Difference between revisions of "Acetal"

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== Description ==
 
== Description ==
  
A colorless, volatile liquid obtained from the reaction of [[hacetaldehyde|acetaldehyde]] and [[ethyl%20alcohol|ethyl alcohol]]. Acetal has a pleasing odor and a nutlike aftertaste. It is used as a solvent, and as an ingredient in cosmetics, perfumes (such as jasmine) and flavorings.
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A colorless, volatile liquid obtained from the reaction of [[acetaldehyde|acetaldehyde]] and [[ethyl%20alcohol|ethyl alcohol]]. Acetal has a pleasing odor and a nutlike aftertaste. It is used as a solvent, and as an ingredient in cosmetics, perfumes (such as jasmine) and flavorings.
  
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
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diethylacetal; 1,1-diethoxyethane; ethylidenediethyl ether; acetaldehyde diethyl acetal
 
diethylacetal; 1,1-diethoxyethane; ethylidenediethyl ether; acetaldehyde diethyl acetal
  
[[[SliderGallery rightalign|acetal.jpg~Chemical structure]]]
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== Risks ==
  
== Other Properties ==
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* Highly flammable. Flash point = -12C. 
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* Sensitive to light, moisture and heat. 
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* May form explosive peroxides. 
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* Contact causes irritation.
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* Narcotic in high concentrations. 
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* Fisher Scientific: [https://www.fishersci.com/store/msds?partNumber=AC102220050&productDescription=ACETAL%2C99%25+5ML&vendorId=VN00032119&countryCode=US&language=en SDS]
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== Physical and Chemical Properties ==
  
 
Soluble in hexane, ethanol and ethyl acetate. Slightly soluble in water.
 
Soluble in hexane, ethanol and ethyl acetate. Slightly soluble in water.
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|-
 
|-
 
! scope="row"| Melting Point
 
! scope="row"| Melting Point
| -100
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| -100 C
 
|-
 
|-
 
! scope="row"| Density
 
! scope="row"| Density
| 0.8254
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| 0.8254 g/ml
 
|-
 
|-
 
! scope="row"| Molecular Weight
 
! scope="row"| Molecular Weight
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|-
 
|-
 
! scope="row"| Boiling Point
 
! scope="row"| Boiling Point
| 102.7
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| 102.7 C
 
|}
 
|}
  
== Hazards and Safety ==
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==Resources and Citations==
 
 
Highly flammable. Flash point = -12C.  Sensitive to light, moisture and heat.  May form explosive peroxides.  Contact causes irritation. Narcotic in high concentrations. 
 
 
 
Fisher Scientific: [http://www.fishersci.ca/msds2.nsf/0/6617ED9ADBB1F1B485256CA40083A6D4/$file/MSDS-69052.html?open MSDS]
 
 
 
== Authority ==
 
  
 
* ''Van Nostrand's Scientific Encyclopedia'', Douglas M. Considine (ed.), Van Nostrand Reinhold, New York, 1976
 
* ''Van Nostrand's Scientific Encyclopedia'', Douglas M. Considine (ed.), Van Nostrand Reinhold, New York, 1976
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* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
 
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
 
* Website address 1  Comment: Fisher Scientific at https://www1.fishersci.com/catalogs/acrosgroup.jsp?catalogParamId=8013176&catalogParamType=AG  Flash point = -21C
 
  
  
  
 
[[Category:Materials database]]
 
[[Category:Materials database]]

Latest revision as of 17:20, 18 April 2022

Description

A colorless, volatile liquid obtained from the reaction of Acetaldehyde and Ethyl alcohol. Acetal has a pleasing odor and a nutlike aftertaste. It is used as a solvent, and as an ingredient in cosmetics, perfumes (such as jasmine) and flavorings.

Synonyms and Related Terms

diethylacetal; 1,1-diethoxyethane; ethylidenediethyl ether; acetaldehyde diethyl acetal

Risks

  • Highly flammable. Flash point = -12C.
  • Sensitive to light, moisture and heat.
  • May form explosive peroxides.
  • Contact causes irritation.
  • Narcotic in high concentrations.
  • Fisher Scientific: SDS

Physical and Chemical Properties

Soluble in hexane, ethanol and ethyl acetate. Slightly soluble in water.

Composition CH3CH(OC2H5)2
CAS 105-57-7
Melting Point -100 C
Density 0.8254 g/ml
Molecular Weight mol. wt. = 118.18
Refractive Index 1.379-1.385
Boiling Point 102.7 C

Resources and Citations

  • Van Nostrand's Scientific Encyclopedia, Douglas M. Considine (ed.), Van Nostrand Reinhold, New York, 1976
  • G.S.Brady, Materials Handbook, McGraw-Hill Book Co., New York, 1971
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993