752460
聚乙二醇双(胺)
average MN 10,000, cross-linking reagent carboxyl reactive, amine
别名:
O,O′-双(2-氨基乙基)聚乙二醇, 二氨基聚乙二醇, 聚乙二醇二胺, 聚氧乙烯二胺
Product Name
聚乙二醇双(胺), average Mn 10,000
表单
powder or solid (or chunk(s))
质量水平
分子量
average Mn 10,000
反应适用性
reagent type: cross-linking reagent
reactivity: carboxyl reactive
mp
56-60 °C
Ω端
amine
α端
amine
聚合物结构设计
shape: linear
functionality: homobifunctional
SMILES字符串
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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应用
Polymer for preparing enzyme conjugates soluble in organic solvents†; promising drug carrier†
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Malar A. Azagarsamy, et al.
Material Matters, 7 (2012)
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
Phaedria M St Hilaire et al.
Journal of medicinal chemistry, 45(10), 1971-1982 (2002-05-03)
A one-bead-two-compound inhibitor library was synthesized by the split-mix method for the identification of inhibitors of a recombinant cysteine protease from Leishmania mexicana, CPB2.8DeltaCTE. The inhibitor library was composed of octapeptides with a centrally located reduced bond introduced by reductive
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
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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