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752460

Sigma-Aldrich

Poly(ethylene glycol) diamine

average MN 10,000, cross-linking reagent carboxyl reactive, amine

Synonym(s):

Poly(ethylene glycol) bis(amine), Polyethylene glycol, O,O′-Bis(2-aminoethyl)polyethylene glycol, Diaminopolyethylene glycol, PEG-diamine, Polyoxyethylene bis(amine)

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1 G
$205.20
5 G
$790.00

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1 G
$205.20
5 G
$790.00

About This Item

Linear Formula:
H2N(CH2CH2O)nCH2CH2NH2
CAS Number:
24991-53-5
MDL number:
MFCD00132004
UNSPSC Code:
12162002
NACRES:
NA.23

$205.20

List Price$216.00Save 5%
Web-Only Promotion

Available to ship onApril 15, 2025Details

Request a Bulk Order

Product Name

Poly(ethylene glycol) diamine, average Mn 10,000

form

powder or solid (or chunk(s))

mol wt

average Mn 10,000

reaction suitability

reagent type: cross-linking reagent
reactivity: carboxyl reactive

mp

56-60 °C

Ω-end

amine

α-end

amine

polymer architecture

shape: linear
functionality: homobifunctional

SMILES string

NCCOCCOCCN

InChI

1S/C6H16N2O2/c7-1-3-9-5-6-10-4-2-8/h1-8H2

Inchi Key

IWBOPFCKHIJFMS-UHFFFAOYSA-N

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1 of 4

This Item
75245275244414508
Poly(ethylene glycol) diamine average Mn 10,000

752460

Poly(ethylene glycol) diamine

Poly(ethylene glycol) diamine average Mn 3,000

752452

Poly(ethylene glycol) diamine

Poly(ethylene glycol) diamine average Mn 6,000

752444

Poly(ethylene glycol) diamine

Poly(ethylene glycol) bis(amine) Mw 10,000

14508

Poly(ethylene glycol) bis(amine)

polymer architecture

shape: linear
functionality: homobifunctional

polymer architecture

shape: linear
functionality: homobifunctional

polymer architecture

shape: linear
functionality: homobifunctional

polymer architecture

shape: linear
functionality: homobifunctional

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

reaction suitability

reagent type: cross-linking reagent
reactivity: carboxyl reactive

reaction suitability

reagent type: cross-linking reagent
reactivity: carboxyl reactive

reaction suitability

reagent type: cross-linking reagent
reactivity: carboxyl reactive

reaction suitability

reagent type: cross-linking reagent
reactivity: carboxyl reactive

mol wt

average Mn 10,000

mol wt

average Mn 3,000

mol wt

average Mn 6,000

mol wt

Mw 10,000

mp

56-60 °C

mp

55-60 °C

mp

54-60 °C

mp

-

Application

Polymer for preparing enzyme conjugates soluble in organic solvents†; promising drug carrier†

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV6408
MKCT5032
MKCS3786
MKCR2454
MKCM6821

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Malar A. Azagarsamy, et al.
Material Matters, 7 (2012)
C S Lee et al.
Artificial organs, 21(9), 1002-1006 (1997-09-01)
Various modifications of alginate-poly-L-lysine microcapsules were made, such as the inclusion of polyethylenimine (PEI) or carboxyl methyl cellulose (CMC) in the core and the coating of bis(polyoxyethylene bis[amine]) (PEGA) onto the microcapsule membrane surface. A characterization of the modified microcapsules
Stephen J Connon et al.
Bioorganic & medicinal chemistry letters, 12(14), 1873-1876 (2002-06-28)
The synthesis and olefin metathesis activity in protic solvents of 7, a phosphine-free ruthenium alkylidene bound to a hydrophilic solid support are reported. This heterogeneous catalyst promotes relatively efficient ring closing- and cross-metathesis reactions in both methanol and water. The
Alison G Patrick et al.
Macromolecular bioscience, 10(10), 1184-1193 (2010-07-02)
The design of hydrogels that simultaneously report protease activity and remove excess protease from solution is elucidated. The hydrogels, based on amino-PEGA, combine enzyme-specific peptides flanked with FRET complimented by charged amino acid residues that facilitate protease uptake via short
Gaëlle-Anne Cremer et al.
Journal of peptide science : an official publication of the European Peptide Society, 12(6), 437-442 (2006-01-25)
This paper describes the optimization of a synthesis of a difficult sequence related to a 12-mer sequence of a Pan DR epitope (PADRE). Elongation was followed by on-line monitoring of the N(alpha)-Fmoc removal adapted for the batch methodology. Studying the
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