RU2016141980A - Простые эфирамины на основе 1,2-диспиртов - Google Patents
Простые эфирамины на основе 1,2-диспиртов Download PDFInfo
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- RU2016141980A RU2016141980A RU2016141980A RU2016141980A RU2016141980A RU 2016141980 A RU2016141980 A RU 2016141980A RU 2016141980 A RU2016141980 A RU 2016141980A RU 2016141980 A RU2016141980 A RU 2016141980A RU 2016141980 A RU2016141980 A RU 2016141980A
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- ether
- carbon atoms
- alkyl group
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 25
- -1 ether amine Chemical class 0.000 claims 15
- 125000004432 carbon atom Chemical group C* 0.000 claims 9
- 125000002947 alkylene group Chemical group 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 4
- 150000002170 ethers Chemical class 0.000 claims 3
- XWAMHGPDZOVVND-UHFFFAOYSA-N (+-)-Octadecan-1,2-diol Natural products CCCCCCCCCCCCCCCCC(O)CO XWAMHGPDZOVVND-UHFFFAOYSA-N 0.000 claims 2
- DWANEFRJKWXRSG-UHFFFAOYSA-N 1,2-tetradecanediol Chemical compound CCCCCCCCCCCCC(O)CO DWANEFRJKWXRSG-UHFFFAOYSA-N 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 2
- 238000005576 amination reaction Methods 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 229910017052 cobalt Inorganic materials 0.000 claims 2
- 239000010941 cobalt Substances 0.000 claims 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 2
- 229910052802 copper Inorganic materials 0.000 claims 2
- 239000010949 copper Substances 0.000 claims 2
- 229910052759 nickel Inorganic materials 0.000 claims 2
- 150000002927 oxygen compounds Chemical class 0.000 claims 2
- BTOOAFQCTJZDRC-UHFFFAOYSA-N 1,2-hexadecanediol Chemical compound CCCCCCCCCCCCCCC(O)CO BTOOAFQCTJZDRC-UHFFFAOYSA-N 0.000 claims 1
- 229940015975 1,2-hexanediol Drugs 0.000 claims 1
- 229940031723 1,2-octanediol Drugs 0.000 claims 1
- 229920002396 Polyurea Polymers 0.000 claims 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- YSRSBDQINUMTIF-UHFFFAOYSA-N decane-1,2-diol Chemical compound CCCCCCCCC(O)CO YSRSBDQINUMTIF-UHFFFAOYSA-N 0.000 claims 1
- ZITKDVFRMRXIJQ-UHFFFAOYSA-N dodecane-1,2-diol Chemical compound CCCCCCCCCCC(O)CO ZITKDVFRMRXIJQ-UHFFFAOYSA-N 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims 1
- GCXZDAKFJKCPGK-UHFFFAOYSA-N heptane-1,2-diol Chemical compound CCCCCC(O)CO GCXZDAKFJKCPGK-UHFFFAOYSA-N 0.000 claims 1
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- LJZULWUXNKDPCG-UHFFFAOYSA-N nonane-1,2-diol Chemical compound CCCCCCCC(O)CO LJZULWUXNKDPCG-UHFFFAOYSA-N 0.000 claims 1
- AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 claims 1
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 claims 1
- 229920000647 polyepoxide Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 229920002635 polyurethane Polymers 0.000 claims 1
- 239000004814 polyurethane Substances 0.000 claims 1
- 239000002453 shampoo Substances 0.000 claims 1
- 229920006345 thermoplastic polyamide Polymers 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/04—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reaction of ammonia or amines with olefin oxides or halohydrins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/45—Derivatives containing from 2 to 10 oxyalkylene groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/883—Molybdenum and nickel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/885—Molybdenum and copper
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
- C07C217/08—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/28—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having one amino group and at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the carbon skeleton, e.g. ethers of polyhydroxy amines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/504—Amines containing an atom other than nitrogen belonging to the amine group, carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/42—Amino alcohols or amino ethers
- C11D1/44—Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Dermatology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Polyurethanes Or Polyureas (AREA)
- Polyethers (AREA)
- Lubricants (AREA)
- External Artificial Organs (AREA)
Claims (34)
1. Простой эфирамин формулы (I) или формулы (II),
или смесь простых эфираминов формулы (I) и формулы (II), где
R1 представляет собой линейную или разветвленную алкильную группу с 2-16 атомами углерода,
R2 представляет собой водород или алкильную группу с 1-16 атомами углерода,
х≥1 и y≥1, и сумма x+y составляет от 2 до 10, и
А1, А2, А3 и A4 независимо выбираются из группы, состоящей из линейных и/или разветвленных алкиленов, имеющих 2-18 атомов углерода,
где Z1-Z4 независимо выбираются из ОН, NH2, NHR' или NR'Rʺ, где по меньшей мере один из Z1-Z2 и по меньшей мере один из Z3-Z4 представляет собой NH2, NHR' или NR'Rʺ, где R' и Rʺ независимо выбираются из алкиленов, имеющих 2-6 атомов углерода.
