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7311-30-0

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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

7311-30-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (L07025)  N-Dodecylmethylamine, 98%   

  • 7311-30-0

  • 1g

  • 203.0CNY

  • Detail
  • Alfa Aesar

  • (L07025)  N-Dodecylmethylamine, 98%   

  • 7311-30-0

  • 5g

  • 1074.0CNY

  • Detail
  • Alfa Aesar

  • (L07025)  N-Dodecylmethylamine, 98%   

  • 7311-30-0

  • 25g

  • 4562.0CNY

  • Detail

7311-30-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-METHYLDODECYLAMINE

1.2 Other means of identification

Product number -
Other names n-dodecyl-n-methylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7311-30-0 SDS

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

-

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.

N-Methylation of amines and nitroarenes with methanol using heterogeneous platinum catalysts

Jamil, Md.A.R.,Touchy, Abeda S.,Rashed, Md. Nurnobi,Ting, Kah Wei,Siddiki, S.M.A. Hakim,Toyao, Takashi,Maeno, Zen,Shimizu, Ken-ichi

, p. 47 - 56 (2019/02/07)

We report herein the selective N-methylation of amines and nitroarenes with methanol under basic conditions using carbon-supported Pt nanoparticles (Pt/C) as a heterogeneous catalyst. This method is widely applicable to four types of N-methylation reactions: (1) N,N-dimethylation of aliphatic amines under N2, (2) N-monomethylation of aliphatic amines under 40 bar H2, (3) N-monomethylation of aromatic amines under N2, and (4) tandem synthesis of N-methyl anilines from nitroarenes and methanol under 2 bar H2. All these reactions under the same catalytic system showed high yields of the corresponding methylamines for a wide range of substrates, high turnover number (TON), and good catalyst reusability. Mechanistic studies suggested that the reaction proceeded via a borrowing hydrogen methodology. Kinetic results combined with density functional theory (DFT) calculations revealed that the high performance of Pt/C was ascribed to the moderate metal–hydrogen bond strength of Pt.

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