Difference between revisions of "Anthracene"

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== Description ==
 
== Description ==
  
A colorless, crystalline compound composed of three attached aromatic rings. Anthracene is derived from the fractional distillation of [http://cameo.mfa.org/materials/fullrecord.asp?name=coal tar coal tar]. Anthracene is used to make [http://cameo.mfa.org/materials/fullrecord.asp?name=alizarin, synthetic synthetic alizarin]. It is also used to manufacture other organic dyes, resins, plasticizers, and tanning agents.
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A colorless, crystalline compound composed of three attached aromatic rings. Anthracene is derived from the fractional distillation of [http://cameo.mfa.org/materials/fullrecord.asp?name=coal%20tar coal tar]. Anthracene is used to make [http://cameo.mfa.org/materials/fullrecord.asp?name=alizarin%2C%20synthetic synthetic alizarin]. It is also used to manufacture other organic dyes, resins, plasticizers, and tanning agents.
  
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
anthracin; paranaphthalene; antracen (Ces., Pol.); Anthracen (Deut.); antraceno(Esp.); anthracne (Fr.); anthraceen (Ned.);
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anthracin; paranaphthalene; antracen (Ces., Pol.); Anthracen (Deut.); antraceno(Esp.); anthracène (Fr.); anthraceen (Ned.);
  
 
[[[SliderGallery rightalign|anthracene.jpg~Chemical structure]]]
 
[[[SliderGallery rightalign|anthracene.jpg~Chemical structure]]]
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== Authority ==
 
== Authority ==
  
* G.S.Brady, G.S.Brady, ''Materials Handbook'', McGraw-Hill Book Co., New York, 1971  Comment: p. 801
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* G.S.Brady, ''Materials Handbook'', McGraw-Hill Book Co., New York, 1971  Comment: p. 801
  
* Richard S. Lewis, Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
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* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
  
* John and Margaret Cannon, John and Margaret Cannon, ''Dye Plants and Dyeing'', Herbert Press, London, 1994
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* John and Margaret Cannon, ''Dye Plants and Dyeing'', Herbert Press, London, 1994
  
 
* ''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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* Wikipedia, the free encyclopedia, at http://www.wikipedia.com  Comment: http://en.wikipedia.org/wiki/Anthracene (Accessed Mar. 20, 2006) -for non-English terms
 
* Wikipedia, the free encyclopedia, at http://www.wikipedia.com  Comment: http://en.wikipedia.org/wiki/Anthracene (Accessed Mar. 20, 2006) -for non-English terms
  
* Random House, Random House, ''Webster's Encyclopedic Unabridged Dictionary of the English Language'', Grammercy Book, New York, 1997
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* Random House, ''Webster's Encyclopedic Unabridged Dictionary of the English Language'', Grammercy Book, New York, 1997
  
 
* ''The American Heritage Dictionary'' or ''Encarta'', via Microsoft Bookshelf 98, Microsoft Corp., 1998
 
* ''The American Heritage Dictionary'' or ''Encarta'', via Microsoft Bookshelf 98, Microsoft Corp., 1998

Revision as of 06:22, 24 July 2013

Absorption and fluorescence emission spectra

Description

A colorless, crystalline compound composed of three attached aromatic rings. Anthracene is derived from the fractional distillation of coal tar. Anthracene is used to make synthetic alizarin. It is also used to manufacture other organic dyes, resins, plasticizers, and tanning agents.

Synonyms and Related Terms

anthracin; paranaphthalene; antracen (Ces., Pol.); Anthracen (Deut.); antraceno(Esp.); anthracène (Fr.); anthraceen (Ned.);

Chemical structure

Anthracene.jpg


Other Properties

Slightly soluble in ethanol, ether and benzene. Insoluble in water.

Violet fluorescence when pure, yellow-green when impure.

Composition C14H10
CAS 120-12-7
Melting Point 218
Density 1.1-1.2
Molecular Weight mol. wt. = 178.2
Boiling Point 342

Hazards and Safety

Combustible. Carcinogenic.

International Chemical Safety Card

Authority

  • G.S.Brady, Materials Handbook, McGraw-Hill Book Co., New York, 1971 Comment: p. 801
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • John and Margaret Cannon, Dye Plants and Dyeing, Herbert Press, London, 1994
  • Van Nostrand's Scientific Encyclopedia, Douglas M. Considine (ed.), Van Nostrand Reinhold, New York, 1976
  • The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 721
  • Random House, Webster's Encyclopedic Unabridged Dictionary of the English Language, Grammercy Book, New York, 1997
  • The American Heritage Dictionary or Encarta, via Microsoft Bookshelf 98, Microsoft Corp., 1998

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