≥98%, containing stabilizer MEHQ 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Propargyl acrylate is a propargyl ester of acrylic acid. It participates in the preparation of lipid nanoparticles for use in siRNA delivery.Propargyl acrylate may be used to synthesize:linear poly(N-isopropylacrylamide)(PNIPAM)1-[3-(2-methyl-2-dodecylsulfanylthiocarbonylsulfanylpropionyloxy)propyl]-1H-[1,2,3]triazol-4-ylmethyl acrylate, an acryloyl trithiocarbonate chain transfer agentpropranolol-imprinted core–shell nanoparticles (mipCS)
| Pubchem Sid | 488186114 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488186114 |
| Sorrisi canonici | C=CC(=O)OCC#C |
| IUPAC Name | prop-2-ynyl prop-2-enoate |
| InChIKey | WPBNLDNIZUGLJL-UHFFFAOYSA-N |
| INCHI | 1S/C6H6O2/c1-3-5-8-6(7)4-2/h1,4H,2,5H2 |
| Isomeri SMILES | C=CC(=O)OCC#C |
| WGK Germania | 3 |
| PubChem CID | 82655 |
| Numero UN | 3272 |
| Gruppo di imballaggio | III |
| Peso molecolare | 110.11 |
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 |
| Classe | Carboxylic acids and derivatives |
| Subclass | Acrylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acrylic acid esters |
| Alternative Parents | Enoate esters Monocarboxylic acids and derivatives Acetylides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acrylic acid ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Acetylide - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Descrizione | 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 | Data | Oggetto |
|---|---|---|---|
 G2516498 | Certificate of Analysis | Mar 27, 2025 | P472190 |
| G2516499 | Certificate of Analysis | Mar 27, 2025 | P472190 |
| D23231342 | Certificate of Analysis | Apr 15, 2023 | P472190 |
| D23231346 | Certificate of Analysis | Apr 15, 2023 | P472190 |
| D2323189 | Certificate of Analysis | Apr 15, 2023 | P472190 |
| D2323191 | Certificate of Analysis | Apr 15, 2023 | P472190 |
| Sensibilità | Light sensitive； Heat sensitive |
|---|---|
| Indice di rifrazione | 1.4460 |
| Punto di infiammabilità (°F) | 109.4 °F |
| Punto di infiammabilità (°C) | 43 °C |
| Punto di ebollizione (°C) | 142-143° C (lit.) |
| Peso molecolare | 110.110 g/mol |
| XLogP3 | 0.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 110.037 Da |
| Monoisotopic Mass | 110.037 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 138.000 |
| 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. Chao Huang, Hongwei Wang, Yunjia Xu, Shujuan Ma, Bolin Gong, Junjie Ou. (2022) Carbon dot-functionalized macroporous adsorption resin for bifunctional ultra-sensitive detection and fast removal of iron(III) ions. Analytical Methods, 14 (38): (3727-3738). [PMID:36106929] [10.1039/D2AY01366E] |
| 2. Yu Liu, Xiaochuan Shui, Meng Wang, Chenguang Zhang, Yuechuan Wang. (2017) Rational design of soluble and clickable polymers prepared by conventional free radical polymerization of acetylene-functionalized acrylate. Polymer Chemistry, 8 (15): (2363-2369). [PMID:] [10.1039/C6PY02104B] |
| 3. Bo Zhao, Yaochen Zheng, Zhulin Weng, Shengying Cai, Chao Gao. (2015) The electrophilic effect of thiol groups on thiol–yne thermal click polymerization for hyperbranched polythioether. Polymer Chemistry, 6 (20): (3747-3753). [PMID:] [10.1039/C5PY00307E] |
