23734-54-5

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 7585-39-9 β‐cyclodextrin 
• 2232-08-8 N-tosylimidazole 
• 7585-39-9 β-cyclodextrin 

Downstream Products

• 53784-83-1 heptakis(6-bromo-6-deoxy)-β-cyclodextrin 

Relevant academic research and scientific papers

Per-3,6-anhydro-α-cyclodextrin and Per-3,6-anhydro-β-cyclodextrin

The synthesis of the per-3,6-anhydro derivatives of α- and β-cyclodextrins (CDs) is described starting from the corresponding per-6-tosylates.These could only be obtained as pure compounds following repeated HPLC under reversed-phase conditions of the cru

The influence of cyclodextrin modification on cellular uptake and transfection efficiency of polyplexes

Cyclodextrin-modified polycations have been studied widely due to their low cytotoxicity, low immunogenicity and the ability to form inclusion complexes. However, the influence of CD modification on cellular uptake and transfection efficiency of polyplexe

Novel hybridized SWCNT-PCD: Synthesis and host-guest inclusion for electrical sensing recognition of persistent organic pollutants

Fabrication of a hybridized single-walled carbon nanotube (SWCNT) device based on novel sensing material mono-6-deoxy-6-(p-aminophenylamino)-β- cyclodextrin (PCD) via a facile approach has been reported for the first time; moreover, the hybridized materia

Preparation of cyclodextrin-modified multi-walled carbon nanotubes through acylamide bond and its application in capturing b-naphthol from wastewater

Multi-walled carbon nanotubes (MWNTs) were covalently modified with water-soluble b-cyclodextrin (b-CD) through acylamide bond. The products cyclodextrin modified multi-walled carbon nanotubes [MWNTs-CO-NH-(CH 2)2-NH-CD] were charact

Synthesis of a novel β-cyclodextrin-functionalized Fe3O4/BaMoO4:Dy3+magnetic luminescent hybrid nanomaterial and its application as a drug carrier

Magnetic luminescent hybrid nanoparticles Fe3O4/BaMoO4:Dy3+ (MLHNPs) were successfully synthesized by the co-precipitation method using ethylene glycol. The MLHNPs are functionalized with β-cyclodextrin (CD) using 3-aminopropyl triethoxysilane (APTES). The surface functionalization of nanoparticles and their conjugation have been confirmed via powder XRD, FTIR, HRTEM, and PL analyses. The feasibility of functionalized MLHNPs as nanocarriers for hydrophobic drugs (triazole derivatives) was verified by studying the uptake and release profile using a triazole derivative as a hydrophobic drug. In addition, the photoluminescence spectroscopy results confirmed the optical imaging capability of MLHNPs. The outcomes of loading and release disclose that this system is likely to be a suitable tool as a hydrophobic drug carrier. This journal is

Construction of micelles based on biocompatible pseudo-graft polymers via β-cyclodextrin/cholesterol interaction for protein delivery

A novel pseudo-graft copolymer was developed for protein delivery, based on the self-assembly of (6-(2-aminoethyl)-amino-6-deoxy)-cyclodextrin (β-CDen)-modified poly(aspartic acid) (PASP-CD) with cholesterol-modified poly(d,l-lactide) (PLA-Chol) by host-g

Magnetic calcined oyster shell functionalized with taurine immobilized on β-cyclodextrin (Fe3O4/COS@β-CD-SO3H NPs) as green and magnetically reusable nanocatalyst for efficient and rapid synthesis of spirooxindoles

Abstract: Magnetic calcined oyster shell functionalized with taurine immobilized on β-cyclodextrin (Fe3O4/COS@β-CD-SO3H NPs) was prepared as a new stable, long-lived, highly efficient, and exceptional reusable magnetic nan

β-Cyclodextrin modified silica nanoparticles for Nafion based proton exchange membranes with significantly enhanced transport properties

In the current study, a composite proton exchange membrane (PEM) was prepared by incorporating β-cyclodextrin (β-CD) modified silica nanoparticles (SN-β-CD) into a Nafion matrix. Due to the decoration of β-CD on the SN surface, SN-β-CD possesses excellent

Polycationic glycosides

Cationic lipids have long been known to serve as antibacterial and antifungal agents. Prior efforts with attachment of cationic lipids to carbohydrate-based surfaces have suggested the possibility that carbohydrate-attached cationic lipids might serve as antibacterial and antifungal pharmaceutical agents. Toward the understanding of this possibility, we have synthesized several series of cationic lipids attached to a variety of glycosides with the intent of generating antimicrobial agents that would meet the requirement for serving as a pharmaceutical agent, specifically that the agent be effective at a very low concentration as well as being biodegradable within the organism being treated. The initial results of our approach to this goal are presented.

Zinc bromide-promoted tosylation of alcohols allows efficient temperature-controlled primary hydroxy sulfonylation

The combination of zinc bromide with tosyl chloride promoted sulfonylation, allowing temperature-controlled regioselective sulfonylation of carbohydrates which possess both primary and secondary hydroxy groups.