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Acetone

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Not to be confused with Acetoin.
Acetone[1]
Full structural formula of acetone with dimensions
Full structural formula of acetone with dimensions
Skeletal formula of acetone
Skeletal formula of acetone
Ball-and-stick model of acetone
Ball-and-stick model of acetone
Space-filling model of acetone
Space-filling model of acetone
Sample of acetone
Names
Preferred IUPAC name
Propan-2-one[7]
Other names
  • Acetone
  • Dimethyl ketone[2]
  • Dimethyl carbonyl
  • β-Ketopropane[2]
  • Propanone[3]
  • 2-Propanone[2]
  • Dimethyl formaldehyde[4]
  • Pyroacetic spirit (archaic)[5]
  • Ketone propane[6]
Identifiers
3D model (JSmol)
3DMet
635680
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.602 Edit this at Wikidata
EC Number
  • 200-662-2
1466
KEGG
MeSH Acetone
RTECS number
  • AL3150000
UNII
UN number 1090
  • InChI=1S/C3H6O/c1-3(2)4/h1-2H3 checkY
    Key: CSCPPACGZOOCGX-UHFFFAOYSA-N checkY
  • InChI=1/C3H6O/c1-3(2)4/h1-2H3
    Key: CSCPPACGZOOCGX-UHFFFAOYAF
  • CC(=O)C
Properties
C3H6O
Molar mass 58.080 g·mol−1
Appearance Colorless liquid
Odor Pungent, irritating, floral, cucumber like
Density 0.7845 g/cm3 (25 °C)
Melting point −94.7 °C (−138.5 °F; 178.5 K)[12]
Boiling point 56.05 °C (132.89 °F; 329.20 K)[12]
Miscible
Solubility Miscible in benzene, diethyl ether, methanol, chloroform, ethanol[8]
log P -0.16[9]
Vapor pressure
  • 9.39 kPa (0 °C)
  • 30.6 kPa (25 °C)
  • 374 kPa (100 °C)
  • 2.8 MPa (200 °C)[2]
Acidity (pKa)
−33.78·10−6 cm3/mol
1.3588 (VD = 54.46)
Viscosity 0.295 mPa·s (25 °C)[8]
Structure
Trigonal planar at C2
Dihedral at C2
2.91 D
Thermochemistry
125.45 J/(mol·K)
200.4 J/(mol·K)
(−250.03) – (−248.77) kJ/mol
−1.772 MJ/mol
Hazards
GHS labelling:
GHS02: Flammable GHS07: Exclamation mark
Danger
H225, H319, H336, H373
P210, P235, P260, P305+P351+P338
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
3
0
Flash point −20 °C (−4 °F; 253 K)
465 °C (869 °F; 738 K)
Explosive limits 2.6–12.8%[13]
1185 mg/m3 (TWA), 2375 mg/m3 (STEL)
Lethal dose or concentration (LD, LC):
  • 5800 mg/kg (rat, oral)
  • 3000 mg/kg (mouse, oral)
  • 5340 mg/kg (rabbit, oral)[14]
20,702 ppm (rat, 8 h)[14]
45,455 ppm (mouse, 1 h)[14]
NIOSH (US health exposure limits):
PEL (Permissible)
 1000 ppm (2400 mg/m3)[6]
REL (Recommended)
 TWA 250 ppm (590 mg/m3)[6]
IDLH (Immediate danger)
 2500 ppm[6]
Related compounds
Related compounds
Supplementary data page
Acetone (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Acetone, or propanone, is the organic compound with the formula (CH3)2CO.[15] It is a colorless, volatile, flammable liquid and is the simplest and smallest ketone.

