Propanol

2-Methyl-1-propanol

2-Methyl-1-propanol (Isobutyl alcohol) is widely used organic solvent. Application 2-Methyl-1-propanol (Isobutyl alcohol) may be used to prepare the isobutyl alcohol-benzene solution for use in the quantification of inorganic phosphates.

2-Methyl-1-propanol (Isobutyl alcohol) is widely used organic solvent. Application 2-Methyl-1-propanol (Isobutyl alcohol) may be used to prepare the isobutyl alcohol-benzene solution for use in the quantification of inorganic phosphates.

2-Methyl-1-propanol, also known as isobutyl alcohol, is an aliphatic alcohol. The densities, viscosities and refractive indices of the binary mixtures of diglyme and 2-methyl-1-propanol have been evaluated.

2-Methyl-1-propanol, also known as isobutyl alcohol, is an aliphatic alcohol. The densities, viscosities and refractive indices of the binary mixtures of diglyme and 2-methyl-1-propanol have been evaluated.

Other Notes Butanol concentration of DNA

Other Notes Butanol concentration of DNA

2-Methyl-1-propanol can be obtained via hydroformylation of alkenes with fuel gas mixture in particular, carbon monoxide being the main reactant. 2-Methyl-1-propanol is a potential biofuel, which can be obtained as a major product in the yeast,

2-Methyl-1-propanol can be obtained via hydroformylation of alkenes with fuel gas mixture in particular, carbon monoxide being the main reactant. 2-Methyl-1-propanol is a potential biofuel, which can be obtained as a major product in the yeast,

2-Methyl-1-propanol can be obtained via hydroformylation of alkenes with fuel gas mixture in particular, carbon monoxide being the main reactant. 2-Methyl-1-propanol is a potential biofuel, which can be obtained as a major product in the yeast,

The mass spectra of 2-phenyl-1-propanol was studied by positive- and negative-ion-fast atom bombardment-mass spectrometric ionization technique . Application 2-Phenyl-1-propanol was used to study the synergism between enzyme catalysis and microwave

Application 2-Propanethiol can react with 6-nitroquinoline in the presence of excess sodium hydride to form 5-isopropylthio-6-nitroquinoline as the major product.