US2016286851A1PendingUtilityA1
Smoking composition comprising flavour precursor
Est. expiryNov 22, 2033(~7.3 yrs left)· nominal 20-yr term from priority
A24B 15/302A24D 1/002A24B 15/30A24F 47/006A24F 47/004A24F 42/10A24B 15/303A24D 1/22
39
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Claims
Abstract
A smoking composition comprises an aerosol-forming substrate and a flavour precursor compound. Upon heating, the precursor compound releases a thiol-containing flavour compound or intermediate that enhances the flavour experience of the aerosol- forming substrate when used in a smoking article. The smoking article may include tobacco and may be configured to heat, but not combust, the tobacco.
Claims
exact text as granted — not AI-modified1 . A smoking article comprising:
an aerosol forming substrate; a heating element configured to heat, but not combust, the aerosol forming substrate; a flavour precursor compound added to the aerosol forming substrate, wherein the flavour precursor compound releases at thiol-containing flavour compound upon heating of the aerosol forming substrate by the heating element.
2 . A smoking article according to claim 1 , wherein the thiol-containing flavour compound is hydrogen sulphide or methanethiol.
3 . A smoking article according to claim 1 , wherein the flavour precursor compound has the following structure:
where:
R 1 is OH or an amino acid residue,
R 2 is H, C(O)CH 3 , or an amino acid residue,
R 3 is H or C1-C3 unsubstituted alkyl,
R 4 is optional and, if present, is C1-C3 unsubstituted alkyl, and
x is an integer from 1 to 3.
4 . A smoking article according to claim 3 , wherein R 1 is OH or a glycine residue, R 2 is H, C(O)CH 3 , or a glutamate residue, R 3 is H or CH 3 , R 4 is not present; and x is 1 or 2.
5 . A smoking article according to claim 1 , wherein the flavour precursor compound has the following structure:
where:
R 1 is OH or an amino acid residue,
R 2 is H, C(O)CH 3 , or an amino acid residue,
R 3 is H, C1-C3 unsubstituted alkyl or a cysteine residue, and
x is an integer from 1 to 3.
6 . A smoking article according to claim 5 , wherein R 1 is OH or a glycine residue, R 2 is H, C(O)CH 3 , or a glutamate residue, R 3 is H or CH 3 , and x is 1 or 2.
7 . A smoking article according to claim 1 , wherein the flavour precursor compound has the following structure:
where:
R 1 is OH or an amino acid residue,
R 2 is H, C(O)CH 3 , or an amino acid residue, and
x is an integer from 1 to 3.
8 . A smoking article according to claim 7 , wherein R 1 is OH or a glycine residue, R 2 is H, C(O)CH 3 , or a glutamate residue, and x is 1 or 2.
9 . A smoking article according to claim 1 , wherein the flavour precursor compound has the following structure:
where:
R 1 is OH or an amino acid residue, and
R 2 is H, C(O)CH 3 , or an amino acid residue.
10 . A smoking article according to claim 9 , wherein R 1 is OH or a glycine residue and R 2 is H, C(O)CH 3 , or a glutamate residue.
11 . A smoking article according to claim 1 , wherein the flavour precursor compound comprises a cysteine residue.
12 . A smoking article according to claim 11 , wherein the flavour precursor compound is selected from the group consisting of cysteine, glutathione, N-acetyl cysteine, S-methyl cysteine, and cystine.
13 . A smoking article according to claim 1 , wherein the flavour precursor compound is selected from the group consisting of cysteine, cystine, glutathione, methionine, DL methionine methylsulfonium, N-acetyl cysteine, S-methyl cysteine, DL-homocyceteine, N-acetyl methionine, Farnesyl-Met-Ome, Albumin and 2-hydroxy-4-(methylthio)butyric acid.
14 . A smoking article according to claim 13 , wherein the flavour precursor compound is cysteine or glutathione.
15 . A smoking article according to claim 1 , wherein flavour precursor compound is cysteine.
16 . A smoking article according to claim 1 wherein the aerosol forming substrate comprises tobacco.
17 . A smoking article according to claim 16 , wherein heating of the tobacco and the flavour precursor compound results in the production of furfurylthiol.
18 . A smoking article according to claim 1 , wherein the flavour precursor compound is configured to release hydrogen sulfide or methanethiol at a temperature of from about 200° C. to about 450° C.
19 . A smoking article according to claim 1 , further comprising nicotine or a source of nicotine.Join the waitlist — get patent alerts
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