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methyl (RS)-3-hydroxybutyrate

group of enantiomers
ChemicalSubstance group_of_stereoisomers Q27288521
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methyl (RS)-3-hydroxybutyrate

Summary

methyl (RS)-3-hydroxybutyrate is a group of stereoisomers[1].

Key Facts

  • methyl (RS)-3-hydroxybutyrate's instance of is recorded as group of stereoisomers[2].
  • methyl (RS)-3-hydroxybutyrate's CAS Registry Number is recorded as 1487-49-6[3].
  • methyl (RS)-3-hydroxybutyrate's EC number is recorded as 216-068-1[4].
  • methyl (RS)-3-hydroxybutyrate's canonical SMILES is recorded as CC(CC(=O)OC)O[5].
  • methyl (RS)-3-hydroxybutyrate's InChI is recorded as InChI=1S/C5H10O3/c1-4(6)3-5(7)8-2/h4,6H,3H2,1-2H3[6].
  • methyl (RS)-3-hydroxybutyrate's InChIKey is recorded as LDLDJEAVRNAEBW-UHFFFAOYSA-N[7].
  • methyl (RS)-3-hydroxybutyrate's chemical formula is recorded as C₅H₁₀O₃[8].
  • methyl (RS)-3-hydroxybutyrate's subclass of is recorded as wax monoester[9].
  • methyl (RS)-3-hydroxybutyrate's UNII is recorded as S36O46U3EA[10].
  • methyl (RS)-3-hydroxybutyrate's ChemSpider ID is recorded as 14417[11].
  • methyl (RS)-3-hydroxybutyrate's PubChem CID is recorded as 15146[12].
  • methyl (RS)-3-hydroxybutyrate's ChEBI ID is recorded as 173462[13].
  • methyl (RS)-3-hydroxybutyrate's found in taxon is recorded as Mangifera indica[14].
  • methyl (RS)-3-hydroxybutyrate's found in taxon is recorded as Annona muricata[15].
  • methyl (RS)-3-hydroxybutyrate's found in taxon is recorded as Carica papaya[16].
  • methyl (RS)-3-hydroxybutyrate's Human Metabolome Database ID is recorded as HMDB0041603[17].
  • methyl (RS)-3-hydroxybutyrate's LIPID MAPS ID is recorded as LMFA07010513[18].
  • methyl (RS)-3-hydroxybutyrate's KNApSAcK ID is recorded as C00060023[19].
  • methyl (RS)-3-hydroxybutyrate's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+118.063'}[20].
  • methyl (RS)-3-hydroxybutyrate's ECHA Substance Infocard ID is recorded as 100.014.608[21].
  • methyl (RS)-3-hydroxybutyrate's SureChEMBL ID is recorded as 53570[22].
  • methyl (RS)-3-hydroxybutyrate's DSSTox substance ID is recorded as DTXSID70862677[23].
  • methyl (RS)-3-hydroxybutyrate's NMRShiftDB structure ID is recorded as 20209164[24].
  • methyl (RS)-3-hydroxybutyrate's UniChem compound ID is recorded as 25584305[25].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  10. [11] ↑ . Q2311683. Retrieved . wikidata.org.
  11. [12] ↑ . PubChem. Retrieved . wikidata.org.
  12. [13] ↑ . ChEBI release 2022-06-13. wikidata.org.
  13. [14] ↑ . Volatile components from mango (Mangifera indica L.) cultivars. wikidata.org.
  14. [15] ↑ . Equilibrium headspace analysis of volatile flavor compounds extracted from soursop (Annona muricata) using solid-phase microextraction. wikidata.org.
  15. [16] ↑ . Volatile components of papaya (Carica papaya L., Maradol variety) fruit. wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . PubChem. Retrieved . wikidata.org.
  20. [21] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_methyl-rs-3-hydroxybutyrate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{methyl (RS)-3-hydroxybutyrate}}, year = {2026}, url = {https://4ort.xyz/entity/methyl-rs-3-hydroxybutyrate}, note = {Accessed: 2026-05-03}}
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