M1296
Malonic acid
ReagentPlus®, 99%
Synonym(s):
Propanedioic acid
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About This Item
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Quality Level
product line
ReagentPlus®
Assay
99%
form
chunks
granular
powder or crystals
mp
132-135 °C (dec.) (lit.)
solubility
1 M NaOH: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow
SMILES string
OC(=O)CC(O)=O
InChI
1S/C3H4O4/c4-2(5)1-3(6)7/h1H2,(H,4,5)(H,6,7)
InChI key
OFOBLEOULBTSOW-UHFFFAOYSA-N
Gene Information
human ... SRC(6714)
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General description
Malonic acid (MA), also known as propanedioic acid, is a dicarboxylic acid. The crystals of MA are triclinic at room temperature. The oxidation of malonic acid by cerium (IV) in sulfuric acid solution has been studied. The reaction kinetics of the photocatalytic decomposition of MA in aqueous suspensions of titanium dioxide (TiO2) have been described.
Application
Malonic acid may be used as a cross-linking agent between corn starch and potato starch to improve its mechanical properties.
Other Notes
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
314.6 °F - closed cup
Flash Point(C)
157 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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On the oxidation of malonic acid by ceric ions.
International Journal of Chemical Kinetics, 10(6), 619-636 (1978)
The crystal structure of malonic acid.
Acta Crystallographica, 10(2), 125-127 (1957)
Photocatalytic degradation of malonic acid in aqueous suspensions of titanium dioxide: an initial kinetic investigation of CO2 photogeneration.
Journal of Photochemistry and Photobiology A: Chemistry, 96(1), 175-180 (1996)
Refinement of the crystal structure of malonic acid, C3H4O4.
Journal of Chemical Crystallography, 24(1), 75-78 (1994)
International journal of pharmaceutics, 436(1-2), 403-409 (2012-07-04)
Cocrystallization and salt formation have been shown to entail substantial promise in tailoring the physicochemical properties of drug compounds, in particular, their dissolution and hygroscopicity. In this work, we report on the preparation and comparative evaluation of a new cocrystal
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