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General Material Information

Preferred name acetone
Trivial Name Acetone
Short Description dimethyl ketone
Formula C3 H6 O
CAS Number 67-64-1
FEMA Number 3326
Flavis Number 7.05
ECHA Number 200-662-2
FDA UNII 1364PS73AF
Nikkaji Number J2.365E
Beilstein Number 0635680
MDL MFCD00008765
COE Number 737
xLogP3-AA -0.10 (est)
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 139 acetone
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 67-64-1 ; ACETONE
Synonyms
  • acetone 99%, (naturals)
  • acetone FCC
  • acetone min. 99%, natural
  • acetone natural
  • acetone, natural
  • chevron acetone
  • dimethyl formaldehyde
  • dimethyl ketal
  • dimethyl ketone
  • dimethylformaldehyde
  • dimethylketal
  • ketone propane
  • ketone, dimethyl
  • methyl ketone
  • propan-2-one
  • 2-oxo propane
  • beta-keto propane
  • propanone
  • 2-propanone
  • pyroacetic acid
  • pyroacetic ether
  • 2-Propanone
  • β-Ketopropane
  • NSC 135802
  • Taimax
  • A 1060
  • A 0140
  • MeSH ID: D000096

US / EU / FDA / JECFA / FEMA / Scholar / Patents

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Literature & References

propan-2-one
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:67-64-1
Pubchem (cid):180
Pubchem (sid):134970724
Pherobase:View
Publications by Info
Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.)
Publications by PubMed
Ultrahigh performance liquid chromatography analysis of volatile carbonyl compounds in virgin olive oils.
The effect of germination on phenolic content and antioxidant activity of chickpea.
Milk volatile organic compounds and fatty acid profile in cows fed timothy as hay, pasture, or silage.
Headspace volatile components of Canadian grown low-tannin faba bean (Vicia faba L.) genotypes.
Biological activity and fatty acid composition of Caesar's mushroom.
Formulation and evaluation of microsphere based oro dispersible tablets of itopride hcl.
Determination of 3-methyl-2,4-nonanedione in red wines using methanol chemical ionization ion trap mass spectrometry.
Monitoring of cocoa volatiles produced during roasting by selected ion flow tube-mass spectrometry (SIFT-MS).
Variation in phenolic composition and antioxidant activity during flower development of safflower (Carthamus tinctorius L.).
Volatile flavor compounds in yogurt: a review.
Chemical and biochemical study of industrially produced San Simón da Costa smoked semi-hard cow's milk cheeses: Effects of storage under vacuum and different modified atmospheres.
Flavor authentication studies of alpha-ionone, beta-ionone, and alpha-ionol from various sources.
An efficient oxidative lactonization of 1,4-diols catalyzed by Cp*Ru(PN) complexes.
Development of a LC-ESI/MS/MS assay for the quantification of vanillin using a simple off-line dansyl chloride derivatization reaction to enhance signal intensity.
[Determination of major flavor components in chinese spirits using a special domestic gas chromatograph with DNP packed column].
A simple and efficient system for green note compound biogenesis by use of certain lipoxygenase and hydroperoxide lyase sources.
Flavor release measurement from gum model system.
C-27 apocarotenoids in the flowers of Boronia megastigma (Nees).
Flavor release measurement by atmospheric pressure chemical ionization ion trap mass spectrometry, construction of interface and mathematical modeling of release profiles.
Headspace gas chromatography-mass spectrometry of volatile compounds in murici (Byrsonima crassifolia l. Rich).
Flavor composition of cashew (Anacardium occidentale) and marmeleiro (Croton species) honeys.
Simple and rapid analysis for quantitation of the most important volatile flavor compounds in yogurt by headspace gas chromatography-mass spectrometry.
Formation of volatile compounds during heating of spice paprika (Capsicum annuum) powder.
Enzymatic synthesis of stable, odorless, and powdered furanone glucosides by sucrose phosphorylase.
Toxicologic evaluation of flavor ingredients added to cigarette tobacco: skin painting bioassay of cigarette smoke condensate in SENCAR mice.
Effect of ethanol in feed on milk flavor and chemical composition.
Inhibition of cytochrome P-450 2E1 by diallyl sulfide and its metabolites.
[Shortened dough preparation of wheat bread and its effect on the flavor. 1. Carbonyl compounds and ethanol].

