Difference between revisions of "Rubiadin"

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1,3-hydroxy-2-methylanthraquinone; CI  75350; rubiadina (Port.)
 
1,3-hydroxy-2-methylanthraquinone; CI  75350; rubiadina (Port.)
  
== Other Properties ==
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==Risks==
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* Millipore Sigma: [https://www.sigmaaldrich.com/US/en/product/sial/74553 SDS]
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==Physical and Chemical Properties==
  
Soluble in ethanol, ether, benzene. Insoluble in boiling water, lime water.  
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* Soluble in ethanol, ether, benzene. Insoluble in boiling water, lime water.  
 
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* Absorption max = 246, 280, 415 nm.
Absorption max = 246, 280, 415 nm.
 
  
 
{| class="wikitable"
 
{| class="wikitable"
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|-
 
|-
 
! scope="row"| Melting Point
 
! scope="row"| Melting Point
| 302
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| 302 C
 
|-
 
|-
 
! scope="row"| Molecular Weight
 
! scope="row"| Molecular Weight
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|}
 
|}
  
== Additional Information ==
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==Resources and Citations==
 
 
H.Schweppe, J.Winter, "Madder and Alizarin", ''Artists Pigments'', Volume 3, E. West FitzHugh (ed.), Oxford University Press: Oxford, 1997.
 
 
 
== Authority ==
 
  
 
* ''Artists' Pigments: A Handbook of their History and Characteristics'', Elisabeth West FitzHugh, Oxford University Press, Oxford, Vol. 3, 1997  Comment: H.Schweppe, J.Winter, "Madder and Alizarin"
 
* ''Artists' Pigments: A Handbook of their History and Characteristics'', Elisabeth West FitzHugh, Oxford University Press, Oxford, Vol. 3, 1997  Comment: H.Schweppe, J.Winter, "Madder and Alizarin"

Latest revision as of 08:39, 28 June 2022

Description

Yellow plate-like crystals. Rubiadin is one of the natural dyes extracted from madder roots and other Rubiaceae family plants. It dissolves in alkalis to form a red solution and turns yellow in acids.

Synonyms and Related Terms

1,3-hydroxy-2-methylanthraquinone; CI 75350; rubiadina (Port.)

Risks

  • Millipore Sigma: SDS

Physical and Chemical Properties

  • Soluble in ethanol, ether, benzene. Insoluble in boiling water, lime water.
  • Absorption max = 246, 280, 415 nm.
Composition C15H10O4
Melting Point 302 C
Molecular Weight mol. wt. = 254.24

Resources and Citations

  • Artists' Pigments: A Handbook of their History and Characteristics, Elisabeth West FitzHugh, Oxford University Press, Oxford, Vol. 3, 1997 Comment: H.Schweppe, J.Winter, "Madder and Alizarin"