Mandelic acid
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| Mandelic acid | |
|---|---|
| Image:Mandelic acid.png | |
| IUPAC name | 2-Phenyl-2-hydroxyacetic acid |
| Other names | Mandelic acid Phenylglycolic acid |
| Identifiers | |
| CAS number | |
| SMILES | OC(C(O)c1ccccc1)=O |
| Properties | |
| Molecular formula | C8H8O3 |
| Molar mass | 152.14 g/mol |
| Density | 1.30 g/cm3 |
| Melting point |
119 °C |
| Boiling point |
°C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
Mandelic acid is an aromatic alpha hydroxy acid with the molecular formula C8H8O3. It is a white crystalline solid that is soluble in water and most common organic solvents.
Discovery and name
Mandelic acid was discovered while heating an extract of bitter almonds with diluted hydrochloric acid. The name is derived from the German "Mandel" for "almond".
Chemistry
It is an isomer of cresotinic acid (2-hydroxy-3-methylbenzoic acid) and oxymethylbenzoic acid (2-methoxybenzoic acid). Derivatives of mandelic acid are formed as a result of metabolism of adrenaline and noradrenaline by monoamine oxidase and catechol-o-methyl transferase. It is also present in certain skin care products, is an intermediate molecule in the production of other biochemicals, may be used as an analytical reagent and is a precursor in the manufacture of dyes.
Since the molecule contains a chiral carbon atom, the acid exists in either of two optically active forms. The racemic mixture of the two is known as paramandelic acid.
It may be prepared by the action of hydrochloric acid on the addition compound of benzaldehyde and hydrocyanic acid, by boiling phenylchloracetic acid with alkalis, by heating benzoyl formaldehyde with alkalis or by the action of dilute alkalis on ω-dibromacetophenone.
References
| The references in this article would be clearer with a different or consistent style of citation, footnoting, or external linking. |
- Merck Index, 11th Edition, 5599.
- This article incorporates text from the Encyclopædia Britannica Eleventh Edition, a publication now in the public domain.
See also
Antibacterials for systemic use: others (J01X) | |
|---|---|
| Glycopeptide | Vancomycin (Oritavancin, Telavancin) - Teicoplanin (Dalbavancin) |
| Polymyxins | Colistin - Polymyxin B |
| Steroid antibacterials | Fusidic acid |
| Imidazole derivatives | Metronidazole - Tinidazole - Ornidazole |
| Nitrofuran derivatives | Nitrofurantoin - Nifurtoinol |
| Other | -mycin (Fosfomycin, Spectinomycin, Daptomycin, Hitachimycin) Xibornol - Clofoctol - Methenamine - Iclaprim - Mandelic acid - Nitroxoline - Linezolid |
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

