BE610351A - - Google Patents
Info
- Publication number
- BE610351A BE610351A BE610351DA BE610351A BE 610351 A BE610351 A BE 610351A BE 610351D A BE610351D A BE 610351DA BE 610351 A BE610351 A BE 610351A
- Authority
- BE
- Belgium
- Prior art keywords
- carbon atoms
- butyl
- fading
- copolymer
- vinyl
- Prior art date
Links
- 238000005562 fading Methods 0.000 claims description 22
- 229920001577 copolymer Polymers 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000011230 binding agent Substances 0.000 claims description 8
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- -1 hydroxy-substituted benzophenone Chemical class 0.000 claims description 5
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 229940124543 ultraviolet light absorber Drugs 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims 2
- 150000002894 organic compounds Chemical class 0.000 claims 1
- 239000000126 substance Substances 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 6
- 230000002745 absorbent Effects 0.000 description 5
- 239000002250 absorbent Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 108010010803 Gelatin Proteins 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 239000008273 gelatin Substances 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 235000011852 gelatine desserts Nutrition 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- VBQMOUFTQANISV-UHFFFAOYSA-N (2-butylphenyl)-phenylmethanone Chemical group CCCCC1=CC=CC=C1C(=O)C1=CC=CC=C1 VBQMOUFTQANISV-UHFFFAOYSA-N 0.000 description 1
- HUYKZYIAFUBPAQ-UHFFFAOYSA-N (2-hydroxyphenyl)-(4-hydroxyphenyl)methanone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1O HUYKZYIAFUBPAQ-UHFFFAOYSA-N 0.000 description 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- RZNHSEZOLFEFGB-UHFFFAOYSA-N 2-methoxybenzoyl chloride Chemical compound COC1=CC=CC=C1C(Cl)=O RZNHSEZOLFEFGB-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000008064 anhydrides Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- DMVOXQPQNTYEKQ-UHFFFAOYSA-N biphenyl-4-amine Chemical compound C1=CC(N)=CC=C1C1=CC=CC=C1 DMVOXQPQNTYEKQ-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE610351T |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE610351A true BE610351A (https=) |
Family
ID=3875265
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE610351D BE610351A (https=) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE610351A (https=) |
-
0
- BE BE610351D patent/BE610351A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0402228B1 (fr) | Composés photochromiques de type indolino-spiro-oxazine à cycle à 5 chaînons, leur procédé de préparation, compositions et articles photochromiques contenant de tels composés | |
| EP0407237B1 (fr) | Composés photochromiques de type indolino-spiro-oxazine, leur procédé de préparation, compositions et article photochromiques contenant de tels composés | |
| FR2793244A1 (fr) | 4-formylphenylmethacrylate, procede de preparation et polymeres qu'il permet d'obtenir | |
| FR2546544A1 (fr) | Nouvelles compositions utilisables comme auxiliaires de teinture | |
| CA2433984C (fr) | Procede d'obtention d'un latex photochromique stabilise, latex obtenu et application a l'optique ophtalmique | |
| FR2567516A1 (fr) | Procede de preparation de xanthones et de thioxanthones et utilisation de ces composes comme initiateurs de photopolymerisation | |
| CA1043495A (fr) | Polymeres anti-solaires et compositions cosmetiques les contenant | |
| BE610351A (https=) | ||
| FR2500835A1 (fr) | Procede de synthese des mononitrates d'isosorbide | |
| CA1292700C (fr) | Compositions cosmetiques destinees a proteger la peau contre les effets indesires des radiations ultraviolettes | |
| CH623305A5 (https=) | ||
| CH628365A5 (fr) | Polymeres structurellement colores a base de monomeres acryliques. | |
| FR2601365A1 (fr) | Nouveaux derives d'acrylamide, leur preparation et leur utilisation dans la realisation de polymeres absorbant les radiations ultraviolettes. | |
| BE1019713A3 (fr) | Peinture repulsive a base de derives de capsaicine. | |
| CA2045762A1 (fr) | Acrylates a fonction alcool, aldehyde et/ou ether, leur procede de fabrication et leur application a l'obtention de nouveaux polymeres et copolymeres | |
| EP0011520A1 (fr) | Résine à cycle thiétane réticulable par irradiation électronique ou photonique, et procédé d'utilisation d'une telle résine | |
| CH616410A5 (https=) | ||
| BE506674A (https=) | ||
| CH590303A5 (en) | Anti-solar polymers compsn - useful esp in cosmetics | |
| FR2487832A1 (fr) | Polyhydroxyphenyl-2, 2h-benzotriazoles et leurs procedes d'obtention et leurs utilisations a titre de stabilisant anti-uv | |
| CH470430A (fr) | Procédé de préparation de nouveaux polymères colorés | |
| CH618727A5 (en) | Process for the preparation of new cationic dyes and product | |
| LU86937A1 (fr) | Nouveaux composes insatures a chromophore absorbeur d'u.v.leur preparation et leur utilisation pour la realisation de polymeres anti-solaires | |
| FR2487831A1 (fr) | Etheroxydes de polyhydroxyphenyl-2, 2h-benzotriazoles, leurs procedes d'obtention et leurs utilisations a titre de stabilisant anti-uv | |
| FR2662693A1 (fr) | Nouvelles oxazolidones acryliques et methacryliques, leur procede de preparation et nouveaux polymeres en derivant. |