DE1040525B - Verfahren zur Herstellung von Estersalzen von Zuckern - Google Patents
Verfahren zur Herstellung von Estersalzen von ZuckernInfo
- Publication number
- DE1040525B DE1040525B DEF23598A DEF0023598A DE1040525B DE 1040525 B DE1040525 B DE 1040525B DE F23598 A DEF23598 A DE F23598A DE F0023598 A DEF0023598 A DE F0023598A DE 1040525 B DE1040525 B DE 1040525B
- Authority
- DE
- Germany
- Prior art keywords
- sugars
- ester salts
- preparation
- parts
- salts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- -1 ester salts Chemical class 0.000 title claims description 12
- 235000000346 sugar Nutrition 0.000 title claims description 10
- 150000008163 sugars Chemical class 0.000 title claims description 10
- 238000000034 method Methods 0.000 title claims description 7
- 238000002360 preparation method Methods 0.000 title description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 7
- 239000000194 fatty acid Substances 0.000 claims description 7
- 229930195729 fatty acid Natural products 0.000 claims description 7
- 230000002378 acidificating effect Effects 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- QIZPVNNYFKFJAD-UHFFFAOYSA-N 1-chloro-2-prop-1-ynylbenzene Chemical compound CC#CC1=CC=CC=C1Cl QIZPVNNYFKFJAD-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 3
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 3
- 229940035023 sucrose monostearate Drugs 0.000 description 3
- GUBGYTABKSRVRQ-PICCSMPSSA-N D-Maltose Chemical compound 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 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Chemical compound OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- MUPFEKGTMRGPLJ-RMMQSMQOSA-N Raffinose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 MUPFEKGTMRGPLJ-RMMQSMQOSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- MUPFEKGTMRGPLJ-UHFFFAOYSA-N UNPD196149 Natural products OC1C(O)C(CO)OC1(CO)OC1C(O)C(O)C(O)C(COC2C(C(O)C(O)C(CO)O2)O)O1 MUPFEKGTMRGPLJ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
- C07H13/06—Fatty acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Saccharide Compounds (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF23598A DE1040525B (de) | 1957-07-26 | 1957-07-26 | Verfahren zur Herstellung von Estersalzen von Zuckern |
| CH6165058A CH373367A (de) | 1957-07-26 | 1958-07-11 | Verfahren zur Herstellung von Estersalzen von Zuckern |
| NL229888D NL229888A (enrdf_load_html_response) | 1957-07-26 | 1958-07-24 | |
| NL229888A NL110818C (enrdf_load_html_response) | 1957-07-26 | 1958-07-24 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF23598A DE1040525B (de) | 1957-07-26 | 1957-07-26 | Verfahren zur Herstellung von Estersalzen von Zuckern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1040525B true DE1040525B (de) | 1958-10-09 |
Family
ID=7090909
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF23598A Pending DE1040525B (de) | 1957-07-26 | 1957-07-26 | Verfahren zur Herstellung von Estersalzen von Zuckern |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH373367A (enrdf_load_html_response) |
| DE (1) | DE1040525B (enrdf_load_html_response) |
| NL (2) | NL229888A (enrdf_load_html_response) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1080090B (de) * | 1958-11-27 | 1960-04-21 | Bayer Ag | Verfahren zur Herstellung von Zuckerderivaten |
| US3063983A (en) * | 1958-11-27 | 1962-11-13 | Bayer Ag | Alkali metal salts of dicarboxylic acid mono-esters of carbamide esters of sugars |
-
1957
- 1957-07-26 DE DEF23598A patent/DE1040525B/de active Pending
-
1958
- 1958-07-11 CH CH6165058A patent/CH373367A/de unknown
- 1958-07-24 NL NL229888D patent/NL229888A/xx unknown
- 1958-07-24 NL NL229888A patent/NL110818C/xx active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1080090B (de) * | 1958-11-27 | 1960-04-21 | Bayer Ag | Verfahren zur Herstellung von Zuckerderivaten |
| US3063983A (en) * | 1958-11-27 | 1962-11-13 | Bayer Ag | Alkali metal salts of dicarboxylic acid mono-esters of carbamide esters of sugars |
Also Published As
| Publication number | Publication date |
|---|---|
| CH373367A (de) | 1963-11-30 |
| NL110818C (enrdf_load_html_response) | 1965-02-16 |
| NL229888A (enrdf_load_html_response) | 1964-10-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1040525B (de) | Verfahren zur Herstellung von Estersalzen von Zuckern | |
| DE720080C (de) | Verfahren zur Herstellung von Titansaeureestern | |
| DE1080090B (de) | Verfahren zur Herstellung von Zuckerderivaten | |
| DE558491C (de) | Verfahren zur Darstellung von sauren Wollfarbstoffen der Anthrachinonreihe | |
| DE915566C (de) | Verfahren zur Herstellung von N-acylierten Aminozuckern | |
| US3063983A (en) | Alkali metal salts of dicarboxylic acid mono-esters of carbamide esters of sugars | |
| DE707024C (de) | Verfahren zur Darstellung von 1-Ascorbinsaeure | |
| DE832152C (de) | Verfahren zur Herstellung von AEthylenimin und seinen Methylabkoemmlingen | |
| DE689714C (de) | Verfahren zur Darstellung von Schwefelsaeureabkoemmlingen organischer Verbindungen | |
| DE649322C (de) | Verfahren zur Herstellung von Persauerstoffverbindungen der Fettalkoholpyrophosphorsaeureester | |
| DE1114177B (de) | Verfahren zur Herstellung von Milchsaeure | |
| DE867592C (de) | Verfahren zur Herstellung von neutralen oder nahezu neutralen Loesungen substituierter Xanthine | |
| DE637808C (de) | Verfahren zur Darstellung von Oxyarylalkylketonen | |
| DE1052388B (de) | Verfahren zur Herstellung von Fettsaeuremonoestern des Rohrzuckers oder der Raffinose | |
| DE1262988B (de) | Verfahren zur Herstellung von Fettsaeurediestern des Rohrzuckers oder der Raffinose | |
| DE731393C (de) | Verfahren zur Herstellung von Carbonsaeureestersulfonsaeuren | |
| AT222100B (de) | Verfahren zur Herstellung neuer saurer Ester | |
| AT209005B (de) | Verfahren zur Herstellung neuer Ester | |
| AT160397B (de) | Verfahren zur Darstellung von l-Ascorbinsäure. | |
| DE854350C (de) | Verfahren zur Herstellung von Succindialdehyd | |
| AT233746B (de) | Verfahren zur Herstellung von Reserpsäurediestern sowie ihren Salzen | |
| SU65065A1 (ru) | Способ получени сахарина | |
| DE1081873B (de) | Verfahren zur Herstellung von Carbamidsaeureestern von Zuckern | |
| DE1767866A1 (de) | Verfahren zur Verhinderung der Verfaerbung und des Nachdunkelns von Vorlauffettsaeuren | |
| SU384819A1 (ru) | Способ получения производных 1,3-имидазолидонов-5 |