JP2016521682A5 - - Google Patents
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- Publication number
- JP2016521682A5 JP2016521682A5 JP2016514396A JP2016514396A JP2016521682A5 JP 2016521682 A5 JP2016521682 A5 JP 2016521682A5 JP 2016514396 A JP2016514396 A JP 2016514396A JP 2016514396 A JP2016514396 A JP 2016514396A JP 2016521682 A5 JP2016521682 A5 JP 2016521682A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- hydroxysilane
- adduct
- optionally
- 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.)
- Granted
Links
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 14
- -1 2-ethoxyethyl Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000005842 heteroatom Chemical group 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 125000005372 silanol group Chemical class 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 239000011593 sulfur Substances 0.000 claims description 5
- 150000003512 tertiary amines Chemical class 0.000 claims description 5
- 150000003568 thioethers Chemical class 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 4
- 125000002723 alicyclic group Chemical group 0.000 claims description 3
- 125000003700 epoxy group Chemical group 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical class C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims 2
- 150000008064 anhydrides Chemical group 0.000 claims 2
- 125000005587 carbonate group Chemical group 0.000 claims 2
- 125000002843 carboxylic acid group Chemical group 0.000 claims 2
- 125000004185 ester group Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 2
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical group CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 claims 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical class C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000003235 pyrrolidines Chemical class 0.000 claims 1
- 239000000565 sealant Substances 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 15
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 10
- 229910000077 silane Inorganic materials 0.000 description 5
- FVCHBWQRIKNLRZ-UHFFFAOYSA-N CCO[Si](CCC1CCC(O)C(C1)N1CCCC1)(OCC)OCC Chemical compound CCO[Si](CCC1CCC(O)C(C1)N1CCCC1)(OCC)OCC FVCHBWQRIKNLRZ-UHFFFAOYSA-N 0.000 description 4
- KUPDLWJEQFXELL-UHFFFAOYSA-N CCO[Si](CCC1CCC(O)C(C1)N1CCOCC1)(OCC)OCC Chemical compound CCO[Si](CCC1CCC(O)C(C1)N1CCOCC1)(OCC)OCC KUPDLWJEQFXELL-UHFFFAOYSA-N 0.000 description 4
- 239000005058 Isophorone diisocyanate Substances 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- KZVBSRUKRPTNGU-UHFFFAOYSA-N 1-amino-2-(2-methoxyethyl)-4-(2-triethoxysilylethyl)cyclohexan-1-ol Chemical compound COCCC1C(CCC(C1)CC[Si](OCC)(OCC)OCC)(O)N KZVBSRUKRPTNGU-UHFFFAOYSA-N 0.000 description 2
- GVPFMCZCTYUHPH-UHFFFAOYSA-N CCO[Si](CCC1CCC(O)C(C1)N(C(C)C)C(C)C)(OCC)OCC Chemical compound CCO[Si](CCC1CCC(O)C(C1)N(C(C)C)C(C)C)(OCC)OCC GVPFMCZCTYUHPH-UHFFFAOYSA-N 0.000 description 2
