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Merck
CN

V800139

Cyclohexanone

AR, ≥99.5%

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About This Item

Linear Formula:
C6H10(=O)
CAS Number:
108-94-1
Molecular Weight:
98.14
EC Number:
203-631-1
UNSPSC Code:
12191502
PubChem Substance ID:
329829187
Beilstein/REAXYS Number:
385735
MDL number:
MFCD00001625
Assay:
≥99.5%
Grade:
AR
Bp:
155 °C (lit.)
Vapor pressure:
3.4 mmHg ( 20 °C)

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InChI key

JHIVVAPYMSGYDF-UHFFFAOYSA-N

InChI

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

SMILES string

O=C1CCCCC1

grade

AR

vapor density

3.4 (vs air)

vapor pressure

3.4 mmHg ( 20 °C)

product line

Vetec™

assay

≥99.5%

form

liquid

autoignition temp.

788 °F

expl. lim.

1.1 %, 100 °F, 9.4 %

dilution

(for analytical testing)

pH

~7 (20 °C, 70 g/L)

bp

155 °C (lit.)

mp

−47 °C (lit.)

density

0.947 g/mL at 25 °C (lit.)

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Legal Information

Vetec 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

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

111.2 °F - closed cup

flash_point_c

44 °C - closed cup

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MMBB4403
MMBB3951
MMBB3863
MMBB3617

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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
Application of fragment screening and merging to the discovery of inhibitors of the Mycobacterium tuberculosis cytochrome P450 CYP121.
Sean A Hudson et al.
Angewandte Chemie (International ed. in English), 51(37), 9311-9316 (2012-08-15)
Viktória Fábos et al.
Chemistry, an Asian journal, 7(11), 2629-2637 (2012-09-07)
Iron (and to a lesser extent manganese) in the wall of a 316 stainless steel (SS) reactor is responsible for the hydrogenation of cyclohexanone to cyclohexanol when using an aqueous formic acid solution under high temperature and pressure water (HTPW)
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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