Bromperidol decanoate

Application 1-Decanol was used to study the thermal properties of polymer-monolithic stationary phases .

Application 1-Decanol was used to study the thermal properties of polymer-monolithic stationary phases .

The interaction of 1-decanol with nanosilicas and silica gels were analyzed using differential scanning calorimetry (DSC) and thermoporometry . Application 1-Decanol was used as an extraction solvent in the determination of several toxic phenolic

Application 10-Bromo-1-decanol was used in the synthesis of (11 Z ,13 Z )-11,13-hexadecadienal, the female sex pheromone of the navel orangeworm ( Amyelois transitella ).

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Analysis Note Assay (GC, area%): &#8805 95.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

2-Hexyl-1-decanol is a branched alcohol. It is one of the constituent of the essential oil, extracted from the roots of Adiantum flabellulatum .

2-Hexyl-1-decanol is a branched alcohol. It is one of the constituent of the essential oil, extracted from the roots of Adiantum flabellulatum .

Reaction between 3-bromo-1-propanol, phenol and a series of phenols having substituents in 4-position has been studied in micellar media and in microemulsions based on cationic or a nonionic surfactant . 3-Bromo-1-propanol is an electrophile used

Reaction between 3-bromo-1-propanol, phenol and a series of phenols having substituents in 4-position has been studied in micellar media and in microemulsions based on cationic or a nonionic surfactant . 3-Bromo-1-propanol is an electrophile used

Reaction between 3-bromo-1-propanol, phenol and a series of phenols having substituents in 4-position has been studied in micellar media and in microemulsions based on cationic or a nonionic surfactant . 3-Bromo-1-propanol is an electrophile used

Application 3-Bromo-2-butanone can be used as a reactant to synthesize: N -(4,5-Dimethyl-1 H -imidazol-2-yl)acetamide by reacting with N -acetylguanidine under acidic conditions. Oxazole derivatives by silver triflate catalyzed cyclization reaction