pivalic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q421509
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pivalic acid

Summary

pivalic acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (45 views/month).[2]

Key Facts

  • pivalic acid's instance of is recorded as type of chemical entity[3].
  • pivalic acid's chemical structure is recorded as Pivalic Acid Structural Formulae V.1.svg[4].
  • pivalic acid's CAS Registry Number is recorded as 75-98-9[5].
  • pivalic acid's EC number is recorded as 200-922-5[6].
  • pivalic acid's canonical SMILES is recorded as CC(C)(C)C(=O)O[7].
  • pivalic acid's InChI is recorded as InChI=1S/C5H10O2/c1-5(2,3)4(6)7/h1-3H3,(H,6,7)[8].
  • pivalic acid's InChIKey is recorded as IUGYQRQAERSCNH-UHFFFAOYSA-N[9].
  • pivalic acid's chemical formula is recorded as C₅H₁₀O₂[10].
  • pivalic acid's subclass of is recorded as branched chain fatty acids[11].
  • pivalic acid's Commons category is recorded as Pivalic acid[12].
  • pivalic acid's has part is recorded as carbon[13].
  • pivalic acid's has part is recorded as oxygen[14].
  • pivalic acid's has part is recorded as hydrogen[15].
  • pivalic acid's ChEMBL ID is recorded as CHEMBL322719[16].
  • pivalic acid's PDB structure ID is recorded as 1SMR[17].
  • pivalic acid's PDB structure ID is recorded as 3ZDA[18].
  • pivalic acid's Freebase ID is recorded as /m/0gq4sn[19].
  • pivalic acid's UNII is recorded as 813RE8BX41[20].
  • pivalic acid's RTECS number is recorded as TO7700000[21].
  • pivalic acid's ChemSpider ID is recorded as 6177[22].
  • pivalic acid's PubChem CID is recorded as 6417[23].
  • pivalic acid's ZVG number is recorded as 37490[24].
  • pivalic acid's ChEBI ID is recorded as 45133[25].
  • pivalic acid's found in taxon is recorded as Streptomyces avermitilis[26].
  • pivalic acid's found in taxon is recorded as Nicotiana tabacum[27].

Why It Matters

pivalic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (45 views/month).[2] It has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[28] It is known by 10 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] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . ChEMBL. Retrieved . 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] . wikidata.org.
  20. [22] . Q2311683. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . ChEMBL. Retrieved . wikidata.org.
  24. [26] . Pivalic acid acts as a starter unit in a fatty acid and antibiotic biosynthetic pathway in Alicyclobacillus, Rhodococcus and Streptomyces. wikidata.org.
  25. [27] . Comparison of different extraction methods: steam distillation, simultaneous distillation and extraction and headspace co-distillation, used for the analysis of the volatile components in aged flue-cured tobacco leaves. 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). pivalic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/pivalic-acid
MLA “pivalic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/pivalic-acid.
BibTeX @misc{4ortxyz_pivalic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{pivalic acid}}, year = {2026}, url = {https://4ort.xyz/entity/pivalic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): pivalic acid — https://4ort.xyz/entity/pivalic-acid (retrieved 2026-05-03)

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