US4774076A
Expired / Lapsed
US
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Oral composition
Assignee: Lion Corp
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Filing: 1986-11-25
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Granted: 1988-09-27
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Expires: 2006-11-25
Abstract
Abstract In an oral composition comprising an amino compound, for example, tranexamic acid and epsilon -aminocaproic acid, a flavor, a surface-active agent, water, and optionally, a humectant, a binder, and an abrasive, the flavor is at least partially comprised of an aldehyde flavor compatible with the amino compound.
Inventors
- 👤 Tetsuo Gomi
- 👤 Nobuo Suganuma
- 👤 Kazuo Ishii
- 👤 Hiroshi Sato
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-27 20:34
CPC Classifications
A; A61; A61Q; A61Q11/00; A61K; A61K8/00; A61K8/18; A61K8/30; A61K8/33; A61K8/34; A61K8/342; A61K8/35; A61K8/40; A61K8/44; A61K8/60; A61K8/602; A61K8/64
Claims Analysis
Total Claims: 13
Claim 1
Independent Claim
199 words
An oral composition selected from the group consisting of a mouthwash, toothpaste, toothpowder, and liquid dentifrice, comprising: an antiplasmin effective amount of an antiplasmin agent selected from the group consisting of transexamic acid, ε-aminocaproic acid and their water-soluble alkyl ester and aryl ester derivatives, a flavor, a surface-active agent and water wherein said flavor is at least comprised of a compatible aldehyde flavor selected from the group consisting of substituted and unsubstituted phenolic hydroxyl-free cyclic aldehyde compounds having an aldehyde group attached to one of their cyclically concatenating carbon atoms, aliphatic aldehyde compounds having 4 to 7 carbon atoms and free of a double bond between the carbon atoms at the α- and β-positions with respect to their aldehyde group, aliphatic aldehyde compounds having 9 to 16 carbon atoms and free of a double bond between the carbon atoms at the α- and β-positions with respect to their aldehyde group, and aliphatic aldehyde compounds having 5 to 6 carbon atoms in total having a double bond between the carbon atoms at the α- and β-positions and a C 1 -C 12 alkyl group or aralkyl group attached at the α-position with respect to their aldehyde group, and mixtures thereof.
Claim 2
Dependent Claim
199 words
An oral composition selected from the group consisting of a mouthwash, toothpaste, toothpowder, and liquid dentifrice, comprising: an antiplasmin effective amount of an antiplasmin agent selected from the group consisting of transexamic acid, ε-aminocaproic acid and their water-soluble alkyl ester and aryl ester derivatives, a flavor, a surface-active agent and water wherein said flavor is at least comprised of a compatible aldehyde flavor selected from the group consisting of substituted and unsubstituted phenolic hydroxyl-free cyclic aldehyde compounds having an aldehyde group attached to one of their cyclically concatenating carbon atoms, aliphatic aldehyde compounds having 4 to 7 carbon atoms and free of a double bond between the carbon atoms at the α- and β-positions with respect to their aldehyde group, aliphatic aldehyde compounds having 9 to 16 carbon atoms and free of a double bond between the carbon atoms at the α- and β-positions with respect to their aldehyde group, and aliphatic aldehyde compounds having 5 to 6 carbon atoms in total having a double bond between the carbon atoms at the α- and β-positions and a C 1 -C 12 alkyl group or aralkyl group attached at the α-position with respect to their aldehyde group, and mixtures thereof.
Claim 3
Dependent Claim
14 words
The oral composition according to claim 1, wherein said oral composition is a mouthwash.
Claim 4
Dependent Claim
24 words
The oral composition according to claim 1, wherein the aldehyde flavor is selected from the group consisting of perillaldehyde, myrtenal, benzaldehyde, anisaldehyde, and heliotropin.
Claim 5
Dependent Claim
22 words
The oral composition according to claim 1, wherein the aldehyde flavor is selected from the group consisting of 4-methylbutanal, 2-methylbutanal, and hexanal.
