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Key Documents

W213403

Sigma-Aldrich

Benzophenone

FCC, FG

Synonym(s):

Diphenyl ketone, Diphenylmethanone, NSC 8077

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About This Item

Linear Formula:
(C6H5)2CO
CAS Number:
Molecular Weight:
182.22
FEMA Number:
2134
Beilstein:
1238185
EC Number:
Council of Europe no.:
166
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
7.032
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

FG
Kosher

Agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FCC

vapor pressure

1 mmHg ( 108 °C)

Assay

99%

form

crystals or chunks (Crystalline)

bp

305 °C (lit.)

mp

47-51 °C (lit.)

solubility

ethanol: soluble 100 mg/mL, clear, colorless (80% ethanol)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

geranium; fruity; sweet

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

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General description

Benzophenone is an aromatic carbonyl compound. Photoinitiated free radical polymerization of benzophenone in the presence of N-methyldiethanolamine as a coinitiator has been reported. Polymeric benzophenone photoinitiator (PBP) has been synthesized by using “Thiol-ene Click Chemistry” and characterized by 1H NMR, FTIR, UV, and phosphorescence spectroscopies.

Application

Benzophenone is suitable anchoring agent used for the surface modification of graphene. It may be used in the preparation of N-(diphenylmethylene)-N′-(tert-butoxycarbonyl)-N′- (4-bromophenyl)-p-phenylenediamine.

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

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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Synthesis of main chain polymeric benzophenone photoinitiator via thiol-ene click chemistry and Its use in free radical polymerization.
Temel G, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 48(23), 5306-5312 (2010)
Photopolymerization and photophysical properties of amine linked benzophenone photoinitiator for free radical polymerization.
Temel G, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 219(1), 26-31 (2011)
Preparation and properties of poly (methacrylamide) s containing oligoaniline side chains.
Chen R and Benicewicz BC.
Macromolecules, 36(17), 6333-6339 (2003)
A powerful tool for graphene functionalization: Benzophenone mediated UV-grafting.
Roppolo I, et al.
Carbon, 77, 226-235 (2014)
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

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