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35800

Supelco

Biphenyl

PESTANAL®, analytical standard

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About This Item

Formula condensata:
C6H5C6H5
Numero CAS:
92-52-4
Peso molecolare:
154.21
Beilstein:
1634058
Numero CE:
202-163-5
Numero MDL:
MFCD00003054
Codice UNSPSC:
41116107
ID PubChem:
329755216
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Densità del vapore

5.31 (vs air)

Tensione di vapore

9.46 mmHg ( 115 °C)

Nome Commerciale

PESTANAL®

Temp. autoaccensione

1004 °F

Durata

limited shelf life, expiry date on the label

Limite di esplosione

0.6 %, 111 °F
5.8 %, 166 °F

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. eboll.

255 °C (lit.)

Punto di fusione

68-70 °C (lit.)

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

c1ccc(cc1)-c2ccccc2

InChI

1S/C12H10/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1-10H
ZUOUZKKEUPVFJK-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

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.

Note legali

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H315 - H319 - H335 - H410

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

230.0 °F - closed cup

Punto d’infiammabilità (°C)

110 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCK2124
BCCH2851
BCCF1061
BCCC2910
BCBV8835

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Sigma-Aldrich

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Benzhydrol United States Pharmacopeia (USP) Reference Standard

USP

1051602

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Sigma-Aldrich

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Supelco

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Sigma-Aldrich

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4-Bromobiphenyl

Electrochemical behavior of biphenyl as polymerizable additive for overcharge protection of lithium ion batteries
Xiao L, et al.
Electrochimica Acta, 49, 4189-4196 (2004)
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
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
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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