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Chemistry

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Also known as: 2-propanone, 67-64-1, Propanone, Dimethyl ketone, Propan-2-one, Methyl ketone
Molecular Formula
C3H6O
Molecular Weight
58.08  g/mol
InChI Key
CSCPPACGZOOCGX-UHFFFAOYSA-N
FDA UNII
1364PS73AF

Acetone
A colorless liquid used as a solvent and an antiseptic. It is one of the ketone bodies produced during ketoacidosis.
1 2D Structure

Acetone

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
propan-2-one
2.1.2 InChI
InChI=1S/C3H6O/c1-3(2)4/h1-2H3
2.1.3 InChI Key
CSCPPACGZOOCGX-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CC(=O)C
2.2 Other Identifiers
2.2.1 UNII
1364PS73AF
2.3 Synonyms
2.3.1 Depositor-Supplied Synonyms

1. 2-propanone

2. 67-64-1

3. Propanone

4. Dimethyl Ketone

5. Propan-2-one

6. Methyl Ketone

7. Pyroacetic Ether

8. Dimethylformaldehyde

9. Beta-ketopropane

10. Dimethylketal

11. Chevron Acetone

12. Ketone Propane

13. Aceton

14. Pyroacetic Acid

15. Ketone, Dimethyl

16. Dimethylketone

17. Fema No. 3326

18. .beta.-ketopropane

19. Rcra Waste Number U002

20. Dimethyl Formaldehyde

21. Taimax

22. Aceton [german, Dutch, Polish]

23. Ketone, Dimethyl-

24. Acetone [nf]

25. Nsc 135802

26. Mfcd00008765

27. Nsc-135802

28. (ch3)2co

29. Chebi:15347

30. 1364ps73af

31. Acetone (nf)

32. Ncgc00091179-01

33. Dsstox_cid_1482

34. Dsstox_rid_76176

35. Acetone (natural)

36. Dsstox_gsid_21482

37. Caswell No. 004

38. 3-methyl-4-(2,2-dimethyl-6-methylenecyclohexyl)-3-buten-2-one

39. Acetone, For Hplc, >=99.8%

40. Acetone, For Hplc, >=99.9%

41. Acetone, Acs Reagent, >=99.5%

42. Cas-67-64-1

43. Hsdb 41

44. Ccris 5953

45. Acetone (1,1,1,3,3,3-d6)

46. Einecs 200-662-2

47. Un1090

48. Rcra Waste No. U002

49. Epa Pesticide Chemical Code 004101

50. Dimethylcetone

51. Isopropanal

52. Methylketone

53. Dimethylketon

54. Propanon

55. Sasetone

56. Methyl-ketone

57. 2propanone

58. B-ketopropane

59. Unii-1364ps73af

60. Ai3-01238

61. 2-propanal

62. Acetone Hp

63. Acetone Acs

64. Acetone, Puriss.

65. Acetone P.a.

66. Acetone (tn)

67. Acetone Hplc Grade

68. Methyl Methyl Ketone

69. Acetone, For Hplc

70. Acetone, Acs Reagent

71. Acetone, Hplc Grade

72. Acetone [vandf]

73. Acetone [fhfi]

74. Acetone [hsdb]

75. Acetone [inci]

76. Acetone Acs Low Benzene

77. Acetone, Technical Grade

78. Acetone [fcc]

79. Acetone [mi]

80. Acetone Oil (salt/mix)

81. Ch3coch3

82. Acetone [mart.]

83. Acetone [usp-rs]

84. Acetone [who-dd]

85. Acetone Reagent Grade Acs

86. Acetone, Histological Grade

87. Ec 200-662-2

88. Acetone, Analytical Standard

89. Acetone, Environmental Grade

90. Acetone, Semiconductor Grade

91. Acetone, Lr, >=99%

92. Acetone, Natural, >=97%

93. Un 1091 (salt/mix)

94. Aceton (german, Polish)

95. Acetone [ep Impurity]

96. Acetone, Puriss., 99.0%

97. Chembl14253

98. Acetone [ep Monograph]

99. Dimethylketone, Pyroacetic Acid

100. Wln: 1v1

101. Acetone, Ar, >=99.5%

102. Dtxsid8021482

103. Acetone, Spectrophotometric Grade

104. Citronellidene Acetone; Baccartol

105. Zinc895111

106. Acetone, Gc, For Residue Analysis

107. Acetone, >=99.5%, Acs Reagent

108. Tox21_111096

109. Tox21_202480

110. C0556

111. Lmfa12000057

112. Nsc135802

113. Acetone 5000 Microg/ml In Methanol

114. Acetone, Purum, >=99.0% (gc)

115. Akos000120890

116. Acetone 100 Microg/ml In Acetonitrile

117. Un 1090

118. Acetone, Saj First Grade, >=99.0%

119. Acetone [un1090] [flammable Liquid]

120. Acetone, For Chromatography, >=99.8%

121. Acetone, Histological Grade, >=99.5%

122. Acetone, Jis Special Grade, >=99.5%

123. Acetone, Laboratory Reagent, >=99.5%

124. Ncgc00260029-01

125. Acetone, For Hplc, >=99.8% (gc)

126. Acetone, Uv Hplc Spectroscopic, 99.8%

127. Acetone, >=99.5%, For Residue Analysis

