ZA200307707B - Polymerization of mono and disaccharides with monocarboxylic acids and lactones. - Google Patents
Polymerization of mono and disaccharides with monocarboxylic acids and lactones. Download PDFInfo
- Publication number
- ZA200307707B ZA200307707B ZA200307707A ZA200307707A ZA200307707B ZA 200307707 B ZA200307707 B ZA 200307707B ZA 200307707 A ZA200307707 A ZA 200307707A ZA 200307707 A ZA200307707 A ZA 200307707A ZA 200307707 B ZA200307707 B ZA 200307707B
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- ZA
- South Africa
- Prior art keywords
- acid
- process according
- organic acid
- monocarboxylic acid
- carbohydrate polymer
- Prior art date
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- 238000006116 polymerization reaction Methods 0.000 title claims description 52
- 150000002596 lactones Chemical class 0.000 title claims description 38
- 150000002772 monosaccharides Chemical class 0.000 title claims description 16
- 150000002016 disaccharides Chemical class 0.000 title claims description 9
- 150000002763 monocarboxylic acids Chemical class 0.000 title description 22
- 238000000034 method Methods 0.000 claims description 134
- DLRVVLDZNNYCBX-UHFFFAOYSA-N Polydextrose Polymers OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(O)O1 DLRVVLDZNNYCBX-UHFFFAOYSA-N 0.000 claims description 115
- 239000000047 product Substances 0.000 claims description 89
- 229920001282 polysaccharide Polymers 0.000 claims description 76
- 229920001100 Polydextrose Polymers 0.000 claims description 57
- 239000001259 polydextrose Substances 0.000 claims description 57
- 235000013856 polydextrose Nutrition 0.000 claims description 57
- 229940035035 polydextrose Drugs 0.000 claims description 57
- 239000002253 acid Substances 0.000 claims description 54
- 125000000217 alkyl group Chemical group 0.000 claims description 52
- 235000000346 sugar Nutrition 0.000 claims description 50
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 48
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 47
- 125000004432 carbon atom Chemical group C* 0.000 claims description 46
- 150000007524 organic acids Chemical class 0.000 claims description 46
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 37
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 37
- 235000013305 food Nutrition 0.000 claims description 37
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims description 37
- 239000000600 sorbitol Substances 0.000 claims description 37
- 235000010356 sorbitol Nutrition 0.000 claims description 37
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 34
- -1 dissacharide Chemical class 0.000 claims description 32
- 125000003118 aryl group Chemical group 0.000 claims description 27
- 125000003342 alkenyl group Chemical group 0.000 claims description 24
- 229920005862 polyol Polymers 0.000 claims description 22
- 150000003077 polyols Chemical class 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 238000000746 purification Methods 0.000 claims description 16
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 14
- 230000003472 neutralizing effect Effects 0.000 claims description 14
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 13
- 125000000623 heterocyclic group Chemical group 0.000 claims description 13
- 230000002829 reductive effect Effects 0.000 claims description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical group OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 12
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 claims description 12
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 12
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 11
- 230000003197 catalytic effect Effects 0.000 claims description 11
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 11
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 10
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 claims description 10
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 claims description 10
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- 238000000354 decomposition reaction Methods 0.000 claims description 9
- 125000005842 heteroatom Chemical group 0.000 claims description 9
- 239000003456 ion exchange resin Substances 0.000 claims description 9
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 9
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 9
