3-heptanol

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q4634146
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3-heptanol

Summary

3-heptanol is a group of stereoisomers[1]. 3-heptanol draws 4 Wikipedia views per month (group_of_stereoisomers category, ranking #214 of 1,063).[2]

Key Facts

  • 3-heptanol's instance of is recorded as group of stereoisomers[3].
  • 3-heptanol's chemical structure is recorded as 3-heptanol.svg[4].
  • 3-heptanol's CAS Registry Number is recorded as 589-82-2[5].
  • 3-heptanol's EC number is recorded as 209-661-1[6].
  • 3-heptanol's canonical SMILES is recorded as CCCCC(CC)O[7].
  • 3-heptanol's InChI is recorded as InChI=1S/C7H16O/c1-3-5-6-7(8)4-2/h7-8H,3-6H2,1-2H3[8].
  • 3-heptanol's InChIKey is recorded as RZKSECIXORKHQS-UHFFFAOYSA-N[9].
  • 3-heptanol's chemical formula is recorded as C₇H₁₆O[10].
  • 3-heptanol's subclass of is recorded as fatty alcohol[11].
  • 3-heptanol's subclass of is recorded as Heptanoles[12].
  • 3-heptanol's Commons category is recorded as 3-Heptanol[13].
  • 3-heptanol's ChEMBL ID is recorded as CHEMBL452729[14].
  • 3-heptanol's Freebase ID is recorded as /m/0g56dk0[15].
  • 3-heptanol's UNII is recorded as 12YBT48HMK[16].
  • 3-heptanol's ChemSpider ID is recorded as 11036[17].
  • 3-heptanol's PubChem CID is recorded as 11520[18].
  • 3-heptanol's ZVG number is recorded as 570042[19].
  • 3-heptanol's ChEBI ID is recorded as 179170[20].
  • 3-heptanol's found in taxon is recorded as Camellia sinensis[21].
  • 3-heptanol's found in taxon is recorded as Coffea arabica[22].
  • 3-heptanol's found in taxon is recorded as Aspalathus linearis[23].
  • 3-heptanol's found in taxon is recorded as Cedronella canariensis[24].
  • 3-heptanol's has characteristic is recorded as bitterness[25].
  • 3-heptanol's Human Metabolome Database ID is recorded as HMDB0031481[26].
  • 3-heptanol's LIPID MAPS ID is recorded as LMFA05000483[27].

Why It Matters

3-heptanol draws 4 Wikipedia views per month (group_of_stereoisomers category, ranking #214 of 1,063).[2] 3-heptanol has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] 3-heptanol is known by 5 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . Freebase Data Dumps. wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] . Q2311683. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . ChEBI release 2022-06-13. wikidata.org.
  19. [21] . Enantiomeric separation of chiral components reported to be in coffee, tea, or cocoa. wikidata.org.
  20. [22] . Enantiomeric separation of chiral components reported to be in coffee, tea, or cocoa. wikidata.org.
  21. [23] . Volatile components of Rooibos tea (Aspalathus linearis). wikidata.org.
  22. [24] . Chavicol β-d-glucoside, a phenylpropanoid heteroside, benzyl-β-d-glucoside and glycosidically bound volatiles from subspecies of Cedronella canariensis. wikidata.org.
  23. [25] . BitterDB. wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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). 3-heptanol. Retrieved May 3, 2026, from https://4ort.xyz/entity/3-heptanol
MLA “3-heptanol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3-heptanol.
BibTeX @misc{4ortxyz_3-heptanol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3-heptanol}}, year = {2026}, url = {https://4ort.xyz/entity/3-heptanol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3-heptanol — https://4ort.xyz/entity/3-heptanol (retrieved 2026-05-03)

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