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Tobacco leaf

C4H N. Almost colourless, ammonia-like liquid, b.p. 88-89 C, which fumes in air. Strong base. It occurs naturally in tobacco leaves, but is made industrially by hydrogenation of pyrrole. [Pg.336]

The leaves and fruit of many plants bear a waxy coating made up of alkanes that prevents loss of water In addition to being present m beeswax (see Problem 2 6) hen triacontane CH3(CH2)29CH3 is a component of the wax of tobacco leaves... [Pg.80]

Additional commercial processes are available for extraction of tea, hops, oriental herbs, tobacco leaves, and pharmaceuticals C02-enhanced oil recovery environmental appHcations such as extraction/flocculation of aqueous wastes reactions with iategrated separations such as aminations (ethylene... [Pg.225]

Ethers, esters, amides and imidazolidines containing an epithio group are said to be effective in enhancing the antiwear and extreme pressure peiformance of lubricants. Other uses of thiiranes are as follows fuel gas odorant (2-methylthiirane), improvement of antistatic and wetting properties of fibers and films [poly(ethyleneglycol) ethers of 2-hydroxymethyl thiirane], inhibition of alkene metathesis (2-methylthiirane), stabilizers for poly(thiirane) (halogen adducts of thiiranes), enhancement of respiration of tobacco leaves (thiirane), tobacco additives to reduce nicotine and to reduce phenol levels in smoke [2-(methoxymethyl)thiirane], stabilizers for trichloroethylene and 1,1,1-trichloroethane (2-methylthiirane, 2-hydroxymethylthiirane) and stabilizers for organic compounds (0,0-dialkyldithiophosphate esters of 2-mercaptomethylthiirane). The product of the reaction of aniline with thiirane is reported to be useful in the flotation of zinc sulfide. [Pg.184]

B Nicotine is a diamino compound isolated from dried tobacco leaves. Nicotine has two rings and M + = 162.1157 by high-resolution mass spectrometry. Give a molecular formula for nicotine, and calculate the number of double bonds. [Pg.435]

Acetaldehyle, CH3CHO, occurs naturally in oak and tobacco leaves, and also is present in automobile and diesel exhaust. The initial rate of decomposition of acetaldehyde at 600°C... [Pg.289]

It should be borne in mind that although it is possible to generalise on sampling procedures, all industries have their own established methods for obtaining a record of the quantity and/or quality of their products. The sampling procedures for tobacco leaves will obviously differ from those used for bales of cotton or for coal. But although the types of samples differ considerably the actual analytical methods used later are of general application. [Pg.155]

Solanesol and other prenyl alcohols are important as metabolites in mulberry and tobacco leaves and in the synthesis of isoprenoid quinones. Hence, Sato and collaborators107 have developed a stereoselective synthesis of all-trans-polyprenol alcohols up to C50. Construction of the requisite skeletons was accomplished by the alkylation of a p-toluenesulphonyl-stabilized carbanion, followed by reductive desulphonylation of the resulting allylic sulphonyl group. This was achieved most efficiently by the use of a large excess of lithium metal in ethylamine (equation (43)), although all reaction conditions led to mixtures. The minor product results from double bond rearrangement. [Pg.945]

Whenham, R.J., Fraser, R.S.S., Brown, L.P. Payne, J.A. (1986). Tobacco-mosaic-virus-induced increase in abscisic-acid concentration in tobacco leaves Intracellular location in light and dark-green areas, and relationship to symptom development. Planta, 168, 592-8. [Pg.10]

Ben-Zioni, A., Itai, C. Vaadia, Y. (1967). Water and salt stresses, kinetin and protein synthesis in tobacco leaves. Plant Physiology, 42, 361-5. [Pg.64]

Exposure to endosulfan residues in tobacco products could be another important source of general population exposure. Endosulfan residues in tobacco leaves and finished tobacco products were reviewed by EPA (1982a). Eor example, auction market tobacco had a mean residue of <0.2-14 ppm endosulfan and endosulfan sulfate in the early 1970s, and cigarettes sold in 1973 contained a mean residue of 0.83 ppm endosulfan. No information was found in the available literature regarding endosulfan concentrations in cigarette smoke. [Pg.236]

C03-0083. Nicotine is an addictive compound found in tobacco leaves. Elemental analysis of nicotine gives these data C 74.0%, H 8.65%, N 17.35%. What is the empirical formula of nicotine The molar mass of nicotine is 162 g/mol. What is the molecular formula of nicotine ... [Pg.190]

