http://lj.rossia.org/users/tryl/ epiKern - LJ.Rossia.org epiKern Tue, 16 Mar 2010 17:11:51 GMT LiveJournal / LJ.Rossia.org http://lj.rossia.org/users/tryl/10700.html Tue, 16 Mar 2010 17:11:51 GMT http://lj.rossia.org/users/tryl/10700.html Re: myristicin&amp;mmda <br>« Reply #1 on: Yesterday at 08:25:55 PM »&nbsp;&nbsp;&nbsp; <br><br><span style="font-style: italic;">Yep.&nbsp; There was talk of forming iodo-safrole back at the hive.&nbsp; Iodine is a much better leaving group than bromine, so primary amines like MDA or, in this case, MMDA&nbsp; are much more easily formed.&nbsp; The idea is to isolate myristicin.&nbsp; There was discussion on another forum that a good fraction of parsley seed oil had myristicin from a source but that the oil did not entirely freeze at the same points.&nbsp; The GC/MS that the company supplied said it had a decent fraction of myristicin.&nbsp; What some don't know is that many parsley seed oils also contain apiol and that the company in question may not have been proficient enough with their equipment to tell the difference between myristicin and apiol.&nbsp; Anyway, keep in mind that apiol might be a fraction you don't want and I think the boiling points are pretty similar.</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">I didn't read the Rhodium link but iodomyristicin would be an excellent way to go.&nbsp; There is a bee named Jon who really nailed down some interesting information on this via a different route.&nbsp; He isolates the terminal alkene and formed bromosafrole in situ by reacting NaBr with H2SO4.&nbsp; He then isolated the bromosafrole and made iodosafrole via the Finkelstein reaction with NaI in acetone.&nbsp; After that MDA was made easily with NH3.&nbsp; Go search that bee's notes on bromo and iodo-safrole and MDA at wetdreams.&nbsp; Some of the best notes on the subject to date can be found by reading his notes and that is probably the best way to get what you want, that is, unless you have access to NaBH3CN and want to make the corresponding ketone.&nbsp; Either way, you are on the right track.</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">Moriarty</span><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/10700.html"><img src="http://lj.rossia.org/numreplies/tryl/10700" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/10700.html http://lj.rossia.org/users/tryl/10288.html Tue, 16 Mar 2010 15:18:09 GMT http://lj.rossia.org/users/tryl/10288.html <img src="http://img59.imageshack.us/img59/8816/hepatent.gif"><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/10288.html"><img src="http://lj.rossia.org/numreplies/tryl/10288" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/10288.html http://lj.rossia.org/users/tryl/9988.html Mon, 15 Mar 2010 08:59:53 GMT http://lj.rossia.org/users/tryl/9988.html <a href="http://www.posterburner.com/">http://www.posterburner.com/</a>&nbsp;&nbsp; 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a more complete rhodium archive<br /><br><br><a href="http://www.pneudart.com/">http://www.pneudart.com/</a>&nbsp; :)<br /><br><br><a href="http://www.youtube.com/watch?v=Vf97Fn11_Lc">http://www.youtube.com/watch?v=Vf97Fn11_<wbr />Lc</a> &nbsp; ancient chinese repeating crossbow<br /><br><br><a href="http://en.wikibooks.org/wiki/Cryptography">http://en.wikibooks.org/wiki/Cryptograph<wbr />y</a>&nbsp; very good one<br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/9787.html"><img src="http://lj.rossia.org/numreplies/tryl/9787" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/9787.html http://lj.rossia.org/users/tryl/9321.html Fri, 12 Mar 2010 07:35:00 GMT http://lj.rossia.org/users/tryl/9321.html <a href="http://www.zoklet.net/bbs/showthread.php?p=1530601">http://www.zoklet.net/bbs/showthread.php?p=1<wbr />530601</a><br><br>dude fucks up at the end - sep funnel spill (and i thought only i was that lame), but still yields enough product.