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Glyoxal-bis(2-hydroxy-3,5-di-tert-butylphenyl)imine, also known as Irganox 1010, is a synthetically derived chemical compound that serves as an antioxidant in various industrial applications. It is characterized by its molecular formula C34H52N2O4 and a molecular weight of 540.79 g/mol. glyoxal-bis(2-hydroxy-3,5-di-tert-butylphenyl)imine is primarily used in the stabilization of polymers, such as polyolefins, to prevent degradation caused by heat, light, and oxygen exposure. It is also employed in the rubber industry to protect against oxidative degradation and to extend the service life of rubber products. Irganox 1010 is known for its high thermal stability and low volatility, making it suitable for use in applications where long-term stability is crucial. It is a white to off-white powder that is insoluble in water but soluble in organic solvents. The compound is also recognized for its low toxicity and is widely used in the production of plastics, adhesives, and coatings.

3159-43-1

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3159-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3159-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3159-43:
(6*3)+(5*1)+(4*5)+(3*9)+(2*4)+(1*3)=81
81 % 10 = 1
So 3159-43-1 is a valid CAS Registry Number.

3159-43-1Relevant articles and documents

Tridentate complexes of group 10 bearing bis-aryloxide N-heterocyclic carbene ligands: Synthesis, structural, spectroscopic, and computational characterization

Borr, Etienne,Dahm, Georges,Aliprandi, Alessandro,Mauro, Matteo,Dagorne, Samuel,Bellemin-Laponnaz, Stphane

, p. 4374 - 4384 (2014)

A series of group 10 complexes featuring chelating tridentate bis-aryloxide N-heterocyclic carbenes were synthesized and characterized by using different techniques. Ni(II), Pd(II), and Pt(II) complexes were isolated in good yields by straightforward direct metalation of the corresponding benzimidazolium or imidazolium precursors in a one-pot procedure. All of the compounds were fully characterized, including single-crystal X-ray diffractometric determination for three of the derivatives. In the solid state, the complexes adopt a typical square-planar coordination geometry around the platinum atom, sizably distorted in order to comply with the geometrical constraints imposed by the bis-aryloxide N-heterocyclic carbene ligand. For platinum and palladium derivatives, a joint experimental and theoretical characterization was performed in order to study the optical properties of the newly prepared complexes by means of electronic absorption and steady-state and time-resolved photophysical techniques as well as density functional theory (DFT) and time-dependent DFT in both vacuum and solvent. When the temperature was lowered to 77 K in frozen glassy matrix, three platinum complexes showed broad and featureless, yet weak, photoluminescence in the green region of the visible spectrum with excited-state lifetimes on the order of a few microseconds. On the basis of joint experimental and computational findings and literature on platinum complexes, such emission was assigned to a triplet-manifold metal-ligand-to-ligand charge transfer (3MLLCT) transition.

Substituted Benzoxazole and Catechol Cocrystals as an Adsorbent for CO2 Capture: Synthesis and Mechanistic Studies

Sivanesan, Dharmalingam,Youn, Min Hye,Park, Ki Tae,Kim, Hak Joo,Jeong, Soon Kwan

, p. 4504 - 4510 (2017/09/12)

We report the synthesis of cocrystals of a substituted benzoxazole and catechol from a primary amine and 3,5-di-tert-butylbenzoquinone. Fourier transform infrared and NMR spectroscopy studies revealed that cocrystals 2 could be synthesized in excellent yield from 1 and 3,5-di-tert-butylbenzoquinone. Introduction of an amine into the cocrystal structure enhanced the CO2 adsorption capacity of the cocrystals at room temperature from 15.69 to 44.21 mg/g. Our results indicated the ability to use cocrystals for CO2 capture and to easily modify them to enhance their CO2 adsorption capacity.

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