In Tobacco. At the time of harvesting, fresh tobacco leaves do not contain measurable amounts of nitrosamines (<5 ppb). However, these compounds are formed during curing, aging and fermentation. Their concentrations depend primarily on the content of proteins, alkaloids, agricultural chemicals and nitrate in the tobacco, as well as on the processing conditions which lead to the reduction of the nitrates. [Pg.249]

Chlorella, aquatic plant, grass, hay, spruce twigs and needles, olive leaves, peach leaves, tobacco leaves Bovine muscle, bovine liver, pig kidney, milk powder, cereals, single cell protein, butterfat, fish oil, animal feed-stuffs, textiles... [Pg.21]

Dybczynski R, Polkowska-Motrenko H, Samczynski Z and Szopa Z (1998) Virginia tobacco leaves (CTA-VTL-z) - new Polish CRM for inorganic trace analysis including microanalysis. Fresenius J Anal Chem 360 384-387. [Pg.44]

Dybczynski R, Poikowska-Motrenko H, Samczynski Z, and Szopa Z (1996) Preparation and Certification of the Polish Reference Material Oriental Tobacco Leaves (CTA-OTL-i) for Inorganic Trace Analysis. Raporty IChTJ Seria A nr 1/96. Institute of Nuclear Chemistry and Technology, Warsawa. [Pg.103]

Thin Laver Chromatography. - The technique has been applied to the determination of tricresyl phosphate in edible oils,265 and insecticides in tobacco leaves.264... [Pg.416]

Cadmium is nutritionally non-essential, toxic and a ubiquitous environmental pollutant. It is found in leafy vegetables, grains and cereals, and since it is present in substantial amounts in tobacco leaves, cigarette smokers on a packet a day can easily double their cadmium intake. It has a long biological half-life (17-30 years in man), accumulates in liver and kidneys and its toxicity involves principally kidney and bone (Goyer, 1997).While Cd interferes primarily with calcium, it also interacts with zinc and can induce the synthesis of metallothionein. Cadmium bound to metallothionein in liver or kidney is thought to be non-toxic, but cadmium in plasma... [Pg.343]

The first hurdle encountered during the development of alfalfa as a recombinant protein production system was the relative inefficiency of the available expression cassettes. A study in which a tomato proteinase inhibitor I transgene was expressed in tobacco and alfalfa under the control of the cauliflower mosaic virus (CaMV) 35S promoter showed that 3-4 times more protein accumulated in tobacco leaves compared to alfalfa leaves [5]. Despite the low efficiency of the CaMV 35S promoter in alfalfa, bio-pharmaceutical production using this system has been reported in the scientific literature. Such reports include expression of the foot and mouth disease virus antigen [6], an enzyme to improve phosphorus utilization [7] and the anti-human IgG C5-1 [8]. In this last work, the C5-1 antibody accumulated to 1% total soluble protein [8]. [Pg.4]

Tetanus toxin fragment C Tobacco leaves Systemic IgG and local IgA responses. Immuno- -genic in mice when administered nasally. 113... [Pg.148]

Virus-infected tobacco leaves Spatial distribution of acidic chitinases and their messenger RNAs in tobacco plants infected with cherry leaf roll virus Balsalobre et al. (5)... [Pg.115]


See other pages where Tobacco leaf is mentioned: [Pg.31]    [Pg.267]    [Pg.379]    [Pg.215]    [Pg.333]    [Pg.58]    [Pg.25]    [Pg.26]    [Pg.48]    [Pg.92]    [Pg.92]    [Pg.142]    [Pg.166]    [Pg.176]    [Pg.178]    [Pg.194]    [Pg.209]    [Pg.211]    [Pg.223]    [Pg.228]    [Pg.275]    [Pg.280]    [Pg.283]    [Pg.284]    [Pg.818]    [Pg.68]    [Pg.1]   
See also in sourсe #XX -- [ Pg.64 , Pg.73 ]

See also in sourсe #XX -- [ Pg.64 ]

See also in sourсe #XX -- [ Pg.3 ]

See also in sourсe #XX -- [ Pg.11 ]




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Biosynthesis tobacco leaves

Conversion of tobacco leaf constituents to total mainstream smoke polycyclic aromatic hydrocarbons

Subunit tobacco leaf

Tobacco leaf cell

Tobacco leaf disks

Tobacco leaf protein synthesis

Tobacco leaves, nicotine

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