Propanone

The simplest ketone, connecting carbonyl addition with secondary-alcohol formation.

Formula
C3H6O
Functional group
Ketones; Methyl ketones
Molar mass
58.08 g/mol
Also known as
propan-2-one, acetone, 2-propanone, Dimethyl ketone, Pyroacetic ether, Methyl ketone

Overview

The simplest ketone, connecting carbonyl addition with secondary-alcohol formation.

Its carbonyl carbon is bonded to two methyl groups. Reduction converts the carbonyl into the secondary alcohol propan-2-ol without extending the carbon chain. The polar C=O bond explains nucleophilic attack at carbon; a carbonyl absorption alone does not uniquely identify propanone.

Identifiers

Formula
C3H6O
Functional group
Ketones; Methyl ketones
Molar mass
58.08 g/mol
Also known as
propan-2-one, acetone, 2-propanone, Dimethyl ketone, Pyroacetic ether, Methyl ketone
Chemical identifiers
SMILES
CC(=O)C
InChI
InChI=1S/C3H6O/c1-3(2)4/h1-2H3
PubChem CID
180

Properties

Melting Point
-94.9 °C
Boiling Point
56.08 °C
Density
0.7845 g/cu cm at 20 °C
Water solubility
Miscible with water

Diagnostic tests

Brady’s carbonyl test

Reagent
prepared 2,4-dinitrophenylhydrazine reagent
Conditions
Small-scale comparison using the source method; allow time for precipitation.
Positive observation
Yellow precipitate develops; propanone can respond more slowly than ethanal.
Negative observation
No precipitate in a valid reagent blank.
Interpretation
Hydrazone formation supports a reactive aldehyde or ketone carbonyl.
Scope
Expected positive for propanone.
Limitations
Observe the prepared reagent response; handle and dispose of residues by the laboratory method.
Evidence
reference experiment

Related compounds

Connected reactions

References

  1. PubChem Compound Summary: Propanone (CID 180)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: Nucleophilic addition of hydride and Grignard reagents: alcohol formationJohn 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): Propanone — melting pointHazardous Substances Data Bank (HSDB)

    Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/180#section=Melting-Point. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-4

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

    Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/180#section=Boiling-Point. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-4

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

    Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/180#section=Density. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-4

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

    Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/180#section=Solubility. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 13

  7. Brady’s test for aldehydes and ketonesRoyal Society of Chemistry · RSC Education

    Source-supported qualitative reference observations.