article

Propionaldehyde
Methylacetaldehyde
Propionic aldehyde
Propaldehyde
C2, C3: sp3

Propionaldehyde
Systematic name Propanal
Synonyms
Chemical formula C3H6O
SMILES CCC=O
Molecular mass 58.080 g mol−1
Appearance Colorless liquid
Pungent, fruity odor
CAS number *
UN number 1275
Properties
Density 0.81 g cm−3
Solubility in water 20 g/100 ml (? °C)
Melting point −81°C (192 K)
Boiling point 46-50°C (321 K)
Viscosity 0.6 cP at 20°C
Structure
Molecular shape C1, O: sp2
Dipole moment 2.52 D
Hazards
MSDS External MSDS
EU classification Highly flammable (F)
Irritant (Xi)
R-phrases ,
S-phrases , ,
Flash point −26°C
Autoignition temperature 175°C
RTECS number ?
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Related compounds
Related aldehydes Formaldehyde
Acetaldehyde
Butanal
Chemical infobox
''Note that propanol is a different compound.

In organic chemistry, propanal or propionaldehyde is the aldehyde of the 3 carbon propyl group. It has a chemical formula of CH3CH2CHO, and is a structural isomer of propanone. At room temperature, it is a colourless liquid with a slightly irritating, fruity odour.

Production


Propanal is mainly produced through the Fischer-Tropsch synthesis, combining synthesis gas (carbon monoxide and hydrogen) with ethene over a metal catalyst:
CO + H2 + C2H4 → CH3CH2CHO

Uses


It is principally used to make trimethylolethane through condensation with methanol; this process is important in the production of alkyd resins.

External links


Aldehydes

Propanal | Προπανάλη | Propanal | プロピオンアルデヒド | Propanal

 

This article is licensed under the GNU Free Documentation License. It uses material from the "Propionaldehyde".

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