3c-p - Drugs Forum
Drugs-Forum  
News Groups Blog Forum Chat Video Audio Images Documents Wiki Home
Go Back   Drugs Forum > CHEMICAL & (SEMI-) SYNTHETIC DRUGS > Research Chemicals
Register Tags Mark Forums Read

Notices

Research Chemicals Piperazines, Phenethylamines, Tryptamines & other Research Chemicals or designer drugs.

Reply
 
Thread Tools Display Modes
  #1  
Old 02-09-2004, 21:46
nikonikad's Avatar
nikonikad nikonikad is offline
Account Awaiting Email Confirmation.
 
Join Date: 07-08-2004
Location: Swiss
Posts: 113
nikonikad is a decent SWIMmer.nikonikad is a decent SWIMmer.
Points: 914, Level: 4 Points: 914, Level: 4 Points: 914, Level: 4
Activity: 0% Activity: 0% Activity: 0%
Has somebody ever tried this chem
Reply With Quote
  #2  
Old 02-09-2004, 22:01
P4nic P4nic is offline
Account Awaiting Email Confirmation.
 
Join Date: 28-06-2004
Location: Belgium
Posts: 243
P4nic is an unknown quantity at this point
Points: 488, Level: 3 Points: 488, Level: 3 Points: 488, Level: 3
Activity: 0% Activity: 0% Activity: 0%


Never heard of it, looked it up on google and almost no information about it only on erowid there's a report of it with that guy going totally loss but it was in combination with other drugs so no really objective information about this drugs.


experience story: http://www.erowid.org/experiences/exp.php?ID=32073
Reply With Quote
  #3  
Old 12-09-2004, 05:50
HeavenBound HeavenBound is offline
Account Awaiting Email Confirmation.
 
Join Date: 12-09-2004
Location: United States
Posts: 4
HeavenBound is an unknown quantity at this point
Points: 27, Level: 1 Points: 27, Level: 1 Points: 27, Level: 1
Activity: 0% Activity: 0% Activity: 0%
I have read in other forums that it was a "dud." The small amount of feedback i have seen in regard to its effects were generally not positive.
Reply With Quote
  #4  
Old 25-10-2004, 19:05
Ximot's Avatar
Ximot Ximot is offline
Ximot is re-establishing his respect for the sacraments
Account Awaiting Email Confirmation.
 
Join Date: 26-06-2004
Location: Europe! Where is Belize anyway?
Posts: 155
Ximot is learning how to SWIM.
Points: 290, Level: 2 Points: 290, Level: 2 Points: 290, Level: 2
Activity: 0% Activity: 0% Activity: 0%
I think it's from the piperazine family, or related. I have seen this sold in Japan openly, but I know of nobody who has tried it. I'd steer clear of anything related to bzp or tfmpp and all that. too many side effects.
Reply With Quote
  #5  
Old 26-10-2004, 06:01
taka taka is offline
Newbie
 
Join Date: 12-10-2004
Location: Japan
Posts: 7
taka is an unknown quantity at this point
Points: 27, Level: 1 Points: 27, Level: 1 Points: 27, Level: 1
Activity: 0% Activity: 0% Activity: 0%
Is it "3CPP" ?
If it is so, it's 1-(3-Chlorophenyl)piperazine.
But I haven't tried it.
Reply With Quote
  #6  
Old 28-10-2004, 07:57
Lynchx Lynchx is offline
Newbie
 
Join Date: 21-10-2004
Location: United States
Age: 26
Posts: 87
Lynchx should urgently read the rules.
Points: 597, Level: 3 Points: 597, Level: 3 Points: 597, Level: 3
Activity: 0% Activity: 0% Activity: 0%
never even heard of it
Reply With Quote
  #7  
Old 26-01-2005, 17:46
midnight577 midnight577 is offline
Account Awaiting Email Confirmation.
 
Join Date: 20-12-2004
Posts: 1
midnight577 is an unknown quantity at this point
Points: 16, Level: 1 Points: 16, Level: 1 Points: 16, Level: 1
Activity: 0% Activity: 0% Activity: 0%
The amphetamine homologue of proscaline, 3,5-dimethoxy-4-(n)-propoxy-amphetamine is an unexplored compound. Its synthesis could not be achieved in parallel to the description given for P. Rather, the propylation of syringaldehyde to give 3,5-dimethoxy-4-(n)-propoxybenzaldehyde, followed by coupling with nitroethane and the reduction of the formed nitrostyrene with lithium aluminum hydride would be the logical process. Following the reasoning given under E, the initials for this base would be 3C-P, and I would guess it would be active, and a psychedelic, in the 20 to 40 milligram range.


<H2>#140 P</H2>PROSCALINE; 3,5-DIMETHOXY-4-(n)-PROPOXYPHENETHYLAMINE



<TABLE align=left>
<T>
<TR>
<TD> </TD></TR>
<TR>
<TD align=middle height=24>[3D .mol structure] </TD></TR></T></TABLE>SYNTHESIS: A solution of 5.8 g of homosyringonitrile (see under E for its synthesis), 100 mg decyltriethylammonium iodide, and 10 g n-propyl bromide in 50 mL anhydrous acetone was treated with 6.9 g finely powdered anhydrous K2CO3 and held at reflux for 10 h. An additional 5 g of n-propyl bromide was added to the mixture, and the refluxing continued for another 48 h. The mixture was filtered, the solids washed with acetone, and the combined filtrate and washes stripped of solvent under vacuum. The residue was suspended in acidified H2O, and extracted 3x175 mL CH2Cl2. The pooled extracts were washed with 2x50 mL 5% NaOH, once with dilute HCl (which lightened the color of the extract) and then stripped of solvent under vacuum giving 9.0 g of a deep yellow oil. This was distilled at 132-142 °C at 0.3 mm/Hg to yield 4.8 g of 3,5-dimethoxy-4-(n)-propoxyphenylacetonitrile as a clear yellow oil. Anal. (C13H17NO3) C H N.

