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Disperse Yellow 54

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Identification
Molecular formula
C11H15N3O4
CAS number
61951-86-8
IUPAC name
2-[N-(2-hydroxyethyl)-4-(methylamino)-3-nitro-anilino]ethanol
State
State

Disperse Yellow 54 is typically found as a solid at room temperature.

Melting point (Celsius)
166.00
Melting point (Kelvin)
439.15
Boiling point (Celsius)
470.30
Boiling point (Kelvin)
743.45
General information
Molecular weight
279.27g/mol
Molar mass
279.2850g/mol
Density
1.3850g/cm3
Appearence

Disperse Yellow 54 appears as a yellow crystalline powder. It is commonly used as a dye, and its vibrant yellow color is its most distinguishing feature. The compound may exhibit different shades of yellow when diluted or applied in various media.

Comment on solubility

Solubility of 2-[N-(2-hydroxyethyl)-4-(methylamino)-3-nitro-anilino]ethanol

The solubility of 2-[N-(2-hydroxyethyl)-4-(methylamino)-3-nitro-anilino]ethanol can be characterized by a few key factors:

  • Polar Nature: This compound possesses both hydrophilic (water-attracting) and hydrophobic (water-repelling) regions. Its hydroxyethyl and amino groups contribute to its polar characteristics, making it more likely to be soluble in water.
  • Temperature Influence: Like many organic compounds, the solubility of this substance can change with temperature. Typically, increased temperature enhances solubility for solids in liquids.
  • pH Sensitivity: The presence of amino groups may make this compound sensitive to pH changes, affecting its solubility. Under varying pH conditions, the ionization state of the amino group can significantly alter solubility.
  • Solvent Compatibility: While it may exhibit good solubility in polar solvents like water, its solubility in organic solvents can vary. Testing in various solvents is essential for a thorough understanding.

In summary, the solubility of 2-[N-(2-hydroxyethyl)-4-(methylamino)-3-nitro-anilino]ethanol is influenced by its structural attributes and environmental conditions. As quoted by scientists, "Understanding solubility is fundamental to predicting the utility of chemical compounds in various applications.” Therefore, further empirical studies are recommended to fully characterize its solubility profile.

Interesting facts

Interesting Facts about 2-[N-(2-hydroxyethyl)-4-(methylamino)-3-nitro-anilino]ethanol

This intriguing chemical compound represents a blend of functional groups, making it a rich subject of study in medicinal chemistry. One of the most notable aspects of this compound is its potential use in pharmaceutical applications, particularly due to the aniline structure that favors interactions with biological systems. Here are some key points of interest:

  • Structure Complexity: The compound contains an aniline derivative which is central to many biologically active compounds. Its structure is characterized by the presence of a nitro group, a hydroxyethyl moiety, and a methylamino substituent, all contributing to its reactivity and biological properties.
  • Biological Activity: Due to its specific functional groups, it may exhibit various biological activities, including potential antioxidant properties. The presence of the hydroxyethyl group enhances its solubility in biological environments, possibly allowing for better bioavailability.
  • Signal Mimetics: This compound could potentially act as a mimic for biological signals, which can be crucial for developing targeted therapies in drug design. The versatility in its structure allows for various modifications, leading to derivatives that might have improved efficacy.
  • Research Potential: Aspects of this compound are likely to be explored in fields such as chemotherapy and biomedical engineering. The capability to fine-tune the properties of compounds such as these can pave the way for advancements in treating complex diseases.
  • Environmental Considerations: As research on similar compounds progresses, understanding their environmental impact will be essential. Studies on how these chemicals break down and their interactions with ecosystems can lead to safer pharmaceutical practices.

In summary, 2-[N-(2-hydroxyethyl)-4-(methylamino)-3-nitro-anilino]ethanol not only showcases the intricacies of organic synthesis but also highlights the ongoing relationship between chemical structure and biological function. As stated by many chemists, "The structure dictates function," making this compound a fascinating study for researchers seeking to unlock new therapeutic avenues.

