54800
4-Hydroxybenzophenone
purum, ≥99.0% (HPLC)
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About This Item
Linear Formula:
HOC6H4COC6H5
CAS Number:
Molecular Weight:
198.22
EC Number:
214-507-1
UNSPSC Code:
12162002
PubChem Substance ID:
Beilstein/REAXYS Number:
777776
MDL number:
InChI key
NPFYZDNDJHZQKY-UHFFFAOYSA-N
InChI
1S/C13H10O2/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h1-9,14H
SMILES string
Oc1ccc(cc1)C(=O)c2ccccc2
grade
purum
assay
≥99.0% (HPLC)
mp
132-134 °C, 132-135 °C (lit.)
Gene Information
rat ... Ar(24208)
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Benzophenone metabolism. I. Isolation of p-hydroxybenzophenone from rat urine.
A W Stocklinski et al.
Life sciences, 26(5), 365-369 (1980-02-04)
Hui-chen Liu et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 40(2), 168-172 (2005-05-07)
To investigate the metabolic pathways of dipfluzine in rats. After an oral dose of dipfluzine (80 mg x kg(-1)) to rats, urine was collected for 12 h. The metabolites of dipfluzine in urine were chromatographed and identified by LC/DAD/MS methods.
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
Hanne Frederiksen et al.
International journal of hygiene and environmental health, 220(2 Pt A), 244-253 (2016-09-18)
Experimental studies indicate that some chemicals with UV blocking properties (known as UV filters) can act as endocrine disruptors. UV filters are used in sunscreens and other cosmetic- and personal care products, as well as in other consumer products such
Jose Serrano et al.
Xenobiotica; the fate of foreign compounds in biological systems, 50(2), 192-208 (2019-03-20)
1. Cyclic phenones are chemicals of interest to the USEPA due to their potential for endocrine disruption to aquatic and terrestrial species.2. Prior to this report, there was very limited information addressing metabolism of cyclic phenones by fish species and
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