JPWO2020212149A5 - - Google Patents
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- JPWO2020212149A5 JPWO2020212149A5 JP2021561650A JP2021561650A JPWO2020212149A5 JP WO2020212149 A5 JPWO2020212149 A5 JP WO2020212149A5 JP 2021561650 A JP2021561650 A JP 2021561650A JP 2021561650 A JP2021561650 A JP 2021561650A JP WO2020212149 A5 JPWO2020212149 A5 JP WO2020212149A5
- Authority
- JP
- Japan
- Prior art keywords
- groups
- jeffamine
- epoxide
- available
- amine
- 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
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- 239000000203 mixture Substances 0.000 description 14
- -1 epoxide compound Chemical class 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- 150000002924 oxiranes Chemical group 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 7
- 150000004985 diamines Chemical class 0.000 description 6
- 229920000768 polyamine Polymers 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 description 4
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 229920000647 polyepoxide Chemical class 0.000 description 4
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical class CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- QOTQFLOTGBBMEX-UHFFFAOYSA-N alpha-angelica lactone Chemical compound CC1=CCC(=O)O1 QOTQFLOTGBBMEX-UHFFFAOYSA-N 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 description 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- BIWBFFZTZOHCRG-UHFFFAOYSA-N 4-(2-nitrophenyl)-1,2-dihydropyridine Chemical compound [O-][N+](=O)C1=CC=CC=C1C1=CCNC=C1 BIWBFFZTZOHCRG-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- JOBBTVPTPXRUBP-UHFFFAOYSA-N [3-(3-sulfanylpropanoyloxy)-2,2-bis(3-sulfanylpropanoyloxymethyl)propyl] 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(COC(=O)CCS)(COC(=O)CCS)COC(=O)CCS JOBBTVPTPXRUBP-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000005576 amination reaction Methods 0.000 description 2
- IVHKZGYFKJRXBD-UHFFFAOYSA-N amino carbamate Chemical compound NOC(N)=O IVHKZGYFKJRXBD-UHFFFAOYSA-N 0.000 description 2
- PUJDIJCNWFYVJX-UHFFFAOYSA-N benzyl carbamate Chemical compound NC(=O)OCC1=CC=CC=C1 PUJDIJCNWFYVJX-UHFFFAOYSA-N 0.000 description 2
- MRNZSTMRDWRNNR-UHFFFAOYSA-N bis(hexamethylene)triamine Chemical compound NCCCCCCNCCCCCCN MRNZSTMRDWRNNR-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- IRRKWKXMRZQNDM-UHFFFAOYSA-N carbamic acid;2-hydroxy-1,2-diphenylethanone Chemical compound NC(O)=O.C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 IRRKWKXMRZQNDM-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 229960001330 hydroxycarbamide Drugs 0.000 description 2
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- DTSDBGVDESRKKD-UHFFFAOYSA-N n'-(2-aminoethyl)propane-1,3-diamine Chemical compound NCCCNCCN DTSDBGVDESRKKD-UHFFFAOYSA-N 0.000 description 2
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 229940124530 sulfonamide Drugs 0.000 description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 description 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 1
- XPNHFNJYPSXRRG-UHFFFAOYSA-N 1-[2-(2-aminobutoxy)ethoxy]butan-2-amine Chemical compound CCC(N)COCCOCC(N)CC XPNHFNJYPSXRRG-UHFFFAOYSA-N 0.000 description 1
- VTAMQDCTAXRISX-UHFFFAOYSA-N 1-[2-(2-aminopropoxy)ethoxy]propan-2-amine Chemical compound CC(N)COCCOCC(C)N VTAMQDCTAXRISX-UHFFFAOYSA-N 0.000 description 1
