19014-04-1 Usage
Uses
Used in Antimicrobial Applications:
Dodecyltrimethylammonium iodide is used as an antimicrobial agent for its effectiveness against a range of microorganisms, including bacteria, fungi, and viruses. Its quaternary ammonium structure allows it to disrupt cell membranes and inhibit microbial growth, making it a valuable component in sanitizing and disinfecting products.
Used in Scientific Research:
In the field of scientific research, Dodecyltrimethylammonium iodide is used as a surfactant in nanoparticle synthesis. Its amphiphilic nature facilitates the formation of stable nanoparticles, which are essential in various applications such as drug delivery, imaging, and sensing.
Used in Phase Transfer Catalysts:
Dodecyltrimethylammonium iodide is employed as a phase transfer catalyst in chemical reactions involving the transfer of reactants between immiscible phases. Its ability to interact with both organic and inorganic compounds makes it a useful tool in organic synthesis and selective transformations.
Used in Environmental Management:
While Dodecyltrimethylammonium iodide offers numerous benefits, its potential toxicity and environmental impact must be carefully managed. It is essential to consider the proper use and disposal of Dodecyltrimethylammonium iodide to minimize its adverse effects on ecosystems and human health.
Used in Various Industries:
Dodecyltrimethylammonium iodide is used in various industries, such as:
Cleaning and Sanitization: As a surfactant and antimicrobial agent in cleaning products.
Pharmaceutical: In the synthesis of drug delivery systems and as a component in antimicrobial formulations.
Chemical Synthesis: As a phase transfer catalyst in organic reactions.
Nanotechnology: In the production of nanoparticles for various applications, including medical and environmental uses.
Check Digit Verification of cas no
The CAS Registry Mumber 19014-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,1 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19014-04:
(7*1)+(6*9)+(5*0)+(4*1)+(3*4)+(2*0)+(1*4)=81
81 % 10 = 1
So 19014-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H34N.HI/c1-5-6-7-8-9-10-11-12-13-14-15-16(2,3)4;/h5-15H2,1-4H3;1H/q+1;/p-1
19014-04-1Relevant academic research and scientific papers
Roitershtein, Dmitrii M.,Puntus, Lada N.,Lyssenko, Konstantin A.,Taidakov, Ilya V.,Varaksina, Evgenia A.,Minyaev, Mikhail E.,Gerasin, Victor A.,Guseva, Maria A.,Vinogradov, Alexey A.,Savchenko, Maria S.,Nifant'Ev, Ilya E.
, p. 13663 - 13672 (2017)
Luminescent composite materials based on linear polyethylene doped by a well dispersed tetrakis dibenzoylmethanate europium complex have been developed. The anion of the latter serves as an efficient light harvesting antenna and possesses the desired photophysical properties. The targeted modification of the Eu complex, namely introduction of a long hydrocarbon chain into the tetraalkylammonium cation [RNEt3]+, has ensured the compatibility of the complex with the polyethylene matrix. The [RNEt3]+ cation has been obtained by using long-chained 1-iodoalkanes synthesized via the Nd-catalyzed ethylene oligomerization process. The photophysical properties and the homogeneity of the obtained composites have been controlled by optical spectroscopy, luminescence intensity mapping as well as scanning electron microscopy.
Synthesis and biological activity of azasqualenes, bis-azasqualenes and derivatives
Ceruti, Maurizio,Balliano, Gianni,Viola, Franca,Cattel, Luigi,Gerst, Nicolas,Schuber, Francis
, p. 199 - 208 (2007/10/02)
Azasqualenes, bis-azasqualenes and derivatives, designed as inhibitors of squalene 2,3-epoxide cyclase, a key enzyme in sterol biosynthesis, were synthesized and their in vitro activities against a variety of yeasts, fungi, gram-positive and gram-negative bacteria were determined.The synthesis involves a new method of squalene degradation, together with an unusual procedure for the aminative reduction of lipophilic aldehydes.A study of the structure-activity relationship was attempted for different biological parameters: anti-bacterial and anti-fungal activities (MIC), inhibition of mycelial growth (GTT), surfactant activity (CMC) and membrane perturbation activity (induction of leakage in liposomes).
