Determine the necessary mass, volume, or concentration for preparing a solution.
≥96%(GC),stabilized with TBC for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504756514 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504756514 |
| Sonrisas canónicas | CC(=C)C(=O)OCC(C(C(C(C(C(F)F)(F)F)(F)F)(F)F)(F)F)(F)F |
| IUPAC Name | 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluoroheptyl 2-methylprop-2-enoate |
| InChIKey | YJKHMSPWWGBKTN-UHFFFAOYSA-N |
| INCHI | 1S/C11H8F12O2/c1-4(2)5(24)25-3-7(14,15)9(18,19)11(22,23)10(20,21)8(16,17)6(12)13/h6H,1,3H2,2H3 |
| Isómeros SMILES | CC(=C)C(=O)OCC(C(C(C(C(C(F)F)(F)F)(F)F)(F)F)(F)F)(F)F |
| Peso molecular | 400.16 |
| Reaxy-Rn | 2305962 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2305962&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 Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Enoate ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organofluoride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl fluoride - 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 |
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 | Apr 24, 2026 | D616485 | |
| Certificate of Analysis | Apr 24, 2026 | D616485 | |
| Certificate of Analysis | Apr 24, 2026 | D616485 | |
| Certificate of Analysis | Sep 15, 2023 | D616485 | |
| Certificate of Analysis | Sep 15, 2023 | D616485 | |
| Certificate of Analysis | Sep 15, 2023 | D616485 | |
| Certificate of Analysis | Sep 15, 2023 | D616485 | |
| Certificate of Analysis | Sep 15, 2023 | D616485 | |
| Certificate of Analysis | Sep 15, 2023 | D616485 | |
| Certificate of Analysis | Sep 15, 2023 | D616485 |
| Sensibilidad | heat sensitive |
|---|---|
| Índice de refracción | 1.35 |
| Punto de inflamación (°F) | 104°C |
| Punto de inflamación (°C) | 104°C |
| Punto de ebullición (°C) | 112°C |
| Peso molecular | 400.160 g/mol |
| XLogP3 | 5.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 9 |
| Exact Mass | 400.033 Da |
| Monoisotopic Mass | 400.033 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 525.000 |
| 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. Penghao Zhang, Cheng Zhang, Chuansheng Zhang, Fei Kong, Ping Yan, Tao Shao. (2020) Low-temperature plasma polymerized fluorocarbon coating promotes surface charge dissipation in polystyrene. NANOTECHNOLOGY, 32 (12): (125703). [PMID:33382042] [10.1088/1361-6528/abcfe9] |
| 2. Zhentao Li, Zhenkun Mao, Changjun Hu, Qiaoyan Li, Zilin Chen. (2020) Fluoro-functionalized stationary phases for electrochromatographic separation of organic fluorides. JOURNAL OF CHROMATOGRAPHY A, [PMID:32709321] [10.1016/j.chroma.2020.461269] |
| 3. Tao Yu, Jiangjiexing Wu, Yuhe Shen, Anastasia Penkova, Wei Qi, Rongxin Su. (2024) Transparent coating based on multienzyme-mimicking Janus nanozyme for synergetic biofouling control in seawater. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2024.155144] |
| 4. Wei-Long Bi, An Tang, Yu Tian, Zhijie Zhu, Su Chen. (2024) Robust and Durable Photonic Crystal with Liquid-Repellent Property for Self-Cleaning Coatings and Structural Colored Textiles. ACS Applied Materials & Interfaces, [PMID:38916253] [10.1021/acsami.4c09497] |