H20202
4-Hydroxybenzophenone
98%
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About This Item
Fórmula lineal:
HOC6H4COC6H5
Número de CAS:
Peso molecular:
198.22
Beilstein/REAXYS Number:
777776
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Productos recomendados
Quality Level
assay
98%
mp
132-135 °C (lit.)
SMILES string
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
InChI key
NPFYZDNDJHZQKY-UHFFFAOYSA-N
Gene Information
rat ... Ar(24208)
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signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3 - STOT RE 2
target_organs
Liver,Kidney
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Los clientes también vieron
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
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
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
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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