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59647

Supelco

Oxybenzone

analytical standard

Synonym(s):

2-Hydroxy-4-methoxybenzophenone, 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:
85151701
eCl@ss:
39023842
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥98% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

150-160 °C/5 mmHg (lit.)

mp

62-64 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-8°C

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

Oxybenzone (Benzophenone-3), an organic filter, is an active ingredient used in sunscreens to protect against the damage caused by the UV radiation of the sun. It belongs to the class of benzophenones, widely used in personal care products including cosmetics, sunscreens, toothpaste, additives in food commodities, pharmaceuticals, industrial products, etc. BP-3 is reportedly identified as a pollutant in lakes, rivers, raw and treated wastewaters, sewage sludge, effluents from washing activity in households, environmental sediments, etc.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Application

Oxybenzone has been used as an analytical reference standard for the quantification of the analyte in environmental samples using gas chromatography coupled to mass spectrometry (GC-MS) and ultra-performance liquid chromatography-electrospray-tandem mass spectrometry (UPLC-ES-MS/MS). It may be used as an analytical reference standard for the determination of the analyte in zebrafish using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) and liquid chromatography with diode array detection (LC-DAD).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

This compound is commonly found in plants of the genus: hypericum

Pictograms

Environment

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


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Environmentally relevant microplastic exposure affects sediment-dwelling bivalves
Bour A, et al.
Environmental Pollution (Barking, Essex : 1987), 236, 652-660 (2018)
Occurrence of benzophenones, parabens and triclosan in the Yangtze River of China, and the implications for human exposure
Ma X, et al.
Chemosphere, 213, 517-525 (2018)
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
N M Siqueira et al.
Skin pharmacology and physiology, 24(3), 166-174 (2011-01-29)
To evaluate the effect of cationic coating of polymeric nanocapsules in sunscreen formulations on the in vitro skin penetration of benzophenone-3. Benzophenone-3-loaded nanocapsules were prepared by the interfacial deposition of poly(ε-caprolactone) and coated by using a chitosan solution. The nanoparticles
Chi-Feng Hung et al.
Journal of dermatological science, 68(3), 135-148 (2012-10-03)
Ultraviolet (UV) exposure is the predominant cause of skin aging. A systematic evaluation of drug skin permeation via photoaged skin is lacking. The aim of this work was to investigate whether UVA and UVB affect absorption by the skin of

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