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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-096-4
Beilstein/REAXYS Number:
508068
MDL number:
Product Name
Bibenzyl, ReagentPlus®, 99%
InChI key
QWUWMCYKGHVNAV-UHFFFAOYSA-N
InChI
1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2
SMILES string
C(Cc1ccccc1)c2ccccc2
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.)
Quality Level
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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
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
Geunhyeong Jo et al.
Magnetic resonance in chemistry : MRC, 49(6), 374-377 (2011-04-01)
Resveratrol is a polyphenol isolated from many natural sources including grapes, mulberries, eucalyptus, spruce, lilies, and peanuts. The hydroxyl groups in polyphenols can be substituted with various functional groups, allowing production of multiple derivatives. NMR spectroscopy is used to identify
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