Tiglic acid

Tiglic acid
Names
	IUPAC name (E)-2-methylbut-2-enoic acid
	Other names cevadic acid, sabadillic acid, tiglinic acid
Identifiers
CAS Number	80-59-1 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:9592 ;
ChemSpider	111629 ;
ECHA InfoCard	100.001.178
IUPHAR/BPS	6499;
PubChem CID	125468;
CompTox Dashboard (EPA)	DTXSID80883257 ;
	InChI InChI=1S/C5H8O2/c1-3-4(2)5(6)7/h3H,1-2H3,(H,6,7)/b4-3+ Key: UIERETOOQGIECD-ONEGZZNKSA-N ; InChI=1/C5H8O2/c1-3-4(2)5(6)7/h3H,1-2H3,(H,6,7)/b4-3+ Key: UIERETOOQGIECD-ONEGZZNKBL;
	SMILES O=C(O)/C(=C/C)C;
Properties
Chemical formula	C5H8O2
Molar mass	100.116 g/mol
Density	0.9641 g/cm3 (76 °C)
Melting point	63.5 to 64 °C (146.3 to 147.2 °F; 336.6 to 337.1 K)
Boiling point	198.5 °C (389.3 °F; 471.6 K)
Acidity (pKa)	4.96
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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.^[1]

Properties and uses

Tiglic acid has a double bond between the second and third carbons of the chain. Tiglic acid and 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. The salts and esters of tiglic acid are called tiglates.

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).

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.^[2] The compound was shown to be identical with the previously described methyl-crotonic acid.

References

^ Attygalle, A. B.; Wu, X.; Will, K. W. (2007). "Biosynthesis of tiglic, ethacrylic, and 2-methylbutyric acids in a carabid beetle, Pterostichus (Hypherpes) californicus". J Chem Ecol. 33: 963–970. PMID 17404818.
^ Lloyd, J. U. (1898). "Croton tiglium". Lloyd Brothers plant drug pamphlets, Lloyd Brothers Pharmacy: Cincinnati.

[1] Attygalle, A. B.; Wu, X.; Will, K. W. (2007). "Biosynthesis of tiglic, ethacrylic, and 2-methylbutyric acids in a carabid beetle, Pterostichus (Hypherpes) californicus". J Chem Ecol. 33: 963–970. PMID 17404818.

[2] Lloyd, J. U. (1898). "Croton tiglium". Lloyd Brothers plant drug pamphlets, Lloyd Brothers Pharmacy: Cincinnati.

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