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Aminacrine Lactate

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Identification
Molecular formula
C17H17N3O·C3H6O3
CAS number
9001-45-0
IUPAC name
7-ethoxyacridine-3,9-diamine;2-hydroxypropanoic acid
State
State

At room temperature, aminacrine lactate is typically a solid.

Melting point (Celsius)
243.00
Melting point (Kelvin)
516.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
352.40g/mol
Molar mass
352.4010g/mol
Density
1.3000g/cm3
Appearence

Aminacrine lactate appears as a yellow crystalline solid. It is known for its bright yellow crystalline form when in a pure state.

Comment on solubility

Solubility of 7-ethoxyacridine-3,9-diamine and 2-hydroxypropanoic acid

The solubility characteristics of the compound comprising 7-ethoxyacridine-3,9-diamine and 2-hydroxypropanoic acid present an interesting study in molecular interactions. Here’s a closer look at the solubility of both components:

7-ethoxyacridine-3,9-diamine

  • Moderate solubility in polar solvents, such as water, due to the presence of amino groups that can form hydrogen bonds.
  • Lower solubility in non-polar solvents, as the ethoxy group adds hydrophobic character.
  • The interaction of the acridine moiety with other compounds can further influence solubility, making it dependent on the specific environment.

2-hydroxypropanoic acid

  • Highly soluble in water, attributed to its hydroxyl group which promotes hydrogen bonding.
  • Good solubility in a variety of alcohols, enhancing its functional versatility.
  • Low solubility in non-polar solvents, consistent with carboxylic acids.

In summary, the solubility of this compound can be viewed as a complex interplay of structural features and solvent interactions. As stated, “Solubility is not only about the chemical nature of the compounds but also about the **environmental conditions** and **solvent choices**.” Understanding these factors is essential in predicting the behavior of compounds in various applications.

Interesting facts

Interesting Facts about 7-Ethoxyacridine-3,9-diamine; 2-Hydroxypropanoic Acid

7-Ethoxyacridine-3,9-diamine is a fascinating compound resulting from the combination of ethoxyacridine and diamine functionalities, while 2-hydroxypropanoic acid, commonly known as lactic acid, plays a supporting role. Here are some captivating aspects about these compounds:

1. Dual Nature

  • 7-Ethoxyacridine-3,9-diamine: This compound is noteworthy for its unique structure which may contribute to potential applications in the realm of pharmaceuticals and organic electronics.
  • 2-Hydroxypropanoic Acid: A crucial metabolite in various biological systems, lactic acid is produced during anaerobic respiration and is significant in muscle metabolism.

2. Applications in Medicine

The dual properties of these compounds can lead to intriguing applications:

  • Potential use in drug development due to the inherent bioactivity of the acridine moiety.
  • In the case of lactic acid, its role in biochemistry makes it a subject of interest in fields such as sports medicine and nutrition.

3. Environmental Relevance

Lactic acid, derived from renewable resources, aligns with the growing trend towards sustainable chemistry. Its biodegradability enhances its appeal as a green solvent and a precursor for the synthesis of biodegradable polymers.

4. Chemical Versatility

The functionality of both compounds opens doors to synthetic chemistry explorations, leading to:

  • New derivatives that exhibit enhanced properties for specific applications.
  • Studies on how molecular interactions can impact reactivity and stability.

In conclusion, the combination of 7-ethoxyacridine-3,9-diamine and 2-hydroxypropanoic acid not only highlights the essence of compound diversity but also underscores the multifaceted roles that chemical compounds play in biological and synthetic realms. The study of these compounds is an enriching journey for any chemistry enthusiast!

Synonyms
ETHACRIDINE LACTATE
1837-57-6
acrinol
Rivanol
Acrolactine
Rivinol
6,9-Diamino-2-ethoxyacridine lactate
Flavitrol
Hectalin
Amoebin
Akron
7-ethoxyacridine-3,9-diamine 2-hydroxypropanoate
Metifex
Antidiar 200
Rimaon
Vucine
Ethacridine (lactate)
2-Ethoxy-6,9-diaminoacridine lactate
NSC 36333
TCMDC-123983
2,5-Diamino-7-ethoxyacridine lactate
2-Ethoxy-6,9-diaminoacridinium lactate
3,9-Diamino-7-ethoxyacridinium lactate
Acrinolum
CHEBI:31172
NSC-36333
7T7T2I9823
ETHACRIDINE LACTATE ANHYDROUS
CCRIS 5165
NCGC00096056-02
EINECS 217-408-1
Acridine, 6,9-diamino-2-ethoxy-, lactate
2-Aethoxy-6,9-diaminoacridinlactat [German]
UNII-7T7T2I9823
Acridine, 6,9-diamino-2-ethoxy-, monolactate
2-Aethoxy-6,9-diaminoacridinlactat
Propanoic acid, 2-hydroxy-, compd. with 7-ethoxy-3,9-acridinediamine (1:1); 6,9-Diamino-2-ethoxyacridine lactate; Lactic acid compd. with 6,9-diamino-2-ethoxyacridine (1:1); 7-Ethoxy-3,9-acridinediamine 2-hydroxypropanoate (1:1); 6,9-Diamino-2-ethoxyacrid
Antidian 200
MFCD00013149
6,9-Acridinediamine, 2-ethoxy-, 2-hydroxypropanoate (1:1)
SCHEMBL138154
SPECTRUM1505168
CHEMBL582355
DTXSID10872472
IYLLULUTZPKQBW-UHFFFAOYSA-N
HMS3264O11
Pharmakon1600-01505168
BCP10467
HY-B2174
NSC36333
ETHACRIDINE LACTATE [WHO-DD]
NSC758932
s4945
AKOS015896231
Acridine,9-diamino-2-ethoxy-, lactate
CCG-213965
CS-7625
KS-5135
NSC-758932
WLN: T C666 BNJ EZ IZ LO2
NCGC00096056-01
Acridine,9-diamino-2-ethoxy-, monolactate
7-ethoxy-3,9-acridinediamine, lactate salt
DB-044505
(+/-)-ETHACRIDINE LACTATE ANHYDROUS
6, 2-ethoxy-, 2-hydroxypropanoate (1:1)
A0136
NS00093573
SJ000012756
D81748
ETHACRIDINE LACTATE ANHYDROUS, (+/-)-
Lactic acid,9-diamino-2-ethoxyacridine (1:1)
Q426220
SR-01000872749
SR-01000872749-1
7-ethoxyacridine-3,9-diamine;2-hydroxypropanoic acid
Acridine,9-diamino-2-ethoxy-, cpd with lactic acid (1:1)
Acrino;Acrolactine;NSC 36333; NSC-36333; NSC36333