Merck
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07965

Sigma-Aldrich

Methoxypolyethylene glycol amine

10,000

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Synonym(s):
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
PubChem Substance ID:
24846129
NACRES:
NA.22

Quality Level

100

form

powder

InChI

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

InChI key

ASUDFOJKTJLAIK-UHFFFAOYSA-N

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This Item
066790667607964
Methoxypolyethylene glycol amine 10,000

Sigma-Aldrich

07965

Methoxypolyethylene glycol amine

Methoxypolyethylene glycol amine 5,000, extent of labeling: ≥0.17 mmol/g NH2 loading

Sigma-Aldrich

06679

Methoxypolyethylene glycol amine

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

Sigma-Aldrich

06676

Methoxypolyethylene glycol amine

Methoxypolyethylene glycol amine 750

Sigma-Aldrich

07964

Methoxypolyethylene glycol amine

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

Other Notes

Polymeric support suitable for liquid-phase peptide synthesis

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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R Colombo
Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 362(10), 1393-1403 (1981-10-01)
The liquid-phase synthesis of three tetradecapeptideamides corresponding to the amino acid sequences of the wasp venoms mastoparan, mastoparan X, and Polistes mastoparan is described. The 4-(aminomethyl)-3-nitrobenzoyl-amino-poly(ethylene glycol) monomethyl ether was employed as the soluble support, and the completed peptideamides were
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

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