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141984

Sigma-Aldrich

4,4′-Dimethoxybenzophenone

97%

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About This Item

Linear Formula:
(CH3OC6H4)2CO
CAS Number:
90-96-0
Molecular Weight:
242.27
Beilstein:
1878026
EC Number:
202-028-0
MDL number:
MFCD00008404
UNSPSC Code:
12352100
PubChem Substance ID:
24848516
NACRES:
NA.22

Assay

97%

form

powder

mp

141-143 °C (lit.)

SMILES string

COc1ccc(cc1)C(=O)c2ccc(OC)cc2

InChI

1S/C15H14O3/c1-17-13-7-3-11(4-8-13)15(16)12-5-9-14(18-2)10-6-12/h3-10H,1-2H3

InChI key

RFVHVYKVRGKLNK-UHFFFAOYSA-N

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General description

Photoreactivity of 4,4′-dimethoxybenzophenone with 2-aminobenzimidazole has been examined. It is an ultraviolet absorbing additive in plastic products.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Hirofumi Hirai et al.
Chemosphere, 55(4), 641-645 (2004-03-10)
Ligninolytic enzymes, manganese peroxidase (MnP), laccase, and lignin peroxidase (LiP), from white-rot fungi were used in an attempt to treat methoxychlor (MC), a chemical widely used as a pesticide. MnP and laccase in the presence of Tween 80 and 1-hydroxybenzotriazole
Xinggui Gu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(49), 17973-17980 (2015-10-23)
We present a nitrogen-containing polycyclic aromatic hydrocarbon (N-PAH), namely 12-methoxy-9-(4-methoxyphenyl)-5,8-diphenyl-4-(pyridin-4-yl)pyreno[1,10,9-h,i,j]isoquinoline (c-TPE-ON), which exhibits high quantum-yield emission both in solution (blue) and in the solid state (yellow). This molecule was unexpectedly obtained by a three-fold, highly regioselective photocyclodehydrogenation of a tetraphenylethylene-derived
Daisuke Nakajima et al.
Journal of UOEH, 28(2), 143-156 (2006-06-20)
This study examines the activities relating to the carcinogenicity of six types of benzophenone derivatives (benzophenone, 2-hydroxy-4-octyloxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2,4-dihydroxybenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone and 2,2'-dihydroxy-4,4'-dimethoxybenzophenone) currently used in plastic products as additives to serve as ultraviolet absorbing agents. The evaluation of the initiation
Dolors Jornet et al.
The journal of physical chemistry. B, 114(36), 11920-11926 (2010-08-26)
This work has examined the photoreactivity of benzophenone (3), 2-benzoylthiophene (4), 4-methoxybenzophenone (5), 4,4'-dimethoxybenzophenone (6), and 4-carboxybenzophenone (7) with 2-aminobenzimidazole (1). Laser flash photolysis (LFP) revealed quenching of the aromatic ketone triplets by 1, leading to formation of ketyl radicals

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