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Chemical compound From Wikipedia, the free encyclopedia
Propiolic acid is the organic compound with the formula HC2CO2H. It is the simplest acetylenic carboxylic acid. It is a colourless liquid that crystallises to give silky crystals. Near its boiling point, it decomposes.
Names | |
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Preferred IUPAC name
Prop-2-ynoic acid[1] | |
Other names
Propiolic acid Acetylene carboxylic acid Propargylic acid Acetylene mono-carboxylic acid | |
Identifiers | |
3D model (JSmol) |
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878176 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.006.763 |
EC Number |
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81893 | |
KEGG | |
MeSH | C011537 |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C3H2O2 | |
Molar mass | 70.047 g·mol−1 |
Density | 1.1325 g/cm3 |
Melting point | 9 °C (48 °F; 282 K) |
Boiling point | 144 °C (291 °F; 417 K) (decomposes) |
Acidity (pKa) | pka = 1.89 [2] |
Hazards | |
GHS labelling:[3] | |
Danger | |
H226, H301, H310, H315, H335 | |
P210, P233, P240, P241, P242, P243, P261, P262, P264, P270, P271, P280, P301+P310, P302+P350, P302+P352, P303+P361+P353, P304+P340, P310, P312, P321, P322, P330, P332+P313, P361, P362, P363, P370+P378, P403+P233, P403+P235, P405, P501 | |
Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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It is soluble in water and possesses an odor like that of acetic acid.[4][5]
It is prepared commercially by oxidizing propargyl alcohol at a lead electrode.[6] It can also be prepared by decarboxylation of acetylenedicarboxylic acid.
Exposure to sunlight converts it into trimesic acid (benzene-1,3,5-tricarboxylic acid).[5] It undergoes bromination to give dibromoacrylic acid. With hydrogen chloride it forms chloroacrylic acid. Its ethyl ester condenses with hydrazine to form pyrazolone.[5]
It forms a characteristic explosive solid upon treatment to its aqueous solution with ammoniacal silver nitrate.[5] An amorphous explosive precipitate forms with ammoniacal cuprous chloride.
Propiolates are esters or salts of propiolic acid. Common examples include methyl propiolate and ethyl propiolate.
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