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182028

Sigma-Aldrich

聚环氧乙烷

average MV 600,000 (nominal), powder, hydroxyl, BHT as inhibitor

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别名:
PEO
线性分子式:
(-CH2CH2O-)n
CAS号:
25322-68-3
MDL编号:
MFCD00081839
UNSPSC代码:
12352104
PubChem化学物质编号:
24850972
NACRES:
NA.23

形式

powder

质量水平

100

分子量

average Mv 600,000 (nominal)

包含

200-500 ppm BHT as inhibitor

粘度

4,500-8,800 cP, 5 % in H2O(25 °C, Brookfield)(lit.)

转变温度

Tm 65 °C

Ω端

hydroxyl

α端

hydroxyl

应用

battery manufacturing

SMILES字符串

[H]OCCO

InChI

1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2

InChI key

LYCAIKOWRPUZTN-UHFFFAOYSA-N

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相关类别

一般描述

聚环氧乙烷（PEO）2是一种高分子量、非离子水溶性聚合物。它在水化时形成凝胶，并具有良好的膨胀能力。EPO聚合物无毒，广泛用于药物递送系统以改善药物可溶性。

应用

聚环氧乙烷可用于制备：
  • 用于药物缓释的可生物吸收、可注射水凝胶。
  • 用于燃料电池的PEO/氧化石墨烯复合电极膜。
  • 聚环氧乙烷-b-聚ε-己内酯（PEO-b-PC）二嵌段共聚物。内含氯沙坦钾的（PEO-b-PCL）共聚物可用作药物载体。

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

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Angeliki Chroni et al.
Nanomaterials (Basel, Switzerland), 10(9) (2020-09-24)
We report on the preparation of drug nanocarriers by encapsulating losartan potassium (LSR) into amphiphilic block copolymer micelles, utilizing the biocompatible/biodegradable poly(ethylene oxide)-b-poly(ε-caprolactone) (PEO-b-PCL) diblock copolymer. The PEO-b-PCL micelles and LSR-loaded PEO-b-PCL nanocarriers were prepared by organic solvent evaporation method
Jun Li et al.
Journal of biomedical materials research. Part A, 65(2), 196-202 (2003-05-08)
Polymeric hydrogels long have attracted interest for biomaterials applications because of their generally favorable biocompatibility. High in water content, they are particularly attractive for delivery of delicate bioactive agents, such as proteins. However, because they require covalent crosslinking for gelation
I L Konorova et al.
Patologicheskaia fiziologiia i eksperimental'naia terapiia, (4)(4), 7-9 (1991-07-01)
The search for antiaggregatory compounds is undertaken, as a rule, under in vitro conditions which do not reflect the dynamics of the real process. The present work deals with study of the peculiarities of the development of the collagen induced
M Patel Geeta et al.
Current drug delivery, 6(2), 159-165 (2009-05-20)
Carbamazepine indicated for the control of epilepsy, undergoes extensive hepatic first-pass metabolism after oral administration. A vaginal dosage form of carbamazepine is not commercially available. Conventional suppository having poor retention in the vaginal tract, as they are removed in a
D D Smyth et al.
Cardiovascular drugs and therapy, 4(1), 297-300 (1990-02-01)
Previous studies have demonstrated that Separan AP-30, a drag-reducing polymer, significantly decreased the formation of atherosclerotic plaques in rabbits fed a high-cholesterol diet. Furthermore, Separan AP-273, a polymer similar to but longer than Separan AP-30, markedly increased cardiac output in
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