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55489-58-2

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55489-58-2 Usage

Description

Triethylene glycol monobenzyl ether, also known as Benzyl-PEG4-alcohol, is a PEG (polyethylene glycol) linker with an acid-labile benzyl protecting group and a reactive primary alcohol. The primary alcohol allows for further derivatization of the compound, while the hydrophilic PEG linker enhances its water solubility in aqueous media.

Uses

Used in Biosensor Applications:
Triethylene glycol monobenzyl ether is used as a component in the preparation of self-assembled monolayers with multiple binding sites and biocompatible imprinted cavities, which are essential for the development of biosensors. The hydrophilic PEG linker contributes to the stability and performance of these biosensors in aqueous environments.
Used in Surfactant Synthesis:
In the chemical industry, Triethylene glycol monobenzyl ether is utilized in the synthesis of novel ethoxylated inositol surfactants. These surfactants have various applications, including detergents, emulsifiers, and stabilizers in the formulation of personal care products, pharmaceuticals, and other industrial products. The presence of the PEG linker and benzyl protecting group in Triethylene glycol monobenzyl ether plays a crucial role in the properties and performance of the resulting surfactants.

Check Digit Verification of cas no

The CAS Registry Mumber 55489-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,8 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55489-58:
(7*5)+(6*5)+(5*4)+(4*8)+(3*9)+(2*5)+(1*8)=162
162 % 10 = 2
So 55489-58-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O4/c14-6-7-15-8-9-16-10-11-17-12-13-4-2-1-3-5-13/h1-5,14H,6-12H2

55489-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Triethylene Glycol Monobenzyl Ether

1.2 Other means of identification

Product number -
Other names 2-[2-(2-phenylmethoxyethoxy)ethoxy]ethanol

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:55489-58-2 SDS

55489-58-2Downstream Products

55489-58-2Relevant articles and documents

Synthesis of β-damascone from 2,6-dimethylcyclohexanone

Chaumont-Olive, Pauline,Plevová, Kristína,Collado Pérez, Ana María,Sánchez-Quesada, Jorge,?ebesta, Radovan,Cossy, Janine

supporting information, p. 140 - 150 (2022/02/10)

The synthesis of β-damascone can be achieved from 2,6-dimethylcyclohexanone using a Rupe rearrangement or a Barton vinyl iodation as the key steps.

INDAZOLE BASED COMPOUNDS AND ASSOCIATED METHODS OF USE

-

Paragraph 00228, (2021/10/02)

Bifunctional compounds, which find utility as modulators of leucine-rich repeat kinase 2 (LRRK2), are described herein. In particular, the hetero-bifunctional compounds of the present disclosure contain on one end a moiety that binds to the cereblon E3 ubiquitin ligase and on the other end a moiety which binds LRRK2, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The hetero-bifunctional compounds of the present disclosure exhibit a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aberrant regulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.

Design of nanosystems for the delivery of quorum sensing inhibitors: A preliminary study

Bortolotti, Daria,Cortesi, Rita,Esposito, Elisabetta,Hallan, Supandeep Singh,Marchetti, Paolo,Mariani, Paolo,Rizzo, Roberta,Sguizzato, Maddalena,Trapella, Claudio

, (2021/06/14)

Biofilm production is regulated by the Quorum Sensing system. Nowadays, Quorum Sensing represents an appealing target to design new compounds to increase antibiotics effects and avoid development of antibiotics multiresistance. In this research the use of liposomes to target two novel synthetic biofilm inhibitors is presented, focusing on a preformulation study to select a liposome composition for in vitro test. Five different liposome (LP) formulations, composed of phosphatidyl choline, cholesterol and charged surfactant (2:1:1, molar ratio) have been prepared by direct hydration and extrusion. As charged surfactants dicetyl phosphate didecyldimethylammonium chloride, di isobutyl phenoxy ethyl dimethyl benzyl ammonium chloride and stearylamine (SA) and have been used. Liposome charge, size and morphology were investigated by zeta potential, photon correlation spectroscopy, small angle x-ray spectroscopy and electron microscopy. LP-SA was selected for the loading of biofilm inhibitors and subjected to high performance liquid chromatography for entrapment capacity evaluation. LP-SA loaded inhibitors showed a higher diameter (223.6 nm) as compared to unloaded ones (205.7 nm) and a dose-dependent anti-biofilm effect mainly after 48 h of treatment, while free biofilm inhibitors loose activity. In conclusion, our data supported the use of liposomes as a strategy to enhance biofilm inhibitors effect.

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