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02474

Supelco

4-Methyl-2-pentanone

analytical standard

Synonym(s):

Isobutyl methyl ketone, Isopropylacetone, MIBK, Methyl isobutyl ketone

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About This Item

Linear Formula:
(CH3)2CHCH2COCH3
CAS Number:
Molecular Weight:
100.16
Beilstein:
605399
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor density

3.5 (vs air)

Assay

≥99.7% (GC)

autoignition temp.

840 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

1.2-8 %, 93 °F

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.395 (lit.)
n20/D 1.396

bp

117-118 °C

mp

−80 °C (lit.)

density

0.801 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

CC(C)CC(C)=O

InChI

1S/C6H12O/c1-5(2)4-6(3)7/h5H,4H2,1-3H3

InChI key

NTIZESTWPVYFNL-UHFFFAOYSA-N

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General description

4-Methyl-2-pentanone (Methyl isobutyl ketone (MBK)) is an organic solvent widely used in various industrial applications, and exists as a clear colorless liquid with a pleasant odor. It is occasionally found as a volatile component of urine making it a biological marker of occupational exposure to this solvent. It is used as is used as a solvent for gums, resins, paints, varnishes, lacquers, and nitrocellulose.

Application

MBK may have been used as internal standard in GC/MS analysis for determining off-flavors in milk extracted using solid-phase microextraction, mass spectrometry, and multivariate analysis (SPME-MS-MVA). 4-Methyl-2-pentanone may be used as an analytical reference standard for the quantification of the analyte in hydro-alcoholic matrices using high-performance liquid chromatography with diode array detection.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

recommended

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Carc. 2 Inhalation - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

57.2 °F - closed cup

Flash Point(C)

14 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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SPME-MS-MVA as an electronic nose for the study of off-flavors in milk.
Marsili RT
Journal of Agricultural and Food Chemistry, 47(2), 648-654 (1999)
HPLC-DAD analysis of ketones as their 2, 4-dinitrophenylhydrazones in Brazilian sugar-cane spirits and rum
Cardoso D, et al.
J. Food Compos. Anal., 16(5), 563-573 (2003)
H J Shim et al.
Journal of chromatography. B, Biomedical applications, 656(2), 407-414 (1994-06-17)
A high-performance liquid chromatographic method was developed for the simultaneous determination of a new anthracycline, DA-125 (I), and its metabolites (M1, M2, M3, and M4) in rat plasma and urine using fluorescein as an internal standard. Compound I, a prodrug
Sebastian L Riedel et al.
Biotechnology and bioengineering, 110(2), 461-470 (2012-08-21)
Reduced downstream costs, together with high purity recovery of polyhydroxyalkanoate (PHA), will accelerate the commercialization of high quality PHA-based products. In this work, a process was designed for effective recovery of the copolymer poly(hydroxybutyrate-co-hydroxyhexanoate) (P(HB-co-HHx)) containing high levels of HHx
Kieron J Doick et al.
Environmental science & technology, 39(17), 6575-6583 (2005-09-30)
Organic matter is considered to be the single most importantfactor limiting availability and mobility of persistent organic pollutants (POPs) in soil. This study aimed to characterize the distribution of 14C-PCB (congeners 28 and 52) and 14C-PAH (fluoranthene and benzo[a]pyrene) residues

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