GB737392A - Improvements in or relating to organic tin-containing compounds and compositions containing the same - Google Patents
Improvements in or relating to organic tin-containing compounds and compositions containing the sameInfo
- Publication number
- GB737392A GB737392A GB23613/52A GB2361352A GB737392A GB 737392 A GB737392 A GB 737392A GB 23613/52 A GB23613/52 A GB 23613/52A GB 2361352 A GB2361352 A GB 2361352A GB 737392 A GB737392 A GB 737392A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radicals
- tin
- sulphur
- referred
- organo
- 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
- 239000000203 mixture Substances 0.000 title abstract 6
- 150000001875 compounds Chemical class 0.000 title abstract 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 title 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 5
- 239000005864 Sulphur Substances 0.000 abstract 5
- -1 amine salts Chemical class 0.000 abstract 5
- 239000003381 stabilizer Substances 0.000 abstract 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 4
- 239000002480 mineral oil Substances 0.000 abstract 4
- 150000001768 cations Chemical class 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000003438 dodecyl group Chemical group [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])* 0.000 abstract 2
- 150000004820 halides Chemical class 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 235000010446 mineral oil Nutrition 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052700 potassium Inorganic materials 0.000 abstract 2
- 239000011591 potassium Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- NPAZWTIGHVUCMK-UHFFFAOYSA-N 2,2-diphenylethylcarbamodithioic acid Chemical class C1(=CC=CC=C1)C(CNC(S)=S)C1=CC=CC=C1 NPAZWTIGHVUCMK-UHFFFAOYSA-N 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 abstract 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052788 barium Inorganic materials 0.000 abstract 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- XTHRTLHUMOKINM-UHFFFAOYSA-N benzylsulfanylmethanedithioic acid Chemical class SC(=S)SCC1=CC=CC=C1 XTHRTLHUMOKINM-UHFFFAOYSA-N 0.000 abstract 1
- SFIWAVRBROEWBI-UHFFFAOYSA-N bis(butylsulfanyloxy)-sulfanyl-sulfanylidene-lambda5-phosphane Chemical class C(CCC)SOP(S)(OSCCCC)=S SFIWAVRBROEWBI-UHFFFAOYSA-N 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 235000019864 coconut oil Nutrition 0.000 abstract 1
- 239000003240 coconut oil Substances 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- YTMAENIETQSSKL-UHFFFAOYSA-L dibromo(dihexyl)stannane Chemical compound [Br-].[Br-].CCCCCC[Sn+2]CCCCCC YTMAENIETQSSKL-UHFFFAOYSA-L 0.000 abstract 1
- RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical group CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-UHFFFAOYSA-L 0.000 abstract 1
- YREAYUWMESCMHJ-UHFFFAOYSA-L didodecyltin(2+);dichloride Chemical compound CCCCCCCCCCCC[Sn](Cl)(Cl)CCCCCCCCCCCC YREAYUWMESCMHJ-UHFFFAOYSA-L 0.000 abstract 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000295 fuel oil Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 229910052744 lithium Inorganic materials 0.000 abstract 1
- 239000000314 lubricant Substances 0.000 abstract 1
- 239000010687 lubricating oil Substances 0.000 abstract 1
- YICRPERKKBDRSP-UHFFFAOYSA-N methyl 3-amino-4-methylthiophene-2-carboxylate Chemical compound COC(=O)C=1SC=C(C)C=1N YICRPERKKBDRSP-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000010705 motor oil Substances 0.000 abstract 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000002347 octyl 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])[H] 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 235000019198 oils Nutrition 0.000 abstract 1
- 125000000913 palmityl 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])[H] 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 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
- C07F9/02—Phosphorus compounds
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/226—Compounds with one or more Sn-S linkages
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/102—Polyesters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/08—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
- C10M2227/083—Sn compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/042—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/044—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/046—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/135—Steam engines or turbines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/17—Electric or magnetic purposes for electric contacts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Lubricants (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention comprises organo-tin compounds of the general formula RwSnGy wherein G represents any of the radicals <FORM:0737392/IV (b)/1> w being 2 or 3, y being 1 or 2 so that w + y is 4, Z represents oxygen or sulphur and R, R1 and R11 represent hydrocarbon radicals, and a process for the preparation thereof by reacting an organo-tin halide of the general formula RwSnXy, wherein R, w and y have the significance indicated above and X is a reactive halogen, with at least one salt of a sulphur containing compound of the general formula GY wherein Y represents a cation and G has the significance indicated above. The R, R1 and R11 radicals preferably have 1 to 20 carbon atoms and may be alkyl, alkenyl, cycloalkyl, aryl, aralkyl and alkaryl radicals. Alkyl radicals referred to are the methyl, isopropyl, octyl, dodecyl and octadecyl radicals. Other radicals referred to are the phenyl, naphthyl, benzyl, octaphenyl and ethylcyclohexyl radicals. The process may be carried out in a substantially inert solvent. The preferred reaction temperature is in the range of 10 DEG to 100 DEG