2,2,6,6-Tetramethyl...

2,2,6,6-Tetramethylpiperidinooxy	2564-83-2
2,2,6,6-Tetramethylpiperidinooxy	2564-83-2
2,2,6,6-Tetramethylpiperidinooxy	2564-83-2
2,2,6,6-Tetramethylpiperidinooxy	2564-83-2
2,2,6,6-Tetramethylpiperidinooxy	2564-83-2

2,2,6,6-Tetramethylpiperidinooxy 2564-83-2

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1 Kilogram

FOB Price:USD 95.0000 -98.0000

  • Min.Order :1 Kilogram
  • Purity: 99.0%
  • Payment Terms : L/C,D/A,D/P,T/T,

Keywords

2,2,6,6-Tetramethylpiperidinooxy 2564-83-2 2,2,6,6-Tetramethyl-1-piperinedinyloxy

Quick Details

  • Appearance:Yellow to green powder
  • Application:TEMPO(2,2,6,6-Tetramethylpiperidinooxy) 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 scav
  • PackAge: Aluminum foil bag /Fiber drum / as customers' request.
  • ProductionCapacity:10000|Metric Ton|Month
  • Storage:Room temperature
  • Transportation:by air; by sea; or as customers' request.

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Details:

2,2,6,6-Tetramethylpiperidinooxy Basic information
Product Name: 2,2,6,6-Tetramethylpiperidinooxy
Synonyms: 2,2,6,6-Tetramethyl-1-piperinedinyloxy;TEMPO, FREE RADICAL;TEMPO;2,2,6,6-Tetramethyl-1-piperidyloxy;2,2,6,6-Tetramethylpiperidin-1-oxy;2,2',6,6'-Tetramethylpiperidin-1-oxyl;2,2,6,6-Tetramethylpiperidin-1-oxyl;2,2,6,6-Tetramethylpiperidine 1-oxide
CAS: 2564-83-2
MF: C9H18NO*
MW: 156.25
EINECS: 219-888-8
Product Categories: Spin Labels;Synthetic Organic Chemistry;Analytical Chemistry;Environmentally-friendly Oxidation;ESR Spectrometry;Fine Chemical;Oxidation;Redox Catalysts (Environmentally-friendly Oxidation)
Mol File: 2564-83-2.mol
2,2,6,6-Tetramethylpiperidinooxy Structure
 
2,2,6,6-Tetramethylpiperidinooxy Chemical Properties
Melting point  36-38 °C(lit.)
Boiling point  193°C
density  1 g/cm3
vapor pressure  0.4 hPa (20 °C)
refractive index  1.4350 (estimate)
Fp  154 °F
storage temp.  Store below +30°C.
solubility  9.7g/l
form  Powder
color  Yellow to green
PH 8.3 (9g/l, H2O, 20℃)
Water Solubility  Soluble in all organic solvents. Insoluble in water.
Merck  14,9140
BRN  1422418
Stability: Stable. Incompatible with strong acids, strong oxidizing agents. Refrigerate.
InChIKey RVWUHFFPEOKYLB-UHFFFAOYSA-N
CAS DataBase Reference 2564-83-2(CAS DataBase Reference)
NIST Chemistry Reference 1-Piperidinyloxy, 2,2,6,6-tetramethyl-(2564-83-2)
EPA Substance Registry System 1-Piperidinyloxy, 2,2,6,6-tetramethyl- (2564-83-2)
 
Safety Information
Hazard Codes  C,Xi
Risk Statements  34-36/37/38
Safety Statements  26-36/37/39-45-24/25
RIDADR  UN 3263 8/PG 2
WGK Germany  3
RTECS  TN8991900
Autoignition Temperature 275 °C
TSCA  Yes
HazardClass  8
PackingGroup  III
HS Code  29333999
MSDS Information
Provider Language
2,2,6,6-Tetramethylpiperidine 1-oxyl English
SigmaAldrich English
ACROS English
ALFA English
 
2,2,6,6-Tetramethylpiperidinooxy Usage And Synthesis
Chemical Properties orange crystals or powder
Uses TEMPO(2,2,6,6-Tetramethylpiperidinooxy) 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 synthe sis and as a structural probe in electron spin resonance spectroscopy. TEMPO can also be used as a mediator in free radical polymerization.
Uses In organic chemistry as a radical trap, 2,2,6,6-Tetramethylpiperidinooxy can be used as a catalyst and in polymerization mediation.
Uses TEMPO can be used:
  • As a catalytic oxidant for copper-catalyzed, greener oxidation of alcohols under aerobic conditions.
  • As a catalytic oxidant in the iodobenzene diacetae oxidation of nerol to neral.
  • For trapping the styrenyl radical generated from benzoyl peroxide during nitroxide-mediated radical polymerization of styrene.
  • In the carboxylation of water-resistant nanofibrillated cellulose (NFC) films.

Copper(I)/TEMPO-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air
General Description For a synthetic protocol using NMP initiators, contributed by Prof. Karen Wooley, please visit our technology spotlight.
Purification Methods Purify TEMPO by sublimation (33o, water aspirator) [Hay & Fincke J Am Chem Soc 109 8012 1987, Keana Chem Rev 78 37 1978].

 

 

 

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