- 239000003463 adsorbent Substances 0.000 claims description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 125000001072 heteroaryl group Chemical group 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 229920001542 oligosaccharide Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 150000001261 hydroxy acids Chemical class 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 150000002482 oligosaccharides Chemical class 0.000 claims description 7
- 239000005711 Benzoic acid Substances 0.000 claims description 6
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- 230000000379 polymerizing effect Effects 0.000 claims description 6
- 229940107700 pyruvic acid Drugs 0.000 claims description 6
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical group OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 claims description 5
- 235000012209 glucono delta-lactone Nutrition 0.000 claims description 5
- 239000000182 glucono-delta-lactone Substances 0.000 claims description 5
- 229960003681 gluconolactone Drugs 0.000 claims description 5
- 239000000413 hydrolysate Substances 0.000 claims description 5
- 150000004715 keto acids Chemical class 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 229960004889 salicylic acid Drugs 0.000 claims description 5
- 241001465754 Metazoa Species 0.000 claims description 4
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- 125000005343 heterocyclic alkyl group Chemical group 0.000 claims description 4
- 125000004043 oxo group Chemical group O=* 0.000 claims description 4
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 claims description 3
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 3
- 239000004386 Erythritol Substances 0.000 claims description 3
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims description 3
- 229930195725 Mannitol Natural products 0.000 claims description 3
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims description 3
- 235000019414 erythritol Nutrition 0.000 claims description 3
- 229940009714 erythritol Drugs 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 claims description 3
- 229960005150 glycerol Drugs 0.000 claims description 3
- 235000011187 glycerol Nutrition 0.000 claims description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- 238000005984 hydrogenation reaction Methods 0.000 claims description 3
- 239000000594 mannitol Substances 0.000 claims description 3
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- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 3
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- 125000006413 ring segment Chemical group 0.000 claims 4
- 239000002808 molecular sieve Substances 0.000 claims 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims 3
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 24
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- 125000000304 alkynyl group Chemical group 0.000 description 11
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Classifications
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- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/125—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives containing carbohydrate syrups; containing sugars; containing sugar alcohols; containing starch hydrolysates
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/30—Foods or foodstuffs containing additives; Preparation or treatment thereof containing carbohydrate syrups; containing sugars; containing sugar alcohols, e.g. xylitol; containing starch hydrolysates, e.g. dextrin
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/20—Reducing nutritive value; Dietetic products with reduced nutritive value
- A23L33/21—Addition of substantially indigestible substances, e.g. dietary fibres
- A23L33/25—Synthetic polymers, e.g. vinylic or acrylic polymers
- A23L33/26—Polyol polyesters, e.g. sucrose polyesters; Synthetic sugar polymers, e.g. polydextrose
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- General Health & Medical Sciences (AREA)
- Mycology (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Polyamides (AREA)
- Saccharide Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
- Fodder In General (AREA)
- Jellies, Jams, And Syrups (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Biological Depolymerization Polymers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28280501P | 2001-04-10 | 2001-04-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200307707B true ZA200307707B (en) | 2005-04-21 |
