CAS 2226-96-2

templo

Descripción:

templo, con el número CAS 2226-96-2, es un radical nitroxilo estable que se utiliza a menudo en investigaciones bioquímicas y farmacológicas. Se caracteriza por su capacidad para actuar como un captador de radicales libres, lo que lo hace valioso en estudios relacionados con el estrés oxidativo y el daño celular. templo posee propiedades antioxidantes, ayudando a neutralizar especies reactivas de oxígeno (ROS) dañinas en sistemas biológicos. Este compuesto es típicamente soluble en agua y disolventes orgánicos, lo que permite aplicaciones versátiles en diversas condiciones experimentales. Además, se ha investigado templo por sus posibles efectos terapéuticos en condiciones como enfermedades cardiovasculares, trastornos neurodegenerativos e inflamación. Su estabilidad y reactividad lo convierten en una herramienta útil para comprender la biología redox y los mecanismos de daño oxidativo. En general, templo sirve como un compuesto importante tanto en la investigación como en aplicaciones clínicas potenciales debido a sus propiedades químicas únicas y su significado biológico.

Fórmula: C₉H₁₈NO₂

InChI: InChI=1S/C9H18NO2/c1-8(2)5-7(11)6-9(3,4)10(8)12/h7,11H,5-6H2,1-4H3

Clave InChI: InChIKey=UZFMOKQJFYMBGY-UHFFFAOYSA-N

SMILES: CC1(C)CC(CC(C)(C)N1O)O

Sinónimos:

• (4-Hydroxy-2,2,6,6-Tetramethylpiperidin-1-Yl)Oxidanyl
• 1-Oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine
• 1-Oxyl-2,2,6,6-tetramethyl-4-piperidinol
• 1-Piperidinyloxy, 4-hydroxy-2,2,6,6-tetramethyl-
• 2,2,6,6-Tetramethyl-1-oxy-4-hydroxypiperidine
• 2,2,6,6-Tetramethyl-4-hydroxy-1-piperidinyloxy radical
• 2,2,6,6-Tetramethyl-4-hydroxylpiperidine-1-oxyl
• 2,2,6,6-Tetramethyl-4-hydroxypiperidin-1-oxyl
• 2,2,6,6-Tetramethyl-4-hydroxypiperidine 1-oxide radical
• 2,2,6,6-Tetramethyl-4-hydroxypiperidine N-oxide
• 2,2,6,6-Tetramethyl-4-hydroxypiperidine oxide
• 2,2,6,6-Tetramethyl-4-hydroxypiperidine-1-hydroxyl
• 2,2,6,6-Tetramethyl-4-hydroxypiperidine-1-oxyl
• 2,2,6,6-Tetramethyl-4-hydroxypiperidine-1-oxyl radical
• 2,2,6,6-Tetramethyl-4-hydroxypiperidinooxy
• 2,2,6,6-Tetramethyl-4-hydroxypiperidinooxy radical
• 2,2,6,6-Tetramethyl-4-hydroxypiperidinyl-1-oxy
• 2,2,6,6-Tetramethyl-4-hydroxypiperidinyl-1-oxyl
• 2,2,6,6-Tetramethyl-4-hydroxypiperidinyloxy radical
• 2,2,6,6-Tetramethyl-4-hydroxypiperidinyloxyl radical
• 2,2,6,6-Tetramethyl-4-hydroxypiperidyl 1-oxyl
• 2,2,6,6-Tetramethyl-4-oxypiperidine-1-oxyl
• 2,2,6,6-Tetramethyl-4-piperidinol 1-oxide
• 2,2,6,6-Tetramethyl-4-piperidinol 1-oxyl
• 2,2,6,6-Tetramethyl-4-piperidinol N-oxyl
• 2,2,6,6-Tetramethyl-4-piperidinol nitroxide
• 2,2,6,6-Tetramethyl-4-piperidinol-1-oxy
• 2,2,6,6-Tetramethyl-4-piperidinol-1-oxyl radical
• 2,2,6,6-Tetramethylpiperidine-4-hydroxy-1-oxyl
• 2,2,6,6-Tetramethylpiperidine-N-oxyl-4-ol
• 2,2,6,6-Tetramethylpiperidinol-4-oxyl-1
• 2.2.6.6-Tetramethyl-Freeagaoxy-4-Piperidyl
• 4-Hidroxi-2,2,6,6-Tetrametilpiperidinoxil
• 4-Ho-Tempo
• 4-Hydroxy-1-oxyl-2,2,6,6-tetramethylpiperidine
• 4-Hydroxy-2,2,6,6-Tetramethylpiperidinoxyl
• 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinoxy
• 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinoxyl
• 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy
• 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy radical
• 4-Hydroxy-2,2,6,6-tetramethyl-piperidinyloxy
• 4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-oxide radical
• 4-Hydroxy-2,2,6,6-tetramethylpiperidine N-oxide
• 4-Hydroxy-2,2,6,6-tetramethylpiperidine oxide
• 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl
• 4-Hydroxy-2,2,6,6-tetramethylpiperidine-N-oxy
• 4-Hydroxy-2,2,6,6-tetramethylpiperidine-N-oxyl
• 4-Hydroxy-2,2,6,6-tetramethylpiperidino-1-oxyl
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinooxy
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinooxy radical
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinoxy
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinoxyle
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinyl-1-oxyl
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinyl-N-oxy
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinyl-N-oxyl
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinyloxy
• 4-Hydroxy-2,2,6,6-tetramethylpiperidinyloxyl
• 4-Hydroxy-2,2,6,6-tetramethylpiperidyl-1-oxyl
• 4-Hydroxy-2,6-Tetramethyl-Piperidine-1-Oxide
• 4-Hydroxy-TEMPO
• 4-OH-Tempo
• 4-Oxypiperidol
• 4-hydroxyl-2,2,6,6-tetramethylpiperidine-1-Oxyl
• 4H-Tempo
• ADK Stab LA 7RD
• ADK Stab NA 7RD
• H 0865
• H-Tempo
• Hotempo
• Htempo
• HyTEMPO
• In701
• La 7Rd
• Nitroxyl 2
• Nr I
• Petroflo 20Y104
• Piperidine, 4-Hydroxy-2,2,6,6-Tetramethyl-1-Oxy-
• Piperidinooxy, 4-hydroxy-2,2,6,6-tetramethyl-
• Polystast 7200P
• Polystop 7010
• Polystop 7300P
• Prostab 5198
• Spj 701
• Tanol
• Tempo OH
• Tempol
• Tempole
• Tetramethyl-2,2,6,6-aza-1-cyclohexanol-4-oxide-1
• Tmhpo
• Tmpn
• Uv-1198
• Zj 01
• Zj 705

