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Sigma-Aldrich

2-Methyl-2-hexanol

97%

Synonym(s):

1,1-Dimethyl-1-pentanol

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About This Item

Linear Formula:
CH3(CH2)3C(CH3)2OH
CAS Number:
Molecular Weight:
116.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.417 (lit.)

bp

141-142 °C (lit.)

density

0.812 g/mL at 25 °C (lit.)

SMILES string

CCCCC(C)(C)O

InChI

1S/C7H16O/c1-4-5-6-7(2,3)8/h8H,4-6H2,1-3H3

InChI key

KRIMXCDMVRMCTC-UHFFFAOYSA-N

Related Categories

Application

2-Methyl-2-hexanol was used in the preparation of esterified phenol. It is used to study the effect of organic solvent on the equillibrium of lipase-catalyzed esterification of glycerol and decanoic acid.
2-Methyl-2-hexanol was used to study the mass accommodation coefficient (α) on 1-methylnaphthalene as a function of temperature (267 K to 298 K) for gas-phase of the product.

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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An achiral, anticlinic-promoting, smectic liquid crystal architecture.
Thisayukta J and Samulski ET.
Journal of Materials Chemistry, 14(10), 1554-1559 (2004)
H Z Zhang et al.
The journal of physical chemistry. A, 109(17), 3941-3949 (2006-07-13)
Organic compounds are a significant component of tropospheric aerosols. In the present study, 1-methylnaphthalene was selected as a surrogate for aromatic hydrocarbons (PAHs) found in tropospheric aerosols. Mass accommodation coefficients (alpha) on 1-methylnaphthalene were determined as a function of temperature
A E Janseen et al.
Biotechnology and bioengineering, 41(1), 95-103 (1993-01-05)
The effect of organic solvents on the equilibrium position of lipase-catalyzed esterification of glycerol and decanoic acid has been investigated. The reaction is carried out in an aqueous-organic two-phase system. In polar solvents, high mole fractions of monoacylglycerol and low

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