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4-Methyl-2-pentanone

CAS No.
108-10-1
Chemical Name:
4-Methyl-2-pentanone
Synonyms
MIBK;METHYL ISOBUTYL KETONE;4-METHYLPENTAN-2-ONE;MIK;MIKB;Hexon;ISOBUTYL METHYL KETONE;HEXONE;4-Methyl-2-pen;ISOPROPYLACETONE
CBNumber:
CB8691781
Molecular Formula:
C6H12O
Lewis structure
c6h12o lewis structure
Molecular Weight:
100.16
MDL Number:
MFCD00008938
MOL File:
108-10-1.mol
MSDS File:
SDS
Last updated:2024-10-30 18:52:02

4-Methyl-2-pentanone Properties

Melting point -80 °C (lit.)
Boiling point 117-118 °C
Density 0.801 g/mL at 25 °C (lit.)
vapor density 3.5 (vs air)
vapor pressure 15 mm Hg ( 20 °C)
refractive index n20/D 1.395(lit.)
FEMA 2731 | 4-METHYL-2-PENTANONE
Flash point 56 °F
storage temp. Store at +5°C to +30°C.
solubility water: soluble20g/L, soluble in alcohol, miscible with oils. Soluble in Propylene glycol and Glycerin.
form Liquid
color APHA: ≤15
Specific Gravity 0.80
Odor Pleasant; mild, characteristic; sharp; non-residual; ketonic.
Odor Threshold 0.17ppm
explosive limit 1.2-8%, 93°F
Odor Type green
Water Solubility 17 g/L (20 ºC)
λmax λ: 335 nm Amax: 1.00
λ: 340 nm Amax: 0.50
λ: 360 nm Amax: 0.15
λ: 380 nm Amax: 0.02
λ: 400 nm Amax: 0.01
Merck 14,5207
JECFA Number 301
BRN 605399
Henry's Law Constant 2.56 at 25 °C (batch stripping method-GC, Kim et al., 2000)
Exposure limits TLV-TWA 205 mg/m3 (50 ppm); STEL 300 mg/m3 (75 ppm) (ACGIH); IDLH 3000 ppm (NIOSH).
Dielectric constant 13.0(Ambient)
Stability Volatile
LogP 1.3-1.9 at 20℃
Substances Added to Food (formerly EAFUS) METHYL ISOBUTYL KETONE
FDA 21 CFR 172.515; 175.105; 177.1650
CAS DataBase Reference 108-10-1(CAS DataBase Reference)
EWG's Food Scores 5-8
FDA UNII U5T7B88CNP
Proposition 65 List Methyl Isobutyl Ketone (MIBK)
NIST Chemistry Reference Methyl isobutyl ketone(108-10-1)
IARC 2B (Vol. 101) 2013
EPA Substance Registry System Methyl isobutyl ketone (108-10-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H319-H332-H335
Precautionary statements  P210-P233-P240-P241-P304+P340+P312-P305+P351+P338
Hazard Codes  F,Xn,T
Risk Statements  11-20-36/37-66-39/23/24/25-23/24/25
Safety Statements  9-16-29-45-36/37-7
RIDADR  UN 1245 3/PG 2
OEB A
OEL TWA: 50 ppm (205 mg/m3), STEL: 75 ppm (300 mg/m3)
WGK Germany  1
RTECS  SA9275000
Autoignition Temperature 840 °F
TSCA  Yes
HS Code  2914 13 00
HazardClass  3
PackingGroup  II
Toxicity LD50 orally in rats: 2.08 g/kg (Smyth)
IDLA 500 ppm
NFPA 704
3
2 1

