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07671

Supelco

Anthracene

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Sinónimos:

Anthraxcene, Paranaphthalene

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About This Item

Fórmula empírica (notación de Hill):
C14H10
Número de CAS:
120-12-7
Peso molecular:
178.23
Número de índice de color:
10790
Beilstein:
1905429
Número CE:
204-371-1
Número MDL:
MFCD00001240
Código UNSPSC:
41116107
eCl@ss:
39011608
ID de la sustancia en PubChem:
329748502
NACRES:
NA.24

grado

certified reference material
TraceCERT®

Nivel de calidad

300

densidad de vapor

6.15 (vs air)

presión de vapor

1 mmHg ( 145 °C)

Línea del producto

TraceCERT®

Formulario

powder or crystals

temp. de autoignición

1004 °F

caducidad

limited shelf life, expiry date on the label

fabricante / nombre comercial

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

condiciones de almacenamiento

under inert gas

técnicas

HPLC: suitable
gas chromatography (GC): suitable

bp

340 °C (lit.)

mp

210-215 °C (lit.)

solubilidad

alcohols: soluble
benzene: soluble
chloroform: soluble
hydronaphthalenes: soluble
supercritical carbon dioxide: soluble

aplicaciones

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

cadena SMILES

c1ccc2cc3ccccc3cc2c1

InChI

1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H

Clave InChI

MWPLVEDNUUSJAV-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

Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol .

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

H319,H410

Clasificaciones de peligro

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

249.8 °F - closed cup

Punto de inflamabilidad (°C)

121.0 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number

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Kohei Yazaki et al.
Chemical communications (Cambridge, England), 49(16), 1630-1632 (2013-01-23)
A bowl-shaped organic host was prepared by linking two anthracene-embedded bispyridine ligands with two methylene spacers. The water-soluble host has a hemispherical hydrophobic cavity (∼1 nm in diameter) with two cationic methylenebispyridinyl (Lewis acidic) moieties and shows the selective recognition
Jiang-Fei Xu et al.
Organic letters, 15(24), 6148-6151 (2013-11-19)
Dynamic covalent bonds supplied by reversible anthracene dimerization were combined with pillar[5]arene/imidazole host-guest interactions to construct double-dynamic polymers. Heating such polymers (in solution or as a gel) led to depolymerization by dissociation of either the host-guest complexes alone or the
Ling-Bao Xing et al.
Langmuir : the ACS journal of surfaces and colloids, 29(9), 2843-2848 (2013-02-12)
A new type of anthracene organogelator based on uracil was obtained using organic aromatic solvents, cyclohexane, DMSO, ethanol, and ethyl acetate. It was further characterized by field-emission scanning electron microscopy and transmission electron microscopy. Specifically, the resulting organogels were demonstrated
Mohammed S Almeataq et al.
Chemical communications (Cambridge, England), 49(22), 2252-2254 (2013-02-12)
The preparation of anthracene-based low band gap conjugated polymers comprising 2,6-linked anthracene and dithienyl-benzo[c][1,2,5]thiadiazole or dibithiophenyl-benzo[c][1,2,5]thiadiazole alternate repeat units is presented. The photophysical, electrochemical and photovoltaic properties of the polymers in bulk heterojunction solar cells using PC(71)BM as an acceptor
Qiuli Zhao et al.
Chemical communications (Cambridge, England), 48(95), 11671-11673 (2012-10-26)
Perylene bisimide derivatives substituted with one and two tetraphenylethene moieties at 1 and 1,7-postions show distinct optical properties. The former displays characteristic emission features of perylene bisimides in solution and red emission in the aggregate state, while the latter is
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