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caprylyl glucoside

chemical compound
ChemicalSubstance type_of_chemical_entity Q7077127
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caprylyl glucoside

Summary

caprylyl glucoside is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2]

Key Facts

  • caprylyl glucoside's instance of is recorded as type of chemical entity[3].
  • caprylyl glucoside's chemical structure is recorded as Octyl glucoside.png[4].
  • caprylyl glucoside's CAS Registry Number is recorded as 29836-26-8[5].
  • caprylyl glucoside's EC number is recorded as 249-887-8[6].
  • caprylyl glucoside's canonical SMILES is recorded as CCCCCCCCOC1C(C(C(C(O1)CO)O)O)O[7].
  • caprylyl glucoside's InChI is recorded as InChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1[8].
  • caprylyl glucoside's InChIKey is recorded as HEGSGKPQLMEBJL-RKQHYHRCSA-N[9].
  • caprylyl glucoside's chemical formula is recorded as C₁₄H₂₈O₆[10].
  • caprylyl glucoside's subclass of is recorded as Octyl D-glucopyranoside[11].
  • caprylyl glucoside's has use is recorded as detergent[12].
  • caprylyl glucoside's MeSH descriptor ID is recorded as C018619[13].
  • caprylyl glucoside's ChEMBL ID is recorded as CHEMBL446037[14].
  • caprylyl glucoside's Freebase ID is recorded as /m/054t1sm[15].
  • caprylyl glucoside's UNII is recorded as V109WUT6RL[16].
  • caprylyl glucoside's ChemSpider ID is recorded as 56585[17].
  • caprylyl glucoside's PubChem CID is recorded as 62852[18].
  • caprylyl glucoside's ChEBI ID is recorded as 41128[19].
  • caprylyl glucoside's found in taxon is recorded as Rhodiola sachalinensis[20].
  • caprylyl glucoside's found in taxon is recorded as Rhodiola rosea[21].
  • caprylyl glucoside's found in taxon is recorded as Eucalyptus globulus[22].
  • caprylyl glucoside's isomeric SMILES is recorded as CCCCCCCCO[C@H]1C@@HOC@@HO">[23].
  • caprylyl glucoside's mass is recorded as {'unit': 'Q483261', 'amount': '+292.189'}[24].
  • caprylyl glucoside's ECHA Substance Infocard ID is recorded as 100.045.337[25].
  • caprylyl glucoside's SureChEMBL ID is recorded as 61562[26].
  • caprylyl glucoside's CosIng number is recorded as 55138[27].

Why It Matters

caprylyl glucoside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2]

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] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  11. [13] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . 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] ↑ . ChEBI release 2019-10-02. wikidata.org.
  18. [20] ↑ . Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis. wikidata.org.
  19. [21] ↑ . Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis. wikidata.org.
  20. [22] ↑ . Eucalyptone G, a new phloroglucinol derivative and other constituents from Eucalyptus globulus Labill. wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . CosIng database. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). caprylyl glucoside. Retrieved May 3, 2026, from https://4ort.xyz/entity/caprylyl-glucoside
MLA “caprylyl glucoside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/caprylyl-glucoside.
BibTeX @misc{4ortxyz_caprylyl-glucoside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{caprylyl glucoside}}, year = {2026}, url = {https://4ort.xyz/entity/caprylyl-glucoside}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): caprylyl glucoside — https://4ort.xyz/entity/caprylyl-glucoside (retrieved 2026-05-03)

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