Hydroxypivaldehyde
Hydroxypivaldehyde is the organic compound with the formula HOCH2(CH3)2CCHO. A colorless liquid, it is produced by condensation of formaldehyde and isobutyraldehyde:[2]
- CH2O + (CH3)2CHCHO → HOCH2(CH3)2CCHO
![]() | |
Identifiers | |
---|---|
3D model (JSmol) |
|
ChemSpider | |
ECHA InfoCard | 100.008.998 |
EC Number |
|
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C5H10O2 | |
Molar mass | 102.133 g·mol−1 |
Appearance | colorless liquid |
Boiling point | 141 °C (286 °F; 414 K) |
Hazards | |
GHS labelling:[1] | |
![]() | |
Warning | |
H319 | |
P264, P280, P305+P351+P338, P337+P313 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
The compound is a rare example of a distillable aldol (3-hydroxyaldehyde). Upon standing, it dimerizes reversibly to the dioxane derivative. Its main use, in terms of scale, is as a precursor to neopentyl glycol:
- HOCH2(CH3)2CCHO + H2 → (CH3)2C(CH2OH)2
References
- "3-Hydroxy-2,2-dimethylpropanal". pubchem.ncbi.nlm.nih.gov. Retrieved 31 December 2021.
- Kohlpaintner, Christian; Schulte, Markus; Falbe, Jürgen; Lappe, Peter; Weber, Jürgen; Frey, Guido D. (2013). "Aldehydes, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_321.pub3.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.