1990
DOI: 10.1016/s0021-9673(01)81487-4
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Gas chromatographic retention indices of monoterpenes and sesquiterpenes on methyl silicon and Carbowax 20M phases

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Cited by 1,986 publications
(726 citation statements)
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“…II apparatus, fitted with a fused silica HP-1 capillary column (30 m x 0.25 mm; 0.33 μm film thickness), coupled to an Agilent Mass Selective Detector MSD 5973; ionization voltage 70 eV; electron multiplier energy 2000 V. Gas chromatographic conditions were as reported above; transfer line temperature, 295 °C. Most constituents were identified through gas chromatography by comparing their retention indices to either those from the literature (Davies, 1990) or with those of authentic compounds available in our laboratories. The retention indices were determined in relation to a homologous series of n-alkanes (C 8 -C 24 ) under the same operating conditions.…”
Section: Plant Materialsmentioning
confidence: 99%
“…II apparatus, fitted with a fused silica HP-1 capillary column (30 m x 0.25 mm; 0.33 μm film thickness), coupled to an Agilent Mass Selective Detector MSD 5973; ionization voltage 70 eV; electron multiplier energy 2000 V. Gas chromatographic conditions were as reported above; transfer line temperature, 295 °C. Most constituents were identified through gas chromatography by comparing their retention indices to either those from the literature (Davies, 1990) or with those of authentic compounds available in our laboratories. The retention indices were determined in relation to a homologous series of n-alkanes (C 8 -C 24 ) under the same operating conditions.…”
Section: Plant Materialsmentioning
confidence: 99%
“…Peak area percent was used for obtaining quantitative data with the HP-Chem Station software (Agilent Technologies) without using correction factors. Identification of the essential oil constituents was performed on the basis of MS library of NIST and Wiley, (Davies 1990 andAdams 1995 …”
Section: Analysis Of Essential Oilsmentioning
confidence: 99%
“…Analytical conditions were as follows: injector and transfer line temperature at 250 and 240 °C, respectively; oven temperature was programmed from 60 to 240 °C at 3 °C min -1 ; carrier gas, helium at 1 ml min -1 ; splitless injection. The identifi cation of the constituents was based on comparison of the retention times with those of authentic samples, comparing their linear retention indices relative to the series of n-hydrocarbons, and on computer matching against commercial (NIST 98 and ADAMS) and home-made library mass spectra built from pure substances and components of known oils and MS literature data (DAVIES, 1990). Moreover, the molecular weights of all the identifi cation substances were confi rmed by GC-CIMS, using MeOH as CI ionising gas.…”
Section: Volatile Compound Analysesmentioning
confidence: 99%