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Benz[b]anthracene - sublimed grade, 99.99% trace metals basis, high purity , CAS No.92-24-0

  • Cas Number:  92-24-0
  • Molecular Weight:  228.29
  • PubChem CID: 7080
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Item Number
B434579
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B434579-1g
1g
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$921.90
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Metabolite (5307)

Basic Description

Synonyms EINECS 202-138-9 | NAPHTHACENE [MI] | N0001 | naphthacene, benz[b]anthracene;tetracene, naphthacene, benz[b]anthracene | Benz(b)anthracene | FT-0695324 | AKOS024290196 | Chrysogen | MFCD00003702 | MLS000028646 | UNII-QYJ5Z6712R | Benz[b]anthracene | Benz[
Specifications & Purity PrimorTrace™, sublimed grade, ≥99.99% metals basis
Grade PrimorTrace™, sublimed grade
Product Description

Benz[ 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. Benz[ b ]anthracene is a fused polycyclic aromatic compound with an electron field-effect mobility of about 10 cm 2 /Vs


Application

p-Type organic conductor and OLED dopant. Sublimed grade for organic electronic device applications. Suitable for organic semiconductor lasers. Benz[ b ]anthracene can be used in a wide range of organic electronics based devices, which include organic light emitting diodes (OLEDs), solar cells, organic photovoltaics (OPVs), thin film transistors (TFTs), and other single crystal based organic semiconductors.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Naphthacenes
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Naphthacenes
Alternative Parents Aromatic hydrocarbons  Polycyclic hydrocarbons  Unsaturated hydrocarbons  
Molecular Framework Aromatic homopolycyclic compounds
Substituents Tetracene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
Description This compound belongs to the class of organic compounds known as naphthacenes. These are compounds containing a naphthacene moiety, which is a polyaromatic hydrocarbon made of four linearly fused benzene rings.
External Descriptors tetracenes - acene

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name tetracene
INCHI InChI=1S/C18H12/c1-2-6-14-10-18-12-16-8-4-3-7-15(16)11-17(18)9-13(14)5-1/h1-12H
InChIKey IFLREYGFSNHWGE-UHFFFAOYSA-N
Smiles C1=CC=C2C=C3C=C4C=CC=CC4=CC3=CC2=C1
Isomeric SMILES C1=CC=C2C=C3C=C4C=CC=CC4=CC3=CC2=C1
WGK Germany 3
Molecular Weight 228.29
Reaxy-Rn 1909299
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1909299&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Melt Point(°C) 357℃
Molecular Weight 228.300 g/mol
XLogP3 5.900
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 0
Exact Mass 228.094 Da
Monoisotopic Mass 228.094 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 236.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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