lithium phenyl-2,4,6-trimethylbenzoylphosphinate
lithium phenyl-2,4,6-trimethylbenzoylphosphinate Basic information
- Product Name:
- lithium phenyl-2,4,6-trimethylbenzoylphosphinate
- Synonyms:
-
- lithium phenyl-2,4,6-trimethylbenzoylphosphinate
- OC2000, Lithium Phenyl(2,4,6-trimethylbenzoyl)phosphinate
- photoinitiator LAP
- P-Phenyl-P-(2,4,6-trimethylbenzoyl)phosphinic acid
- Phenyl(2,4,6-trimethylbenzoyl)phosphinic Acid Lithium Salt
- LAP (Lithium phenyl-2,4,6-trimethylbenzoylphosphinate)
- lithium phenyl-2,4,6-trimethylbenzoylphosphinate N
- Lithium PTMB phosphinate
- CAS:
- 85073-19-4
- MF:
- C16H18LiO3P
- MW:
- 296.23
- Mol File:
- 85073-19-4.mol
lithium phenyl-2,4,6-trimethylbenzoylphosphinate Chemical Properties
- storage temp.
- 2-8°C
- solubility
- Soluble in DMSO
- form
- crystalline powder
- color
- white to off-white
- InChI
- InChI=1S/C16H17O3P.Li.H/c1-11-9-12(2)15(13(3)10-11)16(17)20(18,19)14-7-5-4-6-8-14;;/h4-10H,1-3H3,(H,18,19);;
- InChIKey
- CVDUWYDMNPODNA-UHFFFAOYSA-N
- SMILES
- C(C1C(=CC(C)=CC=1C)C)(=O)P(C1C=CC=CC=1)(O)=O.[LiH]
lithium phenyl-2,4,6-trimethylbenzoylphosphinate Usage And Synthesis
Description
LAP (Lithium phenyl-2,4,6-trimethylbenzoylphosphinate) is a free radical initiator. The free radicals produced by LAP under bioprinting conditions are potentially cytotoxic and mutagenic. In addition, the concentration of LAP affects the mechanical strength of 3D-printed scaffolds. Generally, the concentration range of LAP used for curing is 0.05%-1%. The elastic modulus produced at a concentration of 0.1% is the highest, with enhanced mechanical properties and excellent biocompatibility.
Uses
Lithium phenyl-2,4,6-trimethylbenzoylphosphinate (LAP) is a water soluble, cytocompatible, Type I photoinitiator for use in the polymerization of hydrogels or other polymeric materials. This photoinitator is preferred over Irgacure 2959 for biological applications due to its increased water solubility, increased polymerization rates with 365 nm light, and absorbance at 400 nm allowing for polymerization with visible light. The improved polymerization kinetics enable cell encapsualation at reduced initiator concentration and longer wavelength light, which has been shown to reduce initiator toxicity and increase cell viability.
storage
Store at RT
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