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
FDA Indirect Additives used in Food Contact Substances:View
CHEBI:View
CHEMBL:View
UM BBD:Search
KEGG (GenomeNet):C00207
HMDB (The Human Metabolome Database):HMDB01659
FooDB:FDB008301
Export Tariff Code:2914.11.5000
FDA Listing of Food Additive Status:View
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 58.080020904541
Specific gravity @ 25 °C
Pounds per Gallon 6.557 to 6.59
Refractive Index 1.347 to 1.359 @ 20 °C
Melting Point -95 to -94°C @ 760 mm Hg
Boiling Point 56 to 57°C @ 760 mm Hg
Boiling Point 22 to 23°C @ 200 mm Hg
Vapor Pressure 232 mmHg @ 25 °C
Vapor Density 2
Flash Point TCC Value -17.22 °C TCC
logP (o/w) -0.16
Shelf life 24 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
water, 2.199e+005 mg/L @ 25 °C (est) Yes
water, 1.00E+06 mg/L @ 25 °C (exp) Yes

Organoleptic Properties

Odor Type: Solvent
solvent, ethereal, apple, pear
Odor strength high , recommend smelling in a 1.00 % solution or less
Substantivity < 1 hour(s) at 100.00 %
General comment At 1.00 % in propylene glycol. solvent ethereal apple pear

Occurrences

Potential Uses

Applications
Other purposes Denaturants, Solvents
Cosmetic purposes Denaturants, Solvents

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 11 - Highly flammable.
R 36 - Irritating to eyes.
R 66 - Repeated exposure may cause skin dryness or cracking.
R 67 - Vapours may cause frowsiness and dizziness.
S 02 - Keep out of the reach of children.
S 09 - Keep container in a well-ventilated place.
S 16 - Keep away from sources of ignition - No Smoking.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50 [sex: M] 8452 mg/kg
(Smyth et al., 1970)

oral-rat LD50 8930 mg/kg
(Smyth et al., 1969b)

oral-rat LD50 9750 mg/kg
(FDA, 1975a)

oral-rat LD50 6800 mg/kg
(Kimura et al., 1971a)

oral-rat LD50 3465 mg/kg
(Kohli et al., 1967)

oral-mouse LD50 [sex: M] 5250 mg/kg
(Tanii et al., 1986)

oral-rabbit LD50 5300 mg/kg
(Krasavage et al., 1982)

intraperitoneal-dog LDLo 8000 mg/kg
BEHAVIORAL: COMA GASTROINTESTINAL: ALTERATION IN GASTRIC SECRETION
Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 18, Pg. 218, 1884.

oral-dog LDLo 8000 mg/kg
MUSCULOSKELETAL: JOINTS BEHAVIORAL: COMA BEHAVIORAL: ATAXIA
Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 18, Pg. 218, 1884.

oral-man TDLo 2857 mg/kg
BEHAVIORAL: COMA KIDNEY, URETER, AND BLADDER: OTHER CHANGES
"Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 64, 1969.

oral-man TDLo 2857 mg/kg
BEHAVIORAL: COMA
Diabetes. Vol. 15, Pg. 810, 1966.

intraperitoneal-mouse LD50 1297 mg/kg
Shell Chemical Company. Unpublished Report. Vol. -, Pg. 1, 1961.

oral-mouse LD50 3000 mg/kg
Pharmaceutical Chemistry Journal Vol. 14, Pg. 162, 1980.

intravenous-mouse LDLo 4000 mg/kg
FAO Nutrition Meetings Report Series. Vol. 48A, Pg. 86, 1970.

oral-rabbit LD50 5340 mg/kg
FAO Nutrition Meetings Report Series. Vol. 48A, Pg. 86, 1970.

intravenous-rabbit LDLo 1576 mg/kg
BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY) LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION
Journal of Pharmacology and Experimental Therapeutics. Vol. 33, Pg. 175, 1928.

intravenous-rat LD50 5500 mg/kg
Raw Material Data Handbook, Vol.1: Organic Solvents, 1974. Vol. 1, Pg. 1, 1974.

oral-rat LD50 5800 mg/kg
BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) BEHAVIORAL: TREMOR
Journal of Toxicology and Environmental Health. Vol. 15, Pg. 609, 1985.

intraperitoneal-rat LDLo 500 mg/kg
KIDNEY, URETER, AND BLADDER: RENAL FUNCTION TESTS DEPRESSED BEHAVIORAL: GENERAL ANESTHETIC BEHAVIORAL: MUSCLE WEAKNESS
Journal of Pharmacy and Pharmacology. Vol. 11, Pg. 150, 1959.

