GB1194414A - Organo-Antimony-Tin Compounds - Google Patents
Organo-Antimony-Tin CompoundsInfo
- Publication number
- GB1194414A GB1194414A GB2623567A GB2623567A GB1194414A GB 1194414 A GB1194414 A GB 1194414A GB 2623567 A GB2623567 A GB 2623567A GB 2623567 A GB2623567 A GB 2623567A GB 1194414 A GB1194414 A GB 1194414A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- compounds
- antimony
- atom
- 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
- -1 mercapto compounds Chemical class 0.000 abstract 4
- 125000000962 organic group Chemical group 0.000 abstract 4
- 125000004434 sulfur atom Chemical group 0.000 abstract 3
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 abstract 3
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000003125 aqueous solvent Substances 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- QRMMMWOSHHVOCJ-UHFFFAOYSA-N 2,2-dimethylheptanoic acid Chemical compound CCCCCC(C)(C)C(O)=O QRMMMWOSHHVOCJ-UHFFFAOYSA-N 0.000 abstract 1
- PSYGHMBJXWRQFD-UHFFFAOYSA-N 2-(2-sulfanylacetyl)oxyethyl 2-sulfanylacetate Chemical compound SCC(=O)OCCOC(=O)CS PSYGHMBJXWRQFD-UHFFFAOYSA-N 0.000 abstract 1
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 abstract 1
- RZBBHEJLECUBJT-UHFFFAOYSA-N 6-methylheptyl 2-sulfanylacetate Chemical compound CC(C)CCCCCOC(=O)CS RZBBHEJLECUBJT-UHFFFAOYSA-N 0.000 abstract 1
- XZOYHFBNQHPJRQ-UHFFFAOYSA-N 7-methyloctanoic acid Chemical compound CC(C)CCCCCC(O)=O XZOYHFBNQHPJRQ-UHFFFAOYSA-N 0.000 abstract 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000004703 alkoxides Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910052787 antimony Inorganic materials 0.000 abstract 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 1
- 230000001588 bifunctional effect Effects 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical compound CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-UHFFFAOYSA-L 0.000 abstract 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 abstract 1
- LQRUPWUPINJLMU-UHFFFAOYSA-N dioctyl(oxo)tin Chemical compound CCCCCCCC[Sn](=O)CCCCCCCC LQRUPWUPINJLMU-UHFFFAOYSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- 239000011976 maleic acid Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 abstract 1
- 229910001887 tin oxide Inorganic materials 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin 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
- 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
-
- 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
- C08K5/59—Arsenic- or antimony-containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,194,414. Organo - antimony - tin compounds. CHEMISCHE WERKE MUNCHEN OTTO BARLOCHER G.m.b.H. 7 June, 1967 [1 July, 1966], No. 26235/67. Heading C2J. [Also in Division C3] Organo-antimony-tin compounds are made by reacting at least two mercapto compounds, at least one of which is bifunctional (SH/SH or SH/CO 2 H) with either: (1) dialkyl tin oxide or alkoxide and antimony trioxide with or without an aliphatic carboxylic acid (C 4 or more); or (2) dialkyl tin dihalide and antimony trihalide in presence of an alkali, with or without an alkali derivative of an aliphatic carboxylic acid (C 4 or more). Reaction in either case is effected by heating in presence of a non-aqueous solvent with continuous removal of the water produced in the reaction, and with final removal of the non-aqueous solvent. Typical compounds are: where R<SP>1</SP> is an organic group (which may contain Sn and/or Sb) linked to Sn via a -CO 2 H or -SH group and is the radical of a mercaptan or a carboxylic acid as defined; R<SP>2</SP> is alkyl, R<SP>3</SP> and R<SP>4</SP> are organic groups linked to the S atom via a C atom and are, together with the S atom, radicals of mercapto compounds, and R<SP>5</SP> is an organic group (which may contain Sn and/or Sb) linked to the S atom via a C atom. Specified starting materials are dibutyl tin oxide, dioctyl tin oxide, and dibutyl tin dichloride; maleic acid, α-ethyl hexyl acid, 2,2-dimethyl heptanic acid, isooctanoic acid, and isononanoic acid; thioglycolic acid, #- mercapto-propionic acid, thioglycolic acid isooctyl ester, thioglycolic acid lauryl ester and ethylene glycol dithioglycolate. The compounds are used as polymer stabilizers (Division C3).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEC0039505 | 1966-07-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1194414A true GB1194414A (en) | 1970-06-10 |