Claim 6
Dependent Claim
25 words
The oral composition according to claim 1, wherein the aliphatic aldehyde flavor is selected from the group consisting of 10-undecenal, decanal, citronellal, dodecanal and hydroxycitronellal.
Claim 7
Dependent Claim
13 words
The oral composition according to claim 1, wherein the aldehyde flavor is α-methylcinnamaldehyde.
Claim 8
Dependent Claim
219 words
An oral composition selected from the group consisting of a mouthwash, toothpaste, toothpowder, and liquid dentifrice, comprising: 0.01 to 5% by weight of an antiplasmin agent selected from the group consisting of tranexamic acid, ε-aminocaproic acid and their water-soluble alkyl ester and aryl ester derivatives, 0.01 to 10% by weight of a flavor mixture, a surface-active agent and water wherein said flavor mixture comprises 0.05 to 90% by weight based on the total weight of the flavor mixture of a compatible aldehyde flavor selected from the group consisting of substituted and unsubstituted phenolic hydroxyl-free cyclic aldehyde compounds having an aldehyde group attached to one of their cyclically concatenating carbon atoms, aliphatic aldehyde compounds having 4 to 7 carbon atoms and free of a double bond between the carbon atoms at the α- and β-positions with respect to their aldehyde group, aliphatic aldehyde compounds having 9 to 16 carbon atoms and free of a double bond between the carbon atoms at the α- and β-positions with respect to their aldehyde group, and aliphatic aldehyde compounds possessing 5 to 16 carbon atoms in total having a double bond between the carbon atoms at the α- and β-positions and a C 1 -C 12 alkyl group or aralkyl group attached at the α-position with respect to their aldehyde group, and mixtures thereof.
Claim 9
Dependent Claim
219 words
An oral composition selected from the group consisting of a mouthwash, toothpaste, toothpowder, and liquid dentifrice, comprising: 0.01 to 5% by weight of an antiplasmin agent selected from the group consisting of tranexamic acid, ε-aminocaproic acid and their water-soluble alkyl ester and aryl ester derivatives, 0.01 to 10% by weight of a flavor mixture, a surface-active agent and water wherein said flavor mixture comprises 0.05 to 90% by weight based on the total weight of the flavor mixture of a compatible aldehyde flavor selected from the group consisting of substituted and unsubstituted phenolic hydroxyl-free cyclic aldehyde compounds having an aldehyde group attached to one of their cyclically concatenating carbon atoms, aliphatic aldehyde compounds having 4 to 7 carbon atoms and free of a double bond between the carbon atoms at the α- and β-positions with respect to their aldehyde group, aliphatic aldehyde compounds having 9 to 16 carbon atoms and free of a double bond between the carbon atoms at the α- and β-positions with respect to their aldehyde group, and aliphatic aldehyde compounds possessing 5 to 16 carbon atoms in total having a double bond between the carbon atoms at the α- and β-positions and a C 1 -C 12 alkyl group or aralkyl group attached at the α-position with respect to their aldehyde group, and mixtures thereof.
Claim 10
Dependent Claim
24 words
The oral composition according to claim 7, wherein the aldehyde flavor is selected from the group consisting of perillaldehyde, myrtenal, benzaldehyde, anisaldehyde, and heliotropin.
Claim 11
Dependent Claim
22 words
The oral composition according to claim 7, wherein the aldehyde flavor is selected from the group consisting of 3-methylbutanal, 2-methylbutanal, and hexanal.
Claim 12
Dependent Claim
25 words
The oral composition according to claim 7, wherein the aliphatic aldehyde flavor is selected from the group consisting of 1-undecenal, decanal, citronellal, dodecanal and hydroxycitronellal.
Claim 13
Dependent Claim
13 words
The oral composition according to claim 7, wherein the aldehyde flavor is α-methylcinnamaldehyde.
References Cited (Backward Citations)
US4649044A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1991-09-27 | 1992-03-28 | 1992-09-27 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1995-09-27 | 1996-03-28 | 1996-09-27 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1999-09-27 | 2000-03-28 | 2000-09-27 | $7700.00 | Window Closed / Lapsed |