Acetone is miscible with water and serves as an important solvent in its own right, typically for cleaning purposes in laboratories. About 6.7 million tonnes were produced worldwide in 2010, mainly for use as a solvent and production of methyl methacrylate and bisphenol A.[16][17] It is a common building block in organic chemistry. Familiar household uses of acetone are as the active ingredient in nail polish remover and as paint thinner. It has VOC exempt status in the USA.[18]

Acetone is produced and disposed of in the human body through normal metabolic processes. It is normally present in blood and urine. People with diabetes produce it in larger amounts. Reproductive toxicity tests show that it has low potential to cause reproductive problems. Ketogenic diets that increase ketone bodies (acetone, β-hydroxybutyric acid and acetoacetic acid) in the blood are used to counter epileptic attacks in infants and children who suffer from recalcitrant refractory epilepsy.[19]

History

Acetone was first produced by alchemists during the late Middle Ages via the dry distillation of metal acetates (e.g., lead acetate, which produced "spirit of Saturn" (since the alchemical symbol for lead was also the astrological symbol for the planet Saturn)).[20]

In 1832, French chemist Jean-Baptiste Dumas and German chemist Justus von Liebig determined the empirical formula for acetone.[21][22] In 1833, the French chemist Antoine Bussy named acetone by adding the suffix -one to the stem of the corresponding acid (viz, acetic acid).[23] By 1852, English chemist Alexander William Williamson realized that acetone was methyl acetyl;[24] the following year, the French chemist Charles Frédéric Gerhardt concurred.[25] In 1865, the German chemist August Kekulé published the modern structural formula for acetone.[26][27] Johann Josef Loschmidt had presented the structure of acetone in 1861,[28] but his privately published booklet received little attention. During World War I, Chaim Weizmann developed the process for industrial production of acetone (Weizmann Process).[29]

Metabolism

See also: Ketosis

Biosynthesis

Small amounts of acetone are produced in the body by the decarboxylation of ketone bodies. Certain dietary patterns, including prolonged fasting and high-fat low-carbohydrate dieting, can produce ketosis, in which acetone is formed in body tissue. Certain health conditions, such as alcoholism and diabetes, can produce ketoacidosis, uncontrollable ketosis that leads to a sharp, and potentially fatal, increase in the acidity of the blood. Since it is a byproduct of fermentation, acetone is a byproduct of the distillery industry.

Metabolic use

Although some biochemistry textbooks and current research publications[30] indicate that acetone cannot be metabolized, there is evidence to the contrary, some dating back thirty years.

Acetone can be produced from the oxidation of ingested isopropanol, or from the spontaneous/enzymatic breakdown of acetoacetate (a ketone body) in ketotic individuals. It can then be metabolized either by CYP2E1 via methylglyoxal to D-lactate and pyruvate, and ultimately glucose/energy, or by a different pathway via propylene glycol to pyruvate, lactate, acetate (usable for energy) and propionaldehyde.[31][32][33]

Production

In 2010, the worldwide production capacity for acetone was estimated at 6.7 million tonnes per year.[34] With 1.56 million tonnes per year, the United States had the highest production capacity,[35] followed by Taiwan and mainland China. The largest producer of acetone is INEOS Phenol, owning 17% of the world's capacity, with also significant capacity (7–8%) by Mitsui, Sunoco and Shell in 2010.[34] INEOS Phenol also owns the world's largest production site (420,000 tonnes/annum) in Beveren (Belgium). Spot price of acetone in summer 2011 was 1100–1250 USD/tonne in the United States.[36]

Current method

Acetone is produced directly or indirectly from propylene. Approximately 83% of acetone is produced via the cumene process;[17] as a result, acetone production is tied to phenol production. In the cumene process, benzene is alkylated with propylene to produce cumene, which is oxidized by air to produce phenol and acetone:

Overview of the cumene process

Other processes involve the direct oxidation of propylene (Wacker-Hoechst process), or the hydration of propylene to give 2-propanol, which is oxidized (dehydrogenated) to acetone.[17]

Older methods

Previously, acetone was produced by the dry distillation of acetates, for example calcium acetate in ketonic decarboxylation.