<br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/9321.html"><img src="http://lj.rossia.org/numreplies/tryl/9321" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/9321.html http://lj.rossia.org/users/tryl/9168.html Fri, 12 Mar 2010 04:05:01 GMT http://lj.rossia.org/users/tryl/9168.html <img src="http://img175.imageshack.us/img175/8487/200512834929pc0cw.jpg"><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/9168.html"><img src="http://lj.rossia.org/numreplies/tryl/9168" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/9168.html http://lj.rossia.org/users/tryl/8946.html Fri, 12 Mar 2010 00:58:08 GMT http://lj.rossia.org/users/tryl/8946.html <a href="http://lifehacker.com/%20">http://lifehacker.com/</a>&nbsp;&nbsp;<br />tips and downloads for getting things done<br><a href="http://www.textbookrevolution.org/index.php/Main_Page">http://www.textbookrevolution.org/index.p<wbr />hp/Main_Page</a><br /><br><a href="http://zshare.net/%20">http://zshare.net/</a><br><a href="http://www.securityfocus.com/%20">http://www.securityfocus.com/<br /></a><br><a href="http://www.globalsecurity.org/military/library/policy/army/fm/%20">http://www.globalsecurity.org/military/l<wbr />ibrary/policy/army/fm/</a>&nbsp;&nbsp; US army field manuals<br><a href="http://www.lycaeum.org/rhodium/chemistry/index.html%20">http://www.lycaeum.org/rhodium/chemistry/i<wbr />ndex.html</a>&nbsp; a more complete rhodium archive<br><br><a href="http://www.tuxradar.com/content/newbies-guide-hacking-linux-kernel">http://www.tuxradar.com/content/newbies-g<wbr />uide-hacking-linux-kernel</a><br><br><a href="http://forum.rorta.net/%20">http://forum.rorta.net/</a><br><a href="http://t-militia.org/">http://t-militia.org/</a><br><a href="http://www.zoklet.net/">http://www.zoklet.net/</a><br><br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/8946.html"><img src="http://lj.rossia.org/numreplies/tryl/8946" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/8946.html http://lj.rossia.org/users/tryl/8561.html Fri, 12 Mar 2010 00:51:30 GMT http://lj.rossia.org/users/tryl/8561.html <a href="http://www.lycaeum.org/rhodium/chemistry/mmda.html">http://www.lycaeum.org/rhodium/chemistry/m<wbr />mda.html</a><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/8561.html"><img src="http://lj.rossia.org/numreplies/tryl/8561" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/8561.html http://lj.rossia.org/users/tryl/8274.html Thu, 11 Mar 2010 00:03:55 GMT http://lj.rossia.org/users/tryl/8274.html +inurl:mp3 site:sharebee.com velvet underground <br>+inurl:pdf|doc|lit site:sharebee.com<br>-inurl:htm -inurl:html intitle:”index of” +(“/ebooks”|”/book”) +(chm|pdf|zip) +”For Dummies”<br><span style="font-style: italic;">or</span><br>-inurl:htm -inurl:html intitle:"index of" +("/ebooks"|"/book") +(chm|pdf|zip) +"o'reilly"<br>"<a href="http://*:*@www">http://*:*@www</a>" site&nbsp; <span style="font-style: italic;">passwords for site, stored as the string "<a href="http://username">http://username</a>: password@www..."</span><br>filetype:xls inurl:"email.xls"&nbsp; <span style="font-style: italic;">email.xls files, potentially containing contact information</span><br style="font-style: italic;"><span style="font-style: italic;">"not for distribution" confidential&nbsp; documents containing the confidential clause</span><br><br><span style="text-decoration: underline;">reports for network security scans, penetration tests etc.</span><br>"Network Vulnerability Assessment Report" <br>"Host Vulnerability Summary Report"<br>filetype:pdf "Assessment Report"<br>"This file was generated by Nessus"<br><br style="text-decoration: underline;"><span style="text-decoration: underline;">Queries for locating network devices</span><br>inurl:"printer/main.html" intext:"settings"&nbsp; <span style="font-style: italic;">Brother HL printers</span><br>inurl:hp/device/this.LCDispatcher&nbsp;&nbsp;&nbsp; <span style="font-style: italic;">HP printers</span><br><br>intitle:index.of finances.xls&nbsp;&nbsp; <span style="font-style: italic;">finances.xls files, potentially containing information on bank ac-</span><br style="font-style: italic;"><span style="font-style: italic;">counts, financial summaries and credit card numbers</span><br><br>filetype:ctt "msn"&nbsp;&nbsp; <span style="font-style: italic;">MSN contacts list</span><br>buddylist.blt&nbsp;&nbsp;&nbsp; <span style="font-style: italic;">AIM contacts list</span><br style="font-style: italic;"><br><br><br><br><a href="http://www.hackersforcharity.org/ghdb/">http://www.hackersforcharity.org/ghdb/</a>&nbsp;&nbsp;&nbsp; google hacking database<br><br><br><br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/8274.html"><img src="http://lj.rossia.org/numreplies/tryl/8274" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/8274.html http://lj.rossia.org/users/tryl/7244.html Wed, 10 Mar 2010 21:02:31 GMT http://lj.rossia.org/users/tryl/7244.html <span style="text-decoration: underline; font-style: italic;">Feistel Networks</span><span style="font-style: italic;">&nbsp;&nbsp; --- A Feistel network is a general method of transforming any function (usually called the F function) into a permutation. It was invented by Horst Feistel [FNS75] in his design of Lucifer [Fei73], and popularized by DES [NBS77].</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">All commonly used symmetric block ciphers are product ciphers; they are strong ciphers constructed by many iterations of a round function, which is itself a kind of weak cipher. In a Feistel cipher, the round function consists of taking one part of the data being encrypted, feeding it into some key dependent function F, and then XORing (or otherwise combining) the result into another part of the block. If the part of the data used as input to the F function and the part of the data combined with output from the F function are each half of the block, then the cipher is a “balanced” Feistel network [SK96].</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="text-decoration: underline; font-style: italic;">XOR</span><span style="font-style: italic;"> - The logical operation exclusive disjunction, also called exclusive or (symbolized XOR, EOR, or ⊕), is a type of logical disjunction on two operands that results in a value of true if exactly one of the operands has a value of true.[1] A simple way to state this is "one or the other but not both."</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">XOR truth table </span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">F, F -- F&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 0, 0 -- 0</span><br style="font-style: italic;"><span style="font-style: italic;">F, T -- T&nbsp;&nbsp; or&nbsp;&nbsp;&nbsp; 0, 1 -- 1</span><br style="font-style: italic;"><span style="font-style: italic;">T, F -- T&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 1, 0 -- 1</span><br style="font-style: italic;"><span style="font-style: italic;">T, T -- F&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 1, 1 -- 1</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">symbol: &gt;&lt; </span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">Whitening: The technique of XORing key material before the first round and after the last round, was used by Ralph Merkle in Khufu/Khafre, and independently invented by Ron Rivest for DES-X [KR96a].</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">S-boxes&nbsp; -- An S-box is a table-driven non-linear substitution operation used in most block ciphers. S-boxes vary in both input size and output size, and can be created either randomly or algorithmically. S-boxes were first used in Lucifer, then DES, and afterwards in most encryption algorithms. </span><br><br><br>(from "Wiley - Bruce Schneier - The Twofish Encryption Algorithm - A 128--Bit Block Cipher")<br><br><img style=" " src="http://upload.wikimedia.org/wikipedia/en/d/d2/Feistel.png"><br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/7244.html"><img src="http://lj.rossia.org/numreplies/tryl/7244" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/7244.html http://lj.rossia.org/users/tryl/6942.html Wed, 10 Mar 2010 00:28:27 GMT http://lj.rossia.org/users/tryl/6942.html <span style="font-style: italic;">Easy, High Yield MDA </span><br style="font-style: italic;"><span style="font-style: italic;">Exerpt from something I heard somewhere.......