Compositions comprising non-crystalline forms of cannabidiol

US10993928B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10993928-B2
Application numberUS-201916408428-A
CountryUS
Kind codeB2
Filing dateMay 9, 2019
Priority dateApr 26, 2019
Publication dateMay 4, 2021
Grant dateMay 4, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Various aspects of this patent document relate to liquid compositions comprising cannabidiol, which have either freezing points or glass-liquid transition temperatures less than the melting point of pure cannabidiol.

First claim

Opening claim text (preview).

What is claimed is: 1. A composition, comprising cannabidiol at a concentration of 50% to 99.5% by mass and one or more solutes selected from terpenes, terpene alcohols, and terpenoids at a combined concentration of 0.5% to 40% by mass, in which: the one or more solutes are dissolved in the cannabidiol; the composition has either a freezing point or a glass-liquid transition temperature; and the freezing point or the glass-liquid transition temperature is either at least 50 degrees Fahrenheit less than the freezing point of pure cannabidiol or at least 27 degrees Celsius less than the freezing point of pure cannabidiol. 2. The composition of claim 1 , in which: the composition has a freezing point; the composition lacks a glass-liquid transition temperature; and the freezing point is less than either 70 degrees Fahrenheit or 21 degrees Celsius. 3. The composition of claim 1 , in which: the composition has a glass-liquid transition temperature; the composition lacks a freezing point; and the glass-liquid transition temperature is less than either 70 degrees Fahrenheit or 21 degrees Celsius. 4. The composition of claim 1 , in which the composition lacks crystals of cannabidiol. 5. The composition of claim 1 , in which the composition comprises cannabidiol at a concentration of 75% to 99% by mass. 6. The composition of claim 1 , in which the composition lacks tetrahydrocannabinol at a concentration greater than 0.3% by mass. 7. The composition of claim 1 , in which: the composition comprises tetrahydrocannabinol at a concentration greater than 0.3% by mass; the tetrahydrocannabinol is dissolved in the cannabidiol; and the composition comprises cannabidiol and tetrahydrocannabinol at a ratio of 3:1 to 200:1 by mass. 8. The composition of claim 1 , comprising (6aS,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol at a concentration of 0.05% to 5% by mass, in which the (6aS,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol is dissolved in the cannabidiol. 9. The composition of claim 1 , in which the composition comprises molecules having a boiling point lower than either 360 degrees Fahrenheit or 182 degrees Celsius at a combined concentration of at least 95% by mass. 10. The composition of claim 1 , in which the composition lacks propylene glycol, glycerol, triglycerides, phospholipids, fatty acids, and waxes at a combined concentration greater than 5% by mass. 11. The composition of claim 1 , in which the composition is a liquid. 12. The composition of claim 11 , in which the composition has a viscosity, and the viscosity is less than 100 pascal-seconds at a temperature of either 70 degrees Fahrenheit or 21 degrees Celsius. 13. The composition of claim 12 , in which the viscosity is 50 millipascal-seconds to 50 pascal-seconds at a temperature of either 70 degrees Fahrenheit or 21 degrees Celsius. 14. The composition of claim 1 , in which the one or more solutes comprise one or more of alpha-bisabolol, alpha-phellandrene, alpha-pinene, alpha-terpinene, alpha-terpineol, beta-caryophyllene, beta-pinene, borneol, cadinene, camphene, camphor, caryophyllene oxide, citral, citronellol, delta-3-carene, eucalyptol, eugenol, gamma-terpinene, geraniol, guaiol, humulene, isopulegol, limonene, linalool, myrcene, nerol, nerolidol, ocimene, para-cymene, phytol, pulegone, terpineol, terpinolene, and valencene at a combined concentration of 0.5% to 40% by mass. 15. The composition of claim 1 , in which the one or more solutes comprise one or more of alpha-bisabolol, beta-caryophyllene, guaiol, humulene, limonene, myrcene, and terpinolene at a combined concentration of 0.5% to 40% by mass. 16. The composition of claim 1 , in which: the composition comprises cannabidiol at a concentration of 65% to 99% by mass; the composition lacks crystals of cannabidiol; the composition lacks tetrahydrocannabinol at a concentration greater than 0.3% by mass; the one or more solutes comprise one or more of alpha-bisabolol, beta-caryophyllene, guaiol, humulene, limonene, myrcene, and terpinolene at a combined concentration of 0.5% to 35% by mass; the composition comprises molecules having a boiling point lower than either 360 degrees Fahrenheit or 182 degrees Celsius at a combined concentration of at least 95% by mass; the composition lacks propylene glycol, glycerol, triglycerides, phospholipids, fatty acids, and waxes at a combined concentration greater than 5% by mass; the composition has a glass-liquid transition temperature; the glass-liquid transition temperature is less than either 70 degrees Fahrenheit or 21 degrees Celsius; the composition lacks a freezing point; the composition is a liquid; and the composition has a viscosity, and the viscosity is 50 millipascal-seconds to 50 pascal-seconds at a temperature of either 70 degrees Fahrenheit or 21 degrees Celsius. 17. The composition of claim 1 , in which: the composition comprises cannabidiol at a concentration of 65% to 99% by mass; the composition lacks crystals of cannabidiol; the composition comprises tetrahydrocannabinol at a concentration greater than 0.3% by mass; the tetrahydrocannabinol is dissolved in the cannabidiol; the composition comprises cannabidiol and tetrahydrocannabinol at a ratio of 3:1 to 200:1 by mass; the one or more solutes comprise one or more of alpha-bisabolol, beta-caryophyllene, guaiol, humulene, limonene, myrcene, and terpinolene at a combined concentration of 0.5% to 35% by mass; the composition comprises molecules having a boiling point lower than either 360 degrees Fahrenheit or 182 degrees Celsius at a combined concentration of at least 95% by mass; the composition lacks propylene glycol, glycerol, triglycerides, phospholipids, fatty acids, and waxes at a combined concentration greater than 5% by mass; the composition has a glass-liquid transition temperature; the glass-liquid transition temperature is less than either 70 degrees Fahrenheit or 21 degrees Celsius; the composition lacks a freezing point; the composition is a liquid; and the composition has a viscosity, and the viscosity is 50 millipascal-seconds to 50 pascal-seconds at a temperature of either 70 degrees Fahrenheit or 21 degrees Celsius.

Assignees

Inventors

Classifications

  • Cannabis · CPC title

  • A61K31/658Primary

    o-phenolic cannabinoids, e.g. cannabidiol, cannabigerolic acid, cannabichromene or tetrahydrocannabinol · CPC title

  • Cannabaceae · CPC title

  • Theobroma, e.g. cocao or cocoa · CPC title

  • Humulus · CPC title

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Frequently asked questions

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What does patent US10993928B2 cover?
Various aspects of this patent document relate to liquid compositions comprising cannabidiol, which have either freezing points or glass-liquid transition temperatures less than the melting point of pure cannabidiol.
Who is the assignee on this patent?
Natural Extraction Sys Llc
What technology area does this patent fall under?
Primary CPC classification A61K31/658. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue May 04 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).