128. Acetone, For Residue Analysis, >=99.5%

129. Isoflurane Impurity F [ep Impurity]

130. A0054

131. Acetone, For Luminescence, >=99.5% (gc)

132. Ft-0621803

133. Acetone, Suitable For Determination Of Dioxins

134. Chlorobutanol Impurity B [ep Impurity]

135. Acetone, Glass Distilled Hrgc/hplc Trace Grade

136. C00207

137. D02311

138. Q49546

139. Acetone, Acs Spectrophotometric Grade, >=99.5%

140. Acetone, Reagentplus(r), Phenol Free, >=99.5%

141. Acetone, >=99%, Meets Fcc Analytical Specifications

142. Acetone, Acs Reagent, >=99.5%, <=2 Ppm Low Benzene

143. Acetone, Contains 20.0 % (v/v) Acetonitrile, For Hplc

144. Acetone, For Residue Analysis, Suitable For 5000 Per Jis

145. Acetone, For Uv-spectroscopy, Acs Reagent, >=99.7% (gc)

146. Acetone, United States Pharmacopeia (usp) Reference Standard

147. Acetone Solution, Contains 20.0 % (v/v) Acetonitrile, For Hplc

148. Acetone, Hplc Plus, For Hplc, Gc, And Residue Analysis, >=99.9%

149. Acetone, Semiconductor Grade Mos Puranal(tm) (honeywell 17921)

150. Acetone, Semiconductor Grade Ulsi Puranal(tm) (honeywell 17014)

151. Acetone, Semiconductor Grade Vlsi Puranal(tm) (honeywell 17617)

152. Acetone, Pharmaceutical Secondary Standard; Certified Reference Material

153. Acetone Solution, Certified Reference Material, 2000 Mug/ml In Methanol: Water (9:1)

154. Acetone, Puriss. P.a., Acs Reagent, Reag. Iso, Reag. Ph. Eur., >=99.5% (gc)

155. Acetone, Puriss., Meets Analytical Specification Of Ph. Eur., Bp, Nf, >=99% (gc)

2.4 Create Date
2004-09-16
3 Chemical and Physical Properties
Molecular Weight 58.08 g/mol
Molecular Formula C3H6O
XLogP3-0.1
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass58.041864811 g/mol
Monoisotopic Mass58.041864811 g/mol
Topological Polar Surface Area17.1 Ų
Heavy Atom Count4
Formal Charge0
Complexity26.3
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Solvents

Liquids that dissolve other substances (solutes), generally solids, without any change in chemical composition, as, water containing sugar. (Grant and Hackh's Chemical Dictionary, 5th ed) (See all compounds classified as Solvents.)


4.2 Absorption, Distribution and Excretion

In rats receiving acetone in drinking water (7.5% v/v) for 11 consecutive days, plasma concentrations of acetone on day 1 were in the range of 315-800 ug/mL. The plasma concentration appeared to plateau at about 1,200 ug/mL by day 4.

DHHS/ATSDR; Addendum to the Toxicological Profile for Acetone p.? (August 2011). Available from, as of January 7, 2015: https://www.atsdr.cdc.gov/toxprofiles/index.asp


Physiologically based toxicokinetic (PBTK) modeling of human experimental data suggests difficulties to simultaneously describe the time courses of inhaled polar solvents in blood and breath, especially if exposures occur during physical exercise. We attribute this to the washin-washout effect in the airways. The aim was to develop a PBTK-model that explains the behavior of acetone in blood and exhaled air at different levels of physical exercise. The model includes exchange of inhaled solvent vapor with the blood flow via the mucosa and separate compartments to describe working and resting muscles. The developed model was contrasted to a traditional PBTK-model where the conducting airways were regarded as an inert tube. Our model predictions agrees well with experimentally observed acetone levels in both arterial blood and end- and mixed-exhaled air from 26 inhalation experiments conducted with 18 human volunteers at 0, 50, 100 and 150 W workload. In contrast, the inert-tube model was unable to describe the data. The developed model is to our knowledge the first which explains the toxicokinetics of acetone at such various levels of physical exercise. It may be useful in breath monitoring and to obtain more accurate estimates of absorbed dose during inhalation of polar volatiles.

