GB1008002A - Stannous salt complexes - Google Patents
Stannous salt complexesInfo
- Publication number
- GB1008002A GB1008002A GB1156765A GB1156765A GB1008002A GB 1008002 A GB1008002 A GB 1008002A GB 1156765 A GB1156765 A GB 1156765A GB 1156765 A GB1156765 A GB 1156765A GB 1008002 A GB1008002 A GB 1008002A
- Authority
- GB
- United Kingdom
- Prior art keywords
- salt complexes
- stannous salt
- production
- components
- stannous
- 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
- 150000003839 salts Chemical class 0.000 title abstract 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 abstract 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 abstract 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 abstract 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 abstract 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 125000005341 metaphosphate group Chemical group 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 125000005474 octanoate group Chemical group 0.000 abstract 1
- 229940049964 oleate Drugs 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- 235000011150 stannous chloride Nutrition 0.000 abstract 1
- 239000001119 stannous chloride Substances 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- 229940095064 tartrate Drugs 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/24—Catalysts containing metal compounds of tin
-
- 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
- C07F7/003—Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention comprises complex compounds of stannous salts of inorganic or organic acids with N-substituted organic carboxylic amides, and their production by mixing the components, optionally in the presence of an inert solvent. Specified components are stannous chloride, bromide, fluoride, sulphate, orthophosphate, hypophosphite, metaphosphate, oxalate, tartrate, acetate, butyrate, hexoate, octoate, oleate and p-toluenesulphonate; and N,N-dimethylformamide, N,N - diethylformamide, N,N - dimethylacetamide and N - methylacetamide. The complexes are catalysts for polyurethane production (see Specification 1,003,201 in Division C3).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1156763 | 1963-03-15 | ||
GB1035163A GB1003201A (en) | 1963-03-15 | 1963-03-15 | Improvements in or relating to the manufacture of polyurethanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1008002A true GB1008002A (en) | 1965-10-22 |
Family
ID=26247463
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1035163A Expired GB1003201A (en) | 1963-03-15 | 1963-03-15 | Improvements in or relating to the manufacture of polyurethanes |
GB1156765A Expired GB1008002A (en) | 1963-03-15 | 1963-03-15 | Stannous salt complexes |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1035163A Expired GB1003201A (en) | 1963-03-15 | 1963-03-15 | Improvements in or relating to the manufacture of polyurethanes |
Country Status (4)
Country | Link |
---|---|
DE (1) | DE1235576B (en) |
FR (1) | FR1391255A (en) |
GB (2) | GB1003201A (en) |
NL (1) | NL6402613A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112851498A (en) * | 2020-12-31 | 2021-05-28 | 潍坊加易加生物科技有限公司 | Preparation method and application of stannous isooctenoate |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4085072A (en) * | 1975-12-18 | 1978-04-18 | M&T Chemicals Inc. | Process for preparing oxidatively stable polyurethane foam |
US4251636A (en) * | 1979-04-30 | 1981-02-17 | Texaco Development Corporation | Stannous halide complexes and their use in preparing polyurethane foams |
FR2496107A1 (en) * | 1980-12-12 | 1982-06-18 | Texaco Development Corp | Stannous halide-alcohol complex gelling catalysts - for polyurethane prodn., low blowing activity, allowing prodn. of non-foamed prods. |
US4867892A (en) * | 1987-12-28 | 1989-09-19 | Exxon Research And Engineering Company | Antiwear additives for lubricating oils |
EP3575282A4 (en) * | 2017-01-27 | 2021-03-17 | Kyoto University | Complex and method for producing same |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE584911A (en) * | 1958-11-24 |
-
1963
- 1963-03-15 GB GB1035163A patent/GB1003201A/en not_active Expired
- 1963-03-15 GB GB1156765A patent/GB1008002A/en not_active Expired
-
1964
- 1964-03-12 NL NL6402613A patent/NL6402613A/xx unknown
- 1964-03-13 FR FR967416A patent/FR1391255A/en not_active Expired
- 1964-03-16 DE DEJ25464A patent/DE1235576B/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112851498A (en) * | 2020-12-31 | 2021-05-28 | 潍坊加易加生物科技有限公司 | Preparation method and application of stannous isooctenoate |
Also Published As
Publication number | Publication date |
---|---|
FR1391255A (en) | 1965-03-05 |
DE1235576B (en) | 1967-03-02 |
NL6402613A (en) | 1964-09-16 |
GB1003201A (en) | 1965-09-02 |
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