5910-75-8 Usage
Uses
Used in Personal Care Products:
N-tridecyltridecan-1-amine is used as a surfactant and emulsifier for its ability to reduce surface tension and enhance the mixing of immiscible substances, which is crucial in the formulation of personal care products for improved texture, stability, and performance.
Used in Household Detergents:
In the household detergent industry, N-tridecyltridecan-1-amine serves as a surfactant and emulsifier, contributing to the cleaning power of detergents by facilitating the dispersion of dirt and grease in water, thus enhancing the overall cleaning efficiency.
Used in Agricultural Chemicals:
N-tridecyltridecan-1-amine is utilized as a surfactant and emulsifier in agricultural chemicals to improve the solubility and distribution of active ingredients, ensuring even application and absorption by crops, which can lead to better pest control and crop protection.
Used in Surface Cleaning and Coating:
Due to its long alkyl chain, N-tridecyltridecan-1-amine is effective in cleaning and coating surfaces, making it suitable for applications where a high level of cleaning or protective coating is required, such as in industrial settings or manufacturing processes.
Used as a Corrosion Inhibitor:
N-tridecyltridecan-1-amine also acts as a corrosion inhibitor, protecting metal surfaces from degradation and wear, which is particularly useful in industries where equipment and structures are exposed to harsh environments or corrosive substances.
Check Digit Verification of cas no
The CAS Registry Mumber 5910-75-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,1 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5910-75:
(6*5)+(5*9)+(4*1)+(3*0)+(2*7)+(1*5)=98
98 % 10 = 8
So 5910-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C26H55N/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-26-24-22-20-18-16-14-12-10-8-6-4-2/h27H,3-26H2,1-2H3
5910-75-8Relevant academic research and scientific papers
Bálint, Ana-Maria,Bodor, Andrea,G?m?ry, ágnes,Vékey, Károly,Szabó, Dénes,Rábai, József
, p. 1524 - 1530 (2005)
Trifluoromethanesulfonamides (triflamides) having the structure CF 3SO2N[(CH2)3R]2 (R = CnF2n + 1 or CnH2n + 1, n = 4, 6, 8, 10) are obtained in high yields, when CF3SO2NH 2 is reacted with 3-perfluoroalkyl-1-propanols or the parent aliphatic alcohols in a Mitsunobu reaction (Ph3P/[i-PrO 2CNNCO2-i-Pr]/ether). Products are isolated easily by fluorous extraction, fluorous solid-organic liquid filtration or n-heptane/CH3OH extraction. Consecutive deprotection of triflamides with LiAlH4 in boiling ether or dioxane solution affords the title amines in good overall yields. Fluorous partition coefficients of the F-tagged amides and amines are determined and qualitatively analyzed.
Sequential hydroaminomethylation/Pd-catalyzed hydrogenolysis as an atom efficient route to valuable primary and secondary amines
October, Jacquin,Mapolie, Selwyn F.
supporting information, (2021/04/12)
The facile synthesis of valuable primary and secondary amines is reported using a sequential procedure of hydroaminomethylation and Pd-catalyzed hydrogenolysis. The hydroaminomethylation reaction was catalyzed by a cationic Rh(I) iminopyridyl complex and the N-alkylated benzylamines were produced with high chemoselectivity, albeit as mixtures of linear and branched products. Performing the hydrogenolysis reaction using 10% Pd/C, provided access to valuable primary and secondary amines which have applications in the surfactant, pharmaceutical and polymer industries.
