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Benzyl ether

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Benzyl ether Basic information

Product Name:
Benzyl ether
Synonyms:
  • Tribenoside impurity D
  • [(Benzyloxy)methyl]benzene
  • 1,1-[oxybis(methylene)]bis[benzene]
  • 1,1’-(oxybis(methylene))bis-benzen
  • 1,1’-[oxybis(methylene)]bis-benzen
  • 1,1’-[oxybis(methylene)]bis-Benzene
  • 1,1’-oxybis(methylene-benzen
  • BA (Plasticizer)
CAS:
103-50-4
MF:
C14H14O
MW:
198.26
EINECS:
203-118-2
Product Categories:
  • Building Blocks
  • C13 to C14
  • Chemical Synthesis
  • Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • Organics
Mol File:
103-50-4.mol
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Benzyl ether Chemical Properties

Melting point:
1.5-3.5 °C(lit.)
Boiling point:
298 °C(lit.)
Density 
1.043 g/mL at 25 °C(lit.)
vapor pressure 
<1 Pa (25 °C)
FEMA 
2371 | DIBENZYL ETHER
refractive index 
n20/D 1.562
Flash point:
275 °F
storage temp. 
2-8°C
solubility 
42mg/l insoluble
form 
Liquid
color 
Clear colorless to pale yellow
Relative polarity
3.3
Odor
at 100.00 %. sweet fruity cherry earthy mushroom rose plastic
Odor Type
earthy
Water Solubility 
insoluble
JECFA Number
1256
Merck 
14,1132
BRN 
1911156
Dielectric constant
3.8599999999999999
Stability:
Stable. Combustible. Incompatible with strong acids, strong oxidizing agents.
LogP
3.31
CAS DataBase Reference
103-50-4(CAS DataBase Reference)
NIST Chemistry Reference
Benzene, 1,1'-[oxybis(methylene)]bis-(103-50-4)
EPA Substance Registry System
Benzyl ether (103-50-4)
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Safety Information

Hazard Codes 
Xi,N
Risk Statements 
36/37/38-51/53
Safety Statements 
23-61
RIDADR 
UN 3082 9/PG 3
WGK Germany 
2
RTECS 
DQ6125000
9
Autoignition Temperature
470 °C
TSCA 
Yes
HS Code 
2909 30 90
HazardClass 
9
PackingGroup 
III
Hazardous Substances Data
103-50-4(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 2500 mg/kg

MSDS

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Benzyl ether Usage And Synthesis

Chemical Properties

Dibenzyl ether has a slightly earthy, mushroom-like odor with a rosy undertone.

Chemical Properties

Dibenzyl ether is a clear, almost colorless liquid. It is miscible with alcohols and ethers, but insoluble in water. Dibenzyl ether is used as special solvent and delustering agent for textiles.

Uses

Plasticizer for nitrocellulose; solvent in perfumery.

Uses

Benzyl ether is used as an effective GFP friendly tissue clearing medium for mouse brains. It is also used in a study to develop a detailed protocol for performing 3D imaging of solvent-cleared organs and its application to various microscopy techniques. It is also employed as a plasticizer for nitrocellulose and synthetic rubber, a solvent in perfumery, and a flavoring agent in chewing gums and baked goods.

Uses

Benzyl ether was used as an effective GFP friendly tissue clearing medium for mouse brains. It was used in a study to develop a detailed protocol for performing 3D imaging of solvent-cleared organs and its application to various microscopy techniques.

Preparation

As a by-product in the preparation of benzyl alcohol by hydrolysis of benzyl chloride; by using a concentrated caustic instead of carbonate, yields can be improved to 50% or higher.

Definition

ChEBI: Dibenzyl ether is a benzyl ether in which the oxygen atom is connected to two benzyl groups. It has a role as a metabolite.

General Description

Colorless liquid with a mild odor.

Air & Water Reactions

Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick, 1979 p.151-154, 164]. Insoluble in water.

Reactivity Profile

Benzyl ether can act as a base to form salts with strong acids and addition complexes with Lewis acids. May react violently with strong oxidizing agents. Burns readily but relatively inert in other reactions, which typically involve the breaking of the carbon-oxygen bond.

Hazard

Moderately toxic by ingestion. A skin irri- tant.

Health Hazard

Inhalation may cause nausea because of disagreeable odor. Contact of liquid with eyes causes mild irritation. Prolonged exposure of skin to liquid causes reddening and irritation. Ingestion produces nausea.

Fire Hazard

Benzyl ether is combustible.

Synthesis

Benzyl ether is formed when benzyl alcohol is heated with strong acids or bases. It is produced almost exclusively by the alkaline hydrolysis of benzyl chloride. Heat treatment decomposes dibenzyl ether into benzaldehyde and toluene.

Purification Methods

Reflux the ether over sodium, then distil it under reduced pressure. It been purified by fractional freezing. [Beilstein 6 IV 2240.]

Benzyl ether Preparation Products And Raw materials

Preparation Products

Raw materials

Benzyl etherSupplier

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