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The Chemistry Behind Alpha-PHP: What We Know So Far
Alpha-PHP (also known as α-Pyrrolidinohexiophenone) is a synthetic stimulant and cathinone derivative that belongs to the broader class of substituted cathinones. These substances typically exhibit stimulant and empathogenic effects and are often compared to other common stimulants like amphetamines.
Chemical Structure and Mechanism of Action
Alpha-PHP shares similarities with other synthetic cathinones like alpha-PVP (α-pyrrolidinopentiophenone) and methylone. Its structure is characterized by a pyrrolidine ring (a five-membered nitrogen-containing heterocyclic structure) attached to a hexyl chain and a ketone functional group (-C=O) on the aromatic ring.
The chemical structure of Alpha-PHP can be broken down into the following components:
1) Pyrrolidine ring: A nitrogen-containing structure that is crucial for its stimulant effects.
2) Aromatic ring (phenyl group): This is part of the molecule that contributes to its interaction with various receptors in the brain.
3) Ketone group: A carbonyl functional group (-C=O) attached to the aromatic ring, which plays a role in the molecule's ability to cross the blood-brain barrier and interact with brain chemistry.
4)Hexyl group: A six-carbon alkyl chain that influences the molecule lipophilicity (ability to dissolve in fat) and affects its potency and pharmacokinetics.
Alpha-PHP (also known as α-Pyrrolidinohexiophenone) is a synthetic stimulant and cathinone derivative that belongs to the broader class of substituted cathinones. These substances typically exhibit stimulant and empathogenic effects and are often compared to other common stimulants like amphetamines.
Chemical Structure and Mechanism of Action
Alpha-PHP shares similarities with other synthetic cathinones like alpha-PVP (α-pyrrolidinopentiophenone) and methylone. Its structure is characterized by a pyrrolidine ring (a five-membered nitrogen-containing heterocyclic structure) attached to a hexyl chain and a ketone functional group (-C=O) on the aromatic ring.
The chemical structure of Alpha-PHP can be broken down into the following components:
Pyrrolidine ring: A nitrogen-containing structure that is crucial for its stimulant effects.
1) Aromatic ring (phenyl group): This is part of the molecule that contributes to its interaction with various receptors in the brain.
2) Ketone group: A carbonyl functional group (-C=O) attached to the aromatic ring, which plays a role in the molecule's ability to cross the blood-brain barrier and interact with brain chemistry.
3) Hexyl group: A six-carbon alkyl chain that influences the molecule lipophilicity (ability to dissolve in fat) and affects its potency and pharmacokinetics.
Our extensive range of products spans chemical and spectroscopy applications.
You can search and buy our chemical compounds and full product range online.
https://narcochems.com/en/product/alpha-php/
https://narcochems.com/es/producto/alfa-php/
telegram: https://t.me/narcochemlab
Alpha-PHP (also known as α-Pyrrolidinohexiophenone) is a synthetic stimulant and cathinone derivative that belongs to the broader class of substituted cathinones. These substances typically exhibit stimulant and empathogenic effects and are often compared to other common stimulants like amphetamines.
Chemical Structure and Mechanism of Action
Alpha-PHP shares similarities with other synthetic cathinones like alpha-PVP (α-pyrrolidinopentiophenone) and methylone. Its structure is characterized by a pyrrolidine ring (a five-membered nitrogen-containing heterocyclic structure) attached to a hexyl chain and a ketone functional group (-C=O) on the aromatic ring.
The chemical structure of Alpha-PHP can be broken down into the following components:
1) Pyrrolidine ring: A nitrogen-containing structure that is crucial for its stimulant effects.
2) Aromatic ring (phenyl group): This is part of the molecule that contributes to its interaction with various receptors in the brain.
3) Ketone group: A carbonyl functional group (-C=O) attached to the aromatic ring, which plays a role in the molecule's ability to cross the blood-brain barrier and interact with brain chemistry.
4)Hexyl group: A six-carbon alkyl chain that influences the molecule lipophilicity (ability to dissolve in fat) and affects its potency and pharmacokinetics.
