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(±)-sec-butyl acetate

pair of enantiomers
ChemicalSubstance group_of_stereoisomers Q421143
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(±)-sec-butyl acetate

Summary

(±)-sec-butyl acetate is a group of stereoisomers[1]. (±)-sec-butyl acetate draws 16 Wikipedia views per month (group_of_stereoisomers category, ranking #208 of 1,063).[2]

Key Facts

  • (±)-sec-butyl acetate's instance of is recorded as group of stereoisomers[3].
  • (±)-sec-butyl acetate's chemical structure is recorded as Sec-Butylacetat.svg[4].
  • (±)-sec-butyl acetate's chemical structure is recorded as Sec-butyl acetate.svg[5].
  • (±)-sec-butyl acetate's CAS Registry Number is recorded as 105-46-4[6].
  • (±)-sec-butyl acetate's EC number is recorded as 203-300-1[7].
  • (±)-sec-butyl acetate's canonical SMILES is recorded as CCC(C)OC(=O)C[8].
  • (±)-sec-butyl acetate's InChI is recorded as InChI=1S/C6H12O2/c1-4-5(2)8-6(3)7/h5H,4H2,1-3H3[9].
  • (±)-sec-butyl acetate's InChIKey is recorded as DCKVNWZUADLDEH-UHFFFAOYSA-N[10].
  • (±)-sec-butyl acetate's chemical formula is recorded as C₆H₁₂O₂[11].
  • (±)-sec-butyl acetate's subclass of is recorded as acetate ester[12].
  • (±)-sec-butyl acetate's subclass of is recorded as butyl ester[13].
  • (±)-sec-butyl acetate's subclass of is recorded as biogenic acyclic ester[14].
  • (±)-sec-butyl acetate's Commons category is recorded as Sec-Butyl acetate[15].
  • (±)-sec-butyl acetate's Freebase ID is recorded as /m/09zb9p[16].
  • (±)-sec-butyl acetate's UNII is recorded as UVH2QII6CG[17].
  • (±)-sec-butyl acetate's RTECS number is recorded as AF7380000[18].
  • (±)-sec-butyl acetate's ChemSpider ID is recorded as 7472[19].
  • (±)-sec-butyl acetate's PubChem CID is recorded as 7758[20].
  • (±)-sec-butyl acetate's ZVG number is recorded as 37250[21].
  • (±)-sec-butyl acetate's found in taxon is recorded as Sauromatum venosum[22].
  • (±)-sec-butyl acetate's found in taxon is recorded as tomato[23].
  • (±)-sec-butyl acetate's found in taxon is recorded as ginger[24].
  • (±)-sec-butyl acetate's has effect is recorded as sec-Butyl acetate exposure[25].
  • (±)-sec-butyl acetate's has characteristic is recorded as Class IB flammable liquid[26].
  • (±)-sec-butyl acetate's NIOSH Pocket Guide ID is recorded as 0073[27].

Why It Matters

(±)-sec-butyl acetate draws 16 Wikipedia views per month (group_of_stereoisomers category, ranking #208 of 1,063).[2] (±)-sec-butyl acetate has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] (±)-sec-butyl acetate is known by 9 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] ↑ . wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . Freebase Data Dumps. wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . Q2311683. Retrieved . wikidata.org.
  18. [20] ↑ . PubChem. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . Dimethyl oligosulphides, major volatiles released from Sauromatum guttatum and Phallus impudicus. wikidata.org.
  21. [23] ↑ . Effect of autochthonous lactic acid bacteria starters on health-promoting and sensory properties of tomato juices. wikidata.org.
  22. [24] ↑ . Determination of volatile components in ginger using gas chromatography-mass spectrometry with resolution improved by data processing techniques. wikidata.org.
  23. [25] ↑ . cdc.gov. cdc.gov. Provenance: wikidata.org.
  24. [26] ↑ . cdc.gov. cdc.gov. Provenance: wikidata.org.
  25. [27] ↑ . 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). (±)-sec-butyl acetate. Retrieved May 3, 2026, from https://4ort.xyz/entity/sec-butyl-acetate
MLA “(±)-sec-butyl acetate.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sec-butyl-acetate.
BibTeX @misc{4ortxyz_sec-butyl-acetate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(±)-sec-butyl acetate}}, year = {2026}, url = {https://4ort.xyz/entity/sec-butyl-acetate}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (±)-sec-butyl acetate — https://4ort.xyz/entity/sec-butyl-acetate (retrieved 2026-05-03)

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