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Anisi

The separation capacity of a TLC method can be easily improved by use of a two-dimensional high performance TLC technique (2D HPTLC). Various plant essential oils (menthae, thymi, anisi, lavandulae, etc.) have been analysed by 2D TLC with florisil (magnesium silicate) as the adsorbent, using dichloromethane/ -heptane (4 6) in the first direction and ethyl acetate/n-heptane (1 9) in the second direction (69). [Pg.243]

Tetra-/>-anisy lhy drazine is green in benzene at room temperature.185 On the other hand, 1,2-diphenyl-1,2-di- >-nitrophenylhydrazine appears not to be dissociated at all. If this difference in degree of dissociation is real, and not a specious one due merely to a difference in color or reactivity of the radicals, it presents a puzzling contrast to the case of diphenylpicrylhydrazyl and to the triphenylmethyl series in which both kinds of substituent stabilize the radical. [Pg.67]

Protonation of ( -l-/ -anisyl-2-(triisopropylsilyl)ethene 17 with FS03H in S02C1F/S02F2 yields a mixture of syn- and anti -p-anisy -2-(triisopropylsilyl)ethyl cations 18 (13, 21). [Pg.24]

Schultz, W., Lange, C. and Heinrich, G. (1 986) Mass spectrometric study of medicinal plants. II. Direct mass spectrometric analysis of Anisi fructus. Deutsche Apotheker-Zeitung 126 (51/52), 2787-2793. [Pg.341]

Cu(I)-complexed [2]-rotaxane 96 was synthesized as follows (Figure 2.32)16f 67 2-rnethy l-9-(p-anisy I)-1, 10-phenanthroline 91 was deprotonated (lithium diisopropylamide) and the resulting anion was alkylated with the... [Pg.157]

The same dilution technique is usually applied in the analysis of ethereal oils [210]. It can be used in the determination of aldehydes such as citral and citronellal in lemon oil (Oleum citri) and in Oleum verbenae, of anisaldehyde in Oleum anisi stellati. Oleum anisi and Oleum foeniculi, of cinnamaldehyde in Oleum cinnamomi, and of ketones, such as car-vone, in Oleum anethi, of pulegone and diosphenol. In all these cases, the oil is first diluted with ethanol and to this solution an aqueous solution of the supporting electrolyte is added, usually only 0.1 M LiCl. [Pg.279]

Di-anisidine.—A derivative of di-phenyl which is related to benzidine, and related also to anisole, CeHs—OCH3 (p. 612) and to anisi-dine, H2N—CeH4—OCH3, is known as di-anisidine. [Pg.732]

Diphenyl-1,2-dithiolium ion leads to 3-amino-1,3-diphenylprop-2-ene-l-thiones when reacted with methylamine, ethylamine, ben-zylamine, 2-aminoethanethiol, piperidine,aniline, toluidines, anisi-dines, and chloranilines. With dimethylamine a double condensation, analogous to the one shown in Eq. (15), occurs. ... [Pg.176]

Conformational factors can determine more than the stereochemistry of rearrangement. In light of Collins findings, let us examine work done earlier by D. Y. Curtin (of the University of Illinois) with 2-amino-1-anisy 1-1-phenyl-1-propanol. This resembles Collins labeled compound (p. 899), except that an anisyl group (p-methoxyphenyl group) takes the place of one of the phenyls. Here, the competition in migration is between a phenyl and an anisyl, instead of between labeled and unlabeled phenyl groups. [Pg.901]

The ferrocenylphosphine ligands L5 and L6 are formally equivalent to L3 but do not fulfill the RSAI. Although one derivative of L5 ortho-anisy instead of... [Pg.734]

Since 2005, the Eur. Pharm. has changed its monograph for Anisi aetheroleum by limiting the source of the oil to Pimpinella anisum L. (formerly P. anisum and Illicium vemm Hook). In general, the monograph conforms with the ISO standard, supplemented by the limitation for foeniculin (max. 0.01%, adulteration with star anise oil) and fenchone (max. 0.01%, mixing or adulteration with fennel oil). [Pg.217]

Olei anisi utriusque drachmam unam. Glycyrrhizae extracti, unciam dimidiam. Mcllis despumati uncias duas. [Pg.222]

Anisi contusi, utriasque unciam unam. Sacchari uncias duas. [Pg.238]

Absinthii herba Aloe capensis Anisi fructus Arnicae flos Blackcurrant Leaf Caraway Cascara Centaury Dandelion Leaf Devil s Claw... [Pg.20]

ANISE, Anisi fructus-inA aetheroleum Amsc is the schizocarp of Pimpinella anisum L., family Apiaceae, with its origin in Egypt and Greece and cultivated in Europe and South America. The drug contains 2% essential oil with the main ingredient anethole (80-90%). The oil is also used as an expectorant (section R05C). [Pg.48]

ANISEED Anisi fructus The drug consists of the schizocarpic fruit of Pimpindlla anisum... [Pg.123]

L., family Apiaceae, a herb endemic to the Eastern Mediterrean Region, and cnltivated in Southern Europe. Aniseed contains 1-3% volatile oil, Anisi aetheroleum. The main ingredient is trans-anethole (80-90%). Anisi aetheroleum can also be obtained by steam distillation of... [Pg.123]

Submitted by Edward C. Taylor, Wendell A. Ehehart, and M. Kaw.anisi Checked by John J. Miller and William D. Emmons... [Pg.98]

Curaimae xanth. rhizonia, Melissae folium Anisi -, Cai vi Caryophylli -, Foeniculiaeth. Lavandulae and Rosmarini aeth. ... [Pg.151]


See other pages where Anisi is mentioned: [Pg.503]    [Pg.329]    [Pg.15]    [Pg.79]    [Pg.228]    [Pg.228]    [Pg.155]    [Pg.92]    [Pg.2156]    [Pg.324]    [Pg.136]    [Pg.168]    [Pg.212]    [Pg.31]    [Pg.47]    [Pg.72]    [Pg.304]    [Pg.146]    [Pg.240]    [Pg.152]    [Pg.153]   


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Anisi fructus

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