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C101400

Sigma-Aldrich

1,2-Cyclohexanedione

97%

Synonym(s):

1,2-Dioxocyclohexane, Cyclohexan-1,2-dione

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About This Item

Linear Formula:
C6H8(=O)2
CAS Number:
765-87-7
Molecular Weight:
112.13
Beilstein:
507419
EC Number:
212-155-3
MDL number:
MFCD00001648
UNSPSC Code:
12352100
PubChem Substance ID:
24892299
NACRES:
NA.22

Quality Level

100

Assay

97%

form

solid

bp

193-195 °C (lit.)

mp

34-38 °C (lit.)

storage temp.

2-8°C

SMILES string

O=C1CCCCC1=O

InChI

1S/C6H8O2/c7-5-3-1-2-4-6(5)8/h1-4H2

InChI key

OILAIQUEIWYQPH-UHFFFAOYSA-N

Gene Information

human ... ACHE(43) , BCHE(590) , CES1(1066)

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Related Categories

Application

Specific reagent for arginine residues.

WGK

WGK 3

Flash Point(F)

No data available

Flash Point(C)

No data available

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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I Heiland et al.
Biochemistry, 18(21), 4605-4612 (1979-10-16)
The primary structure of protein L21 from the 50S subunit of Escherichia coli ribosomes has been completely determined by sequencing the peptides obtained by digestion of L21 with trypsin before and after modification of the arginine residues with 1,2-cyclohexanedione, Staphylococcus
Bellamkonda Ramakrishna et al.
International journal of biological macromolecules, 115, 1225-1232 (2018-05-05)
The recombinant C-terminal domain of chitinase C of Chitinophaga pinensis (CpChiC-GH18C) exhibits the highest activity at pH 6.0 and 35 °C, with a Km of 76.13 (mg-1 ml), a kcat of 10.16 (s-1), and a kcat/Km of 0.133 (mg-1 ml s-1) on colloidal chitin. Analysis
Minyi Han et al.
Food & function, 9(7), 4017-4027 (2018-07-07)
The addition of dietary fibers can alleviate the deteriorated textural properties and water binding capacity (WBC) that may occur when the fat content is lowered directly in the formulas of comminuted meat products. This study investigated the effects of the
M Holmquist et al.
Journal of protein chemistry, 12(6), 749-757 (1993-12-01)
The homologous lipases from Rhizomucor miehei and Humicola lanuginosa showed approximately the same enantioselectivity when 2-methyldecanoic acid esters were used as substrates. Both lipases preferentially hydrolyzed the S-enantiomer of 1-heptyl 2-methyldecanoate (R. miehei: ES = 8.5; H. lanuginosa: ES =
M Ghosh et al.
The Biochemical journal, 298 ( Pt 2), 295-301 (1994-03-01)
The presence of arginine at the active site of Leishmania donovani adenosine kinase was studied by chemical modification, followed by the characterization of the modified enzyme. The arginine-specific reagents phenylglyoxal (PGO), butane-2,3-dione and cyclohexane-1,2-dione all irreversibly inactivated the enzyme. In
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