NAPHTHACENE

NAPHTHACENE
  • CAS No.:92-24-0
Other grades of this product :
NAPHTHACENE Chemical Properties
Melting point >300 °C(lit.)
Boiling point 305.1°C (rough estimate)
density 1.35
refractive index 1.5500 (estimate)
form Crystalline Powder
color Orange
Water Solubility 1.507ug/L(25 ºC)
Merck 14,6369
BRN 1909299
Stability:Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference92-24-0(CAS DataBase Reference)
EPA Substance Registry SystemNaphthacene (92-24-0)
Safety Information
Hazard Codes Xn,N
Risk Statements 40-50/53
Safety Statements 45-36/37-61-60-24/25
RIDADR UN 3077 9/PG 3
WGK Germany 3
RTECS QI7605000
HS Code 29029090
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
NAPHTHACENE Usage And Synthesis
Chemical Propertiesorange powder
Usesp-Type organic conductor and OLED dopant. Sublimed grade for organic electronic device applications.
UsesNaphthacene is a polycyclic aromatic hydrocarbon. Naphthacene is often used as a molecular organic semiconductor in organic field-effect transistors and organic light-emitting diodes. Naphthacene is a lso used in various applications involving the enhancement of photocurrent.
UsesNaphthacene is a polycyclic aromatic hydrocarbon. Naphthacene is often used as a molecular organic semiconductor in organic field-effect transistors and organic light-emitting diodes. Naphthacene is also used in various applications involving the enhancement of photocurrent.
DefinitionChEBI: An acene that consists of four ortho-fused benzene rings in a rectilinear arrangement.
General DescriptionBenz[b]anthracene is an ethylnylated acene that is a conducting polymer, which can be used as a donor material. It has a high photoluminescence and quantum yield that makes it a promising candidate in the development of single crystal electronic material.
HazardExplodes when shocked, reacts with oxidizing materials.
Purification MethodsNaphthacene crystallises in orange needles from EtOH, *C6H6 or toluene. Dissolve it in sodium-dried *benzene and pass it through a column of alumina. The eluent is evaporated under vacuum, and the chromatography is repeated using fresh *benzene. Finally, the naphthacene is sublimed in vacuo at 186o. [Martin & Ubblehode J Chem Soc 4948 1961, UV: Clar Chem Ber 65 517 1932, Clar Chem Ber 69 607 1936, IR: Cannon & Sutherland Spectrochim Acta 4 373 1951, Beilstein 5 H 718, 5 IV 2545.]

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