C. The cation Y may be an alkali or alkaline earth metal such as sodium, potassium or calcium, or ammonium or amine salts of the sulphur containing acid may be used. The following sulphur-containing compounds are referred to: n-butyl, isopropyl, hexadecyl and ethylcyclohexyl, xanthic acids, n-nonyl, lauryl and benzyl thioxanthic acids, dibutyl isopropyl ethyl, diamyl, didodecyl, diethyl and diphenyl ethyl dithiocarbamic acids, di-(methylcyclohexyl), di-(octylphenyl), di-(2-ethylhexyl), dilauryl, dicetyl and di(butylmercapto)dithiophosphoric acids, and dialkyl dithiophosphoric acid where the alkyl groups are derived from a mixture of alcohols obtained from coconut oil and having from 8 to 18 carbon atoms. The cation Y may be an alkali or alkaline earth metal such as sodium, potassium, lithium or barium, or ammonium or amine salts may be used. Organotin halides referred to are dibutyl- and dilauryltin dichloride, di-n-hexyl-tin dibromide, triphenyl- and tri-tert.-octyl-tin iodide and tricyclohexyltin chloride. A number of detailed examples are given.ALSO:Mineral oil fractions and polyether and polyester lubricants contain as a stabilizer an organo-tin compound of the general formula RwSnGy where G represents one of the groups <FORM:0737392/III/1> w is 2 or 3, y is 1 or 2, w plus y is 4, Z is oxygen or sulphur and R, R1 and R11 represent hydrocarbon radicals. The stabilizer may be present in a minor proportion by weight, e.g. in an amount up to 20 per cent of the whole composition such as in an amount from 0.01 to 5 per cent preferably 0.1 to 2.0 per cent by weight based on the total composition. The stabilizer may be present in sufficient quantity to form a concentrated composition having from 20 to 75 per cent by weight of stabilizer based on the whole composition. Mineral oil fractions mentioned are motor and fuel oils, lubricating oils and greases, white mineral oils, hydrogenated mineral oils and heating oils. Organo-tin stabilizers specifically referred to are dilauryltindi-isopropylxanthate, dibutyltindi - n - butylxanthate, triphenyltinlaurylthioxanthate, dilauryltindibutyldithiocarbamate, dibutyltindiamyldithiocarbamate, dilauryltindi-(di-isopropyldithiophosphate), dibutyltindi-[di-(methylcyclohexyl) - dithiophosphate] and dibutyltindi - [di - (octylphenyl) - dithiophosphate.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US737392XA | 1951-11-15 | 1951-11-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB737392A true GB737392A (en) | 1955-09-28 |
Family
ID=22115516
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB23613/52A Expired GB737392A (en) | 1951-11-15 | 1952-09-19 | Improvements in or relating to organic tin-containing compounds and compositions containing the same |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB737392A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0018899A1 (en) * | 1979-05-04 | 1980-11-12 | Societe Nationale Elf Aquitaine | Process for the preparation of organotin compounds |
-
1952
- 1952-09-19 GB GB23613/52A patent/GB737392A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0018899A1 (en) * | 1979-05-04 | 1980-11-12 | Societe Nationale Elf Aquitaine | Process for the preparation of organotin compounds |
| FR2455606A1 (en) * | 1979-05-04 | 1980-11-28 | Elf Aquitaine | NEW PROCESS FOR THE PREPARATION OF ORGANOETANS |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2809492C2 (en) | Trithio- and tetrathiophosphoric acid triesters, processes for their preparation and for the preparation of trithiophosphorous acid esters and use of the trithio- and tetrathiophosphoric acid triesters | |
| CA1126748A (en) | Organotin mercaptoalkanol esters and alkoxides containing sulfide groups | |
| US4255320A (en) | Mixtures of alkyltin sulfides and alkyltin 2-acyloxyethlymecaptides as stabilizer compositons for polyvinyl chloride resin compositions | |
| GB819169A (en) | Phosphorus-and-sulfur-containing materials and lubricants containing them | |
| USRE22830E (en) | Compounded oil | |
| DE1211212B (en) | Process for the production of open-chain or cyclic substitution products of 2,3-dimercaptoquinoxaline | |
| US2866732A (en) | Metal derivatives of organic phosphates and phosphites | |
| US2977382A (en) | Method of preparing esters of phosphorodithioic acids | |
| US2763617A (en) | Lubricating oil containing dicyclopentadienyl iron and a wear inhibiting agent | |
| GB737392A (en) | Improvements in or relating to organic tin-containing compounds and compositions containing the same | |
| US2884431A (en) | Fluorinated diesters of phosphorodithioic acid and salts thereof | |
| US3068259A (en) | Molybdenum and tungsten halides and sulfides of organic substituted dithiophosphoricacids | |
| US3193500A (en) | Extreme pressure lubricant | |
| US2836561A (en) | Lubricating oils | |
| US2894951A (en) | Heterocyclic polyamine salts of phosphorodithioic acid esters and compositions containing the same | |
| GB1099478A (en) | Preparation of metal organo dithiophosphates | |
| US3412118A (en) | Salts of 2, 6-and 2, 4, 6-substituted primary aryl phosphites | |
| Barber | The preparation of some phosphorus compounds and their comparison as load carrying additives by the four-ball machine | |
| US2895983A (en) | Beta hydroxy phosphinothioic esters and method of preparing same | |
| US2961457A (en) | New esters of omicron, omicron-dialkylphosphoric or omicron. omicron-dialkylthionophosphoric acids | |
| US2822374A (en) | Preparation of organic phosphorothioic halides | |
| US3177233A (en) | Oil-soluble polyvalent metal salts of alkyl mercaptomethyl phosphonic acid | |
| US3775451A (en) | Organotin thiocarboxylates and preparation thereof | |
| EP0134063A2 (en) | Grease composition | |
| US4634541A (en) | Color stabilizers for zinc dithiophosphates |