≥95%, stabilized with MEHQ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sonrisas canónicas | C=CC(=O)OCC1CO1 |
|---|---|
| IUPAC Name | oxiran-2-ylmethyl prop-2-enoate |
| InChIKey | RPQRDASANLAFCM-UHFFFAOYSA-N |
| INCHI | 1S/C6H8O3/c1-2-6(7)9-4-5-3-8-5/h2,5H,1,3-4H2 |
| Isómeros SMILES | C=CC(=O)OCC1CO1 |
| Número ONU | 1992 |
| Grupo de embalaje | I |
| Peso molecular | 128.13 |
| Reaxy-Rn | 109092 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=109092&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 | Acrylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acrylic acid esters |
| Alternative Parents | Enoate esters Oxacyclic compounds Monocarboxylic acids and derivatives Epoxides Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Acrylic acid ester - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Dialkyl ether - Oxirane - Ether - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as acrylic acid esters. These are organic compounds containing and ester acrylic acid (CH2=CHC(=O)OH). |
| 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 |
|---|---|---|---|
 G2430539 | Certificate of Analysis | Jun 08, 2026 | G156838 |
| G2430540 | Certificate of Analysis | Jun 08, 2026 | G156838 |
| I2312541 | Certificate of Analysis | Dec 13, 2023 | G156838 |
| I2312542 | Certificate of Analysis | Dec 13, 2023 | G156838 |
| I2312543 | Certificate of Analysis | Dec 13, 2023 | G156838 |
| H2206348 | Certificate of Analysis | Aug 12, 2022 | G156838 |
| H2206349 | Certificate of Analysis | Aug 12, 2022 | G156838 |
| H2206350 | Certificate of Analysis | Aug 12, 2022 | G156838 |
| Sensibilidad | Heat sensitive |
|---|---|
| Índice de refracción | 1.45 |
| Punto de inflamación (°C) | 60 °C |
| Punto de ebullición (°C) | 65 °C/5 mmHg |
| Punto de fusión (°C) | -42 °C |
| Peso molecular | 128.130 g/mol |
| XLogP3 | 0.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 4 |
| Exact Mass | 128.047 Da |
| Monoisotopic Mass | 128.047 Da |
| Topological Polar Surface Area | 38.800 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 130.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Daguang He, Xuefeng Gui, Yonglu Dong, Shudong Lin, Yuanyuan Tu, Jiwen Hu, Shi Li, Jihe Zhao. (2023) An efficient catalytic and solvent-free method for the synthesis of mono-organofunctionalized polymethylhydrosiloxane derivatives. POLYMERS FOR ADVANCED TECHNOLOGIES, 34 (6): (1979-1989). [PMID:] [10.1002/pat.6025] |
