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129380

4-Ethylcyclohexanone

Name: 4-Ethylcyclohexanone
Brand: ALDRICH

97%

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About This Item

Linear Formula:

C₂H₅C₆H₉(=O)

CAS Number:

5441-51-0

Molecular Weight:

126.20

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24847900

EC Number:

226-629-2

Beilstein/REAXYS Number:

1924964

MDL number:

MFCD00001644

Assay:

97%

Form:

liquid

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Properties

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.)

functional group

ketone

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

Description

Application

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

pictograms

GHS07

signalword

Warning

hcodes

H315,H317,H412

pcodes

P261 - P264 - P272 - P273 - P280 - P302 + P352

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

145.4 °F

flash_point_c

63 °C

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Regulatory Information

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Miyazawa M, et al.

Journal of Chemical Technology and Biotechnology, 75(2), 143-146 (2000)

Synthesis of ketones from biomass-derived feedstock.

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

Global Trade Item Number

SKU	GTIN
129380-25G	04061838726179