M6768
Methoxypolyethylene glycol 350
average mol wt 350
Synonym(s):
Polyethylene glycol, Methoxypolyethylene glycol, Poly(ethylene glycol) methyl ether, mono-Methyl polyethylene glycol 350
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About This Item
Linear Formula:
CH3O(CH2CH2O)nH
CAS Number:
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.25
description
non-ionic
Quality Level
mol wt
average mol wt 350
application(s)
microbiology
InChI
1S/C3H8O2/c1-5-3-2-4/h4H,2-3H2,1H3
InChI key
XNWFRZJHXBZDAG-UHFFFAOYSA-N
Related Categories
General description
Methoxypolyethylene glycol 350 is a polymer similar in structure and nomenclature to polyethylene glycols.
Application
Methoxypolyethylene glycol 350 has been used in a study to assess the synthesis of a new class of thermosensitive micellar cyclotriphosphazenes. It has also been used in a study to investigate synthesis of a new amphiphilic poly(organophosphazene) by stepwise nucleophilic substitution.
WGK
WGK 1
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Thermosensitive and biocompatible cyclotriphosphazene micelles
U, Toti.
J. Controlled Release, 119, 7-7 (2007)
S J Hermansky et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(10-11), 1031-1039 (1998-02-17)
The methoxy polyethylene glycols (MPEGs), also referred to as polyethylene glycol methyl ethers, are high molecular weight polymers similar in structure and nomenclature to the polyethylene glycols. Because of the potential for repeated cutaneous exposure of humans to MPEG-350 and
Synthesis, characterization, and tumor selectivity of a polyphosphazene-platinum(II) conjugate
Rita Song et al.
J. Controlled Release, 105, 9-9 (2005)
Yiyi Yu et al.
Journal of pharmaceutical sciences, 102(3), 1054-1062 (2013-01-03)
To promote the application of methoxy poly(ethylene glycol)-cholesterol (mPEG-Chol), mPEG-Chol was used to prepare core-shell micelles encapsulating poorly water-soluble docetaxel (DTX-PM) by modified cosolvent evaporation method. Approaches to enhance DTX entrapment efficiency (EE) and minimize particle size were investigated in
Lina Du et al.
Anti-cancer drugs, 24(2), 172-180 (2012-09-20)
A functionalized poly(amidoamine) (PAMAM) nanocarrier was designed and prepared to deliver anticancer drugs. The nanocarrier is a copolymer with a core-shell structure with 3.0 G PAMAM as the core and sequentially conjugated poly(2-(N,N-diethylamino)ethyl methacrylate) (pDEA) and methoxy-poly(ethylene glycol) 2000 (mPEG)
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