35800
联苯
PESTANAL®, analytical standard
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线性分子式:
C6H5C6H5
化学文摘社编号:
分子量:
154.21
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-163-5
Beilstein/REAXYS Number:
1634058
MDL number:
InChI key
ZUOUZKKEUPVFJK-UHFFFAOYSA-N
InChI
1S/C12H10/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1-10H
SMILES string
c1ccc(cc1)-c2ccccc2
grade
analytical standard
vapor density
5.31 (vs air)
vapor pressure
9.46 mmHg ( 115 °C)
product line
PESTANAL®
autoignition temp.
1004 °F
shelf life
limited shelf life, expiry date on the label
expl. lim.
0.6 %, 111 °F, 5.8 %, 166 °F
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
255 °C (lit.)
Quality Level
application(s)
agriculture
environmental
format
neat
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Application
Biphenyl may also serve as a polymerizable electrolyte additive for overcharge protection of lithium ion batteries.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
危险化学品
此项目有
Electrochemical behavior of biphenyl as polymerizable additive for overcharge protection of lithium ion batteries
Xiao L, et al.
Electrochimica Acta, 49, 4189-4196 (2004)
Shi-Rong Liu et al.
Organic letters, 15(4), 878-881 (2013-02-05)
A BODIPY-based fluorescent probe, HCSe, has been successfully developed for the rapid detection of hypochlorous acid based on the specific HOCl-promoted oxidation of diphenyl selenide in response to the amount of HOCl. Confocal fluorescence microscopy imaging using RAW264.7 cells showed
Susan L Zultanski et al.
Journal of the American Chemical Society, 135(2), 624-627 (2013-01-04)
The first Suzuki cross-couplings of unactivated tertiary alkyl electrophiles are described. The method employs a readily accessible catalyst (NiBr(2)·diglyme/4,4'-di-tert-butyl-2,2'-bipyridine, both commercially available) and represents the initial example of the use of a group 10 catalyst to cross-couple unactivated tertiary electrophiles
Xiaofeng Chen et al.
The Journal of organic chemistry, 77(17), 7572-7578 (2012-08-07)
A highly efficient cross-coupling of diarylborinic acids and anhydrides with aryl chlorides and bromides has been effected by using a palladium catalyst system co-supported by a strong σ-donor N-heterocyclic carbene (NHC), N,N'-bis(2,6-diisopropylphenyl) imidazol-2-ylidene, and a strong π-acceptor phosphite, triphenylphosphite, in
Yang Ou et al.
Chemical communications (Cambridge, England), 49(33), 3473-3475 (2013-03-22)
A novel A21-CuI catalyzed direct nitrogenation of biphenyl halides for the direct synthesis of carbazoles via a direct C-H amination process has been developed. A recyclable and inexpensive Cu-catalyst was successfully employed in N-heterocyclic compound synthesis via tandem azidation and
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