A solution of 4.7 g 3,5-dimethoxy-4-(n)-propoxyphenylacetonitrile in 20 mL THF was treated with 2.4 g powdered sodium borohydride. To this well-stirred suspension there was added, dropwise, 1.5 mL trifluoroacetic acid. There was a vigorous gas evolution from the exothermic reaction. Stirring was continued for 1 h, then all was poured into 300 mL H2O. This was acidified cautiously with dilute H2SO4, and washed with 2x75 mL CH2Cl2. The aqueous phase was made basic with dilute NaOH, extracted with 2x75 mL CH2Cl2, the extracts pooled, and the solvent removed under vacuum. The residue was distilled at 115-125 °C at 0.3 mm/Hg to give 1.5 mL of a colorless oil which upon dissolving in 5 mL IPA, neutralizing with 27 drops concentrated HCl, and dilution with 25 mL anhydrous Et2O yielded 1.5 g 3,5-dimethoxy-4-(n)-propoxyphenethylamine hydrochloride (P) as spectacular white crystals. The catalytic hydrogenation process for reducing the nitrile (see under E) also succeeded with this material. The mp was 170-172 °C. Anal. (C13H22ClNO3) C,H,N.

DOSAGE: 30 - 60 mg.

DURATION: 8 - 12 h.

QUALITATIVE COMMENTS: (with 30 mg) Proscaline dulled my sense of pain and made the other senses really sharp. Everything felt really soft, and clean and clear. I could feel every hair my hand was touching. I felt so relaxed and at ease. I know that under the appropriate circumstances, this material would lead to uninhibited eroticism.

(with 35 mg) The whole experiment was very quiet. There was no nystagmus, no anorexia, and insignificant visuals with the eyes closed. I was restless with a bit of tremor for the first couple of hours, and then became drowsy. Would I do this again? Probably not. It doesn't seem to offer anything except speculation about the nature of the high. The high was pleasant, but quite uneventful.

(with 40 mg) For me there was a deep feeling of peace and contentment. The euphoria grows in intensity for several hours and remains for the rest of the day making this one of the most enjoyable experiences I have ever had. It was marvel-ous talking and joking with the others. However, I was a little disappointed that there was no enhanced clarity and no deep realizations. There was not a problem to be found. There were no motivations to discuss anything serious. If I had any objection, it would be with the name, not the pharmacology.

(with 60 mg) The development of the intoxication was complete in a couple of hours. I feel that there is more physical effect than mental, in that there is considerable irritability. This should probably be the maximum dose. Despite feeling quite drunk, my thinking seems straight. The effects were already waning by the fifth hour, but sleep was not possible until after the twelth hour. There was no hangover the next day.

EXTENSIONS AND COMMENTARY: There is a very early report describing the human use of proscaline tucked away in the Czechoslovakian literature that describes experiments at up to 80 milligrams. At these dosages, there were reported some difficulty with dreams, and the residual effects were still apparent even after 12 hours.
Reply With Quote
  #8  
Old 26-01-2005, 21:19
Lacognac69 Iridium member Lacognac69 is offline
Iridium Member
 
Join Date: 24-01-2005
Location: miami
Posts: 149
Lacognac69 is an unknown quantity at this point
Points: 411, Level: 3 Points: 411, Level: 3 Points: 411, Level: 3
Activity: 0% Activity: 0% Activity: 0%
hmm that stuff sounds decent. Is that source from pihkal or
something else because you mentioned it was a very early report from
czechoslovakian liteature, but it looks like somethin from pihkal.
Reply With Quote
  #9  
Old 26-01-2005, 22:59
psy-marshal's Avatar
psy-marshal psy-marshal is offline
Silver Member
 
Join Date: 25-01-2005
Location: Berlin
Age: 31
Posts: 29
psy-marshal is a decent SWIMmer.psy-marshal is a decent SWIMmer.
Points: 299, Level: 2 Points: 299, Level: 2 Points: 299, Level: 2
Activity: 0% Activity: 0% Activity: 0%
I had some of this, and was all set to try it, but my little bottle fell on the ground and smashed all over the place.

Now I guess I will never ever get to...
Reply With Quote
  #10  
Old 26-01-2005, 23:05
Sasha Gulag Gold member Sasha Gulag is offline
Gold Member
 
Join Date: 28-12-2004
Location: United States
Age: 27
Posts: 271
Sasha Gulag is learning how to SWIM.
Points: 882, Level: 4 Points: 882, Level: 4 Points: 882, Level: 4
Activity: 0% Activity: 0% Activity: 0%


id like to see some of those crazy pihkal chems besides the 2c series of PEAs


what about the ALEPH chems? or Ganesha or ARiadne?


when will these RC's show up??
Reply With Quote
Reply

Bookmarks

Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump


Sitelinks: Site Functions:

All times are GMT +1. The time now is 01:57.


Copyright: Substance Information Network 2003 - 2009, All rights reserved