3,4-Ethylenedioxythiophene

Cat.No ACM126213501-2

Basic Information Description Application Features And Benefits

CAS	126213-50-1
Catalog Number	ACM126213501-2
Synonyms	EDOT
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
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
PubChem ID	24871861
Quality Level	100
Refractive Index	n20/D 1.571 (lit.)
Storage Temperature	2-8°C

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.

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.

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