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Quality Level
Assay
99%
form
powder
mp
164-166 °C (lit.)
SMILES string
OC(=O)c1cccc(c1)C(=O)c2ccccc2
InChI
1S/C14H10O3/c15-13(10-5-2-1-3-6-10)11-7-4-8-12(9-11)14(16)17/h1-9H,(H,16,17)
InChI key
AXJXRLHTQQONQR-UHFFFAOYSA-N
Application
3-Benzoylbenzoic acid has been used in:
- light-induced reactions on benzophenone-terminated boron-doped diamond (BDD) surfaces
- preparation of benzophenone flavonol derivative
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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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Chemical communications (Cambridge, England), (27)(27), 2793-2795 (2007-07-05)
Irradiation of a patterned benzophenone-terminated boron-doped diamond (BDD) surface with UV light (lambda = 350 nm) in the presence of a 15(mer) oligonucleotide resulted in the covalent linking of the DNA strand to the BDD interface.
Synthesis of flavonol derivatives as probes of biological processes.
Tetrahedron Letters, 41(50), 9735-9739 (2000)
The journal of physical chemistry. B, 118(29), 8549-8558 (2014-06-20)
The Met residue oxidation has been studied for decades. Although many efforts have been made on the identification of free radicals, some doubts remain about their final fates, i.e., the nature of stable oxidation products. The photosensitized oxidation processes of
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