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07964

Sigma-Aldrich

Methoxypolyethylene glycol amine

750

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Synonym(s):
mPEG-NH2, O-(2-Aminoethyl)-O′-methylpolyethylene glycol, Aminopolyethylene glycol monomethyl ether, Methoxypolyoxyethylene amine
Linear Formula:
H2NCH2CH2(OCH2CH2)nOCH3
CAS Number:
MDL number:
NACRES:
NA.22

Quality Level

form

solid

color

white to yellow

storage temp.

room temp

InChI

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

InChI key

ASUDFOJKTJLAIK-UHFFFAOYSA-N

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1 of 4

This Item
066790667614508
vibrant-m

07964

Methoxypolyethylene glycol amine

vibrant-m

06679

Methoxypolyethylene glycol amine

vibrant-m

06676

Methoxypolyethylene glycol amine

vibrant-m

14508

Poly(ethylene glycol) bis(amine)

form

solid

form

-

form

powder

form

-

storage temp.

−20°C

storage temp.

-

storage temp.

-

storage temp.

-

color

white to yellow

color

-

color

-

color

-

Application

Methoxypolyethylene glycol amine can:
  • Form dendritic micelles to enhance the solubility of hydrophobic compounds.
  • Conjugate with an anticancer drug methotrexate (MTX) to form MTX-PEG with potential application as drug carriers.
  • Couple with polyethylenimine (PEI) to form graft copolymers which can be used as nonviral gene vectors.

Other Notes

Oligomer used to prepare PEG-ylated conjugates having the advantage of reduced immunogenicity and increased serum half life

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Customers Also Viewed

Slide 1 of 7

1 of 7

Effect of polyethylene glycol on gene delivery of polyethylenimine.
Sung SJ, et al.
Biological & Pharmaceutical Bulletin, 26(4), 492-500 (2003)
Polyethylene Glycol Conjugates of Methotrexate Varying in Their Molecular Weight from MW 750 to MW 40000: Synthesis, Characterization, and Structure- Activity Relationships in Vitro and in Vivo.
Riebeseel K, et al.
Bioconjugate Chemistry, 13(4), 773-785 (2002)
Polyethylene glycol-polyamidoamine dendritic micelle as solubility enhancer and the effect of the length of polyethylene glycol arms on the solubility of pyrene in water.
Yang H, et al.
Journal of Colloid and Interface Science, 273(1), 148-154 (2004)
M Yokoyama et al.
Bioconjugate chemistry, 3(4), 295-301 (1992-07-01)
Adriamycin, a hydrophobic anticancer drug, was conjugated with poly(ethylene oxide)-poly(aspartic acid) block copolymers composed of various lengths of each block copolymer segment ranging from 1000 to 12,000 in molecular weight and from 10 to 80 units, respectively. Conjugation was achieved
T.P. Kogan
Synthetic Communications, 22, 2417-2417 (1992)

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