CH396863A - Verfahren zur Herstellung von Zuckerabkömmlingen - Google Patents

Verfahren zur Herstellung von Zuckerabkömmlingen

Info

Publication number: CH396863A
Authority: CH; Switzerland
Prior art keywords: sucrose; glycol ether; octapropylene; octapropylene glycol; sugar
Prior art date: 1960-08-16

Application number

CH925461A

Other languages

German (de)

English (en)

Inventor

Walter Dr Hagge

Guenther Dr Boehmke

Georg Dr Matthaeus

Mathieu Dr Quaedvlieg

Original Assignee

Bayer Ag

Priority date (The priority date 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 date listed.)

1960-08-16

Filing date

1961-08-07

Publication date

1965-08-15

1961-08-07 Application filed by Bayer Ag filed Critical Bayer Ag

1965-08-15 Publication of CH396863A publication Critical patent/CH396863A/de

Links

235000000346 sugar Nutrition 0.000 title claims description 16
238000000034 method Methods 0.000 title claims description 10
238000004519 manufacturing process Methods 0.000 title claims description 5
-1 fatty acid esters Chemical class 0.000 claims description 21
235000014113 dietary fatty acids Nutrition 0.000 claims description 7
229930195729 fatty acid Natural products 0.000 claims description 7
239000000194 fatty acid Substances 0.000 claims description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
150000004043 trisaccharides Chemical class 0.000 claims description 4
150000001298 alcohols Chemical class 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 2
150000002016 disaccharides Chemical class 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
150000002772 monosaccharides Chemical class 0.000 claims description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 34
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 33
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 20
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 18
229930006000 Sucrose Natural products 0.000 description 18
239000005720 sucrose Substances 0.000 description 18
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 12
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 12
ZZEANNAZZVVPKU-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-(2-hydroxypropoxy)propoxy]propoxy]propoxy]propoxy]propoxy]propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)COC(C)COC(C)COC(C)COC(C)COC(C)CO ZZEANNAZZVVPKU-UHFFFAOYSA-N 0.000 description 11
239000000243 solution Substances 0.000 description 11
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 10
UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 10
229910000027 potassium carbonate Inorganic materials 0.000 description 10
239000002904 solvent Substances 0.000 description 9
239000007864 aqueous solution Substances 0.000 description 8
239000005639 Lauric acid Substances 0.000 description 7
235000021355 Stearic acid Nutrition 0.000 description 7
150000002148 esters Chemical class 0.000 description 7
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 7
239000011780 sodium chloride Substances 0.000 description 7
239000008117 stearic acid Substances 0.000 description 7
CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 6
239000000203 mixture Substances 0.000 description 6
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 5
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
239000005642 Oleic acid Substances 0.000 description 5
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 5
QVHMSMOUDQXMRS-UHFFFAOYSA-N PPG n4 Chemical compound CC(O)COC(C)COC(C)COC(C)CO QVHMSMOUDQXMRS-UHFFFAOYSA-N 0.000 description 5
239000007795 chemical reaction product Substances 0.000 description 5
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 5
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 4
QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 4
239000000047 product Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
150000008163 sugars Chemical class 0.000 description 4
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000004702 methyl esters Chemical class 0.000 description 3
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
AOHAPDDBNAPPIN-UHFFFAOYSA-N 3-Methoxy-4,5-methylenedioxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC2=C1OCO2 AOHAPDDBNAPPIN-UHFFFAOYSA-N 0.000 description 2
LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000003925 fat Substances 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
239000006260 foam Substances 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000008096 xylene Substances 0.000 description 2
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 description 1
UDOJNGPPRYJMKR-UHFFFAOYSA-N 2-[2-[2-[2-[2-(2-hydroxypropoxy)propoxy]propoxy]propoxy]propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)COC(C)COC(C)COC(C)CO UDOJNGPPRYJMKR-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose 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)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
229930091371 Fructose Natural products 0.000 description 1
239000005715 Fructose Substances 0.000 description 1
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products 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 1
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 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
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-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
125000001931 aliphatic group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
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 description 1
239000003054 catalyst Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000003599 detergent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000004872 foam stabilizing agent Substances 0.000 description 1
239000011888 foil Substances 0.000 description 1
150000002314 glycerols Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000008101 lactose Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
239000004014 plasticizer Substances 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
239000002994 raw material Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000005060 rubber Substances 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
- C07H15/06—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical being a hydroxyalkyl group esterified by a fatty acid

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Crystallography & Structural Chemistry (AREA)
Polymers & Plastics (AREA)
Medicinal Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Biochemistry (AREA)
Biotechnology (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Molecular Biology (AREA)
Saccharide Compounds (AREA)

CH925461A 1960-08-16 1961-08-07 Verfahren zur Herstellung von Zuckerabkömmlingen CH396863A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DEF0031889		1960-08-16

Publications (1)

