Interesting facts
Interesting Facts about Acridine-3,6-Diamine
Acridine-3,6-diamine, also known as 3,6-diaminoacridine, is a fascinating organic compound that has drawn attention in the fields of medicinal chemistry and materials science. Here are some intriguing aspects of this compound:
- Biological Significance: Acridine derivatives, including acridine-3,6-diamine, have been studied for their potential antibacterial and antitumor activities. Their ability to intercalate with DNA can disrupt the duplication process of cancer cells.
- Fluorescent Properties: This compound is known for its fluorescent properties, which makes it useful in biological imaging and as a fluorescent probe in various experimental settings.
- Structure and Reactivity: The unique acridine structure contributes to its reactivity and interaction with various biological systems. Its nitrogen atoms create sites for hydrogen bonding and coordination with metal ions.
- Applications in Dyes: Acridine-3,6-diamine is utilized in the synthesis of dyes and pigments. Its bright colors make it invaluable in the textile industry.
- Potential Complexes: Researchers are exploring acridine-3,6-diamine's ability to form complexes with metal ions, which could lead to advancements in catalysis and materials science.
In the words of a chemist, "Acridine-3,6-diamine stands at the intersection of biology and materials science, showcasing how organic compounds can bridge diverse fields." This compound continues to be a subject of ongoing research, unlocking new perspectives and possibilities in science.
Synonyms
Proflavine
acridine-3,6-diamine
Proflavin
92-62-6
3,6-ACRIDINEDIAMINE
3,6-Diaminoacridine
Isoflav base
Proflavina
Proflavine hemisulfate
Proflavine [INN]
Acridine, 3,6-diamino-
2,8-Diaminoacridinium
Proflavinum
Progarmed
Profura
3,6-Diaminoacridinium
3,7-Diamino-5-azaanthracene
Proflavinum [INN-Latin]
Proflavina [INN-Spanish]
2,8-Diaminoacridine (European)
2,8-Diaminoacridine
Diaminoacridine
CCRIS 1244
HSDB 7071
UNII-CY3RNB3K4T
CY3RNB3K4T
EINECS 202-172-4
BRN 0166050
AI3-52128
PROFLAVINE [MI]
Proflavine (hemisulfate)
PROFLAVINE [HSDB]
PROFLAVINE [VANDF]
PROFLAVINE [WHO-DD]
CHEBI:8452
DTXSID9043776
WDVSHHCDHLJJJR-UHFFFAOYSA-
5-22-11-00322 (Beilstein Handbook Reference)
Proflavinum (INN-Latin)
3,6-Diaminoacridine hemisulfate salt
Proflavina (INN-Spanish)
PRL
Proflavin hemisulfate;3,6-Diaminoacridine hemisulfate
Proflavine hemisulfate salt hydrate
3,6 diaminoacridine
MFCD00149650
3,6-diamino acridine
3,6 Diamino Acridine
NCGC00166245-01
Acridine, 3,6-Diamino
1bcu
1qvt
1qvu
3,6-Acridinediamine hydrochloride
3,6Acridinediamine
3,6Diaminoacridine
3,6-diaminoacridin
MFCD00005030
proflavine-hemisulfate
2,8Diaminoacridinium
3,6Diaminoacridinium
Acridine, 3,6diamino
3,7Diamino5azaanthracene
NCIMech_000209
SCHEMBL27386
AE-562/12222295
CHEMBL55400
2,8Diaminoacridine (European)
Proflavine;3,6-Diaminoacridine
SCHEMBL8149677
YSCH0132
DTXCID7023776
BDBM12590
2v57
AAA53173
ALBB-024962
HY-B1741
STK380650
AKOS005449844
AT13412
CCG-339542
DB01123
NCGC00166245-02
DA-77083
NCI60_004643
NCI60_004767
NCI60_032077
TS-08258
A3219
CS-0013756
NS00008797
S5776
AB00375967-03
AB00375967_04
(6-aminoacridin-3-yl)amine;sulfuric acid;hydrate
Q420454
SR-01000883943
SR-01000883943-1
BRD-K68408467-065-01-8
202-172-4
Solubility of Acridine-3,6-diamine
Acridine-3,6-diamine, with its unique chemical structure, exhibits notable solubility characteristics. Primarily, it can be characterized by its behavior in various solvents:
It is important to note that solubility is highly influenced by temperature, often increasing as the temperature rises. This behavior can lead to interesting applications in biological and pharmaceutical fields where solubility affects bioavailability.
In summary, acridine-3,6-diamine's solubility properties make it a versatile compound for various applications, but care should be taken to consider the solvent choice in practice.