=CC=C(C=C1)C(C(=O)O)O | |
| 152.149 | |
| CHEBI:35825 | |
| 99% | |
| Light sensitive |
| 90-64-2 | |
| C8H8O3 | |
| 510011 | |
| mandelic acid, dl-mandelic acid, phenylglycolic acid, amygdalic acid, almond acid, uromaline, p-mandelic acid, racemic mandelic acid, paramandelic acid, rs-mandelic acid | |
| IWYDHOAUDWTVEP-UHFFFAOYSA-N | |
| 2-hydroxy-2-phenylacetic acid | |
| 1292 | |
| 152.15 | |
| 100 g | |
| (±)-Mandelic Acid |
Safety and Handling
GHS H Statement
H318
Causes serious eye damage.
P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
H302-H315-H319-H335
EINECSNumber : 202-007-6
RTECSNumber : OO6300000
TSCA : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only