Gas-chromatographic determination of the composition of the volatile components of the oleoresins of some species of conifers

Using the method of analytical GLC in a glass capillary column, the compositions have been studied of the volatile fractions of the oleoresins of five species of conifers:Larix decidua,Pinus strobus,Pinus mugo,Picea excelsa, andPinus abies. In the oleoresins 21 monoterpene and 22 sesquiterpene compounds were identified from their relative retention times and with the aid of additives. The main components of the volatile fractions of the oleoresins were α- and β-pinenes and 3-carene among the monoterpenes, and longifolene caryophyllene, δ- and γ-cadinenes and α-murolene among the sesquiterpene compounds. The quantitative analysis of the fractions was carried out by the method of internal normalization from averaged correlation coefficients.     

Neutral diterpenoids of oleoresins of five species of conifers of Transcarpathia

The compositions of the neutral diterpenoids of the oleoresins of five species of conifers growing in the Transcarpathia have been studied. It has been found that the oleoresins ofAbies alba M.,Larix decidua M., andPicea excelsa L. contain more than 50% of neutral diterpenoids. The group and qualitative compositions of the oxygen-containing diterpenoids have been determined. In the oleoresins ofAbies alba,Picea excelsa, andPicea abies tertiary alcohols — cis-abienol and isocembrol — predominate, while inLarix decidua the main component is the hydroxy ester larixyl acetate. Primary alcohols related to the resin acids have been found in all the oleoresins investigated. Features of the distribution of diterpenoids according to the species of conifers have been revealed. The results obtained are necessary for the chemotaxonomy of conifers of the family Pinceae.     

Neutral diterpenoids of oleoresins of five species of conifers of Transcarpathia

The compositions of the neutral diterpenoids of the oleoresins of five species of conifers growing in the Transcarpathia have been studied. It has been found that the oleoresins ofAbies alba M.,Larix decidua M., andPicea excelsa L. contain more than 50% of neutral diterpenoids. The group and qualitative compositions of the oxygen-containing diterpenoids have been determined. In the oleoresins ofAbies alba,Picea excelsa, andPicea abies tertiary alcohols — cis-abienol and isocembrol — predominate, while inLarix decidua the main component is the hydroxy ester larixyl acetate. Primary alcohols related to the resin acids have been found in all the oleoresins investigated. Features of the distribution of diterpenoids according to the species of conifers have been revealed. The results obtained are necessary for the chemotaxonomy of conifers of the family Pinceae.Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Translated from Khimiya Prirodynkh Soedinenii, No. 6, pp. 812–816, November–December, 1988.     

Resin acids of the oleoresins of conifers growing in Transcarpathia

The chemical composition of the resin acids of the oleoresins of five species of the conifers of Transcarpathia has been studied. The oleoresins contain eight resin acids. ^8,9-Isopimaric and anticopalic acids have been found in the acid part of the oleoresin of the Weymouth pine.Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 212–214, March–April, 1987.     

Gas-chromatographic determination of the distribution ratios of volatile substances in gas-liquid systems

Methods for determining the distribution ratios of volatile substances between liquid and gas phases, based on gas-liquid chromatography or gas extraction in systems with constant or variable volume under static or dynamic conditions, are classified and described, and their application fields are indicated.     

Chemical composition and variability of the volatile components from inflorescences of Cirsium species

The present study aimed to investigate the chemical composition of the essential oils of inflorescences Cirsium spp. (Asteraceae) by GC/MS method. Essential oils were extracted from the inflorescences of Cirsium pannonicum (Link), Cirsium ligulare Boiss., Cirsium heterophyllum (L.) Hill., Cirsium acaule (L.) Scop., Cirsium oleraceum (L.) Scop., Cirsium dissectum (L.) Hill., Cirsium decussatum (Janka) and Cirsium eriophorum (L.) Scop., using the steam distillation method. A gas chromatography–mass spectrometry method was employed for the analysis of essential oils. Our study shows the differences in chemical composition of volatile oils in the inflorescences of Cirsium spp. The main components of the essential oil were ketones and aldehydes with a long carbon side-chain. Volatile oils also contained small amounts of terpenes: thymol, β-linalool, eugenol, carvacrol and fatty acids with odd number of carbon atoms–waxes. The compounds in the essential oils obtained from inflorescences Cirsium L. species have been identified for the first time.     

Gas-chromatographic determination of volatile sulfur-containing impurities in industrial emissions and aqueous solutions

Procedures are developed for determining volatile sulfur-containing impurities, hydrogen sulfide, simple mercaptans, sulfides, and disulfides in air and aqueous solutions. The procedures are based on the principle’s headspace gas chromatography and equilibrium preconcentration. The procedures differ from the officially approved ones in that the operations of sampling and sample preparation to gas-chromatographic analysis considerably reduce the loss of hydrogen sulfide and mercaptans unstable in humid air. The procedures provide the determination of sulfur-containing substances at the level of their maximum permissible concentrations (MPC) in industrial emissions and natural waters and the analytical range of four orders of magnitude; they can be implemented on gas chromatographs with flame ionization and flame photometric detectors, a quartz capillary column, and a thermostated gas-sampling valve.     

