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Merck

767751

Sigma-Aldrich

2- {2- [2-(2-巯基乙氧基)乙氧基]乙氧基}乙醇

97%

别名:

MEEE, 1-Mercapto-11-hydroxy-3,6,9-trioxaundecane

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About This Item

经验公式(希尔记法):
C8H18O4S
分子量:
210.29
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22

方案

97%

表单

liquid

反应适用性

reagent type: cross-linking reagent

折射率

n20/D 1.481

密度

1.098 g/mL at 25 °C

SMILES字符串

OCCOCCOCCOCCS

InChI

1S/C8H18O4S/c9-1-2-10-3-4-11-5-6-12-7-8-13/h9,13H,1-8H2

InChI key

GKKYNULPAQDGHI-UHFFFAOYSA-N

应用

2-{2-[2-(2-Mercaptoethoxy)ethoxy]ethoxy}ethanol may be used in the synthesis of 2-(2-(2-((7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)thio)ethoxy)ethoxy)ethanol, an nitrobenzoxadiazole (NBD) analog of the anticancer agent 6-((7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)thio)hexan-1-ol (NBDHEX). This analog is a potent glutathione S-transferase (GST) and a potential therapeutic antimelanoma agent with enhanced water solubility and antitumor efficacy when compared to NBDHEX in a study.
  • Oligo-ehtylene glycol of peptides and small molecules (PEGylation)
  • PEG-disulfide formation
  • ultra-thin protein-resistant monolayers
  • Densely packed monolayer and a flexible-hydrophilic oligo ethylene glycol arm for avoiding non-specific adsorption

象形图

Skull and crossbonesCorrosion

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Oral - Skin Corr. 1B

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Click and chemically triggered declick reactions through reversible amine and thiol coupling via a conjugate acceptor
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Nature Chemistry, 8(10) (2016)
Influence of surface functionalization and particle size on the aggregation kinetics of engineered nanoparticles.
Liu J, et al.
Chemosphere, 87(8), 918-924 (2012)
Carbohydrates as the next frontier in pharmaceutical research.
Werz DB & Seeberger PH
Chemistry?A European Journal , 11(11), 3194-3206 (2005)
Thiol functionalized oligo-ethylene glycol, for modification of peptides/small molecules containing thiols or maleimide functional groups
Journal of Materials Chemistry, 9, 1121-1121 (1999)
Oligosaccharide and glycoprotein microarrays as tools in HIV glycobiology: glycan-dependent gp120/protein interactions.
Adams EW, et al.
Chemistry & Biology, 11(6), 875-881 (2004)

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