CAS 2564-83-2
:Tempo
Description:
Tempo, or 2,2,6,6-tetramethylpiperidinyl-1-oxyl, is a stable free radical characterized by its distinctive structure, which includes a piperidine ring and a nitroxide functional group. This compound is known for its stability and ability to act as a radical scavenger, making it useful in various applications, including organic synthesis and polymer chemistry. Tempo exhibits a characteristic deep yellow color and is soluble in organic solvents such as ethanol and acetone, but it is less soluble in water. Its radical nature allows it to participate in redox reactions, and it is often employed as a spin label in electron paramagnetic resonance (EPR) spectroscopy. Additionally, Tempo can serve as an oxidation catalyst in certain chemical reactions, enhancing the efficiency of processes such as the oxidation of alcohols to carbonyl compounds. Its unique properties make it a valuable tool in both academic research and industrial applications.
Formula:C9H18NO
InChI:InChI=1/C9H18NO/c1-8(2)6-5-7-9(3,4)10(8)11/h5-7H2,1-4H3
InChI key:InChIKey=QYTDEUPAUMOIOP-UHFFFAOYSA-N
SMILES:CC1(C)CCCC(C)(C)N1O
Synonyms:- (2,2,6,6-Tetramethylpiperidin-1-Yl)Oxidanyl
- 1,1,5,5-Tetramethylpentamethylene nitroxide
- 1-Oxyl-2,2,6,6-tetramethylpiperidine
- 1-Piperidinyloxy, 2,2,6,6-tetramethyl-
- 2,2,5,6-Tetramethylpiperidin-1-oxyl
- 2,2,6,6-Tetramethyl-1-oxylpiperidine
- 2,2,6,6-Tetramethyl-1-piperadoxyl
- 2,2,6,6-Tetramethyl-1-piperidine-N-oxyl
- 2,2,6,6-Tetramethyl-1-piperidinoxyl
- 2,2,6,6-Tetramethyl-1-piperidinyloxy
- 2,2,6,6-Tetramethyl-1-piperidinyloxy, free radical
- 2,2,6,6-Tetramethyl-1-piperidyloxy
- 2,2,6,6-Tetramethyl-1-piperinedinyloxy
- 2,2,6,6-Tetramethylpiperidin-1-Ol
- 2,2,6,6-Tetramethylpiperidin-1-oxy
- 2,2,6,6-Tetramethylpiperidin-1-oxyl radical
- 2,2,6,6-Tetramethylpiperidin-N-oxyl
- 2,2,6,6-Tetramethylpiperidine 1-oxyl
- 2,2,6,6-Tetramethylpiperidine N-oxide
- 2,2,6,6-Tetramethylpiperidine N-oxide radical
- 2,2,6,6-Tetramethylpiperidine N-oxy
- 2,2,6,6-Tetramethylpiperidine N-oxyl
- 2,2,6,6-Tetramethylpiperidine N-oxyl radical
- 2,2,6,6-Tetramethylpiperidine nitroxide
- 2,2,6,6-Tetramethylpiperidine nitroxide radical
- 2,2,6,6-Tetramethylpiperidine oxide
- 2,2,6,6-Tetramethylpiperidino-1-oxy
- 2,2,6,6-Tetramethylpiperidinooxy
- 2,2,6,6-Tetramethylpiperidinooxy radical
- 2,2,6,6-Tetramethylpiperidinooxyl
- 2,2,6,6-Tetramethylpiperidinoxy
- 2,2,6,6-Tetramethylpiperidinoxyl
- 2,2,6,6-Tetramethylpiperidinoxyl radical
- 2,2,6,6-Tetramethylpiperidinyl-1-oxyl
- 2,2,6,6-Tetramethylpiperidinyl-N-oxy
- 2,2,6,6-Tetramethylpiperidinyloxy
- 2,2,6,6-Tetramethylpiperidoxyl
- 2,2,6,6-Tetrametilpiperidinooxi
- Ho 6
- Piperidinooxy, 2,2,6,6-tetramethyl-
- T 3751
- Tanan
- Tanane
- Tempo
- See more synonyms
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Found 16 products.