2. Простой эфирамин по п. 1, где А1, А2, A3 и А4 независимо выбираются из 1,2-пропилена и 1,2-бутилена.
3. Простой эфирамин по п. 1, где A1, А2, A3 и А4 независимо выбираются из 1,2-пропилена и 1,2-бутилена, и по меньшей мере один из A1, А2, A3 или А4 представляет собой 1,2-пропилен.
4. Простой эфирамин по п. 1, где А1, А2, A3 и А4 представляют собой 1,2-пропилен.
5. Простой эфирамин по п. 1, где x+y находится в интервале от 3 до 6.
6. Простой эфирамин по п. 1, где R1 представляет собой линейную или разветвленную алкильную группу с 3-16 атомами углерода, и R2 представляет собой водород или алкильную группу с 1-16 атомами углерода.
7. Простой эфирамин по п. 1, где R1 представляет собой линейную алкильную группу с 3-8 атомами углерода, и R2 представляет собой водород.
8. Простой эфирамин по п. 1, где Z1-Z4 представляют собой NH2.
9. Простой эфирамин по п. 1, где простой эфирамин формулы (I) или формулы (II) имеет средневесову. молекулярную массу от около 270 до около 1000 г/моль.
10. Простой эфирамин по любому из пп. 1-9, где простой эфирамин формулы (I) или формулы (II) реагирует с кислотой.
11. Способ получения простого эфирамина формулы (I) или формулы (II), включающий следующие стадии:
a) алкоксилирование 1,2-диспирта формулы (III) С2-С18 алкиленоксидами, где мольное отношение 1,2-диспирта формулы (III) к С2-С18 алкиленоксидам находится в интервале от 1:2 до 1:10,
где R1 представляет собой линейную или разветвленную алкильную группу с 3-16 атомами углерода, и R2 представляет собой водород или алкильную группу с 1-16 атомами углерода,
b) аминирование алкоксилированного 1,2-диспирта аммиаком.
12. Способ по п. 11, где мольное отношение 1,2-диспирта к С2-С18 алкиленоксидам находится в интервале от 1:3 до 1:8.
13. Способ по п. 11, где мольное отношение 1,2-диспирта к С2-С18 алкиленоксидам находится в интервале от 1:4 до 1:6.
14. Способ по п. 11, где С2-С18 алкиленоксиды выбираются из группы, состоящей из пропиленоксида, бутиленоксида или их смеси.
15. Способ по п. 11, где С2-C18 алкиленоксид представляет собой пропиленоксид.
16. Способ по п. 11, где 1,2-диспирт формулы (III) выбирается из группы, состоящей из 1,2-пентандиола, 1,2-гександиола, 1,2-гептандиола, 1,2-октандиола, 1,2-нонандиола, 1,2-декандиола и 1,2-додекандиола, 1,2-тетрадекандиола, 1,2 гексадекандиола и 1,2 октадекандиола.
17. Способ по любому из пп. 11-16, где аминирование осуществляется в присутствии медь-, никель- или кобальт-содержащего катализатора.
