Interesting facts
Interesting Facts About Tris(4-Aminophenyl)methanol
Tris(4-aminophenyl)methanol, often abbreviated as TAPM, is a fascinating compound that captivates the attention of chemists and material scientists alike. Here are some intriguing aspects of this compound:
- Versatile Applications: Due to its unique structure, TAPM is utilized in various fields, ranging from organic electronics to polymer science. It serves as a potential component in the fabrication of conductive polymers and may contribute to advancements in electronic devices.
- Potential in Drug Development: The amino groups in TAPM make it a prospective candidate for drug development, particularly in creating novel pharmaceuticals with targeted therapeutic properties.
- Research Interest: TAPM has gained research interest for its ability to form hydrogen bonds, which play a crucial role in stabilizing molecular structures. The study of its intermolecular interactions is a valuable area of exploration in supramolecular chemistry.
- Colorimetric Applications: Due to its phenyl groups, this compound can undergo various reactions that make it useful in colorimetric assays, enhancing the detection of specific analytes.
- Eco-Friendly Chemistry: The synthesis of TAPM does not typically involve hazardous reagents, making it an excellent example of sustainable chemistry practices aimed at reducing environmental impact.
In summary, tris(4-aminophenyl)methanol is not just an ordinary chemical compound. Its myriad applications and research potential position it as a significant subject in the ever-expanding fields of chemistry and materials science. As researchers continue to uncover the capabilities of TAPM, its contributions could transform various industries, highlighting the importance of studying chemical compounds with unique structures.
Synonyms
Pararosaniline base
Tris(4-aminophenyl)methanol
TRIS(P-AMINOPHENYL)METHANOL
Fuchsin dye base
Parafuchsin carbinol
Tris (4-aminophenyl) carbinol
Methanol, tris(4-aminophenyl)-
Benzenemethanol, 4-amino-.alpha.,.alpha.-bis(4-aminophenyl)-
4,4',4''-Triaminotrityl alcohol
25620-78-4
4,4',4''-Triaminotriphenylcarbinol
UNII-5YB58864V4
HSDB 6128
EINECS 207-395-0
5YB58864V4
Benzenemethanol, 4-amino-alpha,alpha-bis(4-aminophenyl)-
DTXSID7060049
METHANOL, TRIS(P-AMINOPHENYL)-
TRIS(P-AMINOPHENYL)METHANOL [HSDB]
Methanol, tris(4aminophenyl)
Tris (4aminophenyl) carbinol
DTXCID9040502
4,4',4''Triaminotriphenylcarbinol
Benzenemethanol, 4aminoalpha,alphabis(4aminophenyl)
krvruayunoqmov-uhfffaoysa-n
467-62-9
CI 42500
Ci42500
MFCD00036222
Parafuchsin Carbinol; 4-Amino-a,a-bis(4-aminophenyl)benzenemethanol; Tris(4-aminophenyl)methanol; Tris(p-aminophenyl)methanol
Parafuchsin;Paramagenta
tris-(4-aminophenyl)methanol
SCHEMBL301882
Tris(4-aminophenyl)methanol #
CHEMBL119866
Pararosaniline Base, crystalline
STL483083
AKOS024282610
FP52727
HY-W140934
Pararosaniline Base, Dye content 95 %
triphenylcarbinol, 4,4',4''-triamino-
AS-56029
BENZENAMINE,4-[(4-AMINOPHENYL)(4-IMINO-2,5-CYCLOHEXADIEN-1-YLIDENE)METHYL]-, CONJUGATE ACID(1:1)
SY052067
CS-0199432
NS00031634
P0021
D78473
EN300-323064
Q27263046
Z2574927324
Solubility of tris(4-aminophenyl)methanol
Tris(4-aminophenyl)methanol is an intriguing compound when it comes to its solubility characteristics. Being a phenolic compound, its solubility can be influenced by several factors including polarity, intermolecular interactions, and the presence of functional groups. Here are some key points to consider:
In conclusion, tris(4-aminophenyl)methanol displays appreciable solubility in water enabled by its polar nature and the ability to engage in hydrogen bonding, highlighting its functional potential in various chemical applications.