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2-Butoxyethanol (2-Butoxyethanol)

Bargaining 10-21 09:11 Update

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2-Butoxyethanol

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Inquiry
  • 2-Butoxyethanol
  • Ethanol, 2-butoxy-
  • Ethylene Glycol Mono-Butyl Ether
  • ethylene glycol monobutyl ether
  • Myristic acid,2-hydroxyethyl ester
  • 2-butoxy-ethanol
  • 1-O-Tetradecanoyl-1,2-ethandiol
  • 2-hydroxyethyl butyl ether
  • 2-Butoxy ethanol
  • Ethylene glycol butyl ether
  • 2-n-butyloxyethanol
  • 2-butoxy-1-ethanol
  • 2-hydroxyethyl myristate
  • 2-butoxyethyl alcohol
  • Butyl Glycol
  • Ethyleneglycol-monobutyl ether
  • Tetradecanoic acid,2-hydroxyethyl ester
  • Ethylene glycol monomyristate
  • Polyethylene glycol myristate
  • 2-Hydroxyethyl-myristat
  • Ethylene Glycol Monobutyl Ether
  • Butyl Cellosolve
  • Glycol myristate
  • ethylene glycol mono-n-butyl ether
+Expand -Stow
111-76-2 C6H14O2 118.174 2909440000

Nature Description

Colorless flammable liquid with moderate ether flavor. Freezing point-40℃, boiling point 171 ℃, relative density 0.9015(20/4 ℃), refractive index 1.4198, flash point 61.1 ℃, vapor pressure (20℃)0.101kPa, autoignition point 472 ℃. Soluble in 20 times of water, soluble in most organic solvents and mineral oil. It has a high dilution ratio with petroleum hydrocarbon.
0.901 171oC -70oC MISCIBLE 1.418-1.42 MISCIBLE

Product Applications

Used as solvent for paint and ink, metal cleaning agent component and raw material for dye dispersant; Used as reagent and solvent for determination of iron and molybdenum, and also used for separation of calcium and strontium in nitrate; Mainly used as cellulose nitrate, spray paint, quick-drying paint, varnish, enamel and paint remover solvent. It can also be used as fiber..

Production method

It is derived from the addition of ethylene oxide to n-butyl alcohol. N-butyl alcohol was added to the diethyl ether solution of boron trifluoride at 20 °c, and ethylene oxide was introduced under stirring. As the reaction proceeds, the temperature auto rise. After the temperature drops, leave it for three days. The crude product is obtained by neutralization with potassium hydroxide methanol solution to pH = 8. After adding a little p-aminophenol to the crude product, it is fractionated and the fraction 166-170 ℃ is divided to obtain the finished product. Industrial production can adopt the method of non-catalytic reaction under high temperature and high pressure (reaction temperature 180-250 ℃, pressure 2.1-4.6MPa) for 6 hours. Alkali catalysts can also be used at near normal pressure and lower temperature.

Security

Xn

S46: in case of accidental swallowing, seek doctor's advice immediately (display product container or label). S36/37: Wear suitable protective clothing and gloves.

R20/21/22: inhalation, skin contact and accidental swallowing are harmful. R36/38: it can irritate eyes and skin.

UN2369

GHS07

Complete packaging, light loading and unloading, ventilation in the warehouse, away from open flame, high temperature, and separate storage from oxidant

P261;P301+P312+P330;P302+P352+P312;P304+P340+P312;P305+P351+P338;P337+P313

III

Warning

H302+H312+H332;H315;H319

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