Skip to Content
Merck
All Photos(1)

Documents

129380

Sigma-Aldrich

4-Ethylcyclohexanone

97%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C2H5C6H9(=O)
CAS Number:
5441-51-0
Molecular Weight:
126.20
Beilstein:
1924964
EC Number:
226-629-2
MDL number:
MFCD00001644
UNSPSC Code:
12352100
PubChem Substance ID:
24847900
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.452 (lit.)

bp

192-194 °C (lit.)

density

0.895 g/mL at 25 °C (lit.)

SMILES string

CCC1CCC(=O)CC1

InChI

1S/C8H14O/c1-2-7-3-5-8(9)6-4-7/h7H,2-6H2,1H3

InChI key

OKSDJGWHKXFVME-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

4-Ethylcyclohexanone was used to study the biotransformations of 4-Ethylcyclohexanone.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H317 - H412

Hazard Classifications

Aquatic Chronic 3 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

145.4 °F

Flash Point(C)

63 °C

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

N-Methyldiphenylamine 96%

Sigma-Aldrich

524212

N-Methyldiphenylamine

3-Methyl-2-cyclohexenone 98%, Stabilized

Sigma-Aldrich

M39105

3-Methyl-2-cyclohexenone

4-Hydroxybenzhydrazide ≥97%

Sigma-Aldrich

H9882

4-Hydroxybenzhydrazide

Miyazawa M, et al.
Journal of Chemical Technology and Biotechnology, 75(2), 143-146 (2000)
Qinglei Meng et al.
Nature communications, 8, 14190-14190 (2017-02-01)
Cyclohexanone and its derivatives are very important chemicals, which are currently produced mainly by oxidation of cyclohexane or alkylcyclohexane, hydrogenation of phenols, and alkylation of cyclohexanone. Here we report that bromide salt-modified Pd/C in H

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service