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Merck
CN

29135

Supelco

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:
385735
EC Number:
203-631-1
MDL number:
MFCD00001625
UNSPSC Code:
26111700
PubChem Substance ID:
329753314
NACRES:
NB.61

Key Documents

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vapor density

3.4 (vs air)

Quality Level

200

vapor pressure

3.4 mmHg ( 20 °C)

description

for ion-selective electrodes
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.
Visit our Sensor Applications portal to learn more.

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

Signal Word

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

111.2 °F - closed cup

Flash Point(C)

44 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCL8197
BCCL5932
BCCL3072
BCCM3437
BCCK0862

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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)
Selective phenol hydrogenation to cyclohexanone over a dual supported Pd-Lewis acid catalyst.
Liu H
Science, 326 (5957), 1250-1252 (2009)
Raju Adepu et al.
Organic & biomolecular chemistry, 10(29), 5554-5569 (2012-06-20)
Novel thieno[2,3-d]pyrimidines containing a cyclohexane ring fused with a six- or five-membered heterocyclic moiety along with a benzylic nitrile were designed as potential inhibitors of PDE4. Expeditious synthesis of these compounds was carried out via a multi-step sequence consisting of
Viktória Fábos et al.
Chemistry, an Asian journal, 7(11), 2638-2643 (2012-09-07)
The processing of renewable feedstocks to platform chemicals and, to a lesser degree, fuels is a key part of sustainable development. In particular, the combination of lignocellulosic biomass with hydrothermal upgrading (HTU), using high temperature and pressure water (HTPW), is
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