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tert-butylhydroquinone

chemical compound
ChemicalSubstance type_of_chemical_entity Q662443
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tert-butylhydroquinone

Summary

tert-butylhydroquinone is a type of chemical entity[1]. tert-butylhydroquinone ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (159 views/month).[2]

Key Facts

  • tert-butylhydroquinone's instance of is recorded as type of chemical entity[3].
  • tert-butylhydroquinone's chemical structure is recorded as Tert-Butylhydroquinone Structural Formula V1.svg[4].
  • tert-butylhydroquinone's CAS Registry Number is recorded as 1948-33-0[5].
  • tert-butylhydroquinone's EC number is recorded as 217-752-2[6].
  • tert-butylhydroquinone's canonical SMILES is recorded as CC(C)(C)C1=C(C=CC(=C1)O)O[7].
  • tert-butylhydroquinone's InChI is recorded as InChI=1S/C10H14O2/c1-10(2,3)8-6-7(11)4-5-9(8)12/h4-6,11-12H,1-3H3[8].
  • tert-butylhydroquinone's InChIKey is recorded as BGNXCDMCOKJUMV-UHFFFAOYSA-N[9].
  • tert-butylhydroquinone's chemical formula is recorded as C₁₀H₁₄O₂[10].
  • tert-butylhydroquinone's subclass of is recorded as chemical compound[11].
  • tert-butylhydroquinone's has use is recorded as antioxidant[12].
  • tert-butylhydroquinone's has use is recorded as food additive[13].
  • tert-butylhydroquinone's MeSH descriptor ID is recorded as C018855[14].
  • tert-butylhydroquinone's ChEMBL ID is recorded as CHEMBL242080[15].
  • tert-butylhydroquinone's E number is recorded as E319[16].
  • tert-butylhydroquinone's PDB structure ID is recorded as 3EYM[17].
  • tert-butylhydroquinone's PDB structure ID is recorded as 3EYK[18].
  • tert-butylhydroquinone's Freebase ID is recorded as /m/0df6bm[19].
  • tert-butylhydroquinone's UNII is recorded as C12674942B[20].
  • tert-butylhydroquinone's ChemSpider ID is recorded as 15235[21].
  • tert-butylhydroquinone's PubChem CID is recorded as 16043[22].
  • tert-butylhydroquinone's ZVG number is recorded as 490351[23].
  • tert-butylhydroquinone's ChEBI ID is recorded as 78886[24].
  • tert-butylhydroquinone's found in taxon is recorded as Paeonia × suffruticosa[25].
  • tert-butylhydroquinone's found in taxon is recorded as liquorice[26].
  • tert-butylhydroquinone's found in taxon is recorded as Streptosporangium[27].

Why It Matters

tert-butylhydroquinone ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (159 views/month).[2] tert-butylhydroquinone has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[28] tert-butylhydroquinone is known by 24 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] ↑ . Food Chemistry. wikidata.org.
  11. [13] ↑ . Food Chemistry. wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  16. [18] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  17. [19] ↑ . Freebase Data Dumps. wikidata.org.
  18. [20] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  19. [21] ↑ . Q2311683. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . ChEMBL. Retrieved . wikidata.org.
  23. [25] ↑ . The inhibition of phenylhydroquinone-induced oxidative DNA cleavage by constituents of Moutan Cortex and Paeoniae Radix. wikidata.org.
  24. [26] ↑ . Glycybridins A-K, Bioactive Phenolic Compounds from Glycyrrhiza glabra.. wikidata.org.
  25. [27] ↑ . Hexaricins, Pradimicin-like Polyketides from a Marine Sediment-Derived Streptosporangium sp. and Their Antioxidant Effects. 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). tert-butylhydroquinone. Retrieved May 3, 2026, from https://4ort.xyz/entity/tert-butylhydroquinone
MLA “tert-butylhydroquinone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tert-butylhydroquinone.
BibTeX @misc{4ortxyz_tert-butylhydroquinone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tert-butylhydroquinone}}, year = {2026}, url = {https://4ort.xyz/entity/tert-butylhydroquinone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): tert-butylhydroquinone — https://4ort.xyz/entity/tert-butylhydroquinone (retrieved 2026-05-03)

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