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Merck
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B9300

Sigma-Aldrich

Benzophénone

ReagentPlus®, 99%

Synonyme(s) :

Diphenyl ketone, Diphenylmethanone, NSC 8077

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About This Item

Formule linéaire :
(C6H5)2CO
Numéro CAS:
Poids moléculaire :
182.22
Numéro Beilstein :
1238185
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Pression de vapeur

1 mmHg ( 108 °C)

Niveau de qualité

Gamme de produits

ReagentPlus®

Pureté

99%

Forme

flakes

Point d'ébullition

305 °C (lit.)

Pf

47-51 °C (lit.)

Chaîne SMILES 

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

Clé InChI

RWCCWEUUXYIKHB-UHFFFAOYSA-N

Informations sur le gène

rat ... Ar(24208)

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Catégories apparentées

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).

Informations légales

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Health hazard

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Organes cibles

Liver,Kidney

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

280.4 °F - closed cup

Point d'éclair (°C)

138 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Les clients ont également consulté

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
Tao Zhang et al.
The Science of the total environment, 461-462, 49-55 (2013-05-29)
Limited information exists on the exposure of benzophenone (BP)-type UV filters (i.e., sunscreen compounds) in children, adults, and pregnant women in China. In this study, we determined the concentrations of five BP derivatives, BP-1, BP-2, BP-3, BP-8, and 4OH-BP in
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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