|Place of Origin:||China|
|Minimum Order Quantity:||unlimited|
|Packaging Details:||plastic drum/carton drum/bag/|
|Delivery Time:||3-10 working days|
|Grade:||Electronic Grade||Solubility:||Solubility In 20ºC Water Is 2.1g/L|
|Appearance:||Near Colorless To Pale Yellow Liquid||Smell:||Sligtly Unpleasant Odor|
|Cas No.:||126213-50-1||Application:||1. In Solid Electrolytic Capacitor, 2. In Antistatic Coating 3. The Super Material Of Capacitor Elect 3. OEL Display Technology 4. As The Fine Characteristics Of PEDT 5. Other|
|Supply Ability:||35t Per Month|
high purity chemicals,
industrial grade chemicals
3,4-ethylen3dioxythiophene Electronic Grade Chemicals For Conductive Polymers
BeiLi is a leading manufacturer of 3,4-ethylenedioxythiophene(EDOT) 126213-50-1 which has the patented technology for producing high quality EDOT.
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.
3,4-ethylenedioxythiophene(EDOT) Chemical Specification
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.
|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|
|refractive index||n20/D 1.5765(lit.)|
|density||1.331 g/mL at 25 °C(lit.)|
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.
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:
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.
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)Headquartered in Lianyungang which is an international port city, one of China's top ten seaports. 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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