56562-64-2

Usage

Uses

Used in Healthcare and Industrial Applications:
TRIETHYL M-PHENOXYBENZYL AMMOUIUM CHLORIDE is used as a disinfectant and antiseptic for its ability to effectively disrupt the cell membranes of microorganisms, thereby destroying them and preventing the spread of infections.
Used in Pharmaceuticals:
TRIETHYL M-PHENOXYBENZYL AMMOUIUM CHLORIDE is used as a preservative in pharmaceuticals to maintain the sterility and stability of the products, ensuring their safety and efficacy.
Used in Personal Care Products:
TRIETHYL M-PHENOXYBENZYL AMMOUIUM CHLORIDE is used as a preservative in personal care products to prevent microbial contamination and extend the shelf life of these products.
It is crucial to handle TRIETHYL M-PHENOXYBENZYL AMMOUIUM CHLORIDE with caution due to its potential harmful effects if ingested or inhaled, and its capacity to cause skin and eye irritation.

Upstream product

• 51632-16-7 3-phenoxybenzyl bromide 

Downstream Products

• 141041-39-6 cis-Permethrin 
• 121772-10-9 (1R,3R)-3-((Z)-2-Chloro-3-hydroxy-propenyl)-2,2-dimethyl-cyclopropanecarboxylic acid 3-phenoxy-benzyl ester 
• 91176-37-3 (1R,3S)-3-((E)-2-Cyano-2-methyl-vinyl)-2,2-dimethyl-cyclopropanecarboxylic acid 3-phenoxy-benzyl ester 
• 51630-06-9 3'-phenoxybenzyl 4-bromo-α-ethyl-phenyl-acetate 
• 36102-49-5 3'-phenoxybenzyl 2,2-dimethyl-3-vinyl-cyclopropane-carboxylate 

Relevant academic research and scientific papers

A plurality of light-emitting tube having a ceramic metal halide lamp

The purpose of the present invention is to provide a ceramic metal halide lamp with a plurality of light-emitting tubes, wherein other light-emitting tubes light normally when one light-emitting tube is at the end of the life thereof, by setting the gas pressure inside the lamp to a predetermined pressure. The ceramic metal halide lamp (10) comprises: two light-emitting tubes (4-1, 4-2) whereof one light-emitting tube is lit selectively; internal tubes (18H-1, 18H-2) that surround each of the light-emitting tubes; and an outside globe (2) that houses the light-emitting tubes and the internal tubes. The internal tubes are sealed and, when the shortest distance between metal members with different potentials inside the internal tubes is X (mm) and one of the light-emitting tubes has ruptured, the internal tubes are adjusted so as to have an internal gas pressure of Y (kPa) or greater, where Y= -9.44X+72.29, and one atmospheric pressure or lower, and a discharge tube commences discharge without discharge occurring between the metal members with different potentials.

Process for preparing cyclopropane-carboxylic acid esters

A process for preparing an organic acid ester of the formula (I), EQU1 wherein R1 is a hydrogen atom or a methyl group, R2 is a methyl group, a vinyl group, a 2,2-dichlorovinyl group, a 1-propenyl group, a 2-methyl-1-propenyl group, a 2-carbomethoxy-1-propenyl group, a 2-methoxymethyl-1-propenyl group, a 1,3-butadienyl group, a 2-methyl-1,3-butadienyl group or a cyclopentylidenemethyl group when R1 is a hydrogen atom, and R2 is a methyl group when R1 is a methyl group; which comprises reacting an acid of the formula (II), EQU2 wherein R1 and R2 are each as defined above, or its reactive derivative, or mixture of the acid and its reactive derivative with a quaternary ammonium salt of the formula (III), SPC1 wherein X is a halogen atom, A is an alkylamine, pyridine or an N-alkylaniline.