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323578

Sigma-Aldrich

2,2′-Dihydroxy-4-methoxybenzophenone

98%

Sinónimos:

Dioxybenzone

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About This Item

Fórmula lineal:
CH3OC6H3(OH)COC6H4OH
Número de CAS:
131-53-3
Peso molecular:
244.24
EC Number:
205-026-8
MDL number:
MFCD00002218
UNSPSC Code:
12162002
PubChem Substance ID:
24859402
NACRES:
NA.23

assay

98%

form

powder

bp

170-175 °C/1 mmHg (lit.)

mp

73-75 °C (lit.)

SMILES string

COc1ccc(c(O)c1)C(=O)c2ccccc2O

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

MEZZCSHVIGVWFI-UHFFFAOYSA-N

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Categorías relacionadas

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Wen Luo et al.
Journal of enzyme inhibition and medicinal chemistry, 26(5), 706-711 (2011-01-22)
A novel series of N,N'-bis-methylenedioxybenzyl-alkylenediamines 5a-5g have been designed, synthesized and evaluated as bivalent anti-Alzheimer's disease ligands. The enzyme inhibition assay results indicated that compounds 5e-5g inhibit both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) in the micromolar range (IC(50), 2.76-4.24 µM
Vaughn F Sherwood et al.
Cutaneous and ocular toxicology, 31(4), 273-279 (2012-01-20)
Sunscreens are widely utilized due to the adverse effects of ultraviolet (UV) radiation on human health. The safety of their active ingredients as well as that of any modified versions generated during use is thus of concern. Chlorine is used
N Negreira et al.
Analytica chimica acta, 638(1), 36-44 (2009-03-21)
A sensitive procedure for the determination of three UV filters: ethylhexyl salicylate (EHS), 3,3,5-trimethylcyclohexyl salicylate (Homosalate, HMS), 2-hydroxy-4-methoxybenzophenone (BP-3) and two related hydroxylated benzophenones (2,4-dihydroxybenzophenone, BP-1 and 2,2'-dihydroxy-4-methoxybenzophenone, BP-8) in water samples is presented. Analytes were first concentrated on the
Stephen E Duirk et al.
Water research, 47(2), 579-587 (2012-11-22)
The transformation of two benzophenone UV filters (Oxybenzone and Dioxybenzone) was examined over the pH range 6-11 in the presence of excess aqueous chlorine. Under these conditions, both UV filters were rapidly transformed by aqueous chlorine just above circumneutral pH
G Subba Rao et al.
Anticancer research, 33(6), 2535-2540 (2013-06-12)
Sunscreen compounds with added benefit of skin cancer prevention have both public and commercial interests. Our earlier study using the Epstein-Barr virus early antigen in vitro assay reported on skin cancer chemoprevention potential of benzophenone sunscreens. We now report the
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