LT4759B - N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio druskos - Google Patents
N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio druskos Download PDFInfo
- Publication number
- LT4759B LT4759B LT2000026A LT2000026A LT4759B LT 4759 B LT4759 B LT 4759B LT 2000026 A LT2000026 A LT 2000026A LT 2000026 A LT2000026 A LT 2000026A LT 4759 B LT4759 B LT 4759B
- Authority
- LT
- Lithuania
- Prior art keywords
- phenylalanine
- divergent
- salt according
- methyl ester
- dimethylbutyl
- Prior art date
Links
- -1 3,3-DIMETHYL-BUTYL Chemical class 0.000 title claims abstract description 26
- 229960005190 phenylalanine Drugs 0.000 title description 24
- 150000003839 salts Chemical class 0.000 claims abstract description 34
- HLIAVLHNDJUHFG-HOTGVXAUSA-N neotame Chemical class CC(C)(C)CCN[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 HLIAVLHNDJUHFG-HOTGVXAUSA-N 0.000 claims abstract description 20
- 239000007788 liquid Substances 0.000 claims abstract description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims abstract description 9
- 235000013615 non-nutritive sweetener Nutrition 0.000 claims abstract description 9
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims abstract description 8
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims abstract description 7
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims abstract description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims abstract description 6
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 claims abstract description 6
- 229940050410 gluconate Drugs 0.000 claims abstract description 6
- 229940049920 malate Drugs 0.000 claims abstract description 6
- 235000010357 aspartame Nutrition 0.000 claims description 27
- FGOJCPKOOGIRPA-UHFFFAOYSA-N 1-o-tert-butyl 4-o-ethyl 5-oxoazepane-1,4-dicarboxylate Chemical compound CCOC(=O)C1CCN(C(=O)OC(C)(C)C)CCC1=O FGOJCPKOOGIRPA-UHFFFAOYSA-N 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 12
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 8
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 7
- 238000004090 dissolution Methods 0.000 claims description 7
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 239000004384 Neotame Substances 0.000 claims description 5
- 229940022663 acetate Drugs 0.000 claims description 5
- 229940050390 benzoate Drugs 0.000 claims description 5
- 235000019412 neotame Nutrition 0.000 claims description 5
- 108010070257 neotame Proteins 0.000 claims description 5
- 229940095064 tartrate Drugs 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 235000009508 confectionery Nutrition 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 2
- 235000003599 food sweetener Nutrition 0.000 abstract description 14
- 239000003765 sweetening agent Substances 0.000 abstract description 14
- 108010016626 Dipeptides Proteins 0.000 abstract description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 abstract 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 13
- 239000000243 solution Substances 0.000 description 8
- 108010011485 Aspartame Proteins 0.000 description 7
- 239000000605 aspartame Substances 0.000 description 7
- 229960003438 aspartame Drugs 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 230000000007 visual effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 3
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 235000013361 beverage Nutrition 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 238000004108 freeze drying Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- HLIAVLHNDJUHFG-UHFFFAOYSA-N neotame Chemical compound CC(C)(C)CCNC(CC(O)=O)C(=O)NC(C(=O)OC)CC1=CC=CC=C1 HLIAVLHNDJUHFG-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 206010011224 Cough Diseases 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229940024606 amino acid Drugs 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 235000012970 cakes Nutrition 0.000 description 1
