| Identification | More | [Name]
1,4-Bis(vinyloxy)-butane | [CAS]
3891-33-6 | [Synonyms]
1,4-BIS-(VINYLOXY)-BUTANE
1,4-BUTANEDIOL DIVINYL ETHER
1,4-BUTYLDIOL VINYL ETHER
1,4-BUTYLENE GLYCOL DIVINYL ETHER
1,4-DIVINYLOXYBUTANE
BUTANEDIOL DIVINYL ETHER
1,4-bis(ethenyloxy)-butan
1,4-Bis(ethenyloxy)butane
1,4-divinyloxybutane(1,4-butanedioldivinylether)
1-[4-(Vinyloxy)butoxy]ethylene
Butane, 1,4-bis(ethenyloxy)-
Butane, 1,4-bis(vinyloxy)-
1,4-Butanediylbis(vinyl ether)
3,8-Dioxa 1,9-decadiene
Tetramethylenebis(vinyl ether) | [EINECS(EC#)]
223-437-0 | [Molecular Formula]
C8H14O2 | [MDL Number]
MFCD00026065 | [Molecular Weight]
142.2 | [MOL File]
3891-33-6.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
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| Hazard Information | Back Directory | [Uses]
1,4-Bis(vinyloxy)-butane, which also serves as an intermediate in manufacturing higher perfume chemicals, has found some use in perfume compositions, mainly for its diffusive power and “l(fā)ift” in soap fragrances, detergent perfumes, etc. It seems most conceivable that certain Vinyl ethers are the intermediate steps made by Mother Nature in the manufacture (biosynthesis) of some very interesting and important odorous chemicals, including “Rose oxide”. Many Pyran derivatives are made by means of Vinylether synthesis.
| [Production Methods]
1,4-Bis(vinyloxy)-butane was produced from Tetramethylene glycol and Acetylene, using pressure and a catalyst. | [Flammability and Explosibility]
Flammable | [Solubility in water]
Insoluble in water, soluble in alcohol, miscible with oils.
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