3,4-dihydroxybutyric acid

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q27159112
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3,4-dihydroxybutyric acid

Summary

3,4-dihydroxybutyric acid is a group of stereoisomers[1].

Key Facts

  • 3,4-dihydroxybutyric acid's instance of is recorded as group of stereoisomers[2].
  • 3,4-dihydroxybutyric acid's CAS Registry Number is recorded as 1518-61-2[3].
  • 3,4-dihydroxybutyric acid's canonical SMILES is recorded as C(C(CO)O)C(=O)O[4].
  • 3,4-dihydroxybutyric acid's InChI is recorded as InChI=1S/C4H8O4/c5-2-3(6)1-4(7)8/h3,5-6H,1-2H2,(H,7,8)[5].
  • 3,4-dihydroxybutyric acid's InChIKey is recorded as DZAIOXUZHHTJKN-UHFFFAOYSA-N[6].
  • 3,4-dihydroxybutyric acid's chemical formula is recorded as C₄H₈O₄[7].
  • 3,4-dihydroxybutyric acid's subclass of is recorded as hydroxy fatty acid[8].
  • 3,4-dihydroxybutyric acid's ChemSpider ID is recorded as 133026[9].
  • 3,4-dihydroxybutyric acid's PubChem CID is recorded as 150929[10].
  • 3,4-dihydroxybutyric acid's ChEBI ID is recorded as 86371[11].
  • 3,4-dihydroxybutyric acid's found in taxon is recorded as Crocus sativus[12].
  • 3,4-dihydroxybutyric acid's found in taxon is recorded as Homo sapiens[13].
  • 3,4-dihydroxybutyric acid's Reaxys registry number is recorded as 1721709[14].
  • 3,4-dihydroxybutyric acid's Human Metabolome Database ID is recorded as HMDB0000337[15].
  • 3,4-dihydroxybutyric acid's LIPID MAPS ID is recorded as LMFA01050461[16].
  • 3,4-dihydroxybutyric acid's KNApSAcK ID is recorded as C00052139[17].
  • 3,4-dihydroxybutyric acid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+120.042259'}[18].
  • 3,4-dihydroxybutyric acid's SureChEMBL ID is recorded as 415845[19].
  • 3,4-dihydroxybutyric acid's DSSTox substance ID is recorded as DTXSID70934348[20].
  • 3,4-dihydroxybutyric acid's SPLASH is recorded as splash10-0012-0910000000-4054231c9c4cffa8a3c9[21].
  • 3,4-dihydroxybutyric acid's DSSTOX compound identifier is recorded as DTXCID301005620[22].
  • 3,4-dihydroxybutyric acid's UniChem compound ID is recorded as 25712436[23].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . Q2311683. Retrieved . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Antityrosinase principles and constituents of the petals of Crocus sativus. wikidata.org.
  12. [13] ↑ . A Statistical Analysis of the Effects of Urease Pre-treatment on the Measurement of the Urinary Metabolome by Gas Chromatography-Mass Spectrometry. wikidata.org.
  13. [14] ↑ . ChEBI. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . PubChem. Retrieved . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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-dihydroxybutyric acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/3-4-dihydroxybutyric-acid
MLA “3,4-dihydroxybutyric acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3-4-dihydroxybutyric-acid.
BibTeX @misc{4ortxyz_3-4-dihydroxybutyric-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3,4-dihydroxybutyric acid}}, year = {2026}, url = {https://4ort.xyz/entity/3-4-dihydroxybutyric-acid}, note = {Accessed: 2026-05-03}}
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