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(2E)-4-chloro-N,N,N-trimethylbut-2-en-1-aminium, also known as 2-chloro-N,N,N-trimethylbut-2-en-1-aminium or 1-(trimethylammonio)-2-butene chloride, is a quaternary ammonium salt with a molecular formula of C7H15ClN. It features a positively charged nitrogen atom and a chloride anion. This chemical compound is recognized for its role as a phase-transfer catalyst in organic synthesis reactions and for its applications in the production of pharmaceuticals and agrochemicals. Its chemical structure and properties allow it to facilitate the transfer of reactants between immiscible phases, which is beneficial for the synthesis of various organic compounds. Moreover, it exhibits antimicrobial properties, making it a valuable component in disinfectants and antimicrobial agents.

4237-07-4

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4237-07-4 Usage

Uses

Used in Organic Synthesis:
(2E)-4-chloro-N,N,N-trimethylbut-2-en-1-aminium is used as a phase-transfer catalyst in organic synthesis, enabling the efficient transfer of reactants between immiscible phases. This function is crucial for promoting the synthesis of a wide range of organic compounds, thereby enhancing the efficiency and effectiveness of various chemical reactions.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (2E)-4-chloro-N,N,N-trimethylbut-2-en-1-aminium is utilized in the production of certain medications. Its role as a phase-transfer catalyst aids in the synthesis of complex organic molecules that are integral to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, (2E)-4-chloro-N,N,N-trimethylbut-2-en-1-aminium is employed in the production of various agricultural chemicals. Its ability to act as a phase-transfer catalyst is instrumental in synthesizing the organic compounds necessary for the creation of effective pesticides, herbicides, and other agrochemicals.
Used in Disinfectants and Antimicrobial Agents:
(2E)-4-chloro-N,N,N-trimethylbut-2-en-1-aminium is also used as an active ingredient in disinfectants and antimicrobial agents due to its antimicrobial properties. It helps in the formulation of products designed to eliminate or inhibit the growth of microorganisms, contributing to improved hygiene and sanitation in various settings.

Check Digit Verification of cas no

The CAS Registry Mumber 4237-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4237-07:
(6*4)+(5*2)+(4*3)+(3*7)+(2*0)+(1*7)=74
74 % 10 = 4
So 4237-07-4 is a valid CAS Registry Number.

4237-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Chloro-2-butenyl)trimethylammonium chloride

1.2 Other means of identification

Product number -
Other names -

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:4237-07-4 SDS

4237-07-4Downstream Products

4237-07-4Relevant academic research and scientific papers

Properties of onium salts of phosphorus and nitrogen

Ovakimyan,Barsegyan,Kikoyan,Indzhikyan

, p. 1074 - 1076 (2007/10/03)

Ammonium and phosphonium halides when heated with excess dimethyl or diethyl phosphite can undergo anion exchange as a result of alkylation of halide ions with dialkyl phosphites. Experimental data were obtained, that cast some doubt in the commonly accepted opinion that reactions of tertiary amines and phosphines with dihalides in apolar media result in exclusive formation of monosalts. 2005 Pleiades Publishing, Inc.

Facile synthesis of (ω-bromoalkyl)trimethylammonium bromides

Bartsch, Richard A.,Zhao, Wenyi,Zhang, Zhi-Yi

, p. 2393 - 2398 (2007/10/03)

Reaction of a 1,ω-dibromoalkane with trimethylamine in THF at room temperature precipitates the corresponding (ω-bromoalkyl)trimethylammonium bromide to cleanly form the mono-substituted product in the absence of the bis-quat salt.

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