
Dextroamphetamine: Difference between revisions
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{{SubstanceBox/Dextroamphetamine}} | {{SubstanceBox/Dextroamphetamine}} | ||
'''Dextroamphetamine''' ( | '''Dextroamphetamine''' (also known as '''Dexamphetamine''', '''D-Amphetamine''', '''Dex''', or by brand names including '''Adderall''', '''Dexedrine''') is a [[stimulant]] substance and one of the two optical isomers of [[amphetamine]]. | ||
Dextroamphetamine is the more potent isomer of the two, but the effects are also slightly different in character. The small difference in affinity affects the mechanism resulting in a more mentally focused stimulation rather than physical, thus creating a stimulant that is more fit for functionally/therapeutically useful drug rather than a recreational stimulant. Therefore, the dextrorotatory enantiomer is preferred in treatment of attention deficit hyperactivity disorder, whereas a racemic mixture like amphetamine is found when sold on the streets. | Dextroamphetamine is the more potent isomer of the two, but the effects are also slightly different in character. The small difference in affinity affects the mechanism resulting in a more mentally focused stimulation rather than physical, thus creating a stimulant that is more fit for functionally/therapeutically useful drug rather than a recreational stimulant. Therefore, the dextrorotatory enantiomer is preferred in treatment of attention deficit hyperactivity disorder, whereas a racemic mixture like amphetamine is found when sold on the streets. | ||
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==History and culture== | ==History and culture== | ||
In 1935, 3 years after amphetamine became widely marketed, the medical community became aware of the stimulant properties of amphetamine, specifically dextroamphetamine, and in 1937 Smith, Kline, and French introduced tablets under the tradename Dexedrine. Dexedrine is used to treat narcolepsy, attention disorders, and obesity. Additionally, it is used as an athletic performance and cognitive enhancer, and recreationally as an [[aphrodisiac]] and [[euphoriant]]. | In 1935, 3 years after amphetamine became widely marketed, the medical community became aware of the stimulant properties of amphetamine, specifically dextroamphetamine, and in 1937 Smith, Kline, and French introduced tablets under the tradename Dexedrine. Dexedrine is used to treat narcolepsy, attention disorders, and obesity. Additionally, it is used as an athletic performance and cognitive enhancer, and recreationally as an [[aphrodisiac]] and [[euphoriant]]. | ||
==Legal status== | |||
Internationally, [[amphetamine]] (and its isomers '''dextroamphetamine''' and [[levoamphetamine]]) are Schedule II controlled substances under the United Nations 1971 Convention on Psychotropic Substances.<ref>{{cite web|url=http://www.emcdda.europa.eu/system/files/attachments/10451/convention_1971_en.pdf|title=CONVENTION ON PSYCHOTROPIC SUBSTANCES 1971|publisher=United Nations|access-date=December 19, 2019}}</ref> | |||
==See also== | |||
*[[Responsible use]] | |||
*[[Stimulant]] | |||
*[[Amphetamine]] | |||
==External links== | ==External links== | ||
*[[wikipedia:Dextroamphetamine|Dextroamphetamine (Wikipedia)]] | *[[wikipedia:Dextroamphetamine|Dextroamphetamine (Wikipedia)]] | ||
*[https://erowid.org//chemicals/amphetamines/amphetamines.shtml Dextroamphetamine (Erowid Vault)] | *[https://erowid.org//chemicals/amphetamines/amphetamines.shtml Dextroamphetamine (Erowid Vault)] | ||
==References== | |||
{{reflist|2}} | |||
[[Category:Psychoactive substance]] | [[Category:Psychoactive substance]] |
Revision as of 15:00, 4 October 2023
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Summary sheet: Dextroamphetamine |
Dextroamphetamine | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Chemical Nomenclature | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Common names | Dextroamphetamine, Dexamphetamine, D-amphetamine,Dexedrine, Dex, Attentin | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Substitutive name | D-Amphetamine | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Systematic name | (2S)-1-phenylpropan-2-amine | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Class Membership | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Psychoactive class | Stimulant | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical class | Phenethylamine | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Routes of Administration | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Interactions | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Alcohol | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
GHB | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
GBL | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Opioids | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cannabis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Caffeine | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ketamine | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Methoxetamine | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Psychedelics | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cocaine | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DXM | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
PCP | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
25x-NBOMe | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
2C-T-x | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
5-MeO-xxT | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DOx | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tramadol | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
aMT | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
MAOIs |
Dextroamphetamine (also known as Dexamphetamine, D-Amphetamine, Dex, or by brand names including Adderall, Dexedrine) is a stimulant substance and one of the two optical isomers of amphetamine.
Dextroamphetamine is the more potent isomer of the two, but the effects are also slightly different in character. The small difference in affinity affects the mechanism resulting in a more mentally focused stimulation rather than physical, thus creating a stimulant that is more fit for functionally/therapeutically useful drug rather than a recreational stimulant. Therefore, the dextrorotatory enantiomer is preferred in treatment of attention deficit hyperactivity disorder, whereas a racemic mixture like amphetamine is found when sold on the streets.
It is highly advised to use harm reduction practices if using this substance.
Chemistry
With regular synthesis, the resulting product will always be a racemic mixture. An enantiopure can be obtained through a biological synthesis route, where certain proteins form only one of the two isomers or through isolation of one isomer from a previously racemic mixture. Financially it would be beneficial to use the biological process, since it requires only little materials, but instead can be performed by bacteria that can be genetically altered to perform the synthesis for you. Those bacteria multiply by themselves, thus automatically creating a long-term production solution. [citation needed]
History and culture
In 1935, 3 years after amphetamine became widely marketed, the medical community became aware of the stimulant properties of amphetamine, specifically dextroamphetamine, and in 1937 Smith, Kline, and French introduced tablets under the tradename Dexedrine. Dexedrine is used to treat narcolepsy, attention disorders, and obesity. Additionally, it is used as an athletic performance and cognitive enhancer, and recreationally as an aphrodisiac and euphoriant.
Legal status
Internationally, amphetamine (and its isomers dextroamphetamine and levoamphetamine) are Schedule II controlled substances under the United Nations 1971 Convention on Psychotropic Substances.[3]
See also
External links
References
- ↑ "chemeurope.com - Amphetamine
- ↑ "Drugbank - Amphetamine
- ↑ "CONVENTION ON PSYCHOTROPIC SUBSTANCES 1971" (PDF). United Nations. Retrieved December 19, 2019.