Tiglic acid
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| Tiglic acid | |
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| IUPAC name | (E)-2-methylbut-2-enoic acid |
| Other names | cevadic acid, sabadillic acid, tiglinic acid |
| Identifiers | |
| CAS number | [80-59-1] |
| SMILES | CC=C(C)C(=O)O |
| Properties | |
| Molecular formula | C5H8O2 |
| Molar mass | 100.116 g/mol |
| Density | 0.9641 g/cm3 (76 °C) |
| Melting point |
63.5-64 °C |
| Boiling point |
198.5 °C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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Tiglic acid is a monocarboxylic unsaturated organic acid. It is found in croton oil and in several other natural products. It was also isolated from the defensive secretion of certain beetles.
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[edit] Properties and uses
Tiglic acid has a double bond between the second and third carbons of the chain. Together with angelic acid form a pair of cis-trans isomers. Tiglic acid is a volatile and crystallizable substance with a sweet, warm spicy odour. It is used in making perfumes and flavoring agents.
[edit] Toxicity
Tiglic acid is a skin and eye irritant. The inhalation of the substance causes respiratory tract irritation. It is listed on the Toxic Substances Control Act (TSCA).
[edit] Names and discovery
In 1819 Pelletier and Caventou isolated a peculiar volatile and crystallizable acid from the seeds of Schoenocaulon officinalis, a Mexican plant of family Melanthaceae (also called cevadilla or sabadilla). Consequently the substance was named sabadillic or cevadic acid. It was later found to be identical with Frankland and Duppa's methylcrotonic acid (1865). In 1870 Geuther and Fröhlich prepared an acid from croton oil to which they gave the name tiglic acid (or tiglinic acid) after (Croton) tiglium (Linn.), specific name of the croton oil plant. The compound was shown to be identical with the previously described methyl-crotonic acid.
[edit] References
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