Pivaldehyde

Pivaldehyde
Names
Preferred IUPAC name
2,2-Dimethylpropanal
Other names
Trimethylacetaldehyde
Pivalaldehyde
Neopentanal
Neopentaldehyde
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.010.123 Edit this at Wikidata
EC Number
  • 211-134-6
UNII
  • InChI=1S/C5H10O/c1-5(2,3)4-6/h4H,1-3H3
    Key: FJJYHTVHBVXEEQ-UHFFFAOYSA-N
  • CC(C)(C([H])=O)C
Properties
C5H10O
Molar mass 86.134 g·mol−1
Boiling point 74–76 °C (165–169 °F; 347–349 K)[1]
Hazards
GHS labelling:
GHS05: CorrosiveGHS07: Exclamation mark
Danger
H225, H315, H335
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P312, P321, P332+P313, P362, P370+P378, P403+P233, P403+P235, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Pivaldehyde is an organic compound, more specifically an aldehyde. Shown in the infobox image is a line-angle representation of this organic aldehyde, whose systematic name, 2,2-dimethylpropanal, is based on the longest carbon chain (three carbon atoms), ending in "-al" to indicate the aldehyde functionality, and where another descriptive synonym is trimethylacetaldehyde.[2] Pivaldehyde is an example of an aldehyde attached to a sterically bulky alkyl group, the tertiary butyl group (carbon attached to with 3 methyl groups).

See also

References

  1. ^ Conant, J. B.; Webb, C. N.; Mendum, W. C. (April 1929). "TRIMETHYLACETALDEHYDE AND DIMETHYLETHYLACETALDEHYDE". Journal of the American Chemical Society. 51 (4): 1246–1255. doi:10.1021/ja01379a038.
  2. ^ Pubchem. "Trimethylacetaldehyde". nih.gov. Retrieved 1 March 2016.


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