≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships FedEx DG Service 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.
2,4-Dimethyl-3-pentanone is a carbonyl compound used in an experimental method to measure the equilibrium isotopic fractionation factor (αeq ) for C-bound H positions adjacent to carbonyl group in ketones.
| Pubchem Sid | 488181296 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181296 |
| Canonical Smiles | CC(C)C(=O)C(C)C |
| IUPAC Name | 2,4-dimethylpentan-3-one |
| InChIKey | HXVNBWAKAOHACI-UHFFFAOYSA-N |
| INCHI | 1S/C7H14O/c1-5(2)7(8)6(3)4/h5-6H,1-4H3 |
| Isomeric SMILES | CC(C)C(=O)C(C)C |
| WGK Germany | 1 |
| RTECS | SA8575500 |
| UN Number | 1224 |
| Molecular Weight | 114.19 |
| Beilstein | 773782 |
| Reaxy-Rn | 773782 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773782&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 oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Ketones |
| Alternative Parents | Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Ketone - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol. |
| 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 | Item |
|---|---|---|---|
 I1813137 | Certificate of Analysis | Apr 15, 2026 | D111802 |
| L2111175 | Certificate of Analysis | Sep 17, 2025 | D111802 |
| L2111193 | Certificate of Analysis | Sep 17, 2025 | D111802 |
| B1801043 | Certificate of Analysis | Sep 16, 2025 | D111802 |
| B2526089 | Certificate of Analysis | Jul 02, 2024 | D111802 |
| B2526094 | Certificate of Analysis | Jul 02, 2024 | D111802 |
| D2411052 | Certificate of Analysis | Apr 13, 2024 | D111802 |
| C23311539 | Certificate of Analysis | Apr 08, 2023 | D111802 |
| C23311543 | Certificate of Analysis | Apr 08, 2023 | D111802 |
| B2515020 | Certificate of Analysis | Dec 18, 2021 | D111802 |
| Refractive Index | 1.399-1.402 |
|---|---|
| Flash Point(°F) | 59 °F |
| Flash Point(°C) | 15℃ |
| Boil Point(°C) | 124°C |
| Melt Point(°C) | -80°C |
| Molecular Weight | 114.190 g/mol |
| XLogP3 | 1.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 114.104 Da |
| Monoisotopic Mass | 114.104 Da |
| Topological Polar Surface Area | 17.100 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 72.400 |
| 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. Lihui Yang, Xiao Zhao, Manjun Lei, Jie Sun, Lei Yang, Yifeng Shen, Qiangqiang Zhao. (2020) Facile construction of thermo-responsive Pickering emulsion for esterification reaction in phase transfer catalysis system. Molecular Catalysis, [PMID:] [10.1016/j.mcat.2020.111335] |
