724-46-9 Usage
Uses
Used in Plastics Industry:
3,5-DI-TERT-BUTYL-4-HYDROXYBENZYLAMINE is used as a hindered amine light stabilizer (HALS) for plastics to protect them from degradation caused by UV radiation and other environmental stressors. Its ability to scavenge free radicals helps maintain the integrity and longevity of plastic products.
Used in Coatings Industry:
In the coatings industry, 3,5-DI-TERT-BUTYL-4-HYDROXYBENZYLAMINE serves as a HALS to enhance the durability and resistance of coatings against UV-induced degradation. This contributes to the preservation of the color, gloss, and overall appearance of coated surfaces.
Used in Rubber Products:
3,5-DI-TERT-BUTYL-4-HYDROXYBENZYLAMINE is utilized as a HALS in rubber products to prevent the deterioration caused by exposure to sunlight and other environmental factors. Its incorporation into rubber formulations helps to extend the service life and maintain the physical properties of rubber goods.
Used in Pharmaceutical Research:
3,5-DI-TERT-BUTYL-4-HYDROXYBENZYLAMINE is being explored for its potential use in pharmaceuticals due to its antioxidant properties. Research is ongoing to understand its possible applications in the development of new drugs or therapies.
Used in Skincare Products:
The antioxidant properties of 3,5-DI-TERT-BUTYL-4-HYDROXYBENZYLAMINE are also being investigated for their potential benefits in skincare products. Its ability to neutralize free radicals may contribute to anti-aging and skin protection formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 724-46-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 724-46:
(5*7)+(4*2)+(3*4)+(2*4)+(1*6)=69
69 % 10 = 9
So 724-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H25NO/c1-14(2,3)11-7-10(9-16)8-12(13(11)17)15(4,5)6/h7-8,17H,9,16H2,1-6H3
724-46-9Relevant academic research and scientific papers
MULTIFUNCTIONAL SYNERGISTIC MACROMOLECULAR ANTI-OXIDATION STABILIZER AND PREPARATION METHOD AND USE THEREOF
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Paragraph 0048; 0051-0052, (2017/12/27)
Disclosed is an anti-oxidation stabilizer, which has the following structure (A), wherein R1 is a connection chain, and the connection chain is a fatty chain, an aromatic structural chain or a fatty and aromatic structurally combined chain; R2 is (B), and X is O, S, N or NH or —CONR—, Z is O, S, N or NH, and X is different from Z; R is a fatty chain, an aromatic group, a sterically hindered amine or sterically hindered phenol, R3 is a fatty chain, an aromatic group, a sterically hindered amine or sterically hindered phenol, and R is identical to R3, or R is different from R3; n is a positive integer including 1, n1 is a positive integer including 1, and n is identical to n1, or n is different from n1.
Synthesis and antioxidant activities of 3,5-dialkoxy-4-hydroxycinnamamides
Kang, Tae-Souk,Jo, Hyang-Ok,Park, Woo-Kyu,Kim, Jong-Pyung,Konishi, Yasuo,Kong, Jae-Yang,Park, No-Sang,Jung, Young-Sik
, p. 1663 - 1667 (2008/12/21)
A series of 3,5-dialkoxy-4-hydroxycinnamamides 6 and 7 was synthesized, and their antioxidant activity was assessed using the thiobarbituric acid reactive substance (TBARS) assay. Interestingly, cinnamamides with longer alkoxy groups on the C-3 and C-5 positions display enhanced inhibition, and most of the compounds in the series tested exhibit excellent lipid peroxidation inhibitory activities. Some cinamamides bearing hexyloxy or 2,6-di-tert-butyl-4-methyl phenol groups have submicromolar inhibitory activities.
Chemical process
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, (2008/06/13)
Novel 2,4-dihydrocarbylspiro[5.5]undeca-1,4,8-trien-3-one compounds are prepared by reacting an N,N-dihydrocarbyl,2,6-dihydrocarbyl-4-aminomethylphenol with a conjugated diene and an alkyl halide in a liquid solvent medium.
