N-Butyl Glycidyl Ether used as diluent in adhesives

Min.Order / FOB Price:Get Latest Price

1 Metric Ton	Negotiable

1 Metric Ton

Negotiable

Min.Order :1 Metric Ton
Purity: ≥99.0%
Payment Terms : L/C,T/T

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Quick Details

Appearance:Colorless to pale yellow liquid with a strong, slightly unpleasant odor
Application:Electronic industry Insulating bonding materials
PackAge:25kg/drum or 180kg/drum
ProductionCapacity:|Metric Ton|Day
Storage:Store in a cool, dry place. Keep container closed when not in use
Transportation:depends on the goods

Superiority:

Professional:

60 years devoted to chemical industry.

Market segments:

Covering more than 12 industries

Supply chain management:

Customer tailored logistics portfolio

Global vision:

More than 20 years of cooperation with international partners

Application development:

Cross industry New application

Details:

Features of N-Butyl Glycidyl Ether

Product Name: n-Butyl Glycidyl Ether
Chemical Formula: C4H9OCH2(CHCH2)O
CAS No.: 2426-08-6
Dangerous Grade: 3

Technical Data of N-Butyl Glycidyl Ether

ITEMS	SPECIFICATION
Chromaticity	≤30
Viscosity 25℃, mPa.S	≤3
Epoxy value eg/100g	≥0.55
Hydrolyzed chlorine eg/100g	≤0.02
Water content	≤0.2

Package and Storage:

25kg/drum or 180kg/drum
Store in a cool, dry place. Keep container closed when not in use

Application /Application Industries:

Electronic industry
Insulating bonding materials

Colorless to pale yellow liquid with a strong, slightly unpleasant odor. Flash point approximately 164°F. Denser than water. Vapors are heavier than air. Vapors may irritate the nose, throat and respiratory tract. Ingestion or inhalation may cause central nervous system depression. Liquid contact may severely irritate the eyes and skin. Prolonged contact with the skin may cause defatting and drying.

Butyl glycidyl ether, an ether, can act as a base. They form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert.

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