Ca(CH3COO)2 → CaO(s) + CO2(g) + (CH3)2CO (v)

After that time, during World War I, acetone was produced using acetone-butanol-ethanol fermentation with Clostridium acetobutylicum bacteria, which was developed by Chaim Weizmann (later the first president of Israel) in order to help the British war effort,[17] in the preparation of Cordite.[37] This acetone-butanol-ethanol fermentation was eventually abandoned when newer methods with better yields were found.[17]

Uses

About a third of the world's acetone is used as a solvent, and a quarter is consumed as acetone cyanohydrin, a precursor to methyl methacrylate.[16]

Solvent

Acetone is a good solvent for many plastics and some synthetic fibers. It is used for thinning polyester resin, cleaning tools used with it, and dissolving two-part epoxies and superglue before they harden. It is used as one of the volatile components of some paints and varnishes. As a heavy-duty degreaser, it is useful in the preparation of metal prior to painting. It is also useful for high reliability soldering applications to remove rosin flux after soldering is complete; this helps to prevent the rusty bolt effect.

Acetone is used as a solvent by the pharmaceutical industry and as a denaturant in denatured alcohol.[38] Acetone is also present as an excipient in some pharmaceutical drugs.[39]

Although itself flammable, acetone is used extensively as a solvent for the safe transportation and storage of acetylene, which cannot be safely pressurized as a pure compound. Vessels containing a porous material are first filled with acetone followed by acetylene, which dissolves into the acetone. One liter of acetone can dissolve around 250 liters of acetylene at a pressure of 10 bar.[40][41]

Chemical intermediate

Acetone is used to synthesize methyl methacrylate. It begins with the initial conversion of acetone to acetone cyanohydrin:

(CH3)2CO + HCN → (CH3)2C(OH)CN

In a subsequent step, the nitrile is hydrolyzed to the unsaturated amide, which is esterified:

(CH3)2C(OH)CN + CH3OH → CH2=(CH3)CCO2CH3 + NH3

The third major use of acetone (about 20%)[16] is synthesizing bisphenol A. Bisphenol A is a component of many polymers such as polycarbonates, polyurethanes, and epoxy resins. The synthesis involves the condensation of acetone with phenol:

(CH3)2CO + 2 C6H5OH → (CH3)2C(C6H4OH)2 + H2O

Many millions of kilograms of acetone are consumed in the production of the solvents methyl isobutyl alcohol and methyl isobutyl ketone. These products arise via an initial aldol condensation to give diacetone alcohol.[17]

2 (CH3)2CO → (CH3)2C(OH)CH2C(O)CH3

Condensation with acetylene gives 2-methylbut-3-yn-2-ol, precursor to synthetic terpenes and terpenoids.

Laboratory

In the laboratory, acetone is used as a polar, aprotic solvent in a variety of organic reactions, such as SN2 reactions. The use of acetone solvent is critical for the Jones oxidation. It does not form an azeotrope with water (see azeotrope (data)).[42] It is a common solvent for rinsing laboratory glassware because of its low cost and volatility. Despite its common use as a supposed drying agent, it is not effective except by bulk displacement and dilution. Acetone can be cooled with dry ice to −78 °C without freezing; acetone/dry ice baths are commonly used to conduct reactions at low temperatures. Acetone is fluorescent under ultraviolet light, and its vapor can be used as a fluorescent tracer in fluid flow experiments.[43]

Acetone is used to precipitate proteins.[44] Alternatives for protein precipitation is trichloroacetic acid and ethanol.

Medical and cosmetic uses

Acetone is used in a variety of general medical and cosmetic applications and is also listed as a component in food additives and food packaging and also in nail polish remover. Dermatologists use acetone with alcohol for acne treatments to peel dry skin.

