Propanal

A three-carbon aldehyde linking oxidation and carbonyl addition.

Formula
C3H6O
Functional group
Aldehydes
Molar mass
58.08 g/mol
Also known as
Propionaldehyde, Propanaldehyde, Propylaldehyde, Propaldehyde, Methylacetaldehyde, n-Propanal

Overview

A three-carbon aldehyde linking oxidation and carbonyl addition.

The terminal CHO group is oxidised to propanoic acid, or propanoate in alkaline conditions. Its carbonyl carbon bears a hydrogen, unlike that of isomeric propanone. This structural difference underlies the contrasting response to mild aldehyde oxidation tests.

Identifiers

Formula
C3H6O
Functional group
Aldehydes
Molar mass
58.08 g/mol
Also known as
Propionaldehyde, Propanaldehyde, Propylaldehyde, Propaldehyde, Methylacetaldehyde, n-Propanal
Chemical identifiers
SMILES
CCC=O
InChI
InChI=1S/C3H6O/c1-2-3-4/h3H,2H2,1H3
PubChem CID
527

Properties

Melting Point
-80 °C
Boiling Point
48 °C
Density
0.8657 g/cu cm at 25 °C
Water solubility
In water, 3.06X10+5 mg/L at 25 °C

Diagnostic tests

Tollens’ aldehyde test

Reagent
freshly prepared Tollens’ reagent
Conditions
Warm gently in a water bath under the reference method.
Positive observation
Silver deposit or mirror forms.
Negative observation
No silver deposit in the reagent blank.
Interpretation
Propanal is oxidised to propanoate as silver(I) is reduced.
Scope
Expected positive for propanal.
Limitations
Other reducing compounds also react; dispose of the mixture by the laboratory method.
Evidence
reference experiment

Related compounds

Connected reactions

References

  1. PubChem Compound Summary: Propanal (CID 527)National Center for Biotechnology Information · PubChem

    Identity, molecular formula, molecular weight and aliases retrieved via PUG REST on 2026-09-08.

  2. OpenStax Organic Chemistry: Oxidation of aldehydes and ketonesJohn McMurry · OpenStax · 2023

    Supports the qualitative structural interpretation of the recorded molecular structure; no new physical measurement or verified preparative yield is claimed.

  3. Hazardous Substances Data Bank (HSDB): Propanal — melting pointHazardous Substances Data Bank (HSDB)

    Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/527#section=Melting-Point. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Lide, D.R. CRC Handbook of Chemistry and Physics 88TH Edition 2007-2008. CRC Press, Taylor & Francis, Boca Raton, FL 2007, p. 3-414

  4. Hazardous Substances Data Bank (HSDB): Propanal — boiling pointHazardous Substances Data Bank (HSDB)

    Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/527#section=Boiling-Point. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Lide, D.R. CRC Handbook of Chemistry and Physics 88TH Edition 2007-2008. CRC Press, Taylor & Francis, Boca Raton, FL 2007, p. 3-440

  5. Hazardous Substances Data Bank (HSDB): Propanal — densityHazardous Substances Data Bank (HSDB)

    Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/527#section=Density. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Lide, D.R. CRC Handbook of Chemistry and Physics 88TH Edition 2007-2008. CRC Press, Taylor & Francis, Boca Raton, FL 2007, p. 3-440

  6. Hazardous Substances Data Bank (HSDB): Propanal — solubilityHazardous Substances Data Bank (HSDB)

    Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/527#section=Solubility. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Riddick, J.A., W.B. Bunger, Sakano T.K. Techniques of Chemistry 4th ed., Volume II. Organic Solvents. New York, NY: John Wiley and Sons., 1985., p. 329

  7. The silver mirror test with Tollens’ reagentRoyal Society of Chemistry · RSC Education

    Source-supported qualitative reference observations.