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Cyclohexanone

Selectophore™, ≥99.5%

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About This Item

Linear Formula:
C6H10(=O)
CAS Number:
108-94-1
Molecular Weight:
98.14
Beilstein/REAXYS Number:
385735
EC Number:
203-631-1
MDL number:
MFCD00001625
UNSPSC Code:
26111700
PubChem Substance ID:
329753314
NACRES:
NB.61

grade

for ion-selective electrodes

Quality Level

200

vapor density

3.4 (vs air)

vapor pressure

3.4 mmHg ( 20 °C)

description

solvent for preparation of membranes

product line

Selectophore™

assay

≥99.5% (GC)
≥99.5%

autoignition temp.

788 °F

expl. lim.

1.1 %, 100 °F
9.4 %

impurities

≤0.1% water

refractive index

n20/D 1.450 (lit.)
n20/D 1.451

bp

155 °C (lit.)

mp

−47 °C (lit.)

density

0.947 g/mL at 25 °C (lit.)

SMILES string

O=C1CCCCC1

InChI

1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2

InChI key

JHIVVAPYMSGYDF-UHFFFAOYSA-N

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General description

Cyclohexanone is an industrially important reagent. It is also a major intermediate in the synthesis of nylon.
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Other Notes

Solvent for preparing ion-selective membranes for microelectrodes; it is less volatile than other solvents

Legal Information

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 1

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Selective phenol hydrogenation to cyclohexanone over a dual supported Pd-Lewis acid catalyst.
Liu H
Science, 326 (5957), 1250-1252 (2009)
Effect of hydrogen sulphide on the hydrodeoxygenation of aromatic and aliphatic oxygenates on sulphided catalysts.
Senol OI
J. Mol. Catal. A: Chem., 277 (1), 107-112 (2007)
U. Schaller et al.
Pflugers Archiv : European Journal of Physiology (1993)
Alakananda Hajra et al.
Organic letters, 14(21), 5488-5491 (2012-10-18)
Dehydrogenative aromatization of cyclohexanone imines to arylamines has been achieved using a palladium catalyst under aerobic conditions. The reaction is applicable to a variety of imines that are either preformed or generated in situ from cyclohexanone derivatives and aryl or
Brahm J Yachnin et al.
Journal of the American Chemical Society, 134(18), 7788-7795 (2012-04-18)
The Baeyer-Villiger monooxygenases (BVMOs) are a family of bacterial flavoproteins that catalyze the synthetically useful Baeyer-Villiger oxidation reaction. This involves the conversion of ketones into esters or cyclic ketones into lactones by introducing an oxygen atom adjacent to the carbonyl
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