Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Iodine location with

Kushi and Handa (68) described in 1985 a TLC/MS method for the analysis of lipids. Secondary ion mass spectrometry with a liquid matrix of triethanolamine was used for the extraction and ionization of sample spots first located with iodine or Coomassie brilliant blue staining. A piece of TLC plate of size 5 x 20 mm could be attached to the direct insertion probe, and scanning in one-dimension was accomplished by manually inserting the probe into the source of the mass spectrometer. Spectra could be obtained from one microgram of a lipid separated on a silica TLC plate with aluminum- or plastic-backed TLC plates. Although not specifically noted in this paper, since a plastic-backed plate is an electrical insulator, some provision for connecting the surface to the plate platform itself must be made to hold the surface at the source potential. [Pg.260]

Iodine Value A common measurement of unsaturation in a triglyceride is the iodine values. Iodine reacts with the double bonds of the triglyceride and the amount of iodine taken indicates the degree of unsaturation. The iodine value will vary from lot to lot of oil as the composition of the extracted oil varies because of factors such as season, location, and climate. Table 6.2 gives some iodine values for a few triglycerides (20). [Pg.181]

The method presently available for clinical studies does not allow any distinction between inorganic and organic iodine in the thyroid gland and because of the effect of overlying tissue on the specific iodine Ka X-ray (half value layer equals 2 cm of tissue) thyroid tissue not located immediately under the skin (thyroid cancer metastasis) cannot be evaluated. The results of iodine measurements with XRF are expressed in units of weight (mg) of iodine contained in the area scanned. Additional efforts have to be extended if a volume measurement is desired. Then, the units would be mg iodine per volume. The problems concerning the accuracy of the method are discussed elsewhere in this monograph. [Pg.163]

Fig. 11.6a,b. Dynamic helical CT in a patient with hepatic metastasis from lung cancer located at the central liver, a Due to its central location with prohahle portal vein involvement there is a peripheral fan-shaped perfusion abnormality artificially increasing the lesion size, b This finding is exacerbated at a later phase of liver enhancement due to the interstitial diffusion of iodinated contrast material within the metastasis... [Pg.154]

Aliquots of 10 (A of 10 M racemic atenolol, metoprolol, and propranolol were applied to the layers and chromatograms were developed at 17°C in chambers equilibrated with the eluents for 25 min. Development time was 20 min and the migration distance was 15 cm. The spots were located with iodine vapors. Eluents were mixtures of acetonitrile/methanol/water in different ratios. Excellent separations were obtained for metoprolol and, above all, for propranolol, whereas the resolution of atenolol was much more difficult (see Table 5.5). [Pg.121]

In another approach, optically pure (—)-brucine was mixed with ( )-ibuprofen while preparing the solution prior to its application onto TLC plates [16]. The premixing resulted in the formation of diastereomeric salts of the type (-1-)-ibuprofen-(—)-brucine and (—)-ibuprofen-(—)-brucine without resorting to any covalent linkage. It was the movement of these ionic diastereomers on TLC plates that resulted in separation. Chromatograms were developed at 28 2°C for 20 min in acetonitrile/methanol (5 1, v/v), and the spots were located with iodine vapors. [Pg.341]

Solvent front, 15 cm in 45 min Spots located with iodine vapours. [Pg.345]

Iodine plant locations in the United States and Japan are dictated primarily by the availabiHty of natural brines or bitterns containing adequate amounts of iodine. In 1992, the United States had three iodine-producing companies Woodward Iodine Corp., North American Brine Resources, and loChem. In Japan there are five iodine-producing companies, with over 30 plants Ise, Godo, Nippo, Nitten, and Kanto. AH these companies deHver iodine as flaked material except Ise, which also produces pfiUed iodine. [Pg.364]

In the anion electrochemical series, sulfur, being the less noble element compared to its heavier congeners, occupies an intermediate position between iodine and selenium [(+)F, Cl, Br, I, S, Se, Te(-)]. Selenium, regarded as a metalloid, is a relatively noble element. Tellurium is rather an amphoteric element it can enter into solution in the form of both cations and anions. Regarded as a metal, i.e., with respect to its cations, tellurium occupies a position between copper and mercury. Regarded as a metalloid, i.e., with respect to its anions, it is located on the extreme right of the above series. [Pg.57]

Another reversal location method is to expose the TLC plate to iodine vapour in a closed chamber that contains some iodine crystals. Iodine is lipophilic and accumulates in hpophihc sample spots, showing a brown color on a pale yellow-brown background. The same result is obtained by spraying with an iodine solution (250 mg iodine dissolved in 100 ml of heptane). In nearly all cases, this iodine accumulation is totally reversible without altering the sample, because outside the closed chamber iodine evaporates quickly from the plate. Caution should be taken with this iodine treatment in the case of unsaturated compounds because iodine vapor can react with double bonds [16]. [Pg.171]

In nonivamide and RTX derivatives, the antagonist activity depends on the location of iodine, with antagonism being maximal at C-5 in RTX (2b) and at C-6 in nonivamide (4b). Complementary iodination at C-5 in nonivamide (4c) could still reverse activity [68], but iodination of RTX at C-6 (2c) yielded only a partial agonist [72]. [Pg.153]

It is noteworthy that iodine addition in pyridine to 79 takes place regioselectively, with the iodine atom located exclusively in the product at C(7). Steric factors have been invoked again to explain the selectivity of the nucleophilic attack (equation 81). [Pg.592]

Astatine is located just below iodine, which suggests that it should have some of the same chemical properties as iodine, even though it also acts more hke a metal or semimetal than does iodine. It is a fairly heavy element with an odd atomic number, which assisted chemists in learning more about this extremely rare element. The 41 isotopes are man-made in atomic reactors, and most exist for fractions of a second. The elements melting point is about 302°C, its boiling point is approximately 337°C, and its density is about 7g/cm. ... [Pg.258]


See other pages where Iodine location with is mentioned: [Pg.322]    [Pg.1188]    [Pg.293]    [Pg.297]    [Pg.345]    [Pg.961]    [Pg.197]    [Pg.555]    [Pg.282]    [Pg.296]    [Pg.632]    [Pg.348]    [Pg.363]    [Pg.364]    [Pg.87]    [Pg.35]    [Pg.324]    [Pg.796]    [Pg.12]    [Pg.71]    [Pg.84]    [Pg.667]    [Pg.5]    [Pg.216]    [Pg.304]    [Pg.960]    [Pg.117]    [Pg.318]    [Pg.31]    [Pg.399]    [Pg.95]    [Pg.100]    [Pg.100]    [Pg.101]    [Pg.15]    [Pg.20]    [Pg.137]   
See also in sourсe #XX -- [ Pg.147 , Pg.322 , Pg.882 ]




SEARCH



With iodine

© 2024 chempedia.info