(2E)-geranic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q4381113
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(2E)-geranic acid

Summary

(2E)-geranic acid is a type of chemical entity[1]. (2E)-geranic acid is known by 11 alternative names across languages and contexts.[2]

Key Facts

  • (2E)-geranic acid's instance of is recorded as type of chemical entity[3].
  • (2E)-geranic acid's canonical SMILES is recorded as CC(=CCCC(=CC(=O)O)C)C[4].
  • (2E)-geranic acid's chemical formula is recorded as C₁₀H₁₆O₂[5].
  • (2E)-geranic acid is a type of 3,7-dimethylocta-2,6-dienoic acid[6].
  • (2E)-geranic acid's Commons category is recorded as Geranic acid[7].
  • (2E)-geranic acid's found in taxon is recorded as Daphne odora[8].
  • (2E)-geranic acid's found in taxon is recorded as ginger[9].
  • (2E)-geranic acid's found in taxon is recorded as Aloysia citrodora[10].
  • (2E)-geranic acid's found in taxon is recorded as Aloysia triphylla[11].
  • (2E)-geranic acid's found in taxon is recorded as Cymbopogon citratus[12].
  • (2E)-geranic acid's found in taxon is recorded as Monocyclanthus vignei[13].
  • (2E)-geranic acid's found in taxon is recorded as Pectis elongata[14].
  • (2E)-geranic acid's found in taxon is recorded as Pelargonium graveolens[15].
  • (2E)-geranic acid's found in taxon is recorded as Prunus avium[16].
  • (2E)-geranic acid's found in taxon is recorded as Mangifera indica[17].
  • (2E)-geranic acid's found in taxon is recorded as Chenopodium ambrosioides[18].
  • (2E)-geranic acid's found in taxon is recorded as Dysphania ambrosioides[19].
  • (2E)-geranic acid's found in taxon is recorded as Aloysia citriodora[20].
  • (2E)-geranic acid's found in taxon is recorded as Vitis vinifera[21].
  • (2E)-geranic acid's isomeric SMILES is recorded as CC(=CCC/C(=C/C(=O)O)/C)C[22].
  • (2E)-geranic acid's mass is recorded as {'unit': 'Q483261', 'amount': '+168.115'}[23].

Why It Matters

(2E)-geranic acid is known by 11 alternative names across languages and contexts.[2]

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] . wikidata.org.
  6. [8] . Volatile components of zinchoge flower (Daphne odora Thunb.).. wikidata.org.
  7. [9] . Glycosidically bound aroma compounds in ginger (Zingiber officinale Roscoe). wikidata.org.
  8. [10] . Composition of Lemon Verbena (Aloysia triphylla(L'Herit.) Britton) Oil of Moroccan Origin. wikidata.org.
  9. [11] . Composition of Lemon Verbena (Aloysia triphylla(L'Herit.) Britton) Oil of Moroccan Origin. wikidata.org.
  10. [12] . Supercritical fluid extraction ofCymbopogon citratus (DC.) Stapf. wikidata.org.
  11. [13] . Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei. wikidata.org.
  12. [14] . Analysis of the Essential Oil ofPectis elongataKunth. from Martinique. Evaluation of Its Bacteriostatic and Fungistatic Properties. wikidata.org.
  13. [15] . Analysis of the acid fraction of reunion geranium oil (Pelargonium graveolens L'Her. ex Ait). wikidata.org.
  14. [16] . Free and glycosidically bound aroma compounds in cherry (Prunus avium L.).. wikidata.org.
  15. [17] . Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity. wikidata.org.
  16. [18] . Volatile Constituents from the Leaves of Chenopodium ambrosioides L.. wikidata.org.
  17. [19] . Volatile Constituents from the Leaves of Chenopodium ambrosioides L.. wikidata.org.
  18. [20] . Composition of Lemon Verbena (Aloysia triphylla(L'Herit.) Britton) Oil of Moroccan Origin. wikidata.org.
  19. [21] . Free and Bound Volatile Secondary Metabolites of Vitis Vhifera Grape cv. Sauvignon Blanc. wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . 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). (2E)-geranic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/2e-geranic-acid
MLA “(2E)-geranic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2e-geranic-acid.
BibTeX @misc{4ortxyz_2e-geranic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(2E)-geranic acid}}, year = {2026}, url = {https://4ort.xyz/entity/2e-geranic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (2E)-geranic acid — https://4ort.xyz/entity/2e-geranic-acid (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. 5w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Instance of type of chemical entity
    Subclass of
    Aliases
    Human metabolome database id HMDB0036103
    + 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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