Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

128562

Sigma-Aldrich

Hexaketocyclohexane octahydrate

97%

Synonym(s):

Cyclohexanehexone octahydrate, Triquinoyl octahydrate

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

About This Item

Empirical Formula (Hill Notation):
C6O6 · 8H2O
CAS Number:
527-31-1
Molecular Weight:
312.18
MDL number:
MFCD00149074
UNSPSC Code:
12352100
PubChem Substance ID:
24847867
NACRES:
NA.22

Quality Level

100

Assay

97%

form

powder

mp

99 °C (dec.) (lit.)

functional group

ketone

storage temp.

2-8°C

SMILES string

[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].O=C1C(=O)C(=O)C(=O)C(=O)C1=O

InChI

1S/C6O6.8H2O/c7-1-2(8)4(10)6(12)5(11)3(1)9;;;;;;;;/h;8*1H2

InChI key

MQIMWEBORAIJPP-UHFFFAOYSA-N

General description

Hexaketocyclohexane octahydrate also known as Triquinoyl octahydrate is an organic compound, often utilized as a building block in various organic reactions, including the synthesis of water-soluble π-conjugated hexaazatrinaphthylenes and their derivatives.

Application

Hexaketocyclohexane octahydrate has been used in the preparation of hexaazatriphenylenehexacarbonitrile.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBK6592
STBK3788
STBK0736
STBJ6139
STBJ5488

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

Synthesis and some reactions of hexaazatriphenylenehexanitrile, a hydrogen-free polyfunctional heterocycle with D3h symmetry.
Kanakarajan K and Czarnik AW.
The Journal of Organic Chemistry, 51(26), 5241-5243 (1986)
Lei Wang et al.
Nanoscale, 9(12), 4090-4096 (2017-03-16)
Nanostructured semiconducting polymers have emerged as a very promising class of metal-free photocatalytic materials for solar water splitting. However, they generally exhibit low efficiency and lack the ability to utilize long-wavelength photons in a photocatalytic oxygen evolution reaction (OER). Here
Hao Huang et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 7(9), 2000012-2000012 (2020-05-10)
The 2D conductive metal-organic frameworks (MOFs) are expected to be an ideal electrocatalyst due to their high utilization of metal atoms. Exploring a new conjugated ligand with extra active metallic center can further boost the structural advantages of conductive MOFs.

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