H36206
2-Hydroxy-4-methoxybenzophenone
98%
Synonym(s):
Oxybenzone
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About This Item
Linear Formula:
HOC6H3(OCH3)COC6H5
CAS Number:
Molecular Weight:
228.24
Beilstein:
1913145
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
bp
150-160 °C/5 mmHg (lit.)
mp
62-64 °C (lit.)
solubility
95% ethanol: soluble 50 mg/mL, clear, colorless
SMILES string
COc1ccc(c(O)c1)C(=O)c2ccccc2
InChI
1S/C14H12O3/c1-17-11-7-8-12(13(15)9-11)14(16)10-5-3-2-4-6-10/h2-9,15H,1H3
InChI key
DXGLGDHPHMLXJC-UHFFFAOYSA-N
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General description
2-Hydroxy-4-methoxybenzophenone (benzophenone-3) is commonly employed as a broad-band UV-filter in sunscreen cosmetic products. It protects skin from the deleterious effects of the sun. It is one of the sunscreen constituent and its trace determination in water samples by solid-phase microextraction (SPME) and gas chromatography with flame ionization and mass spectrometric detection has been reported.
Application
2-Hydroxy-4-methoxybenzophenone may be used in the following studies:
- Synthesis of as poly[(2-hydroxy-4-methoxybenzophenone) propylene] (HMBP-PD), a polymeric ligand (resin) used for the synthesis of metal/ligand polychelates (metal-polymer complexes).
- Analytical reagent for the gravimetric determination of Cu(II).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 2
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 2
Flash Point(F)
212.0 °F - closed cup
Flash Point(C)
100 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis, characterization, ion-exchange, and antimicrobial study of poly [(2-hydroxy-4-methoxybenzophenone) propylene] resin and its polychelates with lanthanides (III).
Patel MM, et al.
Journal of Applied Polymer Science, 106(2), 1307-1317 (2007)
Purohit, K.; Desai, K.K.
E-Journal of Chemistry, 2 (2005)
Zacarías León et al.
Analytical and bioanalytical chemistry, 398(2), 831-843 (2010-07-14)
2-Hydroxy-4-methoxybenzophenone (HMB), which is one of the most commonly used UV filters in sunscreen cosmetics to protect skin from the deleterious effects of the sun, can be percutaneously absorbed, further metabolized, and finally excreted or bioaccumulated. An analytical method for
D A Lambropoulou et al.
Journal of chromatography. A, 967(2), 243-253 (2003-04-11)
A method has been developed for the trace determination of two sunscreen constituents (2-hydroxy-4-methoxybenzophenone and octyldimethyl-p-aminobenzoic acid) in water samples, which are commonly used in commercial formulations. The method employs solid-phase microextraction (SPME) and gas chromatography with flame ionization and
Pablo Gago-Ferrero et al.
The Science of the total environment, 443, 209-217 (2012-11-29)
The goal of this study was to bring forward new data and insights with respect to the effect of operational variables and reaction pathways during ozonation and peroxone oxidation of the UV filter compound benzophenone-3 (BP3) in water. A systematic
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