Propionaldehyde
|
|||
![]() |
|||
Names | |||
---|---|---|---|
IUPAC name
Propanal
|
|||
Systematic IUPAC name
Propanal
|
|||
Other names
|
|||
Identifiers | |||
123-38-6 ![]() |
|||
ChEBI | CHEBI:17153 ![]() |
||
ChEMBL | ChEMBL275626 ![]() |
||
ChemSpider | 512 ![]() |
||
ECHA InfoCard | 100.004.204 | ||
Jmol 3D model | Interactive image | ||
PubChem | 527 | ||
UNII | AMJ2B4M67V ![]() |
||
UN number | 1275 | ||
|
|||
|
|||
Properties | |||
C3H6O | |||
Molar mass | 58.08 g·mol−1 | ||
Appearance | Colorless liquid Pungent, fruity odor |
||
Density | 0.81 g cm−3 | ||
Melting point | −81 °C (−114 °F; 192 K) | ||
Boiling point | 46 to 50 °C (115 to 122 °F; 319 to 323 K) | ||
20 g/100 mL | |||
Viscosity | 0.6 cP at 20 °C | ||
Structure | |||
C1, O: sp2
C2, C3: sp3 |
|||
2.52 D | |||
Hazards | |||
EU classification (DSD)
|
![]() ![]() |
||
R-phrases | R11, R36/37/38 | ||
S-phrases | S9, S16, S29 | ||
NFPA 704 | |||
Flash point | −26 °C (−15 °F; 247 K) | ||
175 °C (347 °F; 448 K) | |||
Related compounds | |||
Related aldehydes
|
Acetaldehyde Butyraldehyde |
||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|||
![]() ![]() ![]() |
|||
Infobox references | |||
Propionaldehyde or propanal is the organic compound with the formula CH3CH2CHO. It is a saturated 3-carbon aldehyde and is a structural isomer of acetone. It is a colorless liquid with a slightly irritating, fruity odor.
Production[edit]
Propionaldehyde is mainly produced industrially through hydroformylation, by combining synthesis gas (carbon monoxide and hydrogen) with ethylene using a metal (typically rhodium) catalyst:
- CO + H2 + C2H4 → CH3CH2CHO
In this way, several hundred thousand tons are produced annually.[1]
Laboratory preparation[edit]
Propionaldehyde may also be prepared by oxidizing 1-propanol with a mixture of sulfuric acid and potassium dichromate. The reflux condenser contains water heated at 60 °C, which condenses unreacted propanol, but allows propionaldehyde to pass. The propionaldehyde vapor is immediately condensed into a suitable receiver. In this arrangement, any propionaldehyde formed is immediately removed from the reactor, thus it does not get over-oxidized to propionic acid.[2]
Uses[edit]
It is principally used as a precursor to trimethylolethane (CH3C(CH2OH)3) through a condensation reaction with formaldehyde; this triol is an important intermediate in the production of alkyd resins. Other applications include reduction to propanol and oxidation to propionic acid.[1]
Condensation of propionaldehyde with tert-butylamine gives CH3CH2CH=N-t-Bu, a three-carbon building block used in organic synthesis. Deprotonation of this imine with LDA produces CH3CHLiCH=N-t-Bu, which in turn condenses with aldehydes.[3]
Extraterrestrial occurrence[edit]
Astronomers have detected propionaldehyde (along with acrolein) in the molecular cloud Sagittarius B2 near the center of the Milky Way Galaxy, about 26,000 light years from Earth.[4][5][6]
On 30 July 2015, scientists reported that upon the first touchdown of the Philae lander on comet 67/P's surface, measurements by the COSAC and Ptolemy instruments revealed sixteen organic compounds, four of which were seen for the first time on a comet, including acetamide, acetone, methyl isocyanate and propionaldehyde.[7][8][9]
References[edit]
- ^ a b Anthony J. Papa "Propanal" In Ullmann's Encyclopedia of Industrial Chemistry, 2011, WIley-VCH, Weinheim. doi:10.1002/14356007.a22_157.pub2
- ^ Charles D. Hurd and R. N. Meinert (1943). "Propionaldehyde". Org. Synth.; Coll. Vol., 2, p. 541
- ^ Peralta, M. M. "Propionaldehyde t-Butylimine" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi:10.1002/047084289.
- ^ Scientists Discover Two New Interstellar Molecules: Point to Probable Pathways for Chemical Evolution in Space, National Radio Astronomy Observatory, June 21, 2004
- ^ Two newly found space molecules. By: Goho, Alexandra, Science News, 00368423, 7/24/2004, Vol. 166, Issue 4
- ^ Chemical Precursors to Life Found in Space Scientists say that a universal prebiotic chemistry may be at work
- ^ Jordans, Frank (30 July 2015). "Philae probe finds evidence that comets can be cosmic labs". The Washington Post. Associated Press. Retrieved 30 July 2015.
- ^ "Science on the Surface of a Comet". European Space Agency. 30 July 2015. Retrieved 30 July 2015.
- ^ Bibring, J.-P.; Taylor, M.G.G.T.; Alexander, C.; Auster, U.; Biele, J.; Finzi, A. Ercoli; Goesmann, F.; Klingehoefer, G.; Kofman, W.; Mottola, S.; Seidenstiker, K.J.; Spohn, T.; Wright, I. (31 July 2015). "Philae's First Days on the Comet - Introduction to Special Issue". Science. 349 (6247): 493. Bibcode:2015Sci...349..493B. doi:10.1126/science.aac5116. Retrieved 30 July 2015.