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Usage

Uses

Used in UV-curable Inks, Adhesives, and Coatings:
1-(4-dodecylphenyl)-2-hydroxy-2-methylpropan-1-one is used as a photoinitiator for the production of UV-curable inks, adhesives, and coatings. Its capacity to initiate chemical reactions under UV light ensures rapid curing and high-quality performance of these materials.
Used in Electronics Industry for Printed Circuit Boards:
In the electronics industry, 1-(4-dodecylphenyl)-2-hydroxy-2-methylpropan-1-one is utilized as a photoinitiator in the production of printed circuit boards. Its role in the curing process contributes to the creation of reliable and high-precision electronic components.
Used in 3D Printing Processes:
1-(4-dodecylphenyl)-2-hydroxy-2-methylpropan-1-one is also employed as a photoinitiator in 3D printing processes. It plays a crucial role in the rapid curing of materials used in this technology, enabling the production of complex and detailed 3D-printed objects.

InChI:InChI=1/C22H36O2/c1-4-5-6-7-8-9-10-11-12-13-14-19-15-17-20(18-16-19)21(23)22(2,3)24/h15-18,24H,4-14H2,1-3H3

Relevant academic research and scientific papers

Oxygen-containing titanocenes, and the use thereof

Titanocenes of the formula I STR1 in which R1 are cyclopentadienyl? groups and R2 and R3 are aromatic radicals which are substituted in both ortho-positions by fluorine and, in addition, are substituted by an acyloxy group are suitable as photoinitiators for the photopolymerization of ethylenically unsaturated compounds.

Titanocenes, the use thereof, and n-substituted fluoroanilines

Titanocenes containing two 5-membered cyclodienyl gropus, for example cyclopentadienyl, and one or two 6-membered carbocyclic or 5- or 6-membered heterocyclic aromatic rings which are substituted by a fluorine atom in at least one of the two ortho-positions to the titanium-carbon bond and contain, as further substituents, a substituted amino radical, are suitable as photoinitiators for radiation-induced polymerization of ethylenically unsaturated compounds.

Titanocenes, the use thereof, and N-substituted pyrroles

Titanocenes containing two 5-membered cyclodienyl groups, for example cyclopentadienyl, and one or two 6-membered carbocyclic or 5- or 6-membered heterocyclic aromatic rings which are substituted by a fluorine atom in at least one of the two ortho-positions to the titanium-carbon bond and contain, as a further substituent, unsubstituted or substituted 1-pyrryl, are suitable as photoinitiators for radiation-induced polymerization of ethylenically unsaturated compounds.

Novel nitrogen-containing titanocenes, and the use thereof

Titanocenes of the formula I STR1 in which R1 are cyclopentadienyl? groups and R2 and R3 are aromatic radicals which are substituted in both ortho-positions by fluorine and, in addition, are substituted by a pyrrylalkyl group, amidoalkyl group or imidoalkyl group, are suitable as photoinitiators for the photopolymerization of ethylenically unsaturated compounds.

Photosensitive hydroxyalkylphenones

Compounds of the formula STR1 wherein R1 is hydrogen, chlorine, phenyl, dialkylamino of 2-4 carbon atoms or alkyl or alkoxy each of up to 18 carbon atoms; R2 is hydrogen, chlorine, bromine or alkyl or alkoxy each of up to 4 carbon atoms; R3 and R4, which can be the same or different, each is hydrogen or alkyl of up to 6 carbon atoms; R5 is hydrogen or alkyl or alkanoyl each of up to 4 carbon atoms; and R6 is hydrogen or methyl, with the proviso that not all of R1 to R6 simultaneously are hydrogen, are effective photosensitizers, especially for photopolymerization of unsaturated compounds and for hardening of printing dyes.