- WTFAGPBUAGFMQX-UHFFFAOYSA-N 1-[2-[2-(2-aminopropoxy)propoxy]propoxy]propan-2-amine Chemical compound CC(N)COCC(C)OCC(C)OCC(C)N WTFAGPBUAGFMQX-UHFFFAOYSA-N 0.000 description 1
- WDQDOALSJXWMIU-UHFFFAOYSA-N 1-n-(1-aminopentan-3-yl)pentane-1,3-diamine Chemical compound CCC(N)CCNC(CC)CCN WDQDOALSJXWMIU-UHFFFAOYSA-N 0.000 description 1
- IMQFZQVZKBIPCQ-UHFFFAOYSA-N 2,2-bis(3-sulfanylpropanoyloxymethyl)butyl 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(CC)(COC(=O)CCS)COC(=O)CCS IMQFZQVZKBIPCQ-UHFFFAOYSA-N 0.000 description 1
- GXVUZYLYWKWJIM-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanamine Chemical compound NCCOCCN GXVUZYLYWKWJIM-UHFFFAOYSA-N 0.000 description 1
- UCRXZJYCOMRCER-UHFFFAOYSA-N 2-[n,n'-di(propan-2-yl)carbamimidoyl]-1,1,3,3-tetramethylguanidine Chemical compound CC(C)NC(=NC(C)C)N=C(N(C)C)N(C)C UCRXZJYCOMRCER-UHFFFAOYSA-N 0.000 description 1
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- POTQBGGWSWSMCX-UHFFFAOYSA-N 3-[2-(3-aminopropoxy)ethoxy]propan-1-amine Chemical compound NCCCOCCOCCCN POTQBGGWSWSMCX-UHFFFAOYSA-N 0.000 description 1
- YOOSAIJKYCBPFW-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)butoxy]propan-1-amine Chemical compound NCCCOCCCCOCCCN YOOSAIJKYCBPFW-UHFFFAOYSA-N 0.000 description 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 description 1
- 239000009261 D 400 Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 240000002045 Guettarda speciosa Species 0.000 description 1
- 235000001287 Guettarda speciosa Nutrition 0.000 description 1
- HJOVHMDZYOCNQW-UHFFFAOYSA-N Isophorone Natural products CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000005626 carbonium group Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007278 cyanoethylation reaction Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical group 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical group NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- HAPOVYFOVVWLRS-UHFFFAOYSA-N ethosuximide Chemical compound CCC1(C)CC(=O)NC1=O HAPOVYFOVVWLRS-UHFFFAOYSA-N 0.000 description 1
- IWBOPFCKHIJFMS-UHFFFAOYSA-N ethylene glycol bis(2-aminoethyl) ether Chemical compound NCCOCCOCCN IWBOPFCKHIJFMS-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 229940040102 levulinic acid Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- GBTLMWXVQMOHRC-UHFFFAOYSA-N n'-(1-aminopentan-3-yl)-2-methylpentane-1,5-diamine Chemical compound NCCC(CC)NCCCC(C)CN GBTLMWXVQMOHRC-UHFFFAOYSA-N 0.000 description 1
- IRYWPHGCDAOHJJ-UHFFFAOYSA-N n'-(3-aminopropyl)-2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCNCCCN IRYWPHGCDAOHJJ-UHFFFAOYSA-N 0.000 description 1
- AZZHHQHXUXFIJP-UHFFFAOYSA-N n,n'-bis(1-aminopentan-3-yl)-2-methylpentane-1,5-diamine Chemical compound NCCC(CC)NCCCC(C)CNC(CC)CCN AZZHHQHXUXFIJP-UHFFFAOYSA-N 0.000 description 1
- 150000002905 orthoesters Chemical class 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 150000003141 primary amines Chemical group 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- SPVXKVOXSXTJOY-UHFFFAOYSA-O selenonium Chemical compound [SeH3+] SPVXKVOXSXTJOY-UHFFFAOYSA-O 0.000 description 1
- 238000012358 sourcing Methods 0.000 description 1
