ChemicalBook Product Catalog Organic Chemistry Ketones 2-Butanone

2-Butanone

2-Butanone Chemical Properties
Melting point -87 °C (lit.)
Boiling point 80 °C (lit.)
density 0.805 g/mL at 25 °C (lit.)
vapor density 2.49 (vs air)
vapor pressure 71 mm Hg ( 20 °C)
refractive index n20/D 1.379(lit.)
FEMA 2170 | 2-BUTANONE
Fp 26 °F
storage temp. 2-8°C
solubility Miscible with acetone, ethanol, benzene, ether (U.S. EPA, 1985), and many other solvents, particularly ketones and aldehydes
pka14.7 (quoted, Riddick et al., 1986)
form Solution
color Colorless
PHpH(1+4, 25℃):6.0～7.0
Relative polarity0.327
OdorSweet/sharp odor detectable at 2 to 85 ppm (mean = 16 ppm)
Odor Threshold0.44ppm
Odor Typeethereal
explosive limit1.8-11.5%(V)
Water Solubility 290 g/L (20 ºC)
Merck 14,6072
JECFA Number278
BRN 741880
Henry's Law Constant23.0 at 50.00 °C, 34.1 at 60.00 °C, 50.6 at 70.00 °C, 70.4 at 80.00 °C (headspace-GC, Hovorka et al., 2002)
Exposure limitsTLV-TWA, PEL 590 mg/m3 (200 ppm) (ACGIH, OSHA); STEL 885 mg/m3 (300 ppm) (ACGIH); IDLH 3000 ppm (NIOSH).
Stability:Stable. Highly flammable. Incompatible with oxidizing agents, bases, strong reducing agents. Protect from moisture.
LogP0.3 at 40℃
CAS DataBase Reference78-93-3(CAS DataBase Reference)
NIST Chemistry Reference2-Butanone(78-93-3)
EPA Substance Registry SystemMethyl ethyl ketone (78-93-3)
Safety Information
Hazard Codes F,Xi,T
Risk Statements 11-36-66-67-39/23/24/25-23/24/25
Safety Statements 9-16-45-36/37
RIDADR UN 1193 3/PG 2
WGK Germany 1
RTECS EL6475000
Autoignition Temperature516 °C
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29141200
Hazardous Substances Data78-93-3(Hazardous Substances Data)
ToxicityLD50 orally in rats: 6.86 ml/kg (Smyth)
IDLA3,000 ppm
MSDS Information
ProviderLanguage
2-Butanone English
SigmaAldrich English
ALFA English
2-Butanone Usage And Synthesis
Description2-Butanone is a stable, highly flammable chemical. It is incompatible with oxidising agents, bases, and strong reducing agents. It is a colourless liquid with a sharp, sweet odour. 2-Butanone is produced in large quantities. It is used as a solvent and nearly half of its use is in paints and other coatings because it will quickly evaporate into the air and it dissolves many substances. It is also used in glues and as a cleaning agent.
Chemical PropertiesMethyl ethyl ketone (MEK) is a colorless liquid with an odor that has been described as moderately sharp, fragrant, peppermint, or acetone like. It soluble in water up to 28% by weight and is miscible with many other organic solvents. The lower explosive limit is 1.4% and the upper explosive limit is 11.4%. Methyl ethyl ketone may be incompatible with strong oxidizers, amines, ammonia, inorganic acids, caustics, isocyanates, and pyridines. When used industrially, methyl ethyl ketone must be handled with caution, as it is a Class lB flammable liquid NIOSH (2010).
Physical properties2-Butanone is a clear, colorless, volatile, very flammable liquid with a sweet, mint or acetone-like odor. Odor threshold concentration is 10.0 ppmv (Leonardos et al., 1969). Experimentally determined detection and recognition odor threshold concentrations were 5.8 mg/m3 (2.0 ppmv) and 16 mg/m3 (5.4 ppmv), respectively (Hellman and Small, 1974). It is incompatible with oxidizing agents, bases, and strong reducing agents. It is a colorless liquid with a sharp, sweet odor. 2-Butanone is produced in large quantities. It is used as a solvent and nearly half of its use is in paints and other coatings because it quickly evaporates into the air and it dissolves many substances. It is also used in glues and as a cleaning agent.
