CH493592A - Verwendung von Estern der Aethantetracarbonsäure oder der Propantetracarbonsäure oder deren Substitutionsprodukten als ultraviolettes Licht absorbierendes Mittel - Google Patents
Verwendung von Estern der Aethantetracarbonsäure oder der Propantetracarbonsäure oder deren Substitutionsprodukten als ultraviolettes Licht absorbierendes MittelInfo
- Publication number
- CH493592A CH493592A CH42965A CH42965A CH493592A CH 493592 A CH493592 A CH 493592A CH 42965 A CH42965 A CH 42965A CH 42965 A CH42965 A CH 42965A CH 493592 A CH493592 A CH 493592A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- tetracarboxylic acid
- esters
- ethane
- cooch3
- Prior art date
Links
- HFKBPAKZRASAGX-UHFFFAOYSA-N ethane-1,1,1,2-tetracarboxylic acid Chemical class OC(=O)CC(C(O)=O)(C(O)=O)C(O)=O HFKBPAKZRASAGX-UHFFFAOYSA-N 0.000 title claims abstract description 5
- 239000003223 protective agent Substances 0.000 title abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 4
- 125000003118 aryl group Chemical group 0.000 claims abstract description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 4
- 239000006096 absorbing agent Substances 0.000 claims abstract description 3
- 125000005843 halogen group Chemical group 0.000 claims abstract description 3
- 150000002148 esters Chemical class 0.000 claims description 19
- SHALVKVVWYJLCA-UHFFFAOYSA-N propane-1,1,1,2-tetracarboxylic acid Chemical compound OC(=O)C(C)C(C(O)=O)(C(O)=O)C(O)=O SHALVKVVWYJLCA-UHFFFAOYSA-N 0.000 claims description 3
- 238000006467 substitution reaction Methods 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000004033 plastic Substances 0.000 abstract description 7
- 229920003023 plastic Polymers 0.000 abstract description 7
- -1 R2-R5 = H Chemical group 0.000 abstract description 4
- 239000003973 paint Substances 0.000 abstract description 3
- 239000000976 ink Substances 0.000 abstract description 2
- 239000002904 solvent Substances 0.000 abstract description 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000012780 transparent material Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000002253 acid Substances 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 101100005001 Caenorhabditis elegans cah-5 gene Proteins 0.000 description 2
- 125000006364 carbonyl oxy methylene group Chemical group [H]C([H])([*:2])OC([*:1])=O 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- QNAPYKYKJNQLOF-UHFFFAOYSA-N 2-phenylpropane-1,1,3,3-tetracarboxylic acid Chemical compound OC(=O)C(C(O)=O)C(C(C(O)=O)C(O)=O)C1=CC=CC=C1 QNAPYKYKJNQLOF-UHFFFAOYSA-N 0.000 description 1
- DWXSMRQBBFSNRM-UHFFFAOYSA-N C(C(CCCC)C(=O)OC)(C(=O)OC)(C(=O)OC)C(=O)OC Chemical compound C(C(CCCC)C(=O)OC)(C(=O)OC)(C(=O)OC)C(=O)OC DWXSMRQBBFSNRM-UHFFFAOYSA-N 0.000 description 1
- DVHUADPRAZUCNW-UHFFFAOYSA-N CCCCCCCCOC(C(C(C(C(OCCCCCCCC)=O)C(OCCCCCCCC)=O)C1=CC=CC=C1)C(OCCCCCCCC)=O)=O Chemical compound CCCCCCCCOC(C(C(C(C(OCCCCCCCC)=O)C(OCCCCCCCC)=O)C1=CC=CC=C1)C(OCCCCCCCC)=O)=O DVHUADPRAZUCNW-UHFFFAOYSA-N 0.000 description 1
- NCLDKBHZANMFCZ-UHFFFAOYSA-N COC(C(CC1=CC=CC=C1)C(C(OC)=O)(C(OC)=O)C(OC)=O)=O Chemical compound COC(C(CC1=CC=CC=C1)C(C(OC)=O)(C(OC)=O)C(OC)=O)=O NCLDKBHZANMFCZ-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- NJEVMKZODGWUQT-UHFFFAOYSA-N propane-1,1,3,3-tetracarboxylic acid Chemical compound OC(=O)C(C(O)=O)CC(C(O)=O)C(O)=O NJEVMKZODGWUQT-UHFFFAOYSA-N 0.000 description 1