4-Methyl-2-pentanone price More Price(56)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W273104 4-Methyl-2-pentanone ≥99%, FCC 108-10-1 1kg $80.9 2024-03-01 Buy
Sigma-Aldrich W273104 4-Methyl-2-pentanone ≥99%, FCC 108-10-1 8kg $268 2024-03-01 Buy
Sigma-Aldrich MX1301 4-Methyl-2-pentanone OmniSolv? 108-10-1 4L $448 2024-03-01 Buy
Sigma-Aldrich 8.20820 Isobutyl methyl ketone EMPLURA? 108-10-1 2.5L $183 2024-03-01 Buy
Sigma-Aldrich 8.20820 Isobutyl methyl ketone EMPLURA? 108-10-1 10L $597 2024-03-01 Buy
Product number Packaging Price Buy
W273104 1kg $80.9 Buy
W273104 8kg $268 Buy
MX1301 4L $448 Buy
8.20820 2.5L $183 Buy
8.20820 10L $597 Buy

4-Methyl-2-pentanone Chemical Properties,Uses,Production

Description

4-Methyl-2-pentanone has a pleasant odor. May be prepared by hydrogenation of mesityl oxide over Ni at 160 - 190°C; also by oxidation of methyl isobutyl carbinol.

Chemical Properties

4-Methyl-2-pentanone has a fruity, ethereal, spicy (on dilution) odor.

Chemical Properties

4-Methyl-2-pentanone, also known as Methyl isobutyl ketone (MIBK), is a colorless liquid with a pleasant, sweet, fruity odor. The odor threshold can be as low as 0.10 ppm. It is 2% soluble in water by weight and with several other organic solvents. The lower explosive limit is 1.2% and the upper explosive limit is 8.0% at 200 °F. Methyl isobutyl ketone may be incompatible with strong oxidizers and potassium tert-butoxide.

Physical properties

Clear, colorless, watery liquid with a mild, pleasant odor. Odor threshold concentration is 47 ppbv (Leonardos et al., 1969). Experimentally determined detection and recognition odor threshold concentrations were 400 μg/m3 (100 ppbv) and 1.1 mg/m3 (270 ppbv), respectively (Hellman and Small, 1974).

Occurrence

Reported found in orange and lemon juice, grape; vinegar, baked potato, papaya, ginger, wheat bread, cheeses, milk, cooked egg, roast chicken, cooked beef, lamb fat, pork liver, hop oil, beer, cognac, coffee, tea, plumcot, plum brandy, mushroom, trassi, sesame seed, buckwheat, wort, elder flower, Bourbon vanilla, clary and red sage, crab, clam and Chinese quince.

Uses

In paints, glues, and cleaning agents; used in the plastic and petrol industries

Uses

MIBK is used as a solvent for gums, resins,nitrocellulose and cellulose ethers, and various fats, oils, and waxes.

Uses

Methyl isobutyl ketone (hexone, isobutyl methyl ketone, 4-methyl-2-pentanone) is an organic solvent similar in structure and use to methyl butyl ketone. In addition to its use as a solvent for paints, lacquers, and varnishes, methyl isobutyl ketone is used in extraction processes and as a denaturant for rubbing alcohol. Methyl isobutyl ketone is also used as a synthetic flavoring in some varieties of rum, candy, and cheese. Unlike methyl butyl ketone, methyl isobutyl ketone has not been found to occur naturally.

Definition

ChEBI: Methyl isobutyl ketone is a ketone.

Production Methods

Methyl isobutyl ketone can be manufactured by two processes . The first is a mixed ketone process where MiBK, diisobutyl ketone, and acetone are coproduced in a single reaction using isopropanol as a starting material. The second method is used to produce the majority of MiBK and involves a three-step reaction sequence in which diacetone alcohol and mesityl oxide are formed as intermediates.

Preparation

By hydrogenation of mesityl oxide over Ni at 160 to 190°C; also by oxidation of methyl isobutyl carbinol.

