1960
DOI: 10.1071/ch9600498
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Sugar-Cane Wax. II. An Examination of the Constituents of Sugar-Cane Cuticle Wax by Gas Chromatography

Abstract: Sugar-cane cuticle wax previously found to consist of long-chain aldehydes, alcohols, acids, and hydrocarbons (Lamberton and Redcliffe 1960) has been re-examined by gas chromatography to identify and estimate the individual constituents. The aldehydes, alcohols, and acids, all straight chain, are principally of even carbon number in each instance with the C28 member predominant, but appreciable amounts of odd carbon homologues are also present. The hydrocarbons are also of odd and even carbon number but with t… Show more

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Cited by 45 publications
(8 citation statements)
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“…The significant amounts of even alkanes C 24 (10.1%), C 26 (13.1%) and C 28 (6.4 %) can be pointed out. These values are in agreement with literature for sugarcane cuticle waxes [6].Free n-fatty acids [(fraction V; 8.2% in crude wax, R f 0.32 (CH 2 Cl 2 /AcOEt:7/3)], fatty acid esters [fraction II; R f 0.85 (heptane/CH 2 Cl 2 :5/5) FAE -4%, ketosteroids -2%], and triglycerides [fraction III; 2.4%, R f 0.8 (CH 2 Cl 2 )] were isolated from the waxy material and identified by NMR. Their compositions were determined by GC after transmethylation (triglycerides) or GC/MS (free fatty acids and esters) ( Table 2).…”
supporting
confidence: 93%
“…The significant amounts of even alkanes C 24 (10.1%), C 26 (13.1%) and C 28 (6.4 %) can be pointed out. These values are in agreement with literature for sugarcane cuticle waxes [6].Free n-fatty acids [(fraction V; 8.2% in crude wax, R f 0.32 (CH 2 Cl 2 /AcOEt:7/3)], fatty acid esters [fraction II; R f 0.85 (heptane/CH 2 Cl 2 :5/5) FAE -4%, ketosteroids -2%], and triglycerides [fraction III; 2.4%, R f 0.8 (CH 2 Cl 2 )] were isolated from the waxy material and identified by NMR. Their compositions were determined by GC after transmethylation (triglycerides) or GC/MS (free fatty acids and esters) ( Table 2).…”
supporting
confidence: 93%
“…Analysis of the chain length composition of these methyl esters as well as of the aldehydes was accomplished using a Varian Aerograph Model 1700 Gas Chromatograph with flame ionization detectors coupled with an Infotronics Model CRS-100 digital Isothermal and programmed chromatograms were run using column temperatures from 140 to 290°C and nitrogen, helium and air streams adjusted to yield optimum separations. The chain length of the aldehydes was established using internal standards isolated from sugar cane wax [6].…”
Section: Methodsmentioning
confidence: 99%
“…Reduction of the dimethyl esters with lithium aluminium hydride gave diols, m.p. 95-97 "C, w-hich were converted into hydrocarbons by methods which hare been described previously (Downing, Kranz, and Murray Kranz et al 1960). The conditions used in the gas chromatographic separations and the basis for identification of the hydrocarbons have been fully described in the papers cited immediately above.…”
Section: Methodsmentioning
confidence: 99%