Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2-Tridecanone was used to study the impact of soil amendments in onion bulbs.
| Pubchem Sid | 488181399 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181399 |
| Sorrisi canonici | CCCCCCCCCCCC(=O)C |
| IUPAC Name | tridecan-2-one |
| InChIKey | CYIFVRUOHKNECG-UHFFFAOYSA-N |
| INCHI | 1S/C13H26O/c1-3-4-5-6-7-8-9-10-11-12-13(2)14/h3-12H2,1-2H3 |
| Isomeri SMILES | CCCCCCCCCCCC(=O)C |
| WGK Germania | 2 |
| PubChem CID | 11622 |
| Peso molecolare | 198.34 |
| Beilstein | 1757402 |
| Reaxy-Rn | 1757402 |
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 |
| Classe | 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 |
| Descrizione | 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 | a ketone |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Jul 06, 2026 | T106563 | |
| Certificate of Analysis | Jan 21, 2026 | T106563 | |
| Certificate of Analysis | Oct 29, 2025 | T106563 | |
| Certificate of Analysis | Jul 01, 2024 | T106563 | |
| Certificate of Analysis | Jul 01, 2024 | T106563 | |
| Certificate of Analysis | Jul 01, 2024 | T106563 | |
| Certificate of Analysis | Jul 01, 2024 | T106563 | |
| Certificate of Analysis | Feb 07, 2023 | T106563 | |
| Certificate of Analysis | Dec 27, 2021 | T106563 | |
| Certificate of Analysis | Dec 27, 2021 | T106563 | |
| Certificate of Analysis | Dec 27, 2021 | T106563 |
| Punto di congelamento (°C) | 27 °C |
|---|---|
| Indice di rifrazione | 1.435 |
| Punto di infiammabilità (°F) | 224.6 °F |
| Punto di infiammabilità (°C) | 107℃ |
| Punto di ebollizione (°C) | 263°C |
| Punto di fusione (°C) | 24-27°C |
| Peso molecolare | 198.340 g/mol |
| XLogP3 | 5.200 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 10 |
| Exact Mass | 198.198 Da |
| Monoisotopic Mass | 198.198 Da |
| Topological Polar Surface Area | 17.100 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 129.000 |
| 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. Wenwen Song, Mingming Dai, Shasha Gao, Yindong Mi, Shijia Zhang, Jianyong Wei, Honghai Zhao, Fangmeng Duan, Chen Liang, Qianqian Shi. (2023) Volatile organic compounds produced by Paenibacillus polymyxa J2-4 exhibit toxic activity against Meloidogyne incognita. PEST MANAGEMENT SCIENCE, [PMID:37899496] [10.1002/ps.7859] |
| 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. Chengrui Liang, Shuxiao Wang, Bin Zhao, Boyang Feng, Qipeng Qu, Liang Zhu, Jiming Hao. (2025) Impact of Molecular Structure on Secondary Organic Aerosol Formation from Aliphatic Carbonyls. ENVIRONMENTAL SCIENCE & TECHNOLOGY, [PMID:40552609] [10.1021/acs.est.5c00793] |
| 4. Deng Zhongyuan, Fang Liying, Cheng Lan, Yang Lihong, Zong Ruyi, Ding Qian, Wang Lixiang, Ni Xinzhi, Li Xianchun. (2025) Specialist/generalist divergence: phylogenetic constraints on the correlation between allelochemical tolerance spectra and host ranges of herbivorous insects. JOURNAL OF PEST SCIENCE, 99 (1): (10). [PMID:] [10.1007/s10340-025-02005-x] |
| 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] |
| 6. Lingling Cao, Junjie Lu, Yinglu Chen, Yajie Du, Shuqiong Yang, Zhiqiang Yan, Qingling Zheng, Pengfei Duan. (2026) Biocontrol potential of endophytic strain Pseudomonas chlororaphis subsp. piscium YX-3 isolated from Morchella against white mold disease. BIOLOGICAL CONTROL, [PMID:] [10.1016/j.biocontrol.2026.106024] |