PMID:16364574 Mork AK, Johanson G; Toxicol Lett 164 (1): 6-15 (2006)


Patients with severe diabetic ketoacidosis can have plasma acetone levels as high as 750 mg/L, which is up to 300 times the normal limit.

European Chemicals Bureau; IUCLID Dataset, ACETONE (67-64-1). Available from, as of January 22, 2007: https://esis.jrc.ec.europa.eu/


Acetone is one of the least hazardous industrial solvents, but is highly volatile and may be inhaled in large quantities. It may be absorbed into the blood through the lungs and diffused throughout the body. Small quantities may be absorbed through the skin.

International Labour Office. Encyclopedia of Occupational Health and Safety. Vols. I&II. Geneva, Switzerland: International Labour Office, 1983., p. 38


For more Absorption, Distribution and Excretion (Complete) data for ACETONE (19 total), please visit the HSDB record page.


4.3 Metabolism/Metabolites

... The role of CYP2E1 in acetone catabolism /was assessed/ by measuring acetone levels at different time points in rats that had been treated with diallyl sulfide (DAS, a CYP2E1 inhibitor) at a variety of dose levels. The study noted DAS dose-dependent increases in the time to peak blood acetone level and in the time to return to pre-dose levels, suggesting an important role of CYP2E1 in acetone catabolism.

DHHS/ATSDR; Addendum to the Toxicological Profile for Acetone p.6 (August 2011). Available from, as of January 7, 2015: https://www.atsdr.cdc.gov/toxprofiles/index.asp


Acetone, one of the principal ketone bodies elevated during treatment with the ketogenic diet, exhibits anticonvulsant properties that may contribute to the seizure protection conferred by the diet. The anticonvulsant mechanism of acetone is unknown, but it is metabolized to several bioactive substances that could play a role. Acetone and its major metabolites-acetol, 1,2-propanediol, methylglyoxal, and pyruvic acid-were assessed for anticonvulsant activity in two mouse seizure models. Various doses of the substances administered intraperitoneally were characterized for their ability to elevate the threshold for clonic seizures induced by intravenous infusion of pentylenetetrazol (PTZ) and for protection against tonic seizures induced by subcutaneous bolus administration of 4-aminopyridine (4-AP). The inverted-screen test was used to assess acute neurological toxicity. Acetone (1-32 mmol/kg, i.p.), in a dose-dependent fashion, elevated the PTZ threshold and conferred protection against 4-AP seizures (ED(50), 26.3 mmol/kg). Effective doses of acetone (10-32 mmol/kg) did not cause motor impairment in the inverted-screen test (TD(50), 45.7 mmol/kg). In doses 10-fold greater than the minimally effective dose ofacetone (3.2 mmol/kg), the metabolites acetol, 1,2-propanediol, and pyruvic acid were inactive in the PTZ model. At higher doses that produced motor impairment, acetol and 1,2-propanediol (but not pyruvic acid) did elevate the PTZ threshold. Methylglyoxal had both proconvulsant and anticonvulsant actions, and had substantial toxicity, producing respiratory distress, motor impairment, and death. None of the acetone metabolites protected against 4-AP seizures. This study confirms the broad-spectrum anticonvulsant properties of acetone and indicates that the seizure protection conferred is unlikely to result from its major metabolic products.

PMID:17386058 Gasior M et al; Epilepsia 48 (4): 793-800 (2007)


Two pathways for the conversion of acetone to glucose are proposed, the methylglyoxal & the propanediol pathways. The methylglyoxal pathway is responsible for the conversion to acetol, acetol to methylglyoxal, & subsequent conversion of methylglyoxal to glucose. The propanediol pathway involves the conversion of acetol to L-1,2-propanediol by an as yet unknown process. L-1,2-propanediol is converted to L-lactaldehyde by alcohol dehydrogenase, & L-lactaldehyde is converted to L-lactic acid by aldehyde dehydrogenase. Expression of these metabolic pathways in rat appears to be dependent on the induction of /acetone/ oxygenase & acetol monooxygenase by acetone.

PMID:6706932 Casazza JP et al; J Biol Chem 259 (1): 231-6 (1984)


Hepatic NAD-dependent alcohol dehydrogenase... enzyme is capable of catalyzing reverse reaction in which... acetone.../is reduced to alcohol/.

Testa, B. and P. Jenner. Drug Metabolism: Chemical & Biochemical Aspects. New York: Marcel Dekker, Inc., 1976., p. 310


For more Metabolism/Metabolites (Complete) data for ACETONE (8 total), please visit the HSDB record page.


