Interesting facts
Interesting Facts about 2,4,6-Trimethylpyridine
2,4,6-Trimethylpyridine, also known as collidine, is a fascinating compound with various applications in both industrial and academic settings. This nitrogen-containing heterocycle is a member of the pyridine family, where the basic structure is enriched with methyl groups at the 2, 4, and 6 positions of the ring. Here are some noteworthy points about 2,4,6-trimethylpyridine:
- Solvent and Reagent: 2,4,6-Trimethylpyridine serves as an excellent solvent and reagent in diverse chemical reactions. Its unique electron-rich nature makes it particularly useful in reactions involving electron-deficient compounds.
- Role in Catalysis: The compound is recognized for its ability to act as a catalyst in various reactions, notably in the synthesis of aromatic compounds and pharmaceutical intermediates. It promotes chemical transformations, enhancing yields and selectivity.
- Chemical Structure: The presence of three methyl groups contributes to its steric and electronic properties, making it quite distinct within the pyridine series. This structural characteristic allows for increased solubility in organic solvents.
- Applications in Industry: Collidine finds its place in the manufacturing of agriculture chemicals, antioxidants, and dyestuffs. Its versatility in chemical processes is a significant advantage in industrial chemistry.
- Biological Insights: Recent studies have shown that some derivatives of collidine exhibit interesting biological properties, including potential antimicrobial activity, prompting further research into its medicinal uses.
- Safety Considerations: Like many organic compounds, 2,4,6-trimethylpyridine should be handled with care, as it can pose health risks if ingested or inhaled. Proper safety protocols should always be observed in the lab.
As explored, 2,4,6-trimethylpyridine is more than just a simple chemical compound—it is a crucial player in various scientific fields, pushing the boundaries of what is achievable through organic chemistry. Its blend of industrial relevance and intriguing chemical behavior makes it a compound worth studying.
Synonyms
2,4,6-Trimethylpyridine
108-75-8
2,4,6-COLLIDINE
s-Collidine
gamma-Collidine
Pyridine, 2,4,6-trimethyl-
COLLIDINE
sym-Collidine
.gamma.-Collidine
2,4,6-trimethyl-pyridine
2,4,6-Kollidin
HSDB 57
NSC 460
UNII-7IE4BK5J5V
2,4,6-trimethyl pyridine
EINECS 203-613-3
MFCD00006338
BRN 0107283
AI3-10050
NSC-460
.alpha.,.gamma.,.alpha.'-Collidine
7IE4BK5J5V
CHEMBL1209580
DTXSID1051561
2,4,6-COLLIDINE [HSDB]
5-20-06-00093 (Beilstein Handbook Reference)
2,4,6-TRIMETHYLPYRIDINE [MI]
2,4,6-Collidine (2,4,6-Trimethylpyridine)
2,4,6-Kollidin [Czech]
alpha,gamma,alpha'-Collidine
2,4,6 Trimethylpyridine
collidin
2,4,6 COLLIDINE
gammaCollidine
sCollidine
2,4,6Kollidin
2,4,6-collidin
2,4,6-Collinine
2,4,6- collidine
2,4,6trimethylpyridine
2,4,6-trimethypyridine
Pyridine,4,6-trimethyl-
2,4,6-tri-methylpyridine
alpha,gamma,alpha'Collidine
2,4,6-Trimethylpyridinium
Pyridine, 2,4,6trimethyl
SCHEMBL7489
NCIOpen2_009389
pyridine, 2,4,6-trimethyl
.alpha.,.alpha.'-Collidine
2,4,6-Collidine;s-Collidine
NSC460
DTXCID5030113
CHEBI:189131
STR03652
BDBM50416505
STL146741
AKOS000119121
CS-W018506
PS-5252
SB52289
BP-30156
DB-015912
NS00014381
T0716
2,4,6-Trimethylpyridine, >=98.0% (GC)
EN300-19114
D77846
2,4,6-Trimethylpyridine, ReagentPlus(R), 99%
Q409155
2,4,6-Trimethylpyridine, Vetec(TM) reagent grade, 98%
F0001-0178
Z104472822
2,4,6-Trimethylpyridine, puriss. p.a., >=99.0% (GC)
203-613-3
Solubility of 2,4,6-Trimethylpyridine
2,4,6-trimethylpyridine, with the chemical formula C9H11N, exhibits unique solubility characteristics that are important for its applications in various chemical processes. This compound is known to be a pyridine derivative, which influences its interactions with different solvents.
The solubility profile of 2,4,6-trimethylpyridine can be summarized as follows:
2,4,6-trimethylpyridine's moderate solubility in water coupled with its high solubility in organic solvents makes it an interesting compound for synthesis and reaction environments. As noted, the distinctive structure of this compound allows it to act effectively within various chemical frameworks, thus highlighting the importance of understanding solubility in the context of its utility in chemistry.
In summary, “the choice of solvent can significantly impact the behavior of 2,4,6-trimethylpyridine in chemical processes”, making a thorough understanding of its solubility essential for optimizing experimental conditions.