CA1035781A - Orgonotin mercaptides bearing polysulfanediyl groups - Google Patents
Orgonotin mercaptides bearing polysulfanediyl groupsInfo
- Publication number
- CA1035781A CA1035781A CA199,889A CA199889A CA1035781A CA 1035781 A CA1035781 A CA 1035781A CA 199889 A CA199889 A CA 199889A CA 1035781 A CA1035781 A CA 1035781A
- Authority
- CA
- Canada
- Prior art keywords
- atomes
- carbone
- ayant
- groupement
- les
- 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
- -1 polysulfanediyl groups Polymers 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 150000002009 diols Chemical class 0.000 claims description 22
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 8
- 230000009471 action Effects 0.000 abstract description 7
- 238000001125 extrusion Methods 0.000 abstract description 4
- 239000003381 stabilizer Substances 0.000 abstract description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- 238000004383 yellowing Methods 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 description 2
- RZBBHEJLECUBJT-UHFFFAOYSA-N 6-methylheptyl 2-sulfanylacetate Chemical compound CC(C)CCCCCOC(=O)CS RZBBHEJLECUBJT-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 101100421144 Danio rerio selenoo1 gene Proteins 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- HJEINPVZRDJRBY-UHFFFAOYSA-N Disul Chemical compound OS(=O)(=O)OCCOC1=CC=C(Cl)C=C1Cl HJEINPVZRDJRBY-UHFFFAOYSA-N 0.000 description 1
- 241001482630 Epinnula magistralis Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 101100202896 Mus musculus Selenoo gene Proteins 0.000 description 1
- 102100026933 Myelin-associated neurite-outgrowth inhibitor Human genes 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- KYNFOMQIXZUKRK-UHFFFAOYSA-N bishydroxyethyldisulfide Natural products OCCSSCCO KYNFOMQIXZUKRK-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 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
- C08G79/12—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 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
- C07F7/22—Tin compounds
- C07F7/226—Compounds with one or more Sn-S linkages
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/14—Polysulfides
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/14—Polysulfides
- C08G75/16—Polysulfides by polycondensation of organic compounds with inorganic polysulfides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
- C08K5/57—Organo-tin compounds
- C08K5/58—Organo-tin compounds containing sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7317326A FR2229702B1 (xx) | 1973-05-14 | 1973-05-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1035781A true CA1035781A (en) | 1978-08-01 |
Family
ID=9119272
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA199,889A Expired CA1035781A (en) | 1973-05-14 | 1974-05-13 | Orgonotin mercaptides bearing polysulfanediyl groups |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4001178A (xx) |
| JP (1) | JPS5014634A (xx) |
| BE (1) | BE814954A (xx) |
| BR (1) | BR7403813D0 (xx) |
| CA (1) | CA1035781A (xx) |
| CH (1) | CH591508A5 (xx) |
| DE (1) | DE2423406A1 (xx) |
| ES (1) | ES426334A1 (xx) |
| FR (1) | FR2229702B1 (xx) |
| GB (1) | GB1474108A (xx) |
| IE (1) | IE39703B1 (xx) |
| IT (1) | IT1012343B (xx) |
| LU (1) | LU70059A1 (xx) |
| NL (1) | NL7406066A (xx) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5542101B2 (xx) * | 1973-10-25 | 1980-10-28 | ||
| JPS53118272A (en) * | 1977-03-25 | 1978-10-16 | Kobashi Kogyo Kk | Forming method of rolling for cultivate nail |
| CN107417589A (zh) * | 2017-07-20 | 2017-12-01 | 温州大学 | 二‑3‑巯基丙酸‑2.2‑二硫二乙酯及其制备方法和应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2752325A (en) * | 1952-05-23 | 1956-06-26 | Argus Chemical Lab Inc | Reaction products of an organic tin compound with a glycol ester of a mercaptocarboxylic acid, and high molecular weight halogenated materials stabilized therewith |
| FR1138451A (fr) * | 1954-11-17 | 1957-06-14 | Advance Solvents & Chemical Co | Nouveaux composés organiques de l'étain, et résines halogénées stabilisées à l'aide de ces nouveaux composés |
