CAS 2564-83-2

Zeit

Beschreibung:

Zeit, oder 2,2,6,6-Tetramethylpiperidinyloxyl, ist ein stabiler freier Radikal, der durch seine charakteristische Struktur gekennzeichnet ist, die einen Piperidinring und eine Nitroxid-Funktionalgruppe umfasst. Diese Verbindung ist bekannt für ihre Stabilität und Fähigkeit, als Radikalfänger zu wirken, was sie in verschiedenen Anwendungen nützlich macht, einschließlich organischer Synthese und Polymerchemie. Zeit zeigt eine charakteristische tiefgelbe Farbe und ist in organischen Lösungsmitteln wie Ethanol und Aceton löslich, aber weniger löslich in Wasser. Ihre radikale Natur ermöglicht es ihr, an Redoxreaktionen teilzunehmen, und sie wird häufig als Spinmarkierung in der Elektronenspinresonanz (EPR) Spektroskopie eingesetzt. Darüber hinaus kann Zeit als Oxidationskatalysator in bestimmten chemischen Reaktionen dienen, wodurch die Effizienz von Prozessen wie der Oxidation von Alkoholen zu Carbonylverbindungen erhöht wird. Ihre einzigartigen Eigenschaften machen sie zu einem wertvollen Werkzeug sowohl in der akademischen Forschung als auch in industriellen Anwendungen.

Formel: C₉H₁₈NO

InChl: 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

Synonyme:

• (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

Formel: C₉H₁₈NO

Reinheit: >99.0%(GC)(T)

Farbe und Form: Orange to Brown powder to crystal

Molekulargewicht: 156.25

Ref: 3B-T3751

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

CAS: 2564-83-2

Formel: C₉H₁₈NO

Reinheit: >98.0%(GC)(T)

Farbe und Form: Orange to Brown powder to crystal

Molekulargewicht: 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

Formel: C₉H₁₈NO

Reinheit: 98+%

Farbe und Form: Orange-red to red to dark red, Crystalline powder or powder or crystals or fused solid and/or chunks

Molekulargewicht: 156.25

Ref: 02-A12733

Tempo, 10mM (in DMSO)

CAS: 2564-83-2

Tempo, 10mM (in DMSO)

Formel: C₉H₁₈NO

Reinheit: ≥98%, 10 mM in DMSO

Molekulargewicht: 156.25

Ref: 54-BUP19082

2,2,6,6-Tetramethylpiperidoxyl

CAS: 2564-83-2

Formel: C₉H₁₈NO

Reinheit: 95%

Farbe und Form: Solid

Molekulargewicht: 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

Formel: C₉H₁₈NO

Reinheit: ≥95%

Farbe und Form: Red Solid-Crystals

Molekulargewicht: 156.24532

Ref: 54-OR59926

Medetomidine Impurity 33

CAS: 2564-83-2

Formel: C₉H₁₈NO

Farbe und Form: Orange Red Solid

Molekulargewicht: 156.25

Ref: 4Z-M-6840

TEMPO

CAS: 2564-83-2

Formel: C₉H₁₈NO

Reinheit: ≥ 97.5%

Farbe und Form: Orange, red or dark red crystals or solid

Molekulargewicht: 156.25

Ref: 7W-GK6347

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

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

Reinheit: 98 atom % D

Farbe und Form: Red Solid

Molekulargewicht: 174.36

Ref: 3U-D7184

2,2,6,6-Tetramethylpiperidinoxy free radical

CAS: 2564-83-2

Formel: C₉H₁₈NO

Reinheit: 99.0%

Farbe und Form: Solid

Molekulargewicht: 156.249

Ref: 10-F013714

Tempo

CAS: 2564-83-2

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

Formel: C₉H₁₈NO

Reinheit: 97%

Molekulargewicht: 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

Formel: C₉H₁₈NO

Reinheit: 99.90%

Farbe und Form: Orange Solid

Molekulargewicht: 156.25

Ref: TM-T5363

TEMPO

Kontrolliertes Produkt

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);

Formel: C₉H₁₈NO

Farbe und Form: Neat

Molekulargewicht: 156.25

Ref: TR-T017850

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.

Formel: C₉H₁₈NO

Reinheit: Min. 98 Area-%

Farbe und Form: Orange Red Powder

Molekulargewicht: 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.

Formel: C₉H₁₈NO

Reinheit: Min. 98 Area-%

Farbe und Form: Orange Red Powder

Molekulargewicht: 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.

Formel: C₉H₁₈NO

Reinheit: Min. 95%

Farbe und Form: Powder

Molekulargewicht: 156.25 g/mol

Ref: 3D-FT167208

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

CAS: 2564-83-2

Formel: C₉H₁₈NO

Reinheit: min. 98%

Farbe und Form: Orange red, Crystalline hygroscopic compound, Clear

Molekulargewicht: 156.25

Ref: SR-91902