7311-30-0 Usage
Description
N-Methyldodecylamine, a secondary fatty acid amine, is a colorless liquid that is formed during the pyrolysis of N-(2-cyanoethyl)-N-methyldodecylamine under reduced pressure. It is a versatile compound with various applications across different industries.
Uses
1. Used in Chemical Synthesis:
N-Methyldodecylamine is used as a precursor for the preparation of N,N,N,N,N,N-trimethyldodecylammonium bromide, which is an important compound in various chemical processes and applications.
2. Used in Surfactant Production:
In the chemical industry, N-Methyldodecylamine can be used as a building block for the synthesis of surfactants. These surfactants are essential in various applications, such as detergents, emulsifiers, and dispersants, due to their ability to reduce surface tension and stabilize mixtures.
3. Used in Pharmaceutical Industry:
N-Methyldodecylamine may also find applications in the pharmaceutical industry, where it can be used as an intermediate in the synthesis of various drugs and active pharmaceutical ingredients.
4. Used in Cosmetics Industry:
In the cosmetics industry, N-Methyldodecylamine can be utilized as a component in the formulation of personal care products, such as creams, lotions, and shampoos, due to its emulsifying and conditioning properties.
5. Used in Agriculture:
N-Methyldodecylamine may also have potential applications in the agricultural sector, where it can be used as an additive in the formulation of pesticides, herbicides, and fertilizers to enhance their effectiveness and improve crop yield.
6. Used in Textile Industry:
In the textile industry, N-Methyldodecylamine can be employed as a softening agent, providing a smooth and soft feel to fabrics, as well as improving their durability and resistance to wear and tear.
7. Used in Water Treatment:
N-Methyldodecylamine can be used in water treatment processes, where it can act as a coagulant or flocculant to help remove impurities and contaminants from water, making it suitable for various applications, such as drinking water, industrial water supply, and wastewater treatment.
8. Used in Energy Industry:
In the energy sector, N-Methyldodecylamine may be used as an additive in the formulation of drilling fluids, enhancing their performance and improving the efficiency of oil and gas extraction processes.
Check Digit Verification of cas no
The CAS Registry Mumber 7311-30-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7311-30:
(6*7)+(5*3)+(4*1)+(3*1)+(2*3)+(1*0)=70
70 % 10 = 0
So 7311-30-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H29N/c1-3-4-5-6-7-8-9-10-11-12-13-14-2/h14H,3-13H2,1-2H3
7311-30-0Relevant articles and documents
SYNTHESIS AND BACTERICIDAL ACTIVITY OF QUATERNARY AMMONIUM COMPOUNDS CONTAINING AN ASYMMETRIC NITROGEN ATOM
Limanov, V. E.,Myazina, N. V.,Tsivrova, I. M.
, p. 47 - 51 (1990)
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PRODUCTION OF AMINES VIA A HYDROAMINOMETHYLATION REACTION USING IMINIUM REACTANTS
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Page/Page column 29-30, (2020/05/14)
Provided is a process for producing an amine via a hydroaminomethylation reaction of a non- aromatic C-C double bond, said process comprising a step of reacting a compound comprising a non-aromatic C-C double bond with an iminium ion in a solvent comprising an alcohol, wherein the iminium ion is represented by the following formula (I): wherein R1 and R2 are independently hydrogen or selected from the group consisting of an aliphatic hydrocarbon group which may be substituted, an aromatic hydrocarbon group which may be substituted, an aliphatic heterocyclic group which may be substituted, an aromatic heterocyclic group which may be substituted and of combinations thereof, such as an aralkyl group which may be substituted; and R1 and R2 may be bonded to each other to form a ring together with the nitrogen atom to which they are bound; and wherein R1 and R2 are not both hydrogen and at least one of R1 and R2 carries a hydrogen atom at a carbon atom in ex? position to the nitrogen atom of the iminium ion.
A General Acid-Mediated Hydroaminomethylation of Unactivated Alkenes and Alkynes
Kaiser, Daniel,Tona, Veronica,Gon?alves, Carlos R.,Shaaban, Saad,Oppedisano, Alberto,Maulide, Nuno
supporting information, p. 14639 - 14643 (2019/09/17)
In comparison to the extensively studied metal-catalyzed hydroamination reaction, hydroaminomethylation has received significantly less attention despite its considerable potential to streamline amine synthesis. State-of-the-art protocols for hydroaminomethylation of alkenes rely largely on transition-metal catalysis, enabling this transformation only under highly designed and controlled conditions. Here we report a broadly applicable, acid-mediated approach to the hydroaminomethylation of unactivated alkenes and alkynes. This methodology employs cheap, readily available, and bench-stable reactants and affords the desired amines with excellent functional group tolerance and impeccable regioselectivity. The broad scope of this transformation, as well as mechanistic investigations and in situ domino functionalization reactions are reported.
