CAS 2564-83-2

Temps

Description :

Temps, ou 2,2,6,6-tétraméthylpyridinyle-1-oxyle, est un radical libre stable caractérisé par sa structure distinctive, qui comprend un cycle de pipéridine et un groupe fonctionnel nitroxyle. Ce composé est connu pour sa stabilité et sa capacité à agir comme un piégeur de radicaux, ce qui le rend utile dans diverses applications, y compris la synthèse organique et la chimie des polymères. Temps présente une couleur jaune profond caractéristique et est soluble dans des solvants organiques tels que l'éthanol et l'acétone, mais il est moins soluble dans l'eau. Sa nature radicale lui permet de participer à des réactions redox, et il est souvent utilisé comme étiquette de spin en résonance paramagnétique électronique (EPR). De plus, Temps peut servir de catalyseur d'oxydation dans certaines réactions chimiques, améliorant l'efficacité de processus tels que l'oxydation des alcools en composés carbonylés. Ses propriétés uniques en font un outil précieux tant dans la recherche académique que dans les applications industrielles.

Formule : C₉H₁₈NO

InChI : InChI=1/C9H18NO/c1-8(2)6-5-7-9(3,4)10(8)11/h5-7H2,1-4H3

Code InChI : InChIKey=QYTDEUPAUMOIOP-UHFFFAOYSA-N

SMILES : CC1(C)CCCC(C)(C)N1O

Synonymes :

• (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

Formule : C₉H₁₈NO

Degré de pureté : >99.0%(GC)(T)

Couleur et forme : Orange to Brown powder to crystal

Masse moléculaire : 156.25

Ref: 3B-T3751

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

CAS : 2564-83-2

Formule : C₉H₁₈NO

Degré de pureté : >98.0%(GC)(T)

Couleur et forme : Orange to Brown powder to crystal

Masse moléculaire : 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

Formule : C₉H₁₈NO

Degré de pureté : 98+%

Couleur et forme : Orange-red to red to dark red, Crystalline powder or powder or crystals or fused solid and/or chunks

Masse moléculaire : 156.25

Ref: 02-A12733

2,2,6,6-Tetramethylpiperidoxyl

CAS : 2564-83-2

Formule : C₉H₁₈NO

Degré de pureté : 97%

Couleur et forme : Solid

Masse moléculaire : 156.2453

Ref: IN-DA0035MS

Medetomidine Impurity 33

CAS : 2564-83-2

Formule : C₉H₁₈NO

Couleur et forme : Orange Red Solid

Masse moléculaire : 156.25

Ref: 4Z-M-6840

Tempo, 10mM (in DMSO)

CAS : 2564-83-2

Tempo, 10mM (in DMSO)

Degré de pureté : ≥98%

Masse moléculaire : 156.25g/mol

Ref: 54-BUP19082

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

CAS : 2564-83-2

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

Formule : C₉H₁₈NO

Degré de pureté : ≥95%

Couleur et forme : dark red crystals

Masse moléculaire : 156.24532g/mol

Ref: 54-OR59926

TEMPO

CAS : 2564-83-2

Formule : C₉H₁₈NO

Degré de pureté : ≥ 97.5%

Couleur et forme : Orange, red or dark red crystals or solid

Masse moléculaire : 156.25

Ref: 7W-GK6347

2,2,6,6-Tetramethylpiperidinoxy free radical

CAS : 2564-83-2

Formule : C₉H₁₈NO

Degré de pureté : 99.0%

Couleur et forme : Solid, Powder or Crystalline Powder or Solid or Chunks

Masse moléculaire : 156.249

Ref: 10-F013714

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

Formule : C₉H₁₈NO

Degré de pureté : 98.35%

Couleur et forme : Orange Crystals Or Powder

Masse moléculaire : 156.25

Ref: TM-T5363

TEMPO

Produit contrôlé

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);

Formule : C₉H₁₈NO

Couleur et forme : Neat

Masse moléculaire : 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.

Formule : C₉H₁₈NO

Degré de pureté : Min. 98 Area-%

Masse moléculaire : 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.

Formule : C₉H₁₈NO

Degré de pureté : Min. 98 Area-%

Couleur et forme : Orange Red Powder

Masse moléculaire : 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.

Formule : C₉H₁₈NO

Degré de pureté : Min. 98 Area-%

Couleur et forme : Orange Red Powder

Masse moléculaire : 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.

Formule : C₉H₁₈NO

Degré de pureté : Min. 95%

Couleur et forme : Powder

Masse moléculaire : 156.25 g/mol

Ref: 3D-FT167208

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

CAS : 2564-83-2

Formule : C₉H₁₈NO

Degré de pureté : min. 98%

Couleur et forme : Orange red, Crystalline hygroscopic compound, Clear

Masse moléculaire : 156.25

Ref: SR-91902