Aroma threshold values

Detection: 240 to 640 ppb

Taste threshold values

Taste characteristics at 25 ppm: sweet, ethereal, banana and fruity with dairy nuances

Synthesis Reference(s)

Journal of the American Chemical Society, 100, p. 5437, 1978 DOI: 10.1021/ja00485a031
Tetrahedron Letters, 36, p. 2285, 1995 DOI: 10.1016/0040-4039(95)00191-E
Tetrahedron, 37, p. 3073, 1981 DOI: 10.1016/S0040-4020(01)98839-8

General Description

A clear colorless liquid with a pleasant odor. Flash point 73°F. Less dense than water. Vapors heavier than air.

Air & Water Reactions

Highly flammable. 4-Methyl-2-pentanone is sensitive to air (may form explosive peroxides). Slightly soluble in water.

Reactivity Profile

4-Methyl-2-pentanone is incompatible with caustic soda and other strong alkalis, hydrochloric acid, sulfuric acid and other strong inorganic acids, amines and oxidizing agents such as hydrogen peroxide, nitric acid, perchloric acid and chromium trioxide. 4-Methyl-2-pentanone reacts violently with potassium tert-butoxide. 4-Methyl-2-pentanone reacts vigorously with reducing materials. .

Hazard

Flammable, dangerous fire risk, explosivelimits in air 1.4–7.5%. Avoid ingestion and inhala-tion. Upper respiratory tract irritant, dizziness, andheadache. Possible carcinogen.

Health Hazard

Vapor causes irritation of eyes and nose; high concentrations cause anesthesia and depression. Liquid dries out skin and may cause dermatitis; irritates eyes but does not injure them.

Health Hazard

MIBK exhibits low to moderate toxicity.It is more toxic than acetone. Exposureto 200 ppm can cause irritation of theeyes, mucous membranes, and skin. Prolonged skin contact can leach out fat fromthe skin. Exposure to high concentrationscan cause nausea, headache, and narcosis. Animal studies indicate that this compound could probably cause kidney damage,with symptoms of a heavier kidney, higherkidney-to-body weight ratio, and tubularnecrosis. An increase in liver weight wasnoted, too, associated with its exposure inanimal subjects. In male rats the effect wasobserved at 2000 ppm on 2 weeks’ exposure(6 hours/day) (Phillips et al. 1987). Otherthan for the male rat kidney effect, the levelsup to 1000 ppm for 14 weeks had no significant toxicological effect. In another study,exposure to 3000 ppm in rats and mice wasfound to cause increased liver and kidneyweights, decrease in food consumption, incidence of dead fetuses, and reduced fetal bodyweight (Tyl et al. 1987).
Ingestion of MIBK can result in narcosis and coma. A genetic toxicology studyof MIBK showed a negative response inthe bacterial mutation assays and the yeastmitotic gene conversion assay (Brooks et al.1988).
LD50 value, oral (rat): 2080 mg/kg
LD50 value, intraperitoneal (rat): 400 mg/kg.

Flammability and Explosibility

Highly flammable

Chemical Reactivity

Reactivity 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.

Potential Exposure

MIBK is used as a solvent; a denaturant; and as an extractant; in the manufacture of methyl amyl alcohol; as a solvent in paints, varnishes, and lacquers; as an alcohol denaturant; as a solvent in uranium extraction from fission products.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.

Carcinogenicity

The National Toxicology Program conducted cancer bioassays by exposing groups of 50 male and 50 female F344 rats and B6C3F1 mice to MiBK vapor at 0, 450, 900, or 1800 ppm 6h/day, 5 days/ week for 2 years. Survival and body weight gain were decreased in male rats at 1800 ppm. Body weight gain was also decreased in male rats at 900 and in female mice at 1800ppm. A higher incidence of mineralization of the renal papilla was observed in male rats at all MiBK exposure levels. Chronic progressive nephropathy (CPN) and the incidences of adenoma and adenoma or carcinoma (combined) were increased for the male 1800 ppm exposure group. The severity of CPN and renal tubular hyperplasia was increased in all male rat exposure groups. An uncertain increase in mononuclear cell leukemia, adrenal medulla hyperplasia, and a positive trend for increases in benign or malignant pheochromocytomas (combined) were reported for the 1800 ppm male group. The NTP considered that there was some evidence of carcinogenic activity in male rats based on increased incidences of renal tubule neoplasms.
None of the rodent bioassay results were considered clear evidence of carcinogenicity by NTP.