18. Способ по п. 17, где каталитически активное вещество катализаторов, перед его восстановлением водородом, содержит кислородные соединения алюминия, меди, никеля и кобальта, и в интервале от 0.2 до 5.0 мас. % кислородных соединений олова, вычисленных как SnO.
19. Применение простого эфирамина по любому из пп. 1-10 в личной гигиене.
20. Применение простого эфирамина по любому из пп. 1-10 в шампунях и составах для мытья тела.
21. Применение смеси простых эфираминов по любому из пп. 1-10 в качестве вулканизирующего средства для эпоксидных смол или в качестве восстановителя в получении полимеров.
22. Применение смеси простых эфираминов по любому из пп. 1-9 в полиуретанах, полимочевинах и в качестве термопластичных полиамидных клеев.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14162047 | 2014-03-27 | ||
| EP14162047.6 | 2014-03-27 | ||
| PCT/EP2015/055562 WO2015144497A1 (en) | 2014-03-27 | 2015-03-17 | Etheramines based on 1,2-dialcohols |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| RU2016141980A3 RU2016141980A3 (ru) | 2018-04-27 |
| RU2016141980A true RU2016141980A (ru) | 2018-04-27 |
| RU2680249C2 RU2680249C2 (ru) | 2019-02-19 |
Family
ID=50389885
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2016141980A RU2680249C2 (ru) | 2014-03-27 | 2015-03-17 | Простые эфирамины на основе 1,2-диспиртов |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP3122717B1 (ru) |
| JP (1) | JP6418621B2 (ru) |
| KR (1) | KR101903976B1 (ru) |
| CN (1) | CN106132918A (ru) |
| BR (1) | BR112016022047A2 (ru) |
| CA (1) | CA2943229A1 (ru) |
| ES (1) | ES2722301T3 (ru) |
| MX (1) | MX378408B (ru) |
| PL (1) | PL3122717T3 (ru) |
| RU (1) | RU2680249C2 (ru) |
| TR (1) | TR201904958T4 (ru) |
| WO (1) | WO2015144497A1 (ru) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6193801B2 (ja) | 2014-04-28 | 2017-09-06 | 株式会社ハイレックスコーポレーション | 嵌合部材および長尺部材の取り替えユニット |
| WO2017200737A1 (en) | 2016-05-20 | 2017-11-23 | Stepan Company | Polyetheramine compositions for laundry detergents |
| BR112019021951A2 (pt) | 2017-06-28 | 2020-05-05 | Huntsman Petrochemical Llc | polieteramina, processos para produzir a polieteramina e o dispersante, dispersante, solução aquosa, e, dispersão aquosa de pigmento. |
| EP4290224A3 (en) | 2018-07-20 | 2024-05-22 | Stepan Company | Reduced-residue hard surface cleaner and method for determining film/streak |
| CA3113923A1 (en) | 2018-09-25 | 2020-04-02 | Huntsman Petrochemical Llc | Cyclic amide initialized polyetheramine and uses thereof |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3654370A (en) | 1970-08-28 | 1972-04-04 | Jefferson Chem Co Inc | Process for preparing polyoxyalkylene polyamines |
| SU968029A1 (ru) * | 1981-01-14 | 1982-10-23 | Предприятие П/Я В-8469 | Способ совместного получени 2-амино-2-оксиэтилового эфира и морфолина |
| JP2566821B2 (ja) * | 1989-02-03 | 1996-12-25 | 花王株式会社 | 洗浄剤組成物 |
| DE4428004A1 (de) | 1994-08-08 | 1996-02-15 | Basf Ag | Verfahren zur Herstellung von Aminen |
