had a proper dose of 3Cl-PCP by now. this stuff is disguisting, as bad as 2-fdck. dont know if 3F-PCP is similar. can anybody make a comparison about these two? 3meo-pcp was miles better. so anybody with experience of 3cl-pcp and 3f-pcp?
To me,
I've had both a dozen times or more now, as well as FXE, and I think
3C-PCP is pretty close in qualitative effects to 3F-PCP, which makes sense given how
both fluorine and chlorine are halogens and in the same column on the periodic table. So
your instincts are right – the two drugs are similar…
…
yet they're also distinct. I'll take the 3-fluorinated compound over the 3-chlorinated, but still much prefer either 3-MeO-PCP or 3-HO-PCP. Or MXE, PCP, PCE, 3-MeO-PCE, or 3-HO-PCE, in that order of preference. I personally rank all as superior to 3F-PCP, which itself is superior to 3Cl-PCP. These 3-halogen-substituted compounds are not without their own charms though. For me, the
dose needs to be low – 15 mg to 25 mg seems about right. Any lower and I won't feel a thing; any higher and I risk getting the spins, nausea and/or vomiting. It's best to
keep expectations low, and then the minor buzz they provide is pleasant, bubbly & social, somewhat disinhibiting, and perhaps even a worthwhile antidepressant of sorts. I find this is true of both drugs, with 3F-PCP feeling smoother and 3Cl-PCP feeling spacier yet slightly more manic-prone.
It's very painful to insufflate either drug, but especially 3C-PCP.
Hope that helps.
I imagine 3F-PCP is to PCP as 2-fluoromethamphetamine (2-FMA) is to methamphetamine. That is, very different.
Pretty accurate, especially insofar as to say: with 2-FMA and 3F-PCP/3C-PCP, I'm limited in RoA and the dose window where it's enjoyable is pretty small. Conversely, Methamphetamine and PCP are both open to a number of routes of administration and it has a wider, dose-dependant breadth of action.
However, if you take very large doses of 2-FMA it does eventually resemble methamphetamine somewhat. I imagine this is the case with 3F-PCP; it is a very different drug than PCP but at high enough doses it will begin to resemble the parent compound.
In theory, both drugs should lead to full anesthesia, but otherwise I don't consider 3C-PCP or 3F-PCP to come close to some of the profound states I experience on many of the other compounds in the family such as PCP, 3-HO-PCP, and 3-MeO-PCP. This is fairly consistent, too. Large doses of 3CL-PCP or 3F-PCP are not euphoric or pleasant at all. Bad times.
Similarly I disagree that "if you take very large doses of 2-FMA it does eventually resemble methamphetamine somewhat." This is true maybe in only the loosest sense. Large doses of 2FMA are uncomfortable and lack the euphoria central to the large-dose methamphetamine experience. At least this is my experience. So there is a corollary, but I don't think either RC ever reaches the full potential of their respective parent compounds. Just my proverbial two cents anyway…