Gas-chromatographic determination of the components of the catalytic oxidation of ethylene glycol to glyoxal

The gas-chromatographic retention of formaldehyde, acetaldehyde, glyoxal, formic acid, and ethylene glycol on polar and nonpolar polymeric adsorbents was studied, and a procedure was developed for the determination of these components. The time of analysis was 12–14 min. The detection limits were 0.02 (acetaldehyde) to 0.7 (formic acid) ppm.     

Gas-chromatographic determination of selenium

Selenium(IV) is reacted with 2,3-diaminonaphthalene at pH 2 to form the well established complex, which is extracted into hexane. An aliquot of the hexane layer is analyzed gas chromatographically with an electron-capture detector. As little as 510^?10 g of selenium could be detected; 0.01μg of selenium could be determined in a sample by extracting int 0.1 ml of hexane and injecting a 5-μl aliquot of the extract. The method was applied to the determination of physiological amounts of selenium in human blood and urine. Averages of 0.38 p.p.m. and 0.007 p.p.m. selenium were found in blood and urine. respectively. River water samples were also analyzed. Complete analysis time for a single sample is less than 3 h. including time for digestion of the sample and 2 h for formation of the complex.     

Gas-chromatographic determination of mutual solubility of components in heterophase binary systems of organic solvents

A general gas-chromatographic method is proposed for determining mutual solubility of partially miscible organic solvents. The method involves gradual increase of the concentration of one component in the other component in the region below their mutual solubility limit, determining parameters of the linear regression c = aS + b (c is the concentration, and S is the peak area), analysis of saturated solutions of components of binary systems in each other (at S ≈ const), and calculating c values from the obtained equation. The method was tested by known data on mutual solubility of components of the hexane-acetonitrile and hexane-nitromethane binary systems. Data for the hexane-2,2,2-trifluoroethanol and perfluorodecalin-acetonitrile binary systems are obtained for the first time; in the latter case, abnormally low mutual solubility of components is revealed.     

Gas-chromatographic determination of deltamethrin in crops

A rapid and economical method is described for the determination of deltamethrin in wheat, rice, peanuts and corn. It is based on simultaneous extraction and clean-up on a column packed with alumina and silica gel using n-hexane-ethyl ether (8:2, v/v), followed by a derivatization step and gas-chromatographic analysis. Recoveries from fortified cereal and peanut samples were determined at four concentration levels and ranged from 73 to 109%. The detection limits were 0.01 to 0.03 mg/ kg. This method simplifies the traditional procedures in terms of sample size, solvent consumption and analysis time. Received: 25 March 1997 / Revised: 3 June 1997 / Accepted: 4 June 1997     

Gas-chromatographic determination of deltamethrin in crops

A rapid and economical method is described for the determination of deltamethrin in wheat, rice, peanuts and corn. It is based on simultaneous extraction and clean-up on a column packed with alumina and silica gel using n-hexane-ethyl ether (8:2, v/v), followed by a derivatization step and gas-chromatographic analysis. Recoveries from fortified cereal and peanut samples were determined at four concentration levels and ranged from 73 to 109%. The detection limits were 0.01 to 0.03 mg/ kg. This method simplifies the traditional procedures in terms of sample size, solvent consumption and analysis time. Received: 25 March 1997 / Revised: 3 June 1997 / Accepted: 4 June 1997     

Gas-chromatographic determination of the enantiomeric composition of optically active alcohols and amines using achiral bifunctional reagents

A technique for determining the enantiomeric composition of 2-octanol and -phenylethylamine with the use of gas chromatography on optically inactive stationary phases is proposed. The technique is based on the formation of symmetrical diastereomeric derivatives upon the interaction of enantiomers with bifunctional achiral reagents: dimethyldichlorosilane, bromochloromethane, and dibromoethane. The reagents were chosen from the viewpoint of the synthesis of diastereomers with a minimum distance between the chiral centers. This minimum distance is responsible for a difference in the energies of interaction of the derivatives with the stationary liquid phase, which is sufficient for the separation of these derivatives.Translated from Zhurnal Analiticheskoi Khimii, Vol. 60, No. 3, 2005, pp. 297–306.Original Russian Text Copyright © 2005 by Stankov, Sitnikov, Sadovnikov, Sergeeva, Derevyagina, Morozova, Mylova, Kuzmina, Gurenko.     

Gas-chromatographic determination of 1,1-dimethylhydrazine in water

A gas-chromatographic procedure for the determination of 1,1-dimethylhydrazine in water was developed on the basis of its reaction with 4-nitrobenzaldehyde yielding the corresponding hydrazone, the extraction of the latter from water with an organic solvent, its subsequent preconcentration by evaporation, and the determination on a gas chromatograph with a nitrogen-phosphorus detector. The determination limit of 1,1-dimethylhydrazine is 0.03 μg/L. The relative error of the determination is no larger than 22% in the concentration range 0.06–0.60 μg/L and 33% at a level of 0.03 μg/L.     

An investigation by gas liquid chromatography into the composition of the essential oils of some Siberian conifers

Summary Eighteen monoterpene hydrocarbons have been isolated from the essential oils of Siberian species of cedar, larch, and fir. Fourteen components have been identified by gas-liquid chromatography.Khimiya Prirodnykh Soedinenii, Vol. 1, No. 6, pp. 382–384, 1965.