</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">The Finkelstein reaction is the word for the day! Bromosafrole in acetone treated with KI to form the iodide (iodine is a much better leaving group). Iodosafrole forms the amine with NH3 alone at normal pressure. Start to finish MDA in the +90%! </span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">Or, as per twodogs:</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">Quote:The following reactions make use of a commercially available product that goes under various trade names eg Helional, Floramelon.</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">The aldoxime of this aldehyde undergoes the Beckman rearrangement with Nickel Acetate to give the amide that is then easily transformed to the amine by the Hoffman reaction. The Hoffman reaction can be achieved with 4.2% NaOCl sold in supermarkets as bleach.</span><br style="font-style: italic;"><span style="font-style: italic;">I don't have any references as this was done a while ago. The aldoxime and Hoffman reactions are pretty standard. The Beckman rearrangement of this particular product using Nickel Acetate is my own work.</span><br style="font-style: italic;"><span style="font-style: italic;">It doesn't get any easier that this.</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">The aldoxime.</span><br style="font-style: italic;"><span style="font-style: italic;">100 grms of the aldehyde is placed in 200 mls of ETOH with 50-60 grms of Hydroxylamine Hydrochloride * in 100 mls of H2O. 40 grms of Sodium Carbonate in 100 mls of H2O is slowly added with stirring. Once addition is complete the mixture is stirred overnight then filtered to give about 100 grms of the aldoxime. If the aldoxime doesn't solidify add more hydroxylamine and base.</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">The amide.</span><br style="font-style: italic;"><span style="font-style: italic;">100 grms of the aldoxime is mixed with 300 mls of xylene and 2 grms of Nickel Acetate ** is added and refluxed for 5 hours. About 100 mls of xylene is distilled off and the mixture is left to cool. About 70 grms of the amide separates and is filtered and dried,. Can be recrystallized with xylene.</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">The amine.</span><br style="font-style: italic;"><span style="font-style: italic;">To a solution of 10 grms NaOH in 200 mls H2O in a 500 mls flask is added 20 grms of the amide and 250 grms of 4.2 % NaOCl . The mixture is then heated to 80C with stirring. At about 50 to 60C the mixture can become white as the carbonate forms. At 70 – 80C an oil separates. (This is crude MDA). The solution was cooled and extracted with xylene. The solution was filtered and the filtrate washed with xylene and the xylene portions added together. About 100 mls of conc HCL was added to the xylene shaken and separated. The aqueous solution was extracted with xylene and the xylene separated. The amine was then liberated from the aqueous portion with NaOH and worked up in the usual way to give MDA</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">* Hydroxylamine HCL</span><br style="font-style: italic;"><span style="font-style: italic;">200 mls nitromethane, 300 mls Acetic acid and 300 mls HCL are heated to just below reflux and held there for 2 hours then refluxed for 12 hours. The solution is reduced to half gone the cooled in fridge overnight and filtered.