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Buy Proscaline Online
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Proscaline

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Buy Proscaline Online

Proscaline is a designer drug, 4 propoxy 3,5 DMPEA, psychedelic-hallucinogen. Proscaline has properties like mescaline, isoproscaline, and also escaline.
Catalog No.
S689650
CAS No.
39201-78-0
M.F
C13H21NO3
M. Wt
239.31 g/mol
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Buy Proscaline Online

Buy Proscaline Online, chemically known as 4-propoxy-3,5-dimethoxyphenethylamine, is a psychedelic substance belonging to the phenethylamine class. It is structurally related to mescaline and its analogs, such as isoproscaline and escaline. Proscaline was first synthesized by David E. Nichols in 1977, and its effects were later documented by Alexander Shulgin in his book PiHKAL (Phenethylamines I Have Known and Loved), where it was noted to have a potency estimated to be five times that of mescaline

Where to Buy Proscaline | 39201-78-0

Where to Buy Proscaline Online (3,4-dimethoxy-4-propoxyphenethylamine) is a psychedelic substance with a chemical structure similar to mescaline. However, unlike mescaline, which is derived from the peyote cactus, proscaline does not occur naturally. Because of this, and its psychoactive properties, proscaline is a Schedule I controlled substance in the United States, making it difficult to obtain for scientific research purposes [US Drug Enforcement Administration.

Potential Research Areas:

Despite the limitations, Order Proscaline Online could be a valuable tool in studying consciousness and perception. Studies on other psychedelic drugs, such as LSD and psilocybin, have shown promise in treating mental health conditions like depression and anxiety [National Institute of Mental Health].The mechanism by which these drugs produce these effects is not fully understood, but proscaline’s similarity to mescaline, which has also been shown to have therapeutic potential [Passie et al., 2008], could provide insights into the neurological basis of these conditions. Purchase Proscaline Online

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Chemical Reactions

Typical of phenethylamines:

  • Oxidation: Proscaline can be oxidized to form quinones using reagents such as potassium permanganate or chromium trioxide.
  • Reduction: The nitro group in intermediates can be reduced to an amine, typically using lithium aluminum hydride.
  • Substitution: The methoxy groups can participate in nucleophilic substitution reactions with nucleophiles like sodium methoxide

Common Reagents and Conditions

Reaction Type Reagents Major Products
Oxidation Potassium permanganate Quinones
Reduction Lithium aluminum hydride Amines
Substitution Sodium methoxide Substituted phenethylamines

Synthesis Methods | Order Proscaline Online

The synthesis of proscaline typically follows these steps:

  • Starting Material: 3,5-dimethoxybenzaldehyde is reacted with nitroethane in the presence of a base to form 3,5-dimethoxy-4-nitrostyrene.
  • Reduction: The nitrostyrene is reduced using lithium aluminum hydride to yield 3,5-dimethoxy-4-aminostyrene.
  • Alkylation: Alkylation occurs with propyl bromide to form 4-propoxy-3,5-dimethoxyphenethylamine.
  • Hydrochloride Formation: The free base is converted into its hydrochloride salt using hydrochloric acid

Similar Compounds: Comparison with Other Compounds

Proscaline shares structural similarities with several other compounds within the phenethylamine class. Below is a comparison highlighting its uniqueness:

Compound Structural Feature Unique Characteristics
Mescaline No propoxy group Classic psychedelic known for strong visual effects
Isoproscaline Isopropoxy group Similar structure but different potency profile
Escaline Ethoxy group Different pharmacological properties compared to proscaline
Allylescaline Allyloxy group Varies in effects due to structural differences
Methallylescaline Methallyloxy group Distinct from proscaline in terms of psychoactive effects

Proscaline’s unique propoxy group differentiates it from these compounds, contributing to distinct pharmacological effects and potency levels

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