GB959282A - Improvements relating to organic aluminium compounds - Google Patents
Improvements relating to organic aluminium compoundsInfo
- Publication number
- GB959282A GB959282A GB28308/59A GB2830859A GB959282A GB 959282 A GB959282 A GB 959282A GB 28308/59 A GB28308/59 A GB 28308/59A GB 2830859 A GB2830859 A GB 2830859A GB 959282 A GB959282 A GB 959282A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aluminium
- polyoxo
- hydrolysis
- oleate
- compound
- 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.)
- Expired
Links
- 150000001399 aluminium compounds Chemical class 0.000 title abstract 3
- 229940077746 antacid containing aluminium compound Drugs 0.000 title 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 22
- 239000004411 aluminium Substances 0.000 abstract 22
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 8
- 239000000126 substance Substances 0.000 abstract 8
- 239000013543 active substance Substances 0.000 abstract 6
- -1 aluminium alkoxide Chemical class 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 6
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 abstract 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N n-octadecyl alcohol Natural products CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 abstract 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 4
- 239000000344 soap Substances 0.000 abstract 4
- CSTRPYAGFNTOEQ-MGMRMFRLSA-N (2r)-2-[(1s)-1,2-dihydroxyethyl]-3,4-dihydroxy-2h-furan-5-one;octadecanoic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O.CCCCCCCCCCCCCCCCCC(O)=O CSTRPYAGFNTOEQ-MGMRMFRLSA-N 0.000 abstract 3
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 abstract 3
- 229940068372 acetyl salicylate Drugs 0.000 abstract 3
- 230000007062 hydrolysis Effects 0.000 abstract 3
- 238000006460 hydrolysis reaction Methods 0.000 abstract 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 2
- 239000005711 Benzoic acid Substances 0.000 abstract 2
- NDJDZOBKJDUVKK-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)O.NC=1C=C(C(C(=O)O)=CC1)O Chemical compound C(C1=CC=CC=C1)(=O)O.NC=1C=C(C(C(=O)O)=CC1)O NDJDZOBKJDUVKK-UHFFFAOYSA-N 0.000 abstract 2
- 239000005642 Oleic acid Substances 0.000 abstract 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 2
- 235000021355 Stearic acid Nutrition 0.000 abstract 2
- 230000002378 acidificating effect Effects 0.000 abstract 2
- 229910021502 aluminium hydroxide Inorganic materials 0.000 abstract 2
- 229940072107 ascorbate Drugs 0.000 abstract 2
- 235000010323 ascorbic acid Nutrition 0.000 abstract 2
- 239000011668 ascorbic acid Substances 0.000 abstract 2
- 235000010233 benzoic acid Nutrition 0.000 abstract 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 2
- 239000004359 castor oil Substances 0.000 abstract 2
- 235000019438 castor oil Nutrition 0.000 abstract 2
- 229940082500 cetostearyl alcohol Drugs 0.000 abstract 2
- 230000005494 condensation Effects 0.000 abstract 2
- 238000009833 condensation Methods 0.000 abstract 2
- 230000008030 elimination Effects 0.000 abstract 2
- 238000003379 elimination reaction Methods 0.000 abstract 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 abstract 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 abstract 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 2
- 229940049964 oleate Drugs 0.000 abstract 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 2
- 150000002888 oleic acid derivatives Chemical class 0.000 abstract 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 239000007858 starting material Substances 0.000 abstract 2
- 239000008117 stearic acid Substances 0.000 abstract 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 2
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 abstract 2
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 abstract 1
- 229940113720 aminosalicylate Drugs 0.000 abstract 1
- 229960002327 chloral hydrate Drugs 0.000 abstract 1
- 229960005235 piperonyl butoxide Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/10—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/069—Aluminium compounds without C-aluminium linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB28308/59A GB959282A (en) | 1959-08-19 | 1959-08-19 | Improvements relating to organic aluminium compounds |
| US49137A US3173934A (en) | 1959-08-19 | 1960-08-12 | Organic aluminum compounds |
| SE7920/60A SE308914B (enExample) | 1959-08-19 | 1960-08-17 | |
| CH942460A CH447159A (fr) | 1959-08-19 | 1960-08-19 | Procédé de préparation de composés organiques de l'aluminium |
