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181994

Sigma-Aldrich

Poly(ethylene oxide)

average MV 200,000 (nominal), powder, hydroxyl, BHT as inhibitor

Synonym(s):

Polyethylene oxide, PEO

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About This Item

Linear Formula:
(-CH2CH2O-)n
CAS Number:
MDL number:
UNSPSC Code:
12352104
PubChem Substance ID:
NACRES:
NA.23

product name

Poly(ethylene oxide), average Mv 200,000 (nominal), powder

form

powder

mol wt

average Mv 200,000 (nominal)

contains

200-500 ppm BHT as inhibitor

viscosity

65-115 cP, 5 % in H2O(25 °C, Brookfield)(lit.)

transition temp

Tm 65 °C

Ω-end

hydroxyl

α-end

hydroxyl

application(s)

battery manufacturing

SMILES string

[H]OCCO

InChI

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

InChI key

LYCAIKOWRPUZTN-UHFFFAOYSA-N

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General description

Poly(ethylene oxide) (PEO) is a synthetichydrophilic polymer available in several molecular weights. It can be obtained by the ring-opening polymerization ofethylene oxide. It is a semicrystalline polymer with high ionic conductivitycommonly used as a solid polymer electrolyte.

Application

Poly(ethylene oxide) can be used to prepare polymer electrolyte systems for energy storage and conversion devices such as all-solid-state lithium-ion batteries (ASLBs).

This biocompatible polymer can be widely used in the field of biomedical research and tissue engineering. For example, it can be used in the fabrication of biodegradable polyurethane/graphene oxide scaffolds.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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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
P I Polimeni et al.
Journal of cardiovascular pharmacology, 14(3), 374-380 (1989-09-01)
The acute hemodynamic effects of an intravenously (i.v.) injected poly(ethylene oxide), Polyox WSR N-60K (dose 50 mg/kg), were studied in the open-chest rat anesthetized with sodium pentobarbital. The injectate is one of four drag-reducing polymers known to augment in vitro

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