OccurrenceReported found as an impurity among products from the dry distillation of wood and in the oil (extracted with ether) of black tea; it is also present in coffee, cheese, bread, some citrus oils and some other natural products (grape, raspberry).
UsesMethyl ethyl ketone (2-butanone, ethyl methyl ketone, methyl acetone) is an organic solvent of relatively low toxicity, which is found in many applications. It is used in industrial and commercial products as a solvent for adhesives, paints, and cleaning agents and as a de-waxing solvent. A natural component of some foods, methyl ethyl ketone can be released into the environment by volcanoes and forest fires.It is used in themanufacture of smokeless powder and colorless synthetic resins, as a solvent, and insurface coating. It is also used as a flavoringsubstance in food.
UsesMEK is used as a solvent for various coating systems, for example, vinyl, adhesives, nitrocellulose, and acrylic coatings. It is used in paint removers, lacquers, varnishes, spray paints, sealers, glues, magnetic tapes, printing inks, resins, rosins, cleaning solutions, and for polymerization. It is found in other consumer products, for example, household and hobby cements, and wood-filling products. MEK is used in dewaxing lubricating oils, the degreasing of metals, in the production of synthetic leathers, transparent paper and aluminum foil, and as a chemical intermediate and catalyst. It is an extraction solvent in the processing of foodstuffs and food ingredients. MEK can also be used to sterilize surgical and dental equipment.
In addition to its manufacture, environmental sources of MEK include exhaust from jet and internal combustion engines, and industrial activities such as gasification of coal. It is found in substantial amounts in tobacco smoke. MEK is produced biologically and has been identified as a product of microbial metabolism. It has also been found in plants, insect pheromones, and animal tissues, and MEK is probably a minor product of normal mammalian metabolism. It is stable under ordinary conditions but can form peroxides on prolonged storage; these may be explosive.
Uses2-Butanone is an eye irritant that has been used as a water soluble photoinitiator for the photopolymerization of methacrylic acid (MAA). As solvent; in the surface coating industry; manufacture of smokeless powder; colorless synthetic resins.
DefinitionChEBI: A dialkyl ketone that is a four-carbon ketone carrying a single keto- group at position C-2.
Production MethodsMethyl ethyl ketone is commercially manufactured from nbutene in a metal-catalyzed hydrogenation reaction that proceeds through the intermediate formation of 2-butanol . A second method of synthesis involves the liquid- phase oxidation of n-butane with the formation of acetic acid as a coproduct.
DefinitionA colorless volatile liquid ketone. It is manufactured by the oxidation of butane and used as a solvent.
PreparationBy catalytic dehydrogenation of secondary butyl alcohol; by dehydration of butane-2,3-diol by refluxing with 25% aqueous H2SO4. Industrially, it is also prepared by controlled oxidation of butane, by dry distillation of calcium acetate and calcium propionate, or by refluxing methyl acetoacetate and diluted H2SO4.
Taste threshold valuesTaste characteristics at 5 ppm: chemical-like and slightly fruity green.
General DescriptionMethyl ethyl ketone (MEK) is a colourless liquid with a sweet and sharp odour. It is soluble in alcohol, ether, acetone benzene, and water. It is a solvent often found in mixtures with acetone, ethyl acetate, n-hexane, toluene, or alcohols. It has applications in the surface coating industry and in the de-waxing of lubricating oils. MEK is used in the manufacture of colourless synthetic resins, artificial leather, rubbers, lacquers, varnishes, and glues.
Air & Water ReactionsHighly flammable. Slightly soluble in water.
Reactivity ProfileAmines are chemical bases. They neutralize acids to form salts plus water.These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides.They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.
HazardFlammable, dangerous fire risk. Toxic by ingestion.
