10570-68-0 Usage
Uses
Used in Personal Care Products:
4-cyclohexyl-2,6-xylenol is used as an antimicrobial agent in personal care products for its ability to inhibit the growth of bacteria and fungi, contributing to the maintenance of hygiene and prevention of infections.
Used in Household Products:
In household products, 4-cyclohexyl-2,6-xylenol is used as a disinfectant to ensure cleanliness and prevent the spread of harmful microorganisms.
Used in Hand Soaps:
4-cyclohexyl-2,6-xylenol is used as an active ingredient in hand soaps to provide effective antimicrobial action, promoting hand hygiene and reducing the transmission of bacteria and fungi.
Used in Deodorants:
CHX is used in deodorants as an antimicrobial agent to control odor-causing bacteria, offering long-lasting freshness and reducing body odor.
Used in Lotions:
4-cyclohexyl-2,6-xylenol is used in lotions to provide antimicrobial properties, ensuring skin health and preventing potential infections.
Used in Disinfectants:
In disinfectants, 4-cyclohexyl-2,6-xylenol is used as a key component to eliminate a broad spectrum of microorganisms, ensuring a clean and hygienic environment.
Overall, 4-cyclohexyl-2,6-xylenol is an important ingredient in the personal care and household product industries due to its wide range of practical applications and compatibility with other ingredients. It is considered relatively safe for use in consumer products when used in accordance with regulatory guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 10570-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10570-68:
(7*1)+(6*0)+(5*5)+(4*7)+(3*0)+(2*6)+(1*8)=80
80 % 10 = 0
So 10570-68-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O/c1-10-8-13(9-11(2)14(10)15)12-6-4-3-5-7-12/h8-9,12,15H,3-7H2,1-2H3
10570-68-0Relevant articles and documents
Acid catalyzed alkylation of phenols with cyclohexene: Comparison between homogeneous and heterogeneous catalysis, influence of cyclohexyl phenyl ether equilibrium and of the substituent on reaction rate and selectivity
Ronchin,Vavasori,Toniolo
scheme or table, p. 134 - 141 (2012/03/09)
The reactivity of several phenols toward liquid phase alkylation with cyclohexene in the presence of heterogeneous and homogeneous acid catalyst at 358 K is studied. The comparison between Amberlyst 15 and CH3SO 3H, as examples of heterogeneous and homogeneous systems, shows a higher activity of the former with different behavior of selectivity between the two systems, anyway, in both systems O-alkylation and ring alkylations occur. A remarkable difference in the selectivity of the ring alkylation between heterogeneous and homogeneous systems is observed: Amberlyst 15 shows a constant ortho/para ratio close to 2, while in the presence of CH3SO 3H ortho/para is variable from 3 to 5, suggesting an involvement of the cyclohexyl phenyl ether rearrangement. This is proved also by a direct relationship between the ortho/para ratio and the concentration of the cyclohexyl phenyl ether when CH3SO3H is used as a catalyst. The formation of cyclohexyl aryl ethers is reversible; on the contrary, ring alkylation appears irreversible. The reactivity of the dimethylphenols shows a strong influence of the steric hindrance of the substituent on the electrophilic attack of the cyclohexyl cation, which is poorly influenced by the inductive effect of the methyl group.
