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Merck
CN

902586

Sigma-Aldrich

Hydroxy-PEG4-t-butyl ester

别名:

tert-Butyl-1-hydroxy-3,6,9,12-tetraoxapentadecan-15-oate, HO-PEG4-CO-OtBu

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关于此项目

经验公式(希尔记法):
C15H30O7
化学文摘社编号:
分子量:
322.39
MDL编号:
UNSPSC代码:
51171641
NACRES:
NA.22
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方案

≥95%

表单

liquid

反应适用性

reagent type: cross-linking reagent

折射率

n/D 1.4492

密度

1.04746 g/mL

官能团

ester
hydroxyl

储存温度

2-8°C

SMILES字符串

O=C(OC(C)(C)C)CCOCCOCCOCCOCCO

InChI

1S/C15H30O7/c1-15(2,3)22-14(17)4-6-18-8-10-20-12-13-21-11-9-19-7-5-16/h16H,4-13H2,1-3H3

InChI key

FJRDXEGYAVAMLB-UHFFFAOYSA-N

应用

This heterobifunctional, PEGylated crosslinker features a hydroxyl group at one end and t-butyl-protected carboxylic acid at the other, which can be deprotected with acidic conditions. The hydrophillic PEG linker facilitates solubility in biological applications. Hydroxy-PEG4-t-butyl ester can be used for bioconjugation or as a building block for synthesis of small molecules, conjugates of small molecules and/or biomolecules, or other tool compounds for chemical biology and medicinal chemistry that require ligation. Examples of applications include its synthetic incorporation into antibody-drug conjugates or proteolysis-targeting chimeras (PROTAC® molecules) for targeted protein degradation.

法律信息

PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Sara V Orski et al.
Journal of the American Chemical Society, 132(32), 11024-11026 (2010-08-12)
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Bioorganic & medicinal chemistry letters, 17(2), 501-506 (2006-10-24)
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Yacob Z, et al
Advanced Synthesis & Catalysis, 354(17), 3259-3264 (2012)
A new route for the synthesis of 1-amino-3,6,9,12-?tetraoxapentadecan-15-oic acid.
Wu X, et al.
J. Chem. Res. (M), 40(6), 368-370 (2016)

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