3,4-Ethylenedioxythiophene

3,4-Ethylenedioxythiophene Basic information
Product Name:3,4-Ethylenedioxythiophene
Synonyms:EDOT;EDT;3,4-ETHYLENEDIOXOTHIOPHENE;3,4-ETHYLENEDIOXYTHIOPHENE;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 98+% GC
CAS:126213-50-1
MF:C6H6O2S
MW:142.18
EINECS:415-450-7
Product Categories:Thiophen;Sulphur Derivatives;Thiophenes;Thiophens;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, functional materials;EDOT;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, thiophen;OLED materials,pharm chemical,electronic;Pharmaceutical intermediates;126213-50-1
Mol File:126213-50-1.mol
3,4-Ethylenedioxythiophene Structure
3,4-Ethylenedioxythiophene Chemical Properties
Melting point 10 °C
Boiling point 193 °C (lit.)
density 1.331 g/mL at 25 °C (lit.)
vapor pressure 11.9Pa at 25℃
refractive index n20/D 1.5765(lit.)
Fp 230 °F
storage temp. 2-8°C
form clear liquid
color Colorless to Yellow
Water Solubility Immsicible with water. Miscible with alcohol and ether.
InChIKeyGKWLILHTTGWKLQ-UHFFFAOYSA-N
LogP1.976 at 25℃ and pH7.1
CAS DataBase Reference126213-50-1(CAS DataBase Reference)
EPA Substance Registry SystemThieno[3,4-b]-1,4-dioxin, 2,3-dihydro- (126213-50-1)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 21/22-36
Safety Statements 26-36
RIDADR UN 2810 6.1/PG 3
WGK Germany 2
TSCA Yes
HazardClass 6.1
PackingGroup III
HS Code 29349990
MSDS Information
ProviderLanguage
SigmaAldrich English
3,4-Ethylenedioxythiophene Usage And Synthesis
Chemical PropertiesLight yellow liquid
Uses3,4-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.
General Description3,4-Ethylenedioxythiophene (EDOT) is an electro-active conductive monomer with a thiol group that combines an electron donor and electron acceptor in a donor-acceptor-donor arrangement.
3,4-Ethylenedioxythiophene Preparation Products And Raw materials
Preparation Products2,3-DIHYDRO-5-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YL)THIENO[3,4-B][1,4]DIOXINE
5,7-Dibromo-2,3-dihydrothieno[3,4-b][1,4]dioxine 2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5-CARBALDEHYDE N-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YLMETHYL)-N-METHYLAMINE 2,2',3,3'-TETRAHYDRO-[5,5'-BITHIENO[3,4-B]-1,4-DIOXIN]-7,7'-DICARBOXALDEHYDE 7-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5-CARBOXALDEHYDE 97 5-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE 5-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE 2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5-CARBOXYLIC ACID 3,4-Ethylenedioxythiophene 7-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5-CARBONYL CHLORIDE 90 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN Thieno[3,4-b]-1,4-dioxin-5,7-dicarboxylic acid, 2,3-dihydro-, diethyl ester Selenium dioxide 5-(TRIBUTYLSTANNYL)-7-(5-(TRIBUTYLSTANNYL)-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-7-YL)-2,3-DIHYDROTHIENE DIOXOPROMETHAZINE HCL Tetrahydrothiophene Cephalothin sodium 7-BROMO-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5-CARBOXYLIC ACID

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