| FR2129974B1 (xx) * | 1971-03-24 | 1974-02-15 | Silicones Ste Indle |
-
1973
- 1973-05-14 FR FR7317326A patent/FR2229702B1/fr not_active Expired
-
1974
- 1974-05-06 NL NL7406066A patent/NL7406066A/xx active Search and Examination
- 1974-05-10 JP JP49052161A patent/JPS5014634A/ja active Pending
- 1974-05-10 IE IE998/74A patent/IE39703B1/xx unknown
- 1974-05-10 US US05/468,997 patent/US4001178A/en not_active Expired - Lifetime
- 1974-05-10 BR BR3813/74A patent/BR7403813D0/pt unknown
- 1974-05-13 BE BE144260A patent/BE814954A/xx unknown
- 1974-05-13 CA CA199,889A patent/CA1035781A/en not_active Expired
- 1974-05-13 LU LU70059A patent/LU70059A1/xx unknown
- 1974-05-13 GB GB2108374A patent/GB1474108A/en not_active Expired
- 1974-05-13 CH CH651174A patent/CH591508A5/xx not_active IP Right Cessation
- 1974-05-14 DE DE2423406A patent/DE2423406A1/de not_active Withdrawn
- 1974-05-14 ES ES426334A patent/ES426334A1/es not_active Expired
- 1974-05-14 IT IT22686/74A patent/IT1012343B/it active
Also Published As
| Publication number | Publication date |
|---|---|
| US4001178A (en) | 1977-01-04 |
| CH591508A5 (xx) | 1977-09-30 |
| LU70059A1 (xx) | 1975-02-24 |
| GB1474108A (en) | 1977-05-18 |
| IT1012343B (it) | 1977-03-10 |
| JPS5014634A (xx) | 1975-02-15 |
| FR2229702A1 (xx) | 1974-12-13 |
| NL7406066A (xx) | 1974-11-18 |
| IE39703B1 (en) | 1978-12-06 |
| FR2229702B1 (xx) | 1976-05-07 |
| BR7403813D0 (pt) | 1974-12-03 |
| DE2423406A1 (de) | 1974-12-05 |
| ES426334A1 (es) | 1976-07-01 |
| BE814954A (fr) | 1974-11-13 |
| IE39703L (en) | 1974-11-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Matzner et al. | The chemistry of chloroformates | |
| EP0263038B1 (fr) | Diorganopolysiloxane à fonction bétacétoester utile comme stabilisant des polymères à base de polychlorure de vinyle | |
| EP0358584B1 (fr) | Diorganopolysiloxane à fonction benzalmalonate | |
| FR2483437A1 (fr) | Nouveaux derives du type diorganopolysiloxane | |
| CA1035781A (en) | Orgonotin mercaptides bearing polysulfanediyl groups | |
| US2719165A (en) | Triorganosilylmethyl sulfur derivatives | |
| CA1082726A (en) | Organotin compounds and vinyl halide resin compositions stabilized therewith | |
| FR2645156A1 (fr) | Compose organosilicie a groupes hydroxyles | |
| EP3966218A1 (de) | Herstellung von siloxanen in gegenwart von kationischen germanium(ii)-verbindungen | |
| EP0354146B1 (fr) | Diorganopolysiloxane à fonction dibenzoylmethane | |
| EP0963368B1 (fr) | Composition a base de maleates d'organoetain utilisable pour stabiliser et lubrifier des polymeres thermoplastiques. procede d'obtention de ladite composition | |
| US8691198B2 (en) | Environmentally benign plasticizers based on derivatives of acetone | |
| CA1178607A (fr) | Telomeres photoreticulables et procede d'obtention | |
| US3478074A (en) | Preparation of organosilicon compounds from hydrosilicon compounds | |
| CA1095073A (en) | Mercaptocarboxylic acid esters and process for their manufacture | |
| CA1333610C (fr) | Diorganopolysiloxane a fonction benzylidene-3 camphre | |
| DE2749083A1 (de) | Verfahren zur herstellung von organozinnverbindungen | |
| EP0021033B2 (fr) | Compositions stabilisatrices contenant des composés monoorgano tris-thioalkyl étain et leur application à la stabilisation de polymères halogéno-vinyliques | |
| EP0369359A2 (de) | Verfahren zur Herstellung von Ketoximosilanen | |
| EP0696608B1 (de) | Organosilan- und Organopolysiloxan-Radikalinitiatoren und damit herstellbare Makromonomere und Pfropfcopolymerisate | |
| FR2611730A1 (fr) | Diorganopolysiloxane a fonction alpha-mercaptoester utile comme stabilisant des polymeres a base de chlorure de polyvinyle | |
| EP0549775B1 (fr) | Composes du germanium et leur utilisation comme huile biocompatible | |
| FR2605634A1 (fr) | Procede d'hydrolyse d'organodichlorosilanes | |
| CA1250306A (fr) | Procede de preparation de derives acetyleniques, derives obtenus et leur emploi | |
| FR2641782A1 (fr) | Composes chlorofluores fonctionnels et leur preparation |