Health HazardOccupational workers are exposed to 2-butanone by breathing contaminated air in workplaces associated with the production or use of paints, glues, coatings, or cleaning agents. Prolonged exposures to 2-butanone cause symptoms of poisoning such as cough, dizziness, drowsiness, headache, nausea, vomiting, dermatitis, irritation of the nose, throat, skin, and eyes and at very high levels cause drooping eyelids, uncoordinated muscle movements, loss of consciousness, and birth defects. Chronic inhalation studies in animals have reported slight neurological, liver, kidney, and respiratory effects. However, information on the chronic (long-term) effects of 2-butanone (methyl ethyl ketone) in humans is limited.
Health HazardThe acute toxicity of methyl ethyl ketone is low. Exposure to high concentrations can cause headache, dizziness, drowsiness, vomiting, and numbness of the extremities. Irritation of the eyes, nose, and throat can also occur. Methyl ethyl ketone is considered to have adequate warning properties.
Repeated or prolonged skin exposure to methyl ethyl ketone can cause defatting of the skin, leading to cracking, secondary infection, and dermatitis. This compound has not been found to be carcinogenic or to show reproductive or developmental toxicity in humans. Methyl ethyl ketone has exhibited developmental toxicity in some animal tests
Fire HazardFlammable/combustible material. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Flammability and ExplosibilityMethyl ethyl ketone is extremely flammable (NFPA rating = 3), and its vapor can travel a considerable distance to an ignition source and "flash back." MEK vapor forms explosive mixtures with air at concentrations of 1.9 to 11% (by volume). Carbon dioxide or dry chemical extinguishers should be used for MEK fires.
Chemical ReactivityReactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
PharmacologyAnticonvulsant activity was demonstrated in rats given orally a dose of 805 mg MEK/kg, which significantly delayed the onset of isonicotinic acid hydrazide-induced convulsions and provided 60% protection against electroshock convulsions, but failed to protect against metrazole convulsions (Kohli, Kishor, Dua & Saxena, 1967). Golubev (1969) reported that 0.25 M-MEK caused contraction of the rabbit pupil, and MEK and other volatile substances isolated from human urine and injected iv into rabbits damaged cerebral and coronary arteries and caused increased capillary permeability, but did not alter the blood-sugar level (Mabuchi, 1969). In dogs, MEK caused vomiting, muscular debility and the formation of large quantities of urinary magnesium ammonium phosphate crystals (Verstraete, van der Stock & Mattheeuws, 1964).
Combined ip administration of MBK and MEK (1:3) to guinea-pigs increased the urinary excretion of the MBK metabolites 2-hexanol and 2,5-hexanedione (Couri, Abdel-Rahman & Hetland, 1976). If the neurotoxic action of MBK is mediated by a metabolite, stimulation of MBK metabolism by simultaneous exposure to MEK may help to explain the marked enhancement of neurotoxicity that is observed with combined MBK/MEK exposures (Hetland et al. 1976).
Safety ProfileModerately toxic by ingestion, skin contact, and intraperitoneal routes. Human systemic effects by inhalation: conjunctiva irritation and unspecified effects on the nose and respiratory system. An experimental teratogen. A strong irritant. Human eye irritation @ 350 ppm. Affects peripheral nervous system and central nervous system. Highly flammable liquid. Reaction with hydrogen peroxide + nitric acid forms a heatand shock-sensitive explosive product. Ignition on contact with potassium tert-butoxide. Mixture with 2- propanol will produce explosive peroxides during storage. Vigorous reaction with chloroform + alkali. Incompatible with chlorosulfonic acid, oleum. To fight fire, use alcohol foam, CO2, dry chemical. Used in production of drugs of abuse. When heated to decomposition it emits acrid smoke and fumes.
