26468-13-3

Usage

Uses

Used in Organic Synthesis:
1-(2-Hydroxyethyl)lepidiniuM BroMide is used as a synthetic building block for the creation of various organic compounds. Its chemical properties make it a versatile and valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(2-Hydroxyethyl)lepidiniuM BroMide is used as a key intermediate in the development of new drugs. Its unique structure allows for the formation of novel molecular entities with potential therapeutic applications, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
1-(2-Hydroxyethyl)lepidiniuM BroMide is also employed in the agrochemical industry as a component in the synthesis of new pesticides, herbicides, and other crop protection agents. Its incorporation into these products can lead to improved efficacy and selectivity, ultimately benefiting agricultural productivity and sustainability.
Used in Specialty Chemicals:
In the specialty chemicals sector, 1-(2-Hydroxyethyl)lepidiniuM BroMide is used as a crucial component in the synthesis of various high-value chemicals. These can include dyes, fragrances, and other additives that are used across a wide range of industries, from textiles to cosmetics.

Upstream product

• 60-29-7 diethyl ether 
• 540-51-2 2-bromoethanol 
• 491-35-0 C₆H₄NCH₂CHCCH₂ 

Downstream Products

• 1334475-52-3 Br^(1-)*C₂₇H₂₄N₃O₂S⁽¹⁺⁾ 

Relevant academic research and scientific papers

Synthesis of chloro-substituted analogs of Thiazole orange - Fluorophores for flow cytometric analyses

Synthesis, absorption and fluorescence properties of a series of asymmetrical monomethine cyanine dyes, chloro-containing analogs of Thiazole orange, are reported. Their staining ability was studied by flow cytometry. The saturating concentrations of each dye that gives a stable staining intensity have been determined. The ability of dyes B9, B11, B13 to stain live macrophages and apoptotic splenocytes was investigated. Positive signal in nucleus of adherent macrophages detected by fluorescent microscopy showed good specificity of B9, B11 and B13 dyes for DNA. In apoptotic assay cells positive for Annexin V were stained more brightly with the dyes B9, B11 and B13 than with propidium iodide. Despite that B13 showed high DNA selectivity it induces apoptosis of splenocytes and it is not suitable for detection of dead cells. The other synthesized chloro-containing analogs of Thiazole orange B9 and B11 can be successfully used for flow cytometric analyses of DNA content in live cells and for analyses of cell apoptosis.

Synthesis and fluorescence characteristics of novel asymmetric cyanine dyes for DNA detection

Sixteen new asymmetric monomethine cyanine dyes have been synthesized and their spectral characteristics and interaction with double stranded DNA have been investigated. The dyes absorb in the region 453-519 nm and have molar absorptivities in the range 3

Heteroaromatic compounds having two-photon absorption activity

The present invention relates to new heteroaromatic compounds having two-photon absorption activity. According to the invention, said compounds are suitable for use as optical power limiting agents via two-photon absorption or for use as imaging agents with two-photon absorbing activity for application in two-photon laser scanning confocal fluorescence microscopy. Compositions including said compounds and intermediates for their preparations are also within the scope of the present invention.