Bromo-DragonFLY: Difference between revisions
>Dextromethorphan No edit summary |
>Dextromethorphan No edit summary |
(No difference)
| |
Revision as of 00:54, 19 October 2016
|
|
| Bromo-DragonFLY | |||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
 |
|||||||||||||||||||||||||||||||||
| Chemical Nomenclature | |||||||||||||||||||||||||||||||||
| Common names | Bromo-DragonFLY, DOB-DragonFLY, B-DFLY, Dragonfly | ||||||||||||||||||||||||||||||||
| Substitutive name | 8-bromo-4-(2-aminopropyl)benzodifuran | ||||||||||||||||||||||||||||||||
| Systematic name | (1-(8-bromobenzo[1,2-b;4,5-b']difuran-4-yl)-2-aminopropane | ||||||||||||||||||||||||||||||||
| Class Membership | |||||||||||||||||||||||||||||||||
| Psychoactive class | Psychedelic | ||||||||||||||||||||||||||||||||
| Chemical class | Amphetamine / Benzodifuran | ||||||||||||||||||||||||||||||||
| Routes of Administration | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
| Interactions | |||||||||||||||||||||||||||||||||
| Summary sheet: Bromo-DragonFLY |
Bromo-DragonFLY is a psychedelic phenethylamine of the DOx family. It produces unusually long psychedelic effects which can last up to several days. It is considered as mild in comparison to LSD.
Very little is known about this substance, but it gained popularity about a decade ago after several deaths occurred in October 2009 after the ingestion of a substance that was mislabelled and sold as 2C-B-FLY or 2C-E but was actually Bromo-DragonFLY.[1]
Chemistry
2C-H or 2,5-dimethoxyphenethylamine is a substituted phenethylamine featuring a phenyl ring bound to an amino (NH2) group through an ethyl chain. 2C-H contains methoxy functional groups CH3O- attached to carbons R2 and R5 as well as a hydrogen atom attached to carbon R4 of the phenyl ring. 2C-H belongs to the 2C family of phenethylamines which contain methoxy groups on the 2 and 5 positions of the benzene ring, and is also their simplest member. It is commonly used as a precursor to other compounds of the 2C family, including, but not limited to 2C-B, 2C-C, 2C-I, 2C-N and 2C-TFM.
Pharmacology
 |
This pharmacology section is incomplete. You can help by adding to it. |
It is believed that 2C-H has little to no affinity for the 5-HT2A receptor, thus being not psychedelic. It does however, have affinity for the 5-HT2C receptor, which is responsible for some stimulant effects.
Subjective effects
 |
This subjective effects section is a stub. As such, it is still in progress and may contain incomplete or wrong information. You can help by expanding or correcting it. |
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
- Stimulation
- Abnormal heartbeat
- Appetite suppression
- Bronchodilation
- Dehydration
- Frequent urination
- Increased bodily temperature
- Increased blood pressure
- Increased heart rate
- Increased perspiration
- Nausea
- Pupil dilation
- Stamina enhancement
- Teeth grinding
- Temporary erectile dysfunction
- Vasoconstriction
Cognitive effects
- Analysis enhancement
- Cognitive euphoria
- Compulsive redosing
- Dream suppression
- Ego inflation
- Focus enhancement - This component is most effective at low to moderate doses as anything higher will usually impair concentration.
- Increased libido
- Increased music appreciation
- Memory enhancement
- Motivation enhancement
- Thought acceleration
- Thought organization
- Wakefulness
Toxicity and harm potential
 |
This toxicity and harm potential section is a stub. As a result, it may contain incomplete or even dangerously wrong information! You can help by expanding upon or correcting it. |
The toxicity and long-term health effects of recreational 2C-H use do not seem to have been studied in any scientific context and the exact toxic dose is unknown. This is because 2C-H is a research chemical with very little history of human usage. 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.
Legal issues
Canada: As of October 31st, 2016, 2C-H is a controlled substance (Schedule III) in Canada, and is thus illegal to possess, produce and sell.[2]
United States: As of July 9, 2012, 2C-H is a Schedule I controlled substance in the United States, under the Synthetic Drug Abuse Prevention Act of 2012.[3]