Synonyms
HC Blue 1
HC Blue No. 1
2784-94-3
HC Blue Number 1
HC BLUE NO 1
CCRIS 1362
HSDB 4182
NCI-C04159
EINECS 220-495-9
UH430IGW0C
BRN 2134980
2,2'-((4-(Methylamino)-3-nitrophenyl)imino)diethanol
1-Methylamino-2-nitro-4-(bis-2-hydroxyethyl)aminobenzene
Ethanol, 2,2'-((4-(methylamino)-3-nitrophenyl)imino)bis-
Ethanol, 2,2'-((4-(methylamino)-3-nitrophenyl)imino)di-
2,2'-[[4-(METHYLAMINO)-3-NITROPHENYL]IMINO]BISETHANOL
2,2'-((4-(Methylamino)-3-nitrophenyl)imino)bisethanol
DTXSID6020191
N,N-Bis(2-hydroxyethyl)-N'-methyl-3-nitro-p-phenylenediamine
HC BLUE NO. 1 [HSDB]
HC BLUE NO. 1 [IARC]
N',N'-Bis(2-hydroxyethyl)-N-methyl-2-nitro-p-phenylenediamine
N1,N1-Bis(2-hydroxyethyl)-N4-methyl-3-nitro-p-phenylenediamine
p-Phenylenediamine, N,N-bis(2-hydroxyethyl)-N'-methyl-2-nitro-
N-Methyl-amino-2-nitro-4-N',N'-bis-(2-hydroxyethyl)-aminobenzene
2,2'-{[4-(methylamino)-3-nitrophenyl]imino}diethanol
N4,N4-bis(2-hydroxyethyl)-N1-methyl-2-nitro-p-phenylenediamine
HC BLUE NO. 1 (IARC)
Ethanol, 2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bis-
N-methylamino-2-nitro-4-N',N'-bis(2-hydroxyethyl)aminobenzene
N-METHYL-N',N'-BIS(2-HYDROXYETHYL)-2-NITRO-P-PHENYLENEDIAMINE
1-METHYLAMINO-2-NITRO-4-N,N-(BIS-.BETA.-HYDROXYETHYL)AMINOBENZENE
N1-METHYL-N4,N4-BIS(2-HYDROXYETHYL)-2-NITRO-P-PHENYLENEDIAMINE
N4,N4-BIS(2'-HYDROXYETHYL)-N1-METHYL-2-NITRO-P-PHENYLENEDIAMINE
ETHANOL, 2,2'-[[4-(METHYLAMINO)-3-NITROPHENYL]IMINO]DI-
DTXCID20191
1Methylamino2nitro4(bis2hydroxyethyl)aminobenzene
2,2'((4(Methylamino)3nitrophenyl)imino)diethanol
N,NBis(2hydroxyethyl)N'methyl3nitropphenylenediamine
Ethanol, 2,2'((4(methylamino)3nitrophenyl)imino)bis
Ethanol, 2,2'((4(methylamino)3nitrophenyl)imino)di
N',N'Bis(2hydroxyethyl)Nmethyl2nitropphenylenediamine
N1,N1Bis(2hydroxyethyl)N4methyl3nitropphenylenediamine
NMethylamino2nitro4N',N'bis(2hydroxyethyl)aminobenzene
pPhenylenediamine, N,Nbis(2hydroxyethyl)N'methyl2nitro
1-METHYLAMINO-2-NITRO-4-N,N-(BIS-BETA-HYDROXYETHYL)AMINOBENZENE
N,N-BIS(2-HYDROXYETHYL)-N'-METHYL-2-NITRO-P-PHENYLENEDIAMINE
220-495-9
HC blue no.1
HC blue no. 1 (purified)
2-[N-(2-hydroxyethyl)-4-(methylamino)-3-nitroanilino]ethanol
CHEBI:82333
UNII-UH430IGW0C
HC Azul 1
HC Bleu 1
HC Blu 1
CHEMBL259863
SCHEMBL2467623
MWJSMPQOVHQYTE-UHFFFAOYSA-N
NS00020784
C19247
Q27155882
N-METHYLAMINO-2-NITRO-4-N',N'-BIS(2- HYDROXYETHYL)AMINOBENZENE