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224,000+ research products · Triple ISO certified · COA & SDS available for every product · Same-day shipping on in-stock items 2-Decanone - ≥97% , CAS No.693-54-9
Synonyms
2-Decanone|Decan-2-one|693-54-9|METHYL OCTYL KETONE|Methyl n-octyl ketone|Octyl methyl ketone|n-C8H17COCH3|MFCD00009571|GX543OLT0R|CHEMBL47127|DTXSID9022104|CHEBI:77929|2-Decanone, >=98%|EINECS 211-752-6|UNII-GX543OLT0R|BRN 1747463|2-Decanone, 98%|2-DECAN
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
2-Decanone | Decan-2-one | 693-54-9 | METHYL OCTYL KETONE | Methyl n-octyl ketone | Octyl methyl ketone | n-C8H17COCH3 | MFCD00009571 | GX543OLT0R | CHEMBL47127 | DTXSID9022104 | CHEBI:77929 | 2-Decanone, >=98% | EINECS 211-752-6 | UNII-GX543OLT0R | BRN 1747463 | 2-Decanone, 98% | 2-DECAN
Specifications & Purity
≥97%
Names and Identifiers Pubchem Sid 488181723 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488181723 Canonical Smiles CCCCCCCCC(=O)C IUPAC Name decan-2-one InChIKey ZAJNGDIORYACQU-UHFFFAOYSA-N INCHI 1S/C10H20O/c1-3-4-5-6-7-8-9-10(2)11/h3-9H2,1-2H3 Isomeric SMILES CCCCCCCCC(=O)C Molecular Weight 156.27 Beilstein 1747463 Reaxy-Rn 1747463 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1747463&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification 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 Oxygenated hydrocarbons Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates(CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in alcohol. Insoluble in water. Refractive Index 1.43 Flash Point(°F) 187°F Flash Point(°C) 86℃ Boil Point(°C) 210-212℃ Melt Point(°C) 3℃ Molecular Weight 156.260 g/mol XLogP3 3.700 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 7 Exact Mass 156.151 Da Monoisotopic Mass 156.151 Da Topological Polar Surface Area 17.100 Ų Heavy Atom Count 11 Formal Charge 0 Complexity 97.000 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
Citations of This Product References 1. Yanmei Xi, Sana Ikram, Tong Zhao, Yiwei Shao, Ruirui Liu, Fuhang Song, Baoguo Sun, Nasi Ai. (2023) 2-Heptanone, 2-nonanone, and 2-undecanone confer oxidation off-flavor in cow milk storage. JOURNAL OF DAIRY SCIENCE, [PMID:37641261 ] [10.3168/jds.2022-23056 ] 2. Tao Tang, Fanfan Wang, Houyun Huang, Nengneng Xie, Jie Guo, Xiaoliang Guo, Yuanyuan Duan, Xiaoyue Wang, Qingfang Wang, Jingmao You. (2024) Antipathogenic Activities of Volatile Organic Compounds Produced by Bacillus velezensis LT1 against Sclerotium rolfsii LC1, the Pathogen of Southern Blight in Coptis chinensis. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:38657235 ] [10.1021/acs.jafc.4c00984 ] 3. Yimeng Ren, Longzhu Zhou, Yujie Shi, Yanan Yu, Weihai Xing, Qingyu Zhao, Junmin Zhang, Yueyu Bai, Jing Li, Chaohua Tang. (2024) Effect of alterations in phospholipids and free fatty acids on aroma-active compounds in instant-boiled chuck tender, sirloin and silverside beef. Heliyon, [PMID:39253161 ] [10.1016/j.heliyon.2024.e36382 ] 4. Bin Lin, Fen Wang, Hongliang Wang, Xinsheng Huang, Xueqin Liu, Xuechun Wang, Chihua Wang, Yan Xing, Chunqing Dai, Yi Zheng. (2025) Determination of Theophylline Across Biological, Environmental and Food Matrices Using Liquid-Phase Microextraction Coupled with LC-MS/MS. MOLECULES, 30 (18): (3797). [PMID:41011689 ] [10.3390/molecules30183797 ] 5. Qiangbo Zhao, Ruhan Xia, Pengxiang Han, Jiangyuan Han, Weihua Zhao, Xiangyan Zhou, Fuqiang Xu, Wenzhi Yao, Jianhe Wei, Miaoyin Dong, Mengfei Li. (2026) Biocontrol efficiency and potential mechanism of Bacillus subtilis GNRP-01A against Astragalus mongholicus root rot. INDUSTRIAL CROPS AND PRODUCTS, [PMID: ] [10.1016/j.indcrop.2026.122842 ]
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