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| | 3,4-Ethylenedioxythiophene Basic information |
| Product Name: | 3,4-Ethylenedioxythiophene | | Synonyms: | 3,4-ETHYLENEDIOXOTHIOPHENE;3,4-ETHYLENEDIOXYTHIOPHENE;AKOS BBS-00006360;2,3-DIHYDROTHIENO[3,4-B]-1,4-DIOXIN;3,4-ETHYLENEDIOXO THIOPHENE 98+% GC;3,4-ethylenedioxythiophene,EDOT,EDT;Thieno3,4-b-1,4-dioxin, 2,3-dihydro-;3,4-Ethylenedioxythiophene(EDOT) | | CAS: | 126213-50-1 | | MF: | C6H6O2S | | MW: | 142.18 | | EINECS: | 415-450-7 | | Product Categories: | Thiophen;Sulphur Derivatives;Thiophens;Thiophenes;EDOT;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, functional materials;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 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. | | InChIKey | GKWLILHTTGWKLQ-UHFFFAOYSA-N | | LogP | 1.976 at 25℃ and pH7.1 | | CAS DataBase Reference | 126213-50-1(CAS DataBase Reference) | | EPA Substance Registry System | Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro- (126213-50-1) |
| 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 |
| | 3,4-Ethylenedioxythiophene Usage And Synthesis |
| Chemical Properties | Light yellow liquid | | Uses | 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. | | General Description | 3,4-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 |
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