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3-(4-hydroxyphenyl)propionic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q7186527
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3-(4-hydroxyphenyl)propionic acid

Summary

3-(4-hydroxyphenyl)propionic acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2]

Key Facts

  • 3-(4-hydroxyphenyl)propionic acid's instance of is recorded as type of chemical entity[3].
  • 3-(4-hydroxyphenyl)propionic acid's canonical SMILES is recorded as C1=CC(=CC=C1CCC(=O)O)O[4].
  • 3-(4-hydroxyphenyl)propionic acid's chemical formula is recorded as C₉H₁₀O₃[5].
  • 3-(4-hydroxyphenyl)propionic acid is a type of chemical compound[6].
  • 3-(4-hydroxyphenyl)propionic acid's Commons category is recorded as Phloretic acid[7].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Ginkgo biloba[8].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Camellia sinensis[9].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Anigozanthos preissii[10].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Aguacate[11].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Colchicum kotschyi[12].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Polyscias murrayi[13].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Spiranthes sinensis[14].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Lepisorus contortus[15].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Olea europaea[16].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Aloe africana[17].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Annona cherimola[18].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Bulbine frutescens[19].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Cestrum parqui[20].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Cinnamomum reticulatum[21].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Cucurbita pepo[22].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Dendrobium plicatile[23].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Iryanthera sagotiana[24].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Picea glauca[25].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Malva sylvestris[26].
  • 3-(4-hydroxyphenyl)propionic acid's found in taxon is recorded as Chenopodium formosanum[27].

Why It Matters

3-(4-hydroxyphenyl)propionic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 51 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] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Trolox equivalent antioxidant capacity (TEAC) of Ginkgo biloba flavonol and Camellia sinensis catechin metabolites. wikidata.org.
  7. [9] ↑ . Trolox equivalent antioxidant capacity (TEAC) of Ginkgo biloba flavonol and Camellia sinensis catechin metabolites. wikidata.org.
  8. [10] ↑ . Phenylpropanoid interconversion inAnigozanthos preissii observed by high-performance liquid chromatography-nuclear magnetic resonance spectroscopy. wikidata.org.
  9. [11] ↑ . Flavonoid metabolites in urine after oral administration of aqueous extract of Persea americana to rats. wikidata.org.
  10. [12] ↑ . Alkaloids and phenolics of Colchicum turcicum. wikidata.org.
  11. [13] ↑ . Tyrosine kinase inhibitors from the rainforest tree Polyscias murrayi. wikidata.org.
  12. [14] ↑ . Homocyclotirucallane and two dihydrophenanthrenes from Spiranthes sinensis. wikidata.org.
  13. [15] ↑ . Bioactive compounds from the fern Lepisorus contortus. wikidata.org.
  14. [16] ↑ . Antioxidant Capacity and Phenolic Profile of Table Olives from the Greek Market. wikidata.org.
  15. [17] ↑ . Aloe ferox leaf gel phytochemical content, antioxidant capacity, and possible health benefits. wikidata.org.
  16. [18] ↑ . Cheritamine, A NewN-Fatty Acyl Tryptamine and Other Constituents from the Stems ofAnnona cherimola. wikidata.org.
  17. [19] ↑ . Joziknipholones A and B: the first dimeric phenylanthraquinones, from the roots of Bulbine frutescens. wikidata.org.
  18. [20] ↑ . Low molecular weight phenols from the bioactive aqueous fraction of Cestrum parqui. wikidata.org.
  19. [21] ↑ . Chemical constituents from the roots of Cinnamomum reticulatum. wikidata.org.
  20. [22] ↑ . Phenolic plant growth inhibitors from the flowers of Cucurbita pepo. wikidata.org.
  21. [23] ↑ . Constituents of Ephemerantha fimbriata. Isolation and Structure Elucidation of Two New Phenanthrenes, Fimbriol-A and Fimbriol-B, and a New Dihydrophenanthrene, Ephemeranthol-C.. wikidata.org.
  22. [24] ↑ . Flavonoids from Iryanthera sagotiana. wikidata.org.
  23. [25] ↑ . Comparison of phenolic compounds from galls and shoots of Picea glauca. wikidata.org.
  24. [26] ↑ . Terpenoids and phenol derivatives from Malva silvestris. wikidata.org.
  25. [27] ↑ . Phenols and lignans from Chenopodium album. 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-(4-hydroxyphenyl)propionic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/3-4-hydroxyphenyl-propionic-acid
MLA “3-(4-hydroxyphenyl)propionic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3-4-hydroxyphenyl-propionic-acid.
BibTeX @misc{4ortxyz_3-4-hydroxyphenyl-propionic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3-(4-hydroxyphenyl)propionic acid}}, year = {2026}, url = {https://4ort.xyz/entity/3-4-hydroxyphenyl-propionic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3-(4-hydroxyphenyl)propionic acid — https://4ort.xyz/entity/3-4-hydroxyphenyl-propionic-acid (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. 29d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Aliases → —
    Subclass of → chemical compound
    Mass → {'unit': 'Q483261', 'amount': '+166.063'}
    Found in taxon → Ginkgo biloba, Camellia sinensis, Anigozanthos preissii +25
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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