4912-58-7

Basic information

• Product Name: 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL
• Synonyms: RARECHEM AL BD 0103;3-ETHOXY-4-HYDROXYBENZYL ALCOHOL
• CAS NO: 4912-58-7
• Molecular Formula: C₉H₁₂O₃
• Molecular Weight: 168.19
• Product Categories: Benzhydrols, Benzyl & Special Alcohols
• Mol File: 4912-58-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 73-75°C
• Boiling Point: 323.3 °C at 760 mmHg
• Flash Point: 149.3 °C
• Appearance: /
• Density: 1.182 g/cm³
• Vapor Pressure: 0.000109mmHg at 25°C
• Refractive Index: 1.558
• CAS DataBase Reference: 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL(4912-58-7)
• EPA Substance Registry System: 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL(4912-58-7)

Safety Data

• Hazardous Substances Data: 4912-58-7(Hazardous Substances Data)

Usage

General Description

3-Ethoxy-4-hydroxybenzyl alcohol is a chemical compound with the molecular formula C10H14O3. It is a white crystalline solid that is often used in the synthesis of pharmaceuticals and as a building block in organic chemistry. 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL is derived from ethyl phenyl ether and has both ethoxy and hydroxy groups attached to a benzene ring. It has been identified as a potential antioxidant and has shown promise in various biological and medicinal applications. Additionally, it is an important intermediate in the production of various compounds used in the pharmaceutical industry.

InChI:InChI=1/C9H12O3/c1-2-12-9-5-7(6-10)3-4-8(9)11/h3-5,10-11H,2,6H2,1H3

Upstream product

• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 64-17-5 ethanol 

Downstream Products

• 1000378-07-3 8-methylnonanoic acid (3-ethoxy-4-hydroxyphenyl)methyl ester 
• 70959-77-2 5-{2-[2-(2-Ethoxy-4-hydroxymethyl-phenoxy)-ethylamino]-1-hydroxy-ethyl}-2-methoxy-benzenesulfonamide 
• 70958-89-3 5-{1-Hydroxy-2-[2-(2-ethoxy-4-hydroxymethylphenoxy)ethylamino]ethyl}-2-methylbenzenesulfonamide 
• 70958-73-5 [4-(2-Benzylamino-ethoxy)-3-ethoxy-phenyl]-methanol 
• 96840-56-1 2-ethoxy-4-isopropoxymethylphenol 
• 71119-07-8 2-ethoxy-4-ethoxymethylphenol 
• 5595-79-9 2-ethoxy-4-(methoxymethyl)phenol 
• 78826-07-0 (+/-)-2-(2-ethoxy-4-hydroxymethylphenoxy)propionic acid 

Relevant articles and documents

Phosphoric acid-modified commercial kieselguhr supported palladium nanoparticles as efficient catalysts for low-temperature hydrodeoxygenation of lignin derivatives in water

Efficient production of high value-added chemicals and biofuels via low-temperature chemoselective HDO of lignin derivatives in water is still a challenge. Here, we construct a low-cost, active and stable Pd/PCE catalyst using phosphoric acid-modified commercial Celite (PCE) as the support, and this catalyst exhibits excellent activity in low-temperature HDO of vanillin as well as other lignin derivatives in water. The superior catalytic performance is due to the presence of P species on the surface of Pd/PCE, accelerating the selective conversion of the intermediate into the final product. Detailed experimental and mechanistic studies reveal that the rapid conversion of the intermediate to the final product proceeds via a free-radical process in an interfacial microenvironment created by intimate interacting between the P species and Pd NPs. The insights of this work provide a new low-cost catalytic system for efficient production of valuable chemicals and future biofuels from lignin derivatives. This journal is

Thioether type compound as well as synthesis method and application thereof

The invention provides a thioether type compound and also relates to a synthesis method of the thioether type compound and application of the thioether type compound. A chemical structure of the thioether type compound enables the thioether type compound to have a relatively high melting point and be not easily sublimated, so that the thioether type compound has relatively good thermal stability;the thioether type compound has an excellent anti-oxidization capability and has no toxic and side effects, so that the thioether type compound has relatively high utilization safety; secondly, a target compound is synthesized by the synthesis method of the thioether type compound, provided by the invention, by adopting one-step reaction; visibly, the synthesis method is simple to operate, moderate in technological conditions, green and environmentally friendly, and is very suitable for large-scale industrial production. A series of experiments prove that the thioether type compound has an obvious inhibition effect on oxidization of various foods and an anti-oxidization effect of the compound has a certain dose-effect relationship with the concentration of the compound; therefore, the thioether type compound provided by the invention has a wide application prospect and a good market potential.