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一般描述
4-Hydroxybenzophenone is characterized by its ability to absorb UV radiation and convert it into lower-energy radiation. This property makes it an effective photostabilizer. Its molecular structure features two aromatic rings connected by a carbonyl group, allowing for strong π-π stacking interactions, which enhance its stability and efficacy in polymer matrices. Incorporating 4-Hydroxybenzophenone into polymer matrices increases the longevity and performance of materials used in outdoor applications, such as coatings and plastics.
应用
4-Hydroxybenzophenone can be used:
- As a photoinitiator to synthesize fluorescent triblock copolymer micelles for targeted release of cancer drugs and intracellular bioimaging. It facilitates controlled release, improving therapeutic efficacy while minimizing side effects.
- As a photoacid catalyst for ring opening polymerization of lactones to prepare biodegradable polyesters.
- As a precursor to synthesize functional copolymer for fabrication of nanostructured transparent metal electrodes for flexible optoelectronic devices.
警示用语：
Warning
危险声明
预防措施声明
危险分类
Aquatic Chronic 3 - STOT RE 2
靶器官
Liver,Kidney
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Daniel Molins-Delgado et al.
The Science of the total environment, 601-602, 975-986 (2017-06-06)
The increased use of beauty and other daily use products, in particular those containing UV filters (UV-Fs) and benzotriazoles, results in their introduction in significant amounts into the aquatic environment. In this study, we aim to assess the occurrence and
Aneesh Karkhanis et al.
Biochemical pharmacology, 146, 188-198 (2017-09-30)
Cardiac enzymes such as cytochrome P450 2J2 (CYP2J2) metabolize arachidonic acid (AA) to cardioprotective epoxyeicosatrienoic acids (EETs), which in turn are metabolized by soluble epoxide hydrolase (sEH) to dihydroxyeicosatrienoic acids (DHETs). As EETs and less potent DHETs exhibit cardioprotective and
Benzophenone metabolism. I. Isolation of p-hydroxybenzophenone from rat urine.
A W Stocklinski et al.
Life sciences, 26(5), 365-369 (1980-02-04)
Francesco Barsotti et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 16(4), 527-538 (2017-01-20)
The photophysics and photochemistry of 4-hydroxybenzophenone (4HOBP) are interesting because they can give some insight into the behavior of humic material. Here we show that 4HOBP has a number of fluorescence peaks: (i) an intense one at excitation/emission wavelengths Ex/Em
S E Blanco et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(13), 2985-2995 (2003-10-30)
The anomalous UV spectroscopic behavior of 4-hydroxy-benzophenone and 2,4-dihydroxy-benzophenone in ethanol-acetonitrile mixtures has been investigated using theoretical and experimental methods. Band I of these compounds, associated to strong pi-->pi* transitions, suffers a blue shift when the polarity of the ethanol-acetonitrile
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