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H20202
4-Hydroxybenzophenon
98%
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About This Item
Lineare Formel:
HOC6H4COC6H5
CAS-Nummer:
Molekulargewicht:
198.22
Beilstein:
777776
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12162002
PubChem Substanz-ID:
NACRES:
NA.23
Empfohlene Produkte
Qualitätsniveau
Assay
98%
mp (Schmelzpunkt)
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
InChIKey
NPFYZDNDJHZQKY-UHFFFAOYSA-N
Angaben zum Gen
rat ... Ar(24208)
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Signalwort
Warning
H-Sätze
P-Sätze
Gefahreneinstufungen
Aquatic Chronic 3 - STOT RE 2
Zielorgane
Liver,Kidney
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 2
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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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
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