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2424-01-3

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2424-01-3 Usage

Description

Methyldiallylamine, also known as N-Methyl-N-(2-propenyl)-2-propen-1-amine, is a tertiary amine derived from the reaction between aqueous methylamine and allyl chloride in the presence of polyglycol-400 as a phase transfer catalyst. It is a colorless to pale yellow liquid with a characteristic amine-like odor.

Uses

Used in Chemical Synthesis:
Methyldiallylamine is used as a key intermediate in the synthesis of various quaternary ammonium compounds, which have a wide range of applications in different industries. These include diallyldimethylammonium iodide, diallylethylmethylammonium bromide, diallylbenzylmethylammonium chloride, and alkyl-substituted diallylmethyl quaternary ammonium salt monomers.
Used in Pharmaceutical Industry:
Methyldiallylamine is used as a building block for the synthesis of pharmaceutical compounds, particularly those with antimicrobial, antifungal, and antiviral properties. The quaternary ammonium compounds derived from methyldiallylamine are known for their biocidal activities and are often used in the formulation of disinfectants and sanitizers.
Used in Agrochemical Industry:
In the agrochemical industry, methyldiallylamine is utilized in the production of biocidal agents for crop protection. The quaternary ammonium compounds synthesized from methyldiallylamine exhibit pesticidal properties, helping to control pests and diseases in agricultural crops.
Used in Cosmetics and Personal Care Industry:
Methyldiallylamine and its derivatives are also used in the cosmetics and personal care industry, where they serve as preservatives and antimicrobial agents. These compounds help maintain the shelf life and safety of cosmetic and personal care products by preventing the growth of harmful microorganisms.
Used in Water Treatment Industry:
In the water treatment industry, methyldiallylamine-derived quaternary ammonium compounds are employed as coagulants and flocculants. They help in the removal of suspended solids and impurities from water, making it suitable for various applications, including drinking, irrigation, and industrial use.
Used in Textile Industry:
Methyldiallylamine is used in the textile industry for the production of cationic dyes and finishing agents. These compounds enhance the colorfastness and durability of textiles, as well as provide antimicrobial properties to fabrics, making them more resistant to microbial degradation and odor formation.

Check Digit Verification of cas no

The CAS Registry Mumber 2424-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2424-01:
(6*2)+(5*4)+(4*2)+(3*4)+(2*0)+(1*1)=53
53 % 10 = 3
So 2424-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N/c1-3-5-7(8)6-4-2/h3-4,7H,1-2,5-6,8H2

2424-01-3SDS

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 Methyldiallylamine

1.2 Other means of identification

Product number -
Other names n-methyl-n-2-propenyl-2-propen-1-amin

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:2424-01-3 SDS

2424-01-3Relevant articles and documents

Synthesis of high-molecular-weight polyamine by radical polymerization of N,N-diallyl-N-methylamine

Vasilieva,Kleshcheva,Gromova,Rebrov,Filatova,Krut'ko,Timofeeva,Topchiev

, p. 431 - 437 (2000)

The first synthesis of high-molecular-weight poly( N,N-diallyl-N-methylamine) by thermal (at 30 and 50 °C) and photoinduced (at 21 °C) radical polymerization of N,N-diallyl-N-methylamine (DAMA) in aqueous solution in the presence of an equimolar amount of trifluoroacetic acid (TFA) and by polymerization of the newly synthesized equimolar DAMA · TFA salt is reported. Data of 1H NMR spectroscopy indicate that the molecules of the monomer under chosen conditions are in the protonated form. This leads to a decrease in the contribution of the reaction of degradative chain transfer to the monomer and its transformation into effective chain transfer to the monomer. A bimolecular chain termination mechanism was established and the possibility of controlling the polymerization rate and the molecular weight of the polymer was demonstrated.

Dieck,Friedel

, p. 173,176, 178, 179 (1968)

Production method of N-methyldiallylamine

-

Paragraph 0022-0045, (2021/09/04)

The invention discloses a production method of N-methyldiallylamine. The method comprises the following steps: adding monomethylamine and water into a high-pressure reaction kettle, adding a phase transfer catalyst, and dropwise adding chloropropene and an alkali liquor catalyst into the high-pressure reaction kettle to obtain a reaction solution; and layering the reaction solution, wherein the upper oil phase is a N-methyldiallylamine crude product; and pumping the crude product into a rectifying still for refinement. According to the method, the amination reaction is adopted, the reaction speed is high, the raw materials can fully react, the yield is high (99% or above), few byproducts are generated, and meanwhile, the byproduct N-methylallylamine can be repeatedly reacted; through the method, the prepared N-methyldiallylamine is colorless transparent liquid in appearance; when the chromaticity is measured by a colorimeter, the chromaticity is smaller than or equal to 17, the content detected by a GC gas chromatography is larger than or equal to 98.5%, and the moisture is smaller than or equal to 0.1%; the purity of the N-methyldiallylamine is high; and lower-layer wastewater is easy to treat, and the cost of subsequent wastewater treatment is saved.

1,4-Dioxane-Tuned Catalyst-Free Methylation of Amines by CO2 and NaBH4

Guo, Zhiqiang,Zhang, Bo,Wei, Xuehong,Xi, Chanjuan

, p. 2296 - 2299 (2018/07/31)

A catalyst-free reductive functionalization of CO2 with amines and NaBH4 was developed. The N-methylation of amines was carried out with CO2 as a C1 building block and 1,4-dioxane as the solvent. Notably, the six-electron reduction of CO2 to form the methyl group occurred simultaneously with formation of the C?N bond to give the N-methylated amine.

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