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Glycidic acid information


Glycidic acid
Names
Preferred IUPAC name
Oxiranecarboxylic acid
Identifiers
CAS Number
  • 503-11-7
3D model (JSmol)
  • Interactive image
ChemSpider
  • 84975
ECHA InfoCard 100.007.238 Edit this at Wikidata
PubChem CID
  • 94158
CompTox Dashboard (EPA)
  • DTXSID70964569 Edit this at Wikidata
InChI
  • InChI=1S/C3H4O3/c4-3(5)2-1-6-2/h2H,1H2,(H,4,5)
    Key: OTGHWLKHGCENJV-UHFFFAOYSA-N
  • InChI=1/C3H4O3/c4-3(5)2-1-6-2/h2H,1H2,(H,4,5)
    Key: OTGHWLKHGCENJV-UHFFFAOYAU
SMILES
  • C1C(O1)C(=O)O
Properties
Chemical formula
C3H4O3
Molar mass 88.062 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Glycidic acid is an organic compound that has both epoxide and carboxylic acid functions. It may be prepared by the oxidation of glycidol,[1] or by the epoxidation of acrylic acid.[2] This compound is commercially available as well.

  1. ^ More, Swati S.; Vince, Robert (2008). "Design, Synthesis and Biological Evaluation of Glutathione Peptidomimetics as Components of Anti-Parkinson Prodrugs". Journal of Medicinal Chemistry. 51 (15): 4581–8. doi:10.1021/jm800239v. PMID 18651729.
  2. ^ Kamata, Keigo; Sugahara, Kosei; Yonehara, Kazuhiro; Ishimoto, Ryo; Mizuno, Noritaka (2011). "Efficient Epoxidation of Electron-Deficient Alkenes with Hydrogen Peroxide Catalyzed by \γ-PW10O38V2(μ-OH)2]3−". Chemistry: A European Journal. 17 (27): 7549–59. doi:10.1002/chem.201101001. PMID 21647994.

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Glycidic acid

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Brazilian Controlled Drugs and Substances Act

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DEA list of chemicals

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methyl ethyl ketone or MEK) Toluene Hydrochloric acid (including anhydrous hydrogen chloride) Sulfuric acid Methyl isobutyl ketone (MIBK) Sodium permanganate...

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C3H4O3

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refer to: Acetic formic anhydride Ethylene carbonate Glucic acid Glycidic acid Pyruvic acid This set index page lists chemical structure articles associated...

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European law on drug precursors

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glycidate) 2-methyl-3-phenyloxirane-2-carboxylic acid (BMK glycidic acid) N-acetylanthranilic acid alpha-phenylacetoacetamide (APAA) alpha-phenylacetoacetonitrile...

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Glycidol

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be carcinogenic in rats. Epichlorohydrin Ethylene oxide Glycidamide Glycidic acid Merck Index, 11th Edition, 4385 NIOSH Pocket Guide to Chemical Hazards...

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Darzens reaction

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The Darzens reaction (also known as the Darzens condensation or glycidic ester condensation) is the chemical reaction of a ketone or aldehyde with an α-haloester...

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Glycidamide

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Saturated fatty acids protect the acrylamide from forming glycidamide. When during food processing, oil is used that contains unsaturated fatty acids, the amount...

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companies. In Canada, a wide range of basic laboratory reagents such as nitric acid and hydrogen peroxide are restricted as "explosives precursors". Two of the...

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benzannulation Darapsky degradation Darzens condensation, Darzens–Claisen reaction, Glycidic ester condensation Darzens halogenation Darzens synthesis of unsaturated...

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Picrotoxin

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reduction of an epoxy ketone, and a stereo­specific construction of a glycidic ester. The June 2020 synthesis instead employed the quick formation of...

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Asymmetric nucleophilic epoxidation

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aldehydes and (alpha)-haloesters is an effective method for the synthesis of glycidic esters. Chiral auxiliaries, chiral boron enolates, and asymmetric phase...

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