5345-94-8

Usage

Physical properties

Viscous, colorless to pale yellow liquid with a faint amine odor

Chemical class

Ethanolamines

Uses

Corrosion inhibitor in metalworking fluids, lubricant additive, surfactant in industrial applications, production of oil well drilling and completion fluids, formulation of agricultural products, solvent, intermediate in the synthesis of other compounds

Safety precautions

Can cause skin and eye irritation, may be harmful if ingested or inhaled, handle with care.

Upstream product

• 1120-48-5 n-dioctylamine 
• 107-07-3 2-chloro-ethanol 
• 111-83-1 1-bromo-octane 
• 141-43-5 ethanolamine 
• 16156-52-8 n-octyl methanesulfonate 

Relevant academic research and scientific papers

COMPOUNDS AND COMPOSITIONS FOR INTRACELLULAR DELIVERY OF AGENTS

The disclosure features amino lipids and compositions involving the same. Nanoparticle compositions include an amino lipid as well as additional lipids such as phospholipids, structural lipids, PEG lipids, or a combination thereof. Nanoparticle compositions further including therapeutic and/or prophylactic agents such as RNA are useful in the delivery of therapeutic and/or prophylactic agents to mammalian cells or organs to, for example, regulate polypeptide, protein, or gene expression.

COMPOUNDS AND COMPOSITIONS FOR INTRACELLULAR DELIVERY OF AGENTS

The disclosure features amino lipids and compositions involving the same. Nanoparticle compositions include an amino lipid as well as additional lipids such as phospholipids, structural lipids, PEG lipids, or a combination thereof. Nanoparticle compositions further including therapeutic and/or prophylactic agents such as RNA are useful in the delivery of therapeutic and/or prophylactic agents to mammalian cells or organs to, for example, regulate polypeptide, protein, or gene expression.

Preparation and antitubercular activities of alkylated amino alcohols and their glycosylated derivatives

A series of N- and C-alkylated amino alcohols and of their protected galactopyranosyl derivatives was synthesized and evaluated for antitubercular activity. Five of these compounds displayed good activity, with a MIC below 12.5 μg/mL. The presence of the carbohydrate slightly affected the antibacterial activity.