Environmental Fate

Biological. Bridié et al. (1979) reported BOD and COD values of 2.06 and 2.16 g/g using filtered effluent from a biological sanitary waste treatment plant. These values were determined using a standard dilution method at 20 °C and stirred for a period of 5 d. Heukelekian and Rand (1955) reported a 5-d BOD value of 1.51 g/g which is 55.5% of the ThOD value of 2.72 g/g.
Photolytic. When synthetic air containing gaseous nitrous acid and 4-methyl-2-pentanone was exposed to artificial sunlight (λ = 300–450 nm), photooxidation products identified were acetone, peroxyacetal nitrate, and methyl nitrate (Cox et al., 1980). In a subsequent experiment, the OHinitiated photooxidation of 4-methyl-2-pentanone in a smog chamber produced acetone (90% yield) and peroxyacetal nitrate (Cox et al., 1981). Irradiation at 3130 ? resulted in the formation of acetone, propyldiene, and free radicals (Calvert and Pitts, 1966).
Second-order photooxidation rate constants for the reaction of 4-methyl-2-butanone and OH radicals in the atmosphere are 1.4 x 10-10, 1.42 x 10-10, and 1.32 x 10-10 cm3/molecule?sec at 295, 299, and 300 K, respectively (Atkinson, 1985). The atmospheric lifetime was estimated to be 1–5 d (Kelly et al., 1994).
Photolytic. Cox et al. (1980) reported a rate constant of 1.24 x 10-11 cm3/molecule?sec for the reaction of gaseous 4-methyl-2-pentanone with OH radicals based on a value of 8 x 10-12 cm3/molecule?sec for the reaction of ethylene with OH radicals.
Chemical/Physical. 4-Methyl-2-pentanone will not hydrolyze in water because it does not contain a hydrolyzable functional group (Kollig, 1993).

storage

Color Code—Red: Flammability Hazard: Store ina flammable liquid storage area or approved cabinet awayfrom ignition sources and corrosive and reactive materials.Prior to working with this chemical you should be trainedon its proper handling and storage. Before entering confinedspace where this chemical may be present, check to makesure that an explosive concentration does not exist. Methylisobutyl ketone must be stored to avoid contact with strongoxidizers because violent reactions occur. Store in tightlyclosed containers in a cool, well-ventilated area away fromheat, sparks, and flames. Sources of ignition, such as smoking and open flames, are prohibited where methyl isobutylketone is used, handled, or stored in a manner that couldcrate a potential fire or explosion hazard. Metal containersinvolving the transfer of 5 gallons or more of methyl isobutyl ketone should be grounded and bonded. Drums must beequipped with self-closing valves, pressure vacuum bungs,and flame arresters. Use only nonsparking tools and equipment, especially when opening and closing containers ofmethyl isobutyl ketone.

Shipping

UN1245 Methyl isobutyl ketone, Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

Reflux the ketone with a little KMnO4, wash it with aqueous NaHCO3, dry with CaSO4 and distil it. Acidic impurities are removed by passage through a small column of activated alumina. [Beilstein 1 IV 3305.]

Incompatibilities

Able to form unstable and explosive peroxides on contact with air. Reacts violently with strong oxidizers, potassium tert-butoxide; strong acids; aliphatic amines; reducing agents

Waste Disposal

Consult 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.

