- Formula: C12H24O3
- Molecular weight: 216.3172
- IUPAC Standard InChIKey: XYIANCZIPATGDH-UHFFFAOYSA-N
- CAS Registry Number: 7580-12-3
- Chemical structure:
This structure is also available as a 2d Mol file
- Species with the same structure:
- Other names: s-Trioxane, 2,4,6-triisopropyl-; Sunsubly B; Triisopropyl-s-trioxane; 1,3,5-Trioxane, 2,4,6-triisopropyl-; 2,4,6-Triisopropyl-1,3,5-trioxane; 2,4,6-Triisopropyltrioxane; 2,4,6-Tri-isopropyl-[1,3,5]trioxane, stereoisomer 2
- Information on this page:
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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Normal alkane RI, polar column, temperature ramp
View large format table.
|Column type||Active phase||I||Reference||Comment|
|Capillary||FFAP||1230.||Vernin, Metzger, et al., 1993||60. C @ 8. min, 2. K/min; Column length: 50. m; Column diameter: 0.22 mm; Tend: 230. C|
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Vernin, Metzger, et al., 1993
Vernin, G.; Metzger, J.; Sultan, A.A.M.; El-Shafei, A.K.; Párkányi, C., Heterocyclic compounds in model systems for the Maillard reaction. Reactions of aldehydes with ammonium sulfide in the presence or absence of acetoin, Am. Chem. Soc. Symp. Ser., 1993, 528, 36-55. [all data]
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- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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