Difference between revisions of "Chrysophanic acid"

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m (Text replace - "== Authority ==" to "== Sources Checked for Data in Record ==")
 
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A natural yellow dyestuff found in the roots of rhubarb plants and also in a yellow colored lichen, ''Xanthoria parietina'', in the form of parietin. Chrysophanic acid is extracted from the ground plant in an alkaline solution. The yellow colorant precipitates when the solution is neutralized with an acid.
 
A natural yellow dyestuff found in the roots of rhubarb plants and also in a yellow colored lichen, ''Xanthoria parietina'', in the form of parietin. Chrysophanic acid is extracted from the ground plant in an alkaline solution. The yellow colorant precipitates when the solution is neutralized with an acid.
 
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[[[SliderGallery rightalign|chrysophanic acid.jpg~Chemical structure]]]
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
 
''Xanthoria parietina''; 1,8-dihydroxy-3-methylanthraquinone; chrysophanol; 3-methylchrysazin; 1,8-dihydroxy-3-methyl-9,10-anthracenedione; rhenic acid; acido crisofanico (It.)
 
''Xanthoria parietina''; 1,8-dihydroxy-3-methylanthraquinone; chrysophanol; 3-methylchrysazin; 1,8-dihydroxy-3-methyl-9,10-anthracenedione; rhenic acid; acido crisofanico (It.)
  
[[[SliderGallery rightalign|chrysophanic acid.jpg~Chemical structure]]]
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== Risks ==
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* Contact may cause irritation. 
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* Ingestion may cause nausea and vomiting. 
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* Fisher Scientific: [https://fscimage.fishersci.com/msds/43573.htm MSDS]
  
== Other Properties ==
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==Physical and Chemical Properties==
  
Soluble in ethanol, benzene, chloroform, ether, acetone, acids, alkalis.  Insoluble in water. Absorption max. = 226, 256, 278, 288, 436 nm.
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* Soluble in ethanol, benzene, chloroform, ether, acetone, acids, alkalis.  Insoluble in water.  
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* Absorption max. = 226, 256, 278, 288, 436 nm.
  
 
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! scope="row"| Melting Point
 
! scope="row"| Melting Point
| 196
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| 196 C
 
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! scope="row"| Molecular Weight
 
! scope="row"| Molecular Weight
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== Hazards and Safety ==
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==Resources and Citations==
 
 
Contact may cause irritation.  Ingestion may cause nausea and vomiting. 
 
 
 
Fisher Scientific: [https://fscimage.fishersci.com/msds/43573.htm MSDS]
 
 
 
== Sources Checked for Data in Record ==
 
  
 
* 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

Latest revision as of 14:55, 29 May 2022

Description

A natural yellow dyestuff found in the roots of rhubarb plants and also in a yellow colored lichen, Xanthoria parietina, in the form of parietin. Chrysophanic acid is extracted from the ground plant in an alkaline solution. The yellow colorant precipitates when the solution is neutralized with an acid.

Chemical structure

Chrysophanic acid.jpg

Synonyms and Related Terms

Xanthoria parietina; 1,8-dihydroxy-3-methylanthraquinone; chrysophanol; 3-methylchrysazin; 1,8-dihydroxy-3-methyl-9,10-anthracenedione; rhenic acid; acido crisofanico (It.)

Risks

  • Contact may cause irritation.
  • Ingestion may cause nausea and vomiting.
  • Fisher Scientific: MSDS

Physical and Chemical Properties

  • Soluble in ethanol, benzene, chloroform, ether, acetone, acids, alkalis. Insoluble in water.
  • Absorption max. = 226, 256, 278, 288, 436 nm.
Composition C15H10O4
CAS 481-74-3
Melting Point 196 C
Molecular Weight mol. wt.=254.24

Resources and Citations

  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 2318
  • F. Crace-Calvert, Dyeing and Calico Printing, Palmer & Howe, London, 1876 Comment: pp. 296 and 298
  • Sigma Dyes, Stains and Natural Pigments, Infrared Library, Nicolet, 1991-1995 Comment: OMNIC: formula= C15H10O4, CAS= 481-74-3