JP2009530428A5 - - Google Patents
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- JP2009530428A5 JP2009530428A5 JP2008558784A JP2008558784A JP2009530428A5 JP 2009530428 A5 JP2009530428 A5 JP 2009530428A5 JP 2008558784 A JP2008558784 A JP 2008558784A JP 2008558784 A JP2008558784 A JP 2008558784A JP 2009530428 A5 JP2009530428 A5 JP 2009530428A5
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- JP
- Japan
- Prior art keywords
- formula
- alkyl
- compound
- group
- hydrogen
- 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.)
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- 125000000217 alkyl group Chemical group 0.000 claims description 48
- 150000001875 compounds Chemical class 0.000 claims description 42
- 229910052739 hydrogen Inorganic materials 0.000 claims description 28
- 239000001257 hydrogen Substances 0.000 claims description 28
- 125000004432 carbon atom Chemical group C* 0.000 claims description 24
- 150000002431 hydrogen Chemical group 0.000 claims description 19
- 229910052736 halogen Inorganic materials 0.000 claims description 16
- 150000002367 halogens Chemical class 0.000 claims description 16
- -1 cyano, carboxyl Chemical group 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
- 125000000962 organic group Chemical group 0.000 claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 239000003381 stabilizer Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 229910004013 NO 2 Inorganic materials 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 6
- 239000003063 flame retardant Substances 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims description 6
- 239000011574 phosphorus Substances 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 4
- VDVUCLWJZJHFAV-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1 VDVUCLWJZJHFAV-UHFFFAOYSA-N 0.000 claims description 4
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 claims description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- JWUXJYZVKZKLTJ-UHFFFAOYSA-N Triacetonamine Chemical compound CC1(C)CC(=O)CC(C)(C)N1 JWUXJYZVKZKLTJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- FJZCFGKQFDPNHS-UHFFFAOYSA-N henicosanal Chemical compound CCCCCCCCCCCCCCCCCCCCC=O FJZCFGKQFDPNHS-UHFFFAOYSA-N 0.000 claims description 4
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 150000002736 metal compounds Chemical class 0.000 claims description 4
- WQZXJTWTIYVJLT-UHFFFAOYSA-N n-ethylpiperidin-1-amine Chemical compound CCNN1CCCCC1 WQZXJTWTIYVJLT-UHFFFAOYSA-N 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 239000000049 pigment Substances 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 239000004611 light stabiliser Substances 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 3
- CWGBFIRHYJNILV-UHFFFAOYSA-N (1,4-diphenyl-1,2,4-triazol-4-ium-3-yl)-phenylazanide Chemical compound C=1C=CC=CC=1[N-]C1=NN(C=2C=CC=CC=2)C=[N+]1C1=CC=CC=C1 CWGBFIRHYJNILV-UHFFFAOYSA-N 0.000 claims description 2
- FMZUHGYZWYNSOA-VVBFYGJXSA-N (1r)-1-[(4r,4ar,8as)-2,6-diphenyl-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C([C@@H]1OC(O[C@@H]([C@@H]1O1)[C@H](O)CO)C=2C=CC=CC=2)OC1C1=CC=CC=C1 FMZUHGYZWYNSOA-VVBFYGJXSA-N 0.000 claims description 2
- HZVFRKSYUGFFEJ-YVECIDJPSA-N (2r,3r,4s,5r)-7-phenylhept-6-ene-1,2,3,4,5,6-hexol Chemical class OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=CC1=CC=CC=C1 HZVFRKSYUGFFEJ-YVECIDJPSA-N 0.000 claims description 2
