2,6-Dimethyl-4-heptanone

2,6-Dimethyl-4-heptanone Basic information
Product Name:2,6-Dimethyl-4-heptanone
Synonyms:2,6-DIMETHYL-4-HEPTANONE;2,6-Dimethyl-4-heptanone, remainder mainly 4,6-dimethyl-2-heptanone;Diisobutyl ketone~Isovalerone;Dimethylheptanone;2 6-DIMETHYL-4-HEPTANONE 99+%;2,6-DIMETHYL-4-HEPTANONE, TECH., 80%;2,6-Dimethyl-4-Heptanone,Purified;2,6-Dimethyl-4-heptanone, remainder mainly 4,6-dimethyl-2-heptanone, tech., 80%
CAS:108-83-8
MF:C9H18O
MW:142.24
EINECS:203-620-1
Product Categories:
Mol File:108-83-8.mol
2,6-Dimethyl-4-heptanone Structure
2,6-Dimethyl-4-heptanone Chemical Properties
Melting point -46 °C
Boiling point 165-170 °C(lit.)
density 0.808 g/mL at 25 °C(lit.)
vapor density 4.9 (vs air)
vapor pressure 1.7 mm Hg ( 20 °C)
refractive index n20/D 1.412(lit.)
FEMA 3537 | 2,6-DIMETHYL-4-HEPTANONE
Fp 120 °F
storage temp. Store below +30°C.
solubility Miscible with ethanol, ether, carbon tetrachloride, chloroform, benzene and most organic liquids.
form Liquid
Specific Gravity0.810 (20/4℃)
color Clear colorless to slightly yellow
OdorMild; characteristic ketonic.
Odor Typegreen
explosive limit0.8-6.2%, 100°F
Water Solubility 0.05 g/100 mL
JECFA Number302
BRN 1743163
Henry's Law Constant6.36(x 10-4 atm?m3/mol) at 20 °C (approximate - calculated from water solubility and vapor pressure)
Exposure limitsTLV-TWA 150 mg/m3 (25 ppm); IDLH 1000 ppm.
Stability:Stable. Flammable. Incompatible with strong oxidizing agents.
LogP3.71 at 20℃
CAS DataBase Reference108-83-8(CAS DataBase Reference)
NIST Chemistry Reference4-Heptanone, 2,6-dimethyl-(108-83-8)
EPA Substance Registry SystemDiisobutyl ketone (108-83-8)
Safety Information
Hazard Codes Xi
Risk Statements 10-37
Safety Statements 24
RIDADR UN 1157 3/PG 3
WGK Germany 1
RTECS MJ5775000
Autoignition Temperature745 °F
TSCA Yes
HazardClass 3
PackingGroup III
HS Code 29141990
Hazardous Substances Data108-83-8(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 5750 mg/kg LD50 dermal Rabbit 16000 mg/kg
IDLA500 ppm
MSDS Information
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2,6-Dimethyl-4-heptanone Usage And Synthesis
Description2, 6-Dimethyl-4-heptanone, also known as diisobutyl ketone, belongs to the family of ketones, being a flavoring ingredient. It can also be used as the extraction solvent for the determination of ten trace metals (V, Cr, Fe, Co, Ni, Cu, Zn, Mo, Cd, Pb) in aqueous samples with plasma atomic emission spectrometry. Similar logic can also be applied to the measurement of phosphorus using 2, 6-dimethyl-4-heptanone as the extraction agent. It is also an important organic solvent widely used as industrial intermediates.
Chemical Propertiescolourless liquid
Physical propertiesClear, colorless liquid with a mild, sweet, ether-like odor. Odor threshold concentration is 0.11 ppm (quoted, Amoore and Hautala, 1983).
OccurrenceReported found in baked potato and wheaten bread.
Uses2,6-Dimethyl-4-heptanone is used as a coating solvent. It is an active component of mint oil. It acts as a dispersant for organosol type resins. It is involved in the antigerminative treatment of bulbs and tubers. Further, it is used as a solvent for nitrocellulose. In addition to this, it acts as an intermediate in the preparation of inhibitors, active pharmaceutical ingredients and dyes.
UsesDiisobutyl ketone is used as a solvent fornitrocellulose, lacquers, and synthetic resins;in organic syntheses.
