Terpene-based compositions, processes, methodologies for creation and products thereby
Compositions which are fragrant and contain at least a member set culled from a library of compositions, each being comprised of sub-combinations of selected terpenes. Fragrances that mimic that of various states of organic and synthetic aromatics including products, processes and those from non-combusted plant products, among other things, uniquitous products, processes, medicinals, and related moieties leverage databases of all known terpene groupings are offered for consideration, and have been provided, according to the instant teachings.
1. A process for preparing a synthetic blend; wherein the process comprises:
(i) obtaining a sample from a plant;
(ii) analyzing a chemical profile of the sample to identify two or more compounds in the sample; wherein the two or more compounds have a fragrance, and
(iii) preparing a synthetic blend that mimics the fragrance of the two or more compounds identified in the sample;
wherein the two or more compounds function as entourage compounds, and
wherein the synthetic blend in step (iii) comprises only terpenes or terpenoids.
2. The process according to claim 1 , wherein the process comprises quantifying the two or more compounds identified in the sample.
3. The process according to claim 1 , wherein at least one of the compounds identified in step (ii) is a terpene or terpenoid.
4. The process according to claim 3 , wherein the terpene or terpenoid is selected from the group consisting of alpha-bisabolol, borneol, camphene, camphor, beta-caryophyllene, delta-3-carene, caryophyllene oxide, alpha-cedrene, beta-eudesmol, fenchol, geraniol, guaiol, alpha-humulene, isoborneol, limonene, linalool, menthol, myrcene, nerol, cis-ocimene, trans-ocimene, alpha-phellandrene, alpha-pinene, beta-pinene, sabinene, alpha-terpinene, alpha-terpineol, terpinolene, alpha-guaiene, elemene, farnesene, germacrene, guaiol, pinanol, selina-3,7(11)-diene, eudesm-7(11)-en-4-ol, valencene, and mixtures thereof.
5. The process according to claim 1 , wherein the compounds identified in the sample in step (ii) are terpenes and/or terpenoids.
6. The process according to claim 1 , wherein the synthetic blend in step (iii) comprises at least one synthetic form of the compounds identified in the sample.
7. The process according to claim 1 , wherein the synthetic blend in step (iii) comprises only synthetic forms of the compounds identified in the sample.
8. The process according to claim 1 , wherein the synthetic blend in step (iii) comprises at least one natural form of the compounds identified in the sample.
9. The process according to claim 1 , wherein the synthetic blend in step (iii) comprises only natural forms of the compounds identified in the sample.
10. The process according to claim 1 , wherein the synthetic blend in step (iii) comprises at least one purified form of the compounds identified in the sample.
11. The process according to claim 10 , wherein the purified form comprises a purity greater than 90%.
12. The process according to claim 10 , wherein the purified form comprises a purity greater than 80%.
13. The process according to claim 10 , wherein the purified form comprises a purity greater than 70%.
14. The process according to claim 10 , wherein the purified form comprises a purity greater than 60%.
15. The process according to claim 10 , wherein the purified form is obtained from a natural source.
16. The process according to claim 1 , wherein the synthetic blend in step (iii) comprises only purified forms of the compounds identified in the sample.
17. The process according to claim 1 , wherein the synthetic blend in step (iii) comprises at least one-terpene or terpenoid is selected from the group consisting of alpha-bisabolol, borneol, camphene, camphor, beta-caryophyllene, delta-3-carene, caryophyllene oxide, alpha-cedrene, beta-eudesmol, fenchol, geraniol, guaiol, alpha-humulene, isoborneol, limonene, linalool, menthol, myrcene, nerol, cis-ocimene, trans-ocimene, alpha-phellandrene, alpha-pinene, beta-pinene, sabinene, alpha-terpinene, alpha-terpineol, terpinolene, alpha-guaiene, elemene, farnesene, germacrene, guaiol, pinanol, selina-3,7(11)-diene, eudesm-7(11)-en-4-ol, valencene, and mixtures thereof.
18. The process according to claim 1 , wherein the synthetic blend in step (iii) comprises at least one or more selected from the group consisting of thiol, ester, ketone, and aldehyde.
19. The process according to claim 1 , wherein the plant in step (i) is a cannabis plant.
20. The process according to claim 1 , wherein at least one of the two or more compounds in step (ii) is a cannabinoid.
21. A process for preparing a database comprising combinations of two or more compounds, wherein the two or more compounds function as entourage compounds, the process comprising:
(i) obtaining samples from cannabis plants;
(ii) analyzing a chemical profile of the samples to identify a combination of compounds in the samples; and
(iii) preparing a database comprising combinations of compounds identified in the samples.
22. The process according to claim 21 , wherein the process further comprises quantifying the combination of compounds identified in the sample.
23. The process according to claim 21 , wherein the terpene or terpenoid is selected from the group consisting of alpha-bisabolol, borneol, camphene, camphor, beta-caryophyllene, delta-3-carene, caryophyllene oxide, alpha-cedrene, beta-eudesmol, fenchol, geraniol, guaiol, alpha-humulene, isoborneol, limonene, linalool, menthol, myrcene, nerol, cis-ocimene, trans-ocimene, alpha-phellandrene, alpha-pinene, beta-pinene, sabinene, alpha-terpinene, alpha-terpineol, terpinolene, alpha-guaiene, elemene, farnesene, germacrene, guaiol, pinanol, selina-3,7(11)-diene, eudesm-7(11)-en-4-ol, valencene, and mixtures thereof.
24. The process according to claim 21 , wherein at least one of the two or more compounds is a cannabinoid.
25. A process for preparing a synthetic blend; wherein the process comprises:
(i) obtaining a sample from a cannabis plant;
(ii) analyzing a chemical profile of the sample to identify two or more compounds in the sample; wherein the two or more compounds have a fragrance, and
(iii) preparing a synthetic blend that mimics the fragrance of the two or more compounds identified in the sample.
26. The process according to claim 25 , wherein at least one of the two or more compounds in step (ii) is a cannabinoid.
27. The process according to claim 25 , wherein the two or more compounds function as entourage compounds.
28. A synthetic blend prepared by the process according to claim 1 .
29. A database prepared by the process according to claim 21 .