17540-75-9 Usage
Uses
Used in Polyols:
4-SEC-BUTYL-2,6-DI-TERT-BUTYLPHENOL is used as a stabilizer for polyols to enhance their performance and extend their shelf life. It provides protection against degradation, ensuring the stability and quality of the final product.
Used in PVC:
In the PVC industry, 4-SEC-BUTYL-2,6-DI-TERT-BUTYLPHENOL is used as a stabilizer to prevent the degradation of PVC, which can lead to discoloration and loss of mechanical properties. Its use ensures the longevity and durability of PVC products.
Used in Adhesives:
4-SEC-BUTYL-2,6-DI-TERT-BUTYLPHENOL is used as a stabilizer in the adhesives industry to improve the bonding strength and durability of adhesive formulations. It helps maintain the adhesive's performance over time and under various environmental conditions.
Used in Functional Fluids:
In the production of functional fluids, 4-SEC-BUTYL-2,6-DI-TERT-BUTYLPHENOL is used as a stabilizer to enhance the fluid's performance and resistance to degradation. This ensures the fluid's effectiveness and longevity in various applications, such as lubricants, hydraulic fluids, and heat transfer fluids.
Overall, 4-SEC-BUTYL-2,6-DI-TERT-BUTYLPHENOL is a versatile and cost-effective stabilizer with a wide range of applications in various industries, contributing to the enhancement of product performance and stability.
Check Digit Verification of cas no
The CAS Registry Mumber 17540-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,4 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17540-75:
(7*1)+(6*7)+(5*5)+(4*4)+(3*0)+(2*7)+(1*5)=109
109 % 10 = 9
So 17540-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H30O/c1-9-12(2)13-10-14(17(3,4)5)16(19)15(11-13)18(6,7)8/h10-12,19H,9H2,1-8H3/t12-/m0/s1
17540-75-9Relevant academic research and scientific papers
Highly selective conversion of guaiacol to: Tert -butylphenols in supercritical ethanol over a H2WO4 catalyst
Mai, Fuhang,Cui, Kai,Wen, Zhe,Wu, Kai,Yan, Fei,Chen, Mengmeng,Chen, Hong,Li, Yongdan
, p. 2764 - 2771 (2019/02/01)
The conversion of guaiacol is examined at 300 °C in supercritical ethanol over a H2WO4 catalyst. Guaiacol is consumed completely, meanwhile, 16.7% aromatic ethers and 80.0% alkylphenols are obtained. Interestingly, tert-butylphenols are produced mainly with a high selectivity of 71.8%, and the overall selectivity of 2,6-di-tert-butylphenol and 2,6-di-tert-butyl-4-ethylphenol is as high as 63.7%. The experimental results indicate that catechol and 2-ethoxyphenol are the intermediates. Meanwhile, the WO3 sites play an important role in the conversion of guaiacol and the Br?nsted acid sites on H2WO4 enhance the conversion and favour a high selectivity of the tert-butylphenols. The recycling tests show that the carbon deposition on the catalyst surface, the dehydration and partial reduction of the catalyst itself are responsible for the decay of the H2WO4 catalyst. Finally, the possible reaction pathways proposed involve the transetherification process and the alkylation process during guaiacol conversion.
METHODS AND COMPOSITIONS FOR INHIBITING VINYL AROMATIC MONOMER POLYMERIZATION
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, (2013/03/26)
Methods and compositions are provided for inhibiting the polymerization of a vinyl aromatic monomer, such as styrene monomer, during elevated temperature processing thereof or during storage or shipment of polymer containing product. The compositions comprise a combination of a quinone methide derivative A) and a phenol compound B). The methods comprise adding from about 1-10,000 ppm of the combination to the monomer containing medium, per one million parts of the monomer.
