109916
4-Methyl-2-pentanol
98%
Synonym(s):
3-MIC, Isobutyl methyl carbinol, MAOH, MIBC
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About This Item
Linear Formula:
(CH3)2CHCH2CH(OH)CH3
CAS Number:
Molecular Weight:
102.17
Beilstein:
1098268
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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vapor density
3.5 (vs air)
vapor pressure
3.7 mmHg ( 20 °C)
Assay
98%
expl. lim.
5.5 %
refractive index
n20/D 1.410 (lit.)
bp
132 °C (lit.)
mp
−90 °C (lit.)
density
0.802 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
CC(C)CC(C)O
InChI
1S/C6H14O/c1-5(2)4-6(3)7/h5-7H,4H2,1-3H3
InChI key
WVYWICLMDOOCFB-UHFFFAOYSA-N
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General description
4-Methyl-2-pentanol is a member of the fragrance structural group, branched chain saturated alcohol.
Application
4-Methyl-2-pentanol has been used as an internal standard in the characterization of volatile fraction of monovarietal wines.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
105.8 °F - closed cup
Flash Point(C)
41 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Hongxiang Gong et al.
The journal of physical chemistry. B, 116(37), 11482-11487 (2012-08-24)
The dielectric strength of the Debye relaxation in the binary mixtures of two isomeric monohydroxy alcohols, 2-ethyl-1-butanol (2E1B) and 4-methyl-2-pentanol (4M2P), is studied at low temperature near glass transition. Enhanced dielectric strength is exhibited in the mixtures, remarkably different from
Xiaofeng Yue et al.
Food research international (Ottawa, Ont.), 131, 109028-109028 (2020-04-06)
Monoterpenes contribute to the varietal aromas of grapes and wines. We determined the effects of cluster zone leaf removal on the monoterpene profiles of Sauvignon Blanc grape berries and wines, and on the expression of key genes in the terpenoid
Characterisation of volatile fraction of monovarietal wines: influence of winemaking practices.
Analytica Chimica Acta, 563(1-2), 165-172 (2006)
Laura Quintana Gomez et al.
ChemSusChem, 13(3), 647-658 (2019-12-04)
The synthesis of oxygenate products, including cyclic ketones and phenol, from carbon dioxide and water in the absence of gas-phase hydrogen has been demonstrated. The reaction takes place in subcritical conditions at 300 °C and pressure at room temperature of 25 barg.
Chi M Phan et al.
The journal of physical chemistry. B, 116(3), 980-986 (2011-12-17)
The surface potential (ΔV) and surface tension (γ) of MIBC (methyl isobutyl carbinol) were measured on the subphase of pure water and electrolyte solutions (NaCl at 0.02 and 2 M). In contrast to ionic surfactants, it was found that surface
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