Acetone is commonly used in chemical peeling. Common agents used today for chemical peels are salicylic acid, glycolic acid, 30% salicylic acid in ethanol, and trichloroacetic acid (TCA). Prior to chemexfoliation, the skin is cleaned and excess fat removed in a process called defatting. Acetone, Septisol, or a combination of these agents is commonly used in this process.[citation needed]

Acetone is used in the field of pathology to find lymph nodes in fatty tissues for tumor staging (such as looking for lymph nodes in the fat surrounding the intestines).[45] This helps dissolve the fat, and hardens the nodes, making finding them easier.[46]

It's also used for destaining microscope slides of certain stains.[47]

Domestic and other niche uses

Acetone is often the primary component in cleaning agents such as nail polish remover. Acetone is a component of superglue remover and easily removes residues from glass and porcelain. Make-up artists use acetone to remove skin adhesive from the netting of wigs and mustaches by immersing the item in an acetone bath, then removing the softened glue residue with a stiff brush.

Acetone is often used for vapor polishing of printing artifacts on 3D-printed models printed with ABS plastic. The technique, called acetone vapor bath smoothing, involves placing the printed part in a sealed chamber containing a small amount of acetone, and heating to around 80 degrees Celsius for 10 minutes. This creates a vapor of acetone in the container. The acetone condenses evenly all over the part, causing the surface to soften and liquefy. Surface tension then smooths the semi-liquid plastic. When the part is removed from the chamber, the acetone component evaporates leaving a glassy-smooth part free of striation, patterning, and visible layer edges, common features in untreated 3D printed parts.[48]

Low-grade acetone is also commonly used in academic laboratory settings as a glassware rinsing agent for removing residue and solids before a final wash.[49]

Safety

Flammability

The most hazardous property of acetone is its extreme flammability. At temperatures greater than acetone's flash point of −20 °C (−4 °F), air mixtures of between 2.5% and 12.8% acetone, by volume, may explode or cause a flash fire. Vapors can flow along surfaces to distant ignition sources and flash back. Static discharge may also ignite acetone vapors, though acetone has a very high ignition initiation energy point and therefore accidental ignition is rare. Even pouring or spraying acetone over red-glowing coal will not ignite it, due to the high concentration of vapour and the cooling effect of evaporation of the liquid.[50] It auto-ignites at 465 °C (869 °F). Auto-ignition temperature is also dependent upon the exposure time, thus at some tests it is quoted as 525 °C. Also, industrial acetone is likely to contain a small amount of water which also inhibits ignition.

Acetone peroxide

Main article: Acetone peroxide

When oxidized, acetone forms acetone peroxide as a by product, which is a highly unstable, primary high explosive compound. It may be formed accidentally, e.g. when waste hydrogen peroxide is poured into waste solvent containing acetone. Due to its instability, it is rarely used, despite its simple chemical synthesis.

Health information

Acetone has been studied extensively and is generally recognized to have low acute and chronic toxicity if ingested and/or inhaled.[51] Acetone is not currently regarded as a carcinogen, a mutagenic chemical nor a concern for chronic neurotoxicity effects.[50]

Acetone can be found as an ingredient in a variety of consumer products ranging from cosmetics to processed and unprocessed foods. Acetone has been rated as a generally recognized as safe (GRAS) substance when present in beverages, baked foods, desserts, and preserves at concentrations ranging from 5 to 8 mg/L.[51]

Acetone has been shown to have anticonvulsant effects in animal models of epilepsy, in the absence of toxicity, when administered in millimolar concentrations.[52] It has been hypothesized that the high-fat low-carbohydrate ketogenic diet used clinically to control drug-resistant epilepsy in children works by elevating acetone in the brain.[52] Because of their higher energy requirements, children have higher acetone production than most adults – and the younger the child, the higher the expected production. This indicates that children are not uniquely susceptible to acetone exposure. External exposures are small compared to the exposures associated with the ketogenic diet.[53]

Toxicology

Acetone is believed to exhibit only slight toxicity in normal use, and there is no strong evidence of chronic health effects if basic precautions are followed.[54]