4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-Oxyl Free Radical

CAS: 2226-96-2

Fórmula: C₉H₁₈NO₂

Pureza: >98.0%(GC)

Forma y color: Light yellow to Brown powder to lump

Peso molecular: 172.25

Ref: 3B-H0865

4-Hydroxy-TEMPO, free radical, 98+%

CAS: 2226-96-2

Superoxide scavenger with neuroprotective, anti-inflammatory and analgesic effects4-Hydroxy-TEMPO free radical is used as a catalyst and a chemical oxidant by virtue of being a stable radical. It is used for detoxifying reactive oxygen species in medicinal chemistry. It is involved in the catalysis

Fórmula: C₉H₁₈NO₂

Pureza: 98+%

Forma y color: Crystals or powder or crystalline powder or flakes, Orange

Peso molecular: 172.25

Ref: 02-A12497

4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy

CAS: 2226-96-2

Fórmula: C₉H₁₈NO₂

Pureza: 98%

Forma y color: Solid

Peso molecular: 172.2447

Ref: IN-DA00342N

4-Hydroxy TEMPO, free radical

CAS: 2226-96-2

Fórmula: C₉H₁₈NO₂

Pureza: (GC) ≥ 98%

Forma y color: Yellow to orange-red crystalline powder or solid

Peso molecular: 172.25

Ref: 7W-GE0239

Tempol

CAS: 2226-96-2

Tempol

Pureza: ≥95%

Peso molecular: 172.25g/mol

Ref: 54-BUP18148

4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl

CAS: 2226-96-2

4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl

Pureza: 98%

Forma y color: Solid

Peso molecular: 172.24g/mol

Ref: 54-OR480623

Tempol

CAS: 2226-96-2

Tempol (Tanol) is a superoxide scavenger. It has anti-inflammatory, neuroprotective and analgesic effects.

Fórmula: C₉H₁₈NO₂

Pureza: 97% - 99.98%

Forma y color: 4-Hydroxy-Tempo Appears As Orange Flakes Solid Flakes

Peso molecular: 172.25

Ref: TM-T6699

4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy

Producto controlado

CAS: 2226-96-2

Applications A free radical scavenger; may be used for prophylaxis and treatment of IRI.
References Flather, M., et al.: Lancet, 355, 1575 (2000), Sasso, F., et al.: Metabolism, 52, 675 (2003), Kass, D., et al.: Circ. Res., 94, 1533 (2004), Murdoch, C., et al.: Cardiovasc Res., 71, 208 (2006),

Fórmula: C₉H₁₈NO₂

Forma y color: Light Orange To Orange

Peso molecular: 172.24

Ref: TR-H956500

4-Hydroxy-2,2,6,6-tetramethyl piperidinyloxy free radical

CAS: 2226-96-2

Fórmula: C₉H₁₈NO₂

Pureza: 98%

Forma y color: Solid, Dark orange solid

Peso molecular: 172.248

Ref: 10-F013608

2,2,6,6-Tetramethyl-4-piperidinol 1-oxyl, free radical

CAS: 2226-96-2

2,2,6,6-Tetramethyl-4-piperidinol 1-oxyl (TEMPO) is a reactive oxygen species that belongs to the group of nitroxide radicals. It can be used as a radical scavenger and has been shown to inhibit the production of pro-apoptotic proteins in human macrophages. TEMPO has also been shown to bind to DNA and prevent the binding of HIV viral protein gp120. TEMPO can be used as an inhibitor for glycol ethers in laboratory experiments. The most common use is as a water vapor scavenger during polymerization reactions in organic chemistry.

Fórmula: C₉H₁₈NO₂

Pureza: Min. 98 Area-%

Forma y color: Orange Solid

Peso molecular: 172.24 g/mol

Ref: 3D-FT02559