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2,2,6,6-Tetramethylpiperidinyl amide, also known as TMP-amid, is a chemical compound with the molecular formula C10H21NO. It is a derivative of piperidine, an alkaloid found in many plants, and is characterized by the presence of four methyl groups attached to the 2, 2, 6, and 6 positions of the piperidine ring. 2,2,6,6-tetramethylpiperidinyl amide is often used as a radical scavenger and an antioxidant in various industrial applications, including the stabilization of polymers and the protection of materials against oxidative degradation. Its ability to neutralize free radicals makes it a valuable component in formulations that require enhanced resistance to heat, light, and atmospheric exposure.

89806-88-2

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89806-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89806-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,0 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89806-88:
(7*8)+(6*9)+(5*8)+(4*0)+(3*6)+(2*8)+(1*8)=192
192 % 10 = 2
So 89806-88-2 is a valid CAS Registry Number.

89806-88-2Downstream Products

89806-88-2Relevant academic research and scientific papers

THE PREPARATION AND PROPERTIES OF NEUTRAL DIAMIDE IONOPHORES FOR GROUP IIA METAL CATIONS-II

Borowitz, Irving J.,Readio, Josephine D.,Li, Ven-Shun

, p. 1009 - 1016 (1984)

The elaboration of a series of neutral ligands featuring vicinal ether and N,N-dialkylacetamido groups is described.Several of these ligands were previously described.The ligands are moderate binders with Kapp=1E3-1E5 in methanol of the Group IIA cations for wich they are sensitive.Binding constants by Scatchard method are reported for number of ligands mainly with Ca, Sr, Mn and Ba.The ligands in methylene chloride solution extract these cations via their picrate salts from water.The electrochemical Kijpot (selectivity) values for some of the ligands when they are incorporated into liquid membrane electrodes and tested with various cations as determined by Simon et al. (ETH Zurich) are reported.Selectivity ratios of over 100:1 for Na vs Ca were found for several piperidenyl amides of 1,2-phenylenedioxydiacetic acid.Incorporation of N-methylamino instead of ether oxygen groups into the basic structure gives a stronger cation binder which is still selective for Group IIA vs Group IA cations but with binding capacity for transition metal cations also.Limitations of the Scatchard plots for these ligands and the non-correspondance of electrochemical selectivities with the ordering of binding of cations in single liquid phase are discussed.

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