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%, stabilized with 100ppm MEHQ 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 13 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sonrisas canónicas | CCCCCCOC(=O)C(=C)C |
|---|---|
| IUPAC Name | hexyl 2-methylprop-2-enoate |
| InChIKey | LNCPIMCVTKXXOY-UHFFFAOYSA-N |
| INCHI | 1S/C10H18O2/c1-4-5-6-7-8-12-10(11)9(2)3/h2,4-8H2,1,3H3 |
| Isómeros SMILES | CCCCCCOC(=O)C(=C)C |
| WGK Alemania | 2 |
| Número ONU | 3082 |
| Grupo de embalaje | III |
| Peso molecular | 170.25 |
| Reaxy-Rn | 1754703 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1754703&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 | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Carboxylic acid esters - Alpha,beta-unsaturated carboxylic esters |
| Direct Parent | Enoate esters |
| Alternative Parents | Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Enoate ester - Monocarboxylic acid or derivatives - 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 enoate esters. These are an alpha,beta-unsaturated carboxylic ester of general formula R1C(R2)=C(R3)C(=O)OR4 (R4= organyl compound) in which the ester C=O function is conjugated to a C=C double bond at the alpha,beta position. |
| External Descriptors | Not available |
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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 | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Jun 09, 2026 | H102084 | |
| Certificate of Analysis | May 21, 2026 | H102084 | |
| Certificate of Analysis | Apr 07, 2026 | H102084 | |
| Certificate of Analysis | Jan 19, 2026 | H102084 | |
| Certificate of Analysis | Jan 19, 2026 | H102084 | |
| Certificate of Analysis | Oct 15, 2025 | H102084 | |
| Certificate of Analysis | Jan 22, 2025 | H102084 | |
| Certificate of Analysis | Jan 22, 2025 | H102084 | |
| Certificate of Analysis | Jan 22, 2025 | H102084 | |
| Certificate of Analysis | Jun 04, 2022 | H102084 |
| Solubilidad | Soluble in Benzene,Ether,Acetone,Ethanol |
|---|---|
| Sensibilidad | Light sensitive |
| Índice de refracción | 1.432 |
| Punto de inflamación (°F) | 170.6 °F |
| Punto de inflamación (°C) | 80℃ |
| Punto de ebullición (°C) | 203°C |
| Peso molecular | 170.250 g/mol |
| XLogP3 | 4.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 7 |
| Exact Mass | 170.131 Da |
| Monoisotopic Mass | 170.131 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 150.000 |
| 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. Jiao He, Lin Yun, Xinjian Cheng. (2023) Organic-soluble chitosan-g-PHMA (PEMA/PBMA)-bodipy fluorescent probes and film by RAFT method for selective detection of Hg2+/Hg+ ions. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:36996960] [10.1016/j.ijbiomac.2023.124255] |
| 2. Yang Huanhuan, Wu Shilong, Chen Quan. (2022) Linear viscoelasticity of double associative polymers with varied density of the secondary interaction. JOURNAL OF RHEOLOGY, 66 (6): (1113-1123). [PMID:] [10.1122/8.0000394] |
| 3. Shuyue Zhao, Wenjun Huang, Changrong Wang, Yaping Wang, YuFeng Zhang, Zhanpeng Ye, Jianhua Zhang, Liandong Deng, Anjie Dong. (2020) Screening and Matching Amphiphilic Cationic Polymers for Efficient Antibiosis. BIOMACROMOLECULES, [PMID:33226784] [10.1021/acs.biomac.0c01330] |
| 4. Wenwen Jiang, Xinyue Zhang, Yafei Luan, Rensheng Wang, Hanzhou Liu, Dan Li, Liang Hu. (2019) Using γ-Ray Polymerization-Induced Assemblies to Synthesize Polydopamine Nanocapsules. Polymers, 11 (11): (1754). [PMID:31731483] [10.3390/polym11111754] |
| 5. Ding Zhang, Ping Xing, Renming Pan, Xiangyang Lin, Min Sha, Biao Jiang. (2018) Preparation and Surface Properties Study of Novel Fluorine-Containing Methacrylate Polymers for Coating. Materials, 11 (11): (2258). [PMID:30428523] [10.3390/ma11112258] |
| 6. Anna Zheng, Ling Su, Zheng Li, Guijin Zou, Xiang Xu, Yong Guan. (2017) Synthesis of poly(n-hexyl methacrylate)-b-poly(methyl methacrylate) via anionic polymerization with t-BuOK as the initiator at ambient temperature. RSC Advances, 7 (85): (53996-54001). [PMID:] [10.1039/C7RA10978D] |
| 7. Yang Gao, Lijie Duan, Shuang Guan, Guanghui Gao, Ya Cheng, Xiuyan Ren, Yuanrui Wang. (2017) The effect of hydrophobic alkyl chain length on the mechanical properties of latex particle hydrogels. RSC Advances, 7 (71): (44673-44679). [PMID:] [10.1039/C7RA07983D] |
| 8. Weixing Xu, Jianfei Zhou, Ya’nan Wang, Bi Shi. (2016) Modification of Leather Split by In Situ Polymerization of Acrylates. International Journal of Polymer Science, [PMID:] [10.1155/2016/7460572] |
| 9. Lichao Jiang, Feiyang Li, Yunting Li, Menghan Pi, Jiacen Xie, Jie Zhang, Hui Guo, Rong Ran, Wei Cui. (2025) Solvent-Free Fabrication of Robust Physical Hydrogels via Bulk Copolymerization for Underwater Acoustics. ADVANCED MATERIALS, [PMID:40538263] [10.1002/adma.202508162] |
| 10. Jinsong Wang, Huining Xiao, Haijiao Xie, Yang Huang, Farzad Seidi. (2025) Tailoring disulfide-embedded lignin-based hydrophobic self-healing coatings for metal protection. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:40280525] [10.1016/j.ijbiomac.2025.143448] |
| 11. Shilong Wu, Huanhuan Yang, Quan Chen. (2025) Enhancement of Transient Elongational Hardening of Poly(alkyl methacrylate) via Increase of Side-Chain Length Distribution. MACROMOLECULES, [PMID:] [10.1021/acs.macromol.5c00042] |
| 12. Zhangjie Luo, Yiying Li, Xingyu Liu, Qiang Chen, Chunmei Ding, Jie Zheng, Hong Chen, Jianshu Li. (2026) Transforming a general design strategy into elastomer-crosslinked hybrid hydrogels with co-constructed hydrophobic–hydrophilic networks for electronic skin. Materials Today, [PMID:] [10.1016/j.mattod.2026.103196] |
| 13. Yusong Xiao, Lijuan Zhu, Juntao Li, Yi Li, Ce Liang. (2026) Amphiphilic terpolymer sizing enabling an interfacial toughening layer for enhanced interfacial and mechanical properties of CF/EP composites. COMPOSITES SCIENCE AND TECHNOLOGY, [PMID:] [10.1016/j.compscitech.2026.111609] |