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1 See also  





2 References  





3 External links  














Homodihydrocapsaicin






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Homodihydrocapsaicin
Names
Preferred IUPAC name

N-[(4-Hydroxy-3-methoxyphenyl)methyl]-9-methyldecanamide

Other names

  • Homodihydrocapsaicin
  • N-Vanillyl-9-methyldecanamide
  • Vanillylamide of 9-methyldecanoic acid
  • HDHC
  • Identifiers

    CAS Number

    3D model (JSmol)

    ChemSpider

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C19H31NO3/c1-15(2)9-7-5-4-6-8-10-19(22)20-14-16-11-12-17(21)18(13-16)23-3/h11-13,15,21H,4-10,14H2,1-3H3,(H,20,22) ☒N

      Key: AKDLSISGGARWFP-UHFFFAOYSA-N ☒N

    • InChI=1/C19H31NO3/c1-15(2)9-7-5-4-6-8-10-19(22)20-14-16-11-12-17(21)18(13-16)23-3/h11-13,15,21H,4-10,14H2,1-3H3,(H,20,22)

      Key: AKDLSISGGARWFP-UHFFFAOYAS

    • O=C(NCc1cc(OC)c(O)cc1)CCCCCCCC(C)C

    Properties

    Chemical formula

    C19H31NO3
    Molar mass 321.461 g·mol−1

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Homodihydrocapsaicin
    HeatAbove peak
    Scoville scale8,600,000[1] SHU

    Homodihydrocapsaicin is a capsaicinoid and analog and congenerofcapsaicininchili peppers (Capsicum). Like capsaicin it is an irritant. Homodihydrocapsaicin accounts for about 1% of the total capsaicinoids mixture[2] and has about half the pungency of capsaicin. Pure homodihydrocapsaicin is a lipophilic colorless odorless crystalline to waxy compound. It produces "numbing burn" in the throat and is one of the most prolonged and difficult to rinse out. On the Scoville scale it has 8,600,000 SHU (Scoville heat units).[1]

    See also[edit]

    References[edit]

    1. ^ a b Govindarajan, Sathyanarayana (1991). "Capsicum — Production, Technology, Chemistry, and Quality. Part V. Impact on Physiology, Pharmacology, Nutrition, and Metabolism; Structure, Pungency, Pain, and Desensitization Sequences". Critical Reviews in Food Science and Nutrition. 29 (6): 435–474. doi:10.1080/10408399109527536. PMID 2039598.
  • ^ Bennett DJ, Kirby GW (1968). "Constitution and biosynthesis of capsaicin". J. Chem. Soc. C: 442. doi:10.1039/j39680000442.
  • External links[edit]


    Retrieved from "https://en.wikipedia.org/w/index.php?title=Homodihydrocapsaicin&oldid=1180265276"

    Categories: 
    Capsaicinoids
    Acetamides
    Hidden categories: 
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    Articles without KEGG source
    Articles with changed ChemSpider identifier
    Articles with changed InChI identifier
    Articles containing unverified chemical infoboxes
    Chembox image size set
    Articles with short description
    Short description matches Wikidata
     



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