Mar 4, 2017
2c-cNbome I laid along time ago
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2c-cNbome I laid along time ago
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This fits perfectly with the Shulgin and 2C-B presentation I just did on tuesday :D This Index is simply wonderful!
2C-C
Sampled 25mg of 2C-C earlier, administered via plugging. The one hour peak was marvelously visual, mild to moderate effects persisted for an hour to an hour and a half after the peak. I'm now in the afterglow stage, reflecting on a wonderful experience.
This is the strangest life I've ever known
My last 2C-C trip on Sunday focused around the need to find another person to be with, the very next day an absolutely gorgeous 18 year old woman gives me her number at work. Strange magic :)
2C-C is quickly becoming one of my favorite psychedelic phenethylamines. I plugged 25mg this morning, my third trial with the compound. The visuals are quite lovely and the body feel is very refreshing and relaxing. It is a marvelous compound.
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2C-C follow up
I opted to try 2C-C again, and I plugged 20mg at 5:30PM. There was some mild discomfort after administration which faded after ~2 minutes as is typical when plugging the 2C-X series. I spent the duration of the come up in the shower basking in its warmth, relaxing after work. I exited the bathroom to find myself in the midst of a clear-headed psychedelic experience. The peak of the experience only lasted about an hour or so, which I spent laying in bed listening to Sticky Fingers by the Rolling Stones. The visuals of 2C-C at 20mg were impressive to say the least, very colorful indeed. The visual style was of a very gentle, flowing nature and each new musical note sent ripples of neon colors throughout the room. Had some CEVs which resembled erotic scenes at some points. Tactile sensations were enhanced greatly and I again found no traces of the metallic overtone reported in PiHKAL. After ~55 minutes or so of the peak I actually fell asleep for ~5 minutes which was quite odd. After waking up the experience began to fade quickly, visual effects were mostly gone by 7:30PM except for color enhancement. I vaporized cannabis at this time, but it did not succeed in bringing the visuals back. By 8:00PM most activity had completely faded, it is 8:30PM now and I only have slightly elevated trails and visual static compared to baseline.
2C-C report
"T" and I consumed 28mg of 2C-C orally last night. I felt the body high begin at around T+30 and it continued to rise until about T+110. By T+120 pupils were slightly dilated, but no visual effects were noted. At T+140 I plugged 15mg of 2C-C. It came on in approximately 10-15 minutes and I was peaking 20-30 minutes after administration. Visuals were more animated than 2C-E and had another layer of depth added in which was reminiscent of 25C-NBOMe. Effects were mild and only persisted for 2-3 hours before returning to baseline. No nausea was noted over the course of the entire experience and there was no stomach discomfort. The headspace was very clean and relaxed. I experienced some rushes from the body high but it was more of a relaxed feeling compared to the surges which 2C-E provides. I had no shaking/muscle tremors throughout the experience. I did not experience the metallic overtone which Shulgin discussed in the 2C-C entry in PiHKAL. In fact, it was much less pronounced than 2C-E, if even present at all. Plugging is definitely the best ROA for this compound, oral dosing does not seem to be very efficient. I may have some 4-AcO-DMT later ~17-20 mg or so, I haven't taken it in a fair amount of time.
The halogens represent a small group of atoms that are unique for a couple of reasons. They are all located in a single column of the periodic table, being monovalent and negative. That means that they can be reasonably stable things when attached to an aromatic nucleus. But, being monovalent, they cannot be modified or extended in any way. Thus, they are kind of a dead end, at least as far as the 2C-X series is considered. The heaviest, iodine, was explored as the phenethylamine, as 2C-I, and as the amphetamine as DOI. These are the most potent. The next lighter is bromine, where the phenethylamine is 2C-B and the amphetamine is DOB. These two are a bit less potent, and are by far the most broadly explored of all the halides. Here, in the above recipe, we have the chlorine counterpart, 2C-C. There is also the corresponding amphetamine DOC. These are less potent still, and much less explored. Why? Perhaps because chlorine is a gas and troublesome to handle (bromine is a liquid, and iodine is a solid). The fluorine analogue is yet harder to make, and requires procedures that are indirect, because fluorine (the lightest of all the halides) is not only a gas, but is dangerous to handle and does not react in the usual halogen way. There will be mention made of 2C-F, but DOF is still unexplored.
The treatment of the 2C-B phthalimide described above, with cuprous cyanide rather than cuprous chloride, gave rise to the cyano analog which, on hydrolysis with hydrazine, yielded 2,5-dimethoxy-4-cyanophenethylamine (2C-CN). Hydrolysis of this with hot, strong base gave the corresponding acid, 2,5-dimethoxy-4-carboxyphenethylamine, 2C-COOH. No evaluation of either of these compounds has been made in the human animal, as far as I know.