2035-08-7
108-10-1
Synthesis of 4-Methyl-2-pentanone from 2-Methyl-2-(2-methylpropyl)-1,3-dioxolane
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View Lastest Price from 4-Methyl-2-pentanone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
MIBK / 4-Methyl-2-pentanone pictures 2024-10-30 MIBK / 4-Methyl-2-pentanone
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US $1.00 / KG 1KG 99% 10 mt Hebei Weibang Biotechnology Co., Ltd
4-Methyl-2-pentanone pictures 2024-10-29 4-Methyl-2-pentanone
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US $0.00 / kg 20kg 99% 20 tons Qingdao RENAS Polymer Material Co., Ltd.
Methyl Isobutyl Ketoe  pictures 2024-10-11 Methyl Isobutyl Ketoe
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US $2.70 / kg 10kg 99% 10000kg Hebei Chuanghai Biotechnology Co,.LTD
Methyl Isobutyl Ketone, Reagent Isobutyl methyl ketone, Isopropylacetone, Methyl isobutyl ketone FEMA 2731 Methyl #niso-butyl ketone 4-METHYL-2-PENTANONE, 99+% 4-METHYL-2-PENTANONE, 1X1ML, MEOH, 200UG /ML 4-METHYL-2-PENTANONE REAGENTPLUS(TM) & 4-METHYL-2-PENTANONE, ACS 4-METHYL-2-PENTANONE, 99.5+%, HPLC GRADE METHYL-ISO-BUTYLKETONE FOR EXTRAC-TION ANALYSIS, REAG. ACS, REAG. PH. 4-METHYL-2-PENTANONE, 1X1ML, MEOH, 5000U G/ML 4-METHYL-2-PENTANONE, 1000MG, NEAT METHYL-ISO-BUTYL KETONE OEKANAL 4-METHYL-2-PENTANONE, 99+%, SPECTROPHOTO -METRIC GRADE 4-Methyl-2-pentanone, HPLC, 99.0% min. 4-Methyl-2-pentanone, ACS, 98.5% min. 4-Methyl-2-pentanone4x1L 4-Methyl-2-pentanone4x4L Isobutyl methyl ketone for extraction analysis EMSURE ACS,Reag. Ph Eur. Isobutyl methyl ketone EMPLURA 4-METHYL-2-PENTANONE >=98.5% A.C.S. R& 4-METHYL-2-PENTANONE 99+% FCC 4-METHYL-2-PENTANONE, >=98.5%, A.C.S. REAGENT Methyl-Iso-ButylKetoneGr MethylIsobutylKetoneAcs Methyl-Iso-ButylKetone(Iso-ButylMethylKetone) MethylBlueForMicroscopy 2-Methyl-4-pentanal 2-Methyl-4-Pentanone 2-Methylpropyl methyl ketone 2-methylpropylmethylketone Metyloizobutyloketon metyloizobutyloketon(polish) Rcra waste number U161 rcrawastenumberu161 Shell mibk shellmibk 4-METHYL-2-PENTANONE 4-Methyl-2-pentnone 4-Methyl-2-pentanone, 99.5% 4-methyl-2-pentanone solution 4-methyl-2-pentanone, hplc grade METHYLISOBUTYLKETONE,HPLCGRADE METHYLISOBUTYLKETONE,OMNISOLV METHYLISOBUTYLKETONE,REAGENT,ACS ISOPROPYLACETONE, 4-METHYL-2-PENTANONE, METHYL ISOBUTYL KETONE Methyl isobutyl ketone Odor Standard 4-Methyl-2-pentanone (I) Methyl isobutyl ketone (I) 4-Methyl-2-pentanone, HPLC Grade, 99+% 4-Methyl-2-pentanone, ACS, 98.5+% METHYL ISOBUTYL KETONE, NATURAL 2-Methylpentan-2-one 4-Methyl-2-pentanone, 99+%, electronic use grade, residue free 4-Methyl-2-pentanone, for analysis ACS 1LT 4-Methyl-2-pentanone, for analysis, 99.5% 1LT 4-Methyl-2-pentanone, 99.50% 4-Methyl-2-pentanone, electronic use grade, residue free