- ALWCAMFWHZSQMU-UHFFFAOYSA-N CCO[Si](CCC1CCC(O)C(C1)N1CCSCC1)(OCC)OCC Chemical compound CCO[Si](CCC1CCC(O)C(C1)N1CCSCC1)(OCC)OCC ALWCAMFWHZSQMU-UHFFFAOYSA-N 0.000 description 2
- QDOYYPBUPBKSOF-UHFFFAOYSA-N CO[Si](CCC1CCC(O)C(C1)N1CCOCC1)(OC)OC Chemical compound CO[Si](CCC1CCC(O)C(C1)N1CCOCC1)(OC)OC QDOYYPBUPBKSOF-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- LGXYFPHTBJDQQE-UHFFFAOYSA-N CCCCN(CCCC)C1CC(CC[Si](OCC)(OCC)OCC)CCC1O Chemical compound CCCCN(CCCC)C1CC(CC[Si](OCC)(OCC)OCC)CCC1O LGXYFPHTBJDQQE-UHFFFAOYSA-N 0.000 description 1
- GEONUZNWBOYFIH-UHFFFAOYSA-N CCO[Si](CCC1CCC(C(O)C1)N1CCOCC1)(OCC)OCC Chemical compound CCO[Si](CCC1CCC(C(O)C1)N1CCOCC1)(OCC)OCC GEONUZNWBOYFIH-UHFFFAOYSA-N 0.000 description 1
- ISJPLVPMNVDQQZ-UHFFFAOYSA-N CCO[Si](CCC1CCC(O)C(C1)N1CC(C)OC(C)C1)(OCC)OCC Chemical compound CCO[Si](CCC1CCC(O)C(C1)N1CC(C)OC(C)C1)(OCC)OCC ISJPLVPMNVDQQZ-UHFFFAOYSA-N 0.000 description 1
- BPQXTQAWXQQZHH-UHFFFAOYSA-N CCO[Si](CCC1CCC(O)C(C1)N1CCN(C)CC1)(OCC)OCC Chemical compound CCO[Si](CCC1CCC(O)C(C1)N1CCN(C)CC1)(OCC)OCC BPQXTQAWXQQZHH-UHFFFAOYSA-N 0.000 description 1
- OSFNAYRHZLSNMS-UHFFFAOYSA-N CO[Si](CCC1CCC(O)C(C1)N1CCCC1)(OC)OC Chemical compound CO[Si](CCC1CCC(O)C(C1)N1CCCC1)(OC)OC OSFNAYRHZLSNMS-UHFFFAOYSA-N 0.000 description 1
- 229910018540 Si C Inorganic materials 0.000 description 1
- 229910018557 Si O Inorganic materials 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13168803.8 | 2013-05-22 | ||
| EP13168803.8A EP2805985A1 (de) | 2013-05-22 | 2013-05-22 | Hydroxysilan und Silangruppen-haltiges Polymer |
| PCT/EP2014/060457 WO2014187865A1 (de) | 2013-05-22 | 2014-05-21 | Hydroxysilan und silangruppen-haltiges polymer |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016521682A JP2016521682A (ja) | 2016-07-25 |
| JP2016521682A5 true JP2016521682A5 (enExample) | 2018-09-06 |
| JP6444385B2 JP6444385B2 (ja) | 2018-12-26 |
Family
ID=48463843
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016514396A Expired - Fee Related JP6444385B2 (ja) | 2013-05-22 | 2014-05-21 | ヒドロキシシラン及びシラン基含有ポリマー |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US9751900B2 (enExample) |
| EP (2) | EP2805985A1 (enExample) |
| JP (1) | JP6444385B2 (enExample) |
| CN (1) | CN105473643B (enExample) |
| BR (1) | BR112015029017A2 (enExample) |
| WO (1) | WO2014187865A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10398633B2 (en) | 2014-10-27 | 2019-09-03 | Conopco, Inc. | Anhydrous antiperspirant compositions |
| EP3023429A1 (de) * | 2014-11-24 | 2016-05-25 | Sika Technology AG | Hydroxysilan als Haftvermittler oder Vernetzer |
| CN113004854B (zh) * | 2015-09-30 | 2022-09-30 | 伊英克公司 | 用于电光组件的聚氨酯粘合剂层 |
| EP3255113B1 (en) | 2016-06-08 | 2025-11-05 | Soudal | Adhesive and/or sealant composition with high initial tack |
| EP3309187B1 (de) | 2016-10-17 | 2020-08-05 | Sika Tech Ag | Reaktivweichmacher für feuchtigkeitshärtende zusammensetzungen mit silanfunktionellen polymeren |
| EP3406644A1 (de) | 2017-05-23 | 2018-11-28 | Sika Technology Ag | Lösungsmittelbasierter primer mit langer offenzeit und verbesserter ahäsion |
