16152-65-1 Usage
Uses
Used in Personal Care and Cosmetics Industry:
2-(1-methylcyclohexyl)-p-cresol is utilized as an antioxidant and preservative in personal care and cosmetic products. Its application helps to prevent the oxidative degradation of ingredients, ensuring the freshness and efficacy of these products over time.
Used in Food Industry:
In the food industry, 2-(1-methylcyclohexyl)-p-cresol serves as an antioxidant, which is crucial for maintaining the quality and safety of food products. It helps to extend the shelf life by inhibiting the growth of spoilage-causing microorganisms and preventing the oxidation of fats and oils.
Used in Pharmaceutical Industry:
2-(1-methylcyclohexyl)-p-cresol is employed as a preservative in pharmaceutical formulations. Its antimicrobial properties contribute to the prevention of microbial contamination, thus ensuring the stability and safety of medications.
Used in Industrial Applications:
Beyond consumer products, 2-(1-methylcyclohexyl)-p-cresol is also used in various industrial applications where its antioxidant and antimicrobial properties are beneficial. This includes its use in the manufacturing of plastics, rubber, and other materials where protection against degradation is essential for maintaining product integrity and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 16152-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,5 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16152-65:
(7*1)+(6*6)+(5*1)+(4*5)+(3*2)+(2*6)+(1*5)=91
91 % 10 = 1
So 16152-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O/c1-11-6-7-13(15)12(10-11)14(2)8-4-3-5-9-14/h6-7,10,15H,3-5,8-9H2,1-2H3
16152-65-1Relevant academic research and scientific papers
Titanium salalen catalysts based on cis-1,2-diaminocyclohexane: Enantioselective epoxidation of terminal non-conjugated olefins with H 2O2
Berkessel, Albrecht,Guenther, Thomas,Wang, Qifang,Neudoerfl, Joerg-M.
supporting information, p. 8467 - 8471 (2013/09/02)
Terminal, non-conjugated olefins, such as 1-octene, are difficult to epoxidize asymmetrically. Ti salalen complexes based on cis-1,2- diaminocyclohexane catalyze this demanding reaction giving high yields and enantioselectivities (up to 95 % ee), with H2O2 as the oxidant. The X-ray structures of the μ-oxo and peroxo complexes shed light on the coordination behavior of this novel class of ligands.
Asymmetric Olefin Epoxidation with Sodium Hypochlorite Catalyzed by Easily Prepared Chiral Mn(III) Salen Complexes
Zhang, Wei,Jacobsen, Eric N.
, p. 2296 - 2298 (2007/10/02)
A practical method is described for the asymmetric epoxidation of cis-β-methylstyrene by commercial bleach with up to 86percent ee.