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- SXENQBBEFVGGLF-UHFFFAOYSA-N tetraethyl 2-phenylpropane-1,1,3,3-tetracarboxylate Chemical compound CCOC(=O)C(C(=O)OCC)C(C(C(=O)OCC)C(=O)OCC)C1=CC=CC=C1 SXENQBBEFVGGLF-UHFFFAOYSA-N 0.000 description 1
- KRMLKRWQLHXGNH-UHFFFAOYSA-N tetramethyl 2-(4-methoxyphenyl)propane-1,1,3,3-tetracarboxylate Chemical compound COC(=O)C(C(=O)OC)C(C(C(=O)OC)C(=O)OC)C1=CC=C(OC)C=C1 KRMLKRWQLHXGNH-UHFFFAOYSA-N 0.000 description 1
- UCQHMFFQQBOHTK-UHFFFAOYSA-N tetramethyl 2-phenylpropane-1,1,3,3-tetracarboxylate Chemical compound COC(=O)C(C(=O)OC)C(C(C(=O)OC)C(=O)OC)C1=CC=CC=C1 UCQHMFFQQBOHTK-UHFFFAOYSA-N 0.000 description 1
- OOKYMDWDUVIRGM-UHFFFAOYSA-N tetramethyl 3-(4-nitrophenyl)propane-1,1,1,2-tetracarboxylate Chemical compound [N+](=O)([O-])C1=CC=C(CC(C(C(=O)OC)(C(=O)OC)C(=O)OC)C(=O)OC)C=C1 OOKYMDWDUVIRGM-UHFFFAOYSA-N 0.000 description 1
- XQQGINSCLPSSER-UHFFFAOYSA-N tetramethyl propane-1,1,1,2-tetracarboxylate Chemical compound C(C(C)C(=O)OC)(C(=O)OC)(C(=O)OC)C(=O)OC XQQGINSCLPSSER-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DES89894A DE1232963B (de) | 1964-03-07 | 1964-03-07 | Ultraviolettschutzmittel fuer organische Stoffe |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH493592A true CH493592A (de) | 1970-07-15 |
Family
ID=7515413
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH42965A CH493592A (de) | 1964-03-07 | 1965-01-13 | Verwendung von Estern der Aethantetracarbonsäure oder der Propantetracarbonsäure oder deren Substitutionsprodukten als ultraviolettes Licht absorbierendes Mittel |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE659456A (en)van) |
| CH (1) | CH493592A (en)van) |
| DE (1) | DE1232963B (en)van) |
| FR (1) | FR1493414A (en)van) |
| GB (1) | GB1030629A (en)van) |
| NL (1) | NL6501525A (en)van) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU55702A1 (en)van) * | 1968-03-18 | 1969-10-02 | ||
| EP0341961A3 (en) * | 1988-05-09 | 1990-06-20 | Merck & Co. Inc. | Polymalonic acids as boneaffinity agents |
| GB8917991D0 (en) * | 1989-08-07 | 1989-09-20 | Akzo Nv | Uv-stabilization of polymers using nitro compounds |
| JP3159896B2 (ja) * | 1995-08-24 | 2001-04-23 | ポリプラスチックス株式会社 | ポリアリーレンサルファイド樹脂組成物 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1087902B (de) * | 1956-06-19 | 1960-08-25 | Bayer Ag | Ultraviolett-Schutzfiltermasse oder -schicht |
-
1964
- 1964-03-07 DE DES89894A patent/DE1232963B/de active Granted
-
1965
- 1965-01-13 CH CH42965A patent/CH493592A/de not_active IP Right Cessation
- 1965-02-01 FR FR3918A patent/FR1493414A/fr not_active Expired
- 1965-02-08 NL NL6501525A patent/NL6501525A/xx unknown
- 1965-02-09 BE BE659456D patent/BE659456A/xx unknown
- 1965-02-24 GB GB802365A patent/GB1030629A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE659456A (en)van) | 1965-05-28 |
| GB1030629A (en) | 1966-05-25 |
| FR1493414A (fr) | 1967-09-01 |
| NL6501525A (en)van) | 1965-09-08 |
| DE1232963C2 (en)van) | 1967-08-03 |
| DE1232963B (de) | 1967-01-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |