≥99% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Dimethyl methylmalonate is an ester. Microwave-enhanced Pd(0)/acetic acid catalyzed allylation of C, N and O-nucleophiles with dimethyl methylmalonate has been reported.
A useful biochemical for proteomics research.
| Pubchem Sid | 488184213 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184213 |
| Sourires canoniques | CC(C(=O)OC)C(=O)OC |
| IUPAC Name | dimethyl 2-methylpropanedioate |
| InChIKey | LRBPFPZTIZSOGG-UHFFFAOYSA-N |
| INCHI | 1S/C6H10O4/c1-4(5(7)9-2)6(8)10-3/h4H,1-3H3 |
| Isomères SMILES | CC(C(=O)OC)C(=O)OC |
| Poids moléculaire | 146.14 |
| Reaxy-Rn | 1763727 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1763727&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 |
| Classe | 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 |
| Description | 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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 G1908170 | Certificate of Analysis | Jun 05, 2025 | D137292 |
| K2105240 | Certificate of Analysis | May 07, 2025 | D137292 |
| K2105241 | Certificate of Analysis | May 07, 2025 | D137292 |
| K2105242 | Certificate of Analysis | May 07, 2025 | D137292 |
| F2325384 | Certificate of Analysis | Apr 09, 2025 | D137292 |
| F2325381 | Certificate of Analysis | Apr 09, 2025 | D137292 |
| H2409339 | Certificate of Analysis | Jul 26, 2024 | D137292 |
| H2409340 | Certificate of Analysis | Jul 26, 2024 | D137292 |
| H2409341 | Certificate of Analysis | Jul 26, 2024 | D137292 |
| H2409342 | Certificate of Analysis | Jul 26, 2024 | D137292 |
| K2105259 | Certificate of Analysis | Aug 08, 2023 | D137292 |
| Point d'éclair (°C) | 76 °C |
|---|---|
| Point d'ébullition (°C) | 174 °C |
| Poids moléculaire | 146.140 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 146.058 Da |
| Monoisotopic Mass | 146.058 Da |
| Topological Polar Surface Area | 52.600 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 125.000 |
| 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 |
| 1. Guo Junchen, Wang Shanjie, Wan Xin, Liu Xiaoxuan, Wang Zeng, Liang Chenchen, Zhang Zhenming, Wang Ye, Yan Miao, Wu Pengyan, Fang Shaohong, Yu Bo. (2024) Mitochondria-derived methylmalonic acid aggravates ischemia–reperfusion injury by activating reactive oxygen species-dependent ferroptosis. Cell Communication and Signaling, 22 (1): (1-20). [PMID:38238728] [10.1186/s12964-024-01479-z] |