Acetone is an irritant causing mild skin irritation and moderate to severe eye irritation. At high vapor concentrations, it may depress the central nervous system like many other solvents.[55] In one documented case, ingestion of a substantial amount of acetone led to systemic toxicity, although the patient eventually fully recovered.[citation needed] Some sources estimate LD50 for human ingestion at 0.621 g/kg;[citation needed] Acute toxicity for mice by ingestation (LD50) is 3 g/kg and by inhalation LC50) is 44 g/m3 over 4 hours.[56]

  • EPA EPCRA Delisting (1995). EPA removed acetone from the list of "toxic chemicals" maintained under Section 313 of the Emergency Planning and Community Right to Know Act (EPCRA). In making that decision, EPA conducted an extensive review of the available toxicity data on acetone and found that acetone "exhibits acute toxicity only at levels that greatly exceed releases and resultant exposures", and further that acetone "exhibits low toxicity in chronic studies".
  • Genotoxicity. Acetone has been tested in more than two dozen in vitro and in vivo assays. These studies indicate that acetone is not genotoxic.
  • Carcinogenicity. EPA in 1995 concluded, "There is currently no evidence to suggest a concern for carcinogenicity". (EPCRA Review, described in Section 3.3). NTP scientists have recommended against chronic toxicity/carcinogenicity testing of acetone because "the prechronic studies only demonstrated a very mild toxic response at very high doses in rodents".
  • Neurotoxicity and Developmental Neurotoxicity. The neurotoxic potential of both acetone and isopropanol, the metabolic precursor of acetone, have been extensively studied. These studies demonstrate that although exposure to high doses of acetone may cause transient central nervous system effects, acetone is not a neurotoxicant. A guideline developmental neurotoxicity study has been conducted with isopropanol, and no developmental neurotoxic effects were identified, even at the highest dose tested. (SIAR, pp. 1, 25, 31).
  • Environmental. When the EPA exempted acetone from regulation as a volatile organic compound (VOC) in 1995, EPA stated that this exemption would "contribute to the achievement of several important environmental goals and would support EPA's pollution prevention efforts". 60 Fed. Reg. 31,634 (June 16, 1995). 60 Fed. Reg. 31,634 (June 16, 1995). EPA noted that acetone could be used as a substitute for several compounds that are listed as hazardous air pollutants (HAP) under section 112 of the Clean Air Act.

Environmental effects

Although acetone occurs naturally in the environment in plants, trees, volcanic gases, forest fires, and as a product of the breakdown of body fat,[57] the majority of the acetone released into the environment is of industrial origin. Acetone evaporates rapidly, even from water and soil. Once in the atmosphere, it has a 22-day half-life and is degraded by UV light via photolysis (primarily into methane and ethane.[58]) Consumption by microorganisms contributes to the dissipation of acetone in soil, animals, or waterways.[57] The LD50 of acetone for fish is 8.3 g/L of water (or about 1%) over 96 hours, and its environmental half-life in water is about 1 to 10 days. Acetone may pose a significant risk of oxygen depletion in aquatic systems due to the microbial consumption.[59]

Extraterrestrial occurrence

On 30 July 2015, scientists reported that upon the first touchdown of the Philae lander on comet 67P's surface, measurements by the COSAC and Ptolemy instruments revealed sixteen organic compounds, four of which were seen for the first time on a comet, including acetamide, acetone, methyl isocyanate, and propionaldehyde.[60][61][62]

