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Mimosa hostilis

For our experiment we will be using Mimosa hostilis root-bark to provide a very pure product of NN-DMT without the over powering influence of 5-MeO-DMT or the negative side effects of 5-OH-DMT. For a solvent we will be using common naphtha. Notes on adaptations for chemicals and other variations of this process are described as well. The following is a list of materials ... [Pg.6]

Mimosa hostilis root-bark (30g suggested starting amount - 45/1 OOg)... [Pg.6]

Grind the plant material to a fine powder. The finer ground the material the better your yields will be. The best technique to pulverize and rupture the cell structure of any plant material is to repeatedly freeze and thaw it over and over again. An example of a plant requiring this treatment is Phalaris arundinacea, a strong and limber grass. Mimosa hostilis root-bark is easily pulverized to a fine powder in a blender, releasing a pink haze. [Pg.7]

DMT is found in the South American plants Virola calophylla and Mimosa hostilis, and in grasses, mushrooms, toads, grubs, and fish, and has been used by the Amazon natives for spiritual effects. DMT was synthesized in 1931. [Pg.96]

N.A. Mimosa hostilis Benth. Nigerine.100 An astringent, cure fatigue. [Pg.281]

South American Indian tribes in a religious manner for prophecy, divination, clairvoyance, tribal initiation of male adolescents, or sacred feasts are cohoba snuff, made from the pulverized seeds of Piptadenia the drink vinho de Jurumens, made from the seeds of Mimosa hostilis and the drink caapi, made from Banisteriopsis. These last three products contain... [Pg.146]

In 1946, Goncalves deLima, a Brazilian ethnobotanist and chemist, extracted an alkaloid from roots of Mimosa hostilis, another member of the pea family, which has been used by natives of eastern Brazil to prepare a potent psychoactive drink. He named this "nigerine later it was found to be identical to DMT, first synthesized in 1931 by the British chemist Richard Manske. [Pg.407]

D.V. Siva Sankar s enormous green book LSD—A Total Study lists eleven legumes that contain bufotenine and DMT. Of these, the second most widely used is Mimosa hostilis. Decoctions made from its root play a part in the ceremonies of the ancient Yurema cult of Brazil The decoction is known as the "wine of Jurema. William Emboden describes this "miraculous drink as... [Pg.410]

A,A-dimethyltryptamine was isolated (77). A7,Ar-Dim ethyltry ptamine also occurs in the leaves of Lespedeza bicolor vax. japonica (Leguminosae) (78), and in the roots of Mimosa hostilis Benth. (40, 79). The latter plant is also the source of an extract used by the local (Brazilian) Indians in their mysticoreligious ceremonies for its hallucinogenic properties. These rituals have been described by Gongalves de Lima, who recorded the extraction of nigeiine from Mimosa hostilis, but did not identify it as N,N-dimethyltryptamine (79). [Pg.10]

Fabaceae), Arundo donax, Phalaris spp. (Poaceae), Mucuna prwriens, Mimosa hostilis, Piptadenia peregrina (Fabaceae), Virola sp. (Myristicaceae)... [Pg.197]

DMT (dimethyltryptamine nigerine) is an indole alkaloid from Mimosa hostilis, Acacia spp., Arundo donax, Desmodium... [Pg.103]

N,N-dimethyltrypta mine (MAO 1) phenylalkyl amine Mimosa hostilis, Acacia spp., Arundo donax, Desmodium spp., Phalaris spp., Banisteriopsis argentea, Psychotria spp, Virola peruviana, Zanthoxylum spp. and others (Leguininosae, Gramineae, Malphigiaceae, Rubiaceae, Myristicaceae, Rntacea [167]... [Pg.82]

Pachter, I.J. etal. 1959. Indole alkaloids of Acersaccharinum (the silver maple), Edcty-oloma incanescens, Piptadenia colubrina, and Mimosa hostilis" Journal of Organic Chemistry 24 1285-1287. [Pg.594]


See other pages where Mimosa hostilis is mentioned: [Pg.4]    [Pg.8]    [Pg.13]    [Pg.20]    [Pg.22]    [Pg.60]    [Pg.248]    [Pg.17]    [Pg.33]    [Pg.66]    [Pg.55]    [Pg.200]    [Pg.12]   
See also in sourсe #XX -- [ Pg.268 , Pg.514 ]

See also in sourсe #XX -- [ Pg.248 ]

See also in sourсe #XX -- [ Pg.10 ]

See also in sourсe #XX -- [ Pg.25 , Pg.248 ]

See also in sourсe #XX -- [ Pg.12 ]




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