</span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">**Nickel Acetate</span><br style="font-style: italic;"><span style="font-style: italic;">20 grms of nickel oxide (black) is dissolved in Acetic acid and heated with stirring until the mixture turns pale green. The excess Acetic is drained off , the rest is dried and powdered. </span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">Making Hydroxylamine HCl</span><br style="font-style: italic;"><a href="http://psychonaut.com/post-35899.html?f=43"><span style="font-style: italic;">http://psychonaut.com/post-35899.html?f=4<wbr />3</span></a><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/6942.html"><img src="http://lj.rossia.org/numreplies/tryl/6942" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/6942.html http://lj.rossia.org/users/tryl/6692.html Tue, 09 Mar 2010 14:49:35 GMT http://lj.rossia.org/users/tryl/6692.html <a href="http://www.chemfeeds.com/">http://www.chemfeeds.com/</a><br /><br><a href="http://www.freepatentsonline.com/%20">http://www.freepatentsonline.com/<br /></a><br><a href="http://8bitnyc.com/">http://8bitnyc.com/</a> 8bit NYC map<a href="http://8bitnyc.com/"><br></a><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/6692.html"><img src="http://lj.rossia.org/numreplies/tryl/6692" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/6692.html http://lj.rossia.org/users/tryl/6403.html Tue, 09 Mar 2010 10:21:45 GMT http://lj.rossia.org/users/tryl/6403.html <span style="font-style: italic;">Loperamide -&gt; 4 Day Smack <br /></span><br style="font-style: italic;"><span style="font-style: italic;">« on: January 10, 2010, 08:57:23 PM » <br /><br /></span><br style="font-style: italic;"><br style="font-style: italic;"><span style="font-style: italic;">Thanks to beebo from the Hive &amp; Wetdreams...<br /><br /><br><br>Loperamide is an opioid anti diarrheal, structurally similar to methadone, but not usually a compound that is psychoactive.<br /><br><br>From wiki: "Loperamide is an opioid-receptor agonist and acts on the μ-opioid receptors in the myenteric plexus large intestines; by itself it does not affect the central nervous system like other opioids."<br /><br /><br><br>Well, let's change that, shall we?<br /><br /><br><br>First off, beebo discovered that mannitol has been used for some time to shrink the endothelial cells of the blood brain barrier to let things in to the brain which might seem like a bad idea... Exposing the brain to the unfiltered blood soup &amp; all. Well, it's been done for decades now with cocaine as the typical cutting agent &amp; they use this also for priming heart/lung machines during bypass so one might surmise that there's something else keeping the brain protected. As of this post, I'm unclear what that system is. Perhaps things still need a proper transport mechanism? If you have any information about that issue, please post.<br /><br /><br><br>Now that we've used mannitol about 2 hrs before hand to prime the BBB for passage, we need a proper transport mechanism for the loperamide.<br /><br />Polysorbate 80 is that mechanism. Thank you again, beebo.<br /><br />Mixing PS80 &amp; loperamide under dry conditions causes nanoparticles to form. Basically, the PS80 encapsulates the loperamide. The brain sees the PS80 as usable fuel. These are taken up, enzymatically cleaved, exposing the loperamide &amp; the lope binds to u-opioid receptors in the brain instead of the gut.<br /><br />IV administration is choice for this however it's told to be inactive orally.<br /><br />The potency is said to be near on par with morphine, the reported feel is much like demerol with an activity period often lasting 3 - 4 days.<br /><br /><br>The product can be easily acylated to yield a drug closer to heroin in potency with the same duration.<br><br>Now, it's up to you to learn how to extract your loperamide &amp; find PS80 that isn't mixed with PEG &amp; source your mannitol.<br /><br /><br><br>Enjoy.<br /><br /><br><br>Credit due to beebo (that insane fucking moose) for breaking the paradigm open &amp; to jon for the detailed research into SAR studies, efficacy tweaking &amp; acylation to stronger analogs.</span><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/6403.html"><img src="http://lj.rossia.org/numreplies/tryl/6403" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/6403.html http://lj.rossia.org/users/tryl/6075.html Tue, 09 Mar 2010 09:40:00 GMT http://lj.rossia.org/users/tryl/6075.html <a href="http://duckduckgo.com/">http://duckduckgo.com/</a>&nbsp; simple search engine with clean interface, great for certain purposes<br><a href="http://www.tineye.com/">http://www.tineye.com/</a>&nbsp; <font style="font-style: italic;" size="2">"You can submit an image to TinEye to find out where it came from, how it is being used, if modified versions of the image exist, or to find higher resolution versions. TinEye is the first image search engine on the web to use image identification technology rather than keywords, metadata or watermarks."