References

  1. ^ The Merck Index, 15th Ed. (2013), p. 13, Acetone Monograph 65, O'Neil: The Royal Society of Chemistry.(subscription required)
  2. ^ a b c d Acetone in Linstrom, Peter J.; Mallard, William G. (eds.); NIST Chemistry WebBook, NIST Standard Reference Database Number 69, National Institute of Standards and Technology, Gaithersburg (MD) (retrieved 2014-05-11)
  3. ^ Klamt, Andreas (2005). COSMO-RS: From Quantum Chemistry to Fluid Phase Thermodynamics and Drug Design. Elsevier. pp. 92–94. ISBN 978-0-444-51994-8.
  4. ^ Ash, Michael; Ash, Irene (2004). Handbook of preservatives. Synapse Information Resources, Inc. p. 369. ISBN 1-890595-66-7.
  5. ^ Myers, Richard L. (2007). The 100 Most Important Chemical Compounds: A Reference Guide. Greenwood. pp. 4–6. ISBN 978-0-313-08057-9.
  6. ^ a b c d NIOSH Pocket Guide to Chemical Hazards. "#0004". National Institute for Occupational Safety and Health (NIOSH).
  7. ^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 723. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  8. ^ a b Properties of substance: acetone. chemister.ru.
  9. ^ "acetone". ChemSrc. Retrieved 2018-04-13.
  10. ^ Chiang, Yvonne; Kresge, A. Jerry; Tang, Yui S.; Wirz, Jakob (1984). "The pKa and keto-enol equilibrium constant of acetone in aqueous solution". Journal of the American Chemical Society. 106 (2): 460–462. doi:10.1021/ja00314a055.
  11. ^ Bordwell, Frederick G. (1988). "Equilibrium acidities in dimethyl sulfoxide solution". Accounts of Chemical Research. 21 (12): 456–463. doi:10.1021/ar00156a004.
  12. ^ a b Lide, David R. (ed) (2003). CRC Handbook of Chemistry and Physics, 84th Edition. CRC Press. Boca Raton, Florida; Section 3, Physical Constants of Organic Compounds.
  13. ^ "Working with modern hydrocarbon and oxygenated solvents: a guide to flammability". American Chemistry Council Solvents Industry Group. January 2008. p. 7. Archived from the original on 2009-06-01. {{cite web}}: Unknown parameter |dead-url= ignored (|url-status= suggested) (help)
  14. ^ a b c "Acetone". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  15. ^ Allen, P.W.; Bowen, H.J.M.; Sutton, L.E.; Bastiansen, O. (1952). "The molecular structure of acetone". Transactions of the Faraday Society. 48: 991. doi:10.1039/TF9524800991.
  16. ^ a b c Acetone, World Petrochemicals report, January 2010
  17. ^ a b c d e f Stylianos Sifniades, Alan B. Levy, "Acetone" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.
  18. ^ "Update: U.S. EPA Exempt Volatile Organic Compounds". American Coatings Association. 2018-01-30. Retrieved 2019-03-20.
  19. ^ Freeman JM, Kossoff EH, Hartman AL. The ketogenic diet: one decade later. Pediatrics. 2007 Mar;119(3):535–43. doi:10.1542/peds.2006-2447. PMID 17332207
  20. ^ Gorman, Mel; Doering, Charles (1959). "History of the structure of acetone". Chymia. 5: 202–208. doi:10.2307/27757186. JSTOR 27757186. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
  21. ^ Dumas, J. (1832) "Sur l'esprit pyro-acétique" (On pyro-acetic spirit), Annales de Chimie et de Physique, 2nd series, 49 : 208–210.
  22. ^ Liebig, Justus (1832) "Sur les combinaisons produites par l'action du gas oléfiant et l'esprit acétique" (On compounds produced by the action of ethylene and acetic spirit), Annales de Chimie et de Physique, 2nd series, 49 : 146–204 (especially 193–204).
