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==Reactions== ==Reactions==


Guaiol yields a deep purple color when treated with ] ] reagents.<ref name=waddell>{{cite journal | pmid = 12391567 | year = 2002 | last1 = Waddell | first1 = TG | last2 = Arp | first2 = NW | last3 = Bodine | first3 = KD | last4 = Pagni | first4 = RM | title = The guaiol color reaction | volume = 68 | issue = 10 | pages = 949–50 | doi = 10.1055/s-2002-34931 | journal = Planta Medica}}</ref> Upon heating with sulfur, guaiazulene can yield. Guaiol yields a deep purple color when treated with ] ] reagents.<ref name=waddell>{{cite journal | pmid = 12391567 | year = 2002 | last1 = Waddell | first1 = TG | last2 = Arp | first2 = NW | last3 = Bodine | first3 = KD | last4 = Pagni | first4 = RM | title = The guaiol color reaction | volume = 68 | issue = 10 | pages = 949–50 | doi = 10.1055/s-2002-34931 | journal = Planta Medica}}</ref> Upon heating with ], ] can yield.


==See also== ==See also==

Latest revision as of 06:59, 13 August 2024

Guaiol
Names
IUPAC name Guai-1(5)-en-11-ol
Systematic IUPAC name 2-propan-2-ol
Other names Champacol,
5-Azulenemethanol
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.003 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C15H26O/c1-10-5-7-12(15(3,4)16)9-14-11(2)6-8-13(10)14/h10-12,16H,5-9H2,1-4H3/t10-,11-,12+/m0/s1Key: TWVJWDMOZJXUID-SDDRHHMPSA-N
  • InChI=1/C15H26O/c1-10-5-7-12(15(3,4)16)9-14-11(2)6-8-13(10)14/h10-12,16H,5-9H2,1-4H3/t10-,11-,12+/m0/s1Key: TWVJWDMOZJXUID-SDDRHHMPBW
SMILES
  • OC(1C\C2=C(/(CC1)C)CC2C)(C)C
Properties
Chemical formula C15H26O
Molar mass 222.372 g·mol
Density 0.961 g/mL
Melting point 92 °C (198 °F; 365 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Guaiol or champacol is an organic compound, a sesquiterpenoid alcohol found in several plants, especially in the oil of guaiacum and cypress pine. It is a crystalline solid that melts at 92 °C. Guaiol is one of many terpenes found in Cannabis and it has been associated with anxiolytic activity.

Reactions

Guaiol yields a deep purple color when treated with electrophilic bromine reagents. Upon heating with sulfur, guaiazulene can yield.

See also

References

  1. The Merriam-Webster Dictionary.
  2. Wolfram Alpha Guaiol
  3. Hillig, Karl W (2004-10-01). "A chemotaxonomic analysis of terpenoid variation in Cannabis". Biochemical Systematics and Ecology. 32 (10): 875–891. doi:10.1016/j.bse.2004.04.004.
  4. Kamal, Brishna S.; Kamal, Fatima; Lantela, Daniel E. (2018). "Cannabis and the Anxiety of Fragmentation—A Systems Approach for Finding an Anxiolytic Cannabis Chemotype". Frontiers in Neuroscience. 12: 730. doi:10.3389/fnins.2018.00730. PMC 6204402. PMID 30405331.
  5. Waddell, TG; Arp, NW; Bodine, KD; Pagni, RM (2002). "The guaiol color reaction". Planta Medica. 68 (10): 949–50. doi:10.1055/s-2002-34931. PMID 12391567.


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