2C-I

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2C-I
The skeletal formula of 2C-I
2C-I.png
2CI3D.gif
Chemical Nomenclature
Common names 2C-I
Substitutive name 2,5-Dimethoxy-4-iodophenethylamine
Class Membership
Psychoactive class Psychedelic, Entactogen
Chemical class Phenethylamine
Routes of Administration



Oral
Dosage
WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.
DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.
Threshold 2 - 5 mg
Light 5 - 15 mg
Common 10 - 25 mg
Strong 20 - 30 mg
Heavy 30 mg +
Duration
Total 5 - 10 hours
Onset 20 - 90 minutes
Come up 20 - 30 minutes
Peak 3 - 7 hours
Offset 1 - 2 hours
After effects 2 - 4 hours









Summary sheet: 2C-I

2C-I or 2,5-dimethoxy-4-iodophenethylamine is a psychedelic phenethylamine of the 2C-x family.[1] It was first synthesized by Alexander Shulgin in the 1991 book PiHKAL: A Chemical Love Story. The drug is used recreationally for its psychedelic and entactogenic effects and has been explored as a potential stimulant nootropic in doses between 1-8mg.

2C-I is sometimes confused for the analog 25I-NBOMe and is commonly sold in its hydrochloride salt form which is a fluffy, sparkling, white powder which is sometimes pressed into tablet form.

Chemistry

General formula of phenethylamine molecule

2,5-dimethoxy-4-iodophenethylamine is a substituted phenethylamine featuring a phenyl ring bound to an amino (NH2) group through an ethyl chain. 2C-I contains methoxy functional groups CH3O- attached to carbons R2 and R5 as well as an iodine attached to carbon R4 of the phenyl ring. 2C-I belongs to the 2C family of phenethylamines which contain methoxy groups on the 2 and 5 positions of the benzene ring.[2]

Pharmacology

2C-I's psychedelic effects are believed to come from its efficacy at the 5-HT2A receptor as a partial agonist. However, the role of these interactions and how they result in the psychedelic experience continues to remain elusive.

Subjective effects

The effects listed below are based upon the subjective effects index and personal experiences of PsychonautWiki contributors. The listed effects will rarely (if ever) occur all at once, but heavier dosages will increase the chances and are more likely to induce a full range of effects.

Physical effects

  • Spontaneous tactile sensations - The "body high" of 2C-I is manifested as one of the most proportionally intense in comparison to almost all of the classical psychedelics. The sensation itself can be described as an intense and slightly uncomfortable energetic pins and needles sensation that constantly encompasses a person’s entire body. It is usually felt over every square inch of the skin but occasionally manifests itself in the form of a continuously shifting, tingling sensation that travels up and down the body in spontaneous waves. Alongside of this, many users commonly report that the "body high" can be particularly uncomfortable and sometimes accompanied by dysphoric aches and urges to shift the position of one's body and prolonged tensing of unusual combinations of muscle groups.
  • Bodily control enhancement
  • Increased heart rate
  • Nausea - Mild to extreme nausea is consistently reported when consumed in moderate to high doses and either passes once the tripper has vomited or gradually fades by itself as the peak sets in.
  • Euphoria - Feelings of frequent but unpredictable rushes of warm physical euphoria are extremely common and very pleasurable. These move from the top of the head downwards before enveloping one's whole body.
  • Pupil dilation
  • Stimulation - In terms of its effects on the physical energy levels of the tripper, 2C-I is usually considered to be very energetic and stimulating in a fashion that is quite comparable to that of MDMA although it is encouraged instead of forced.
  • Tactile enhancement
  • Temperature regulation suppression

Cognitive effects

The head space of 2C-I is described by many as one which is relatively normal in its thought processes even at moderate to high doses. It is often said to lack insight when compared to that of 2C-E, 2C-B and LSD.

The total sum of these cognitive components regardless of the setting generally includes:

Visual effects

Enhancements

Distortions

Geometry

The visual geometry that is present throughout this trip can be described as more similar in appearance to that of LSD or 2C-B than that of 2C-E, psilocin, or ayahuasca although it is much more bland and less detailed. They can be comprehensively described as unstructured in their organization, algorithmic in geometric style, intricate in complexity, large in size, fast and smooth in motion, colourful in scheme, glossy in colour, both soft and sharp in their edges as well as equally rounded and angular in their corners. They seem high in algorithmic visuals such as fractals and at higher doses are significantly more likely to result in states of level 8A visual geometry over level 8B.

Hallucinatory states

Like LSD, while 2C-I is capable of producing a full range of low and high level hallucinatory states, this is extremely rare and inconsistent at higher levels but common at lower and generally includes the following effects:

Auditory effects

Multi-sensory effects

Toxicity and harm potential

Lolol.pngMain articles: Research chemicals § Toxicity and harm potential & Responsible use § Hallucinogens

The toxicity and long-term health effects of recreational 2C-I use do not seem to have been studied in any scientific context and the exact toxic dose is unknown. This is because 2C-I is a research chemical with very little history of human usage. Anecdotal evidence from people within the psychonaut community who have tried 2C-I suggests that there are no negative health effects attributed to simply trying the drug by itself at low to moderate doses and using it very sparingly (but nothing can be completely guaranteed). Independent research should always be done to ensure that a combination of two or more substances is safe before consumption.

It is strongly recommended that one use harm reduction practices when using this drug.

Tolerance and addiction potential

2C-I is not habit-forming and the desire to use it can actually decrease with use. It is most often self-regulating.

Tolerance to the effects of 2C-I are built almost immediately after ingestion. After that, it takes about 3 days for the tolerance to be reduced to half and 7 days to be back at baseline (in the absence of further consumption). 2C-I presents cross-tolerance with all psychedelics, meaning that after the consumption of 2C-I all psychedelics will have a reduced effect.

Legal issues

  • European Union: In December 2003, the European Council issued a binding order compelling all EU member states to ban 2C-I within three months.
  • Denmark: It is a controlled substance.[3]
  • Germany: It is a controlled substance.[3]
  • Greece: It is a controlled substance.[3]
  • Ireland: The drug is a controlled substance.[3]
  • Italy: It is a controlled substance.[3]
  • Latvia: 2C-I is a Schedule I controlled substance.[4]
  • Netherlands: It is a controlled substance.[3]
  • Poland: It is a controlled substance.[3]
  • Sweden: Sveriges riksdag added 2C-I to Schedule I ("substances, plant materials and fungi which normally do not have medical use") as a narcotic in Sweden as of March 16, 2004.[5]
  • United Kingdom: It is controlled as a Class A substance.[3]
  • U.S.: As of July 9, 2012, 2C-I is a Schedule I substance in the U.S. under the Synthetic Drug Abuse Prevention Act of 2012, making possession, distribution and manufacture illegal.[3]

See also

External links

References

  1. Alexander Shulgin - TIHKAL | http://www.erowid.org/library/books_online/pihkal/pihkal033.shtml
  2. http://isomerdesign.com/PiHKAL/read.php?id=24
  3. 3.0 3.1 3.2 3.3 3.4 3.5 3.6 3.7 3.8 Erowid.org, Legal Status of 2C-I
  4. Noteikumi par Latvijā kontrolējamajām narkotiskajām vielām, psihotropajām vielām un prekursoriem (2,5-Dimetoksifeniletānamīni) | http://likumi.lv/doc.php?id=121086
  5. http://www.lakemedelsverket.se/upload/lvfs/LVFS_2004-3.pdf