Publication Number	Publication Date
CH396863A true CH396863A (de)	1965-08-15

Family

ID=7094404

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH925461A CH396863A (de)	1960-08-16	1961-08-07	Verfahren zur Herstellung von Zuckerabkömmlingen

Country Status (3)

Country	Link
BE (1)	BE607191A (fr)
CH (1)	CH396863A (fr)
GB (1)	GB982078A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP2439187A1 (fr) *	2008-12-19	2012-04-11	Cognis IP Management GmbH	Esters d'hydrocarbures alcoxylés et leur utilisation

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5028413B1 (fr) *	1967-03-03	1975-09-16
EP1175474B1 (fr)	1999-05-04	2004-12-15	Akzo Nobel N.V.	Utilisation d'esters de sucre alcoxyles dans des compositions aqueuses liquides adoucissantes
EP2218329A1 (fr) *	2009-02-13	2010-08-18	Cognis IP Management GmbH	Compositions agricoles

1961
- 1961-08-07 CH CH925461A patent/CH396863A/de unknown
- 1961-08-14 BE BE607191A patent/BE607191A/fr unknown
- 1961-08-16 GB GB2963861A patent/GB982078A/en not_active Expired

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP2439187A1 (fr) *	2008-12-19	2012-04-11	Cognis IP Management GmbH	Esters d'hydrocarbures alcoxylés et leur utilisation

Also Published As

Publication number	Publication date
BE607191A (fr)	1961-12-01
GB982078A (en)	1965-02-03

Publication	Publication Date	Title
CH500276A (de)	1970-12-15	Verfahren zur Herstellung von oberflächenaktiven Stoffen aus organischen Hydroxylverbindungen, Fettsäureestern und Alkylenoxyden
CH396863A (de)	1965-08-15	Verfahren zur Herstellung von Zuckerabkömmlingen
DE1593216A1 (de)	1969-08-21	Verfahren zur Herstellung von neuen nicht ionogenen oberflaechenaktiven Verbindungen
AT228233B (de)	1963-07-10	Verfahren zur Herstellung von Zuckerabkömmlingen
DE2004156A1 (de)	1970-08-06	Polyfluorierte Aminodiole
DE1050330B (de)	1959-02-12	Verfahren zur Herstellung von Alkalisalzen unsymmetrischer Ester der Thiophosphorsaeure
DE575141C (de)	1933-04-25	Verfahren zur Herstellung von Derivaten der Polyvinylalkohole
DE1959651C3 (de)	1973-11-15	Verfahren zur Herstellung lag kettiger Alkylol und Acylgruppen ent haltender Oligopeptiddenvate
DE554877C (de)	1932-07-15	Verfahren zur Herstellung von Alkylaralkylaethern kolloidaler Kohlenhydrate, wie Cellulose u. dgl.
FR1307430A (fr)	1962-10-26	Compositions améliorées pour le nettoyage à sec de fibres textiles et autres tissus
DE839864C (de)	1952-05-26	Verfahren zur Stabilisierung von Polyvinylacetalen
DE906371C (de)	1954-03-11	Hautschutzmittel
DE888008C (de)	1953-08-27	Verfahren zur Herstellung von licht- und waermestabilen Kondensationsprodukten des Polyvinylalkohols
DE971836C (de)	1959-04-09	Verfahren zur Herstellung von als Infiltrationsanaesthetika wirksamen p-Aminobenzoesaeureestern
DE856186C (de)	1952-11-20	Loesungsmittelseife
AT246303B (de)	1966-04-12	Waschmittel
DE831394C (de)	1952-02-14	Verfahren zur Herstellung hochwertige Kondensationsprodukte
EP0204961B1 (fr)	1990-09-19	Compositions liquides de moussage pour systèmes aqueux, procédé pour les préparer et leur utilisation
DE1954890A1 (de)	1971-06-24	Polyalkylenglykolaether von Acyl-aminoguanaminen
US2668851A (en)	1954-02-09	Surface active agents
DE763625C (de)	1953-03-02	Verfahren zur Herstellung von Estern aus den Kondensationsprodukten von Eiweissstoffen oder peptidartigen Eiweissspaltprodukten und organischen Saeuren
DE541146C (de)	1932-01-08	Verfahren zur Herstellung von Celluloseaethern
DE735009C (de)	1943-05-10	Verfahren zur Herstellung von neuen Imidazol-Abkoemmlingen
DE1045095B (de)	1958-11-27	Verfahren zur Herstellung von hochmolekularen Kunststoffen
DE934500C (de)	1955-10-27	Loesungs-, Weichmachungs- und Gelatinierungsmittel

CH396863A - Verfahren zur Herstellung von Zuckerabkömmlingen - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (1)

Publications (1)

Family

ID=7094404

Family Applications (1)

Country Status (3)

Cited By (1)

Families Citing this family (3)

Cited By (1)

Also Published As

Similar Documents