2,6-Di-tert-butylph...

2,6-Di-tert-butylphenol 128-39-2CAS NO.: 128-39-2

2,6-Di-tert-butylphenol 128-39-2CAS NO.: 128-39-2

Min.Order / FOB Price:Get Latest Price

1 Kilogram

FOB Price:USD 4.0000 -5.0000

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,D/A,D/P,T/T,,MoneyGram,Other

Keywords

2,6-Di-tert-butylphenol 2,6-DI-T-BUTYLPHENOL 99.5% 2,6-Di-tert-butylphenol

Quick Details

  • Appearance:White solid
  • Application:Adhesive and Sealant
  • PackAge:Aluminium foil bag
  • ProductionCapacity:10000|Gram|Day
  • Storage:Room temperature
  • Transportation:By Sea/Air/DHL

Superiority:

We are leading fine chemicals supplier in China and 
 
Our main business covers the fields below:
 
1.Noble Metal Catalysts (Pt.Pd...)
 
2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)
 
3.OLED intermediates (Fluorene,Carbazole,Boric acid...)
 
4.Customs Synthesis
 
Our advantage:
 
1.Higest quality and good package
 
2.Fast delivery
 
3.Better payment term
 
4.Fast response to customer within 6 hours
 
5.Good business credit in Europe ,US ,Japan ,Korea
 
Anyway ,if you need any chemicals from China ,Henan Wentao can help you
 

Details:

Chemical Properties white solid
Uses Antioxidant for Gasoline, Jet Fuels, and Electrical Insulating Oils
Uses Antioxidant Intermediate, Pharmaceuticals
General Description Odorless colorless to light yellow solid or liquid. Floats on water. Freezing point is 97°F.
Air & Water Reactions Insoluble in water.
Reactivity Profile Phenols, such as 2,6-Di-tert-butylphenol, do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid.
Health Hazard Irritates eyes and (on prolonged contact) skin. Ingestion causes irritation of mouth and stomach.
Purification Methods Crystallise the phenol from aqueous EtOH or n-hexane. [Beilstein 6 III 2061.]

 

Related Searches

Confirm to collect the product to my collection?

OKCancel

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View