- 235000012174 carbonated soft drink Nutrition 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 235000015270 fruit-flavoured drink Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005244 neohexyl group Chemical group [H]C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000021395 porridge Nutrition 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- ALDITMKAAPLVJK-UHFFFAOYSA-N prop-1-ene;hydrate Chemical group O.CC=C ALDITMKAAPLVJK-UHFFFAOYSA-N 0.000 description 1
- 230000006340 racemization Effects 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06104—Dipeptides with the first amino acid being acidic
- C07K5/06113—Asp- or Asn-amino acid
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/31—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives
- A23L27/32—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives containing dipeptides or derivatives
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Nutrition Science (AREA)
- Seasonings (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5850597P | 1997-09-11 | 1997-09-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| LT2000026A LT2000026A (en) | 2000-09-25 |
| LT4759B true LT4759B (lt) | 2001-02-26 |
Family
ID=22017224
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LT2000026A LT4759B (lt) | 1997-09-11 | 2000-04-06 | N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio druskos |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US6180156B1 (et) |
| EP (1) | EP1012168A1 (et) |
| CN (1) | CN1278827A (et) |
| AU (1) | AU753013B2 (et) |
| BG (1) | BG104323A (et) |
| BR (1) | BR9812635A (et) |
| CA (1) | CA2303436A1 (et) |
| EE (1) | EE200000119A (et) |
| HU (1) | HUP0003573A3 (et) |
| ID (1) | ID27534A (et) |
| IL (1) | IL134914A0 (et) |
| LT (1) | LT4759B (et) |
| NO (1) | NO20001270L (et) |
| PL (1) | PL339207A1 (et) |
| SI (1) | SI20330A (et) |
| SK (1) | SK3272000A3 (et) |
| TR (1) | TR200000730T2 (et) |
| WO (1) | WO1999012956A1 (et) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6692778B2 (en) * | 1998-06-05 | 2004-02-17 | Wm. Wrigley Jr. Company | Method of controlling release of N-substituted derivatives of aspartame in chewing gum |
| WO2000056176A1 (en) * | 1999-03-25 | 2000-09-28 | The Nutrasweet Company | EDIBLE GELS SWEETENED WITH N-[N-(3,3-DIMETHYLBUTYL)-L-α-ASPARTYL]-L-PHENYLALANINE 1-METHYL ESTER |
| US6365216B1 (en) | 1999-03-26 | 2002-04-02 | The Nutrasweet Company | Particles of N-[N-(3,3-dimethylbutyl)-L-α-aspartyl]-L-phenylalanine 1-methyl ester |
| US6368651B1 (en) * | 1999-05-13 | 2002-04-09 | The Nutrasweet Company | Use of additives to modify the taste characteristics of N-neohexyl-α-aspartyl-L-phenylalanine methyl ester |
| WO2000069282A1 (en) * | 1999-05-13 | 2000-11-23 | The Nutrasweet Company | Modification of the taste and physicochemical properties of neotame using hydrophobic acid additives |
| US7326430B2 (en) * | 2000-07-18 | 2008-02-05 | The Nutrasweet Company | Method of preparing liquid compositions for delivery of N-[N- (3,3-dimethylbutyl-L-α-aspartyl]-L-phenylalanine 1-methyl ester in food and beverage systems |
| US20080008790A1 (en) * | 2006-06-30 | 2008-01-10 | Michael Jensen | Seasoned food, seasoning, and method for seasoning a food product |
| US20080038411A1 (en) * | 2006-06-30 | 2008-02-14 | Michael Jensen | Seasoning and method for enhancing and potentiating food flavor |
| US7923047B2 (en) * | 2006-06-30 | 2011-04-12 | Conagra Foods Rdm, Inc. | Seasoning and method for seasoning a food product while reducing dietary sodium intake |
| US20110097449A1 (en) * | 2006-06-30 | 2011-04-28 | Conagra Foods Rdm, Inc. | Seasoning and method for seasoning a food product while reducing dietary sodium intake |
| WO2008039533A2 (en) * | 2006-09-27 | 2008-04-03 | Conagra Foods, Inc. | Seasoning and method for enhancing and potentiating food flavor utilizing microencapsulation |
| CN109180914B (zh) * | 2018-04-05 | 2021-02-02 | 河南金丹乳酸科技股份有限公司 | 利用l-乳酸经寡聚、熔融缩聚和固相缩聚生产聚l-乳酸的方法 |
