7333-86-0 Usage
Uses
Used in Lubricant Industry:
METHYL, N-OCTADECYL TEREPHATHALAMATE is used as a friction modifier and wear resistance improver in lubricants. Its hydrophobic tail allows it to adhere to surfaces, reducing friction between moving parts and enhancing the performance and longevity of the lubricant.
Used in Coating Industry:
In the coating industry, METHYL, N-OCTADECYL TEREPHATHALAMATE is used as an additive to improve the wear resistance and durability of coatings. Its ability to adhere to surfaces helps in providing a protective layer that reduces wear and tear, thereby extending the life of the coated surfaces.
Used in Polymer Industry:
METHYL, N-OCTADECYL TEREPHATHALAMATE is used as a plasticizer in synthetic polymers to enhance their flexibility and durability. By incorporating METHYL, N-OCTADECYL TEREPHATHALAMATE into polymer formulations, manufacturers can improve the overall performance and longevity of the final product, making it more resistant to wear and environmental factors.
Overall, METHYL, N-OCTADECYL TEREPHATHALAMATE is a versatile compound with a wide range of applications in various industries, including lubricants, coatings, and polymers, where it serves to improve wear resistance, friction reduction, and overall product performance.
Check Digit Verification of cas no
The CAS Registry Mumber 7333-86-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7333-86:
(6*7)+(5*3)+(4*3)+(3*3)+(2*8)+(1*6)=100
100 % 10 = 0
So 7333-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C27H45NO3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-23-28-26(29)24-19-21-25(22-20-24)27(30)31-2/h19-22H,3-18,23H2,1-2H3,(H,28,29)
7333-86-0Relevant academic research and scientific papers
Process for preparing derivatives of the monoamide of terephthalic acid
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, (2008/06/13)
An improved and simplified process for preparing terephthalic acid monoamide derivatives of the formula STR1 in which R denotes hydrogen, an alkaline earth metal or alkali metal cation or methyl, R1 denotes C8 -C30 -alkyl, preferably C12 -C22 -alkyl, and R2 denotes C1 -C30 -alkyl or, preferably hydrogen, in which dimethyl terephthalate is reacted with an amine of the formula in methanol and in the presence of sodium methylate. The compounds thus obtained are used for gelling oils and organic solvents.