</font><br><a href="http://www.piracetam.net/">http://www.piracetam.net/</a>&nbsp; sourcing nootropics and smart drugs at competitive prices<br><a href="http://www.lookchem.com/">http://www.lookchem.com/</a>&nbsp; sourcing chems<br><a href="http://www.ec21.com/">http://www.ec21.com/</a>&nbsp; global b2b marketplace<br><a href="http://www.security-forums.com/index.php">http://www.security-forums.com/index.php</a><br><a href="http://skreemr.com/">http://skreemr.com/</a>&nbsp; great mp3 search engine<br><a href="http://news.ycombinator.com/newest">http://news.ycombinator.com/newest</a> hackernews<br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/6075.html"><img src="http://lj.rossia.org/numreplies/tryl/6075" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/6075.html http://lj.rossia.org/users/tryl/5843.html Tue, 09 Mar 2010 00:37:44 GMT http://lj.rossia.org/users/tryl/5843.html <a href="http://sharebee.com/c1965222">(P122) Shiitake Growers Handbook - Paul Przybylowicz &amp; John Donoghue-Mushroom</a><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/5843.html"><img src="http://lj.rossia.org/numreplies/tryl/5843" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/5843.html http://lj.rossia.org/users/tryl/5529.html Tue, 09 Mar 2010 00:34:52 GMT http://lj.rossia.org/users/tryl/5529.html <a href="http://webcast.berkeley.edu/">http://webcast.berkeley.edu/</a><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/5529.html"><img src="http://lj.rossia.org/numreplies/tryl/5529" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/5529.html http://lj.rossia.org/users/tryl/5143.html Tue, 09 Mar 2010 00:03:17 GMT http://lj.rossia.org/users/tryl/5143.html <br><img src="http://imgur.com/XKWmp.jpg"><br><br><img src="http://i.imgur.com/TkBIl.jpg"><br><br><img src="http://imgur.com/ZKZaz.jpg"><br><br><img src="http://imgur.com/MN8F8.jpg"><br><br><img src="http://imgur.com/DKrnL.jpg"><br><br><br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/5143.html"><img src="http://lj.rossia.org/numreplies/tryl/5143" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/5143.html http://lj.rossia.org/users/tryl/4875.html Mon, 08 Mar 2010 23:46:27 GMT http://lj.rossia.org/users/tryl/4875.html <a href="http://www.adventuregamestudio.co.uk/">Adventure Game Studio allows you to create your own point-and-click adventure games, similar to the early 90's Sierra and Lucasarts adventures. It consists of an easy-to-use editor to create your games, and a run-time engine to play them.</a><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/4875.html"><img src="http://lj.rossia.org/numreplies/tryl/4875" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/4875.html http://lj.rossia.org/users/tryl/4801.html Mon, 08 Mar 2010 23:42:41 GMT http://lj.rossia.org/users/tryl/4801.html <img src="http://i.imgur.com/537HT.jpg"><br><br>анасон - Pimpinella anisum<br>пелин - Artemesia absinthium<br>бергамот - Citrus bergamia<br>копър - Foeniculum vulgare<br>невен - Calendula officinalis<br>женско биле - Glycyrrhiza glabra<br>ангелика (пищялка) <br>Calamus acorus<br>Damiana - Turnera diffusa<br>Sweet worm?