52337-72-1

Usage

General Description

2-[2-(2-hydroxyethoxy)ethoxy]ethyl acetate is a chemical compound with the molecular formula C8H16O5. It is classified as a glycol ether and is commonly used as a solvent in various industrial and commercial applications. The compound is a clear and colorless liquid with a mild, fruity odor. It is highly soluble in water and has a relatively low volatility. It is commonly used as a solvent in cleaning products, coatings, and adhesives. It is also used as a coupling agent in various formulations to improve the mixing of different components. Overall, 2-[2-(2-hydroxyethoxy)ethoxy]ethyl acetate is a versatile chemical with various industrial applications due to its solvent properties and low toxicity.

InChI:InChI=1/C8H16O5/c1-8(10)13-7-6-12-5-4-11-3-2-9/h9H,2-7H2,1H3

Upstream product

• 75-36-5 acetyl chloride 
• 112-27-6 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 
• 108-24-7 acetic anhydride 

Downstream Products

• 239115-69-6 C₆₁H₁₀₆I₂N₁₀O₁₃S 
• 239115-60-7 C₆₁H₁₀₈N₁₀O₁₃S 
• 239115-68-5 10-[2-(2-{2-[5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethoxy]-decanoic acid [(S)-1-{3-[4-(3-amino-propylamino)-butylamino]-propylcarbamoyl}-2-(4-hydroxy-3,5-diiodo-phenyl)-ethyl]-amide 
• 239115-59-4 10-[2-(2-{2-[5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethoxy]-decanoic acid [(S)-1-{3-[4-(3-amino-propylamino)-butylamino]-propylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-amide 
• 239115-70-9 (S)-2-{10-[2-(2-{2-[5-((3aR,5S,6S,6aS)-2,5-Dioxo-octahydro-5λ⁴-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethoxy]-decanoylamino}-3-(4-hydroxy-3,5-diiodo-phenyl)-propionic acid 
• 239115-67-4 (S)-3-(4-Hydroxy-3,5-diiodo-phenyl)-2-{10-[2-(2-{2-[5-((3aR,6S,6aS)-2-oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethoxy]-decanoylamino}-propionic acid 
• 239115-66-3 N-10-<2-(2-<2-(biotinylamino)ethoxy>ethoxy)ethoxy>decanoyl-(L)-(3,5-diiodo)tyrosine methyl ester 
• 239115-63-0 (S)-2-{10-[2-(2-{2-[5-((3aR,5R,6S,6aS)-2,5-Dioxo-octahydro-5λ⁴-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethoxy]-decanoylamino}-3-(4-methoxycarbonyloxy-phenyl)-propionic acid methyl ester 
• 239115-62-9 (S)-3-(4-Methoxycarbonyloxy-phenyl)-2-{10-[2-(2-{2-[5-((3aR,6S,6aS)-2-oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethoxy]-decanoylamino}-propionic acid methyl ester 
• 239115-61-8 N-10-<2-(2-<2-(β-sulfoxybiotinylamino)ethoxy>ethoxy)ethoxy>decanoyl-(L)-tyrosine 
• 239115-57-2 (S)-3-(4-Hydroxy-phenyl)-2-{10-[2-(2-{2-[5-((3aR,6S,6aS)-2-oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethoxy]-decanoylamino}-propionic acid methyl ester 
• 239115-58-3 (S)-3-(4-Hydroxy-phenyl)-2-{10-[2-(2-{2-[5-((3aR,6S,6aS)-2-oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethoxy]-decanoylamino}-propionic acid 
• 239115-65-2 2-(10-{2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethoxy}-decanoylamino)-3-(4-hydroxy-3,5-diiodo-phenyl)-propionic acid methyl ester 
• 239115-64-1 2-(10-{2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethoxy}-decanoylamino)-3-(4-hydroxy-phenyl)-propionic acid methyl ester 

Relevant academic research and scientific papers

Dioxygen binding of water-soluble iron(ii) porphyrins in phosphate buffer at room temperature

Two water-soluble tris(2-aminoethylamine) (tren) capped iron porphyrins were synthesized. The stability of their dioxygen adducts was studied in phosphate buffer, leading to half-life times around 7 min for the oxygenated species. This journal is The Royal Society of Chemistry.

Preparation and biological properties of biotinylated PhTX derivatives

We report the synthesis of several highly functionalized biotinylated philanthotoxin (PhTX) analogues (7, 8, 10, 13-16) designed on the basis of earlier structure-activity relationship studies. Despite the extensive modifications, the binding to nicotinic acetylcholine receptor (nAChR) is in the low micromolar range according to an inhibition assay using 3H-thienylcyclohexyl-piperidine (TCP). A patch clamp functional assay gave comparable results. Compounds exemplified by 16, which consists of a biotinylated ligand linked to a bifunctional photoaffinity probe (BPP), represent a new type of probe which should find use in photo-cross-linking studies of ligand-receptor interactions. Copyright (C) 1999 Elsevier Science Ltd.

Process for preventing consolidation of p-dichlorobenzene

A triethylene glycol derivative is added to p-dichlorobenzene so as to prevent consolidation and improve flowability of p-dichlorobenzene.