B34656
Biphenyl
99.5%, flakes, powder or crystals, ReagentPlus®
Synonyme(s) :
Diphenyl, 1,1′-Biphenyl
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A propos de cet article
Formule linéaire :
C6H5C6H5
Numéro CAS:
Poids moléculaire :
154.21
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-163-5
MDL number:
Beilstein/REAXYS Number:
1634058
Assay:
99.5%
Form:
flakes, powder or crystals
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Laissez-nous vous aiderNom du produit
Biphenyl, ReagentPlus®, 99.5%
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
vapor density
5.31 (vs air)
vapor pressure
9.46 mmHg ( 115 °C)
product line
ReagentPlus®
assay
99.5%
form
flakes, powder or crystals
autoignition temp.
1004 °F
expl. lim.
0.6 %, 111 °F, 5.8 %, 166 °F
bp
255 °C (lit.)
Quality Level
Gene Information
human ... CYP1A2(1544), ESR1(2099)
functional group
phenyl
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General description
Biphenyl (BP) is a p-polyphenyl containing two phenyl rings with a non-planar conformation. Its synthesis from benzene by intermolecular direct C-H homocoupling in the presence of palladium-containing catalytic system has been described. Stereochemical studies of its structure have been reported. The nitration of BP using 95% nitric acid to form mononitrobiphenyl isomers has been investigated.
Application
- Application of Sublimation in the Synthesis and Crystal Growth of Organosulfones: Utilizing sublimation techniques for the synthesis and growth of organosulfone crystals, this study demonstrates how biphenyl derivatives can be integrated into advanced material science applications (Refat et al., 2024).
- Bicarbazole-Benzophenone Based Twisted Donor-Acceptor Derivatives: Research on bicarbazole-benzophenone derivatives highlights their role as potential blue thermally activated delayed fluorescence emitters for OLED applications, showcasing the utility of biphenyl frameworks in the development of electronic materials (Siddiqui et al., 2024).
- Optimization of Gas Chromatography Methods for Organic Contaminants: A study details the optimization of a gas chromatography method coupled with Orbitrap mass spectrometry, emphasizing the detection of biphenyl-based organic contaminants in biological samples, crucial for environmental monitoring (Oró-Nolla et al., 2024).
- Enhanced Solubility and Bioavailability of Antifungal Agents: This investigation presents how biphenyl structures can improve the solubility and bioavailability of clotrimazole, proposing enhanced antifungal treatments through the use of hydrophobized hyperbranched polyglycidol (Jaworska-Krych et al., 2024).
- Bioremediation of Persistent Organic Pollutants: A systematic review discusses the use of microalgae-bacteria consortia for the bioremediation of biphenyl-containing persistent organic pollutants, providing a sustainable approach to environmental cleanup (Guo et al., 2024).
Legal Information
ReagentPlus 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
Classe de stockage
11 - Combustible Solids
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Lujiang Xu et al.
Waste management (New York, N.Y.), 92, 97-106 (2019-06-05)
Terephthalonitrile (TPN) was directly produced from polyethylene terephthalate (PET) plastic via catalytic fast pyrolysis with ammonia. The optimal condition for producing TPN was over 1 g γ-Al2O3-2 wt% catalyst at 500 °C under carrier gas (50% NH3 and 50% N2) with yield of
Zeolite-assisted nitration of biphenyl using nitric acid.
Tai Y, et al.
Research on Chemical Intermediates, 41(2), 867-872 (2015)
Elucidation of the Forces Governing the Stereochemistry of Biphenyl.
Jia J, et al.
European Journal of Organic Chemistry, 2013(3), 611-616 (2013)
Highly Active Palladium-Based Catalyst System for the Aerobic Oxidative Direct Coupling of Benzene to Biphenyl.
Liu Y, et al.
ChemCatChem, 8(2), 448-454 (2016)
Sheng-Hao Hsu et al.
Acta biomaterialia, 8(11), 4151-4161 (2012-07-31)
Low-shrinkage resin-based photocurable liquid crystalline epoxy nanocomposite has been investigated with regard to its application as a dental restoration material. The nanocomposite consists of an organic matrix and an inorganic reinforcing filler. The organic matrix is made of liquid crystalline
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