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02482

Cyclohexanone

analytical standard

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1 mL
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CZK 767.00

About This Item

Linear Formula:
C6H10(=O)
CAS Number:
Molecular Weight:
98.14
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
203-631-1
Beilstein/REAXYS Number:
385735
MDL number:

CZK 767.00


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grade

analytical standard

Quality Level

vapor density

3.4 (vs air)

vapor pressure

3.4 mmHg ( 20 °C)

assay

≥99.9% (GC)

autoignition temp.

788 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

1.1 %, 100 °F, 9.4 %

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

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

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C10218039824129135
technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

technique(s)

-

technique(s)

-

grade

analytical standard

grade

-

grade

ACS reagent

grade

for ion-selective electrodes

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

application(s)

-

application(s)

-

application(s)

-

assay

≥99.9% (GC)

assay

99.8%

assay

≥99.0%

assay

≥99.5% (GC)

format

neat

format

-

format

-

format

-

vapor density

3.4 (vs air)

vapor density

3.4 (vs air)

vapor density

3.4 (vs air)

vapor density

3.4 (vs air)

General description

Cyclohexanone is a cycloalkanone. It is an industrially important intermediate. It is useful for the preparation of raw materials for various chemical intermediates, such as caprolactam for nylon 6 and adipic acid for nylon 66 synthesis of nylon.[1] It can be synthesized industrially by either the oxidation of cyclohexane or the hydrogenation of phenol.[1][2]

Application

Cyclohexanone may be used for the following syntheses:
  • vitamin A
  • 2-cyclohexylidene cyclohexanone via Aldol condensation reaction
  • 2-cyclohexenyl cyclohexanone via Aldol condensation reaction
  • bis-(arylmethylidene)cycloalkanones by cross-aldol condensation with aldehydes[3]

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

ppe

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


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Dodgson I, et al.
Chemistry & Industry, 830 (1989)
Xu LX, et al.
Catalysis Communications, 9, 816-816 (2008)
Lei Liu et al.
Angewandte Chemie (International ed. in English), 48(12), 2206-2209 (2009-02-10)
On their best behavior: Three zirconium compounds with one-, two-, and three-dimensional structures have been successfully synthesized by the ionothermal approach. The 3D zirconium phosphate (see picture; F green, H white, O red, P pink, Zr yellow) exhibits high catalytic
194. A synthesis of vitamin a from cyclohexanone.
Attenburrow J, et al.
Journal of the Chemical Society, 1094-1111 (1952)
Aldol Condensation of Cyclohexanone and Synthesis of Acetal or Ketals [J]. J. Jilin
Yiezhi L, et al.
Journal of Jilin University (Science Edition) / Chi Lin Ta Hsueh Hsueh Pao (Li Hsueh Pan ), 2, 021-021 (1989)

Articles

The aldol condensation reaction is an organic reaction introduced by Charles Wurtz, who first prepared the β-hydroxy aldehyde from acetaldehdye in 1872.

Global Trade Item Number

SKUGTIN
02482-1ML04061838617521
EHNC-024821-20UG04065265332781
EHNC024821-20UG04061841397007
EHNC024821-50UG04061841397014
EHNC-024821-50UG04065265332798

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