Family
ID=23083188
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200307707A ZA200307707B (en) | 2001-04-10 | 2003-10-02 | Polymerization of mono and disaccharides with monocarboxylic acids and lactones. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6821547B2 (fr) |
| EP (1) | EP1377594A4 (fr) |
| JP (1) | JP2005510581A (fr) |
| KR (1) | KR20040026136A (fr) |
| CN (1) | CN1638651A (fr) |
| AR (1) | AR033137A1 (fr) |
| AU (1) | AU2002309541B8 (fr) |
| BR (1) | BR0208778A (fr) |
| CA (1) | CA2443766A1 (fr) |
| IL (1) | IL158299A0 (fr) |
| MX (1) | MXPA03009279A (fr) |
| NO (1) | NO20034533L (fr) |
| NZ (1) | NZ528677A (fr) |
| PL (1) | PL373506A1 (fr) |
| WO (1) | WO2002083739A2 (fr) |
| ZA (1) | ZA200307707B (fr) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6770148B1 (en) * | 1998-12-04 | 2004-08-03 | Baxter International Inc. | Peritoneal dialysis solution containing modified icodextrins |
| US20040121982A1 (en) * | 2002-12-20 | 2004-06-24 | Leo Martis | Biocompatible dialysis fluids containing icodextrins |
| US7053059B2 (en) * | 2003-07-25 | 2006-05-30 | Baxter International Inc. | Dialysis solutions with reduced levels of glucose degradation products |
| US20050209328A1 (en) * | 2004-03-19 | 2005-09-22 | Allgood Charles C | Alphahydroxyacids with ultra-low metal concentration |
| US20050276868A1 (en) * | 2004-06-10 | 2005-12-15 | Bart Degreve | Bicarbonate-based peritoneal dialysis solutions |
| CN101080430A (zh) * | 2004-10-15 | 2007-11-28 | 丹尼斯科有限公司 | 基于异氰酸酯的发泡聚合物、其混合物及其生产方法 |
| US7465757B2 (en) | 2004-10-15 | 2008-12-16 | Danisco A/S | Foamed isocyanate-based polymer, a mix and process for production thereof |
| WO2006040335A1 (fr) * | 2004-10-15 | 2006-04-20 | Danisco A/S | Polysaccharide hautement ramifie derivatise et melange pour la production de polyurethanne a base d'un tel polysaccharide |
| US8722101B2 (en) * | 2005-02-09 | 2014-05-13 | Vifor (International) Ag | Use of iron(III) complex compounds |
| DK2574640T3 (da) | 2005-07-26 | 2023-04-24 | Knauf Insulation Gmbh | Bindemidler og dermed fremstillede materialer |
| EP1757299A1 (fr) | 2005-08-25 | 2007-02-28 | Vifor (International) Ag | Complexes de fer III pour traiter les manques de fer en patients avec la maladie intestinale inflammatoire |
| US9101160B2 (en) | 2005-11-23 | 2015-08-11 | The Coca-Cola Company | Condiments with high-potency sweetener |
| US8017168B2 (en) | 2006-11-02 | 2011-09-13 | The Coca-Cola Company | High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith |
| EP2450493A3 (fr) | 2007-01-25 | 2015-07-29 | Knauf Insulation SPRL | Panneau de fibres minérales |
| DK2108006T3 (da) | 2007-01-25 | 2020-12-21 | Knauf Insulation Gmbh | Bindemidler og materialer lavet dermed |
| US8501838B2 (en) | 2007-01-25 | 2013-08-06 | Knauf Insulation Sprl | Composite wood board |
| WO2008127936A2 (fr) | 2007-04-13 | 2008-10-23 | Knauf Insulation Gmbh | Liants de maillard-résole composites |
| GB0715100D0 (en) | 2007-08-03 | 2007-09-12 | Knauf Insulation Ltd | Binders |
| US8900495B2 (en) | 2009-08-07 | 2014-12-02 | Knauf Insulation | Molasses binder |
| ES2882129T3 (es) | 2010-05-07 | 2021-12-01 | Knauf Insulation | Aglutinantes de poliamina e hidrato de carbono y materiales fabricados con los mismos |
| WO2011138459A1 (fr) | 2010-05-07 | 2011-11-10 | Knauf Insulation | Liants à base de glucides et matières réalisées avec ces liants |
| EP2576882B1 (fr) | 2010-06-07 | 2015-02-25 | Knauf Insulation | Produits à base de fibres contenant des additifs de régulation de la température |
| JP5731784B2 (ja) * | 2010-09-29 | 2015-06-10 | 松谷化学工業株式会社 | 食感食味の優れたベーカリー製品及びその製造法 |
| JP4966429B1 (ja) * | 2011-01-07 | 2012-07-04 | 日本食品化工株式会社 | 糖縮合物並びにその製造方法および用途 |
| US20140186635A1 (en) | 2011-05-07 | 2014-07-03 | Knauf Insulation | Liquid high solids binder composition |
| AR087159A1 (es) | 2011-06-20 | 2014-02-26 | Gen Biscuit | Galletita para desayuno con glucosa de lenta disponibilidad |
| GB201206193D0 (en) | 2012-04-05 | 2012-05-23 | Knauf Insulation Ltd | Binders and associated products |
| GB201214734D0 (en) | 2012-08-17 | 2012-10-03 | Knauf Insulation Ltd | Wood board and process for its production |
| JP5671594B2 (ja) * | 2012-11-28 | 2015-02-18 | 日本食品化工株式会社 | 糖縮合物の製造法 |