- ANYJPOZXIAFCQP-UHFFFAOYSA-N 1,3-dihydrobenzo[g]indol-2-one Chemical class C1=CC=CC2=C(NC(=O)C3)C3=CC=C21 ANYJPOZXIAFCQP-UHFFFAOYSA-N 0.000 claims description 2
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 claims description 2
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 claims description 2
- FBIXXCXCZOZFCO-UHFFFAOYSA-N 3-dodecyl-1-(2,2,6,6-tetramethylpiperidin-4-yl)pyrrolidine-2,5-dione Chemical compound O=C1C(CCCCCCCCCCCC)CC(=O)N1C1CC(C)(C)NC(C)(C)C1 FBIXXCXCZOZFCO-UHFFFAOYSA-N 0.000 claims description 2
- KKEKJPDPXYTDCF-UHFFFAOYSA-N 3-dodecyl-7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical compound O=C1N(CCCCCCCCCCCC)C(=O)NC11CC(C)(C)NC(C)(C)C1 KKEKJPDPXYTDCF-UHFFFAOYSA-N 0.000 claims description 2
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000004604 Blowing Agent Substances 0.000 claims description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 2
- 235000021314 Palmitic acid Nutrition 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 235000021355 Stearic acid Nutrition 0.000 claims description 2
- 239000006096 absorbing agent Substances 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 229910001413 alkali metal ion Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical group 0.000 claims description 2
- 150000001336 alkenes Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 239000002216 antistatic agent Substances 0.000 claims description 2
- IUKQLMGVFMDQDP-UHFFFAOYSA-N azane;piperidine Chemical compound N.C1CCNCC1 IUKQLMGVFMDQDP-UHFFFAOYSA-N 0.000 claims description 2
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 230000003197 catalytic effect Effects 0.000 claims description 2
- 150000001879 copper Chemical class 0.000 claims description 2
- 229940087101 dibenzylidene sorbitol Drugs 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 239000006081 fluorescent whitening agent Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
- 239000006078 metal deactivator Substances 0.000 claims description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 claims description 2
- UONLDZHKYCFZRW-UHFFFAOYSA-N n-[6-[formyl-(2,2,6,6-tetramethylpiperidin-4-yl)amino]hexyl]-n-(2,2,6,6-tetramethylpiperidin-4-yl)formamide Chemical compound C1C(C)(C)NC(C)(C)CC1N(C=O)CCCCCCN(C=O)C1CC(C)(C)NC(C)(C)C1 UONLDZHKYCFZRW-UHFFFAOYSA-N 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 239000002667 nucleating agent Substances 0.000 claims description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 150000002978 peroxides Chemical class 0.000 claims description 2
- 239000002530 phenolic antioxidant Substances 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 125000003367 polycyclic group Chemical group 0.000 claims description 2
- 239000012779 reinforcing material Substances 0.000 claims description 2
- 238000000518 rheometry Methods 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 230000000087 stabilizing effect Effects 0.000 claims description 2
- 239000008117 stearic acid Substances 0.000 claims description 2
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- 229920001187 thermosetting polymer Polymers 0.000 claims description 2
- 239000004634 thermosetting polymer Substances 0.000 claims description 2
- 239000004416 thermosoftening plastic Substances 0.000 claims description 2
- 239000002023 wood Substances 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 239000001993 wax Substances 0.000 claims 1
