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Lucirintpo l ethyl 2 4 6 trimethylbenzoylphenylphosphinate

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LucirinTPO-L® is a chemical compound with the molecular formula C20H23O3P. It is a photoinitiator used in the production of UV-cured coatings, inks, and adhesives. The core function of this product is to initiate the polymerization process when exposed to UV light.

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Lab products found in correlation

2 2 ethylenedioxy diethanethiol deg dichloromethane, by Merck Group (2 mentions) Deuterated chloroform, by Merck Group (2 mentions) 2 ethyl 2 oxazoline etox, by Merck Group (2 mentions) Porcine liver esterase, by Merck Group (2 mentions) Methyl tosylate meots, by Merck Group (2 mentions) Eosin b, by Merck Group (2 mentions)

2 protocols using lucirintpo l ethyl 2 4 6 trimethylbenzoylphenylphosphinate

1

Synthesis and Characterization of Degradable Oxazoline Polymers

Check if the same lab product or an alternative is used in the 5 most similar protocols
2-Ethyl-2-oxazoline (EtOx) and methyl tosylate (MeOTs) were purchased
from Sigma-Aldrich (Vienna, Austria), purified by distillation over sodium
sulfate and stored in inert atmosphere. 2,2′-(Ethylenedioxy)diethanethiol
(DEG), dichloromethane, ethanol and deuterated chloroform were acquired from
Sigma-Aldrich (Vienna, Austria) and used without purification. Glycol
dimercaptoacetate (GDMA) was kindly provided by Bruno Brock (Marschacht,
Germany) and used without any further purification. The photoinitiator Lucirin
TPO-L®, ethyl-2,4,6-trimethylbenzoylphenylphosphinate, was
purchased from abcr GmbH (Karlsruhe, Germany). Deionized water was produced
through reverse osmosis. 2-But-3′-enyl-2-oxazoline (Bu⁼Ox),
2-nonyl-2-oxazoline (NonOx) and 2-dec-9′-enyl-2-oxazoline (Dc⁼Ox)
were synthesized according to literature protocols [22 –24 (link)],
purified by distillation and flash chromatography using chloroform as an eluent.
For the degradation studies, the enzymes (namely porcine liver esterase and
rabbit liver esterase), Eosin B, and the buffer solutions (pH = 4, 6, 8, and 10)
were acquired from Sigma-Aldrich (Vienna, Austria) and used as received.
Luef K.P., Petit C., Ottersböck B., Oreski G., Ehrenfeld F., Grassl B., Reynaud S, & Wiesbrock F. (2016). UV-mediated thiol-ene click reactions for the synthesis of drug-loadable and degradable gels based on copoly(2-oxazoline)s. European polymer journal, 88, 701-712.
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2

Synthesis and Characterization of Degradable Oxazoline Polymers

Check if the same lab product or an alternative is used in the 5 most similar protocols
2-Ethyl-2-oxazoline (EtOx) and methyl tosylate (MeOTs) were purchased
from Sigma-Aldrich (Vienna, Austria), purified by distillation over sodium
sulfate and stored in inert atmosphere. 2,2′-(Ethylenedioxy)diethanethiol
(DEG), dichloromethane, ethanol and deuterated chloroform were acquired from
Sigma-Aldrich (Vienna, Austria) and used without purification. Glycol
dimercaptoacetate (GDMA) was kindly provided by Bruno Brock (Marschacht,
Germany) and used without any further purification. The photoinitiator Lucirin
TPO-L®, ethyl-2,4,6-trimethylbenzoylphenylphosphinate, was
purchased from abcr GmbH (Karlsruhe, Germany). Deionized water was produced
through reverse osmosis. 2-But-3′-enyl-2-oxazoline (Bu⁼Ox),
2-nonyl-2-oxazoline (NonOx) and 2-dec-9′-enyl-2-oxazoline (Dc⁼Ox)
were synthesized according to literature protocols [22 –24 (link)],
purified by distillation and flash chromatography using chloroform as an eluent.
For the degradation studies, the enzymes (namely porcine liver esterase and
rabbit liver esterase), Eosin B, and the buffer solutions (pH = 4, 6, 8, and 10)
were acquired from Sigma-Aldrich (Vienna, Austria) and used as received.
Luef K.P., Petit C., Ottersböck B., Oreski G., Ehrenfeld F., Grassl B., Reynaud S, & Wiesbrock F. (2016). UV-mediated thiol-ene click reactions for the synthesis of drug-loadable and degradable gels based on copoly(2-oxazoline)s. European polymer journal, 88, 701-712.
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+ Expand

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