About This Item
Fórmula linear:
HOC6H4COC6H5
Número CAS:
Peso molecular:
198.22
Beilstein:
777776
Número CE:
Número MDL:
Código UNSPSC:
12162002
ID de substância PubChem:
NACRES:
NA.23
Produtos recomendados
Nível de qualidade
Ensaio
98%
pf
132-135 °C (lit.)
cadeia de caracteres SMILES
Oc1ccc(cc1)C(=O)c2ccccc2
InChI
1S/C13H10O2/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h1-9,14H
chave InChI
NPFYZDNDJHZQKY-UHFFFAOYSA-N
Informações sobre genes
rat ... Ar(24208)
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Descrição geral
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.
Aplicação
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.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Aquatic Chronic 3 - STOT RE 2
Órgãos-alvo
Liver,Kidney
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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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
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
Benzophenone metabolism. I. Isolation of p-hydroxybenzophenone from rat urine.
A W Stocklinski et al.
Life sciences, 26(5), 365-369 (1980-02-04)
Adela Jing Li et al.
Journal of hazardous materials, 337, 115-125 (2017-05-17)
Ethyl-4-aminobenzoate (Et-PABA) is currently used as a substitute for 4-aminobenzoate (PABA) in sunscreens and anesthetic ointments. Despite its widespread use and hydrophilicity, Et-PABA has never been found in environmental waters. This study, probed the occurrence of Et-PABA in both seawater
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| H20202-100G | 4061833604878 |
| H20202-25G | 4061833791738 |
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