2,2,6,6-Tetramethylpiperidine 1-Oxyl Free Radical (purified by sublimation)
CAS:Formula:C9H18NOPurity:>99.0%(GC)(T)Color and Shape:Orange to Brown powder to crystalMolecular weight:156.252,2,6,6-Tetramethylpiperidine 1-Oxyl Free Radical
CAS:Formula:C9H18NOPurity:>98.0%(GC)(T)Color and Shape:Orange to Brown powder to crystalMolecular weight:156.25TEMPO, free radical, 98+%
CAS:<p>TEMPO is used as a catalyst in organic synthesis and for the oxidation of primary alcohols to aldehydes. It finds use in the chemical industry for conversion of bisnoralcohol (a steroid) to bisnoraldehyde. It acts as a free radical scavenger, as a mediator in controlled radical polymerization and as</p>Formula:C9H18NOPurity:98+%Color and Shape:Orange-red to red to dark red, Crystalline powder or powder or crystals or fused solid and/or chunksMolecular weight:156.252,2,6,6-Tetramethylpiperidoxyl
CAS:Formula:C9H18NOPurity:97%Color and Shape:SolidMolecular weight:156.2453Ref: IN-DA0035MS
10g20.00€25g25.00€5kg523.00€100g56.00€10kg1,872.00€500g114.00€100kg15,364.00€340kg50,316.00€500kg73,076.00€950kg142,367.00€1-Oxy-2,2,6,6-tetramethylpiperidine, free radical
CAS:<p>1-Oxy-2,2,6,6-tetramethylpiperidine, free radical</p>Formula:C9H18NOPurity:≥95%Color and Shape: dark red crystalsMolecular weight:156.24532g/mol2,2,6,6-Tetramethylpiperidinoxy free radical
CAS:Formula:C9H18NOPurity:99.0%Color and Shape:Solid, Powder or Crystalline Powder or Solid or ChunksMolecular weight:156.249TEMPO
CAS:Formula:C9H18NOPurity:≥ 97.5%Color and Shape:Orange, red or dark red crystals or solidMolecular weight:156.25Tempo
CAS:<p>Tempo (2,2,6,6-Tetramethylpiperidinooxy) has a wide range of applications including use as a free radical scavenger, a reagent in organic synthesis and as a</p>Formula:C9H18NOPurity:98.35%Color and Shape:Orange Crystals Or PowderMolecular weight:156.25TEMPO
CAS:Controlled Product<p>Applications TEMPO is a stable radical prepared through the oxidation of 2,2,6,6-tetramethylpiperidine. TEMPO has a wide range of applications including use as a free radical scavenger, a reagent in organic synthesis and as a structural probe in electron spin resonance spectroscopy. TEMPO can also be used as a mediator in free radical polymerization.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Seaton, T.A. et al.: Brain Res., 777, 110 (1997); Tanielyan, S.K. et al.: Top. Catal., 55, 556 (2012); Wolinska-Grabczyk, A. et al.: Polymer, 46, 2461 (2005); Keoshkerian, B. et al.: Polym. Prep., 35, 675 (1994);<br></p>Formula:C9H18NOColor and Shape:NeatMolecular weight:156.252,2,6,6-Tetramethylpiperidine 1-oxyl, free radical - solid melt
CAS:<p>2,2,6,6-Tetramethylpiperidine 1-oxyl, commonly known as TEMPO, is a radical catalyst that belongs to the family of niroxyl radicals. These compounds can be used in the catalysis of alcohols to carbonyls when coupled with approriate oxidants. It is interesting to note that when coupled with Cu(II), TEMPO can be a green solution in oxidising primary alcohols to aldehydes under aerobic conditions. If used in conjuction with EPR it can be used to deteremine the structure of biological systems. TEMPO is also employed to mediate polymerisations by mopping up other free radicals.</p>Formula:C9H18NOPurity:Min. 98 Area-%Molecular weight:156.25 g/mol2,2,6,6-Tetramethylpiperidine 1-oxyl, free radical - free flowing milled solid
CAS:<p>2,2,6,6-Tetramethylpiperidine 1-oxyl, commonly known as TEMPO, is a radical catalyst that belongs to the family of niroxyl radicals. These compounds can be used in the catalysis of alcohols to carbonyls when coupled with approriate oxidants. It is interesting to note that when coupled with Cu(II), TEMPO can be a green solution in oxidising primary alcohols to aldehydes under aerobic conditions. If used in conjuction with EPR it can be used to deteremine the structure of biological systems. TEMPO is also employed to mediate polymerisations by mopping up other free radicals.</p>Formula:C9H18NOPurity:Min. 98 Area-%Color and Shape:Orange Red PowderMolecular weight:156.25 g/mol2,2,6,6-Tetramethylpiperidine 1-oxyl, free radical - solid melt
CAS:<p>2,2,6,6-Tetramethylpiperidine 1-oxyl, commonly known as TEMPO, is a radical catalyst that belongs to the family of niroxyl radicals. These compounds can be used in the catalysis of alcohols to carbonyls when coupled with approriate oxidants. It is interesting to note that when coupled with Cu(II), TEMPO can be a green solution in oxidising primary alcohols to aldehydes under aerobic conditions. If used in conjuction with EPR it can be used to deteremine the structure of biological systems. TEMPO is also employed to mediate polymerisations by mopping up other free radicals.</p>Formula:C9H18NOPurity:Min. 98 Area-%Color and Shape:Orange Red PowderMolecular weight:156.25 g/mol2,2,6,6-Tetramethylpiperidine 1-oxyl, free radical - Solid cubes
CAS:<p>2,2,6,6-Tetramethylpiperidine 1-oxyl, commonly known as TEMPO, is a radical catalyst that belongs to the family of niroxyl radicals. These compounds can be used in the catalysis of alcohols to carbonyls when coupled with approriate oxidants. It is interesting to note that when coupled with Cu(II), TEMPO can be a green solution in oxidising primary alcohols to aldehydes under aerobic conditions. If used in conjuction with EPR it can be used to deteremine the structure of biological systems. TEMPO is also employed to mediate polymerisations by mopping up other free radicals.</p>Formula:C9H18NOPurity:Min. 95%Color and Shape:PowderMolecular weight:156.25 g/mol2,2,6,6-Tetramethylpiperidine-1-Oxyl (TEMPO) pure, 98%
CAS:Formula:C9H18NOPurity:min. 98%Color and Shape:Orange red, Crystalline hygroscopic compound, ClearMolecular weight:156.25










