| 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. Monomer used in the synthesis of conducting polymers. |
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| IUPAC Name | 2,3-Dihydrothieno[3,4-b][1,4]dioxine |
| Molecular Weight | 142.18 |
| Molecular Formula | C6H6O2S |
| Canonical SMILES | C1COC2=CSC=C2O1 |
| InChI | InChI=1S/C6H6O2S/c1-2-8-6-4-9-3-5(6)7-1/h3-4H,1-2H2 |
| InChI Key | GKWLILHTTGWKLQ-UHFFFAOYSA-N |
| Boiling Point | 210.5±19.0 °C/760mmHg (lit.) |
| Melting Point | 10 °C |
| Flash Point | 81.1±21.5 °C |
| Purity | 95%+ |
| Density | 1.3±0.1 g/cm³ |
| Solubility | Slightly soluble in water |
| Appearance | Liquid |
| Application | EDOT can be polymerized to form poly(3,4-ethylenedioxythiophene) (PEDOT) for use as an electrochromic polymer (EC) based coating for a variety of s like solid state organic electrochemical supercapacitors (OESCs), electrochromic devices (ECDs), and carbon nanotubes (CNTs) based electrochemical devices for diabetes monitoring. It can be used: As a reductant in a one-pot synthesis of gold nanoparticles from HAuCl4 (254169). As a starting material used in palladium-catalyzed mono- and bis-arylation reactions. In the synthesis of conjugated polymers and copolymers, with potential optical s. |
| Storage | 2-8 °C |
| Assay | 97% |
| EC Number | 415-450-7;603-128-0 |
| MDL Number | MFCD02093622 |
| NACRES | NA.23 |
| Packaging | Packaging 10 g in glass bottle |
| Quality Level | 100 |
| Refractive Index | n20/D 1.571 (lit.) |