| DK330260AA DK110017C (da) | 1959-08-19 | 1960-08-19 | Fremgangsmåde til fremstilling af organiske aluminiumforbindelser. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB28308/59A GB959282A (en) | 1959-08-19 | 1959-08-19 | Improvements relating to organic aluminium compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB959282A true GB959282A (en) | 1964-05-27 |
Family
ID=10273576
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB28308/59A Expired GB959282A (en) | 1959-08-19 | 1959-08-19 | Improvements relating to organic aluminium compounds |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3173934A (enExample) |
| CH (1) | CH447159A (enExample) |
| DK (1) | DK110017C (enExample) |
| GB (1) | GB959282A (enExample) |
| SE (1) | SE308914B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2451713A (en) * | 2007-02-06 | 2009-02-11 | Medical Res Council | Ligand modified poly oxo-hydroxy metal ion materials, their uses and processes for their preparation |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3410856A (en) * | 1965-10-21 | 1968-11-12 | Merck & Co Inc | Intermediates and process for preparing vitamin b6 |
| US3865857A (en) * | 1972-03-20 | 1975-02-11 | Teikoku Hormone Mfg Co Ltd | Tri-substituted aluminum salts or di-substituted aluminum salts of carboxyl group-containing, pharmaceutically effective compounds, and process for preparation thereof |
| US3988333A (en) * | 1971-03-22 | 1976-10-26 | Teikoku Hormone Mfg. Co., Ltd. | Tri-substituted aluminum salts or di-substituted aluminum salts of carboxyl group-containing, pharmaceutically effective compounds |
| GB1397407A (en) * | 1971-07-06 | 1975-06-11 | Hardman & Holden Ltd | Aluminium containing pharmaceutical compounds |
| US4772724A (en) * | 1986-12-02 | 1988-09-20 | Warner-Lambert Canada Inc. | Essentially pure acid hydroxyl ligand aluminum complexes and their preparation |
| CA1276022C (en) * | 1986-11-21 | 1990-11-06 | Arthur P. G. Wright | Essentially pure acidic amine ligand aluminum complexes and their preparation |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2744074A (en) * | 1951-04-18 | 1956-05-01 | Du Pont | Polymeric organic aluminum oxides and method for preparing same |
| US2768138A (en) * | 1952-10-18 | 1956-10-23 | California Research Corp | Complex basic aluminum soap greases |
| US2932659A (en) * | 1953-05-26 | 1960-04-12 | Hoechst Ag | Organic aluminum compounds and a process of preparing them |
| US2948743A (en) * | 1954-09-11 | 1960-08-09 | J W Ayers & Co | Oxo-aluminum acylates, alkoxides and phenoxides |
| US2925430A (en) * | 1955-02-18 | 1960-02-16 | Konink Ind Mij Voorheen Noury | Polymeric basic aluminum compounds of organic acids |
| US2835685A (en) * | 1955-03-17 | 1958-05-20 | J W Ayers & Co | Metal triacylates of unsaturated higher molecular monocarboxylic acids |
| US2913468A (en) * | 1955-03-21 | 1959-11-17 | J W Ayers & Co | Hydroxy-, r-oxy-aluminum acylates and condsensation products thereof |
| NL86609C (enExample) * | 1955-10-06 | 1957-10-15 | Noury & Van Der Lande | |
| US2959606A (en) * | 1956-09-18 | 1960-11-08 | Lewis Howe Company | Production of aluminum acetylsalicylate |
| US2936317A (en) * | 1957-05-17 | 1960-05-10 | Asta Werke Ag Chem Fab | New mixed alcoholates-phenolates of aluminum and a process for the production thereof |
-
1959
- 1959-08-19 GB GB28308/59A patent/GB959282A/en not_active Expired
-
1960
- 1960-08-12 US US49137A patent/US3173934A/en not_active Expired - Lifetime
- 1960-08-17 SE SE7920/60A patent/SE308914B/xx unknown
- 1960-08-19 DK DK330260AA patent/DK110017C/da active
- 1960-08-19 CH CH942460A patent/CH447159A/fr unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2451713A (en) * | 2007-02-06 | 2009-02-11 | Medical Res Council | Ligand modified poly oxo-hydroxy metal ion materials, their uses and processes for their preparation |
| GB2451713B (en) * | 2007-02-06 | 2009-12-16 | Medical Res Council | Ligand modified poly oxo-hydroxy metal ion materials, their uses and processes for their preparation |
| US8058462B2 (en) | 2007-02-06 | 2011-11-15 | Medical Research Council | Ligand modified poly oxo-hydroxy metal ion materials, their uses and processes for their preparation |
Also Published As
| Publication number | Publication date |
|---|---|
| SE308914B (enExample) | 1969-03-03 |
| US3173934A (en) | 1965-03-16 |
| DK110017C (da) | 1968-08-26 |
| CH447159A (fr) | 1967-11-30 |
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