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Tamine

R. P. Eckberg, TAPPIProceedings—1987 Polymers, Taminations and Coatings Conference, Tappi Press, Adanta, Ga., 1987, p. 21. [Pg.68]

Consider the area neeessary for site work to reduee the spread of eon-tamination. [Pg.64]

Site-speeifie information pertinent to hazard eommunieation should be ineluded in the HASP. Eor instanee, if there is eoneern over metal eon-tamination in site soils and dust, this information should be elearly disseminated to anyone who may eome into eontaet with it [4]. Even for those persons who will likely not eome into eontaet with it beeause of administrative eontrols, some training regarding aeeess zones might be... [Pg.80]

For a kitchen hood with a fixed air curtain, good results are possible if the exhaust flow rate is large enough to exhaust the large amounts of con taminants and induced air from the oven. The circular jet around a wdtl-ing or soldering point is usually too cumbersome to use when working at more than one spot. [Pg.1007]

Under the action of alkali, according to Kotake, Sakan and Kusumoto, (/(-strychnine yields tryptamine, and N-methyleijano- -stryehnine produces N-methy Itr yp tamine. [Pg.559]

Since many of the uses of antihistamines involve conditions such as rashes, which should be treatable by local application, there is some rationale for developing drugs for topical use. The known side effects of antihistamines could in principle be avoided if the drug were functionalized so as to avoid systemic absorption. The known poor absorption of quaternary salts make such derivatives attractive for nonabsorbable antihistamines for topical use. Thus, reaction of the well-known anti his-taminic drug promethazine (104) with methyl chloride leads... [Pg.240]

Kurhatow was ihe first chemist U> e. tamine this oil. He found about 5 per cent, of a terpeue boiling at 16b tu 339°, which was probably pineue, whose presence has siaoe been uoofirmed by Summler and SporuitE. [Pg.90]

Pradhan SP, JR Paterek, BY Liu, JR Conrad, VJ Srivastava (1997) Pilot-scale bioremediation of PAH-con-taminated soils. Appl Biochem Biotechnol 63/65 759-773. [Pg.45]

A reaction of the same nature was probably responsible for a detonation that took place one hour after mixing carbon tetrachloride with tetraethylene pen-tamine. This reaction also occurs with monoamines, but it is not thought to be dangerous. [Pg.286]

For each well, prepare transfection mix B, containing 45 ng of the control Firefly luciferase (F-luc) plasmid pGL3 (Promega), 1 fd Lipofec-tamine 2000 (Invitrogen), and 100 fd of optiMEM. [Pg.121]

Bayona, J.M., Fernandez, P., Porte, C., Tolosa, I., Vails, M., Albaiges, J. (1991) Partitioning of urban wastewater organic microcon-taminants among coastal compartments. Chemosphere 23(3), 313-326. [Pg.901]

The affect of Li+ on the metabolism of serotonin (5-hydroxytryp-tamine, 5-HT) is equivocal. A number of studies consistently find a Li+-induced increase in the levels of the major metabolite, 5-hydroxyin-doleacetic acid (5-HIAA), in rat brain and in human CSF [155], which appears to reflect an increase in the rate of synthesis of 5-HT [156]. Li+-induced increases in the level of the amino acid precursor, tryptophan, and in the uptake of tryptophan by brain have also been reported [157], implying elevated tryptophan availability during Li+ treatment. In rat brain, chronic Li+ decreases the activity of tryptophan hydroxylase, the enzyme which, when activated by a Ca2+ and calmodulin-dependent protein kinase, leads to the synthesis of 5-HT [158]. Ca2+ increases the strength of binding of tryptophan to the enzyme, whereas Li+ has the opposite effect [159]. Tryptophan uptake is coupled to 5-HT utilization by a negative feedback mechanism and, therefore, the Li+-induced inhibition of tryptophan hydroxylase with a resultant decrease in 5-HT utilization could produce the observed increase in tryptophan uptake. [Pg.29]

