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

2,2,6,6-Tetramethylpiperidine 1-Oxyl Free Radical (purified by sublimation)

CAS: 2564-83-2

Formula: C₉H₁₈NO

Purity: >99.0%(GC)(T)

Color and Shape: Orange to Brown powder to crystal

Molecular weight: 156.25

Ref: 3B-T3751

2,2,6,6-Tetramethylpiperidine 1-Oxyl Free Radical

CAS: 2564-83-2

Formula: C₉H₁₈NO

Purity: >98.0%(GC)(T)

Color and Shape: Orange to Brown powder to crystal

Molecular weight: 156.25

Ref: 3B-T1560

TEMPO, free radical, 98+%

CAS: 2564-83-2

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

Formula: C₉H₁₈NO

Purity: 98+%

Color and Shape: Orange-red to red to dark red, Crystalline powder or powder or crystals or fused solid and/or chunks

Molecular weight: 156.25

Ref: 02-A12733

Tempo, 10mM (in DMSO)

CAS: 2564-83-2

Tempo, 10mM (in DMSO)

Formula: C₉H₁₈NO

Purity: ≥98%, 10 mM in DMSO

Molecular weight: 156.25

Ref: 54-BUP19082

2,2,6,6-Tetramethylpiperidoxyl

CAS: 2564-83-2

Formula: C₉H₁₈NO

Purity: 95%

Color and Shape: Solid

Molecular weight: 156.2453

Ref: IN-DA0035MS

1-Oxy-2,2,6,6-tetramethylpiperidine, free radical

CAS: 2564-83-2

1-Oxy-2,2,6,6-tetramethylpiperidine, free radical

Formula: C₉H₁₈NO

Purity: ≥95%

Color and Shape: Red Solid-Crystals

Molecular weight: 156.24532

Ref: 54-OR59926

TEMPO

CAS: 2564-83-2

Formula: C₉H₁₈NO

Purity: ≥ 97.5%

Color and Shape: Orange, red or dark red crystals or solid

Molecular weight: 156.25

Ref: 7W-GK6347

Medetomidine Impurity 33

CAS: 2564-83-2

Formula: C₉H₁₈NO

Color and Shape: Orange Red Solid

Molecular weight: 156.25

Ref: 4Z-M-6840

2,2,6,6-Tetramethylpiperidine-d18-1-oxyl"Carboglace"

CAS: 205679-68-1, 2564-83-2

Purity: 98 atom % D

Color and Shape: Red Solid

Molecular weight: 174.36

Ref: 3U-D7184

2,2,6,6-Tetramethylpiperidinoxy free radical

CAS: 2564-83-2

Formula: C₉H₁₈NO

Purity: 99.0%

Color and Shape: Solid, Powder or Crystalline Powder or Solid or Chunks

Molecular weight: 156.249

Ref: 10-F013714

Tempo

CAS: 2564-83-2

2,2,6,6-Tetramethyl-1-oxylpiperidine

Formula: C₉H₁₈NO

Purity: 97%

Molecular weight: 156.25

Ref: IN-DG152556

Tempo

CAS: 2564-83-2

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

Formula: C₉H₁₈NO

Purity: 99.90%

Color and Shape: Orange Solid

Molecular weight: 156.25

Ref: TM-T5363

TEMPO

Controlled Product

CAS: 2564-83-2

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.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
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);

Formula: C₉H₁₈NO

Color and Shape: Neat

Molecular weight: 156.25

Ref: TR-T017850

2,2,6,6-Tetramethylpiperidine 1-oxyl, free radical - solid melt

CAS: 2564-83-2

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.

Formula: C₉H₁₈NO

Purity: Min. 98 Area-%

Molecular weight: 156.25 g/mol

Ref: 3D-Z-1024

2,2,6,6-Tetramethylpiperidine 1-oxyl, free radical - free flowing milled solid

CAS: 2564-83-2

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.

Formula: C₉H₁₈NO

Purity: Min. 98 Area-%

Color and Shape: Orange Red Powder

Molecular weight: 156.25 g/mol

Ref: 3D-FT09614

2,2,6,6-Tetramethylpiperidine 1-oxyl, free radical - solid melt

CAS: 2564-83-2

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.

Formula: C₉H₁₈NO

Purity: Min. 98 Area-%

Color and Shape: Orange Red Powder

Molecular weight: 156.25 g/mol

Ref: 3D-FT04400

2,2,6,6-Tetramethylpiperidine 1-oxyl, free radical - Solid cubes

CAS: 2564-83-2

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.

Formula: C₉H₁₈NO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 156.25 g/mol

Ref: 3D-FT167208

2,2,6,6-Tetramethylpiperidine-1-Oxyl (TEMPO) pure, 98%

CAS: 2564-83-2

Formula: C₉H₁₈NO

Purity: min. 98%

Color and Shape: Orange red, Crystalline hygroscopic compound, Clear

Molecular weight: 156.25

Ref: SR-91902