Family
ID=7023758
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2623567A Expired GB1194414A (en) | 1966-07-01 | 1967-06-07 | Organo-Antimony-Tin Compounds |
Country Status (6)
| Country | Link |
|---|---|
| AT (1) | AT270234B (en) |
| BE (1) | BE691039A (en) |
| DE (1) | DE1568297A1 (en) |
| ES (1) | ES342144A1 (en) |
| GB (1) | GB1194414A (en) |
| NL (1) | NL6703880A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106188144A (en) * | 2016-07-20 | 2016-12-07 | 浙江海普顿新材料股份有限公司 | A kind of liquid organotin antimonial and its preparation method and application |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0031295B1 (en) * | 1979-11-08 | 1983-05-18 | Ciba-Geigy Ag | Organic antimony-sulphur compounds, their use as stabilisers in chloric thermoplastics, and thermoplastics so stabilised |
| US4988750A (en) * | 1981-07-17 | 1991-01-29 | Schering Ag | Non-toxic stabilizer for halogenated polymer |
-
1966
- 1966-07-01 DE DE19661568297 patent/DE1568297A1/en active Pending
- 1966-12-12 BE BE691039D patent/BE691039A/xx unknown
-
1967
- 1967-02-21 AT AT169367A patent/AT270234B/en active
- 1967-03-15 NL NL6703880A patent/NL6703880A/xx unknown
- 1967-06-07 GB GB2623567A patent/GB1194414A/en not_active Expired
- 1967-06-21 ES ES342144A patent/ES342144A1/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106188144A (en) * | 2016-07-20 | 2016-12-07 | 浙江海普顿新材料股份有限公司 | A kind of liquid organotin antimonial and its preparation method and application |
Also Published As
| Publication number | Publication date |
|---|---|
| AT270234B (en) | 1969-04-25 |
| DE1568297A1 (en) | 1970-01-02 |
| NL6703880A (en) | 1968-01-02 |
| BE691039A (en) | 1967-05-16 |
| ES342144A1 (en) | 1968-07-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU5273279A (en) | Organutin mercaptoalkanol esters and alkoxides containing sulfide groups | |
| GB1453428A (en) | Dihydroxy sulphonates containing ether structures | |
| ES440178A1 (en) | Stabilization of xanthophylls | |
| GB1192820A (en) | Process for the Production of Polyesters | |
| GB1464463A (en) | Process for the manufacture of carboxylic acid chlorides | |
| ES458534A1 (en) | Manufacture of glycol esters | |
| GB1177562A (en) | ||
| GB1194414A (en) | Organo-Antimony-Tin Compounds | |
| GB1233036A (en) | ||
| GB1169955A (en) | New halogenated esters and elastomers thereof | |
| GB1382744A (en) | Preparation of polyfluoroalcohols and esters | |
| ES341874A1 (en) | Indanyl-n-methylcarbamic acid esters | |
| GB1130822A (en) | Flourinated compounds containing functional groups | |
| GB1303491A (en) | ||
| GB1265430A (en) | ||
| CA1014331A (en) | Production of light stable antimonous oxide by hydrolysis of antimony trichloride | |
| ES422996A1 (en) | Halogen-containing phosphoric acid esters | |
| ES433740A1 (en) | Preparation of organotin mercaptides | |
| GB1129725A (en) | Poly(organotin) mercaptide polymers and resins stabilised therewith | |
| GB1200768A (en) | Production of chloroformates | |
| GB1143904A (en) | Esters and ethers derived from polyhalogenated alkylene oxides | |
| GB1043517A (en) | A process for the preparation of ª‡,ª‡-disubstituted succinimides, and the compounds thus prepared | |
| GB1207712A (en) | Hydrazine-carboxylic acid esters and their production | |
| GB1445768A (en) | Triorganotin compounds and method of combating fungi and mites using same | |
| GB1198917A (en) | Process for the Manufacture of beta-Alkoxythiocarboxylic Acid Esters |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |