B33706
Bibenzyl
ReagentPlus®, 99%
Synonym(s):
1,2-Diphenylethane, Dibenzyl
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About This Item
Linear Formula:
C6H5CH2CH2C6H5
CAS Number:
Molecular Weight:
182.26
Beilstein/REAXYS Number:
508068
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
product line
ReagentPlus®
assay
99%
form
crystals
autoignition temp.
896 °F
bp
284 °C (lit.)
mp
50-53 °C (lit.)
density
1.014 g/mL at 25 °C (lit.)
SMILES string
C(Cc1ccccc1)c2ccccc2
InChI
1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2
InChI key
QWUWMCYKGHVNAV-UHFFFAOYSA-N
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Application
Bibenzyl is used in the preparation of flame-retardant, high-density rigid polyurethane foams. Additionally, it can also be used to synthesize acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibitors.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Flame?retardant and mechanical properties of high?density rigid polyurethane foams filled with decabrominated dipheny ethane and expandable graphite.
Ye L, et al.
Journal of Applied Polymer Science, 111(5), 2372-2380 (2009)
Design, synthesis, and biological evaluation of a new series of biphenyl/bibenzyl derivatives functioning as dual inhibitors of acetylcholinesterase and butyrylcholinesterase.
Wang D M, et al.
Molecules (Basel), 22(1), 172-172 (2017)
K H Fritzemeier et al.
European journal of biochemistry, 133(3), 545-550 (1983-07-01)
Hydroxy derivatives of 9,10-dihydrophenanthrenes, orchinol and hircinol, were isolated from bulbs of Orchidaceae which had been induced to accumulate phytoalexins. Incorporation of radioactive precursors, L-phenylalanine and various hydroxycinnamic acids, has been investigated by feeding experiments in vivo. m-Coumaric acid and
Evan G Buchanan et al.
The Journal of chemical physics, 138(6), 064308-064308 (2013-02-22)
The spectroscopy of two flexible hydrocarbons, 1,2-diphenylethane (DPE) and 2,2,2-paracyclophane (TCP) is presented, and a predictive theoretical model for describing the alkyl CH stretch region of these hydrocarbons is developed. Ultraviolet hole-burning spectroscopy identified two isomers of DPE and a
Kohei Hosoi et al.
Chemical communications (Cambridge, England), 47(30), 8632-8634 (2011-07-02)
Electron transfer behavior of 1,2-diphenyl-o-carborane was investigated by cyclic voltammetry (CV). In the presence of 1,2-dibromo-1,2-diphenylethane, a significant catalytic current was observed. The macroscale electrocatalytic reduction of the dibromide using a catalytic amount (1 mol%) of the carborane mediator afforded
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