Welcome to LookChem.com Sign In|Join Free

CAS

  • or

107-48-2

Post Buying Request

107-48-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

107-48-2 Usage

Description

1,2-epoxy-2,4,4-trimethylpentane, also known as 3,3,5-trimethyl-1,2-oxepane, is a colorless liquid chemical compound with the molecular formula C8H16O. It has a pungent odor and is highly flammable. 1,2-epoxy-2,4,4-trimethylpentane is recognized for its use as a reactive diluent in the production of epoxy resins, as well as a solvent and additive in various industrial applications.

Uses

Used in Epoxy Resin Production:
1,2-epoxy-2,4,4-trimethylpentane is used as a reactive diluent for enhancing the processability and curing properties of epoxy resins. It helps in reducing the viscosity of the resin, allowing for easier application and improved performance in end-use products.
Used in Adhesives Industry:
In the adhesives industry, 1,2-epoxy-2,4,4-trimethylpentane is used as a solvent and additive to improve the bonding strength and flexibility of adhesive formulations. Its reactive nature contributes to the curing process, resulting in stronger and more durable bonds.
Used in Coatings Industry:
1,2-epoxy-2,4,4-trimethylpentane is utilized as a component in coatings to provide specific properties such as adhesion, flexibility, and chemical resistance. Its ability to reduce the viscosity of coating formulations facilitates easier application and improved coverage.
Used in Sealants Industry:
As a component in sealant formulations, 1,2-epoxy-2,4,4-trimethylpentane serves to enhance the sealing performance by improving the flow and curing characteristics of the sealants. This leads to better adhesion and durability in sealing applications.

Check Digit Verification of cas no

The CAS Registry Mumber 107-48-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 107-48:
(5*1)+(4*0)+(3*7)+(2*4)+(1*8)=42
42 % 10 = 2
So 107-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-7(2,3)5-8(4)6-9-8/h5-6H2,1-4H3

107-48-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,2-dimethylpropyl)-2-methyloxirane

1.2 Other means of identification

Product number -
Other names 2,4,4-Trimethylpent-1-ene oxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107-48-2 SDS

107-48-2Relevant articles and documents

Epoxidation of olefins by molecular oxygen with clay-impregnated nickel catalysts

Bouhlel, Ezzeddine,Laszlo, Pierre,Levart, Michel,Montaufier, Marie-Therese,Singh, Girij Pal

, p. 1123 - 1126 (1993)

With the supported "clayniac" catalyst, in the presence of i- butyraldehyde as a sacrificial reducer, olefins are epoxidized in good yields by compressed air at room temperature, in a convenient procedure.

Green oxidation of alkenes in ionic liquid solvent by hydrogen peroxide over high performance Fe(III) Schiff base complexes immobilized on MCM-41

Goldani, Mohammad Taghi,Mohammadi, Ali,Sandaroos, Reza

, p. 801 - 805 (2014)

A series of Fe(III) Schiff base complexes immobilized on MCM-41 were prepared and characterized by various physicochemical and spectroscopic methods. The complexes were used for oxidation of cyclohexene by 30% hydrogen peroxide in the presence and absence of ethylmethyl imidazolium chloride (EMIM) ionic liquid as solvent. The immobilized complexes proved to be effective catalysts and generally exhibited much higher catalytic performance than their homogeneous analogue. Catalytic performance of the complexes was also found to be closely related to the Schiff base ligands used. Additionally, ion liquid solvent efficiently improved all the catalytic performances. Finally, the reaction was extended to different alkenes using the heterogeneous complex 2-L4. Among all the alkenes, those containing π-electron-withdrawing groups and trans-orientations exhibited lower tendency for oxidation.

METHOD FOR MANUFACTURING AN EPOXY COMPOUND AND METHOD FOR EPOXIDIZING A CARBON-CARBON DOUBLE BOND

-

Page/Page column 12, (2012/05/07)

The present invention provides a method for producing an epoxy compound, comprising oxidizing a carbon-carbon double bond of an organic compound by hydrogen peroxide in the presence of a neutral inorganic salt and a mixed catalyst of a tungsten compound (a), at least one phosphorus compound selected from the group consisting of phosphoric acids, phosphonic acids, and salts thereof (b) and a surfactant (c), and an epoxidizing method comprising oxidizing a carbon-carbon double bond by hydrogen peroxide in the presence of the catalyst and the neutral inorganic salt.

Catalytic process for the preparation of epoxides from alkenes

-

Page/Page column 6, (2008/06/13)

An improved catalytic process for the preparation of epoxides from alkenes using a combination of transition metal salt, an inorganic promoter and an organic additive in absence of solvent or in the presence of a solvent with commercially available hydrogen per oxide has been disclosed. Thus, styrene oxide was prepared at a kilogram scale in 86% isolated yield with purity >95%.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 107-48-2