
CAS 131-53-3: 2,2′-Dihydroxy-4-methoxybenzophenone
Formula:C14H12O4
InChI:InChI=1S/C14H12O4/c1-18-9-6-7-11(13(16)8-9)14(17)10-4-2-3-5-12(10)15/h2-8,15-16H,1H3
InChI key:InChIKey=MEZZCSHVIGVWFI-UHFFFAOYSA-N
SMILES:C(=O)(C1=C(O)C=C(OC)C=C1)C2=C(O)C=CC=C2
Synonyms:- (2-Hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)methanone
- 2,2'-Dihydroxy-4-Methoxy Benzophenone
- 4-Methoxy-2,2′-dihydroxybenzophenone
- Advastab 47
- Benzophenone 8
- Benzophenone, 2,2′-dihydroxy-4-methoxy-
- Bp-8
- Cyasorb UV 24
- Cyasorb UV 24 Light Absorber
- Dioxybenzon
- Dioxybenzone
- See more synonyms
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Found 16 products.
Dioxybenzone
CAS:Ketone-phenols and ketones with other oxygen functionFormula:C14H12O4Color and Shape:PowderMolecular weight:244.07356(2-Hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)methanone
CAS:Purity:95.0%Molecular weight:244.24600219726562Methanone, (2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-
CAS:Formula:C14H12O4Purity:98%Color and Shape:SolidMolecular weight:244.2427Dioxybenzone-d3
CAS:Controlled ProductStability Hygroscopic Applications Dioxybenzone-d3 is an isotopic analog of Dioxybenzone (D486365), a compound used in sunscreen formulations to block out UVB and UVA harmful rays. References Baumgartner, V. et al.: J. Planar. Chrom. Modern. TLC., 22, 19 (2009); Kunisue, T. et al.: Anal. Meth., 2, 707 (2010);Formula:C14D3H9O4Color and Shape:Light YellowMolecular weight:247.26Dioxybenzone
CAS:Dioxybenzone (Benzophenone-8) is an organic agent that blocks UVB and short-wave UVA ultraviolet radiation.Formula:C14H12O4Purity:99.39%Color and Shape:Physical Description Yellow Powder (Ntp 1992)Molecular weight:244.242,2'-Dihydroxy-4-methoxybenzophenone
CAS:Controlled ProductFormula:C14H12O4Color and Shape:NeatMolecular weight:244.242,2'-Dihydroxy-4-methoxybenzophenone
CAS:2,2'-Dihydroxy-4-methoxybenzophenone (DHMB) is a chemical compound used in the manufacturing of sunscreens. It is also used as an antioxidant and antiinflammatory agent in topical preparations. The genotoxic effects of DHMB are well documented, but it is unclear whether these effects are due to UV radiation or other mechanisms. DHMB has been shown to be toxic to cells in vivo and in vitro. There have been reports of skin cancer developing on the ears of rats following chronic exposure to this chemical. DHMB binds to the estrogen receptor, which may be responsible for its genotoxic activity. This chemical has also been shown to inhibit the growth of bacteria such as Pseudomonas aeruginosa and Escherichia coli by binding with fatty acids on the cell membrane surface. DHMB is used for wastewater treatment because it can bind with heavy metals and remove them from water sources.Formula:C14H12O4Purity:Min. 95%Color and Shape:Yellow To Dark Yellow SolidMolecular weight:244.24 g/mol2,2'-Dihydroxy-4-methoxybenzophenone
CAS:2,2'-Dihydroxy-4-methoxybenzophenonePurity:98+%Molecular weight:244.24g/mol2,2'-Dihydroxy-4-methoxybenzophenone
CAS:Formula:C14H12O4Purity:>98.0%(GC)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:244.25