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2,7-Dimethylacridine-3,6-diamine hydrochloride

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Identification
Molecular formula
C15H16N3 · HCl
CAS number
70357-78-5
IUPAC name
2,7-dimethylacridine-3,6-diamine;hydrochloride
State
State
The compound is solid at room temperature. It may be hygroscopic and should be stored in a tightly sealed container.
Melting point (Celsius)
257.00
Melting point (Kelvin)
530.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
280.80g/mol
Molar mass
280.7990g/mol
Density
1.1800g/cm3
Appearence

The compound typically appears as an off-white to pale yellow solid, depending on the level of purity and specific crystal formation. It is usually supplied in crystalline form.

Comment on solubility

Solubility of 2,7-Dimethylacridine-3,6-diamine; Hydrochloride

The solubility of 2,7-dimethylacridine-3,6-diamine; hydrochloride can be quite intriguing due to its unique structural properties. This compound, a salt formed by the reaction of the base with hydrochloric acid, typically exhibits the following characteristics:

  • Water Solubility: Generally soluble in water due to the presence of the hydrochloride group, enhancing ionic interactions.
  • Solvent Compatibility: May also dissolve in polar organic solvents, though less effectively than in water, highlighting the significance of the charged ammonium group.
  • Temperature Dependence: Solubility can be affected by temperature; solubility usually increases at higher temperatures.
  • pH Influence: Being a salt, its solubility can be influenced by the pH of the solution, especially in the presence of other competing ions or acids.

As a result, understanding the solubility profile of 2,7-dimethylacridine-3,6-diamine; hydrochloride is essential for its applications in various chemical processes. The ability to manipulate its solubility properties can lead to more effective formulations and reactions, making it a compound of interest in both research and industry.

Interesting facts

Interesting Facts about 2,7-Dimethylacridine-3,6-Diamine; Hydrochloride

The compound 2,7-dimethylacridine-3,6-diamine; hydrochloride is an intriguing member of the acridine family, a class of compounds known for their diverse biological activities and applications in pharmaceuticals. Here are some compelling insights about this compound:

  • Structural Diversity: Acridines, including this compound, possess a unique tricyclic aromatic structure that contributes to their stability and reactivity. The presence of methyl groups at the 2 and 7 positions enhances its lipophilicity, which can affect its interaction with biological membranes.
  • Biological Relevance: Compounds like 2,7-dimethylacridine-3,6-diamine have been studied for their potential in medicinal chemistry. They exhibit a range of activities such as antimicrobial, antitumor, and anti-inflammatory effects, making them valuable in drug development.
  • Research Applications: The hydrochloride salt form is commonly used in research, as it enhances solubility in water. This property allows scientists to explore its reactivity and applications in biological assays more effectively.
  • Fluorescent Properties: Acridine derivatives often display interesting photophysical properties. Some studies indicate that these compounds can act as fluorescent probes, potentially serving as markers in biological systems or in environmental monitoring.
  • Historical Context: The exploration of acridine derivatives dates back to the late 19th century when they were initially isolated from coal tar. Since then, they have garnered attention due to their effectiveness and versatility in a wide array of scientific fields.

In summary, 2,7-dimethylacridine-3,6-diamine; hydrochloride exemplifies the significant role that acridine derivatives play in scientific research, particularly in pharmacology and organic chemistry. Its unique structure and properties pave the way for exciting discoveries in medicine and beyond.

Synonyms
Acridine Yellow G
135-49-9
Acridine Yellow
Basic Yellow K
Acridine yellow H107
ci 46025
CCRIS 1202
acridine yellow hydrochloride
EINECS 205-194-2
3,6-Acridinediamine, 2,7-dimethyl-, monohydrochloride
NSC 13973
2,7-dimethylacridine-3,6-diamine hydrochloride
3,6-Diamino-2,7-dimethylacridine hydrochloride
UNII-V0923J4F9K
2,7-Dimethylacridin-3,6-yldiamine hydrochloride
V0923J4F9K
MFCD00012661
NSC-13973
2,7-Dimethyl-3,6-acridinediamine monohydrochloride
NSC13973
DTXSID2059649
CHEBI:51742
ACRIDINE, 3,6-DIAMINO-2,7-DIMETHYL-, MONOHYDROCHLORIDE
3,6-Acridinediamine, 2,7-dimethyl-, hydrochloride (1:1)
C.I. 46025
2,8-diamino-3,7-dimethylacridine hydrochloride
3,6-Diamino-2,7-dimethylacridine monohydrochloride
EINECS 202-141-5
BRN 0201478
AI3-52489
5-22-11-00340 (Beilstein Handbook Reference)
ACRIDINEYELLOW
Acridine Yellow G (C.I. 46025)
3,6-Acridinediamine,2,7-dimethyl-, hydrochloride (1:1)
SCHEMBL68756
SCHEMBL607918
CHEMBL1985453
DTXCID9034282
BGLGAKMTYHWWKW-UHFFFAOYSA-N
MIVVOLJUKZMTIN-UHFFFAOYSA-N
Diamondphosphin (Acridin yellow G)
3,7-dimethylacridine, hydrochloride
HY-D0956
3, 2,7-dimethyl-, monohydrochloride
AKOS015916500
3,6-acridinediamine, 2,7-dimethyl-,
Acridine Yellow G, Dye content 90 %
AS-85609
DB-042292
CS-0022144
2,7-dimethylacridine-3,6-diaminehydrochloride
2,7-dimethylacridine-3,6-diamine;hydrochloride
G84002
Acridine,6-diamino-2,7-dimethyl-, monohydrochloride
Q23054729
3,6-Acridinediamine,2,7-dimethyl-,hydrochloride(1:1)