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Names | |
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IUPAC name
2-(14'-hydroxypentadecyl)-4-methyl-5-oxo-2,5-dihydrofuran-3-carboxylic acid
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
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Properties | |
C21H36O5 | |
Molar mass | 368.514 g·mol−1 |
Appearance | white flakes |
Melting point | 108–109° |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Constipatic acid is a fatty acid found in several lichen species. It was isolated, identified, and named by Douglas Chester and John Alan Elix in a 1979 publication. The compound was extracted from the Australian leafy lichen called Xanthoparmelia constipata (after which the compound is named), which was collected on schist boulders west of Springton, South Australia. The related compounds protoconstipatic acid and dehydroconstipatic acid were also reported concurrently.[1] Syo Kurokawa and Rex Filson had previously detected the compounds using thin-layer chromatography when they formally described the lichen as a new species in 1975, but had not characterised them chemically.[2]
After conversion of constipatic acid to methyl constipatate, a mass spectra of the compound revealed four diagnostic peaks at the mass-to-charge ratio (m/e) of 367, 338, 279 and 169. The peaks correspond to the cleavage of a methyl group, the 1-hydroxyethyl moiety, the methoxycarbonyl group (i.e. CH3-O-CO-) and 1-cleavage of the side chain. Additional analysis with proton nuclear magnetic resonance corroborated these results and confirmed the linear nature of the aliphatic chain.[1]
In addition to Xanthoparmelia constipata, constipatic acid has been isolated from several other Xanthoparmelia species, including X. perezdepazii,[3] X. filarskyana, X. flavecentireagens, X. lineola, and X. metaclystoides.[4] It has been isolated from lichens in other genera as well. Examples include Parmelia xanthosorediata, Heterodermia appendiculata, Heterodermia japonica,[5] Protoparmelia nebulosa,[6] Hertelidea wankaensis,[7] Lepraria coriensis,[8] Punctelia negata,[9] and Rhizoplaca melanophthalma.[10]
Some sources consider the molecule to have an unusual or humorous name due to its similarity to the word "constipation".[11][12]
Chester & Elix 1979
was invoked but never defined (see the help page).Kurokawa & Filson 1975
was invoked but never defined (see the help page).Pérez-Vargas et al. 2007
was invoked but never defined (see the help page).Stocker-Wörgötter 2015
was invoked but never defined (see the help page).Din et al. 2010
was invoked but never defined (see the help page).Elix & Kantvilas 2009
was invoked but never defined (see the help page).Kantvilas & Elix 2006
was invoked but never defined (see the help page).Joshi et al. 2010
was invoked but never defined (see the help page).Canêz et al. 2016
was invoked but never defined (see the help page).Shrestha et al. 2014
was invoked but never defined (see the help page).MayWeb
was invoked but never defined (see the help page).Mestel 2002
was invoked but never defined (see the help page).