GB247986A - The manufacture of new complex antimony compounds - Google Patents
The manufacture of new complex antimony compoundsInfo
- Publication number
- GB247986A GB247986A GB486026A GB486026A GB247986A GB 247986 A GB247986 A GB 247986A GB 486026 A GB486026 A GB 486026A GB 486026 A GB486026 A GB 486026A GB 247986 A GB247986 A GB 247986A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- salts
- thioglycollic
- antimony
- product
- 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
- 150000001463 antimony compounds Chemical class 0.000 title abstract 2
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 5
- LJCFOYOSGPHIOO-UHFFFAOYSA-N antimony pentoxide Chemical compound O=[Sb](=O)O[Sb](=O)=O LJCFOYOSGPHIOO-UHFFFAOYSA-N 0.000 abstract 4
- 239000000047 product Substances 0.000 abstract 4
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 abstract 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 2
- 239000007795 chemical reaction product Substances 0.000 abstract 2
- 230000003993 interaction Effects 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 1
- -1 alkaline earth metal salts Chemical class 0.000 abstract 1
- ZDINGUUTWDGGFF-UHFFFAOYSA-N antimony(5+) Chemical compound [Sb+5] ZDINGUUTWDGGFF-UHFFFAOYSA-N 0.000 abstract 1
- 239000002585 base Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical compound O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
- OHZZTXYKLXZFSZ-UHFFFAOYSA-I manganese(3+) 5,10,15-tris(1-methylpyridin-1-ium-4-yl)-20-(1-methylpyridin-4-ylidene)porphyrin-22-ide pentachloride Chemical compound [Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Mn+3].C1=CN(C)C=CC1=C1C(C=C2)=NC2=C(C=2C=C[N+](C)=CC=2)C([N-]2)=CC=C2C(C=2C=C[N+](C)=CC=2)=C(C=C2)N=C2C(C=2C=C[N+](C)=CC=2)=C2N=C1C=C2 OHZZTXYKLXZFSZ-UHFFFAOYSA-I 0.000 abstract 1
- 238000006386 neutralization reaction Methods 0.000 abstract 1
- 230000020477 pH reduction Effects 0.000 abstract 1
- 238000002360 preparation method Methods 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/90—Antimony compounds
- C07F9/902—Compounds without antimony-carbon linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
247,986. Carpmael, W., (I.G. Farbenindustrie Akt.-Ges.). Feb. 19, 1926. Thioglycollates.-A complex antimony compound of thioglycollic acid is produced by interaction of the acid with a compound of pentavalent antimony and either allowing the product to crystallize or nentralizing it and then acidifying. The product may be converted into salts, two series of which are obtainable according to whether the reaction product is neutralized before or after its isolation. The salts obtained by neutralization of the products of interaction of antimony pentoxide or pentachloride with thioglycollic acid appear to be salts or an acid having the formula Sb(S.CH2.COOH)5; acidification of a solution of these salts does not liberate the said acid, but one formed by the splitting off of thioglycollic acid; this new acid is also obtained when the reaction product of antimony pentoxide and thioglycollic acid is allowed to crystallize, and yields salts with bases. Examples are given of the preparation of the acid and the soluble alkali and alkaline earth metal salts. The products possess pharmaceutical properties.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB486026A GB247986A (en) | 1926-02-19 | 1926-02-19 | The manufacture of new complex antimony compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB486026A GB247986A (en) | 1926-02-19 | 1926-02-19 | The manufacture of new complex antimony compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB247986A true GB247986A (en) | 1926-07-22 |
Family
ID=9785164
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB486026A Expired GB247986A (en) | 1926-02-19 | 1926-02-19 | The manufacture of new complex antimony compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB247986A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2473735A (en) * | 1942-03-24 | 1949-06-21 | Burroughs Wellcome Co | Manufacture of complex organic antimony compounds |
| DE1038276B (en) * | 1954-03-10 | 1958-09-04 | Metal & Thermit Corp | Process for the stabilization of synthetic resin compounds containing chlorine |
-
1926
- 1926-02-19 GB GB486026A patent/GB247986A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2473735A (en) * | 1942-03-24 | 1949-06-21 | Burroughs Wellcome Co | Manufacture of complex organic antimony compounds |
| DE1038276B (en) * | 1954-03-10 | 1958-09-04 | Metal & Thermit Corp | Process for the stabilization of synthetic resin compounds containing chlorine |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB247986A (en) | The manufacture of new complex antimony compounds | |
| GB592827A (en) | Improvements in or relating to the manufacture of phenoxyalkylcarboxylic compounds | |
| GB870575A (en) | Benzothiadiazines and the production thereof | |
| GB450592A (en) | Process for the manufacture of polymerisation products of olefines | |
| US1485378A (en) | Antispasmodic compound and process of producing the same | |
| GB442120A (en) | A process for manufacturing novel cyclic ketones | |
| GB306575A (en) | Process for the manufacture of ortho-cyanaryl-thioglycollic acids and intermediate products | |
| GB1164330A (en) | Process for manufacturing Pyridoxal-5-Phosphate | |
| SU93037A1 (en) | Method for preparing dichloroacetic acid esters | |
| GB571628A (en) | Production of unsubstituted or ª‡,ª‡-substituted ª‰,ª‰-thiodihydracrylic acids | |
| GB510167A (en) | Manufacture of 3-hydroxy-4-carbaminobenzene-1-arsonic acid | |
| GB1262607A (en) | PROCESS FOR THE MANUFACTURE OF beta-ACETOXYPIVALIC ALDEHYDE | |
| GB258973A (en) | The manufacture of new complex alkali or alkaline earth antimony compounds | |
| GB822720A (en) | Production of xanthene derivatives | |
| GB367708A (en) | Manufacture of 2-oxyacetic acid-benzimidazole-arsonic acids | |
| GB169025A (en) | Improvements in or relating to the manufacture of chlorinated derivatives of toluene | |
| GB620026A (en) | Improvements in or relating to the manufacture of 2.4-dinitro-6-cyclohexyl-phenol | |
| GB930289A (en) | Improvements in or relating to the preparation of sodium cyclohexylsulphamate | |
| GB306607A (en) | Process for the manufacture of ortho-cyanaryl thioglycollic acids and intermediate products | |
| GB347052A (en) | Manufacture of perfumes | |
| ES261630A1 (en) | New cyclopentano-naphthalene derivatives and their formation | |
| GB398888A (en) | Improvements in or relating to the manufacture of trisodium phosphate | |
| GB200151A (en) | Improved manufacture of thymol | |
| GB874362A (en) | A process for the production of ª--(p-nitrobenzoyl)-ª--phthalimino acetic acid esters | |
| GB307776A (en) | Process for the manufacture of water-soluble products from commercial fatty acids obtained from raw wool fat |