  23. ^ Bussy, Antoine (1833) "De quelques Produits nouveaux obtenus par l’action des Alcalis sur les Corps gras à une haute température" (On some new products obtained by the action of alkalies on fatty substances at a high temperature), Annales de Chimie et de Physique, 2nd series, 53 : 398–412; see footnote on pp. 408–409.
  24. ^ Williamson, A. W. (1852) "On Etherification," Journal of the Chemical Society, 4 : 229–239; (especially pp. 237–239).
  25. ^ Gerhardt, Charles (1853) "Researches sur les acids organiques anhydres" (Research on anhydrous organic acids), Annales de Chimie et de Physique, 3rd series, 37 : 285–342; see p. 339.
  26. ^ Kekulé, Auguste (1865) "Sur la constitution des substances aromatiques," Bulletin de la Société chimique de Paris, 1 : 98–110; (especially p. 110).
  27. ^ Kekulé, Auguste (1866) "Untersuchungen über aromatischen Verbindungen" (Investigations into aromatic compounds), Annalen der Chemie und Pharmacie, 137 : 129–196; (especially pp. 143–144).
  28. ^ Loschmidt, J. (1861) Chemische Studien Vienna, Austria-Hungary: Carl Gerold's Sohn.
  29. ^ Chaim Weizmann. chemistryexplained.com
  30. ^ Vujasinovic, M; Kocar, M; Kramer, K; Bunc, M; Brvar, M (2007). "Poisoning with 1-propanol and 2-propanol". Human & Experimental Toxicology. 26 (12): 975. doi:10.1177/0960327107087794.
  31. ^ Glew, Robert H (2010). "You Can Get There From Here: Acetone, Anionic Ketones and Even-Carbon Fatty Acids can Provide Substrates for Gluconeogenesis". Nig. J. Physiol. Sci. 25: 2–4.
  32. ^ Miller, DN; Bazzano, G (1965). "Propanediol metabolism and its relation to lactic acid metabolism". Ann NY Acad Sci. 119 (3): 957–973. Bibcode:1965NYASA.119..957M. doi:10.1111/j.1749-6632.1965.tb47455.x. PMID 4285478.
  33. ^ Ruddick, JA (1972). "Toxicology, metabolism, and biochemistry of 1,2-propanediol". Toxicol Appl Pharmacol. 21: 102–111. doi:10.1016/0041-008X(72)90032-4.
  34. ^ a b Greiner, Camara; Funada, C (June 2010). "CEH Marketing Research Report: ACETONE". Chemical Economics Handbook. SRI consulting. Retrieved 2 September 2016.(subscription required)
  35. ^ "Acetone Uses and Market Data". ICIS.com. October 2010. Archived from the original on 2009-05-15. Retrieved 2011-03-21. {{cite web}}: Unknown parameter |dead-url= ignored (|url-status= suggested) (help)
  36. ^ Acetone (US Gulf) Price Report – Chemical pricing information. ICIS Pricing. Retrieved on 2012-11-26.
  37. ^ Wittcoff, M.M.; Green, H.A. (2003). Organic chemistry principles and industrial practice (1. ed., 1. reprint. ed.). Weinheim: Wiley-VCH. p. 4. ISBN 3-527-30289-1.
  38. ^ Weiner, Myra L.; Lois A. Kotkoskie (1999). Excipient Toxicity and Safety. p. 32. ISBN 978-0-8247-8210-8.
  39. ^ Inactive Ingredient Search for Approved Drug Products, FDA/Center for Drug Evaluation and Research
  40. ^ Mine Safety and Health Administration (MSHA) – Safety Hazard Information – Special Hazards of Acetylene Archived 2016-01-22 at the Wayback Machine. Msha.gov. Retrieved on 2012-11-26.
  41. ^ History – Acetylene dissolved in acetone Archived 2015-09-15 at the Wayback Machine. Aga.com. Retrieved on 2012-11-26.
  42. ^ What is an Azeotrope?. Solvent—recycling.com. Retrieved on 2012-11-26.
  43. ^ Lozano, A.; Yip, B.; Hanson, R.K. (1992). "Acetone: a tracer for concentration measurements in gaseous flows by planar laser-induced fluorescence". Exp. Fluids. 13 (6): 369–376. Bibcode:1992ExFl...13..369L. doi:10.1007/BF00223244.