| WO2014086777A2 (fr) | 2012-12-05 | 2014-06-12 | Knauf Insulation | Liant |
| MX2016010192A (es) | 2014-02-07 | 2017-01-09 | Knauf Insulation Inc | Articulos no curados con estabilidad en almacen mejorada. |
| GB201408909D0 (en) | 2014-05-20 | 2014-07-02 | Knauf Insulation Ltd | Binders |
| GB201517867D0 (en) | 2015-10-09 | 2015-11-25 | Knauf Insulation Ltd | Wood particle boards |
| GB201610063D0 (en) | 2016-06-09 | 2016-07-27 | Knauf Insulation Ltd | Binders |
| GB201701569D0 (en) | 2017-01-31 | 2017-03-15 | Knauf Insulation Ltd | Improved binder compositions and uses thereof |
| GB201804907D0 (en) | 2018-03-27 | 2018-05-09 | Knauf Insulation Ltd | Composite products |
| GB201804908D0 (en) | 2018-03-27 | 2018-05-09 | Knauf Insulation Ltd | Binder compositions and uses thereof |
| CN115926015B (zh) * | 2023-01-30 | 2023-06-27 | 山东百龙创园生物科技股份有限公司 | 一种低聚合度聚葡萄糖及其制备方法 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3766165A (en) * | 1966-08-17 | 1973-10-16 | Pfizer | Polysaccharides and their preparation |
| US3876794A (en) * | 1972-12-20 | 1975-04-08 | Pfizer | Dietetic foods |
| US4631195A (en) * | 1982-07-06 | 1986-12-23 | Colliopoulos John A | Sweetening composition |
| US5667593A (en) * | 1989-01-26 | 1997-09-16 | Cultor Ltd. | Modified polydextrose and process therefor |
| US5051500A (en) * | 1989-08-11 | 1991-09-24 | A. E. Staley Manufacturing Company | Method of preparing a randomly-bonded polysaccharide |
| NL8902243A (nl) * | 1989-09-07 | 1991-04-02 | Suiker Unie | Laag-calorische polydextrose-derivaten. |
| US5091015A (en) * | 1990-05-22 | 1992-02-25 | Warner-Lambert Company | Polydextrose compositions |
| WO1992012179A1 (fr) * | 1991-01-04 | 1992-07-23 | Warner-Lambert Company | Purification du polydextrose par chromatographie a exclusion granulometrique |
| JPH05262782A (ja) * | 1991-03-22 | 1993-10-12 | Hoechst Ag | グルコースおよび／またはマルトースと多価アルコールとの重縮合物の製造方法 |
| US5728397A (en) * | 1992-05-12 | 1998-03-17 | Fuisz Technologies Ltd. | Polydextrose product and process |
| IE940142A1 (en) * | 1993-02-18 | 1994-08-24 | Fuisz Technologies Ltd | Polydextrose product and process |
| AU6571898A (en) * | 1997-03-19 | 1998-10-12 | Cultor Food Science, Inc. | Polymerization of mono- and disaccharides using low levels of polycarboxylic acids |
| DE19734086C1 (de) * | 1997-08-07 | 1998-08-13 | Merck Patent Gmbh | Verfahren zur Herstellung von L-Ascorbinsäure |
-
2002
- 2002-04-04 AU AU2002309541A patent/AU2002309541B8/en not_active Expired - Fee Related
- 2002-04-04 IL IL15829902A patent/IL158299A0/xx unknown
- 2002-04-04 NZ NZ528677A patent/NZ528677A/en unknown
- 2002-04-04 MX MXPA03009279A patent/MXPA03009279A/es active IP Right Grant
- 2002-04-04 KR KR10-2003-7013256A patent/KR20040026136A/ko not_active Application Discontinuation
- 2002-04-04 WO PCT/US2002/010677 patent/WO2002083739A2/fr active Application Filing
- 2002-04-04 CA CA002443766A patent/CA2443766A1/fr not_active Abandoned
- 2002-04-04 PL PL02373506A patent/PL373506A1/xx not_active Application Discontinuation
- 2002-04-04 JP JP2002581494A patent/JP2005510581A/ja active Pending
- 2002-04-04 CN CNA028116070A patent/CN1638651A/zh active Pending
- 2002-04-04 EP EP02736543A patent/EP1377594A4/fr not_active Ceased
- 2002-04-04 BR BR0208778-2A patent/BR0208778A/pt not_active IP Right Cessation
- 2002-04-04 US US10/117,670 patent/US6821547B2/en not_active Expired - Fee Related
- 2002-04-09 AR ARP020101303A patent/AR033137A1/es unknown
-
2003
- 2003-10-02 ZA ZA200307707A patent/ZA200307707B/en unknown
- 2003-10-09 NO NO20034533A patent/NO20034533L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2002309541B2 (en) | 2008-10-23 |
| US6821547B2 (en) | 2004-11-23 |
| EP1377594A2 (fr) | 2004-01-07 |
| IL158299A0 (en) | 2004-05-12 |
| CA2443766A1 (fr) | 2002-10-24 |
| EP1377594A4 (fr) | 2004-06-30 |
| NZ528677A (en) | 2006-11-30 |
| CN1638651A (zh) | 2005-07-13 |
| NO20034533L (no) | 2003-11-28 |
| AU2002309541B8 (en) | 2008-11-20 |
| KR20040026136A (ko) | 2004-03-27 |
| WO2002083739A3 (fr) | 2002-12-19 |
| NO20034533D0 (no) | 2003-10-09 |
| JP2005510581A (ja) | 2005-04-21 |
| AR033137A1 (es) | 2003-12-03 |
| US20030044513A1 (en) | 2003-03-06 |
| BR0208778A (pt) | 2005-08-02 |
| PL373506A1 (en) | 2005-09-05 |
| WO2002083739A2 (fr) | 2002-10-24 |
| MXPA03009279A (es) | 2004-11-12 |
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