PubChem CID | 16067438 |
Synonyms: (2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)methanol, EDT-methanol, Thieno[3,4-b]-1,4-dioxin-2-methanol
Hydroxymethyl EDOT (CAS NO 146796-02-3) available for purchase. Minimum purity is 97%. This item is an exclusive product from Sarchem Laboratories and in stock.
PubChem CID | 16067438 |
Synonyms: (2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)methanol, EDT-methanol, Thieno[3,4-b]-1,4-dioxin-2-methanol
Hydroxymethyl EDOT (CAS NO 146796-02-3) available for purchase. Minimum purity is 97%. This item is an exclusive product from Sarchem Laboratories and in stock.
Hydroxymethyl EDOT (also known as 3,4-Ethylenedioxythiophene-2,2-dimethanol or H-MeEDOT) is a derivative of the organic compound EDOT (3,4-ethylenedioxythiophene). It is a white crystalline solid that is soluble in water and common organic solvents.
It is a conjugated polymer that serves as a starting material for ethylenedioxythiophene (EDOT) production.
Hydroxymethyl EDOT is commonly used as a monomer for the synthesis of conductive polymers, particularly poly(3,4-ethylenedioxythiophene) or PEDOT. This polymer has excellent electrical conductivity and is used in a wide range of applications, including organic light-emitting diodes (OLEDs), organic solar cells, and electrochromic displays.
Hydroxymethyl EDOT (EDT-methanol) is a conjugated polymer serving as an ethylenedioxythiophene precursor. The hydroxymethyl groups of EDOT monomers promote electropolymerization in a water-based solution, resulting in an electroactive hydrophilic polymer.
EDOT derivatives help create functional electroactive polymers.
EDT-methanol may functionalize poly(L-lactic acid) by organometallic polymerization, yielding biodegradable and conductive macromonomers for biomedical applications. It may be polymerized to produce poly(hydroxymethyl EDOT)-based films, which can then be combined with silver nanoparticles to create nanocomposites on polyethene terephthalate (PET) for flexible plastic devices.
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Melting Point | 42-46°C |
Specific Gravity Approx | Approx. 600 kg/m³ |
Flash Point | 110°C (230°F) |
Linear Formula | C7H8O3S |
IUPAC Name | (2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)methanol |
Formula Weight | 172.2 AMU |
percent purity | Not specified |
Physical Form | Solid (Powder) |
Chemical Name or Material | Hydroxymethyl EDOT |
Classification of the substance or mixture
Not a hazardous substance or mixture.
GHS Label elements, including precautionary statements
Not a hazardous substance or mixture.
Hazards not otherwise classified (HNOC) or not covered by GHS
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none
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Hydroxymethyl EDOT's molecular structure includes a hydroxymethyl group, distinguishing it from conventional EDOT compounds. This redesigned EDOT structure improves reactivity and compatibility for advanced polymer synthesis and specialised electrical applications.
The EDOT structure of hydroxymethyl EDOT, which includes a hydroxymethyl group, improves solubility and cross-linking potential. These qualities make it perfect for making conductive polymers with excellent performance in different technological sectors.
Hydroxymethyl EDOT's modified EDOT structure improves conductivity and stability. Its hydroxymethyl activity makes it an essential EDOT chemical for developing sophisticated electronic materials such as sensors and organic light-emitting diodes (OLEDs).
The hydroxymethyl group in hydroxymethyl EDOT improves the reactivity of the EDOT structure. This alteration provides various applications in creating high-performance conductive polymers and functional coatings.
Hydroxymethyl EDOT is produced by controlled processes introducing a hydroxymethyl group into the EDOT molecule. This assures chemical integrity and compatibility for the production of high-performance materials in various sectors.