  44. ^ Simpson, Deborah M.; Beynon, Robert J. (2009). "Acetone precipitation of proteins and the modification of peptides". Journal of Proteome Research. 9 (1): 444–450. doi:10.1021/pr900806x. ISSN 1535-3907.
  45. ^ Basten, O.; Bandorski, D.; Bismarck, C.; Neumann, K.; Fisseler-Eckhoff, A. (13 December 2009). "Acetonkompression". Der Pathologe (in German). 31 (3): 218–224. doi:10.1007/s00292-009-1256-7. PMID 20012620. Retrieved 20 August 2019.
  46. ^ Leung, C. A. W.; Fazzi, G. E.; Melenhorst, J.; Rennspiess, D.; Grabsch, H. I. (November 2018). "Acetone clearance of mesocolic or mesorectal fat increases lymph node yield and may improve detection of high-risk Stage II colorectal cancer patients". Colorectal Disease. 20 (11): 1014–1019. doi:10.1111/codi.14335. PMID 29989291. Retrieved 20 August 2019.
  47. ^ Engbaek, K; Johansen, KS; Jensen, ME (February 1979). "A new technique for Gram staining paraffin-embedded tissue" (PDF). Journal of clinical pathology. 32 (2): 187–90. doi:10.1136/jcp.32.2.187. PMID 86548.
  48. ^ "Quality Finish 3D Prints with Acetone". instructables.com
  49. ^ "Cleaning Glassware" (PDF). Wesleyan University. September 2009. Retrieved July 7, 2016.
  50. ^ a b Acetone MSDS. Hazard.com (1998-04-21). Retrieved on 2012-11-26.
  51. ^ a b "SIDS Initial Assessment Report: Acetone" (PDF). Environmental Protection Agency. {{cite journal}}: Cite journal requires |journal= (help)
  52. ^ a b Likhodii SS; Serbanescu I; Cortez MA; Murphy P; Snead OC; Burnham WM (2003). "Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet". Ann Neurol. 54 (2): 219–226. doi:10.1002/ana.10634. PMID 12891674.
  53. ^ American Chemistry Council Acetone Panel (September 10, 2003). "Acetone (CAS No. 67-64-1) VCCEP Submission" (PDF). pp. 6, 9. Retrieved 2018-04-14.
  54. ^ Basic Information on Acetone. Ccohs.ca (1999-02-19). Retrieved on 2012-11-26.
  55. ^ "What are the potential health effects of acetone?". Canadian Centre for Occupational Health and Safety. Archived from the original on 2008-10-17. Retrieved 2008-10-21. {{cite web}}: Unknown parameter |dead-url= ignored (|url-status= suggested) (help)
  56. ^ Safety (MSDS) data for propanone. sciencelab.com/msds. Retrieved on 2018-03-19
  57. ^ a b Acetone, Agency for Toxic Substances and Disease Registry ToxFAQs, 1995
  58. ^ Darwent, B. deB.; Allard, M. J.; Hartman, M. F.; Lange, L. J. (1960). "The Photolysis of Acetone". Journal of Physical Chemistry. 64 (12): 1847–1850. doi:10.1021/j100841a010.
  59. ^ "Safety Data Sheet Acetone" (PDF). J.M. Loveridge. Archived from the original (PDF) on 2009-03-20. Retrieved 2012-11-26. {{cite web}}: Unknown parameter |dead-url= ignored (|url-status= suggested) (help)
  60. ^ Jordans, Frank (30 July 2015). "Philae probe finds evidence that comets can be cosmic labs". The Washington Post. Associated Press. Retrieved 30 July 2015.
  61. ^ "Science on the Surface of a Comet". European Space Agency. 30 July 2015. Retrieved 30 July 2015.
  62. ^ Bibring, J.-P.; Taylor, M.G.G.T.; Alexander, C.; Auster, U.; Biele, J.; Finzi, A. Ercoli; Goesmann, F.; Klingehoefer, G.; Kofman, W.; Mottola, S.; Seidenstiker, K.J.; Spohn, T.; Wright, I. (31 July 2015). "Philae's First Days on the Comet – Introduction to Special Issue". Science. 349 (6247): 493. Bibcode:2015Sci...349..493B. doi:10.1126/science.aac5116. PMID 26228139.
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