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Sigma-Aldrich

Cyclohexane

suitable for HPLC, ≥99.9%

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About This Item

Empirical Formula (Hill Notation):
C6H12
CAS Number:
110-82-7
Molecular Weight:
84.16
Beilstein/REAXYS Number:
1900225
EC Number:
203-806-2
MDL number:
MFCD00003814
UNSPSC Code:
12190000
PubChem Substance ID:
329760021
NACRES:
NA.06

vapor density

2.9 (vs air)

Quality Level

100

vapor pressure

168.8 mmHg ( 37.7 °C)
77 mmHg ( 20 °C)

assay

≥99.9%

form

liquid

autoignition temp.

500 °F

expl. lim.

9 %

technique(s)

HPLC: suitable

impurities

≤1.0 ppb Fluorescence (quinine) at 365 nm
<0.01% water

evapn. residue

<0.0001%

halogenated residue

<10 ng/L (as heptachlor epoxide)

refractive index

n20/D 1.426 (lit.)

bp

80.7 °C (lit.)

mp

4-7 °C (lit.)

density

0.779 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 200 nm Amax: 1.00
λ: 225 nm Amax: 0.17
λ: 250 nm Amax: 0.02
λ: 300-400 nm Amax: 0.005

application(s)

food and beverages

SMILES string

C1CCCCC1

InChI

1S/C6H12/c1-2-4-6-5-3-1/h1-6H2

InChI key

XDTMQSROBMDMFD-UHFFFAOYSA-N

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General description

Cyclohexane, a cycloalkane, is a combustible liquid with petrol like odor. It can be synthesized by hydrogenation of benzene in the presence of nickel or platinum catalysts. Cyclohexane is the precursor for the synthesis of polyamides. Cyclohexane ring forms the structural unit of many naturally occurring products. The conformational changes of cyclohexane have been investigated over the temperature range of 100-1200°C. Conversion of cyclohexane to cyclohexanol and cyclohexanone, via oxidation in the presence of Cu-nanoclusters anchored on nanocrystalline Cr2O3 has been reported.

Application

Suitable for HPLC, spectrophotometry, environmental testing

Recommended products

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signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

wgk_germany

WGK 2

Certificates of Analysis (COA)

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Room temperature selective oxidation of cyclohexane over Cu-nanoclusters supported on nanocrystalline Cr2O3.
Sarkar B, et al.
Green Chemistry, 14(9), 2600-2606 (2012)
Conformational transitions in cyclohexane and benzol.
Melker AI, et al.
SPIE Proc., 5127 (2003)
Eagleson M.
Concise Encyclopedia Chemistry, 296-296 (1994)
Sandra Yucra et al.
Environmental health : a global access science source, 7, 59-59 (2008-11-19)
Organophosphates are broad class of chemicals widely used as pesticides throughout the world. We performed a cross-sectional study of associations between dialkylphosphate metabolites of organophosphates and semen quality among pesticide applicators in Majes (Arequipa), Peru. Thirty-one men exposed to organophosphate
Amanda L Pitts et al.
Journal of the American Chemical Society, 136(24), 8614-8625 (2014-05-16)
Carbon-hydrogen bond activation reactions of four cycloalkanes (C5H10, C6H12, C7H14, and C8H16) by the Cp'Rh(CO) fragments (Cp' = η(5)-C5H5 (Cp) or η(5)-C5Me5 (Cp*)) were modeled theoretically by combining density functional and coupled cluster theories, and their reaction rates were measured
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