TEMPO

TEMPO__Stabilized free radical L68

Product Name	TEMPO
Description	Stabilized free radical
Purity	>98%
CAS No.	2564-83-2
Molecular Formula	C9H18NO
Molecular Weight	156.25

Storage Temperature	-20ºC
Shipping Temperature	Shipped Ambient
Product Type	Inhibitor
Solubility	Soluble in 50 mg/ml of ethanol
Source	Synthetic
Appearance	White Solid
SMILES	CC1(CCCC(N1O)(C)C)C
InChI	InChI=1S/C9H18NO/c1-8(2)6-5-7-9(3,4)10(8)11/h5-7H2,1-4H3
InChIKey	QYTDEUPAUMOIOP-UHFFFAOYSA-N
Safety Phrases	Classification: Harmful. May be harmful if inhaled, swallowed or absorbed through skin. Safety Phrases: S22 – Do not breathe dust S36/37/39 – Wear suitable protective clothing, gloves and eye/face protection S45- In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible) Risk Phrases: R34- Causes Burns Hazard Phrases: H314 Precautionary Phrases: P280-P305 + P351 + P338-P310
Cite This Product	TEMPO (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-155)

Alternative Names	2,2,6,6-Tetramethylpiperidine 1-oxyl, 2,2,6,6-Tetramethyl-1-piperidinyloxy, free radical, (2,2,6,6-Tetramethyl-1-piperidinyl)oxidanyl, 1,1,5,5-tetramethylpentamethylene nitroxide, 2,2,6,6-Tetramethylpiperidine-1-oxyl
Research Areas	Cancer, Oxidative Stress
PubChem ID	2724126
Scientific Background	TEMPO is widely used as a radical trap, as a structural probe for biological systems in conjunction with electron spin resonance spectroscopy, as a reagent in organic synthesis, and as a mediator in controlled free radical polymerization (1).
References	1.  Montanari F., Quici S., Henry-Riyad H., Tidwell T.T. (2005) Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons.