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14509

Sigma-Aldrich

Poly(ethylene glycol) bis(amine)

Mw 20,000, carboxyl reactive, amine

Sinônimo(s):

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

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About This Item

Fórmula linear:
H2N(CH2CH2O)nCH2CH2NH2
Número CAS:
24991-53-5
Número MDL:
MFCD00132004
Código UNSPSC:
51171641
ID de substância PubChem:
24848700
NACRES:
NA.23

Nome do produto

Poly(ethylene glycol) bis(amine), Mw 20,000

peso molecular

Mw 20,000

Nível de qualidade

100

adequação da reação

reagent type: cross-linking reagent
reactivity: carboxyl reactive

Ω-final

amine

α-final

amine

arquitetura do polímero

shape: linear
functionality: homobifunctional

cadeia de caracteres SMILES

NCCOCCOCCN

InChI

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

chave InChI

IWBOPFCKHIJFMS-UHFFFAOYSA-N

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Aplicação

With HCl, reduction agent; stereoselective allylation of carbonyl compounds; in situ generation of tinenolates for directed aldol reactions.

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
BCCD4362
BCCC5572
BCCB9331
BCCB0989
BCBW7210

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Huahua Jian et al.
The Journal of organic chemistry, 68(13), 5091-5103 (2003-06-21)
Four caltrop-shaped molecules that might be useful as surface-bound electric field-driven molecular motors have been synthesized. The caltrops are comprised of a pair of electron donor-acceptor arms and a tripod base. The molecular arms are based on a carbazole or
Yamamoto, Y.; Asao, N.
Chemical Reviews, 93, 2207-2207 (1993)
Takahiko Matsushita et al.
The Journal of organic chemistry, 71(8), 3051-3063 (2006-04-08)
A MUC1-related glycopeptide having five core-2 hexasaccharide branches (C330H527N46O207, MW = 8450.9) was synthesized by a new strategy using a combination of microwave-assisted solid-phase synthesis (MA-SPGS) and enzymatic sugar elongation. Synthesis of a key glycopeptide intermediate was best achieved in
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
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Artigos

Degradable Poly(ethylene glycol) Hydrogels for 2D and 3D Cell Culture

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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