32582-32-4

Basic information

• Product Name: 2-tetradecyloctadecan-1-ol
• Synonyms: 2-tetradecyloctadecan-1-ol;TETRADECYLOCTADECANOL;1-Octadecanol, 2-tetradecyl-;2-Tetradecyl-1-octadecanol;2-TETRADECYL OCTADECANOL
• CAS NO: 32582-32-4
• Molecular Formula: C₃₂H₆₆O
• Molecular Weight: 466.86584
• EINECS: 251-110-2
• Mol File: 32582-32-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 38-39 °C
• Boiling Point: 494.8 °C at 760 mmHg
• Flash Point: 134.8 °C
• Appearance: /
• Density: 0.841 g/cm³
• Vapor Pressure: 7.28E-12mmHg at 25°C
• Refractive Index: 1.459
• PKA: 15.02±0.10(Predicted)
• Water Solubility: 0.467ng/L at 25℃
• CAS DataBase Reference: 2-tetradecyloctadecan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-tetradecyloctadecan-1-ol(32582-32-4)
• EPA Substance Registry System: 2-tetradecyloctadecan-1-ol(32582-32-4)

Safety Data

• Hazardous Substances Data: 32582-32-4(Hazardous Substances Data)

Usage

Uses

2-Tetradecyl-1-octadecanol ls used as a reagent to synthesize choline phospholipids. 2-Tetradecyl-1-octadecanol works as a surfactant in cosmetics.

InChI:InChI=1/C32H66O/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32(31-33)29-27-25-23-21-19-16-14-12-10-8-6-4-2/h32-33H,3-31H2,1-2H3

Upstream product

• 36653-82-4 1-Hexadecanol 

Downstream Products

• 77407-31-9 hentriacontan-15-one 
• 73756-39-5 2-tetradecyloctadecanoic acid 

Relevant articles and documents

Iridium catalysts for acceptorless dehydrogenation of alcohols to carboxylic acids: Scope and mechanism

We introduce iridium-based conditions for the conversion of primary alcohols to potassium carboxylates (or carboxylic acids) in the presence of potassium hydroxide and either [Ir(2-PyCH2(C4H5N2))(COD)]OTf (1) or [Ir(2-PyCH2PBu2t)(COD)]OTf (2). The method provides both aliphatic and benzylic carboxylates in high yield and with outstanding functional group tolerance. We illustrate the application of this method to a diverse variety of primary alcohols, including those involving heterocycles and even free amines. Complex 2 reacts with alcohols to form the crystallographically characterized catalytic intermediates [IrH(η1,η3-C8H12)(2-PyCH2PtBu2)] (2a) and [Ir2H3(CO)(2-PyCH2PtBu2){μ-(C5H3N)CH2PtBu2}] (2c). The unexpected similarities in reactivities of 1 and 2 in this reaction, along with synthetic studies on several of our iridium intermediates, enable us to form a general proposal of the mechanisms of catalyst activation that govern the disparate reactivities of 1 and 2, respectively, in glycerol and formic acid dehydrogenation. Moreover, careful analysis of the organic intermediates in the oxidation sequence enable new insights into the role of Tishchenko and Cannizzaro reactions in the overall oxidation.

Novel organic semiconductor compound and organic electronic device using the same

The present invention relates to an organic semiconductor compound and a use thereof. The organic semiconductor of the present invention has high charge mobility, low on/off ratio, high thermal stability, and high solubility; and thereby an organic thin film transistor and an organic solar cell comprising the same can have high efficiency and can be mass-produced based on a solution process.

Novel alkylhalide compounds and method for preparing the same

The present invention refers to new alkylene halide compound and manufacturing method relates to, alkyl halide compound the present invention according to the organic semiconductor which can be used for all new applied to monomolecular polymer and alkyl alkyl novel organic semiconductor material have been introduced having improved solubility is due to various solvent added spin coating, die casting, printing of fluid, e.g., process fabrication of one end of the end, the type and volume of the film element characteristics for modulating determined the objective compound..