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Supelco

5,5-Dimethyl-1,3-cyclohexanedione

for HPLC derivatization, for the determination of aldehyde formaldehyde, ≥99.0%

Synonym(s):

Dimedone, Methone

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About This Item

Linear Formula:
(CH3)2C6H6(=O)2
CAS Number:
Molecular Weight:
140.18
Beilstein/REAXYS Number:
471489
EC Number:
MDL number:
UNSPSC Code:
12164500
PubChem Substance ID:
NACRES:
NA.21

grade

for HPLC derivatization

Quality Level

assay

≥99.0% (GC)
≥99.0%

quality

for the determination of aldehyde formaldehyde

mp

146-148 °C (lit.)

application(s)

general analytical

SMILES string

CC1(C)CC(=O)CC(=O)C1

InChI

1S/C8H12O2/c1-8(2)4-6(9)3-7(10)5-8/h3-5H2,1-2H3

InChI key

BADXJIPKFRBFOT-UHFFFAOYSA-N

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General description

5,5-dimethyl-1,3-cyclohexanedione (Dimedone) is basically a highly sensitive and very specific reagent used for the determination of aldehydes. It is highly advantageous as it is environment friendly, give high yields and is a simple workup procedure.

Application

5,5-dimethyl-1,3-cyclohexanedione may be used in condensation reaction with aromatic aldehyde in ethylene glycol. It may be also be used in trace analysis of aldehydes by HPLC.

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Trace analysis of aldehydes by reversed-phase high-performance liquid chromatography and precolumn fluorigenic labeling with 5, 5-dimethyl-1, 3-cyclohexanedione.
Kenneth M
Journal of Chromatography A, 256, 243-252 (1983)
Solid-State Condensation Reactions Between Aldehydes and 5, 5-Dimethyl-1, 3-cyclohexanedione by Grinding at Room Temperature.
Tong-shou J
Synthetic Communications, 35 (17), 2339-2345 (2005)
Condensation of aromatic aldehydes with 5, 5-dimethyl-1, 3-cyclohexanedione without catalyst.
Shujiang Tu
Synthetic Communications, 32 (19), 3063-3067 (2002)
Joseph R Burgoyne et al.
Biochemical Society transactions, 39(5), 1260-1267 (2011-09-23)
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