- PFNFFQXMRSDOHW-UHFFFAOYSA-N spermine Chemical compound NCCCNCCCCNCCCN PFNFFQXMRSDOHW-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 125000005537 sulfoxonium group Chemical group 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP19169509.7A EP3725820B1 (en) | 2019-04-16 | 2019-04-16 | Use of functionalized alpha-angelica lactones |
| EP19169509.7 | 2019-04-16 | ||
| PCT/EP2020/059347 WO2020212149A1 (en) | 2019-04-16 | 2020-04-02 | Use of functionalized alpha-angelica lactones |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| JP2022529772A JP2022529772A (ja) | 2022-06-24 |
| JP2022529772A5 JP2022529772A5 (https=) | 2023-04-13 |
| JPWO2020212149A5 true JPWO2020212149A5 (https=) | 2023-04-13 |
| JP7577684B2 JP7577684B2 (ja) | 2024-11-05 |
Family
ID=66286096
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021561650A Active JP7577684B2 (ja) | 2019-04-16 | 2020-04-02 | 官能化アルファ－アンゲリカラクトンの使用 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US11697643B2 (https=) |
| EP (1) | EP3725820B1 (https=) |
| JP (1) | JP7577684B2 (https=) |
| KR (1) | KR20210155015A (https=) |
| CN (1) | CN113710723B (https=) |
| WO (1) | WO2020212149A1 (https=) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3747925A1 (en) * | 2019-06-07 | 2020-12-09 | Henkel AG & Co. KGaA | Radiation-curable composition by anionic polymerization |
| EP4001339B1 (en) | 2020-11-16 | 2024-01-24 | Henkel AG & Co. KGaA | An epoxy composition comprising a bio-based epoxy compound |
| EP4001338B1 (en) * | 2020-11-16 | 2024-01-31 | Henkel AG & Co. KGaA | Cationic epoxy compositions |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3113708A (en) | 1961-08-09 | 1963-12-10 | Jr William E Moulic | Magnetic tape drive mechanism and control therefor |
| US3535342A (en) | 1968-02-07 | 1970-10-20 | Dow Chemical Co | Process for making alkylene carbonates |
| GB1512982A (en) | 1974-05-02 | 1978-06-01 | Gen Electric | Salts |
| US4250311A (en) | 1974-05-02 | 1981-02-10 | General Electric Company | P, As, and Sb hexafluoride onium salts as photoinitiators |
| IT1034323B (it) | 1975-03-17 | 1979-09-10 | Anic Spa | Procedimento per la preparazione di alchilencarbonati |
| JPS5325553A (en) * | 1976-08-24 | 1978-03-09 | Yuki Gosei Yakuhin Kogyo Kk | Preparation of 33furancarboxyethyl ester |
| US4216288A (en) | 1978-09-08 | 1980-08-05 | General Electric Company | Heat curable cationically polymerizable compositions and method of curing same with onium salts and reducing agents |
| GB8307613D0 (en) | 1983-03-18 | 1983-04-27 | Bp Chem Int Ltd | Carbonates |
| DE3529263A1 (de) | 1985-08-16 | 1987-02-19 | Hoechst Ag | Verfahren zur herstellung von 2-oxo-1,3-dioxolanen |
| DE3600602A1 (de) | 1986-01-11 | 1987-07-16 | Hoechst Ag | Verfahren zur herstellung von 2-oxo-1,3-dioxolanen |
| EP0417043A3 (en) * | 1989-09-07 | 1992-09-30 | Ciba-Geigy Ag | Curing agents and accelerators for epoxy- and isocyanate resins |
| US5650261A (en) | 1989-10-27 | 1997-07-22 | Rohm And Haas Company | Positive acting photoresist comprising a photoacid, a photobase and a film forming acid-hardening resin system |
| US5084586A (en) | 1990-02-12 | 1992-01-28 | Minnesota Mining And Manufacturing Company | Novel initiators for cationic polymerization |
| US5124417A (en) | 1990-02-12 | 1992-06-23 | Minnesota Mining And Manufacturing Company | Initiators for cationic polymerization |
