Ok so swim got a bit of sceletium and decided to try extract the alkaloids but is unsure of the best route to go.
Information gathered so far.
Found at (http://entheogen.ru/ipb/index.php?showtopic=2026)(im not russian - just came across this)
Mesembrine
Monograph Number: 5933
Title: Mesembrine
CAS Registry Number: 24880-43-1
CAS Name: (3aS-cis)-3a-(3,4-Dimethoxyphenyl)octahydro-1-methyl-6H-indol-6-one
Additional Names: 3a-(3,4-dimethoxyphenyl)tetrahydro-1-methyl-6(3aH)-indolinone
Molecular Formula: C17H23NO3
Molecular Weight: 289.37.
Percent Composition: C 70.56%, H 8.01%, N 4.84%, O 16.59%
Properties: Pale yellow oil. bp0.3 186-190°. [a]D20 –55.4° (CH3OH). Freely sol in alcohol, chloroform, acetone; slightly sol in ether. Practically insol in benzene, petr ether, alkalies.
Boiling point: bp0.3 186-190°
Optical Rotation: [a]D20 –55.4° (CH3OH)
Derivative Type: Hydrochloride
Molecular Formula: C17H23NO3.HCl
Molecular Weight: 325.84.
Percent Composition: C 62.66%, H 7.42%, N 4.30%, O 14.73%, Cl 10.88%
Properties: mp 205-206°. [a]D20 –8.4° (CH3OH).
Melting point: mp 205-206°
Optical Rotation: [a]D20 –8.4° (CH3OH)
This info was given to me by a friend :
The following is copied from an MSc thesis from a S.A.'n university.
Pretty standard A-B extraction to obtain mesembrine and other analogues from S. Tortuosum.
They used DCM as the non-polar solvent, but you can replace that with your more readily available / preferred solvent.
Sulfuric can also be substituted with your acid of choice (diluted to 0.05M).
7.1.2 Bulk Alkaloid Extraction Procedure
Plant material (oven-dried at maximum 40 °C) was finely ground using a rotary
beater mill. Approximately 0.5 – 1.5 kg of the ground plant material was weighed
and mixed with enough 0.05 M H2SO4 to cover the dry plant material. After being
mixed thoroughly, it was left standing at room temperature for 1 hour (during
which it was stirred a further two times).
A Büchner funnel was prepared by placing a piece of filter paper (Whatman No. 4)
in the funnel followed by coarse grade celite-577 (enough to create a layer
approximately 2 cm thick). A small amount of acid washed sand was placed on
top of the celite to prevent the celite from floating. The funnel was placed on top
of a 5 L Büchner flask and the aqueous plant material was filtered under vacuum.
The pH of the filtrate was adjusted to 7.00 by adding 25% ammonia solution. The
filtrate was poured into a separating funnel until it was three-quarters full, and
100 ml DCM was added to it. It was shaken well and left to separate into two
layers. The aqueous layer was rinsed three times with DCM, and the organic
layers were collected and pooled.
A cylindrical glass column (60 cm X 5 cm) was plugged with cotton wool, which
was then covered with an approximately 1 cm thick layer of anhydrous sodium
sulphate and packed with coarse grade celite-577 until three-quarters full. A small
amount of acid washed sand was placed on top of the celite to prevent the celite
from floating. The organic extract was then filtered onto the column and allowed
to filter through. The column was rinsed with two to three column volumes of
87
dichloromethane (DCM, CH2Cl2) and the extract was collected in a flask.
Evaporation under vacuum at 60 °C yielded the alkaloid extract. The crude
alkaloid extract was transferred to a pre-weighed screw-top sample bottle, and its
yield was determined.
I think this was from the Corroboree
"Add calcium carbonate. Dry. Smoke. Small quantities may be safe chewed this way as the calcium oxalate is insoluble, but not sure what happens in the stomach, possibly hydrochloric acid will release the oxalic acid."
Anyone with a bit more knowledge in chemistry amped to design some theoretical extraction procedure more suitable to a kitchen chemist ?
Much appreciated.
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