JP2018511592A5 - - Google Patents
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- JP2018511592A5 JP2018511592A5 JP2017548947A JP2017548947A JP2018511592A5 JP 2018511592 A5 JP2018511592 A5 JP 2018511592A5 JP 2017548947 A JP2017548947 A JP 2017548947A JP 2017548947 A JP2017548947 A JP 2017548947A JP 2018511592 A5 JP2018511592 A5 JP 2018511592A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- butyl
- unsaturated
- polymerization
- alkyl
- 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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- 238000000034 method Methods 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 8
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 6
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 claims 4
- -1 hydroxylamine compound Chemical class 0.000 claims 4
- 238000006116 polymerization reaction Methods 0.000 claims 3
- 238000000746 purification Methods 0.000 claims 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims 2
- 238000000605 extraction Methods 0.000 claims 2
- 238000005194 fractionation Methods 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 229920002554 vinyl polymer Polymers 0.000 claims 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 claims 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
- 238000005865 alkene metathesis reaction Methods 0.000 claims 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 1
- WFYPICNXBKQZGB-UHFFFAOYSA-N butenyne Chemical group C=CC#C WFYPICNXBKQZGB-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
- 238000003763 carbonization Methods 0.000 claims 1
- 230000006835 compression Effects 0.000 claims 1
- 238000007906 compression Methods 0.000 claims 1
- 238000006356 dehydrogenation reaction Methods 0.000 claims 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 1
- 239000000446 fuel Substances 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 230000002401 inhibitory effect Effects 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
- 239000000203 mixture Substances 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 239000001294 propane Substances 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 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
- 230000006641 stabilisation Effects 0.000 claims 1
- 238000011105 stabilization Methods 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 0 CC(*)(CC(CC1(*)*)O*)N1O Chemical compound CC(*)(CC(CC1(*)*)O*)N1O 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562134811P | 2015-03-18 | 2015-03-18 | |
| US62/134,811 | 2015-03-18 | ||
| PCT/US2016/022731 WO2016149433A1 (en) | 2015-03-18 | 2016-03-17 | The use of stable lipophilic hydroxylamine compounds for inhibiting polymerization of vinyl monomers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018511592A JP2018511592A (ja) | 2018-04-26 |
| JP2018511592A5 true JP2018511592A5 (cg-RX-API-DMAC7.html) | 2019-04-25 |
| JP6730303B2 JP6730303B2 (ja) | 2020-07-29 |
Family
ID=56919278
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017548947A Active JP6730303B2 (ja) | 2015-03-18 | 2016-03-17 | ビニルモノマーの重合を阻害するための安定した親油性ヒドロキシルアミン化合物の使用 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US9914701B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3271331B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP6730303B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR102583199B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN107406388B (cg-RX-API-DMAC7.html) |
| AR (1) | AR103961A1 (cg-RX-API-DMAC7.html) |
| BR (1) | BR112017018283B1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2979828C (cg-RX-API-DMAC7.html) |
| ES (1) | ES2912329T3 (cg-RX-API-DMAC7.html) |
| RU (1) | RU2715559C2 (cg-RX-API-DMAC7.html) |
| TW (1) | TWI680964B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2016149433A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018165382A1 (en) * | 2017-03-09 | 2018-09-13 | Ecolab USA, Inc. | Polymerization inhibitor compositions |
| BR112021019660A2 (pt) | 2019-04-02 | 2021-12-07 | Ecolab Usa Inc | Métodos para produzir dióxido de cloro e para tratar água de processo |
| TW202348787A (zh) | 2022-04-01 | 2023-12-16 | 美商藝康美國公司 | 用於乙烯系單體流之高苛刻度加工的防汙劑組成物 |
| TW202404930A (zh) | 2022-04-01 | 2024-02-01 | 美商藝康美國公司 | 在共軛二烯單體之萃取蒸餾期間減少非所要之乳化聚合 |
| TW202348786A (zh) | 2022-04-01 | 2023-12-16 | 美商藝康美國公司 | 用於蒸氣空間應用之防汙劑組成物 |
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-
2016
- 2016-03-17 JP JP2017548947A patent/JP6730303B2/ja active Active
- 2016-03-17 CA CA2979828A patent/CA2979828C/en active Active
- 2016-03-17 CN CN201680016419.3A patent/CN107406388B/zh active Active
- 2016-03-17 RU RU2017132514A patent/RU2715559C2/ru active
- 2016-03-17 WO PCT/US2016/022731 patent/WO2016149433A1/en not_active Ceased
- 2016-03-17 TW TW105108239A patent/TWI680964B/zh active
- 2016-03-17 KR KR1020177030075A patent/KR102583199B1/ko active Active
- 2016-03-17 EP EP16765703.0A patent/EP3271331B1/en active Active
- 2016-03-17 BR BR112017018283-1A patent/BR112017018283B1/pt active IP Right Grant
- 2016-03-17 ES ES16765703T patent/ES2912329T3/es active Active
- 2016-03-17 AR ARP160100716A patent/AR103961A1/es active IP Right Grant
- 2016-03-17 US US15/072,780 patent/US9914701B2/en active Active
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