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14509

Sigma-Aldrich

聚乙二醇双（胺）

Mw 20,000, 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:
24991-53-5
MDL编号:
MFCD00132004
UNSPSC代码:
51171641
PubChem化学物质编号:
24848700
NACRES:
NA.23

产品名称

聚乙二醇双（胺）, Mw 20,000

分子量

Mw 20,000

质量水平

100

反应适用性

reagent type: cross-linking reagent
reactivity: carboxyl reactive

Ω端

amine

α端

amine

聚合物结构设计

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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应用

随着盐酸，还原剂;羰基化合物的立体选择性烯丙基化; tinenolates指示Aldol反应原位生成。

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves

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分析证书(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)
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
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
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
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