Potential ExposureMEK is used as a solvent in nitrocellulose coating and vinyl film manufacture; in smokeless powder manufacture; in cements and adhesives and in the dewaxing of lubricating oils. It is also an intermediate in drug manufacture
CarcinogenicityAlthough MEK has not been specifically examined in a rodent 2-year bioassay, there is little to suggest that the material is carcinogenic. When used as a delivery vehicle in a dermal carcinogenicity bioassay for organic sulfur compounds, Horton et al. found that the application of benzyl disulfide or phenylbenzylthiophene in a 25–29% solution of MEK in dodecylbenzene together failed to increase the incidence of benign skin papillomas in male C3H/HeJmice. The mice used in the experiments were treated twice a week for 52 weeks with the MEKcontaining test solution.
SourceImproper disposal of cleaning fluids, adhesives, paints, and lacquers, and laboratory solvent. Leaches from PVC cement used to join tubing (Wang and Bricker, 1979). Also present in cigarette smoke (500 ppm) and exhaust from gasoline-powered engines (<0.1–2.6 ppm) (Verschueren, 1983).
Gas-phase tailpipe emission rates from California Phase II reformulated gasoline-powered automobiles with and without catalytic converters were 0.47 and 32 mg/km, respectively (Schauer et al., 2002).
Schauer et al. (2001) measured organic compound emission rates for volatile organic compounds, gas-phase semi-volatile organic compounds, and particle phase organic compounds from the residential (fireplace) combustion of pine, oak, and eucalyptus. The gas-phase emission rates of 2-butanone were 215 mg/kg of pine burned, 115 mg/kg of oak burned, and 77 mg/kg of eucalyptus burned.
Environmental fateBiological. Following a lag time of approximately 5 h, 2-butanone degraded in activated sludge (30 mg/L) at a rate constant ranging from 0.021 to 0.025/h (Urano and Kato, 1986).
Bridié et al. (1979) reported BOD and COD values of 2.03 and 2.31 g/g using filtered effluent from a biological sanitary waste treatment plant. These values were determined using a standard dilution method at 20 °C for a period of 5 d. The ThOD for 2-butanone is 2.44 g/g. Using the BOD technique to measure biodegradation, the mean 5-d BOD value (mM BOD/mM 2-butanone) and ThOD were 3.23 and 58.7%, respectively (Vaishnav et al., 1987).
Photolytic. Synthetic air containing gaseous nitrous acid and exposed to artificial sunlight (λ = 300–450 nm) photooxidized 2-butanone into peroxyacetyl nitrate and methyl nitrate (Cox et al., 1980). They reported a rate constant of 2.6 x 10-12 cm3/molecule?sec for the reaction of gaseous 2- butane with OH radicals based on a value of 8 x 10-12 cm3/molecule?sec for the reaction of ethylene with OH radicals.
The OH radical-initiated photooxidation of 2-butanone in a smog chamber produced peroxyacetyl nitrate and acetaldehyde (Cox et al., 1981). Reported rate constants for the reaction of 2-butanone with OH radicals in the atmosphere and in water are 1.15 x 10-13 and 1.50 x 10-13 cm3/molecule?sec, respectively (Wallington and Kurylo, 1987; Wallington et al., 1988a). The rate constant for the reaction of 2-butanone and OH radicals in the atmosphere at 300 K is 2.0 x 10-12 cm3/molecule?sec (Hendry and Kenley, 1979). Cox et al. (1981) reported a photooxidation half-life of 2.3 d for the reaction of 2-butanone and OH radicals in the atmosphere.
Chemical/Physical. 2-Butanone will not hydrolyze because it has no hydrolyzable functional group (Kollig, 1993).
Combustion in air will produce carbon monoxide (incomplete combustion), carbon dioxide, and water vapor.
At an influent concentration of 1.0 g/L, treatment with GAC resulted in an effluent concentration of 532 mg/L. The adsorbability of the carbon used was 94 mg/g carbon (Guisti et al., 1974).
storage2-Butanone should be protected from moisture.
ShippingUN1193 Methyl ethyl ketone or Ethyl methyl ketone, Hazard Class: 3; Labels: 3-Flammable liquid.
