Improved gas chromatographic analysis of fatty and resin acid mixtures with special reference to tall oil

1977 ◽  
Vol 54 (7) ◽  
pp. 289-293 ◽  
Author(s):  
B. Holmbom
Keyword(s):  
Special Reference ◽  
Chromatographic Analysis ◽  
Resin Acid ◽  
Tall Oil ◽  
Gas Chromatographic Analysis

Gas chromatographic analysis of tall oil rosin acids

1965 ◽  
Vol 42 (3) ◽  
pp. 255-256 ◽  
Author(s):  
N. E. Hetman ◽  
H. G. Arlt ◽  
R. Paylor ◽  
R. Feinland
Keyword(s):  
Chromatographic Analysis ◽  
Tall Oil ◽  
Gas Chromatographic Analysis ◽  
Rosin Acids

Gas-chromatographic analysis of tall oil fatty alkyds for monomer and dimer acid content

1968 ◽  
Vol 40 (8) ◽  
pp. 1358-1360 ◽  
Author(s):  
R. A. L. Paylor ◽  
Raymond. Feinland ◽  
N. H. Conroy
Keyword(s):  
Acid Content ◽  
Chromatographic Analysis ◽  
Tall Oil ◽  
Dimer Acid ◽  
Gas Chromatographic Analysis

The mechanism of formation of 2,7-dimethyl-2,6-octadiene in the synthesis of 3-methylene-7-methyl-1,6-octadiene

1983 ◽  
Vol 48 (7) ◽  
pp. 1864-1866
Author(s):  
Jan Bartoň ◽  
Ivan Kmínek
Keyword(s):  
Mass Spectrometry ◽  
Nmr Spectroscopy ◽  
Alkali Metal ◽  
Chromatographic Analysis ◽  
Solid Phase ◽  
Reaction Pathway ◽  
Mechanism Of Formation ◽  
Gas Chromatographic Analysis ◽  
C Nmr ◽  
Visual Observations

2,7-Dimethyl-2,6-octadiene is formed in the catalytic solution for the dimerization of 2-methyl-1,3-butadiene to β-myrcene (3-methylene-7-methyl-1,6-octadiene), as revealed by mass spectrometry and 13C NMR spectroscopy. Visual observations together with the results of gas chromatographic analysis of the catalytic solution suggest that the formation of 2,7-dimethyl-2,6-octadiene is associated with the transition of the alkali metal (sodium) from the solid phase into the solution. A reaction pathway is suggested accounting for the formation of 2,7-dimethyl-2,6-octadiene in the system.

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