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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:
80506-64-5
MDL number:
MFCD00131599
NACRES:
NA.22

Quality Level

100

form

solid

color

white to yellow

storage temp.

−20°C

InChI

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

InChI key

ASUDFOJKTJLAIK-UHFFFAOYSA-N

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This Item
079660796506676
Methoxypolyethylene glycol amine 750

Sigma-Aldrich

07964

Methoxypolyethylene glycol amine

Methoxypolyethylene glycol amine 20,000

Sigma-Aldrich

07966

Methoxypolyethylene glycol amine

Methoxypolyethylene glycol amine 10,000

Sigma-Aldrich

07965

Methoxypolyethylene glycol amine

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

Sigma-Aldrich

06676

Methoxypolyethylene glycol amine

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 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

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T.P. Kogan
Synthetic Communications, 22, 2417-2417 (1992)
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
Effect of polyethylene glycol on gene delivery of polyethylenimine.
Sung SJ, et al.
Biological & Pharmaceutical Bulletin, 26(4), 492-500 (2003)

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