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Merck
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주요 문서

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687553

Sigma-Aldrich

Hydroxymethyl EDOT

95%

동의어(들):

(2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)methanol, EDT-methanol, Thieno[3,4-b]-1,4-dioxin-2-methanol

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크기 선택

500 MG
₩357,788

₩357,788

예상 입고일2025년 4월 21일세부사항

벌크 견적 요청
모든 사진(1)

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500 MG
₩357,788

About This Item

실험식(Hill 표기법):
C7H8O3S
CAS Number:
146796-02-3
Molecular Weight:
172.20
MDL number:
MFCD11045357
UNSPSC 코드:
12352103
PubChem Substance ID:
329761137
NACRES:
NA.23

₩357,788

예상 입고일2025년 4월 21일세부사항

벌크 견적 요청

Quality Level

100

분석

95%

양식

solid

mp

42-46 °C

저장 온도

2-8°C

SMILES string

OCC1COc2cscc2O1

InChI

1S/C7H8O3S/c8-1-5-2-9-6-3-11-4-7(6)10-5/h3-5,8H,1-2H2

InChI key

YFCHAINVYLQVBG-UHFFFAOYSA-N

관련 카테고리

일반 설명

Hydroxymethyl EDOT (EDT-methanol) is a conjugated polymer that is used as a precursor of ethylenedioxythiophene (EDOT). The hydroxymethyl groups in the EDOT monomers enhance the electro-polymerization in an aqueous solution to form an electro-active hydrophilic polymer.[1][2]

애플리케이션

EDOT derivative useful in preparation of functional electroactive polymers[3][4]
EDT-methanol can functionalize poly(L-lactic acid) by using organometallic polymerization, which can be used to form biodegradable and conducting macromonomers for biomedical applications.[5] It can be polymerized to form poly(hydroxymethyl EDOT) based films, which may be incorporated with silver nanoparticles to form nanocomposites on polyethylene terephthalate (PET) for flexible plastic devices.[6]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

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시험 성적서(COA)

Lot/Batch Number
MKCT5710
MKCT2281
MKCV4511
MKCM7782
MKCQ0520

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Perepichka, I.F.; Besbes, M.; Lecillian, E.; Salle, M.; Roncali, J.
Chemistry of Materials, 14, 449-449 (2002)
One pot biocatalytic synthesis of a biodegradable electroactive macromonomer based on 3, 4-ethylenedioxytiophene and poly (l-lactic acid).
da Silva AC, et al.
Materials Science and Engineering, C, 83(1), 35-43 (2018)
Modification of the electrochemical and electronic properties of electrogenerated poly (3, 4-ethylenedioxythiophene) by hydroxymethyl and oligo (oxyethylene) substituents
Akoudad S and Roncali J
Electrochemical Communications, 2(1), 72-76 (2000)
Antonio Dominguez-Alfaro et al.
Polymers, 13(3) (2021-02-13)
Carbon nanomaterials (CNMs) and conjugated polymers (CPs) are actively investigated in applications such as optics, catalysis, solar cells, and tissue engineering. Generally, CNMs are implemented in devices where the relationship between the active elements and the micro and nanostructure has
Hannah C Goldbach et al.
eLife, 10 (2021-02-02)
Primary visual cortex (V1) in the mouse projects to numerous brain areas, including several secondary visual areas, frontal cortex, and basal ganglia. While it has been demonstrated that optogenetic silencing of V1 strongly impairs visually guided behavior, it is not
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문서

Conjugated Polymers for the Engineering of Device/Tissue Interface

Conjugated polymers offer charge transport between inorganic, electrically conducting metals and organic, proton-conducting biological systems.

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