In terrestrial vegetation, copper is usually less than 35 mg/kg DW except near smelters, where it may approach 700 mg/kg DW, and in copper-accumulator plants that may normally contain as much as 13,700 mg/kg DW (Table 3.3). In aquatic vegetation, copper is elevated in metals-con-taminated water bodies, reaching concentrations as high as 1350 mg/kg DW in eelgrass (Zostera spp.) from contaminated bays vs. 36 mg/kg DW in conspecifics from reference sites (Table 3.3). [Pg.143]

Scheme 8. Reagents and conditions (i) 2-ethylallyl bromide, LDA (ii) LiAlH4, THF (iii) MeOH-HCl (iv) NaI04, MeOH (v) HC(OMe)3, pTSA, MeOH (vi) mCPBA, CH2CI2 (vii) tryp-tamine, 160°C, MeOH, sealed tube (viii) aq. AcOH (ix) silica gel chromatography (x) MsCl, pyridine, 0°C (xi) Na, liq. NH3. Scheme 8. Reagents and conditions (i) 2-ethylallyl bromide, LDA (ii) LiAlH4, THF (iii) MeOH-HCl (iv) NaI04, MeOH (v) HC(OMe)3, pTSA, MeOH (vi) mCPBA, CH2CI2 (vii) tryp-tamine, 160°C, MeOH, sealed tube (viii) aq. AcOH (ix) silica gel chromatography (x) MsCl, pyridine, 0°C (xi) Na, liq. NH3.
Typically, it is best to move the sample from the field to the laboratory as quickly as possible and to minimize storage time in the laboratory. A container, often insulated, is commonly used for containing samples during transport. Using an insulated container allows one to maintain a desired temperature between field and laboratory and to isolate the samples from possible con-tamination.Table 7.1 shows the container, preservative, and storage times used for various types of common samples. [Pg.166]

The most successful modifier is cinchonidine and its enantiomer cinchonine, but some work in expanding the repertoire of substrate/modifier/catalyst combinations has been reported (S)-(-)-l-(l-naphthyl)ethylamine or (//)-1 -(I -naphth T)eth Tamine for Pt/alumina [108,231], derivatives of cinchona alkaloid such as 10,11-dihydrocinchonidine [36,71], 2-phenyl-9-deoxy-10, 11-dihydrocinchonidine [55], and O-methyl-cinchonidine for Pt/alumina [133], ephedrine for Pd/alumina [107], (-)-dihydroapovincaminic acid ethyl ester (-)-DHVIN for Pd/TiOz [122], (-)-dihydrovinpocetine for Pt/alumina [42], chiral amines such as 1 -(1 -naphtln I)-2-(I -pyrro 1 idiny 1) ethanol, l-(9-anthracenyl)-2-(l-pyrrolidinyl)ethanol, l-(9-triptycenyl)-2-(l-pyrrol idi nyl)cthanol, (Z )-2-(l-pyrrolidinyl)-l-(l-naphthyl)ethanol for Pt/alumina [37,116], D- and L-histidine and methyl esters of d- and L-tryptophan for Pt/alumina [35], morphine alkaloids [113],... [Pg.511]


See other pages where Tamine is mentioned: [Pg.230]    [Pg.286]    [Pg.14]    [Pg.1476]    [Pg.2174]    [Pg.170]    [Pg.554]    [Pg.7]    [Pg.17]    [Pg.154]    [Pg.207]    [Pg.209]    [Pg.803]    [Pg.487]    [Pg.1017]    [Pg.171]    [Pg.281]    [Pg.87]    [Pg.169]    [Pg.484]    [Pg.85]    [Pg.199]    [Pg.971]    [Pg.174]    [Pg.178]    [Pg.263]    [Pg.191]    [Pg.429]    [Pg.121]    [Pg.81]    [Pg.1164]    [Pg.179]    [Pg.408]   
See also in sourсe #XX -- [ Pg.978 , Pg.979 ]

See also in sourсe #XX -- [ Pg.26 , Pg.965 ]

See also in sourсe #XX -- [ Pg.965 ]




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