Pelargonin
Chemical structure of pelargonin
Names
IUPAC name
7-Hydroxy-2-(4-hydroxyphenyl)-3,5-bis{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ4-benzopyran-1-ylium
Other names
Pelargonidin 3,5-di-β-D-glucoside
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.037.584
KEGG
UNII
  • InChI=1S/C27H30O15/c28-8-17-19(32)21(34)23(36)26(41-17)39-15-6-12(31)5-14-13(15)7-16(25(38-14)10-1-3-11(30)4-2-10)40-27-24(37)22(35)20(33)18(9-29)42-27/h1-7,17-24,26-29,32-37H,8-9H2,(H-,30,31)/p+1/t17-,18-,19-,20-,21+,22+,23-,24-,26-,27-/m1/s1
    Key: SLCKJKWFULXZBD-ZOTFFYTFSA-O
  • InChI=1/C27H30O15/c28-8-17-19(32)21(34)23(36)26(41-17)39-15-6-12(31)5-14-13(15)7-16(25(38-14)10-1-3-11(30)4-2-10)40-27-24(37)22(35)20(33)18(9-29)42-27/h1-7,17-24,26-29,32-37H,8-9H2,(H-,30,31)/p+1/t17-,18-,19-,20-,21+,22+,23-,24-,26-,27-/m1/s1
    Key: SLCKJKWFULXZBD-OJOSBQBKBL
  • c1cc(ccc1c2c(cc3c([o+]2)cc(cc3O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O
Properties
C27H31O15+
Molar mass 595.53 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Pelargonin is an anthocyanin. It is the 3,5-O-diglucoside of pelargonidin.

Natural occurrences

Pelargonin is a pigment, found in barberries,[1] the petals of the scarlet pelargonium flower[2] pomegranates,[3] and red wine.[4]

See also

References

  1. ↑ Duke, James (1992). "Berberis vulgaris (Berberidaceae), United States Department of Agriculture, National Agricultural Library: Dr. Duke's Phytochemical and Ethnobotanical Databases". phytochem.nal.usda.gov.
  2. ↑ Saunders Currey, Geoffrey (1922). "The Colouring Matter of the Scarlet Pelargonium". J. Chem. Soc., Trans. 121: 319–323. doi:10.1039/CT9222100319.
  3. ↑ Gil, M.I.; Cherif, J.; Ayed, N.; Artes, F.; Tomasbarberan, F.A. (1995). "Influence of Cultivar, Maturity Stage and Geographical Location on the Juice Pigmentation of Tunisian Pomegranates". Zeitschrift für Lebensmittel-Untersuchung und Forschung. 201 (4): 361–364. doi:10.1007/BF01192733. S2CID 95566626.
  4. ↑ He, Fei; Liang, Na-Na; Mu, Lin; Pan, Qiu-Hong; Wang, Jun; Reeves, Michael J.; Duan, Chang-Qing (February 2012). "Anthocyanins and Their Variation in Red Wines I. Monomeric Anthocyanins and Their Color Expression". Molecules. 17 (2): 1571–1601. CiteSeerX 10.1.1.399.2775. doi:10.3390/molecules17021571. PMC 6268338. PMID 22314380.


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