CAS 2226-96-2

tempio

Descrizione:

tempio, con il numero CAS 2226-96-2, è un radicale nitrossido stabile che viene spesso utilizzato nella ricerca biochimica e farmacologica. È caratterizzato dalla sua capacità di agire come un catturatore di radicali liberi, il che lo rende prezioso negli studi relativi allo stress ossidativo e ai danni cellulari. tempio possiede proprietà antiossidanti, aiutando a neutralizzare le specie reattive dell'ossigeno (ROS) dannose nei sistemi biologici. Questo composto è tipicamente solubile in acqua e solventi organici, consentendo applicazioni versatili in varie condizioni sperimentali. Inoltre, tempio è stato studiato per i suoi potenziali effetti terapeutici in condizioni come malattie cardiovascolari, disturbi neurodegenerativi e infiammazione. La sua stabilità e reattività lo rendono uno strumento utile per comprendere la biologia redox e i meccanismi di danno ossidativo. In generale, tempio serve come un composto importante sia nella ricerca che nelle potenziali applicazioni cliniche grazie alle sue uniche proprietà chimiche e al suo significato biologico.

Formula: C₉H₁₈NO₂

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

InChI key: InChIKey=UZFMOKQJFYMBGY-UHFFFAOYSA-N

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

Sinonimi:

• (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

Formula: C₉H₁₈NO₂

Purezza: >98.0%(GC)

Colore e forma: Light yellow to Brown powder to lump

Peso molecolare: 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

Formula: C₉H₁₈NO₂

Purezza: 98+%

Colore e forma: Crystals or powder or crystalline powder or flakes, Orange

Peso molecolare: 172.25

Ref: 02-A12497

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

CAS: 2226-96-2

Formula: C₉H₁₈NO₂

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 172.2447

Ref: IN-DA00342N

4-Hydroxy TEMPO, free radical

CAS: 2226-96-2

Formula: C₉H₁₈NO₂

Purezza: (GC) ≥ 98%

Colore e forma: Yellow to orange-red crystalline powder or solid

Peso molecolare: 172.25

Ref: 7W-GE0239

Tempol

CAS: 2226-96-2

Tempol

Purezza: ≥95%

Peso molecolare: 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

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 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.

Formula: C₉H₁₈NO₂

Purezza: 97% - 99.74%

Colore e forma: 4-Hydroxy-Tempo Appears As Orange Flakes Solid Flakes

Peso molecolare: 172.25

Ref: TM-T6699

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

Prodotto controllato

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),

Formula: C₉H₁₈NO₂

Colore e forma: Light Orange To Orange

Peso molecolare: 172.24

Ref: TR-H956500

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

CAS: 2226-96-2

Formula: C₉H₁₈NO₂

Purezza: 98%

Colore e forma: Solid, Dark orange solid

Peso molecolare: 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.

Formula: C₉H₁₈NO₂

Purezza: Min. 98 Area-%

Colore e forma: Orange Solid

Peso molecolare: 172.24 g/mol

Ref: 3D-FT02559