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Aminoemodin

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Identification
Molecular formula
C15H11NO4
CAS number
641-14-3
IUPAC name
1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione
State
State

Aminoemodin is a solid at room temperature, existing in a crystalline form.

Melting point (Celsius)
231.00
Melting point (Kelvin)
504.15
Boiling point (Celsius)
550.00
Boiling point (Kelvin)
823.15
General information
Molecular weight
283.27g/mol
Molar mass
283.2650g/mol
Density
1.5423g/cm3
Appearence

Aminoemodin typically appears as a yellow to orange crystalline powder. It is a derivative of anthraquinone, giving it a solid crystalline structure.

Comment on solubility

Solubility Characteristics of 1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione

1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione, also known as Alizarin Red S, exhibits interesting solubility properties that are worth noting:

  • Solvent Dependency: This compound is primarily soluble in a variety of organic solvents, such as ethanol and acetone, but displays limited solubility in water.
  • pH Influence: The solubility can vary significantly with changes in pH due to its acidic and basic functional groups, impacting its ionization and thus its ability to dissolve.
  • Temperature Effects: Like many organic compounds, its solubility generally increases with temperature; thus heating may aid in dissolving the compound more readily.
  • Complexation: 1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione can form complexes with certain metals, which may enhance solubility in the presence of those metal ions.

In summary, the solubility of 1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione is influenced by its surroundings, making it essential to consider solvent choice, pH levels, and temperature conditions when working with this compound. As the wise say, “simpler solutions often yield more effective results” — choose your solvent wisely!

Interesting facts

Interesting Facts about 1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione

1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione, often referred to as an important derivative of anthraquinone, boasts a fascinating chemical profile and intriguing applications. Here are some remarkable insights about this compound:

  • Structure and Function: The compound features a unique anthracene backbone, which is modified by the presence of amino, hydroxy, and methoxy groups. This structural diversity leads to varied chemical properties and enhances its potential as a versatile building block in organic chemistry.
  • Biological Relevance: Research surrounding this compound has indicated its potential biological activity. It has been studied for its effects on various biological processes, making it a point of interest for medicinal chemistry.
  • Fluorescent Properties: Many derivatives of anthrone compounds exhibit strong fluorescence, which may be useful in biological imaging and detection methods. This characteristic makes them suitable for applications in biochemistry and analytical chemistry.
  • Applications in Dye Chemistry: Anthraquinone derivatives are well-known for their applications in dye production. The vivid color properties and stability of compounds like 1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione render them valuable for creating dyes and pigments.
  • Environmental Implications: The study of anthraquinone compounds often intersects with environmental chemistry, particularly concerning their degradation and behavior in ecological systems. Understanding these properties can aid in pollution control and waste management strategies.

In summary, 1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione represents a prime example of how organic compounds can bridge numerous fields, including medicine, materials science, and environmental chemistry. As researchers continue to explore its full potential, this compound remains an exciting topic for further investigation.

Synonyms
Disperse Red 4
2379-90-0
Palanil Pink RF
Disperse Pink Zh
Disperse Rose Zh
Samaron Pink RFL
Nyloquinone Pink B
Celliton Fast Pink RF
Dianix Fast Pink R
9,10-Anthracenedione, 1-amino-4-hydroxy-2-methoxy-
Cilla Fast Pink RF
Disperse red-4
Fenacet Fast Pink RF
Miketon Fast Pink RL
Supracet Fast Pink 2R
C.I. Disperse Red 4
Perliton Brilliant Pink R
Artisil Brilliant Pink RFS
Celliton Fast Pink RFA-CF
Acetoquinone Light Pink RLZ
1a-2Mo-4oa
Esteroquinone Light Pink RLL
Interchem Acetate Fast Pink DNA
Cerven disperzni 4
1-Amino-4-hydroxy-2-methoxyanthraquinone
Navicet Pink RF
1-Amino-4-hydroxy-2-methoxy-9,10-anthracenedione
C.I. 60755
ANTHRAQUINONE, 1-AMINO-4-HYDROXY-2-METHOXY-
Periliton Brilliant Pink R
Cerven disperzni 4 [Czech]
1A-2MO-4OA [Russian]
NSC 81265
1-Amino-2-methoxy-4-oxyanthraquinone
EINECS 219-170-4
BRN 2420171
088YQ1PU8W
CATULIA RED B
CELLITON PINK RF
NSC-81265
1-Amino-2-methoxy-4-oxyanthraquinone [Russian]
CELLITON VIOLET 6B
1-amino-2-methoxy-4-hydroxyanthraquinone
DTXSID3062360
1-Amino-2-methoxy-4-hydroxy-9,10-anthraquinone
1-AMINO-2-METHOXY-4-HYDROXY-9,10-ANTHRACENEDIONE
DTXCID3036941
219-170-4
1-amino-4-hydroxy-2-methoxyanthracene-9,10-dione
DISPERSERED4
1-amino-4-hydroxy-2-methoxy-anthracene-9,10-dione
1-amino-4-hydroxy-2-methoxy-9,10-dihydroanthracene-9,10-dione
starbld0009571
UNII-088YQ1PU8W
1-Amino-4-hydroxy-2-methoxyanthra-9,10-quinone
SCHEMBL2207839
NSC81265
9, 1-amino-4-hydroxy-2-methoxy-
BBL001188
STK369414
AKOS003631317
VS-00843
WLN: L C666 BV IVJ DZ EO1 GQ
DB-273279
CS-0333518
NS00021070
AB00079999-01
1-Amino-4-hydroxy-2-methoxyanthra-9,10-quinone #