Cannabidiol diacetate: Difference between revisions

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'''Cannabidiol diacetate''' is a [[chemical compound]] derived from [[cannabidiol]], a [[cannabinoid]] found in the [[Cannabis sativa]] plant. It is a type of [[ester]] that is formed when cannabidiol is combined with [[acetic acid]].
== Cannabidiol Diacetate ==


==Chemistry==
[[File:CBDDO_structure.png|thumb|right|Chemical structure of Cannabidiol Diacetate]]
Cannabidiol diacetate is a white, crystalline solid at room temperature. It is soluble in organic solvents such as [[ethanol]] and [[dimethyl sulfoxide]] (DMSO), but insoluble in water. The compound has a molecular formula of C24H34O4 and a molecular weight of 386.53 g/mol.


==Pharmacology==
'''Cannabidiol Diacetate''' (CBDDA) is a synthetic derivative of [[cannabidiol]] (CBD), a major non-psychoactive component of the [[Cannabis sativa]] plant. CBDDA is formed by the acetylation of CBD, resulting in the addition of two acetate groups to the molecule. This modification can alter the pharmacokinetic properties of the compound, potentially affecting its absorption, distribution, metabolism, and excretion.
The pharmacological properties of cannabidiol diacetate are not well-studied. However, it is known that the compound has a similar structure to cannabidiol, which has been shown to have [[anti-inflammatory]], [[antioxidant]], [[neuroprotective]], and [[antipsychotic]] effects. It is possible that cannabidiol diacetate may have similar effects, but further research is needed to confirm this.


==Medical Uses==
== Chemical Structure and Properties ==
There are currently no approved medical uses for cannabidiol diacetate. However, due to its structural similarity to cannabidiol, it is possible that the compound may have potential therapeutic applications in the treatment of conditions such as [[epilepsy]], [[anxiety disorders]], and [[chronic pain]]. Further research is needed to explore these possibilities.


==Safety==
Cannabidiol Diacetate is characterized by the presence of two acetate groups attached to the CBD molecule. The chemical structure of CBDDA can be represented as C23H32O4. The addition of acetate groups increases the lipophilicity of the compound, which may enhance its ability to cross biological membranes.
The safety of cannabidiol diacetate is not well-studied. As with any chemical compound, it is important to handle cannabidiol diacetate with care and to follow appropriate safety protocols when working with it.
 
== Synthesis ==
 
The synthesis of Cannabidiol Diacetate involves the acetylation of cannabidiol. This process typically uses acetic anhydride in the presence of a catalyst to introduce the acetate groups. The reaction is carried out under controlled conditions to ensure the selective acetylation of the hydroxyl groups present in CBD.
 
== Pharmacology ==
 
The pharmacological effects of Cannabidiol Diacetate are not as extensively studied as those of cannabidiol. However, it is hypothesized that the acetylation of CBD may influence its interaction with the [[endocannabinoid system]], potentially altering its affinity for [[cannabinoid receptors]] such as [[CB1 receptor|CB1]] and [[CB2 receptor|CB2]].
 
== Potential Applications ==
 
Research into the potential applications of Cannabidiol Diacetate is ongoing. Like CBD, it may possess anti-inflammatory, analgesic, and neuroprotective properties. However, further studies are needed to fully understand its therapeutic potential and safety profile.
 
== Legal Status ==
 
The legal status of Cannabidiol Diacetate varies by jurisdiction. As a synthetic derivative of CBD, it may be subject to different regulations compared to naturally occurring cannabinoids. It is important to consult local laws and regulations regarding the use and distribution of CBDDA.
 
== Related Pages ==


==See Also==
* [[Cannabidiol]]
* [[Cannabidiol]]
* [[Cannabinoids]]
* [[Cannabis sativa]]
* [[Cannabis sativa]]
* [[Ester]]
* [[Endocannabinoid system]]
* [[Cannabinoid receptor]]


[[Category:Chemical compounds]]
[[Category:Cannabinoids]]
[[Category:Cannabinoids]]
[[Category:Pharmacology]]
{{pharmacology-stub}}
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Latest revision as of 11:09, 15 February 2025

Cannabidiol Diacetate[edit]

Chemical structure of Cannabidiol Diacetate

Cannabidiol Diacetate (CBDDA) is a synthetic derivative of cannabidiol (CBD), a major non-psychoactive component of the Cannabis sativa plant. CBDDA is formed by the acetylation of CBD, resulting in the addition of two acetate groups to the molecule. This modification can alter the pharmacokinetic properties of the compound, potentially affecting its absorption, distribution, metabolism, and excretion.

Chemical Structure and Properties[edit]

Cannabidiol Diacetate is characterized by the presence of two acetate groups attached to the CBD molecule. The chemical structure of CBDDA can be represented as C23H32O4. The addition of acetate groups increases the lipophilicity of the compound, which may enhance its ability to cross biological membranes.

Synthesis[edit]

The synthesis of Cannabidiol Diacetate involves the acetylation of cannabidiol. This process typically uses acetic anhydride in the presence of a catalyst to introduce the acetate groups. The reaction is carried out under controlled conditions to ensure the selective acetylation of the hydroxyl groups present in CBD.

Pharmacology[edit]

The pharmacological effects of Cannabidiol Diacetate are not as extensively studied as those of cannabidiol. However, it is hypothesized that the acetylation of CBD may influence its interaction with the endocannabinoid system, potentially altering its affinity for cannabinoid receptors such as CB1 and CB2.

Potential Applications[edit]

Research into the potential applications of Cannabidiol Diacetate is ongoing. Like CBD, it may possess anti-inflammatory, analgesic, and neuroprotective properties. However, further studies are needed to fully understand its therapeutic potential and safety profile.

Legal Status[edit]

The legal status of Cannabidiol Diacetate varies by jurisdiction. As a synthetic derivative of CBD, it may be subject to different regulations compared to naturally occurring cannabinoids. It is important to consult local laws and regulations regarding the use and distribution of CBDDA.

Related Pages[edit]