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Cannabis

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Patent US10959961


Issued 2021-03-30

Methods Of Administering Anionic Cannabinoid Molecules Dissolved In Water

Various aspects of this patent document relate to methods to administer compositions comprising anionic cannabinoid molecules.


Classification


Slightly More than Average Length Specification


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USPTO Full Text Publication >

3 Independent Claims

  • Independent Claim 1. A method of consuming a cannabinoid, comprising: providing a composition comprising an anionic cannabinoid molecule dissolved in water, in which the composition has acolorcontacting the composition with a Bronsted acid, in which contacting the composition with the Bronsted acid changes the color to either a different color or no colorand consuming the composition after contacting the composition with theBronsted acid, in which a human being consumes the composition by drinking it, wherein the anionic cannabinoid molecule is selected from the group consisting of: 2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-3-hydroxy-5-pentylph- enolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-3-hydroxy-5-- pentylphenolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-5-pentyl-1,4-benzoqu- inone-3-oxide3-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-6-pentyl-1,2-benzoqu-inone-4-oxide2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-5-pentyl-1,4-benzoqu- inone-3-oxide3-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-6-pentyl-1,2-benzoqu- inone-4-oxide(6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chro- men-1-oxide(6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chr- omen-1-oxide2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-5-pentylphenolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-3-hydroxy-5-propylph- enolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-3-hydroxy-5-- propylphenolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-5-propyl-1,4-benzoqu-inone-3-oxide3-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-6-propyl-1,2-benzoqu- inone-4-oxide2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-5-propyl-1,4-benzoqu- inone-3-oxide3-(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-6-propyl-1,2-benzoqui- none-4-oxide(6aR,10aR)-6,6,9-trimethyl-3-propyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chro- men-1-oxide(6aR,10aR)-6,6,9-trimethyl-3-propyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chr-omen-1-oxideand 2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-5-propylphenolate.

  • Independent Claim 14. A method of consuming a cannabinoid, comprising: providing a hermetically-sealed container that contains a composition, in which: the hermetically-sealed container is a glass bottle, plastic bottle, or aluminum canthe container contains25 milliliters to 800 milliliters of the compositionthe composition comprises water and 50 micrograms to 500 milligrams of an anionic cannabinoid moleculethe anionic cannabinoid molecule is dissolved in the waterand the composition has a colorunsealing the containercontacting the composition with a Bronsted acid, in which contacting the composition with the Bronsted acid changes the color to either a different color or no colorand consuming the composition after contacting thecomposition with the Bronsted acid, in which a human being consumes the composition by drinking it, wherein the anionic cannabinoid molecule is selected from the group consisting of:2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-3-hydroxy-5-pentylph- enolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-3-hydroxy-5-- pentylphenolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-5-pentyl-1,4-benzoqu-inone-3-oxide3-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-6-pentyl-1,2-benzoqu- inone-4-oxide2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-5-pentyl-1,4-benzoqu- inone-3-oxide3-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-6-pentyl-1,2-benzoqu- inone-4-oxide(6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chro- men-1-oxide(6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chr-omen-1-oxide2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-5-pentylphenolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-3-hydroxy-5-propylph- enolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-3-hydroxy-5-- propylphenolate2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-5-propyl-1,4-benzoqu- inone-3-oxide3-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-6-propyl-1,2-benzoqu- inone-4-oxide2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-5-propyl-1,4-benzoqu- inone-3-oxide3-(1R,6R)-6-isopropenyl-3-methylcyclohex-3-en-1-yl]-6-propyl-1,2-benzoqui- none-4-oxide(6aR,10aR)-6,6,9-trimethyl-3-propyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chro- men-1-oxide(6aR,10aR)-6,6,9-trimethyl-3-propyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chr- omen-1-oxideand 2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-5-propylphenolate.

  • Independent Claim 18. A method to change the color of a composition, comprising: providing a container that contains a composition, in which: the composition comprises an anionic cannabinoid molecule dissolved in waterthe anionic cannabinoid molecule is2-[(1R,6R)-6-isopropenyl-3-methylcyclohex-2-en-1-yl]-3-hydroxy-5-pentylph- enolatethe composition has a colorand the color is purpleand contacting the composition with a Bronsted acid, in which contacting the composition with the Bronsted acidchanges the color from purple to either a different color or no color.