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Merck
CN

752460

Sigma-Aldrich

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

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About This Item

线性分子式:
H2N(CH2CH2O)nCH2CH2NH2
CAS号:
MDL编号:
UNSPSC代码:
12162002
NACRES:
NA.23

产品名称

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


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Malar A. Azagarsamy, et al.
Material Matters, 7 (2012)
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
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.
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
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

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