Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Natural Products >  Phenols >  alpha-ethoxy-p-cresol

alpha-ethoxy-p-cresol

Basic information Safety Supplier Related

alpha-ethoxy-p-cresol Basic information

Product Name:
alpha-ethoxy-p-cresol
Synonyms:
  • alpha-ethoxy-p-cresol
  • Phenol, 4-(ethoxymethyl)-
  • 4-(Ethoxymethyl)phenol
  • 4-Ethoxymethylphenol
  • alpha-Ethoxy-p-creso
  • p-Hydroxybenzyl ethyl ether
  • 4-hydroxybenzyl ethyl ether
  • p-Hydroxybenzyl Et ether
CAS:
57726-26-8
MF:
C9H12O2
MW:
152.19
EINECS:
260-918-4
Mol File:
57726-26-8.mol
More
Less

alpha-ethoxy-p-cresol Chemical Properties

storage temp. 
Inert atmosphere,Room Temperature
form 
Solid
color 
White to off-white
LogP
1.699 (est)
More
Less

alpha-ethoxy-p-cresol Usage And Synthesis

Uses

4-(Ethoxymethyl)phenol (p-Hydroxybenzyl Et ether) is a potent antioxidant from Amburana cearensis leaf extract, with in vitro cytogenotoxic properties. Amburana cearensis leaves can be used foe the research of respiratory diseases and inflammations[1].

Definition

ChEBI: 4-(Ethoxymethyl)phenol is a benzyl ether.

Synthesis

64-17-5

623-05-2

57726-26-8

General procedure for the synthesis of 4-(ethoxymethyl)phenol from ethanol and p-hydroxybenzyl alcohol: refer to the operation of Example 2, but substitute ethanol for methanol. After completion of the reaction, the residue was purified by reduced pressure distillation (boiling point: 110-119°C/1.5 Torr) to obtain 4-ethoxymethylphenol in 75% yield and 98% HPLC purity. The operation was as follows: in a 200 mL three-necked flask equipped with a thermometer, a three-way stopper and a stirrer, 15.0 g (0.12 mol) of p-hydroxybenzyl alcohol and 69 g of ethanol were added under nitrogen protection, followed by 0.06 g of nitromethane. A mixed solution consisting of 0.45 g of hydrochloric acid and 3.0 g of ethanol was slowly added dropwise under stirring at room temperature, and then the reaction mixture was stirred at 35 °C for 3 hours. At the end of the reaction, HPLC analysis showed an area percentage of 99%. Next, a mixed solution comprising 0.38 g of imidazole (manufactured by Aldrich Co., Ltd.) and 1.1 g of ethanol was added dropwise for neutralization, followed by concentration under reduced pressure to remove ethanol. To the concentrate, 60 g of isopropyl ether (produced by Nacalai Tesque, Inc.) and 22.5 g of water were added and the organic layer was further washed with 27 g of water and 0.26 g of acetic acid (produced by Nacalai Tesque). After washing the organic layer twice with water, the organic layer was concentrated, the crystal seed was added and slowly cooled to about 8°C. The precipitated crystals were filtered and dried to give 12.0 g (yield: 72%) of colorless 4-methoxymethylphenol with 99% HPLC purity.

References

[1] José Rafael da Silva Araujo, et al. Antioxidant and in vitro cytogenotoxic properties of Amburana cearensis (Allem?o) A.C.Sm. leaf extract. Drug Chem Toxicol. 2021 Dec 14;1-9. DOI:10.1080/01480545.2021.2011313

alpha-ethoxy-p-cresolSupplier

Chembest Research Laboratories Limited
Tel
+86-21-20908456
Email
sales@BioChemBest.com
BioBioPha Co., Ltd.
Tel
0871-65217109 13211707573;
Email
y.liu@mail.biobiopha.com
Sichuan Wei Keqi Biological Technology Co., Ltd.
Tel
028-81700200 18116577057
Email
3003855609@qq.com
Wuxi Zhongkun Biochemical Technology Co., Ltd.
Tel
0510-85629785 18013409632
Email
sales@reading-chemicals.com
Shanghai Yongye Biotechnology Co., Ltd.
Tel
86-021-61559134 15921386130
Email
3423497944@qq.com