malvalic acid

chemical compound

Facts

6 properties
🏷️ Also known as
en 2-octyl-1-cyclopropene-1-heptanoic acid en 7-(2-octyl-1-cyclopropenyl)heptanoic acid en 8,9-methylene-8Z-heptadecenoic acid en malvalic acid de Malvensäure de 7-(2-Octylcyclopropen-1-yl)heptansäure de Malvaliasäure de Malvalinsäure de Malvalsäure es Ácido malválico fa مگنولل fr acide malvalique it acido malvalico ja マルバル酸 uk Малвалова кислота zh 锦葵酸
🔖 Identifiers · 19
CAS Registry Number
503-05-9
ChEBI ID
6673
ChemSpider ID
9987
DSSTOX compound identifier
DTXCID40120791
DSSTox substance ID
DTXSID50198300
Freebase ID
/m/03c9gvt
HSDB ID
3905
Human Metabolome Database ID
HMDB0302286
KEGG ID
C08321
KNApSAcK ID
C00001227
Show all 19 identifiers +7
LIPID MAPS ID
LMFA01140002
Microsoft Academic ID (discontinued)
2776490417
PubChem CID
10416
Reaxys registry number
1970279
SureChEMBL ID
25251
UniChem compound ID
1070002

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Summary

malvalic acid is a type of chemical entity[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . PubChem. Retrieved . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Gas chromatographic analysis of cyclopropenoid acids in cottonseed oils. wikidata.org.
  6. [7] ↑ . Cyclopropenoid fatty acids ingnetum scandens and itsterculia pallens seed oils. wikidata.org.
  7. [8] ↑ . Cyclopropenoid fatty acids ingnetum scandens and itsterculia pallens seed oils. wikidata.org.
  8. [9] ↑ . Cyclopropenoid fatty acids ingnetum scandens and itsterculia pallens seed oils. wikidata.org.
  9. [10] ↑ . Eriolaena hookeriana seed oil: A rich source of malvalic acid. wikidata.org.
  10. [11] ↑ . Cassia siamea seed oil: A minor source of vernolic and cyclopropenoid fatty acids. wikidata.org.
  11. [12] ↑ . Cassia siamea seed oil: A minor source of vernolic and cyclopropenoid fatty acids. wikidata.org.
  12. [13] ↑ . Chemical investigation ofJasminum auriculatum (VAHL) leaves. VII. Structure of Jasminol — A new triterpene. wikidata.org.
  13. [14] ↑ . Cyclopropenoid fatty acids in abutilon ramosum seed oil. wikidata.org.
  14. [15] ↑ . Unusual fatty acids ofCordia rothii seed oil. 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). malvalic acid. Retrieved November 4, 2026, from https://4ort.xyz/entity/malvalic-acid
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BibTeX @misc{4ortxyz_malvalic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{malvalic acid}}, year = {2026}, url = {https://4ort.xyz/entity/malvalic-acid}, note = {Accessed: 2026-11-04}}
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