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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)

Quality Level

100

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)
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)
Carmen M Dominguez et al.
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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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