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erature reading lesson to those who
have made these claims. See Proceedings of the Royal Society of
London, Series B, Volume 155, pages 26 to 54 (1961).
Also see US
Patent 3,219,545. You will note while reading these articles detailing
how to get lysergic amide production in a culture medium that these
guys had to scour the globe to find that rare strain of claviceps fungus
that will cooperate in this manner.
The vast majority of claviceps
fungi just will not produce these alkaloids while being cultured. See
the following articles to convince yourself of just how futile it is to
collect a wild strain of claviceps and try to get it to produce lysergic
acid amides in culture: Ann. Rep. Takeda Res. Lab Volume 10, page 73
(1951); and Farmco, Volume 1, page 1 (1946); also Arch. Pharm.
Volume 273, page 348 (1935); also American Journal of
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Botany, Volume 18, page 50 (1931); also Journal of the American
Pharmacy Association Volume 40, page 434 (1951); also US patent
2,809,920; also Canadian Journal of Microbiology, Volume 3, page
55 (1957), and Volume 4, page 611 (1958) and Volume 6, page 355
(1960); also Journal of the American Pharmacy Society Volume 44,
page 736 (1955).
With this matter disposed of,
Yhs 002 Google it is time to move on to what
actually are viable sources of lysergic acid amides for the production of
LSD. This is the farming end of the acid business. It is only through
what is all the synthetic pills sold online ergot-infested rye, or growing morning glories and Hawaiian
baby woodrose that the required feedstocks of lysergic compounds
can be obtained without making a target of oneself. I have for years
seen ads in High Times offering morning glory seeds and Hawaiian
baby woodrose seeds for sale, but these are offered in small amounts at
high prices. I would bet my bottom dollar that these outfits, if they are
not front operations, will at least report to the heat any large orders they
get. To avoid detection, the aspiring LSD manufacturer must be ready
to get his hands dirty, and spend some time as a farmer.
The most difficult farming choice, and as luck would have it, the
one that gives the purest acid, is to grow a patch of ergot-infested rye.
The reason why ergot is superior to growing morning glory seeds or
woodrose seeds is that these seeds have a considerable amount of
another type of alkaloid in them besides the ones that yield lysergic
acid. These other alkaloids are of the clavine type, meaning that they
have the lysergic-acid skeleton, but lack
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the carboxyl grouping. In its
place will be a methyl grouping, an alcohol grouping, a methyl
alcohol grouping or combinations of the
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alkaloids will likely be carried all the way through into the product,
producing both the GIGO situation during the synthetic operations
and a contaminated product when finished. I will present my ideas on
how to remove them, but they are best avoided in the first place.
Ergot is the name given to a dark brow
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cina xxxx cup of water for each 1/2 pint jar you plan to prepare.
If you are using 1 pint jars you need to double the recipe. Mix all of
this stuff up well. This mixture is the substrate material that the fungus
will consume and use for growth.
The next step is to fill each jar with substrate material. Adaptation-20
This document used to suggest gently packing the substrate into the
culture jars. It has been found that keeping the substrate as loose and
full of air as possible is the best way to fill the jars. The jars will
colonize faster this way. Incidentally, the faster the jar colonizes, the
lower the risk that some competitor contamination will get a foot hold
and take over the substrate. Adaptation-3 Fill each jar to within 1/2
inch of the top with substrate material. If you run out of substrate
material, either mix up enough for one more 1/2 pint jar or cannibalize
a jar to fill up the rest of the jars. This is important because you need to
make sure the substrate is high enough in the jars for the spore syringe
to inject spores into it.
The top 1/2 inch of the glass on each culture jar needs to be cleaned.
No substrate material can be left on the glass above the compressed
cake. First wipe it with your finger to get the bulk of the material off of
it and then do a thorough job with a moistened paper towel. The glass
needs to be spotless. The reason this is necessary is that bacteria and
mold can use any material left there as a wick to infect the main
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How To Grow Magic Mushrooms The Magic Mushroom Growers Guide (page 2)
Next, fill the top 1/2 inch of the each culture jar with vermiculite. This
layer is pure, simple, dry vermiculite. Nothing else. Fill the jar level
with the glass edge. This layer is a break through pioneered by
Psylocybe Fanaticus. What this layer does is insulate the sterilized
substrate from any air borne contamination. This layer gets sterilized
with the substrate later and air borne molds and bacteria can not
(usually) get through it to contaminate the substrate. At the same time,
it allows some gas exchange to occur. The fungus needs oxygen and
gasses can filter through the vermiculite.
Now, place the jar lids in place. Normally, the jar lids have a rubber
seal that is placed in contact with the glass of the jar. Traditionally the
rubber seal is not placed in contact with the glass. It was placed on the
upper side of the lid. The reason was that people thought it would
make too tight of a seal. This does not seem to be an issue. If you wish
to follow tradition, place the rubber on the upper side of the lid. Screw
the lid down tight. Note that you need to have the four holes poked in
the lid in Step 1. Otherwise you can have real problems when you heat
these jars up!
Next, place a piece of tin foil over the top of each jar and crumple it
around the sides of the jar. This is to keep water dro
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@Sunday, March 09, 2014 1:46:41 PM