18924-66-8

Basic information

• Product Name: 2,2'-(tetradecylimino)bisethanol
• Synonyms: 2,2'-(tetradecylimino)bisethanol;2,2'-(Tetradecylimino)diethanol
• CAS NO: 18924-66-8
• Molecular Formula: C₁₈H₃₉NO₂
• Molecular Weight: 301.50776
• EINECS: 242-677-7
• Mol File: 18924-66-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 428.8±20.0 °C(Predicted)
• Appearance: /
• Density: 0.919±0.06 g/cm3(Predicted)
• PKA: 14.41±0.10(Predicted)
• CAS DataBase Reference: 2,2'-(tetradecylimino)bisethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-(tetradecylimino)bisethanol(18924-66-8)
• EPA Substance Registry System: 2,2'-(tetradecylimino)bisethanol(18924-66-8)

Safety Data

• Hazardous Substances Data: 18924-66-8(Hazardous Substances Data)

Usage

General Description

2,2'-(tetradecylimino)bisethanol is a chemical compound with the molecular formula C32H67NO2. It is an organic chemical derivative of ethanol, and the presence of the imine group in its molecular structure suggests potential applications in organic synthesis and chemical processes. This chemical may also have surfactant properties due to the long hydrophobic chain, which could find applications in the formulation of industrial and household products such as detergents and cleaning agents. Additionally, its unique molecular structure and properties may make it useful for research and development in the fields of organic chemistry and materials science. However, further research is needed to fully understand the potential uses and properties of this chemical compound.

Upstream product

• 112-71-0 1-Bromotetradecane 
• 111-42-2 2,2'-iminobis[ethanol] 
• 6222-16-8 tetradecyl mesylate 

Relevant articles and documents

Alkynyl quaternary ammonium salt multifunctional surfactants and preparation method thereof

The invention discloses a series of alkynyl quaternary ammonium salt multifunctional surfactants and a preparation method thereof. A structural formula of quaternary ammonium salt is shown in the description, wherein R represents a C4-C22 linear, branched or cycloalkyl, aryl or alkenyl group. The preparation method comprises the following steps: (1) carrying out alkylation on ethanol amine under alkaline and acetonitrile reflux conditions by virtue of bromo-hydrocarbon; and (2) carrying out further alkylation on tertiary amine under an ethanol reflux condition by virtue of propargyl bromide, so as to obtain alkynyl quaternary ammonium salt, namely reddish brown semitransparent viscous liquid or solid. The alkynyl quaternary ammonium salt multifunctional surfactants have very high surface activity, good corrosion resistance and excellent viscoelasticity, the preparation method is simple and feasible, the raw material cost is low, the operation is easy, the yield is high, and the surfactants are environmentally friendly.

Design of new potent and selective secretory phospholipase A2 inhibitors. Part 5: Synthesis and biological activity of 1-alkyl-4-[4,5-dihydro-1,2,4-[4H]-oxadiazol-5-one-3-ylmethylbenz-4′-yl(oyl)] piperazines

Among the different PLA2s identified to date, the group IIA secretory PLA2 (sPLA2 GIIA) is implied in diverse pathological conditions. In this work we describe the synthesis, inhibitory activities, and structure-activity relationships (SAR) of a new class of substituted piperazine derivatives. The in vitro fluorimetric assay using two groups of enzymes, GIB and GIIA, revealed several compounds as highly potent inhibitors (IC50 = 0.1 μM). The in vivo activity assessed by ip or per os administration in a carrageenan-induced edema test in rats showed that two compounds proved to be as potent as indomethacin (10 mg/kg).