3,4-Ethylenedioxythiophene CAS#126213-50-1
3,4-Ethylenedioxythiophene is a synthetic organic compound characterized by its unique structure that includes a thiophene ring with ethylenedioxy substituents at the 3 and 4 positions. This compound is known for its potential applications in the synthesis of various organic materials, including pharmaceuticals and organic electronic devices such as sensors and solar cells. Its stability and reactivity make it a versatile intermediate in the chemical industry.
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3,4-Ethylenedioxythiophene CAS#126213-50-1
| 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) |
| 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 |
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3,4-Ethylenedioxythiophene is a synthetic organic compound characterized by its unique structure that includes a thiophene ring with ethylenedioxy substituents at the 3 and 4 positions. This compound is known for its potential applications in the synthesis of various organic materials, including pharmaceuticals and organic electronic devices such as sensors and solar cells. Its stability and reactivity make it a versatile intermediate in the chemical industry.
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This hydrochloride salt form of PHMG is highly soluble in water and is commonly used in various applications due to its non-irritant and non-toxic nature to human skin and mucous membranes. It is widely recognized for its ability to form a colorless and odorless solution, making it an ideal choice for use in personal care products, medical disinfectants, and water treatment processes.
The versatility of PHMG-HCl lies in its cationic nature, which allows it to bind to negatively charged microbial cell walls, disrupting their integrity and leading to cell death. This mechanism of action contributes to its effectiveness as a preservative and disinfectant. Moreover, its substantivity, or the ability to adhere to surfaces, enhances its long-lasting antimicrobial activity.
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