+86-138-3850-2999
EnglishEnglish

loading

phenol

Molecular formula: C6H5OH
Density: 1.071g/cm3
Melting point: 43℃
Boiling point: 182℃
Flash point: 72.5℃
Refractive index: 1.553
Viscosity: 11.04 (mPa·s, 20ºC)
Saturated vapor pressure: 0.13kPa (40.1℃)
Critical temperature: 419.2℃
Critical pressure: 6.13MPa
Ignition temperature: 715℃
Explosion upper limit (V/V): 8.5%
Lower explosion limit (V/V): 1.3%
Solubility: slightly soluble in cold water, miscible in ethanol, ether, chloroform, glycerol
 
Availability:
facebook sharing button
twitter sharing button
line sharing button
wechat sharing button
linkedin sharing button
pinterest sharing button
whatsapp sharing button
kakao sharing button
snapchat sharing button
telegram sharing button
sharethis sharing button
Phenol (English: Phenol or phenyl hydroxide, commonly known as carbolic acid, carbolic acid), definition: the molecular formula is C6H6O, which is mainly produced by oxidation and decomposition of isopropyl benzene. It is an important organic chemical raw material. It can be used to produce a variety of chemical products and intermediates such as phenolic resins and bisphenol A, and is also used as solvents and disinfectants.

Phenol is an organic compound with the chemical formula C6H5OH. It is a colorless needle-like crystal with a special odor. It is toxic and is an important raw material for the production of certain resins, fungicides, preservatives and drugs (such as aspirin ).

Chemical Properties:

1. Acid-base reaction: Hydrogen of hydroxyl groups is easily dissociated into hydrogen ions, so it manifests as acidity, reacts with sodium hydroxide to produce sodium phenol: PhOH+NaOH→PhONa+H2O

Phenol Ka=1.28×10-10, acidity is between the two stages of carbonic acid ionization, so phenol cannot react with weak bases such as NaHCO3:
PhOˉ+CO2+H2O→PhOH+HCO3ˉ

2. Color reaction: Phenol looks purple when it encounters ferric chloride solution, because phenol root ions form a colored complex with Fe.

6PhOH+FeCl3→H3[Fe(OPh)6](Purple)+3HCl

3. Substitution reaction: The reaction on the phenol aromatic ring is mainly manifested as electrophilic substitution reactions, such as halogenation, nitration, sulfonation, alkylation, acylation, carboxylation and coupling reaction with diazon salt. This is because the hydroxyl group has an electron donation effect, which increases the electron cloud density of benzene ring.

4. Phenol is easily oxidized to form benzenequinone (pink), further oxidizes to form brown polymers

The oxidation product of phenol is generally parabenzoquinone . This reaction can also be used as an oxidant.
When interacting with metal zinc, it can be reduced to benzene; under the action of nickel catalyst, hydrogenation can be reduced to cyclohexanol.
5. Condensation reaction: phenol and formaldehyde condense under the catalysis of acid or base to form phenolic resin.




Previous: 
Next: 
Henan Kelan Wansen Energy Technology Co., Ltd. holds a controlling stake in Henan Lanmeihui New Materials Co., Ltd. The company was established on December 3, 2024 in Zhengzhou, Henan Province.

QUICK LINKS

CONTACT US

  +86-13838502999
  123462841@qq.com
  No. 1101, 11th Floor, Unit 1, Building 2, Phase I, Meisheng Education Harbor, No.58 Boyuan Road, Jinshui District, Zhengzhou, Henan

SEARCH PRODUCT

Copyright © 2025 Henan Kelan Wansen Energy Technology Co., Ltd. All Rights Reserved.  Sitemap  豫ICP备2025114911号-1