Determine the necessary mass, volume, or concentration for preparing a solution.
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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Dimethyl Malonate is a diester derivative of Malonic Acid. It is also a precursor in the synthesis of Barbituric Acids.
A diester derivative of Malonic Acid.
| Pubchem Sid | 488180614 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180614 |
| Sonrisas canónicas | COC(=O)CC(=O)OC |
| IUPAC Name | dimethyl propanedioate |
| InChIKey | BEPAFCGSDWSTEL-UHFFFAOYSA-N |
| INCHI | 1S/C5H8O4/c1-8-4(6)3-5(7)9-2/h3H2,1-2H3 |
| Isómeros SMILES | COC(=O)CC(=O)OC |
| WGK Alemania | 1 |
| RTECS | OO0950000 |
| Peso molecular | 132.11 |
| Beilstein | 774261 |
| Reaxy-Rn | 774261 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=774261&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Carboxylic acids and derivatives |
| Subclass | Dicarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dicarboxylic acids and derivatives |
| Alternative Parents | 1,3-dicarbonyl compounds Methyl esters Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | 1,3-dicarbonyl compound - Dicarboxylic acid or derivatives - Methyl ester - Carboxylic acid ester - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. |
| External Descriptors | Not available |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Apr 23, 2026 | D103051 | |
| Certificate of Analysis | Apr 23, 2026 | D103051 | |
| Certificate of Analysis | Apr 23, 2026 | D103051 | |
| Certificate of Analysis | Oct 30, 2025 | D103051 | |
| Certificate of Analysis | Sep 29, 2025 | D103051 | |
| Certificate of Analysis | Jul 15, 2025 | D103051 | |
| Certificate of Analysis | Jul 15, 2025 | D103051 | |
| Certificate of Analysis | Jul 15, 2025 | D103051 | |
| Certificate of Analysis | Sep 11, 2024 | D103051 | |
| Certificate of Analysis | Sep 11, 2024 | D103051 | |
| Certificate of Analysis | Sep 11, 2024 | D103051 | |
| Certificate of Analysis | Jul 16, 2024 | D103051 | |
| Certificate of Analysis | Dec 15, 2023 | D103051 | |
| Certificate of Analysis | Sep 11, 2023 | D103051 |
| Solubilidad | Soluble in organic solvents such as alcohol and ether, slightly soluble in water. |
|---|---|
| Sensibilidad | Moisture & Air & Light sensitive. |
| Índice de refracción | 1.4149 |
| Punto de inflamación (°F) | 185 °F |
| Punto de inflamación (°C) | 90℃ |
| Punto de ebullición (°C) | 181.4°C |
| Punto de fusión (°C) | -62°C |
| Peso molecular | 132.110 g/mol |
| XLogP3 | 0.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 132.042 Da |
| Monoisotopic Mass | 132.042 Da |
| Topological Polar Surface Area | 52.600 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 104.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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| 5. Jie Yao, Yan Wang, Suleiman Sabo Bello, Guangwen Xu, Lei Shi. (2020) Regulation of Brønsted acid sites in H-MOR for selective methyl methoxyacetate synthesis. APPLIED ORGANOMETALLIC CHEMISTRY, 34 (11): (e5925). [PMID:] [10.1002/aoc.5925] |
| 6. Fei Xia, Zhongtian Du, Junxia Liu, Yangyang Ma, Jie Xu. (2016) Catalytic oxidative C–C bond cleavage route of levulinic acid and methyl levulinate. RSC Advances, 6 (76): (72744-72749). [PMID:] [10.1039/C6RA16149A] |
| 7. Abbas Tanver, Mu-Hua Huang, Yunjun Luo, Syed Khalid, Tariq Hussain. (2015) Energetic interpenetrating polymer network based on orthogonal azido–alkyne click and polyurethane for potential solid propellant. RSC Advances, 5 (79): (64478-64485). [PMID:] [10.1039/C5RA10467J] |
| 8. Xie Tianyu, Hu Wenbo, You Lin, Wang Xin. (2024) Design, synthesis and biological evaluation of thienopyridine derivatives as c-Met kinase inhibitors. MOLECULAR DIVERSITY, [PMID:39356364] [10.1007/s11030-024-10998-3] |