N-Butyl Glycidyl Et...

N-Butyl Glycidyl Ether used as diluent

N-Butyl Glycidyl Ether used as diluent

Min.Order / FOB Price:Get Latest Price

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

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60 years devoted to chemical industry.
 
Market segments:
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Supply chain management:
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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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