| JP7420711B2 (ja) | 2017-10-23 | 2024-01-23 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | プラスチック基材用のプライマーコーティング材料系 |
| EP3759115B1 (en) | 2018-02-27 | 2024-07-17 | Henkel AG & Co. KGaA | Bio-based reactive plasticizer and adhesives and sealants containing them |
| EP3546541A1 (en) | 2018-03-27 | 2019-10-02 | Sika Technology Ag | A waterproofing membrane with a functional layer |
| EP3617249A1 (en) | 2018-08-28 | 2020-03-04 | Soudal | Adhesive and/or sealant composition |
| FR3088325B1 (fr) * | 2018-11-09 | 2021-10-15 | Bostik Sa | Derives 1,3-oxathiolane-2-thione et leurs utilisations |
| CN109666447A (zh) * | 2019-01-16 | 2019-04-23 | 江西奋发科技有限公司 | 一种单组份脱醇型硅橡胶密封剂及其制备方法 |
| NO346733B1 (en) * | 2019-06-28 | 2022-12-05 | Klingelberg Products As | Flame retardant, method for its preparation and article comprising same |
| EP4028405A1 (en) * | 2019-09-09 | 2022-07-20 | Dow Silicones Corporation | Method of preparing alkoxy-functional organosilicon compounds |
| WO2021122593A1 (de) | 2019-12-17 | 2021-06-24 | Sika Technology Ag | Lösungsmittelbasiertes vorbehandlungsmittel mit verbesserter adhäsion auf klebstoff-restraupen |
| US20230054396A1 (en) * | 2020-02-10 | 2023-02-23 | Sika Technology Ag | Silane group-containing branched polymer |
| CN111393611B (zh) * | 2020-04-29 | 2022-04-29 | 浙江皇马科技股份有限公司 | 一种密封胶用硅烷封端树脂及其制备方法 |
| EP4437060A1 (en) | 2021-11-26 | 2024-10-02 | Soudal | Waterborne adhesive and/or sealant composition |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2946701A (en) * | 1957-11-12 | 1960-07-26 | Dow Corning | Method of treating glass with epoxysilanes and their epoxy-amine adducts, and the articles made thereby |
| JPS61229884A (ja) * | 1985-04-03 | 1986-10-14 | Oouchi Shinko Kagaku Kogyo Kk | パラフエニレンジアミン誘導体及びその誘導体を含有してなるゴム状重合体組成物 |
| US5587502A (en) * | 1995-06-02 | 1996-12-24 | Minnesota Mining & Manufacturing Company | Hydroxy functional alkoxysilane and alkoxysilane functional polyurethane made therefrom |
| RU2004120064A (ru) * | 2001-11-30 | 2006-01-10 | Ф.Хоффманн-Ля Рош Аг (Ch) | N-уреидопиперидины в качестве антагонистов viii в отношении ccr-3 рецепторов |
| JP4081573B2 (ja) * | 2002-11-12 | 2008-04-30 | 信越化学工業株式会社 | インク組成物 |
| JP5359585B2 (ja) | 2008-10-22 | 2013-12-04 | 信越化学工業株式会社 | アミノ基を有する有機ケイ素化合物及びその製造方法 |
| EP2468759A1 (de) | 2010-12-17 | 2012-06-27 | Sika Technology AG | Sekundäre Aminosilane |
-
2013
- 2013-05-22 EP EP13168803.8A patent/EP2805985A1/de not_active Withdrawn
-
2014
- 2014-05-21 EP EP14727183.7A patent/EP2999737B1/de not_active Not-in-force
- 2014-05-21 CN CN201480029544.9A patent/CN105473643B/zh not_active Expired - Fee Related
- 2014-05-21 JP JP2016514396A patent/JP6444385B2/ja not_active Expired - Fee Related
- 2014-05-21 WO PCT/EP2014/060457 patent/WO2014187865A1/de not_active Ceased
- 2014-05-21 BR BR112015029017A patent/BR112015029017A2/pt not_active Application Discontinuation
- 2014-05-21 US US14/891,819 patent/US9751900B2/en not_active Expired - Fee Related
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