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B9300

Sigma-Aldrich

Benzophenone

ReagentPlus®, 99%

Synonym(s):

Diphenyl ketone, Diphenylmethanone, NSC 8077

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About This Item

Linear Formula:
(C6H5)2CO
CAS Number:
119-61-9
Molecular Weight:
182.22
Beilstein:
1238185
EC Number:
204-337-6
MDL number:
MFCD00003076
UNSPSC Code:
12352100
PubChem Substance ID:
24892133
NACRES:
NA.22

vapor pressure

1 mmHg ( 108 °C)

Quality Level

200

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

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H350,H373,H412

Hazard Classifications

Aquatic Chronic 3 - Carc. 1B - STOT RE 2 Oral

Target Organs

Liver,Kidney

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

280.4 °F - closed cup

Flash Point(C)

138 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000367266
0000367266
0000263997
BCCL2042
BCCJ8388

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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
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%
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
Feifan Yu et al.
PloS one, 8(2), e56597-e56597 (2013-02-21)
Affinity proteins binding to antibody constant regions have proved to be invaluable tools in biotechnology. Here, protein engineering was used to expand the repertoire of available immunoglobulin binding proteins via improvement of the binding strength between the widely used staphylococcal
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