| CN112321676B (zh) * | 2020-12-12 | 2022-06-14 | 山东诚汇双达药业有限公司 | 一种纽甜的成盐方法 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4029701A (en) | 1972-03-30 | 1977-06-14 | General Foods Corporation | Sweetening with hydrohalide salts of dipeptide sweeteners |
| US4031258A (en) | 1972-03-30 | 1977-06-21 | General Foods Corporation | Inorganic salts of dipeptide sweeteners |
| US4153737A (en) | 1973-04-02 | 1979-05-08 | General Foods Corporation | Concentrated liquid low calorie sweetner |
| US5480668A (en) | 1992-11-12 | 1996-01-02 | Nofre; Claude | N-substituted derivatives of aspartame useful as sweetening agents |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1431057A (en) * | 1972-03-30 | 1976-04-07 | Gen Foods Corp | Sweetining compositions |
| US4448716A (en) | 1982-03-04 | 1984-05-15 | G. D. Searle & Co. | Dipeptide sweetener-metal complexes |
| FR2719590B1 (fr) | 1994-05-09 | 1996-07-26 | Claude Nofre | Procédé perfectionné de préparation d'un composé dérivé de l'aspartame utile comme agent édulcorant. |
| AU3075195A (en) | 1994-06-28 | 1996-01-25 | Twinklestar Investments N.V. | A communication system for supplying information on objects on display by means of hand-held devices |
| US5728862A (en) | 1997-01-29 | 1998-03-17 | The Nutrasweet Company | Method for preparing and purifying an N-alkylated aspartame derivative |
| JPH10259194A (ja) * | 1997-03-18 | 1998-09-29 | Ajinomoto Co Inc | 新規ジペプチド誘導体及び甘味剤 |
-
1998
- 1998-09-04 US US09/146,964 patent/US6180156B1/en not_active Expired - Fee Related
- 1998-09-11 AU AU93844/98A patent/AU753013B2/en not_active Ceased
- 1998-09-11 WO PCT/US1998/018902 patent/WO1999012956A1/en not_active Ceased
- 1998-09-11 CN CN98811056A patent/CN1278827A/zh active Pending
- 1998-09-11 BR BR9812635-0A patent/BR9812635A/pt not_active Application Discontinuation
- 1998-09-11 EE EEP200000119A patent/EE200000119A/et unknown
- 1998-09-11 SI SI9820062A patent/SI20330A/sl unknown
- 1998-09-11 EP EP98946938A patent/EP1012168A1/en not_active Ceased
- 1998-09-11 HU HU0003573A patent/HUP0003573A3/hu unknown
- 1998-09-11 ID IDW20000471D patent/ID27534A/id unknown
- 1998-09-11 PL PL98339207A patent/PL339207A1/xx unknown
- 1998-09-11 SK SK327-2000A patent/SK3272000A3/sk unknown
- 1998-09-11 CA CA002303436A patent/CA2303436A1/en not_active Abandoned
- 1998-09-11 TR TR2000/00730T patent/TR200000730T2/xx unknown
- 1998-09-11 IL IL13491498A patent/IL134914A0/xx unknown
-
2000
- 2000-03-10 NO NO20001270A patent/NO20001270L/no not_active Application Discontinuation
- 2000-04-06 LT LT2000026A patent/LT4759B/lt not_active IP Right Cessation
- 2000-04-10 BG BG104323A patent/BG104323A/xx unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4029701A (en) | 1972-03-30 | 1977-06-14 | General Foods Corporation | Sweetening with hydrohalide salts of dipeptide sweeteners |
| US4031258A (en) | 1972-03-30 | 1977-06-21 | General Foods Corporation | Inorganic salts of dipeptide sweeteners |
| US4153737A (en) | 1973-04-02 | 1979-05-08 | General Foods Corporation | Concentrated liquid low calorie sweetner |
| US5480668A (en) | 1992-11-12 | 1996-01-02 | Nofre; Claude | N-substituted derivatives of aspartame useful as sweetening agents |
Non-Patent Citations (1)
| Title |
|---|
| LABUZA T.P AND BASISIER M.W.: "Physical Chemistry of Foods" |
Also Published As
| Publication number | Publication date |
|---|---|
| EE200000119A (et) | 2000-12-15 |
| CN1278827A (zh) | 2001-01-03 |
| AU9384498A (en) | 1999-03-29 |
| NO20001270D0 (no) | 2000-03-10 |
| BG104323A (en) | 2001-02-28 |
| PL339207A1 (en) | 2000-12-04 |
| HUP0003573A2 (hu) | 2001-05-28 |
| SK3272000A3 (en) | 2000-10-09 |
| NO20001270L (no) | 2000-05-10 |
| BR9812635A (pt) | 2000-08-22 |
| US6180156B1 (en) | 2001-01-30 |
| LT2000026A (en) | 2000-09-25 |
| EP1012168A1 (en) | 2000-06-28 |
| WO1999012956A1 (en) | 1999-03-18 |
| IL134914A0 (en) | 2001-05-20 |
| ID27534A (id) | 2001-04-12 |
| SI20330A (sl) | 2001-02-28 |
| TR200000730T2 (tr) | 2001-06-21 |
| HUP0003573A3 (en) | 2001-08-28 |
| AU753013B2 (en) | 2002-10-03 |
| CA2303436A1 (en) | 1999-03-18 |
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