Toxicity evaluationThere is very limited information on the mechanisms of toxicity of MEK. Relatively high-inhaled concentrations of 1475–29 500 mg m-3 (500–10 000 ppm) caused pulmonary vasoconstriction and hypertension in cats and dogs. There are several human case reports of neurological effects resulting from high exposure to MEK in combination with other solvents, and animal studies have confirmed synergism between MEK and ethyl n-butyl ketone, methyl n-butyl ketone, n-hexane, carbon tetrachloride, 2,5-hexanedione, and chloroform. The main target organs involved in toxicological interactions are the nervous system and liver, and the lung has also been mentioned.
IncompatibilitiesMay form explosive mixture with air. Violent reaction with strong oxidizers, amines, ammonia, inorganic acids; caustics, isocyanates, pyridines. Incompatible with potassium tert-butoxide, 2-propanol, chlorosulfonic acid; oleum. Attacks some plastics. Ketones are incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, nitrated amines, azo, diazo, azido compounds, carbamates, organic cyanates
Waste DisposalConsult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal. Incineration
Precautions2-Butanone vapor and air mixtures are explosive. It reacts violently with strong oxidants and inorganic acids causing fi re and explosion hazard.
2-Butanone Preparation Products And Raw materials
Raw materialsMethanol-->Hydrogen peroxide-->Zinc oxide-->Palladium chloride-->SULFATE STANDARD-->n-Butane-->Isobutylbenzene-->1-BUTENE-->2-Butanol-->Copper chromite-->CUPRIC CHLORIDE SOLUTION-->COPPER ALLOYS SET OF 5 DISCS (35 MM DIAM., 2 MM THICKNESS)-->ZINC-COPPER COUPLE-->Dehydrogenation catalyst
Preparation Products2-PHENOXYACETAMIDINE HYDROCHLORIDE-->Alizapride-->3-Methylbenzofuran-2-carboxylic acid-->Benzofuran-2-carboxylic acid-->TERT-BUTYL 4-(AMINOMETHYL)PYRIDIN-2-YLCARBAMATE-->3-AMINO-5,6-DIMETHYL-3H-THIENO[2,3-D]PYRIMIDIN-4-ONE-->optical diskbase material modified PMMA copolymer-->2-Butanone peroxide-->1-(3-AMINO-BENZOFURAN-2-YL)-ETHANONE-->2-Benzofurancarboxylic acid ethyl ester-->5-METHOXYBENZOFURAN-2-BORONIC ACID-->(5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDIN-4-YL)-HYDRAZINE-->2-IODO-ISONICOTINIC ACID-->(2-TERT-BUTOXYFORMAMIDO-PYRIDIN-4-YL)METHYL METHANESULFONATE-->3',4'-(DIOCTYLOXY)BENZALDEHYDE-->DL-Isoleucine-->Prothiofos-->Coumaphos-->SEC-BUTYLAMINE-->Industrial gear oil-->Saquinavir-->Dimethylglyoxime-->4-CHLORO-5,6-DIMETHYLTHIENO[2,3-D]PYRIMIDINE-->2,3-Pentanedione-->Industrial gear oil,weight load-->Xanthophyll-->5,6-DIMETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE-->TERT-BUTYL 4-(HYDROXYMETHYL)PYRIDIN-2-YLCARBAMATE-->ETHYL 2-AMINO-4,5-DIMETHYLTHIOPHENE-3-CARBOXYLATE-->ASTRAZON PINK FG-->Industrial gear oil,middle load-->2-(AMINOCARBONYL)NICOTINIC ACID-->2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBONITRILE-->sec-Butylamine-->Mivacurium chloride-->Benomyl-->2,3-Butanedione monoxime-->Carboxymethoxylamine hemihydrochloride-->3-Methyl-1-pentyn-3-ol-->2,3-Dimethylindole
Methyl Acetonitrile Acetylacetone Acetoin Benzalacetone Acetylacetaldehyde dimethyl acetal 2-Butanone Calcium pyruvate Pyruvic acid Benzylacetone 2-Butanone peroxide Kresoxim-methyl Chloromethyl ethyl ether Methoxyacetone Methyl salicylate Methyl acrylate 4-Methyl-2-pentanone Methylthioethane
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