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光引發劑是一種能夠在紫外光（UV）、可見光或激光照射下，吸收光能后分解或激發形成活性自由基或陽離子，從而引發單體或低聚物的聚合反應的物質。它的核心作用是將光能轉化為化學能，實現快速固化。具體在以下方面有廣泛應用：
- 現代制造業：作為各類工業涂料、油墨及膠粘劑實現快速固化的核心技術。
- 電子信息技術：是芯片制造和電子顯示行業微細圖形加工的關鍵材料。
- 增材制造（3D 打印）：構成光固化快速成型技術的基礎，實現產品的精準制造。
- 醫療與個人護理：為牙科修復及光固化美容產品提供安全的現場固化解決方案。
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| 產品編號 |
結構式 |
項目名稱規格 |
分子式 |
| B801870 |
|
安息香,99.5%
Benzoin,99.5% |
C14H12O2
|
| H742530 |
|
2-羥基-2-甲基苯丙酮,99%
2-Hydroxy-2-methylpropiophenone,99% |
C10H12O2
|
| H823463 |
|
2-羥基-4′-(2-羥乙氧基)-2-甲基苯丙酮,98%
2-Hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone,98% |
C12H16O4
|
| P831909 |
|
苯基雙(2,4,6-三甲基苯甲酰基)氧化膦,98%
Phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide,98% |
[(CH3)3C6H2CO]2P(O)C6H5
|
| L862544 |
|
苯基(2,4,6-三甲基苯甲酰基)磷酸鋰鹽,98%(HPLC)(T)
Lithium Phenyl(2,4,6-trimethylbenzoyl)phosphinate,98%(HPLC)(T) |
C16H16LiO3P
|
| B802287 |
|
安息香二甲醚,99%
Benzoin dimethyl ether (DMPA),99% |
C16H16O3
|
| H811166 |
|
1-羥環己基苯酮,98%
1-Hydroxycyclohexyl phenyl ketone,98% |
C13H16O2
|
| H810852 |
|
4-羥基苯乙酮,98%
4'-Hydroxyacetophenone,98% |
C8H8O2
|
| F809617 |
|
二茂鐵,99%
Ferrocene,99% |
FeC10H10
|
| B802181 |
|
二苯甲酮,99%
Benzophenone,99% |
C13H10O
|
| D742503 |
|
二苯基(2,4,6-三甲基苯甲酰基)氧化膦,99%
Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO),99% |
C22H21O2P
|
| D834856 |
|
2,2-二乙氧基苯乙酮,≥95%
2,2-Diethoxyacetophenone,≥95% |
C12H16O3
|
| N815087 |
|
硝苯地平,≥98.0%(HPLC)
Nifedipine,≥98.0%(HPLC) |
C17H18N2O6
|
| E843527 |
|
2,4,6-三甲基苯甲酰基苯基膦酸乙酯,97%
Ethyl phenyl(2,4,6-trimethylbenzoyl)phosphinate,97% |
C18H21O3P
|
| B802393 |
|
3,3'4,4'-二苯甲酮四羧酸二酐,99%
Benzophenone-3,3',4,4'-tetracarboxylic dianhydride,99% |
C17H6O7
|
| I834922 |
|
2-異丙基硫雜蒽酮,>98%
2-Isopropylthioxanthone,>98% |
C16H14OS
|
| A800073 |
|
蒽醌,98%
Anthraquinone,98% |
C14H8O2
|
| B802243 |
|
苯偶酰,98%
Benzil,98% |
C14H10O2
|
| C832719 |
|
(±)-樟腦醌,>98.0%(GC)
(±)-Camphorquinone,>98.0%(GC) |
C10H14O2
|
| M838095 |
|
2-甲基-2-(4-嗎啉基)-4'-(甲硫基)苯丙酮,98%
2-Methyl-4'-(methylthio)-2-morpholinopropiophenone,98% |
C15H21NO2S
|
|
|