- 0 CC(C)(*)N(C)C Chemical compound CC(C)(*)N(C)C 0.000 description 3
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 101100516563 Caenorhabditis elegans nhr-6 gene Proteins 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- SBOJXQVPLKSXOG-UHFFFAOYSA-N o-amino-hydroxylamine Chemical class NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006011990.8 | 2006-03-16 | ||
| DE102006011991.6 | 2006-03-16 | ||
| DE102006011989.4 | 2006-03-16 | ||
| DE102006011990 | 2006-03-16 | ||
| DE102006011989 | 2006-03-16 | ||
| DE102006011991 | 2006-03-16 | ||
| PCT/EP2007/052149 WO2007104689A1 (en) | 2006-03-16 | 2007-03-07 | Modified waxes, a process for their preparation, and their use |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013088652A Division JP5706464B2 (ja) | 2006-03-16 | 2013-04-19 | 変性ロウ、それらの製造方法及びそれらの使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009530428A JP2009530428A (ja) | 2009-08-27 |
| JP2009530428A5 true JP2009530428A5 (https=) | 2010-04-15 |
| JP5420911B2 JP5420911B2 (ja) | 2014-02-19 |
Family
ID=38024151
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008558784A Active JP5420911B2 (ja) | 2006-03-16 | 2007-03-07 | 変性ロウ、それらの製造方法及びそれらの使用 |
| JP2013088652A Active JP5706464B2 (ja) | 2006-03-16 | 2013-04-19 | 変性ロウ、それらの製造方法及びそれらの使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013088652A Active JP5706464B2 (ja) | 2006-03-16 | 2013-04-19 | 変性ロウ、それらの製造方法及びそれらの使用 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US8765848B2 (https=) |
| EP (1) | EP1999166B2 (https=) |
| JP (2) | JP5420911B2 (https=) |
| KR (2) | KR101403753B1 (https=) |
| AU (1) | AU2007224516A1 (https=) |
| BR (1) | BRPI0709551B1 (https=) |
| CA (1) | CA2640056C (https=) |
| DE (1) | DE602007006644D1 (https=) |
| ES (1) | ES2342739T5 (https=) |
| MX (1) | MX2008011341A (https=) |
| WO (1) | WO2007104689A1 (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006049090A1 (de) * | 2006-10-18 | 2008-04-30 | Clariant International Limited | Hochgeladene Haftstoffzusammensetzung durch den Einsatz von Metallocenewachsen |
| DE102008039279A1 (de) * | 2008-08-22 | 2010-02-25 | Clariant International Limited | Transparenzverbesserung von Polypropylen mit Metallocenwachsen |
| BR112012025981A2 (pt) | 2010-04-21 | 2017-08-29 | Sabic Innovative Plastics Ip Bv | Composição polimérica de plástico-madeira, artigo de manufatura e método para formação de uma composição polimérica de plástico-madeira |
| CN103502325B (zh) | 2010-12-13 | 2016-08-10 | 塞特克技术公司 | 处理添加剂和其在旋转成型中的用途 |
| US11267951B2 (en) | 2010-12-13 | 2022-03-08 | Cytec Technology Corp. | Stabilizer compositions containing substituted chroman compounds and methods of use |
| JP5693274B2 (ja) * | 2011-02-07 | 2015-04-01 | 積水フィルム株式会社 | 農業用フィルム |
| WO2013188490A1 (en) | 2012-06-13 | 2013-12-19 | Cytec Technology Corp. | Stabilizer compositions containing substituted chroman compounds and methods of use |
| CN104487532B (zh) * | 2012-08-16 | 2017-11-14 | 科莱恩金融(Bvi)有限公司 | 难燃性地毯背涂层 |
| DE102013012487A1 (de) * | 2013-07-26 | 2015-01-29 | Clariant International Ltd. | Zusammensetzung aus einem thermoplastischen Polymer und einer synergistischen Mischung aus bestimmten Aminoethern und feinteiligen Phosphinaten |
| CN103508937B (zh) * | 2013-10-16 | 2015-02-18 | 上海东升新材料有限公司 | 四甲基哌啶醇的催化合成方法 |
| ES2723575T3 (es) | 2016-01-29 | 2019-08-29 | Dow Global Technologies Llc | Películas y composiciones relacionadas y métodos de producción |
