Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

D153303

Sigma-Aldrich

5,5-Dimethyl-1,3-cyclohexanedione

95%

Synonym(s):

Dimedone, Methone

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
(CH3)2C6H6(=O)2
CAS Number:
126-81-8
Molecular Weight:
140.18
Beilstein:
471489
EC Number:
204-804-4
MDL number:
MFCD00001588
UNSPSC Code:
12352100
PubChem Substance ID:
24893475
NACRES:
NA.22

Assay

95%

form

powder

mp

146-148 °C (lit.)

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

Looking for similar products? Visit Product Comparison Guide

Application

Part of furannulation strategy for the synthesis of naturally occurring fused 3-methylfurans.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBL2043
STBJ7716
STBJ2279
STBH0286
STBF2660V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

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 2

1 of 2

Mesityl oxide technical grade, 90%

Sigma-Aldrich

281832

Mesityl oxide

Dde-OH Novabiochem®

Sigma-Aldrich

8.51015

Dde-OH

The Journal of Organic Chemistry, 58, 3960-3960 (1993)
Hooshang Hamidian et al.
Molecules (Basel, Switzerland), 16(11), 9041-9048 (2011-10-28)
A novel synthesis of triazolo[1,2-a]indazole-1,3,8-trione derivatives by reaction of urazole, dimedone and aromatic aldehydes under conventional heating and microwave irradiation and solvent-free conditions using silica nanoparticles prepared from rice husk ash as catalyst is described. The new method features high
Beatriz Alvarez et al.
Methods in enzymology, 473, 117-136 (2010-06-02)
Protein sulfenic acids (R-SOH) are receiving increased interest as intermediates in redox processes. Human serum albumin, the most abundant protein in plasma, possesses a single free thiol. We describe herein the different methodologies that we have employed to study the
Candice E Paulsen et al.
Chemistry & biology, 16(2), 217-225 (2009-02-24)
Saccharomyces cerevisiae responds to elevated levels of hydrogen peroxide in its environment via a redox relay system comprising the thiol peroxidase Gpx3 and transcription factor Yap1. In this signaling pathway, a central unresolved question is whether cysteine sulfenic acid modification
Douglas S Rehder et al.
BMC biochemistry, 11, 25-25 (2010-07-03)
Cysteine sulfenic acid (Cys-SOH) plays important roles in the redox regulation of numerous proteins. As a relatively unstable posttranslational protein modification it is difficult to quantify the degree to which any particular protein is modified by Cys-SOH within a complex
View All Related Papers

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