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110388

Sigma-Aldrich

Butylcyclohexane

≥99%

Synonym(s):

1-Cyclohexylbutane

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About This Item

Linear Formula:
CH3(CH2)3C6H11
CAS Number:
1678-93-9
Molecular Weight:
140.27
Beilstein:
1900631
EC Number:
216-837-1
MDL number:
MFCD00001530
UNSPSC Code:
12352100
PubChem Substance ID:
24846981
NACRES:
NA.22

vapor pressure

2.9 mmHg ( 37.7 °C)

Assay

≥99%

autoignition temp.

475 °F

refractive index

n20/D 1.441 (lit.)

bp

178-180 °C (lit.)

mp

−78 °C (lit.)

density

0.818 g/mL at 25 °C (lit.)

SMILES string

CCCCC1CCCCC1

InChI

1S/C10H20/c1-2-3-7-10-8-5-4-6-9-10/h10H,2-9H2,1H3

InChI key

GGBJHURWWWLEQH-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

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General description

Butylcyclohexane reacts with n-butylbenzene by free-radical mechanism to form 1-methylcyclohexene and cyclohexane. Butylcyclohexane, when photo-oxidized by solar light on synthetic seawater, forms cyclohexanone.

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

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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Thermal Decomposition of Jet Fuel Model Compounds under Near-Critical and Supercritical Conditions. 1. n-Butylbenzene and n-Butylcyclohexane.
Industrial & Engineering Chemistry Research, 37(12), 4591-4600 (1998)
Carmen M Dominguez et al.
Journal of environmental management, 261, 110240-110240 (2020-03-10)
Chlorinated pesticides were extensively produced in the XX century, generating high amounts of toxic wastes often dumped in the surroundings of the production sites, resulting in hot points of soil and groundwater pollution worldwide. This is the case of Bailín
Photosensitized oxidation of n-butylcyclohexane as a model for photochemical degradation of n-alkylcyclohexanes in seawater.
Journal of Photochemistry and Photobiology A: Chemistry, 46(3), 347-355 (1989)
Emre Seyyal et al.
Analytica chimica acta, 964, 96-111 (2017-03-30)
Principles of sol-gel chemistry were utilized to create silica- and germania-based dual-ligand surface-bonded sol-gel coatings providing enhanced performance in capillary microextraction (CME) through a combination of ligand superhydrophobicity and π-π interaction. These organic-inorganic hybrid coatings were prepared using sol-gel precursors
Jae-Man Park et al.
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Existing gels are mostly polar, whose nature limits their role in soft devices. The intermolecular interactions of nonpolar polymer-liquid system are typically weak, which makes the gel brittle. Here we report highly soft and transparent nonpolar organogels. Even though their
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