13037-88-2

Basic information

• Product Name: p-Hexadecyloxyphenol
• Synonyms: p-Hexadecyloxyphenol;4-HEXADECYLOXYPHENOL;4-N-HEXADECYLOXYPHENOL,98%;4-(hexadecyloxy)-;4-hexadecoxyphenol
• CAS NO: 13037-88-2
• Molecular Formula: C₂₂H₃₈O₂
• Molecular Weight: 334.54
• Product Categories: API intermediates
• Mol File: 13037-88-2.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 453.4°Cat760mmHg
• Flash Point: 164.9°C
• Appearance: /
• Density: 0.93g/cm³
• Vapor Pressure: 7.72E-09mmHg at 25°C
• Refractive Index: 1.492
• CAS DataBase Reference: p-Hexadecyloxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: p-Hexadecyloxyphenol(13037-88-2)
• EPA Substance Registry System: p-Hexadecyloxyphenol(13037-88-2)

Safety Data

• Hazardous Substances Data: 13037-88-2(Hazardous Substances Data)

Usage

Uses

4-Hexadecyloxyphenol is used as a reactant in the enzyme-mediated two-dimensional polymerization of aromatic derivatives on a Langmuir Trough.

InChI:InChI=1/C22H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20-24-22-18-16-21(23)17-19-22/h16-19,23H,2-15,20H2,1H3

Upstream product

• 6068-28-6 tosylate de n-hexadecyle 
• 30008-10-7 sodium 4-hydroxybenzen-1-olate 
• 36653-82-4 1-Hexadecanol 
• 123-31-9 hydroquinone 
• 59117-18-9 p-n-hexadecyloxybenzaldehyde 
• 123-08-0 4-hydroxy-benzaldehyde 
• 544-77-4 1-iodohexadecane 
• 112-82-3 hexadecanyl bromide 
• 103-16-2 4-Benzyloxyphenol 
• 67399-90-0 4-n-Hexadecyloxy-1-benzyloxybenzol 

Downstream Products

• 140468-11-7 4-(4-Hexadecyloxy-phenoxymethyl)-2,2-dimethyl-[1,3]dioxolane 
• 891999-13-6 terephthalic acid 1-benzyl ester 4-(4-hexadecyloxy-phenyl) ester 
• 130442-05-6 3-(bromomethyl)phenyl 4-(hexadecyloxy)phenyl phosphate 
• 1404166-39-7 2,5-bis[(4-hexadecyloxyphenyl)oxycarbonyl]styrene 
• 1422547-57-6 C₃₁H₄₆O₂ 
• 165614-98-2 5-(hexadecyloxy)-2-hydroxybenzaldehyde 

Relevant articles and documents

Synthesis and spectral properties of lutetium complexes with unsymmetrical phthalocyanines and sandwich complexes based thereon containing tetraanthraquinonoporphyrazine fragments

Joint condensation of 4,5-bis(4-hexadecyloxyphenoxy)phthalonitrile (A) and tetrachlorophthalonitrile (B) in boiling hexan-1-ol in the presence of lithium hexan-1-olate and subsequent reaction with LuCl3 · 6 H 2O gave single-decker lu

Discotic liquid crystals of transition metal complexes 56 ?: Synthesis of mesogenic phthalocyanine-fullerene dyads and influence of the substitution position of alkoxy chains and the kind of terminal groups on appearance of the helical supramolecular stru

We have synthesized twelve novel discotic columnar liquid crystals based on a phenoxy-group-substituted phthalocyaninato copper(II) complex having the same alkoxy chain of C16H33O at different positions in the phenoxy group: The parent compounds {0a~0c-16

METHOD OF PURIFYING ALKOXYPHENOL

PROBLEM TO BE SOLVED: To provide a purifying method that can easily remove a dialkoxybenzene from a crude composition containing an alkoxyphenol, to obtain a high-purity alkoxyphenol, and a production method that allows a high-purity alkoxyphenol to be obtained. SOLUTION: After a C1-5 lower alcohol is added to a crude composition containing an alkoxyphenol, represented by formula (1), and insoluble matter is subjected to solid-liquid separation (where R is a C6-20 alkyl group). SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT