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propionaldehyde

 
Dictionary: pro·pi·on·al·de·hyde   (prō'pē-ŏn-ăl'də-hīd') pronunciation
n.
A flammable liquid, C2H5CHO, used in the manufacture of plastics and rubber chemicals.

[PROPION(IC ACID) + ALDEHYDE.]


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Chemistry Dictionary: propanal
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Variant: propionaldehyde

A colourless liquid aldehyde, C2H5CHO; m.p. –81°C; b.p. 48.8°C.



WordNet: propionaldehyde
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Note: click on a word meaning below to see its connections and related words.

The noun has one meaning:

Meaning #1: a colorless liquid aldehyde
  Synonym: propanal


Wikipedia: Propionaldehyde
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Propionaldehyde
Skeletal structure of propanal
Flat structure
IUPAC name
Systematic name Propanal
Other names Methylacetaldehyde; propionic aldehyde; propaldehyde
Identifiers
CAS number 123-38-6
UN number 1275
SMILES
ChemSpider ID 512
Properties
Molecular formula C3H6O
Molar mass 58.080 g mol−1
Appearance Colorless liquid
Pungent, marty odor
Density 0.81 g cm−3
Melting point

−81 °C (192 K)

Boiling point

46-50 °C (321 K)

Solubility in water 20 g/100 mL
Viscosity 0.6 cP at 20°C
Structure
Molecular shape C1, O: sp2

C2, C3: sp3

Dipole moment 2.52 D
Hazards
EU classification Highly flammable (F)
Irritant (Xi)
R-phrases R11, R36/37/38
S-phrases S9, S16, S29
NFPA 704
3
2
2
 
Flash point −26 °C
Autoignition
temperature
175 °C
Related compounds
Related aldehydes Formaldehyde
Acetaldehyde
Butyraldehyde
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Propionaldehyde or propanal is the organic compound with the formula CH3CH2CHO. It is a saturate 3-carbon aldehyde and is a structural isomer of acetone. It is a colourless liquid with a slightly irritating, fruity odour.

Contents

Production

Propionaldehyde is mainly produced industrially through hydroformylation, by combining synthesis gas (carbon monoxide and hydrogen) with ethylene using a metal catalyst:

CO + H2 + C2H4 → CH3CH2CHO

Laboratory preparation

In the laboratory, it may be prepared by refluxing a mixture of propanol, 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.[1]

Uses

It is principally used as a precursor to trimethylolethane (CH3C(CH2OH)3) through a condensation reaction with methanol; this triol is an important intermediate in the production of alkyd resins.

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.[2]

Recent Interstellar Discoveries

Researchers have recently discovered two new interstellar molecules one of which is propanal. It was located within the Milky Way Galaxy inside an interstellar cloud known as Sagittarius B2. The identity of the carbon-containing molecule, propanal, was discovered by , Jan M. Hollis of the NASA Goddard Space Flight Center in Greenbelt, Md., and his colleagues. For the team to identify the propanal they looked for the emission of specific frequencies of radio waves from the cloud. They did this because different types of molecules emit energy at different frequencies, each producing a unique signal that researchers can detect with powerful telescopes. Located in the July 20th Astrophysical Journal Letters, researchers reported that they had recorded the frequencies associated with two aldehydes called propenal and propanal. Although researchers have found other organic molecules in space before this, the evidence of the two aldehydes will assist them in the understanding of how molecular building blocks are assembled into more-complex organic molecules; in space.

"This is a feat unprecedented in the 35-year history of searching for complex molecules in space and suggests that a universal prebiotic chemistry is at work," said Jan M. Hollis of the NASA Goddard Space Flight Center, leader of the research team.

References

  1. ^ Charles D. Hurd and R. N. Meinert (1943), "Propionaldehyde", Org. Synth., http://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=cv2p0541 ; Coll. Vol. 2: 541 
  2. ^ 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.

3.[1] Chemical Precursors to Life Found in Space Scientists say that a universal prebiotic chemistry may be at work

4.Two newly found space molecules. By: Goho, Alexandra, Science News, 00368423, 7/24/2004, Vol. 166, Issue 4


 
 
Learn More
aldicarb
Molecular isomerism
Propanol

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Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2009. Published by Houghton Mifflin Company. All rights reserved.  Read more
Chemistry Dictionary. A Dictionary of Chemistry. Sixth Edition. Copyright © Market House Books Ltd, 2008. All rights reserved.  Read more
WordNet. WordNet 1.7.1 Copyright © 2001 by Princeton University. All rights reserved.  Read more
Wikipedia. This article is licensed under the Creative Commons Attribution/Share-Alike License. It uses material from the Wikipedia article "Propionaldehyde" Read more