Interesting facts
Interesting Facts about 3-Phenylazopyridine-2,6-diamine
3-Phenylazopyridine-2,6-diamine, also known as a distinctive azo compound, belongs to a class of organic chemicals characterized by the presence of an azo group (–N=N–) which is responsible for its vibrant color and diverse applications. Here are some intriguing facts about this compound:
- Dyes and Pigments: The azo group allows 3-phenylazopyridine-2,6-diamine to be employed in the synthesis of dyes, particularly in the textile industry, where vivid colors are paramount.
- Biological Significance: Azo compounds have been studied for their potential biological activities, including anti-cancer and anti-inflammatory properties, making them interesting candidates for medicinal chemistry.
- Versatile Reactions: Its structure enables various chemical reactions, including substitution and coupling reactions, that can form more complex molecules.
- Photochemical Applications: Azo compounds are known for their ability to undergo photoisomerization, a process that changes the structure of the compound upon exposure to light, making them useful in smart materials and light-responsive systems.
3-Phenylazopyridine-2,6-diamine stands out not only for its unique structure but also for the broad range of applications it finds across different fields—including textiles, pharmaceuticals, and materials science. As scientists continue to investigate its properties, we may uncover even more groundbreaking uses for this fascinating compound in the future.
Synonyms
phenazopyridine
94-78-0
Gastracid
3-(Phenylazo)-2,6-pyridinediamine
Fenazopiridina
Pyrazofen
Pyridiate
2,6-Pyridinediamine, 3-(phenylazo)-
Gastrotest
2,6-Diamino-3-phenylazopyridine
2,6-Diamino-3-(phenylazo)pyridine
Pyridacil
Phenazopyridinum
3-phenyldiazenylpyridine-2,6-diamine
3-[(E)-phenyldiazenyl]pyridine-2,6-diamine hydrochloride
Uridinal
NSC 145895
Baridium
Urogesic
NSC-145895
3-(phenyldiazenyl)pyridine-2,6-diamine
Pyridine, 2,6-diamino-3-(phenylazo)-
K2J09EMJ52
Geridium
Viridium
CHEBI:71416
Gastracid;Gastrotest;NSC 145895
Pirid (Salt/Mix)
Sedural (Salt/Mix)
Urodine (Salt/Mix)
Diridone (Salt/Mix)
Nefrecil (Salt/Mix)
Suladyne (Salt/Mix)
Uridinal (Salt/Mix)
Di-Azo (Salt/Mix)
Mallofeen (Salt/Mix)
Phenazopyridine (INN)
Pyridacil (Salt/Mix)
Eridium
Mallophene (Salt/Mix)
Pyrazodine (Salt/Mix)
Phenazodine (Salt/Mix)
NC 150 (Salt/Mix)
W 1655 (Salt/Mix)
PHENAZOPYRIDINE [INN]
3-Phenylazo-2,6-pyridinediamine
Phenazopyridine [INN:BAN]
Fenazopiridina [INN-Spanish]
Phenazopyridinum [INN-Latin]
3-[Phenyldiazenyl]-2,6-pyridinediamine #
HSDB 3153
NCGC00018130-04
CAS-136-40-3
EINECS 202-363-2
BRN 0184497
UNII-K2J09EMJ52
Phenylazo tablet
Fenazopiridina (TN)
Spectrum_001013
starbld0000241
2, 3-(phenylazo)-
Prestwick0_000752
Prestwick1_000752
Prestwick2_000752
Prestwick3_000752
Spectrum2_000017
Spectrum3_000544
Spectrum4_000474
Spectrum5_001403
3-(2-phenyldiazen-1-yl)pyridine-2,6-diamine
CHEMBL1242
PHENAZOPYRIDINE [MI]
BSPBio_000764
BSPBio_002187
KBioGR_000948
KBioSS_001493
5-22-14-00711 (Beilstein Handbook Reference)
DivK1c_000811
PHENAZOPYRIDINE [HSDB]
SCHEMBL253232
SPBio_000053
SPBio_002703
PHENAZOPYRIDINE [VANDF]
BPBio1_000842
GTPL7616
CHEMBL1355537
CHEMBL1625467
DTXSID1023445
PHENAZOPYRIDINE [WHO-DD]
SCHEMBL14340038
HY-B0985A
KBio1_000811
KBio2_001493
KBio2_004061
KBio2_006629
KBio3_001687
WLN: T6NJ BZ CNUNR& FZ
NINDS_000811
QPFYXYFORQJZEC-FOCLMDBBSA-N
BDBM430637
HMS3604J12
ALBB-023228
Pyridine,6-diamino-3-(phenylazo)-
BDBM50420356
NSC145895
AKOS003343059
AKOS028108443
DB01438
IDI1_000811
3-[(E)-phenylazo]pyridine-2,6-diamine
NCGC00016402-01
NCGC00018130-01
NCGC00018130-02
NCGC00018130-03
NCGC00018130-05
NCGC00018130-06
NCGC00018130-08
NCGC00091334-04
2,6-Diamino-3-phenylazopyridine, (3E)
AC-13546
DA-49478
SBI-0051479.P003
2,6-Pyridinediamine, 3-[(E)-phenylazo]-
3-[(E)-phenyldiazenyl]pyridine-2,6-diamine
CS-0013734
NS00005304
C07429
D08346
G77928
AB00053519_06
AB00053519_07
EN300-7477352
2,6-pyridinediamine, 3-(phenylazo)-, hydrochloride
Q3114549
BRD-K76304753-003-05-4
BRD-K76304753-003-08-8
BRD-K76304753-003-19-5
BRD-K76304753-003-20-3
BRD-K76304753-003-21-1
Solubility of 3-phenylazopyridine-2,6-diamine (C11H11N5)
The solubility of 3-phenylazopyridine-2,6-diamine in various solvents can be quite intriguing due to its unique chemical structure. This compound contains both aromatic rings and amine groups, which play a significant role in its solubility characteristics.
Factors Affecting Solubility
Several factors influence the solubility of this compound:
Practical Observations
In practical terms, you may find that:
In summary, the solubility of 3-phenylazopyridine-2,6-diamine is greatly affected by the choice of solvent, temperature, and intermolecular interactions. Understanding these aspects is crucial for applications in various chemical processes and formulations.