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1,3-Propanedioic acid, Carboxyacetic acid, Dicarboxymethane, Methanedicarboxylic acid, Propanedioic acid
CH2(COOH)2
Recommended Products
grade
for synthesis
Quality Level
vapor pressure
0.002 hPa ( 25 °C)
mp
132-135 °C (dec.) (lit.)
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
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General description
Malonic acid is a 1,3-dicarboxylic acid commonly used in the manufacture of dyes, pharmaceuticals, adhesives, agrochemicals, and fragrances, facilitated by the high reactivity of the central methylene group.
Application
Malonic acid can be used as:
It can also be introduced into the isotropic conductive adhesive formulation to enhance the electrical properties of electrically conductive adhesives.
- A complexing agent in the preparation of Cr-P coatings applicable in engineering tools and components.
- A cross-linker in the synthesis of closed-cell polyurethane foams applicable in the polymer industry.
It can also be introduced into the isotropic conductive adhesive formulation to enhance the electrical properties of electrically conductive adhesives.
Legal Information
Technipur is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
314.6 °F
Flash Point(C)
157 °C
Regulatory Information
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Certificates of Analysis (COA)
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Find documentation for the products that you have recently purchased in the Document Library.
Spectroscopic study of the morphology development of closed-cell polyurethane foam using bio-based malonic acid as chain extender
Polymer, 193, 122344-122344 (2020)
Malonic Acid and Derivatives
Ullmann's Encyclopedia of Industrial Chemistry null
Preparation and characterization of Cr?P coatings by electrodeposition from trivalent chromium electrolytes using malonic acid as complex
Surface and Coatings Technology, 201(6), 2578-2586 (2006)
Electrical property improvement of electrically conductive adhesives through in-situ replacement by short-chain difunctional acids
IEEE Transactions on Components and Packaging Technologies, 29(1), 173-178 (2006)
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