| JP6721458B2 (ja) * | 2016-08-24 | 2020-07-15 | 大日精化工業株式会社 | 難燃性マスターバッチ、難燃性樹脂組成物及び成形品 |
| WO2020176101A1 (en) * | 2019-02-28 | 2020-09-03 | Lehigh Technologies, Inc. | Asphalt modifier composition and rubber modified asphalt having increased storage stability |
| CN112126060B (zh) | 2019-06-25 | 2022-05-31 | 北京天罡助剂有限责任公司 | 一种聚合型高分子空间位阻胺及其制备方法 |
| TW202237726A (zh) * | 2021-01-12 | 2022-10-01 | 瑞士商克萊瑞特國際股份有限公司 | 用於矽基改質聚合物密封劑之穩定劑組成物 |
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| JPS5848580B2 (ja) * | 1975-05-28 | 1983-10-29 | 三共株式会社 | ゴウセイコウブンシザイリヨウヨウアンテイザイ |
| JPS5946911B2 (ja) | 1976-12-16 | 1984-11-15 | 住友化学工業株式会社 | インプラント |
| EP0115940B2 (en) * | 1983-01-25 | 1997-03-19 | Mitsui Petrochemical Industries, Ltd. | Film-forming propylene copolymer, film thereof and process for production of the film |
| US4691015A (en) | 1984-07-23 | 1987-09-01 | Ciba-Geigy Corporation | Hydroxylamines derived from hindered amines |
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| US4921962A (en) | 1988-10-19 | 1990-05-01 | Ciba-Geigy Corporation | Process for preparing N-hydrocarbyloxy derivatives of sterically hindered amines |
| US5096950A (en) | 1988-10-19 | 1992-03-17 | Ciba-Geigy Corporation | Polyolefin compositions stabilized with NOR-substituted hindered amines |
| EP0365481A1 (en) | 1988-10-19 | 1990-04-25 | Ciba-Geigy Ag | Polymeric substrates stabilized with N-substituted hindered amines |
| TW252135B (https=) | 1992-08-01 | 1995-07-21 | Hoechst Ag | |
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| DE19737727A1 (de) | 1997-08-29 | 1999-07-08 | Clariant Gmbh | Synergistische Flammschutzmittel-Kombination für Kunststoffe |
| JP4144771B2 (ja) | 1999-05-31 | 2008-09-03 | 株式会社Ａｄｅｋａ | 高分子量化されたヒンダードアミン化合物の製造方法 |
| JP3912944B2 (ja) | 1999-11-11 | 2007-05-09 | 株式会社Ａｄｅｋａ | 農業用フィルム用樹脂組成物 |
| TW572896B (en) | 2000-05-26 | 2004-01-21 | Ciba Sc Holding Ag | Process for the synthesis of amine ethers from secondary amino oxides |
| EP1038912A3 (en) | 2000-06-22 | 2000-12-27 | Ciba SC Holding AG | High molecular weight hindered hydrocarbyloxyamine stabilizers |
| JP2003286412A (ja) * | 2002-03-28 | 2003-10-10 | Asahi Denka Kogyo Kk | 合成樹脂組成物 |
| JP4155788B2 (ja) | 2002-10-15 | 2008-09-24 | 株式会社Ａｄｅｋａ | 高分子化合物用安定剤及びこれを含有してなる高分子化合物組成物 |
| JP4101242B2 (ja) * | 2004-04-01 | 2008-06-18 | 横浜ゴム株式会社 | ポリマーの変性方法 |
| JP4449751B2 (ja) * | 2005-01-11 | 2010-04-14 | 横浜ゴム株式会社 | 変性ポリマーの製造方法及びそれにより製造された変性ポリマー |
-
2007
- 2007-03-07 WO PCT/EP2007/052149 patent/WO2007104689A1/en not_active Ceased
- 2007-03-07 US US12/225,290 patent/US8765848B2/en active Active
- 2007-03-07 ES ES07712469.1T patent/ES2342739T5/es active Active
- 2007-03-07 JP JP2008558784A patent/JP5420911B2/ja active Active
- 2007-03-07 AU AU2007224516A patent/AU2007224516A1/en not_active Abandoned
- 2007-03-07 CA CA2640056A patent/CA2640056C/en active Active
- 2007-03-07 EP EP07712469.1A patent/EP1999166B2/en active Active
- 2007-03-07 BR BRPI0709551-1A patent/BRPI0709551B1/pt not_active IP Right Cessation
- 2007-03-07 DE DE602007006644T patent/DE602007006644D1/de active Active
- 2007-03-07 KR KR1020087022216A patent/KR101403753B1/ko active Active
- 2007-03-07 KR KR1020147006110A patent/KR20140056326A/ko not_active Withdrawn
- 2007-03-07 MX MX2008011341A patent/MX2008011341A/es unknown
-
2013
- 2013-04-19 JP JP2013088652A patent/JP5706464B2/ja active Active
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