176141-25G Display Image

4-Hydroxy-TEMPO, 97%

Code: 176141-25G D2-231

Application

Spin label for studying biological compounds and polymers.

4-Hydroxy-TEMPO (HO-TEMPO) may be employed as catalyst for the oxidation of alcohols to the corre...


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Your Price
£53.10 25G

Application

Spin label for studying biological compounds and polymers.

4-Hydroxy-TEMPO (HO-TEMPO) may be employed as catalyst for the oxidation of alcohols to the corresponding aldehydes. It may be employed for the preparation of TEMPO based polymer catalyst systems, which are useful for the Anelli oxidation of various primary alcohols. It may be used as starting reagent in the synthesis of 4-(2,2,6,6-tetramethyl-1-oxyl-4-piperidoxyl)butyl bromide.

A fluorous-tagged TEMPO derivative was prepared from the derived TEMPO propargylic ether and subsequent "click" reaction with a fluorous azide. This TEMPO derivative proved to be a highly effective catalyst in the oxidation of alcohols with bleach.

Spin label reagent used in the chatacterization of antagonist and agonist binding sites of NK1 receptor. Also used to measure reactive oxygen generation in heart muscle by electron spin resonance spectroscopy. Cells that overexpress CYP2E1 can be protected from arachidonic acid toxicity damage by TEMPOL.

General description

4-Hydroxy-TEMPO is a 4-substituted 2,2,6,6-tetramethylpiperidyl-1-oxy (TEMPO) derivative. It is a low-molecular weight compound and has been proposed as superoxide dismutase mimic.

Packaging

1, 5, 25 g in glass bottle

assay97%
compositionCarbon content, 60.6-65.0%, Nitrogen content, 7.8-8.4%
formsolid
InChI keyUZFMOKQJFYMBGY-UHFFFAOYSA-N
InChI1S/C9H18NO2/c1-8(2)5-7(11)6-9(3,4)10(8)12/h7,11H,5-6H2,1-4H3
mp69-71 °C (lit.)
Quality Level200
SMILES stringCC1(C)CC(O)CC(C)(C)N1[O]
storage temp.2-8°C
Code
Description
Unit Size
List Price
Qty
176141-5G
Unit:5G
List Price: £43.70
Source:List Price
ADD
176141-1G
Unit:1G
List Price: £35.60
Source:List Price
ADD
Cas Number2226-96-2
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