Fine Chemicals: Catalsts and Auxiliary Agents

Home - Products List - Fine Chemicals: Catalsts and Auxiliary Agents

2,2,6,6-Tetramethylpiperidinooxy (TEMPO)

  • Product Name: 2,2,6,6-Tetramethylpiperidinooxy (TEMPO)
  • CAS: 2564-83-2
  • Purity:
  • Appearance: orange crystals or powder

Contact Us: +86-15508631887(WhatsApp/WeChat)

Email:sales@finerchem.com

Inquiry

Factory supply 2,2,6,6-Tetramethylpiperidinooxy (TEMPO) 2564-83-2 with sufficient production capacity

  • Molecular Formula:C9H18NO
  • Molecular Weight:158.264
  • Appearance/Colour:orange crystals or powder 
  • Vapor Pressure:0.4 hPa (20 °C) 
  • Melting Point:36-38 °C(lit.) 
  • Refractive Index:1.4350 (estimate) 
  • Boiling Point:193 °C 
  • Flash Point:154 °F 
  • PSA:3.24000 
  • Density:1 g/cm3 
  • LogP:2.31290 

2,2,6,6-Tetramethylpiperidinooxy(Cas 2564-83-2) Usage

Purification Methods

Purify TEMPO by sublimation (33o, water aspirator) [Hay & Fincke J Am Chem Soc 109 8012 1987, Keana Chem Rev 78 37 1978].

General Description

2,2,6,6-Tetramethylpiperidinooxy (TEMPO) is a stable nitroxide radical widely used in catalysis, dynamic nuclear polarization (DNP) for NMR, and polymer chemistry. It exhibits high reactivity in alcohol oxidation and serves as a key component in biradical systems for enhancing DNP efficiency. TEMPO derivatives can be modified for recyclability in catalytic processes or incorporated into stimuli-responsive polymers, demonstrating versatility in both synthetic and materials applications.

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

2564-83-2 Relevant articles

A Structurally Characterized Nonheme Cobalt-Hydroperoxo Complex Derived from Its Superoxo Intermediate via Hydrogen Atom Abstraction

Wang, Chun-Chieh,Chang, Hao-Ching,Lai, Yei-Chen,Fang, Huayi,Li, Chieh-Chin,Hsu, Hung-Kai,Li, Zong-Yan,Lin, Tien-Sung,Kuo, Ting-Shen,Neese, Frank,Ye, Shengfa,Chiang, Yun-Wei,Tsai, Ming-Li,Liaw, Wen-Feng,Lee, Way-Zen

, p. 14186 - 14189 (2016)

Bubbling O2 into a THF solution of CoII(...

Mechanism of electrochemical oxidation of 1-chloro-2,2,6,6- tetramethylpiperidine

Kagan,Yanilkin,Morozov,Nastapova,Zhukova,Kashparov,Kashparova

, p. 1001 - 1003 (2009)

In contrast to 2,2,6,6-tetramethylpiperi...

An Iron(III) Superoxide Corrole from Iron(II) and Dioxygen

Albert, Therese,Goldberg, David P.,Mo?nne-Loccoz, Pierre,Sacramento, Jireh Joy D.,Siegler, Maxime

, (2021/12/03)

A new structurally characterized ferrous...

The effect of viscosity on the coupling and hydrogen-abstraction reaction between transient and persistent radicals

Li, Xiaopei,Kato, Tatsuhisa,Nakamura, Yasuyuki,Yamago, Shigeru

supporting information, p. 966 - 972 (2021/04/29)

The effect of viscosity on the radical t...

Transformation of Formazanate at Nickel(II) Centers to Give a Singly Reduced Nickel Complex with Azoiminate Radical Ligands and Its Reactivity toward Dioxygen

Ar, Deniz,Kilpatrick, Alexander F. R.,Cula, Beatrice,Herwig, Christian,Limberg, Christian

supporting information, p. 13844 - 13853 (2021/05/04)

The heteroleptic (formazanato)nickel bro...

Controlling the Reactivity of a Metal-Hydroxo Adduct with a Hydrogen Bond

Day, Victor W.,Hessefort, Logan,Jackson, Timothy A.,Opalade, Adedamola A.

supporting information, p. 15159 - 15175 (2021/09/29)

The enzymes manganese lipoxygenase (MnLO...

2564-83-2 Process route

2,2,6,6-tetramethylpiperidin-1-oxoammonium chloride
26864-01-7

2,2,6,6-tetramethylpiperidin-1-oxoammonium chloride

2,2,6,6-tetramethylpiperidin-1-ol
7031-93-8

2,2,6,6-tetramethylpiperidin-1-ol

2,2,6,6-Tetramethyl-1-piperidinyloxy free radical
2564-83-2,45842-10-2,126517-51-9,25657-03-8,26933-82-4,54637-06-8,64104-42-3

2,2,6,6-Tetramethyl-1-piperidinyloxy free radical

N-methyl-N-phenylformamide
93-61-8

N-methyl-N-phenylformamide

N-methylaniline
100-61-8

N-methylaniline

Conditions
Conditions Yield
With N,N-dimethyl-aniline; In dichloromethane; at -78 ℃; for 0.5h; Further byproducts given;
2,2,6,6-tetramethylpiperidin-1-oxoammonium chloride
26864-01-7

2,2,6,6-tetramethylpiperidin-1-oxoammonium chloride

<i>N</i>,<i>N</i>-dimethyl-aniline
121-69-7,77733-26-7

N,N-dimethyl-aniline

formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

2,2,6,6-tetramethylpiperidin-1-ol
7031-93-8

2,2,6,6-tetramethylpiperidin-1-ol

2,2,6,6-Tetramethyl-1-piperidinyloxy free radical
2564-83-2,45842-10-2,126517-51-9,25657-03-8,26933-82-4,54637-06-8,64104-42-3

2,2,6,6-Tetramethyl-1-piperidinyloxy free radical

N-methyl-N-phenylformamide
93-61-8

N-methyl-N-phenylformamide

N-methylaniline
100-61-8

N-methylaniline

Conditions
Conditions Yield
In dichloromethane; at 0 ℃; for 0.5h; Product distribution; Mechanism; var. ratio of oxoimonium ion/substrate, reactions at -80 deg C, var. N,N-dialkylanilines;

2564-83-2 Upstream products

  • 768-66-1
    768-66-1

    2,2,6,6-tetramethyl-piperidine

  • 65587-46-4
    65587-46-4

    1-benzoyl-2,3-di-indol-3-yl-1,2,3,4-tetrahydro-quinoxaline

  • 7031-93-8
    7031-93-8

    2,2,6,6-tetramethylpiperidin-1-ol

  • 26864-01-7
    26864-01-7

    2,2,6,6-tetramethylpiperidin-1-oxoammonium chloride

2564-83-2 Downstream products

  • 291-64-5
    291-64-5

    cycloheptane

  • 628-92-2
    628-92-2

    Cycloheptene

  • 23183-11-1
    23183-11-1

    bicycloheptane

  • 120881-31-4
    120881-31-4

    1-(cycloheptyloxy)-2,2,6,6-tetramethylpiperidine

Leave Your Message

Relevant Products