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2,6-xylenol

chemical compound
ChemicalSubstance type_of_chemical_entity Q1055852
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2,6-xylenol

Summary

2,6-xylenol is a type of chemical entity[1]. 2,6-xylenol has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • 2,6-xylenol's instance of is recorded as type of chemical entity[3].
  • 2,6-xylenol's canonical SMILES is recorded as CC1=C(C(=CC=C1)C)O[4].
  • 2,6-xylenol's chemical formula is recorded as C₈H₁₀O[5].
  • 2,6-xylenol is a type of chemical compound[6].
  • 2,6-xylenol's found in taxon is recorded as Coffea arabica[7].
  • 2,6-xylenol's mass is recorded as {'unit': 'Q483261', 'amount': '+122.073165'}[8].
  • 2,6-xylenol's melting point is recorded as {'unit': 'Q25267', 'amount': '+46.0'}[9].
  • 2,6-xylenol's melting point is recorded as {'unit': 'Q25267', 'amount': '+45.7'}[10].
  • 2,6-xylenol's boiling point is recorded as {'unit': 'Q25267', 'amount': '+201.07'}[11].
  • 2,6-xylenol's ionization energy is recorded as {'unit': 'Q83327', 'amount': '+8.05'}[12].
  • 2,6-xylenol's monomer of is recorded as poly(p-phenylene oxide)[13].

Why It Matters

2,6-xylenol has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] 2,6-xylenol is known by 9 alternative names across languages and contexts.[14]

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] ↑ . New volatile components of roasted coffee. wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . Jean-Claude Bradley Open Melting Point Dataset. wikidata.org.
  8. [10] ↑ . Basic laboratory and industrial chemicals: A CRC quick reference handbook. wikidata.org.
  9. [11] ↑ . Basic laboratory and industrial chemicals: A CRC quick reference handbook. wikidata.org.
  10. [12] ↑ . Basic laboratory and industrial chemicals: A CRC quick reference handbook. wikidata.org.
  11. [13] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.
  2. [14] ↑ . 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). 2,6-xylenol. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-6-xylenol
MLA “2,6-xylenol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2-6-xylenol.
BibTeX @misc{4ortxyz_2-6-xylenol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2,6-xylenol}}, year = {2026}, url = {https://4ort.xyz/entity/2-6-xylenol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 2,6-xylenol — https://4ort.xyz/entity/2-6-xylenol (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 ↗
    Monomer of → poly(p-phenylene oxide)
    Instance of → type of chemical entity
    Subclass of → —
    Ionization energy → {'unit': 'Q83327', 'amount': '+8.05'}
    + 7 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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