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Glucic acid: Difference between revisions

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Revision as of 07:21, 7 January 2022 editJJMC89 bot III (talk | contribs)Bots, Administrators3,690,100 editsm Moving Category:3-hydroxypropenals to Category:3-Hydroxypropenals per Misplaced Pages:Categories for discussion/Speedy← Previous edit Latest revision as of 21:45, 24 March 2024 edit undoMazewaxie (talk | contribs)Extended confirmed users, Pending changes reviewers, Rollbackers113,605 editsm WP:GENFIXESTag: AWB 
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| Density = 1.38 g/mL | Density = 1.38 g/mL
| MeltingPtC = 149 | MeltingPtC = 149
| MeltingPt_notes = (decomposes)<ref>{{cite journal|last1=Holker|first1=J. R.|title=Oxidation of Some Enediols with Selenium Dioxide|journal=J. Chem. Soc.|date=1955|pages=579-580|doi=10.1039/JR9550000574}}</ref> | MeltingPt_notes = (decomposes)<ref>{{cite journal|last1=Holker|first1=J. R.|title=Oxidation of Some Enediols with Selenium Dioxide|journal=J. Chem. Soc.|date=1955|pages=579–580|doi=10.1039/JR9550000574}}</ref>
| BoilingPtC = 274 | BoilingPtC = 274
| Solubility = | Solubility =
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}} }}


'''Glucic acid''' is an ] produced by the action of acids on cane-sugar or of ] on ].{{citation-needed|date=September 2016}} '''Glucic acid''' is an ] produced by the action of acids on cane-sugar or of ] on ].{{citation needed|date=September 2016}}


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== References == == References ==
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{{alcohol-stub}} {{alcohol-stub}}

Latest revision as of 21:45, 24 March 2024

Glucic acid
Names
Preferred IUPAC name Hydroxypropanedial
Other names Hydroxymalonaldehyde
2-Hydroxypropanedial
Reductone
Tartronaldehyde
2-Hydroxymalonaldehyde
2-Hydroxymalondialdehyde
Glucose-reductone
Tartronal
Tartronic aldehyde
Triose reductone
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
InChI
  • InChI=1S/C3H4O3/c4-1-3(6)2-5/h1-3,6HKey: NVXLIZQNSVLKPO-UHFFFAOYSA-N
  • InChI=1/C3H4O3/c4-1-3(6)2-5/h1-3,6HKey: NVXLIZQNSVLKPO-UHFFFAOYAQ
SMILES
  • O=CC(O)C=O
Properties
Chemical formula C3H4O3
Molar mass 88.062 g·mol
Density 1.38 g/mL
Melting point 149 °C (300 °F; 422 K) (decomposes)
Boiling point 274 °C (525 °F; 547 K)
Related compounds
Related alkenals 4-Hydroxynonenal

Malondialdehyde

Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Glucic acid is an acid produced by the action of acids on cane-sugar or of alkalis on glucose.

Tautomeric forms of glucic acid

References

  1. Holker, J. R. (1955). "Oxidation of Some Enediols with Selenium Dioxide". J. Chem. Soc.: 579–580. doi:10.1039/JR9550000574.


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