|bulk dried Mitragyna speciosa||Bookmark|
Is there anywhere offering this for sale?
I think it would be a very interesting project to obtain the alkaloids as a nice white powder of the hydrochloride salts. Principaly mitragynine (9-methoxy-corynantheidine)
Chemfinder has the structure of corynantheidine if your interested. Anyone know where the MeO goes?
Living in a cold country in a small house means growing it would be a pain in dee butt.
Anyone know about the legal status of the alkaloids?
Seems to be seen as a reasonably dirty drug in Thailand. Still quite novel to the western world.
Mitragynine, 9-methoxyCorynantheidine, isolation
(Rated as: excellent)
the alkaloids are commertially available, somewhere
can't name sources so you'll have to find it on your own
The methoxy is right where the 4-hydroxy is on psilocin, now ya know.
the other name Mitragynine,
the longggg name Indolo[2,3-a]quinolizine-2-acetic acid, 3-ethyl-1,2,3,4,6,7,12,12b-octahydro-8-m
CAS RN: 4098-40-2
Here is an article for you to check out
Structure revision of mitragynaline, an indole alkaloid in Mitragyna speciosa
Tetrahedron Letters (2001), 42(9), Pgs 1741-1743
Hiromitsu Takayama, Hayato Ishikawa, Mika Kurihara, Mariko Kitajima, Shin-ichiro Sakai, Norio Aimi, Hiroko Seki, Kentaro Yamaguchi, Ikram M. Said and Peter J. Houghton
Since You wanted to know, I dug up an extraction procedure.
Alkaloids from Mitragyna speciosa
Phytochemistry, Volume 30, Issue 1, 1991, Pages 347-350
Peter J. Houghton, Aishah Latiff and Ikram M. Said
The major alkaloids present in very young leaves of Mitragyna speciosa from Malaysia were shown to be highly conjugated indoles, mitragynaline and corynantheidaline. Related compounds are also present in smaller amounts and two others were isolated and characterized (named mitragynalinic acid and corynantheidalinic acid). Mitragynaline is also present as a minor component in mature leaves of the plant.
Isolation and extraction of mitragynaline(1). Dried, very young
leaves (135 g) were collected from trees of Mitrugyna speciosu
Korth. growing on the campus of Universiti Kebangsaan Mal-
aysia. The material was authenticated at source and a specimen
voucher is deposited in the herbarium of the Botany Depart-
ment, Universiti Kebangsaan Malaysia. The leaves were ex-
tracted with cold MeOH for 3 days and the extract filtered off.
After concn under red. pres. the extract was treated with 10%
HOAc and washed with 2 x 50 ml petrol (bp 60-80C). The aq.
acid layer was made alkaline with Na2CO3, and extracted with 3
x 30 ml CHCl3,. The CHCl3, layers were combined, washed with
H2O and concd under red. pres. to yield 3.24 g of a dark brown
TLC examination of this residue showed the presence of
several yellow zones. Prep. TLC was used (Merck Kieselgel
PF,254: CHCl3,-EtOAc, 4:l) to separate five bands IKl-IK5
with a yellow or orange colour in daylight and giving fluore-
scence under UV light 365 nm. Yields after elution from the silica
were low and decomposition appeared to be taking place.
However a sufficient yield of IKl(70 mg) and IK5 (55 mg) were
obtained for a full range of spectra to be performed. IKl and IK5
were seen to be mixts of two compounds each from the spectra
obtained and after some difficulty the mixts were finally separ-
ated using RP-18 silica gel TLC plates (Merck) with
MeOH-H2O (4: 1) as the mobile phase. Prep. TLC using this
system resulted in the isolation of the two separate components
in each case which were designated IKlA (30 mg), IKlB (25 mg),
IK5A(20 mg) and IK5B (16 mg) and named mitragynaline, cor-
yn~theidaiin~ mitragynalinic acid and coryn~th~dinalic acid
Amounts of IK2, IK3 and IK4 were sufficient only for UV and
MS (2 mg each).
TLC examination of an alcoholic extract of 500g mature
leaves of M. speciosa obtained from Perlis State (voucher
specimen deposited in the herbarium of the Department of
Pharmacy, Universiti Sains Malaysia, Penang) showed the pre-
sence of IKl in small amounts. The concd extract (50 g) was
dissolved in HOAc, diluted with H2O and after standing over-
night the mixt. was filtered. The filtrate was made alkaline with
Na2CO3 and extracted with 3 x 50 ml CHCl3,. The organic layer
was taken to dryness under red. pres. to yield 1.8 g residue. The
residue was dissolved in CHCl3, and treated to vacuum liquid CC
using TLC grade silica gel (Merck Kieselgel G) 5 x 1 cm eluting
with CNCl3, (15 x 25 ml) and CHCl3,-MeOH, 19: 1(10x 25 ml).
The eluates were monitored by TLC and IKl was detected in the
latter eluates. Mitragynine was also present so the two were
separated from the coned bulked frs by prep TLC (Merck
Kieselgel PF, 254, CHCl3,-Et20 (4: 1) and eluted with (Me2CO) to
give mitragynine (5) 55 mg and IKI (1) 30 mg after recrystalliz-
ation from dry EtOH. Analytical TLC on RP-18 SG plates
showed no trace of IKlB in the IKl and so it was presumed that
only mitragynaline IKlA was present; this was confirmed when
spectra were run. Mitragynine was identified by spectral and
TLC comparison with literature values and samples previously
isolated in the laboratory at King's College. NMR spectral
features for both compounds were identified by 2D COSY,
NOESY and 'H-13C ~rrelation spectra.
Those who give up essential liberties for temporary safety deserve neither liberty nor safety
I did a fair bit of work on this plant some years ago.My main interest was in its use to detoxify from opiatesI gathered together every paer ever published and in turn had a hand in publishing a further paper.You need to search back issues of J.Ethnopharmacology (1986 87)Dont be misled by embodens book of narcotic plants the raw plant material is nothing like mushrooms amphetamine or opiates.I tried raw plant material from many sources.There is a very big difference in alkaloid content according to area.There is also a couple of different versions of kratom both M.speciosa.The plant is both a stimulant and depr.In folk medicine it substitutes for opium.A decoction is gently boiled down so it kooks like hash or opium and it is smoked in an opium pipe.The Malay name for this is chandu which is the same as the name for opium.It does help a lot with withdrawel symptoms but a lot of body,mind,spirit work as used by the Malay and Thai traditional healer must also be done.Some years ago one of the Mckenna mafia published a paer inJ.Pschoactive Drugsthe planted at least on of the trees in a Hawian herberium.Smith Kline and co did full assays on the alkaloids and gave up on them because of lack of activity.There are a couple ofr published british articles from the 1930 s in I think the british medical journalwhere the activity of plant material and mitiginine,The plant material was much more potent than the alkaloid.The activity of the plant was speculated to be either a synergic or non alkaloidal part.Dont waste your time and money ,.if you a looking for a legal high there are much stronger plants
|just thought SWIM should...||Bookmark|
Just thought SWIM should report back on the kratom scene.
Right now, acetate-based kratom extracts are widely available, as is bulk kratom.
SWIM is participating in R&D of a HCl-based tek, and is very close to fruition.
Most kratom products available in today's market are high-quality and exceptionally active.