<br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/4801.html"><img src="http://lj.rossia.org/numreplies/tryl/4801" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/4801.html http://lj.rossia.org/users/tryl/4557.html Mon, 08 Mar 2010 23:38:32 GMT http://lj.rossia.org/users/tryl/4557.html <a href="http://en.wikipedia.org/wiki/Eleutherococcus_senticosus">http://en.wikipedia.org/wiki/Eleutheroco<wbr />ccus_senticosus</a><br><br><br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/4557.html"><img src="http://lj.rossia.org/numreplies/tryl/4557" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/4557.html http://lj.rossia.org/users/tryl/4121.html Mon, 08 Mar 2010 23:30:37 GMT http://lj.rossia.org/users/tryl/4121.html <span style="text-decoration: underline;"><a href="http://www.actahort.org/books/306/306_2.htm">http://www.actahort.org/books/306/306_2.h<wbr />tm</a><br><br>Authors</span>: D. Palevitch, A. Levy<br /><br /><br><br><span style="text-decoration: underline;">Abstract</span>: <br />Alternative sources for opium drugs are urgently needed due to increase in abuse of opiates. Papaver bracteatum is considered to be a potential source of raw material for the production of codeine and anti-addiction drugs, without the involvement of morphine. During the last 14 years efforts have been made in Israel to domesticate this wild species by breeding cultivars with high thebaine content and by development of modern cultural practices for the production of capsules or roots. A large variation in thebaine content was found within the wild populations originating from two locations in Iran. Significance negative correlations were found among some of the thebaine yield components. Thebaine yield showed the lowest heritability and therefore a low selection response. However, high selection response was obtained for the thebaine content in the capsules. A significant increase in the thebaine content of the capsules was found in colchicine-induced tetraploid plants. However, the thebaine yield was slightly reduced due to the low number of capsules in the autotetraploid plants. <br /><br />Through selection, early planting and cultivation in locations with cold winters, a high flowering rate was achieved during the first growing season despite the perennial habit of this plant. Foliar application of gibberellic acid enhanced the flowering, especially in late-flowering clones. The concentration of thebaine was not affected by GA3. However, the thebaine yield per plant was increased due to the increase in number and mass of the capsules. Studies of the accumulation of thebaine in the roots showed that the maximum concentrations were obtained at the start of the flowering stage. However, the mass of the roots and thus the thebaine yield increased until full flowering. The lower parts of the roots contained the highest thebaine concentration.<br><br><a href="http://www.backyardgardener.com/seeds/product/484.html"><br>http://www.backyardgardener.com/seeds/pr<wbr />oduct/484.html</a>&nbsp; seed packs<br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/4121.html"><img src="http://lj.rossia.org/numreplies/tryl/4121" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/4121.html http://lj.rossia.org/users/tryl/3968.html Sun, 07 Mar 2010 18:14:52 GMT http://lj.rossia.org/users/tryl/3968.html <a href="http://wiki.dmt-nexus.com/Category:Extraction_Tek">http://wiki.dmt-nexus.com/Category:Extra<wbr />ction_Tek</a><br><br><br>particularly of interest:<br><br><font size="3"><a href="http://wiki.dmt-nexus.com/BLAB_-_The_Big_Leisurely_A/B">DMT fumarate precip from d-Limonene</a><br></font><font size="2"><font size="3"><a href="http://wiki.dmt-nexus.com/Lextek">Acacia obtusifolia A/B</a><br><a href="http://wiki.dmt-nexus.com/Shaggy%27s_Jungle_Tek">jungle tek</a><br></font></font><br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/3968.html"><img src="http://lj.rossia.org/numreplies/tryl/3968" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/3968.html http://lj.rossia.org/users/tryl/3741.html Sun, 07 Mar 2010 17:51:15 GMT http://lj.rossia.org/users/tryl/3741.html <a href="http://en.wikipedia.org/wiki/Yuremamine">http://en.wikipedia.org/wiki/Yurema<wbr />mine</a><br /><br /><br /><br /><br /><br /><br><br><br><a style="font-style: italic;" href="http://wiki.dmt-nexus.com/Jungle_Spice">Jungle Spice <br /><br /><br><br>Jungle spice is one of many names that have been applied to an intriguing non-DMT alkaloid fraction that can be isolated from much of the commercially available Mimosa root bark (See V. Botanical Confustication).