4.4 Biological Half-Life

Blood: 3 hours; whole body: 19-31 hours; [TDR, p. 17]

TDR - Ryan RP, Terry CE, Leffingwell SS (eds). Toxicology Desk Reference: The Toxic Exposure and Medical Monitoring Index, 5th Ed. Washington DC: Taylor & Francis, 1999., p. 17


Half-times for blood elimination of 3-3.9 hrs have been estimated in humans exposed to 100-500 ppm for 2-4 hrs. Elimination half-times of 3.9 hrs and 6.2 hrs have been estimated for arterial and venous blood, respectively. No differences in elimination half-times were found between men and women.

DHHS/ATSDR; Toxicological Profile for Acetone p. 79 (1994)


Tissue distribution of 2(14)C-acetone following inhalation exposure to 1,200 mg/cu m (500 ppm) was studied in mice. .... Half-times for acetone elimination were 2-3 hr for blood, kidney, lung, brain, and muscle, and greater than 5 hr for subcutaneous adipose tissue. By 24 hr after exposure, acetone concentrations had returned to endogenous levels in all tissues.

European Chemicals Bureau; IUCLID Dataset, ACETONE (67-64-1). Available from, as of January 22, 2007: https://esis.jrc.ec.europa.eu/


Two instances of finding abnormally high concentrations of acetone in urine (0.10 g/dL and 0.052 g/dL) without any measurable amounts of ethanol (<0.005 g/dL) or isopropanol (<0.005 g/dL) prompted a survey of the elimination kinetics of isopropanol and its metabolite acetone in humans. In a hospital patient who had ingested denatured alcohol, the elimination half-life (t(1/2)) of acetone during detoxification was 27 hr and not 3-5 hr as reported by other workers. Several other literature reports of individuals who had ingested isopropanol as well as controlled studies after administration of moderate amounts of acetone and/or isopropanol support the notion of a long elimination half-life of 17-27 hr for acetone compared with a t(1/2) of 1-3 hr for isopropanol.

PMID:10654562 Jones AW; J Anal Toxicol 24 (1): 8-10


The elimination half life in mice for acetone in various tissues was between 2 and 5 hr, with the subcutaneous adipose tissue showing the slowest release of acetone. Daily exposure of mice to 500 ppm acetone for 6 hr did not result in any day-to-day accumulation of acetone.

European Chemicals Bureau; IUCLID Dataset, ACETONE (67-64-1). Available from, as of January 22, 2007: https://esis.jrc.ec.europa.eu/


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03-Jan-2022
31-May-2025
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PharmaCompass offers a list of Acetone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Acetone manufacturer or Acetone supplier for your needs.

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PharmaCompass also assists you with knowing the Acetone API Price utilized in the formulation of products. Acetone API Price is not always fixed or binding as the Acetone Price is obtained through a variety of data sources. The Acetone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Acetone

Synonyms

2-propanone, 67-64-1, Propanone, Dimethyl ketone, Propan-2-one, Methyl ketone

Cas Number

67-64-1

Unique Ingredient Identifier (UNII)

1364PS73AF

About Acetone

A colorless liquid used as a solvent and an antiseptic. It is one of the ketone bodies produced during ketoacidosis.

2941-EP2295423A1 Manufacturers

A 2941-EP2295423A1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2941-EP2295423A1, including repackagers and relabelers. The FDA regulates 2941-EP2295423A1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2941-EP2295423A1 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of 2941-EP2295423A1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

2941-EP2295423A1 Suppliers

A 2941-EP2295423A1 supplier is an individual or a company that provides 2941-EP2295423A1 active pharmaceutical ingredient (API) or 2941-EP2295423A1 finished formulations upon request. The 2941-EP2295423A1 suppliers may include 2941-EP2295423A1 API manufacturers, exporters, distributors and traders.

click here to find a list of 2941-EP2295423A1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

2941-EP2295423A1 GMP

2941-EP2295423A1 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of 2941-EP2295423A1 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right 2941-EP2295423A1 GMP manufacturer or 2941-EP2295423A1 GMP API supplier for your needs.

2941-EP2295423A1 CoA

A 2941-EP2295423A1 CoA (Certificate of Analysis) is a formal document that attests to 2941-EP2295423A1's compliance with 2941-EP2295423A1 specifications and serves as a tool for batch-level quality control.

2941-EP2295423A1 CoA mostly includes findings from lab analyses of a specific batch. For each 2941-EP2295423A1 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

2941-EP2295423A1 may be tested according to a variety of international standards, such as European Pharmacopoeia (2941-EP2295423A1 EP), 2941-EP2295423A1 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2941-EP2295423A1 USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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