| DE19645047A1 (de) * | 1996-10-31 | 1998-05-07 | Basf Ag | Katalysatoren für die Aminierung von Alkylenoxiden, Alkoholen, Aldehyden und Ketonen |
| JP2001014840A (ja) | 1999-06-24 | 2001-01-19 | Nec Corp | 複数ラインバッファ型メモリｌｓｉ |
| US7550550B2 (en) | 2002-08-30 | 2009-06-23 | Huntsman Petrochemical Corporation | Polyether polyamine agents and mixtures therefor |
| WO2009138387A1 (de) | 2008-05-14 | 2009-11-19 | Basf Se | Verwendung eines cyclohexandiolgemisches zur herstellung von polymeren |
| JP2011524451A (ja) | 2008-06-16 | 2011-09-01 | ビーエーエスエフ ソシエタス・ヨーロピア | ポリマー製造のための、ｃ１１ジオール、又はｃ１１ジオール混合物の使用 |
| KR20110053969A (ko) | 2008-07-23 | 2011-05-24 | 바스프 에스이 | 중합체 제조를 위한 2-이소프로필-2-알킬-1,3-프로판디올의 용도 |
| JP2012500874A (ja) | 2008-08-26 | 2012-01-12 | ビーエーエスエフ ソシエタス・ヨーロピア | ポリマーを製造するための、１，１−ジメチロールシクロアルカン又は１，１−ジメチロールシクロアルケンの使用 |
| JP2012502124A (ja) | 2008-09-04 | 2012-01-26 | ビーエーエスエフ ソシエタス・ヨーロピア | ポリマーを製造するための置換された２−アリール−２−アルキル−１，３−プロパンジオールまたは置換された２−シクロヘキシル−２−アルキル−１，３−プロパンジオールの使用 |
| SG181100A1 (en) * | 2009-12-03 | 2012-07-30 | Basf Se | Catalyst and method for producing an amine |
| JP5755237B2 (ja) * | 2009-12-03 | 2015-07-29 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 触媒及びアミンの製造方法 |
| JP2013181000A (ja) * | 2012-03-02 | 2013-09-12 | Matsumoto Yushi Seiyaku Co Ltd | 脂肪族アミンアルキレンオキサイド付加物およびその製造方法 |
-
2015
- 2015-03-17 PL PL15710192T patent/PL3122717T3/pl unknown
- 2015-03-17 CA CA2943229A patent/CA2943229A1/en not_active Abandoned
- 2015-03-17 ES ES15710192T patent/ES2722301T3/es active Active
- 2015-03-17 KR KR1020167029409A patent/KR101903976B1/ko not_active Expired - Fee Related
- 2015-03-17 WO PCT/EP2015/055562 patent/WO2015144497A1/en not_active Ceased
- 2015-03-17 CN CN201580016191.3A patent/CN106132918A/zh active Pending
- 2015-03-17 EP EP15710192.4A patent/EP3122717B1/en not_active Not-in-force
- 2015-03-17 TR TR2019/04958T patent/TR201904958T4/tr unknown
- 2015-03-17 JP JP2017501480A patent/JP6418621B2/ja not_active Expired - Fee Related
- 2015-03-17 RU RU2016141980A patent/RU2680249C2/ru active
- 2015-03-17 MX MX2016012652A patent/MX378408B/es unknown
- 2015-03-17 BR BR112016022047A patent/BR112016022047A2/pt active Search and Examination
Also Published As
| Publication number | Publication date |
|---|---|
| RU2680249C2 (ru) | 2019-02-19 |
| EP3122717A1 (en) | 2017-02-01 |
| KR101903976B1 (ko) | 2018-10-04 |
| RU2016141980A3 (ru) | 2018-04-27 |
| EP3122717B1 (en) | 2019-02-06 |
| KR20160136397A (ko) | 2016-11-29 |
| PL3122717T3 (pl) | 2019-08-30 |
| WO2015144497A1 (en) | 2015-10-01 |
| CN106132918A (zh) | 2016-11-16 |
| JP2017516841A (ja) | 2017-06-22 |
| JP6418621B2 (ja) | 2018-11-07 |
| ES2722301T3 (es) | 2019-08-09 |
| TR201904958T4 (tr) | 2019-05-21 |
| BR112016022047A2 (pt) | 2017-08-15 |
| MX2016012652A (es) | 2017-01-09 |
| CA2943229A1 (en) | 2015-10-01 |
| MX378408B (es) | 2025-03-10 |
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