| JPH051225A (ja) | 1991-06-25 | 1993-01-08 | Kanegafuchi Chem Ind Co Ltd | 硬化性組成物 |
| US5554664A (en) | 1995-03-06 | 1996-09-10 | Minnesota Mining And Manufacturing Company | Energy-activatable salts with fluorocarbon anions |
| DE29706235U1 (de) | 1997-04-08 | 1998-08-27 | Ernst Mühlbauer KG, 22547 Hamburg | Anordnung zum Ausgeben einer gemischten dentaltechnischen Mehrkomponentenmasse |
| WO2003106434A1 (ja) | 2002-06-14 | 2003-12-24 | 味の素株式会社 | ピリミジン化合物の製造方法 |
| DE602006004507D1 (de) * | 2005-07-08 | 2009-02-12 | Rohm & Haas | Härtbare Zusammensetzungen, die reaktive Beta-Hydroxylamide aus Lactonen enthalten |
| JP4304251B2 (ja) | 2005-09-09 | 2009-07-29 | 独立行政法人産業技術総合研究所 | エポキシ樹脂組成物の製造方法 |
| SG144183A1 (en) | 2005-11-22 | 2008-08-28 | Aromagen Corp | Adducts of levulinic derivatives with epoxidized fatty acid esters and uses thereof |
| WO2009049378A1 (en) * | 2007-10-17 | 2009-04-23 | Qbiotics Limited | Lactone derivatives |
| JP5239743B2 (ja) * | 2007-10-29 | 2013-07-17 | 三菱瓦斯化学株式会社 | 樹脂組成物並びにこれを用いたプリプレグ及び積層板 |
| WO2009124998A2 (de) * | 2008-04-11 | 2009-10-15 | Basf Se | Hochverzweigte polymere und oligomere mit terminalen aminogruppen als härter für epoxidharze |
| DE102008040738A1 (de) | 2008-07-25 | 2010-01-28 | Hilti Aktiengesellschaft | Foliengebinde |
| CN101348558B (zh) | 2008-09-12 | 2010-11-03 | 福州大学 | 一种酶解木质素环氧树脂及其制备方法 |
| CN102558507B (zh) | 2010-12-14 | 2013-12-25 | 财团法人工业技术研究院 | 生质环氧树脂的原料及生质环氧树脂的制备方法 |
| WO2013148933A1 (en) * | 2012-03-30 | 2013-10-03 | Segetis, Inc. | Reactive diluents, methods of reacting, and thermoset polymers derived therefrom |
| US8883897B2 (en) * | 2012-05-25 | 2014-11-11 | New Functional Polymers LLC | Functional norbornanyl ester derivatives, polymers and process for preparing same |
| EP2752437A1 (de) * | 2013-01-08 | 2014-07-09 | Sika Technology AG | Härter für emissionsarme Epoxidharz-Produkte |
| WO2014108304A2 (de) * | 2013-01-08 | 2014-07-17 | Sika Technology Ag | Härter für emissionsarme epoxidharz-produkte |
| CN104650009A (zh) * | 2013-11-20 | 2015-05-27 | 陶氏环球技术有限公司 | 低粘度环氧树脂和由其制备的低voc可固化制剂 |
| WO2015124792A1 (en) * | 2014-02-24 | 2015-08-27 | Sika Technology Ag | Furan-based amines as curing agents for epoxy resins in low voc applications |
| JP6993781B2 (ja) * | 2017-02-24 | 2022-01-14 | 株式会社Adeka | 硬化性組成物 |
| EP3672947A4 (en) * | 2017-08-21 | 2020-12-16 | Drexel University | RENEWABLE FURAN AMINE CURING AGENTS FOR THERMOSETTING EPOXIDIC PLASTIC |
| CN107556955B (zh) * | 2017-10-17 | 2020-04-24 | 烟台信友新材料有限公司 | 一种高隐蔽性紫外光深层固化胶粘剂的制备方法 |
| CN108440741B (zh) * | 2018-03-13 | 2020-04-28 | 广东工业大学 | 一种可阳离子光固化脲-异丁醛-甲醛树脂及其制备方法 |
| EP3725784B1 (en) | 2019-04-16 | 2022-06-29 | Henkel AG & Co. KGaA | A process for the chain growth polymerization of functionalized alpha-angelica lactone monomers |
-
2019
- 2019-04-16 EP EP19169509.7A patent/EP3725820B1/en active Active
-
2020
- 2020-04-02 CN CN202080029128.4A patent/CN113710723B/zh active Active
- 2020-04-02 JP JP2021561650A patent/JP7577684B2/ja active Active
- 2020-04-02 KR KR1020217033108A patent/KR20210155015A/ko active Pending
- 2020-04-02 WO PCT/EP2020/059347 patent/WO2020212149A1/en not_active Ceased
-
2021
- 2021-10-18 US US17/451,165 patent/US11697643B2/en active Active
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