Alpha-PHP (also known as α-Pyrrolidinohexiophenone) is a synthetic stimulant and cathinone derivative that belongs to the broader class of substituted cathinones. These substances typically exhibit stimulant and empathogenic effects and are often compared to other common stimulants like amphetamines.
Chemical Structure and Mechanism of Action
Alpha-PHP shares similarities with other synthetic cathinones like alpha-PVP (α-pyrrolidinopentiophenone) and methylone. Its structure is characterized by a pyrrolidine ring (a five-membered nitrogen-containing heterocyclic structure) attached to a hexyl chain and a ketone functional group (-C=O) on the aromatic ring.
The chemical structure of Alpha-PHP can be broken down into the following components:
Pyrrolidine ring: A nitrogen-containing structure that is crucial for its stimulant effects.
1) Aromatic ring (phenyl group): This is part of the molecule that contributes to its interaction with various receptors in the brain.
2) Ketone group: A carbonyl functional group (-C=O) attached to the aromatic ring, which plays a role in the molecule's ability to cross the blood-brain barrier and interact with brain chemistry.
3) Hexyl group: A six-carbon alkyl chain that influences the molecule lipophilicity (ability to dissolve in fat) and affects its potency and pharmacokinetics.
Our extensive range of products spans chemical and spectroscopy applications.
You can search and buy our chemical compounds and full product range online.
https://narcochems.com/en/product/alpha-php/
https://narcochems.com/es/producto/alfa-php/
telegram: https://t.me/narcochemlab
The Chemistry Behind Alpha-PHP: What We Know So Far
Alpha-PHP (also known as α-Pyrrolidinohexiophenone) is a synthetic stimulant and cathinone derivative that belongs to the broader class of substituted cathinones. These substances typically exhibit stimulant and empathogenic effects and are often compared to other common stimulants like amphetamines.
Chemical Structure and Mechanism of Action
Alpha-PHP shares similarities with other synthetic cathinones like alpha-PVP (α-pyrrolidinopentiophenone) and methylone. Its structure is characterized by a pyrrolidine ring (a five-membered nitrogen-containing heterocyclic structure) attached to a hexyl chain and a ketone functional group (-C=O) on the aromatic ring.
The chemical structure of Alpha-PHP can be broken down into the following components:
1) Pyrrolidine ring: A nitrogen-containing structure that is crucial for its stimulant effects.
2) Aromatic ring (phenyl group): This is part of the molecule that contributes to its interaction with various receptors in the brain.
3) Ketone group: A carbonyl functional group (-C=O) attached to the aromatic ring, which plays a role in the molecule's ability to cross the blood-brain barrier and interact with brain chemistry.
4)Hexyl group: A six-carbon alkyl chain that influences the molecule lipophilicity (ability to dissolve in fat) and affects its potency and pharmacokinetics.
Alpha-PHP (also known as α-Pyrrolidinohexiophenone) is a synthetic stimulant and cathinone derivative that belongs to the broader class of substituted cathinones. These substances typically exhibit stimulant and empathogenic effects and are often compared to other common stimulants like amphetamines.
Chemical Structure and Mechanism of Action
Alpha-PHP shares similarities with other synthetic cathinones like alpha-PVP (α-pyrrolidinopentiophenone) and methylone. Its structure is characterized by a pyrrolidine ring (a five-membered nitrogen-containing heterocyclic structure) attached to a hexyl chain and a ketone functional group (-C=O) on the aromatic ring.
The chemical structure of Alpha-PHP can be broken down into the following components:
Pyrrolidine ring: A nitrogen-containing structure that is crucial for its stimulant effects.
1) Aromatic ring (phenyl group): This is part of the molecule that contributes to its interaction with various receptors in the brain.
2) Ketone group: A carbonyl functional group (-C=O) attached to the aromatic ring, which plays a role in the molecule's ability to cross the blood-brain barrier and interact with brain chemistry.
3) Hexyl group: A six-carbon alkyl chain that influences the molecule lipophilicity (ability to dissolve in fat) and affects its potency and pharmacokinetics.
Our extensive range of products spans chemical and spectroscopy applications.
You can search and buy our chemical compounds and full product range online.
https://narcochems.com/en/product/alpha-php/
https://narcochems.com/es/producto/alfa-php/
telegram: https://t.me/narcochemlab
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