GB831346A - Improvements relating to organic aluminium compounds - Google Patents
Improvements relating to organic aluminium compoundsInfo
- Publication number
- GB831346A GB831346A GB505657A GB505657A GB831346A GB 831346 A GB831346 A GB 831346A GB 505657 A GB505657 A GB 505657A GB 505657 A GB505657 A GB 505657A GB 831346 A GB831346 A GB 831346A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aluminium
- monochlor
- monophenoxide
- dichlor
- isopropoxide
- 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 2
- 229940077746 antacid containing aluminium compound Drugs 0.000 title abstract 2
- ILXDAXZQNSOSAE-UHFFFAOYSA-N [AlH3].[Cl] Chemical compound [AlH3].[Cl] ILXDAXZQNSOSAE-UHFFFAOYSA-N 0.000 abstract 17
- 229910052782 aluminium Inorganic materials 0.000 abstract 11
- 239000004411 aluminium Substances 0.000 abstract 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 10
- -1 aluminium dichlor Chemical compound 0.000 abstract 6
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 4
- UXFIDFBXVFVKIB-UHFFFAOYSA-L [octadecanoyloxy(propan-2-yloxy)alumanyl] octadecanoate Chemical compound [Al+3].CC(C)[O-].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UXFIDFBXVFVKIB-UHFFFAOYSA-L 0.000 abstract 2
- 125000004423 acyloxy group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- LXVDSDPFRBWEFN-UHFFFAOYSA-M di(propan-2-yloxy)alumanyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[Al](OC(C)C)OC(C)C LXVDSDPFRBWEFN-UHFFFAOYSA-M 0.000 abstract 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 2
- 229960005235 piperonyl butoxide Drugs 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 abstract 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 abstract 1
- ZHQRYWQRFJNYPY-UHFFFAOYSA-L aluminum propan-2-olate diphenoxide Chemical compound [O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1.CC([O-])C.[Al+3] ZHQRYWQRFJNYPY-UHFFFAOYSA-L 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- PZWDHVKNXVLHOV-UHFFFAOYSA-K di(hexadecanoyloxy)alumanyl hexadecanoate Chemical compound [Al+3].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O PZWDHVKNXVLHOV-UHFFFAOYSA-K 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- OPSWAWSNPREEFQ-UHFFFAOYSA-K triphenoxyalumane Chemical compound [Al+3].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 OPSWAWSNPREEFQ-UHFFFAOYSA-K 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
Classifications
-
- 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)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Abstract
Compounds of the formula <FORM:0831346/IV (b)/1> where X and Y represent alkoxy, phenoxy or acyloxy groups and where only an acyloxy group may occur twice, by reacting together n mols. of one or more substances selected from the group consisting of: aluminium trichloride, aluminium dichlor - monoalkoxide, aluminium dichlor - monophenoxide, aluminium dichlormonoacylate, aluminium monochlor - dialkoxide, aluminium monochlor-diphenoxide, aluminium monochlor - diacylate, aluminium monochlormonoalkoxide - monophenoxide, aluminium monochlor - monoalkoxide - monoacylate, aluminium monochlor - monophenoxide-monoacylate, with m mols. of one or more different substances selected from the group consisting of: aluminium triacylate, aluminium triphenoxide, aluminium trialkoxide, aluminium dichlor - monoalkoxide, aluminium dichlor - monophenoxide, aluminium dichlormonoacylate, aluminium monochlor-dialkoxide, aluminium monochlor - diphenoxide, aluminium monochlor - monoalkoxide - monophenoxide, aluminium monochlor - diacylate, aluminium monochlor - monoalkoxide - monoacylate, aluminium monochlor - monophenoxide-monoacylate, where n and m are integers. The process of Specification 806,182 where the organic aluminium compounds are prepared by reacting aluminium trichloride with aluminium alkoxides, phenoxides, triacylates or alkoxy (or phenoxy) acylates is disclaimed. The reaction is effected by heating the reactants together until a homogeneous liquid melt is obtained and an inert solvent such as xylene may be used if desired. The examples describe the preparation of aluminium monochlor-monoisopropoxide mono stearate from aluminium trichloride, aluminium tristearate and aluminium isopropoxide; aluminium trichloride, aluminium monostearate-di-isopropoxide and aluminium di - stearate - mono - isopropoxide; aluminium dichlor monoisopropoxide and aluminium di-stearate-mono isopropoxide; aluminium dichlor-monostearate and aluminium di - isopropoxide monostearate; aluminium monochlor - distearate and aluminium monochlor - di - isopropoxide; aluminium monochlor - monophenoxide - monostearate from aluminium monochlor - diphenoxide and aluminium monochlor - distearate; aluminium monochlor - monoisopropoxide - monophenoxide from aluminium dichlormonoisopropoxide and aluminium monoisopropoxide - diphenoxide and aluminium monochlor - mono - sec.-butoxide monopalmitate from aluminium monochlor - di - sec. butoxide and aluminium tripalmitate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB505657A GB831346A (en) | 1957-02-14 | 1957-02-14 | Improvements relating to organic aluminium compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB505657A GB831346A (en) | 1957-02-14 | 1957-02-14 | Improvements relating to organic aluminium compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB831346A true GB831346A (en) | 1960-03-30 |
Family
ID=9788933
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB505657A Expired GB831346A (en) | 1957-02-14 | 1957-02-14 | Improvements relating to organic aluminium compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB831346A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0049498A1 (en) * | 1980-10-03 | 1982-04-14 | Richardson-Vicks, Inc. | Aluminium compounds that contain an organic rest, anti-sudorific agent containing these compounds as active components and application of this agent as an anti-sudorific agent |
-
1957
- 1957-02-14 GB GB505657A patent/GB831346A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0049498A1 (en) * | 1980-10-03 | 1982-04-14 | Richardson-Vicks, Inc. | Aluminium compounds that contain an organic rest, anti-sudorific agent containing these compounds as active components and application of this agent as an anti-sudorific agent |
| US4434178A (en) | 1980-10-03 | 1984-02-28 | Hoffmann-La Roche, Inc. | Antiperspirants |
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