147834
Michler′s ketone
98%
Synonym(s):
4,4′-Bis(dimethylamino)benzophenone
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About This Item
Linear Formula:
[(CH3)2NC6H4]2CO
CAS Number:
Molecular Weight:
268.35
Beilstein:
790733
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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Quality Level
Assay
98%
form
powder
mp
174-176 °C (lit.)
SMILES string
CN(C)c1ccc(cc1)C(=O)c2ccc(cc2)N(C)C
InChI
1S/C17H20N2O/c1-18(2)15-9-5-13(6-10-15)17(20)14-7-11-16(12-8-14)19(3)4/h5-12H,1-4H3
InChI key
VVBLNCFGVYUYGU-UHFFFAOYSA-N
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General description
Michler′s ketone (MK) is a derivative of benzophenone that shows temperature dependent phosphorescence. It also exhibits triplet-triplet absorption spectra at a lower temperature.
Application
MK can be used as an additive that acts as a photoinitiator in the preparation of dyes. It can also be used as a precursor material in the synthesis of 4,4′-bis{N,N,dimethyl, N (2-ethoxy carbonyl-1-propenyl) ammonium hexafluoro antimonate}benzophenone (MKEA).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Carc. 1B - Eye Dam. 1 - Muta. 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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New Push-Pull Dyes Derived from Michler?s Ketone For Polymerization Reactions Upon Visible Lights.
Tehfe M, et al.
Macromolecules, 46(10), 3761-3770 (2013)
Michler's ketone.
Report on carcinogens : carcinogen profiles, 12, 270-271 (2011-08-24)
Excited state dynamics of Michler's ketone: a laser flash photolysis study
Singh AK, et al.
Research on Chemical Intermediates, 27(1-2), 125-136 (2001)
Synthesis of a novel addition-fragmentation agent based on Michler's ketone and its use as photo-initiator for cationic polymerization
Onen A and Yagci Y
Polymer, 42(16), 6681-6685 (2001)
M C Rezende et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(6), 1183-1190 (2001-06-23)
The preparation and the solvatochromic behavior of two dyes, obtained by condensation of N,N'-dimethylbarbituric acid with dimethylaminobenzaldehyde and with 4,4'-bis(N,N-dimethylamino)benzophenone (Michler's ketone) are described. The latter dye is rather sensitive to the polarity of the medium, and in particular, to
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