52184-13-1 Usage
General Description
4-SEC-BUTYL-2-TERT-BUTYLPHENOL, also known as 2-tert-butyl-4-sec-butylphenol, is an aromatic compound commonly used as an antioxidant and ultraviolet stabilizer in various industrial products such as lubricants, plastics, and polymers. It is synthesized through the reaction of phenol and isobutene, resulting in a structure with a tert-butyl group and a sec-butyl group attached to the benzene ring. This chemical is valued for its ability to prevent degradation and prolong the shelf life of various materials by inhibiting the formation of free radicals and other reactive species that can cause oxidative damage. Despite its beneficial properties, 4-SEC-BUTYL-2-TERT-BUTYLPHENOL should be handled with care and proper safety precautions due to its potential for skin and eye irritation, as well as its flammability.
Check Digit Verification of cas no
The CAS Registry Mumber 52184-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,8 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52184-13:
(7*5)+(6*2)+(5*1)+(4*8)+(3*4)+(2*1)+(1*3)=101
101 % 10 = 1
So 52184-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O/c1-6-10(2)11-7-8-13(15)12(9-11)14(3,4)5/h7-10,15H,6H2,1-5H3
52184-13-1Relevant articles and documents
Process for the production of 2-aryl-2H-benzotriazoles
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, (2008/06/13)
A process for the production of 2-aryl-2H-benzotriazoles comprises reducing and cyclizing the corresponding o-nitroazobenzenes with hydrogen at a temperature in the range of about 20° C. to about 100° C. and at a pressure in the range of about 15 psia (1 atmosphere) to about 1000 psia (66 atmospheres) in an alkaline medium at a pH over 10 in the presence of a nickel catalyst, preferably molybdenum-promoted Raney nickel. High yields of pure product are obtained directly with a concomitant reduction of undesired by-product and a reduction in effluent pollution problems.
Process for the production of 2-aryl-2H-benzotriazoles
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, (2008/06/13)
An improved process for the production of 2-aryl-2H-benzotriazoles by the reduction of o-nitroazobenzene intermediates with zinc in alkaline medium comprises employing a ratio of moles of alkali to moles of o-nitroazobenzene intermediate in the range of 0.2-1.7/1 in the presence of less than 150 ppm of iron based on zinc used. The improved process results in higher yields of high purity products with a concomitant reduction in the amount of undesired cleavage amine by-products and a reduction in effluent pollution problems. The process is carried out in a polar/non-polar solvent mixture.