[1],[2],[3] In the most general terms, it is the alkaloid fraction obtained from the aqueous basic phase of an extraction by pulling with xylene or toluene after DMT ceases to be pulled by an aliphatic hydrocarbon solvent (naphtha, heptane, etc.). This product will almost always contain some N,N-DMT in addition to the more mysterious alkaloids; some extractors choose to remove the DMT in a hot naphtha wash to obtain a pure "jungle" experience, while others use the jungle/DMT mixture as it is. <br /><br />There is a great deal of ambiguity surrounding jungle spice, owing to a wide array of factors. First and foremost, there appears to be a great diversity of compounds which can be isolated by extracting the aqueous basic phase with xylene or toluene.[4],[5] Which compounds are actually isolated depends on some several of the following factors: the source and botanical identity of the root bark, the conditions of cultivation/harvest, and various pH, temperature, and airflow considerations throughout the extraction process.[6],[7],[8],[9] About all that is certain about it at this point is that it contains some psychoactive material that isn't N,N-DMT. <br /><br />There has been a lot of speculation going around that this compound may be yuremamine, the novel phytoindole isolated from Mimosa Tenuiflora and characterized in 2005.[10],[11],[12] Looking at the evidence, this scenario appears exceedingly unlikely based on yuremamine's known instability to base and speculated instability to heat.[13],[14] It can't yet be ruled out completely, but there remains a substantial body of evidence against this identification. Until an LC-MS of jungle spice emerges with a molecular ion at 477.1 m/z, I think it's safe to assume that yuremamine is not the red alkaloid that has been isolated by home extractors.</a><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/3741.html"><img src="http://lj.rossia.org/numreplies/tryl/3741" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/3741.html http://lj.rossia.org/users/tryl/3512.html Sun, 07 Mar 2010 16:55:51 GMT http://lj.rossia.org/users/tryl/3512.html #9 Posted : Monday, February 08, 2010 10:25:51 AM <br /><br /><br /><br><br><span style="font-style: italic;">You don't need to be too careful and baby the boils. Mimosa/Acid juice can withstand a fast boil. I just completed an extraction of 200gr whole bark. I broke it up with my hands, slow boiled in 1lt water at pH3 (HCL). When the bark gets softer, I remove small amounts of it with some liquid and blend it with a hand-blender. Bit by bit with juice. Makes a nice Mimosa Milkshake.<br /><br />I reduce this to about 300ml. Then I drain it, strain it, and SQUEEZE all the juice out.<br /><br />I do this again, boiling, reducing, draining, straining, SQUEEZE all the juice out.<br /><br />At the end I take a little fresh water and soak the left over plant matter till the squeezings come out clear. This way I know I have exhausted it's extract.<br /><br />I end up with 1lt mimosa soup.<br /><br />- decant over night in the fridge<br />- pour off the clear soup and filter the dregs. If you are using a sep-funnel, the dregs will block it, so get them out.<br />- I use 150gr NaOH for 200gr MHRB/1lt Juice. I mix the NaOH with water, WAIT FOR IT TO COOL, then add it to the cool MHRB soup<br />- Proceed with your solvent pulls<br /><br />It's very simple and easy once you've done a few :-)<br /><br />I like using whole bark because it makes the filtering process easier.</span><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/3512.html"><img src="http://lj.rossia.org/numreplies/tryl/3512" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/3512.html http://lj.rossia.org/users/tryl/2854.html Sun, 07 Mar 2010 00:38:53 GMT http://lj.rossia.org/users/tryl/2854.html <a href="http://sharebee.com/cb97f8be">here</a><br><br><br><br /><br /><div style="text-align:left"><font size="-2"><a href="http://lj.rossia.org/users/tryl/2854.html"><img src="http://lj.rossia.org/numreplies/tryl/2854" border=0 width=26 height=17 alt="number of comments" style="border:0px;" /> <strong>Comments</strong></a></font></div> http://lj.rossia.org/users/tryl/2854.html