tridecan-2-ol

chemical compound
ChemicalSubstance group_of_stereoisomers Q81988429
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tridecan-2-ol

Summary

tridecan-2-ol is a group of stereoisomers[1].

Key Facts

  • tridecan-2-ol's instance of is recorded as group of stereoisomers[2].
  • tridecan-2-ol's CAS Registry Number is recorded as 1653-31-2[3].
  • tridecan-2-ol's EC number is recorded as 216-723-1[4].
  • tridecan-2-ol's canonical SMILES is recorded as OC(C)CCCCCCCCCCC[5].
  • tridecan-2-ol's InChI is recorded as InChI=1S/C13H28O/c1-3-4-5-6-7-8-9-10-11-12-13(2)14/h13-14H,3-12H2,1-2H3[6].
  • tridecan-2-ol's InChIKey is recorded as HKOLRKVMHVYNGG-UHFFFAOYSA-N[7].
  • tridecan-2-ol's chemical formula is recorded as C₁₃H₂₈O[8].
  • tridecan-2-ol's subclass of is recorded as fatty alcohol[9].
  • tridecan-2-ol's UNII is recorded as V4E4P9GZB5[10].
  • tridecan-2-ol's PubChem CID is recorded as 15449[11].
  • tridecan-2-ol's ChEBI ID is recorded as 195621[12].
  • tridecan-2-ol's found in taxon is recorded as Zingiber mioga[13].
  • tridecan-2-ol's found in taxon is recorded as Cistus creticus[14].
  • tridecan-2-ol's found in taxon is recorded as Carica papaya[15].
  • tridecan-2-ol's LIPID MAPS ID is recorded as LMFA05000523[16].
  • tridecan-2-ol's KNApSAcK ID is recorded as C00060265[17].
  • tridecan-2-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+200.214015516'}[18].
  • tridecan-2-ol's melting point is recorded as {'unit': 'http://www.wikidata.org/entity/Q25267', 'amount': '+25.0'}[19].
  • tridecan-2-ol's ECHA Substance Infocard ID is recorded as 100.015.204[20].
  • tridecan-2-ol's NSC number is recorded as 9499[21].
  • tridecan-2-ol's SureChEMBL ID is recorded as 20639[22].
  • tridecan-2-ol's DSSTox substance ID is recorded as DTXSID40987402[23].
  • tridecan-2-ol's MassBank accession ID is recorded as MSBNK-Fac_Eng_Univ_Tokyo-JP006867[24].
  • tridecan-2-ol's DSSTOX compound identifier is recorded as DTXCID9029431[25].
  • tridecan-2-ol's UniChem compound ID is recorded as 24404121[26].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . PubChem. Retrieved . wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . Volatile Flavor Compounds of Myoga (Zingiber Mioga).. wikidata.org.
  13. [14] . Morphological, chemical and genetic differentiation of two subspecies of Cistus creticus L. (C. creticus subsp. eriocephalus and C. creticus subsp. corsicus).. wikidata.org.
  14. [15] . Volatile components of papaya (Carica papaya L., Maradol variety) fruit. wikidata.org.
  15. [16] . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . Jean-Claude Bradley Open Melting Point Dataset. wikidata.org.
  19. [20] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . wikidata.org.
  22. [23] . wikidata.org.
  23. [24] . wikidata.org.
  24. [25] . wikidata.org.
  25. [26] . UniChem. wikidata.org.

Class ancestry

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

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APA 4ort.xyz Knowledge Graph. (2026). tridecan-2-ol. Retrieved May 3, 2026, from https://4ort.xyz/entity/tridecan-2-ol
MLA “tridecan-2-ol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tridecan-2-ol.
BibTeX @misc{4ortxyz_tridecan-2-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tridecan-2-ol}}, year = {2026}, url = {https://4ort.xyz/entity/tridecan-2-ol}, note = {Accessed: 2026-05-03}}
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