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US4029701A Expired / Lapsed US ⏱️ 0.0 years remaining

Sweetening with hydrohalide salts of dipeptide sweeteners

Assignee: General Foods Corp
•
Filing: 1972-03-30
•
Granted: 1977-06-14
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Expires: 1992-03-30
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Abstract

Abstract Readily soluble, sweetening compositions comprising the hydrohalide salts of dipeptide sweeteners.

Inventors

  • 👤 Gerhard J. Haas
  • 👤 Jeffrey H. Berg

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 09:19
CPC Classifications
A; A23; A23L; A23L27/00; A23L27/30; A23L27/31; A23L27/32; Y; Y10; Y10S; Y10S530/00; Y10S530/801

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 133 words
An artifically sweetened foodstuff comprising a foodstuff and a dry dipeptide sweetener from the formula ##STR6## wherein: the stereochemical configuration is DL-DL, DL-L, L-DL, or L-D; X represents a halide; n represents an integer of 0 to 5; R represents lower alkyl, lower alkylaryl and cycloalkyl; R 1 represents a. lower alkyl, b. a substituted or unstubstituted unsaturated, partially saturated or totally saturated six carbon hydrocarbon ring provided that when substituted, the substituent is at the four position and is hydroxy, lower alkoxy, lower alkyl or halogen; and c. S(O) m (lower alkyl) provided that n is 1 or 2 and m is 0, or 2, said dry dipeptide sweetener being present in an amount effective to sweeten the foodstuff, said dipeptide salt being faster to dissolve than the corresponding unsubstituted dipeptide sweetener.
Claim 2
Dependent Claim 133 words
An artifically sweetened foodstuff comprising a foodstuff and a dry dipeptide sweetener from the formula ##STR6## wherein: the stereochemical configuration is DL-DL, DL-L, L-DL, or L-D; X represents a halide; n represents an integer of 0 to 5; R represents lower alkyl, lower alkylaryl and cycloalkyl; R 1 represents a. lower alkyl, b. a substituted or unstubstituted unsaturated, partially saturated or totally saturated six carbon hydrocarbon ring provided that when substituted, the substituent is at the four position and is hydroxy, lower alkoxy, lower alkyl or halogen; and c. S(O) m (lower alkyl) provided that n is 1 or 2 and m is 0, or 2, said dry dipeptide sweetener being present in an amount effective to sweeten the foodstuff, said dipeptide salt being faster to dissolve than the corresponding unsubstituted dipeptide sweetener.
Claim 3
Dependent Claim 28 words
The foodstuff of claim 1 wherein; n represents 0 to 1; X represents chloride; R represents lower alkyl; and R 1 represents phenyl, cyclohexyl, benzyl, 1,4-cyclohexadienyl or 1-cyclohexenyl.
Claim 4
Dependent Claim 19 words
The foodstuff of claim 2 wherein; the stereochemical configuration is L-L; R is methyl, and R 1 is phenyl
Claim 5
Dependent Claim 13 words
The foodstuff of claim 3 wherein the sweetener is L-aspartyl-L-phenylalanine methyl ester hydrochloride.
Claim 6
Independent Claim 135 words
A method of sweetening a foodstuff which comprises adding thereto a dry dipeptide salt sweetener of the formula ##STR7## wherein: the stereochemical configuration is DL-DI, DL-L, L-DL, or L-L; X represents a halide; n represents an integer of 0 to 5; R represents lower alkyl, lower alkylaryl R 1 represents a. lower alkyl, b. a substituted or unsubstituted unsaturated, partially saturated or totally saturated six carbon hydrocarbon ring provided that when substituted, the substituent is at the four position and is hydroxy, lower alkoxy, lower alkyl or halogen; and c. S(O) m (lower alkyl) provided that n is 1 or 2 and m is 0, or 2, said dry dipeptide salt sweetener being present in an amount effective to sweeten the foodstuff, said dipeptide salt being faster to dissolve than the corresponding unsubstituted dipeptide sweetener.
Claim 7
Independent Claim 135 words
A method of sweetening a foodstuff which comprises adding thereto a dry dipeptide salt sweetener of the formula ##STR7## wherein: the stereochemical configuration is DL-DI, DL-L, L-DL, or L-L; X represents a halide; n represents an integer of 0 to 5; R represents lower alkyl, lower alkylaryl R 1 represents a. lower alkyl, b. a substituted or unsubstituted unsaturated, partially saturated or totally saturated six carbon hydrocarbon ring provided that when substituted, the substituent is at the four position and is hydroxy, lower alkoxy, lower alkyl or halogen; and c. S(O) m (lower alkyl) provided that n is 1 or 2 and m is 0, or 2, said dry dipeptide salt sweetener being present in an amount effective to sweeten the foodstuff, said dipeptide salt being faster to dissolve than the corresponding unsubstituted dipeptide sweetener.
Claim 8
Dependent Claim 28 words
The method of claim 5 wherein; n represents 0 or 1; X represents chloride; R represents lower alkyl; and R 1 represents phenyl, cyclohexyl, benzyl, 1,4-cyclohexadienyl or 1-cyclohexenyl.
Claim 9
Dependent Claim 19 words
The method of claim 6 wherein; the stereochemical configuration is L-L; R is methyl, and R 1 is phenyl.
Claim 10
Dependent Claim 13 words
The method of claim 7 wherein the sweetener is L-aspartyl-L-phenylalanine methyl ester hydrochloride.
Claim 11
Dependent Claim 59 words
A dry sweetening composition comprising a dipeptide salt sweetener selected from the formula ##STR8## encased in a dry, edible carrier selected from the group consisting of hydrophilic colloids not having free amine groups, water dispersible dextrins, partially hydrolyzed starches, sugars, and mixtures of any of these, said dipeptide salt being faster to dissolve than the corresponding unsubstituted dipeptide sweetener.
Claim 12
Dependent Claim 59 words
A dry sweetening composition comprising a dipeptide salt sweetener selected from the formula ##STR8## encased in a dry, edible carrier selected from the group consisting of hydrophilic colloids not having free amine groups, water dispersible dextrins, partially hydrolyzed starches, sugars, and mixtures of any of these, said dipeptide salt being faster to dissolve than the corresponding unsubstituted dipeptide sweetener.
Claim 13
Dependent Claim 28 words
The composition of claim 9 wherein: n represents 0 or 1; X represents chloride; R represents lower alkyl; and R 1 represents phenyl, cyclohexyl, benzyl, 1,4-cyclohexadienyl or 1-cyclohexenyl.
Claim 14
Dependent Claim 18 words
The composition of claim 10 wherein: stereochemical configuration is L-1; R is methyl, and R 1 is phenyl.
Claim 15
Dependent Claim 13 words
The composition of claim 11 wherein the sweetener is L-aspartyl-L-phenylalanine methyl ester hydrochloride.
Claim 16
Dependent Claim 12 words
The composition of claim 12 wherein the carrier is a non-hygroscopic carbohydrate.
Claim 17
Dependent Claim 11 words
The composition of claim 9 wherein the sweetener is L-aspartyl-L-cyclohexylalanine hydrochloride.
Claim 18
Dependent Claim 12 words
The composition of claim 9 wherein the carrier is a non-hygroscopic carbohydrate.

References Cited (Backward Citations)

US3492131A Cited
US3475403A Cited
US3678026A Cited
US3642491A Cited
US3695898A Cited
US3798204A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-06-13 1980-12-13 1981-06-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-06-13 1984-12-13 1985-06-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-06-13 1988-12-13 1989-06-14 $7700.00 Window Closed / Lapsed

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