| Names | |
|---|---|
Other names
| |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.009.902 |
| EC Number |
|
| 362641 | |
PubChem CID | |
CompTox Dashboard (EPA) | |
| |
| |
| Properties | |
| C4H6O2 | |
| Molar mass | 86.090 g·mol−1 |
| Appearance | Clear light yellow liquid |
| Density | 1.013 g/mL |
| Melting point | −39 °C (−38 °F; 234 K) |
| Boiling point | 163 °C (325 °F; 436 K) |
| Well-soluble | |
| Hazards | |
| GHS labelling: [1] | |
| | |
| Danger | |
| H314, H317, H335, H341, H351, H411 | |
| P202, P273, P280, P303, P304, P305, P310, P338, P340, P351, P353, P361 | |
| Related compounds | |
Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
But-3-enoic acid (or 3-butenoic acid) is a short-chain unsaturated carboxylic acid, with the linear formula CH2=CHCH2CO2H. [2]
The acid is obtained via a reaction of allyl cyanide and concentrated hydrochloric acid. The mixture is gently heated with occasional shaking. The reaction produces a voluminous precipitate of ammonium chloride. Then water is introduced, and the upper acid layer is separated. [3]
The acid forms a clear light yellow liquid. Causes skin burns. [6]
The compound is well-soluble in water, ethanol, and diethyl ether.
The acid has been employed in preparing specialized coatings and complex organic compounds, including those involving Diels-Alder reactions. [1]