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BeiLi Chemicals (Zhangjiagang) Co., Ltd.

Organic Printed Electronic Grade Chemicals 3,4-ethylene Dioxythiophene PEDOT

    • Organic Printed Electronic Grade Chemicals 3,4-ethylene Dioxythiophene  PEDOT
    • Organic Printed Electronic Grade Chemicals 3,4-ethylene Dioxythiophene  PEDOT
  • Organic Printed Electronic Grade Chemicals 3,4-ethylene Dioxythiophene  PEDOT

    Product Details:

    Place of Origin: China
    Brand Name: Bacavi
    Certification: ISO 9001:2008
    Model Number: EDT.99E.Y

    Payment & Shipping Terms:

    Minimum Order Quantity: unlimited
    Price: negotiation
    Packaging Details: plastic drum/carton drum/bag/
    Delivery Time: 3-10 working days
    Payment Terms: negotiation
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    Detailed Product Description
    Classification: Phenolic Compounds Cas No.: 126213-50-1
    Reach PR#: 05-2118156116-47-0000 Molecular Formula: C6H6O2S
    Synonyms:: EDT; 3,4-Ethylenedioxothiophene; AKOS BBS-00006360; 2,3-Dihydrothieno[3,4-B]-1,4-DIOXIN; 2,3-Dihydrothieno[3,4-B][1,4]DIOXINE; 3,4-Ethylenedioxo Thiophene; 3,4-ethylenedioxythiophene,EDOT,EDT; Thieno3,4-b-1,4-dioxin, 2,3-dihydro-; 3,4-Ethylenedioxythiophen P/N#: EDT.99E.Y
    Grade: Electronic Grade Smell: Sligtly Unpleasant Odor
    Density: 1.34g/cm3 Storage Condition: Store In A Cool, Dry Place
    Supply Ability: 35t Per Month

     

    Organic Printed Electronic Grade Chemicals 3,4-ethylene Dioxythiophene  PEDOT

     

     

    3,4-ethylene dioxythiophene, also known as 3,4-ethylenedioxythiophene, referred to as EDOT, colorless to pale yellow liquid, melting point of 10.5 ℃. Slightly soluble in water, 20 ℃ under the conditions of water solubility of 2.1g / L, a slight unpleasant odor.

     

    BeiLi is a leading manufacturer of 3,4-ethylenedioxythiophene(EDOT) 126213-50-1 which has the patented technology for producing high quality EDOT.

     

     

    EDOT/3,4-Ethylenedioxythiophene Description

     

    Spectroscopic and electrochemical studies of the oligomers revealed some general dependencies of their electronic properties on the total number and position of EDOT groups. It was the number of consecutive EDOT units rather than total number of these units which was found to have the most profound effect on electronic energy gap and conjugation length. This influence originates from the especially strong planarization induced in the conjugated backbone by the incorporation of EDOT units.

     

    In contrast, incorporation of thiophene units was found to result in loss of the conformational stabilization. This phenomenon was analyzed using the natural bond orbital computational approach, which revealed the predominantly hyperconjugative nature of the EDOT-induced conformational stabilization. Whereas shorter oligomers, in agreement with the general consensus, were found to be inert toward electrochemical polymerization due to low reactivity of electrochemically generated cation radical and dication species, the longest oligomer showed an unprecedentedly efficient electropolymerization to yield a stable thin film of an electroactive polymer.

     

     

    EDOT/3,4-Ethylenedioxythiophene Specification

     

    BeiLi Brand CAS 126213-50-1 99.9% 3,4-Ethylenedioxythiophene EDOT is using technology patents developed by the company with reliable quality assurance.Our patented technology makes it easy to obtain the target-3,4-Ethylenedioxythiophene EDOT with a short route, high product yield, mild reaction conditions, recyclable materials such as raw materials and solvents, which greatly reduces production costs, reducing the emission of waste, less pollution, with good prospects for industrial applications.

     

    P/N# EDT.99E.Y Grade Electronic grade
    Purity ≥99.90% Melting range 10.5ºC
    Water ≤0.1% Quality standard meets company specification

     

     

     

    3,4-ethylenedioxythiophene(EDOT) Chemical properties

     

    Related Categories Organic and Printed Electronics, Synthetic Tools and Reagents, Thiophene Monomers and Building Blocks
    InChI Key GKWLILHTTGWKLQ-UHFFFAOYSA-N
    assay 99.9%
    refractive index n20/D 1.5765(lit.)
    bp 193 °C(lit.)
    density 1.331 g/mL at 25 °C(lit.)
    storage temp. 2-8°C

     

     

    3,4-ethylenedioxythiophene(EDOT) application

     

    3,4-Ethylenedioxythiophene is used as a monomer to synthesize the conductive polymers and used as a reductant in the one-pot synthesis of gold nanoparticles from chloroauric acid, as starting material used in palladium-catalyzed mono and bis-arylation reactions and in the synthesis of conjugated polymers and copolymers, with potential optical applications. It is also used in redox activity, electroactivity and conductivity.

     

    Thiophene, also known as thiofuran, is a cyclic compound containing four carbon atoms and one sulphur atom in a ring. It is a toxic, flammable, highly reactive, colorless liquid insoluble in water (soluble in alcohol and ether) and melts at 38 C, boils at 84 C. It is used as a solvent and chemical intermediate. Its derivatives are widely used in manufacturing dyes, aroma compounds and pharmaceuticals. They are used as monomers to make condensation copolymers.

     

    Due to extended pi-electron cloud overlaps, organometallic molecules or aromatic oligometers such as anthracene exhibit semiconductor properties. Conductive polymers have extended delocalized bonds that creates electrical conductivity when charge carriers generated make positive charges (holes) and negative charges (electrons) move to opposite electrodes. Doping is the intentional impurities in a pure semiconductor to generate charge carriers. The transportation of charges is responsible for fluorescence and electrical energy. These can form well-ordered thin crystalline films. Organic semiconductors have some merits of self radiation, flexibility, light weight, easy fabrication, and low cost. Organic electroluminescence materials have lead to the rapid development of photovoltaic and display devices such as organic solar cells, biosensitizers, OLED(Organic Light Emiting Diode), OTFT(Organic Thin Film Transistor), Wearable Display, and e-Paper. Some examples of organic electroluminescence materials are:

    • Oligomer Electro Luminescence Materials
      • 8-hydroxyquinoline aluminum
      • Anthracene
      • Pentacene
      • Penyl substituent cyclopentadiene derivatives
      • Phthaloperinone derivatives
      • Perylene derivatives
      • Rubrene
    • Polymer Electro Luminescence Materials
      • Polyanilines
      • Poly(p-phenylenevinylene)s
      • Poly(thiophene)s
      • Poly(alkylfluorene)s
      • Poly(acetylene)s

    3,4-Ethylenedioxythiophene is a monomer for the manufacture of conjugated polymer [ poly(3,4-ethylenedioxythiophene)] for the applications of redox activity, electroactivity, and conductivity.

     

     

    Competitive Advantage

     

    1) We can provide customers with "one-stop" packaging service ,from research, development, production, export and so on.

    2) Powerful R&D strength let our technology in a leading level, forever, in turn, to provide customers with better service.

    3) We have ISO certificate which let the customers more satisfied and rest assured.

    4) More than 20 years of export experience, we can provide customers with more professional service.

    5) Mix and different products in ONE PCL, increase the working efficiency for customers.

    6) At the same time, BeiLi has a branch in Shanghai. Shanghai, is one of the world's largest port, convenient for the customers provide logistics services.

     

     

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