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Merck
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96996

Supelco

Biphenyl

certified reference material, TraceCERT®

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About This Item

Fórmula lineal:
C6H5C6H5
Número de CAS:
92-52-4
Peso molecular:
154.21
Beilstein:
1634058
Número CE:
202-163-5
Número MDL:
MFCD00003054
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329770538
Número E:
E230
NACRES:
NA.24

grado

certified reference material
TraceCERT®

Nivel de calidad

300

densidad de vapor

5.31 (vs air)

presión de vapor

9.46 mmHg ( 115 °C)

Línea del producto

TraceCERT®

temp. de autoignición

1004 °F

caducidad

limited shelf life, expiry date on the label

lim. expl.

0.6 %, 111 °F
5.8 %, 166 °F

técnicas

HPLC: suitable
gas chromatography (GC): suitable

bp

255 °C (lit.)

mp

68-70 °C (lit.)

aplicaciones

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Formato

neat

cadena SMILES

c1ccc(cc1)-c2ccccc2

InChI

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

Clave InChI

ZUOUZKKEUPVFJK-UHFFFAOYSA-N

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Descripción general

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

Información legal

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

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palabra de señalización

Warning

Frases de peligro

H315,H319,H335,H410

Clasificaciones de peligro

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

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

13 - Non Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

230.0 °F - closed cup

Punto de inflamabilidad (°C)

110 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number

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Sigma-Aldrich

32299

Éter de petróleo (bencina)

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Sigma-Aldrich

270989

Acetato de etilo

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Sigma-Aldrich

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Jiyoung Seo et al.
Applied microbiology and biotechnology, 91(2), 219-228 (2011-06-01)
This review details recent progresses in the flavonoid biotransformation by bacterial non-heme dioxygenases, biphenyl dioxygenase (BDO), and naphthalene dioxygenase (NDO), which can initially activate biphenyl and naphthalene with insertion of dioxygen in stereospecfic and regiospecific manners. Flavone, isoflavone, flavanone, and
Pasha M Khan et al.
Bioorganic & medicinal chemistry letters, 23(2), 532-536 (2012-12-13)
The structure-activity relationship study of a diphenylpropanamide series of ROR-γ selective modulators is reported. Compounds were screened using chimeric receptor Gal4 DNA-binding domain (DBD)-NR ligand binding domain cotransfection assay in a two-step format. Three different regions of the scaffold were
Kathy D Miller et al.
Breast cancer research and treatment, 148(1), 99-106 (2014-09-27)
Preclinical data suggest that medroxyprogesterone acetate (MPA) has both anti-metastatic and anti-angiogenic activity in the absence of hormone receptors (HR). This phase II trial assessed the activity of MPA alone or in combination with low-dose chemotherapy in patients with metastatic
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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