UsesDiisobutyl ketone (DIBK) is a transparent liquid with a distinct odor and a high boiling point. It is an heavy-end byproduct of producing MIBK. DIBK is used in many applications such as nitrocellulose lacquers, synthetic resins, coatings and stains, paint strippers, leather finishings, adhesives, printing and coating inks, cleaning and dregreasing, Flavors and fragrances, solvent and re-crystallization aid for pharmaceuticals, mining, and as a chemical intermediate. DIBK has good activity for many synthetic resins including nitrocellulose, rosin esters, phenolics, hydrocarbons, alkyds, polyesters, and acrylics. It is useful as a retarder solvent to improve flow and minimize humidity blushing. The low density and low surface tension of DIBK enables formulators to develop high-solids coatings with low VOC content and excellent flow and leveling properties. DIBK has excellent viscosity reduction for and reduces surface tension in high solid’s coatings. It has good volume-to-weight advantage over other classes of solvents used in coatings. It is a non-HAP (Hazardous Air Pollutant) solvent.
UsesDiisobutyl Ketone is a component of mint oil and L-carvone solutions for fungicidal and antigerminative treatment of bulbs and tubers.
Production MethodsDiisobutyl ketone is produced by hydrogenation of phorone or by metal-catalyzed decomposition of isovaleric acid.It is also a by-product in the manufacture of methyl isobutyl ketone.
DefinitionChEBI: 2-Methyl-4-heptanone is a ketone.
Synthesis Reference(s)Journal of the American Chemical Society, 95, p. 6876, 1973 DOI: 10.1021/ja00801a081
General DescriptionA clear colorless liquid. Flash point 140°F. Less dense than water and insoluble in water. Vapors heavier than air.
Air & Water ReactionsFlammable. Insoluble in water.
Reactivity Profile2,6-Dimethyl-4-heptanone may attack some plastics. 2,6-Dimethyl-4-heptanone reacts with oxidizers.
Health HazardInhalation of vapor causes irritation of nose and throat. Ingestion causes irritation of mouth and stomach. Vaporirritates eyes. Contact with liquid irritates skin.
Health HazardInhalation of the vapors of diisobutyl ketonecan produce irritation of the eyes, nose, andthroat. At 25 ppm its odor was unpleasant, but the irritation effect on humanswas insignificant. At 50 ppm the irritationwas mild. A 7- hour exposure to 125 ppmhad no adverse effect on rats; however, at250 ppm, female rats developed increasedliver and kidney weights. An 8-hour exposure to 2000 ppm was lethal. Ingestion ofthis compound can cause the symptoms ofheadache, dizziness, and dermatitis.
LD50 value, oral (rats): 5.8 g/kg.
Flammability and ExplosibilityNotclassified
Chemical ReactivityReactivity with Water No reaction; Reactivity with Common Materials: May attack some forms of plastics; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
Safety ProfileModerately toxic by ingestion and inhalation. Mddly toxic by skin contact. Human systemic effects by inhalation: headache, nausea or vomiting, and unspecified eye effects. An eye and skin irritant. Narcotic in high concentrations. Flammable liquid when exposed to heat or flame; can react with oxidizing materials. To fight fire, use Con, dry chemical, water spray, mist or fog. When heated to decomposition it emits acrid smoke and fumes. See also KETONES.
Environmental fateBiological. Using the BOD technique to measure biodegradation, the mean 5-d BOD value (mM BOD/mM diisobutyl ketone) and ThOD were 4.86 and 37.4%, respectively (Vaishnav et al., 1987).
Chemical/Physical. Diisobutyl ketone will not hydrolyze because it has no hydrolyzable functional group.
At an influent concentration of 300 mg/L, treatment with GAC resulted in nondetectable concentrations in the effluent. The adsorbability of the carbon used was 60 mg/g carbon (Guisti et al., 1974).
Waste DisposalIncineration, molten metal salt destruction.
ReferencesBone, K. M., and W. D. Hibbert. "Solvent extraction with ammonium pyrrolidinedithiocarbamate and 2,6-dimethyl-4-heptanone for the determination of trace metals in effluents and natural waters." Analytica Chimica Acta 107.JUN(1979):219-229.
Miyazaki, Akira, A. Kimura, and Y. Umezaki. "Determination of ng ml-1 levels of phosphorus in waters by diisobutyl ketone extraction and inductively coupled plasma atomic emission spectrometry." Analytica Chimica Acta 127.96(1981):93-101.
Zhang, Fagen, et al. "Comparative metabolism and pharmacokinetics of diisobutyl ketone and diisobutyl carbinol in male SD rats." Toxicology Letters 232.1(2015):175-181.
Dacthal DIISOBUTYLALUMINUM CHLORIDE Diisobutylcarbinol ISOBUTYLTRICHLOROSILANE N,N-Dimethylformamide Diisobutylaluminium hydride ETHANE Triisobutylaluminium Benzophenone Dimethyl fumarate Dimethyl sulfoxide Dimethyl disulfide 4-Methyl-2-pentanone Dimethyl ether 2,6-Dimethyl-4-heptanone Dimethyl carbonate Dimethyl phthalate Dimethyl sulfate

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