B9300
Benzophénone
99%, flakes, ReagentPlus®
Synonyme(s) :
Diphenyl ketone, Diphenylmethanone, NSC 8077
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A propos de cet article
Formule linéaire :
(C6H5)2CO
Numéro CAS:
Poids moléculaire :
182.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
204-337-6
MDL number:
Beilstein/REAXYS Number:
1238185
Assay:
99%
Form:
flakes
Service technique
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Laissez-nous vous aiderNom du produit
Benzophénone, ReagentPlus®, 99%
vapor pressure
1 mmHg ( 108 °C)
Quality Level
product line
ReagentPlus®
assay
99%
form
flakes
bp
305 °C (lit.)
mp
47-51 °C (lit.)
functional group
ketone, phenyl
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)
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
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Carc. 1B - STOT RE 2 Oral
target_organs
Liver,Kidney
Classe de stockage
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
280.4 °F - closed cup
flash_point_c
138 °C - closed cup
ppe
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