Angelic acid

Angelic acid
Names
IUPAC name
(Z)-2-methylbut-2-enoic acid
Identifiers
565-63-9 Yes
ChEBI CHEBI:36431 Yes
ChEMBL ChEMBL55941 Yes
ChemSpider 559009 Yes
Jmol-3D images Image
Image
PubChem 643915
Properties
Molecular formula
 C5H8O2
Molar mass 100.12 g·mol−1
Melting point 45.5 °C (113.9 °F; 318.6 K)
Boiling point 185 °C (365 °F; 458 K)
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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Infobox references

Angelic acid is a monocarboxylic unsaturated organic acid. It is mostly found in the plants of the family Apiaceae. German pharmacist Ludwig Andreas Buchner isolated angelic acid in 1842 from the roots of garden angelica (Angelica archangelica) which gave the acid its name. Angelic acid is a volatile solid with a biting taste and pungent sour odor. It is the trans isomer of 2-methyl-2-butenoic acid, which easily converts to the cis isomer, tiglic acid, upon heating or reaction with inorganic acids. The reverse transformation occurs much less readily. The salts and esters of angelic acid are called angelates. Angelic acid esters are the active components of herbal medicine used against a wide range of various health disturbances including pains, fever, gout, heartburn, etc.

Name and discovery

Angelic acid was first isolated by the German pharmacist Ludwig Andreas Buchner (1813–1897) in 1842 from the roots of the garden plant angelica (Angelica archangelica) that gave the acid its name.[1]

Occurrence

Angelic acid occurs in the roots of many plants, especially of the family Apiaceae. These plants include Angelica archangelica, Peucedanum ostruthium (masterwort), Levisticum officinale (lovage),[2][3] Euryangium sumbul and Laserpitium latifolium. In the latter plant, it is present in the resin called laserpicium, and the oil of carrot also contains angelic acid.[4] Sumbul plants might contain not angelic acid itself, but a larger complex which breaks into angelic acid upon processing.[5] The acid can also be extracted from the oil of chamomile flowers, and 85% of Roman chamomile (Anthemis nobilis) oil consists of esters of angelic and tiglic acids;[6][7] it also contains isobutyl angelate and amyl angelate.[8] The acid content is highest in Angelica archangelica[9] where it is about 0.3%.[2]

Properties

Angelic acid is a volatile solid with a biting taste and pungent sour odor. It crystallizes in colorless monoclinic prisms which dissolve rapidly in alcohol[10] or hot water and slowly in cold water. Angelic and tiglic acid are trans and cis isomers of 2-methyl-2-butenoic acid, respectively. The former can be entirely converted to the latter by boiling for about 40 hours, by reaction with sulfuric and other acids,[9] by heating with a base to a temperature above 100 °C,[4] or simply by storing the acid for about 25 years.[11] The reverse transformation occurs much less readily; it can be induced by ultraviolet light, but not with visible light. The conversion rate is low and only 0.36 g of angelic acid could be obtained from 13 g of tiglic acid after 43-day irradiation with a 500-watt lamp. Despite being the trans isomer, angelic acid has a lower melting point and higher acid dissociation constant than tiglic acid,[12] although the opposite trends are usually observed.[13][14]

Angelic acid reacts with hydrobromic acid and bromine producing bromovaleric and dibromovaleric acids, respectively, with a yield of 60–70%. Chlorovaleric and iodovaleric acids are obtained using hydrochloric and hydroiodic acids, respectively. The salts of angelic acid are called angelates. Angelates of alkaline earth metals M have a general formula M(C5H7O2)2 and form white, water-soluble crystals.[9]

Applications

The angelic acid esters of sesquiterpene alcohols, such as petasin, are the active chemical behind the strong pain-relieving and spasmolytic action of extracts from the plant butterbur.[2] Roman chamomile, in which esters of angelic and tiglic acids are the principal components, was used as a sedative and tonic, and as a medicine against nervous problems, fever, colic, heartburn, loss of appetite, gout, headache and other health disturbances.[6]

References

  1. ↑ Buchner, L. A. (1842). "Ueber eine eigenthümliche flüchtige Säure aus der Angelicawurzel: Eine briefliche Mittheilung". Justus Liebigs Ann. Chem. 42: 226–233. doi:10.1002/jlac.18420420211.
  2. ↑ 2.0 2.1 2.2 Rudolf Fritz Weiss Weiss's herbal medicine, Thieme, 2001, ISBN 1-58890-069-X pp. 46, 91, 236
  3. ↑ K. V. Peter Handbook of herbs and spices, Volume 2, Woodhead Publishing, 2004, ISBN 1-85573-721-3 p. 96
  4. ↑ 4.0 4.1 Sonobe, Hiromi; Kamps, Laverne R.; Mazzola, Eugene P.; Roach, John A. G. (1981). "Isolation and identification of a new conjugated carbofuran metabolite in carrots: angelic acid ester of 3-hydroxycarbofuran". Journal of Agricultural and Food Chemistry 29 (6): 1125–9. doi:10.1021/jf00108a006. PMID 7320331.
  5. ↑ J. O. Braithwaite Year-book of pharmacy, J. & A. Churchill, 1887, p. 14
  6. ↑ 6.0 6.1 Ernest Small Culinary herbs, National Research Council Canada, 2006, ISBN 0-660-19073-7 p. 288
  7. ↑ Lyle E. Craker, James E. Simon Herbs, Spices, and Medicinal Plants: Recent Advances in Botany, Horticulture, and Pharmacology, Routledge, 1986, ISBN 1-56022-043-0 p. 257
  8. ↑ Henry Watts, Henry Forster Morley, Matthew Moncrieff Pattison Muir Watts' Dictionary of Chemistry, Volume 1, Longmans, Green, 1888, p. 266
  9. ↑ 9.0 9.1 9.2 William Allen Miller, Herbert McLeod Elements of Chemistry, Vol. 3: Chemical physics, p. 958
  10. ↑ Friedrich Wöhler Wöhler's Outlines of organic chemistry, p. 124
  11. ↑ Year-book of pharmacy, p. 92
  12. ↑ Pelletier, S. W.; McLeish, William L. (1952). "The Ultraviolet-induced Isomerization of Tiglic Acid to Angelic Acid". Journal of the American Chemical Society 74: 6292. doi:10.1021/ja01144a518.
  13. ↑ Vickie Vaclavik, Vickie A. Vaclavik, Elizabeth W. Christian Essentials of food science, Springer, 2007, ISBN 0-387-69939-2, p. 282
  14. ↑ D. Nasipuri Stereochemistry of Organic Compounds: Principles and Applications, New Age International, 1994, ISBN 81-224-0570-3, p. 192