Skip to Content
Merck
All Photos(1)

Documents

06676

Sigma-Aldrich

Methoxypolyethylene glycol amine

2,000, extent of labeling: ≥0.4 mmol/g NH2 loading

Synonym(s):

O-(2-Aminoethyl)-O′-methylpolyethylene glycol, Aminopolyethylene glycol monomethyl ether, Methoxypolyoxyethylene amine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
H2NCH2CH2(OCH2CH2)nOCH3
CAS Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.22

Quality Level

form

powder

extent of labeling

≥0.4 mmol/g NH2 loading

InChI

1S/C3H9NO/c1-5-3-2-4/h2-4H2,1H3

InChI key

ASUDFOJKTJLAIK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Methoxypolyethylene glycol amine (mPEG-NH2) can be used:
  • As a supporting material in the synthesis of polymer-lipid conjugates.
  • As an initiator for ring-opening polymerization (ROP) of N-substituted N-carboxy anhydrides (NNCAs) to prepare polypeptoids.

Other Notes

Soluble polymer support for peptide synthesis; Preparation of various conjugates containing polyethylene glycol; Review

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Schiff base and reductive amination reactions of α-amino acids: a facile route toward N-alkylated amino acids and peptoid synthesis
Fu X, et al.
Polym. Chem., 9(37), 4617-4624 (2018)
M. Mutter et al.
Reactive Polymers, 6, 99-99 (1987)
Synthesis of Poly (ethylene glycol)-Polydiacetylene Conjugates and Their Micellar and Chromic Characteristics
Choi H et al.
Journal of Nanoscience and Nanotechnology, 8(10), 5104-5108 (2008)
R Colombo et al.
Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 362(10), 1385-1391 (1981-10-01)
The liquid-phase synthesis of two pentapeptides corresponding to the amino acid sequence of Leu- and Met-enkephalin is described. Modified monofunctional poly(ethylene glycol) containing a p-alkoxybenzyl alcohol functional group was employed as the soluble polymeric support. Cleavage of the peptides from
M. Leonard et al.
Tetrahedron, 40, 1581-1581 (1984)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service