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139211

Sigma-Aldrich

Cyclohexyl phenyl ketone

98%

Synonym(s):

Benzoylcyclohexane

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About This Item

Linear Formula:
C6H11COC6H5
CAS Number:
712-50-5
Molecular Weight:
188.27
Beilstein:
2046712
EC Number:
211-923-5
MDL number:
MFCD00001467
UNSPSC Code:
12352100
PubChem Substance ID:
24848397
NACRES:
NA.22

Assay

98%

form

solid

mp

55-57 °C (lit.)

functional group

ketone

SMILES string

O=C(C1CCCCC1)c2ccccc2

InChI

1S/C13H16O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1,3-4,7-8,12H,2,5-6,9-10H2

InChI key

BMFYCFSWWDXEPB-UHFFFAOYSA-N

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Application

Cyclohexyl phenyl ketone was used to investigate the crosslinked cyclohexyl phenyl compounds under thermal and aquathermal conditions. It was used to examine the effects of molecular changes in the benzophenone molecule on phototoxic behavior.

Biochem/physiol Actions

Cyclohexyl phenyl ketone induces photohaemolysis after exposure to ultraviolet A-rich irradiation in human erythrocytes.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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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Aqueous organic chemistry. 2. Crosslinked cyclohexyl phenyl compounds.
Siskin M, et al.
Energy and Fuels, 4(5), 482-488 (1990)
Jose Serrano et al.
Xenobiotica; the fate of foreign compounds in biological systems, 50(2), 192-208 (2019-03-20)
1. Cyclic phenones are chemicals of interest to the USEPA due to their potential for endocrine disruption to aquatic and terrestrial species.2. Prior to this report, there was very limited information addressing metabolism of cyclic phenones by fish species and
Marianne Placzek et al.
Acta dermato-venereologica, 93(1), 30-32 (2012-09-18)
Benzophenone is a phototoxic compound with absorption maxima in the ultraviolet A (UVA) and ultraviolet B (UVB) range. Many benzophenone derivatives are known to be photosensitizing. On the other hand, 2-hydroxy-4-methoxybenzophenone is used as a photoprotective agent. The aim of

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