235946
Tetramethylammonium iodide
99%
Sinonimo/i:
N,N,N-trimethyl-methanaminium iodide, TMAI
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About This Item
Prodotti consigliati
Livello qualitativo
Saggio
99%
Stato
solid
Punto di fusione
>300 °C (lit.)
Stringa SMILE
[I-].C[N+](C)(C)C
InChI
1S/C4H12N.HI/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
RXMRGBVLCSYIBO-UHFFFAOYSA-M
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Categorie correlate
Applicazioni
Facile iodination of aromatic compounds including anilines, acids and alcohols.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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The Journal of organic chemistry, 67(24), 8622-8624 (2002-11-26)
Tetramethylammonium dichloroiodate (1, TMADCI) as a mild and efficient iodination reagent was prepared. Iodination of different aromatic compounds with this reagent takes place fast and with high yields under solvent-free conditions.
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A simple and low-cost colorimetric assay utilizing ferrofluidic nanoparticulate probes (FNPs) and a ligase for single-nucleotide polymorphism genotyping is described. Excellent sensitivity and selectivity were accomplished through the engagement of the FNPs and a ligase chain reaction.
The Journal of biological chemistry, 288(52), 37289-37295 (2013-11-15)
Metabolic profiling and structural elucidation of novel secondary metabolites obtained from derived deletion strains of the filamentous fungus Penicillium chrysogenum were used to reassign various previously ascribed synthetase genes of the roquefortine/meleagrin pathway to their corresponding products. Next to the
Proceedings of the National Academy of Sciences of the United States of America, 111(13), E1176-E1181 (2014-03-19)
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