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14502

Sigma-Aldrich

Poly(ethylene glycol) bis(amine)

Mw 3,000, carboxyl reactive, amine

Sinónimos:

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

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About This Item

Fórmula lineal:
H2N(CH2CH2O)nCH2CH2NH2
Número de CAS:
24991-53-5
MDL number:
MFCD00132004
UNSPSC Code:
12162002
PubChem Substance ID:
24848543
NACRES:
NA.23

product name

Poly(ethylene glycol) bis(amine), Mw 3,000

mol wt

Mw 3,000

Quality Level

100

reaction suitability

reagent type: cross-linking reagent
reactivity: carboxyl reactive

Ω-end

amine

α-end

amine

polymer architecture

shape: linear
functionality: homobifunctional

InChI

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

InChI key

IWBOPFCKHIJFMS-UHFFFAOYSA-N

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Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCH5149
BCCJ2836
BCCD5722
BCBP8151V
BCBK2952V

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N P Desai et al.
Journal of microencapsulation, 17(6), 677-690 (2000-11-04)
A mixture of alginate and polyethylene glycol acrylate was investigated as a system for the encapsulation of islets of Langerhans. This system showed dual crosslinkability: the alginate was ionically crosslinked by multivalent cations, and the PEG was covalently crosslinked by
Eric Schopf et al.
Chemical communications (Cambridge, England), (32)(32), 4818-4820 (2009-08-05)
A pyrene-functionalized polymer was patterned via electron beam lithography onto a silicon wafer and shown to selectively bind with carbon nanotubes.
Naoki Yamamoto et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(2), 613-625 (2006-09-16)
This paper describes synthesis of asparagine-linked sialylglycopeptides. The typical feature of our strategy for the synthesis of a sialylglycopeptide is to employ undecadisialyloligosaccharyl Fmoc-asparagine (Fmoc-Asn(CHO)-OH) 1 without protecting groups on its hydroxyl groups except for the benzyl ester of the
Cara E Humphrey et al.
Journal of the American Chemical Society, 125(46), 13952-13953 (2003-11-13)
The lipase-catalyzed kinetic resolution of (R/S)-3-phenylbutyric acid 2 using solid-supported cyclohexane-1,3-dione (CHD) 6 is described. In each case the predominant enantiomer observed, after cleavage from the resin, was (R)-(-)-3-phenylbutyric acid (R)-2 (ee > 99%) rather than the expected (S)-enantiomer of
Joseph Deere et al.
Langmuir : the ACS journal of surfaces and colloids, 24(20), 11762-11769 (2008-09-27)
The use of alpha-chymotrypsin to cleave covalently bound N-acetyl- l-tryptophan (Ac-Trp-OH) from the surfaces of aminopropylated controlled pore glass (CPG) and the polymer PEGA 1,900 was investigated. Oligoglycine spacer chains were used to present the covalently attached Ac-Trp-OH substrate to
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Progress in biotechnology fields such as tissue engineering and drug delivery is accompanied by an increasing demand for diverse functional biomaterials. One class of biomaterials that has been the subject of intense research interest is hydrogels, because they closely mimic the natural environment of cells, both chemically and physically and therefore can be used as support to grow cells. This article specifically discusses poly(ethylene glycol) (PEG) hydrogels, which are good for biological applications because they do not generally elicit an immune response. PEGs offer a readily available, easy to modify polymer for widespread use in hydrogel fabrication, including 2D and 3D scaffold for tissue culture. The degradable linkages also enable a variety of applications for release of therapeutic agents.

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