7173-57-1 Usage
Uses
Used in Surfactant and Emulsifier Applications:
3-aminopropyl(octyl)amine is utilized as a surfactant and emulsifier in various industrial processes. Its amphiphilic nature allows it to reduce surface tension and stabilize mixtures of immiscible liquids, making it an essential component in formulations for cleaning agents, detergents, and personal care products.
Used in Corrosion Inhibition:
In the field of corrosion prevention, 3-aminopropyl(octyl)amine serves as an effective inhibitor. It protects metal surfaces from corrosive agents by forming a protective film, thereby extending the service life of equipment and infrastructure in industries such as oil and gas, automotive, and construction.
Used as a Coupling Agent in Adhesives, Coatings, and Sealants:
3-aminopropyl(octyl)amine is employed as a coupling agent in the production of adhesives, coatings, and sealants. Its ability to bond with various substrates enhances the adhesion and durability of these products, contributing to their performance in a wide range of applications, from construction to electronics.
Used in Pharmaceutical Synthesis:
3-aminopropyl(octyl)amine plays a crucial role in the synthesis of pharmaceuticals. Its reactive amine group allows for the formation of various chemical bonds, facilitating the creation of new drug molecules with potential therapeutic benefits.
Used as a Lubricant Additive in the Automotive Industry:
In the automotive sector, 3-aminopropyl(octyl)amine is used as a lubricant additive. It helps improve the performance and longevity of engine oils and other lubricants by reducing friction and wear on moving parts.
Used as an Antistatic Agent in the Textile Industry:
3-aminopropyl(octyl)amine is also utilized as an antistatic agent in the textile industry. Its ability to dissipate static charges makes it a valuable component in the production of fabrics that are less prone to static cling, enhancing both the comfort and functionality of textile products.
Overall, 3-aminopropyl(octyl)amine is a versatile chemical compound with a wide range of applications across various industries, from personal care and pharmaceuticals to automotive and textiles. Its low toxicity and safe handling with proper precautions make it a preferred choice for many applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7173-57-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7173-57:
(6*7)+(5*1)+(4*7)+(3*3)+(2*5)+(1*7)=101
101 % 10 = 1
So 7173-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H26N2/c1-2-3-4-5-6-7-10-13-11-8-9-12/h13H,2-12H2,1H3
7173-57-1Relevant academic research and scientific papers
A Nanocrystal Catalyst Incorporating a Surface Bound Transition Metal to Induce Photocatalytic Sequential Electron Transfer Events
Beard, Matthew C.,Chen, Xihan,Han, Chuang,Lin, Yixiong,Martin, Jovan San,Miller, Collin,Wang, Xiaoming,Yamamoto, Nobuyuki,Yan, Yanfa,Yan, Yong,Yazdi, Sadegh,Zeng, Xianghua
supporting information, p. 11361 - 11369 (2021/08/16)
Heterogeneous photocatalysis is less common but can provide unique avenues for inducing novel chemical transformations and can also be utilized for energy transductions, i.e., the energy in the photons can be captured in chemical bonds. Here, we developed a novel heterogeneous photocatalytic system that employs a lead-halide perovskite nanocrystal (NC) to capture photons and direct photogenerated holes to a surface bound transition metal Cu-site, resulting in a N-N heterocyclization reaction. The reaction starts from surface coordinated diamine substrates and requires two subsequent photo-oxidation events per reaction cycle. We establish a photocatalytic pathway that incorporates sequential inner sphere electron transfer events, photons absorbed by the NC generate holes that are sequentially funneled to the Cu-surface site to perform the reaction. The photocatalyst is readily prepared via a controlled cation-exchange reaction and provides new opportunities in photodriven heterogeneous catalysis.
Synthesis and antitubercular activity of lipophilic moxifloxacin and gatifloxacin derivatives
de Almeida, Mauro V.,Saraiva, Mauricio F.,de Souza, Marcus V.N.,da Costa, Cristiane F.,Vicente, Felipe R.C.,Lourenco, Maria C.S.
, p. 5661 - 5664 (2008/03/14)
Fluoroquinolone (FQ) has a broad spectrum of activity against several bacteria, mycobacteria, parasites, and other diseases. Moxifloxacin and gatifloxacin are a new generation of fluoroquinolone agents with improved activity against Gram-negative and positive bacteria. As lipophilicity is an important consideration in the design and activity of novel antibacterial agents, we report in this work the synthesis and biological evaluation of 12 lipophilic moxifloxacin or gatifloxacin derivatives, by reaction of 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxoquinoline-3-carboxylic acid 13 with severals N-monoalkyl 1,2-ethanediamine or 1,3-propanediamine.