Dermal Toxicity:
skin-rabbit LDLo 20 ml/kg
Union Carbide Data Sheet. Vol. 5/7/1970

skin-guinea pig LD50 > 9.40 ml/kg
Toxicology and Applied Pharmacology. Vol. 7, Pg. 559, 1965.

subcutaneous-dog LDLo 5000 mg/kg
Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 18, Pg. 218, 1884.

skin-guinea pig LD50 > 9400 uL/kg
Toxicology and Applied Pharmacology. Vol. 7, Pg. 559, 1965.

subcutaneous-guinea pig LDLo 5000 mg/kg
Archiv fuer Gewerbepathologie und Gewerbehygiene. Vol. 5, Pg. 1, 1933.

Inhalation Toxicity:
inhalation-rat LC50 50100 mg/m3/8H
American Industrial Hygiene Association Journal. Vol. 20, Pg. 364, 1959.

inhalation-mouse LC50 44 gm/m3/4H
Current Toxicology. Vol. 1, Pg. 47, 1993.

inhalation-human TCLo 500 ppm
SENSE ORGANS AND SPECIAL SENSES: CONJUNCTIVE IRRITATION: EYE LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES SENSE ORGANS AND SPECIAL SENSES: OTHER CHANGES: OLFACTION
Journal of Industrial Hygiene and Toxicology. Vol. 25, Pg. 282, 1943.

inhalation-man TCLo 440 ug/m3/6M
BRAIN AND COVERINGS: RECORDINGS FROM SPECIFIC AREAS OF CNS
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 42(8), Pg. 42, 1977.

inhalation-man TCLo 10 mg/m3/6H
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 42(8), Pg. 42, 1977.

inhalation-man TCLo 12000 ppm/4H
BEHAVIORAL: MUSCLE WEAKNESS GASTROINTESTINAL: NAUSEA OR VOMITING
Annals of Occupational Hygiene. Vol. 16, Pg. 73, 1973.

inhalation-mouse LC50 44000 mg/m3/4H
Current Toxicology. Vol. 1, Pg. 47, 1993.

Safety in use information

Category:
extraction solvents, flavoring agents
Recommendation for acetone usage levels up to:
not for fragrance use.
Maximised Survey-derived Daily Intakes (MSDI-EU): 6100.00 (μg/capita/day)
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 6
Click here to view publication 6
average usual ppmaverage maximum ppm
baked goods: -8.00000
beverages(nonalcoholic): -5.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -5.00000
fruit ices: -5.00000
gelatins / puddings: -5.00000
granulated sugar: --
gravies: --
hard candy: -8.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: -5.00000
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --

Safety references

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 7 (FGE.07): Saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids from chemical group 5
View page or View pdf

Flavouring Group Evaluation 63 (FGE.63): Consideration of aliphatic secondary alcohols, ketones and related esters evaluated by JECFA (59th meeting) structurally related to saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids evaluated by EFSA in FGE.07 (2005) (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf

Flavouring Group Evaluation 7, Revision 1 (FGE.07Rev1): Saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids from chemical group 5 (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Scientific opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) on a request from the Commission
View page or View pdf

Flavouring Group Evaluation 7, Revision 2 (FGE.07Rev2) : Saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids from chemical group 5
View page or View pdf

EPI System: View
EPA-Iris:IRIS
ClinicalTrials.gov:search
Daily Med:search
NIOSH International Chemical Safety Cards:search
NIOSH Pocket Guide:search
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA GENetic TOXicology:Search
EPA Substance Registry Services (TSCA):67-64-1
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :180
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 1090
WGK Germany:1
propan-2-one
Chemidplus:0000067641
EPA/NOAA CAMEO:hazardous materials
RTECS:67-64-1