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patchouli alcohol

chemical compound
ChemicalSubstance type_of_chemical_entity Q7144372
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patchouli alcohol

Summary

patchouli alcohol is a type of chemical entity[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • patchouli alcohol's instance of is recorded as type of chemical entity[3].
  • patchouli alcohol's canonical SMILES is recorded as CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O[4].
  • patchouli alcohol's chemical formula is recorded as C₁₅H₂₆O[5].
  • patchouli alcohol is a type of patchoulol[6].
  • patchouli alcohol's found in taxon is recorded as Teucrium leucocladum[7].
  • patchouli alcohol's found in taxon is recorded as Pogostemon cablin[8].
  • patchouli alcohol's found in taxon is recorded as Valeriana fauriei[9].
  • patchouli alcohol's found in taxon is recorded as Valeriana oficina los[10].
  • patchouli alcohol's found in taxon is recorded as Valeriana jatamansi[11].
  • patchouli alcohol's found in taxon is recorded as ginger[12].
  • patchouli alcohol's found in taxon is recorded as Valeriana phu[13].
  • patchouli alcohol's found in taxon is recorded as Valeriana celtica[14].
  • patchouli alcohol's found in taxon is recorded as Heterotropa[15].
  • patchouli alcohol's found in taxon is recorded as Asarum[16].
  • patchouli alcohol's found in taxon is recorded as Desmos cochinchinensis[17].
  • patchouli alcohol's found in taxon is recorded as Clinopodium odorum[18].
  • patchouli alcohol's found in taxon is recorded as Clinopodium gilliesii[19].
  • patchouli alcohol's isomeric SMILES is recorded as C[C@H]1CC[C@@]2([C@@]3([C@H]1CC@HCC3)C)OC@HCC3)C)O">[20].
  • patchouli alcohol's mass is recorded as {'unit': 'Q483261', 'amount': '+222.198365'}[21].
  • patchouli alcohol's stereoisomer of is recorded as (1R,3R,6S,7R,8S)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol[22].
  • patchouli alcohol's stereoisomer of is recorded as (1S,3R,6R,7R,8R)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol[23].

Why It Matters

patchouli alcohol has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 7 alternative names across languages and contexts.[24]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Chemical analysis and biological activities of the essential oil of Teucrium leucocladum Boiss. (Lamiaceae). wikidata.org.
  6. [8] ↑ . Biosynthesis of the sesquiterpene patchoulol from farnesyl pyrophosphate in leaf extracts of Pogostemon cablin (patchouli): mechanistic considerations. wikidata.org.
  7. [9] ↑ . Sesquiterpenoids from Valeriana fauriei. wikidata.org.
  8. [10] ↑ . Sesquiterpenoids from Valeriana fauriei. wikidata.org.
  9. [11] ↑ . Antioxidant activity of essential oil and extracts of Valeriana jatamansi roots. wikidata.org.
  10. [12] ↑ . Volatile flavor components of Zingiberis rhizoma (Zingiber officinale Roscoe).. wikidata.org.
  11. [13] ↑ . Composition of the essential oils from underground parts ofValeriana officinalis L.s.l. and several closely related taxa. wikidata.org.
  12. [14] ↑ . Composition of the essential oils from underground parts ofValeriana officinalis L.s.l. and several closely related taxa. wikidata.org.
  13. [15] ↑ . Supplemental Studies on the Volatile Oils of Asarum Group. (2). wikidata.org.
  14. [16] ↑ . Supplemental Studies on the Volatile Oils of Asarum Group. (2). wikidata.org.
  15. [17] ↑ . New Cytotoxic Fatty Acid from Desmos cochinchinensis (Annonaceae). wikidata.org.
  16. [18] ↑ . The Essential Oils ofSatureja odoraandS. parvifoliafrom Argentina. wikidata.org.
  17. [19] ↑ . The Essential Oils ofSatureja odoraandS. parvifoliafrom Argentina. wikidata.org.
  18. [20] ↑ . PubChem. Retrieved . wikidata.org.
  19. [21] ↑ . PubChem. Retrieved . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.
  2. [24] ↑ . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). patchouli alcohol. Retrieved May 3, 2026, from https://4ort.xyz/entity/patchouli-alcohol
MLA “patchouli alcohol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/patchouli-alcohol.
BibTeX @misc{4ortxyz_patchouli-alcohol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{patchouli alcohol}}, year = {2026}, url = {https://4ort.xyz/entity/patchouli-alcohol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): patchouli alcohol — https://4ort.xyz/entity/patchouli-alcohol (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 15d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of → (1R,3R,6S,7R,8S)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol, (1S,3R,6R,7R,8R)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol
    Instance of → type of chemical entity
    Subclass of → —
    Aliases → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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