B9300
Benzophenone
ReagentPlus®, 99%
Synonym(s):
Diphenyl ketone, Diphenylmethanone, NSC 8077
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All Photos(4)
About This Item
Linear Formula:
(C6H5)2CO
CAS Number:
Molecular Weight:
182.22
Beilstein:
1238185
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
vapor pressure
1 mmHg ( 108 °C)
Quality Level
product line
ReagentPlus®
Assay
99%
form
flakes
bp
305 °C (lit.)
mp
47-51 °C (lit.)
SMILES string
O=C(C1=CC=CC=C1)C2=CC=CC=C2
InChI
1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
InChI key
RWCCWEUUXYIKHB-UHFFFAOYSA-N
Gene Information
rat ... Ar(24208)
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Related Categories
Application
- Photo-crosslinkable bioglue development: A study demonstrated the creation of a surface-independent bioglue using a photo-crosslinkable benzophenone moiety, potentially enhancing medical adhesives for diverse applications (Shi et al., 2024).
- Organic explosive trace analysis: Research highlighted the use of benzophenone for improved preconcentration and analysis of organic explosive traces in aqueous samples, advancing forensic methodologies (Setayeshfar et al., 2024).
- OLEDs blue emitters: A publication introduced bicarbazole-benzophenone based twisted donor-acceptor derivatives as potential blue TADF emitters for OLED applications, showcasing the versatility of benzophenone in electronic devices (Siddiqui et al., 2024).
- Photodynamic antibacterial nonwovens: Research focused on the modification of traditional composite nonwovens with benzophenone to enable stable storage of light absorption transients and enhance photodynamic antibacterial effects, contributing to medical textile innovations (Li et al., 2024).
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Carc. 1B - STOT RE 2 Oral
Target Organs
Liver,Kidney
WGK
WGK 1
Flash Point(F)
280.4 °F
Flash Point(C)
138 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Jiawei Yang et al.
ACS applied materials & interfaces, 11(27), 24802-24811 (2019-06-14)
Recent innovations highlight the integration of diverse materials with synthetic and biological hydrogels. Examples include brain-machine interfaces, tissue regeneration, and soft ionic devices. Existing methods of strong adhesion mostly focus on the chemistry of bonds and the mechanics of dissipation
Claire Chatalova-Sazepin et al.
Angewandte Chemie (International ed. in English), 54(18), 5443-5446 (2015-03-05)
A three-component carboetherification of unactivated alkenes has been developed allowing the rapid building of complexity from simple starting materials. A wide range of α-substituted styrenes underwent smooth reactions with unactivated alkyl nitriles and alcohols to afford γ-alkoxy alkyl nitriles with
Masayuki Kyomoto et al.
Biomaterials, 34(32), 7829-7839 (2013-07-31)
We investigated the production of free radicals on a poly(ether-ether-ketone) (PEEK) substrate under ultraviolet (UV) irradiation. The amount of the ketyl radicals produced from the benzophenone (BP) units in the PEEK molecular structure initially increased rapidly and then became almost
Haidong Li et al.
Talanta, 99, 811-815 (2012-09-13)
Benzophenone is one of the most commonly used photoinitiators of UV-cured inks on food packaging materials and can migrate into foodstuffs. In this study, an amperometric benzophenone sensor based on molecularly imprinted polymer (MIP) was successfully constructed for the first
L L Barnkob et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 30(2), 395-402 (2012-11-17)
The aim of this study was to investigate the effect of relative humidity on the migration of benzophenone from paperboard into the food simulant Tenax®. Kinetic migration investigations were carried out with three relative humidities in the interval between 39%
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