Acetone
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This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition
Issued and maintained by the United States Pharmacopeial Convention (USP)
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C3H6O 58.08
2-Propanone;
Acetone CAS RN®: 67-64-1.
1 DEFINITION
Acetone contains NLT 99.0% of C H O, calculated on the anhydrous basis.
[Caution—Acetone is very ammable. Do not use where it may be ignited.]
2 IDENTIFICATION
Change to read:
A. Spectroscopic Identification Tests 〈197〉, Infrared Spectroscopy: 197F (CN 1-May-2020)
B. The retention time of the Sample corresponds to that of USP Acetone RS, as obtained in the Assay.
3 ASSAY
Procedure
Sample: Acetone
System suitability solution: Dilute 1.0 mL of USP Methyl Alcohol RS and 1.0 mL of USP Acetone RS with tetrahydrofuran to 50 mL.
Chromatographic system (See Chromatography 〈621〉, System Suitability.)
Mode: GC
Detector: Flame ionization
Column: 0.32-mm × 30-m fused-silica capillary; 1.8-μm of phase G43
Temperature
Column: See Table 1.
Table 1
Initial Temperature (°) | Temperature Ramp (°/min) | Final Temperature (°) | Hold Time at Final Temperature (min) |
| 40 | 0 | 40 | 5 |
| 40 | 20 | 240 | - |
Injector: 200°
Detector: 280°
Carrier gas: Helium
Flow rate: 35 cm/s (linear velocity)
Split ratio: 400:1
Injection volume: 1 μL
System suitability
Sample: System suitability solution
[Note—The relative retention times for methyl alcohol, acetone, and tetrahydrofuran are about 0.6, 1.0, and 1.9, respectively.]
Suitability requirements
Resolution: NLT 15 between the methyl alcohol and acetone peaks
Analysis
Sample: Sample
Calculate the percentage of acetone (C3H6O) in the portion of Acetone taken:
Result = (rU/rT) × 100
rU = peak area due to the acetone peak in the Sample
rT = sum of the areas of all the peaks in the Sample
[Note—No separate correction is applied for water content, because water does not respond to the ame-ionization detector.]
Acceptance criteria: NLT 99.0% on the anhydrous basis
4 SPECIFIC TESTS
4.1 Specific Gravity 〈841〉: NMT 0.789
4.2 Nonvolatile Residue: Evaporate 50 mL in a tared porcelain dish on a steam bath, and dry at 105° for 1 h.
Acceptance criteria: The weight of the residue does not exceed 2 mg (0.004%).
4.3 Water
Sample: Acetone
Standard solution: Transfer 0.50 mL of water to a dry 100-mL volumetric ask, dilute with dehydrated isopropyl alcohol to volume, and mix.
Blank: Dehydrated isopropyl alcohol
Chromatographic system
(See Chromatography 〈621〉, System Suitability.)
Mode: GC
Detector: Thermal conductivity
Column: 0.32-mm × 50-m capillary; 5.0-μm layer of support S2
Temperature
Column: See Table 2.
Table 2
Initial Temperature (°) | Temperature Ramp (°/min) | Final Temperature (°) | Hold Time at Final Temperature (min) |
| 100 | 25 | 190 | - |
Injector: 250°
Detector: 250°
Carrier gas: Helium
Flow rate: 11 mL/min
Split ratio: 4.5:1
Injection size: 1.0 μL
Analysis
Samples: Acetone, Standard solution, and Blank
[Note—Identify the peaks based on their relative retention times, which are 1.0 for water and about 1.9 for isopropyl alcohol.]
Acceptance criteria: The area of the water peak for Acetone is NMT that from the Standard solution, corrected for the area of the water peak from the Blank (0.5%).
Readily Oxidizable Substances
Analysis: Mix 20 mL with 0.10 mL of 0.10 N potassium permanganate in a glass-stoppered bottle.
Acceptance criteria: The permanganate color of the mixture does not completely disappear within 15 min.
5 ADDITIONAL REQUIREMENTS
Packaging and Storage: Preserve in tight containers, remote from fire.
USP Reference Standards 〈11〉
USP Acetone RS
USP Methyl Alcohol RS

