FI65995C - Stabil koncentrerad glycidyltrimetylammoniumkloridloesning ochfoerfarande foer dess framstaellning - Google Patents
Stabil koncentrerad glycidyltrimetylammoniumkloridloesning ochfoerfarande foer dess framstaellning Download PDFInfo
- Publication number
- FI65995C FI65995C FI790195A FI790195A FI65995C FI 65995 C FI65995 C FI 65995C FI 790195 A FI790195 A FI 790195A FI 790195 A FI790195 A FI 790195A FI 65995 C FI65995 C FI 65995C
- Authority
- FI
- Finland
- Prior art keywords
- water
- solution
- gta
- glycidyltrimethylammonium chloride
- anhydrous
- Prior art date
Links
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 title claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 39
- 239000000243 solution Substances 0.000 claims description 34
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 20
- 239000007864 aqueous solution Substances 0.000 claims description 16
- 238000002360 preparation method Methods 0.000 claims description 7
- 229920002472 Starch Polymers 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- KUSHZUGQEBXZHD-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium chloride hydrate Chemical compound O.[Cl-].C[N+](C)(C)CC1CO1 KUSHZUGQEBXZHD-UHFFFAOYSA-M 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- 239000012895 dilution Substances 0.000 claims 1
- 238000010790 dilution Methods 0.000 claims 1
- 150000004682 monohydrates Chemical class 0.000 description 15
- 150000002924 oxiranes Chemical class 0.000 description 15
- 239000000047 product Substances 0.000 description 12
- 230000003247 decreasing effect Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000002425 crystallisation Methods 0.000 description 6
- 230000008025 crystallization Effects 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 238000004821 distillation Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000012047 saturated solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- SZYJELPVAFJOGJ-UHFFFAOYSA-N trimethylamine hydrochloride Chemical group Cl.CN(C)C SZYJELPVAFJOGJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/36—Compounds containing oxirane rings with hydrocarbon radicals, substituted by nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Epoxy Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NLAANVRAGE7801007,A NL171056B (nl) | 1978-01-27 | 1978-01-27 | Stabiele geconcentreerde oplossing van glycidyltrimethylammoniumchloride in water; monohydraat van glycidyltrimetylammoniumchloride. |
| NL7801007 | 1978-01-27 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI790195A FI790195A (fi) | 1979-07-28 |
| FI65995B FI65995B (fi) | 1984-04-30 |
| FI65995C true FI65995C (fi) | 1984-08-10 |
Family
ID=19830240
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI790195A FI65995C (fi) | 1978-01-27 | 1979-01-19 | Stabil koncentrerad glycidyltrimetylammoniumkloridloesning ochfoerfarande foer dess framstaellning |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4216156A (xx) |
| JP (1) | JPS54112805A (xx) |
| BE (1) | BE873730A (xx) |
| CA (1) | CA1118430A (xx) |
| CH (1) | CH638508A5 (xx) |
| DE (1) | DE2902755C2 (xx) |
| FI (1) | FI65995C (xx) |
| FR (1) | FR2415633A1 (xx) |
| GB (1) | GB2013193B (xx) |
| IT (1) | IT1109865B (xx) |
| NL (1) | NL171056B (xx) |
| SE (1) | SE438334B (xx) |
| YU (1) | YU15679A (xx) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3103713C2 (de) * | 1981-02-04 | 1983-03-03 | Degussa Ag, 6000 Frankfurt | Verfahren zur Reinigung der bei der Herstellung von 2,3-Epoxypropyltrialkylammoniumchloriden entstehenden Umsetzungsgemische |
| US5463127A (en) * | 1995-01-17 | 1995-10-31 | The Dow Chemical Company | Process for preparation of halohydroxypropyl-trialkylammonium halides |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2876217A (en) * | 1956-12-31 | 1959-03-03 | Corn Products Co | Starch ethers containing nitrogen and process for making the same |
| US3342840A (en) * | 1964-03-23 | 1967-09-19 | Shell Oil Co | Cationic ester production |
| GB1056587A (en) * | 1965-10-08 | 1967-01-25 | Shell Int Research | A process of producing a glycidyl trialkyl ammonium halide |
| GB1140520A (en) * | 1966-07-19 | 1969-01-22 | Shell Int Research | Novel cationic ester compounds, novel polymers and copolymers thereof, their preparation and use |
| DE2055046B2 (de) * | 1970-11-09 | 1978-08-03 | Hoffmann's Staerkefabriken Ag, 4902 Bad Salzuflen | Verfahren zur Herstellung von nicht vernetzten kationenaktiven Stärkederivaten |
| NL170146C (nl) * | 1970-11-13 | Hoffmann Staerkefabriken Ag | Werkwijze ter bereiding van glycidyltrialkylammoniumhalogeniden. | |
| US4066673A (en) * | 1974-02-25 | 1978-01-03 | Westvaco Corporation | Process for making quaternary amines of epichlorohydrin |
-
1978
- 1978-01-27 NL NLAANVRAGE7801007,A patent/NL171056B/xx not_active Application Discontinuation
-
1979
- 1979-01-19 FI FI790195A patent/FI65995C/fi not_active IP Right Cessation
- 1979-01-22 US US06/005,589 patent/US4216156A/en not_active Expired - Lifetime
- 1979-01-22 CH CH62979A patent/CH638508A5/de not_active IP Right Cessation
- 1979-01-22 GB GB7902171A patent/GB2013193B/en not_active Expired
- 1979-01-24 CA CA000320178A patent/CA1118430A/en not_active Expired
- 1979-01-24 YU YU00156/79A patent/YU15679A/xx unknown
- 1979-01-25 FR FR7901915A patent/FR2415633A1/fr active Granted
- 1979-01-25 DE DE2902755A patent/DE2902755C2/de not_active Expired
- 1979-01-26 BE BE0/193094A patent/BE873730A/xx not_active IP Right Cessation
- 1979-01-26 SE SE7900703A patent/SE438334B/sv not_active IP Right Cessation
- 1979-01-26 IT IT19667/79A patent/IT1109865B/it active
- 1979-01-26 JP JP865879A patent/JPS54112805A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| IT1109865B (it) | 1985-12-23 |
| SE7900703L (sv) | 1979-07-28 |
| GB2013193B (en) | 1982-06-16 |
| IT7919667A0 (it) | 1979-01-26 |
| JPS6360746B2 (xx) | 1988-11-25 |
| BE873730A (nl) | 1979-07-26 |
| CH638508A5 (de) | 1983-09-30 |
| DE2902755C2 (de) | 1981-10-08 |
| SE438334B (sv) | 1985-04-15 |
| FR2415633A1 (fr) | 1979-08-24 |
| DE2902755A1 (de) | 1979-08-02 |
| JPS54112805A (en) | 1979-09-04 |
| FI790195A (fi) | 1979-07-28 |
| NL7801007A (nl) | 1979-07-31 |
| FR2415633B1 (xx) | 1982-08-27 |
| GB2013193A (en) | 1979-08-08 |
| US4216156A (en) | 1980-08-05 |
| CA1118430A (en) | 1982-02-16 |
| FI65995B (fi) | 1984-04-30 |
| NL171056B (nl) | 1982-09-01 |
| YU15679A (en) | 1983-10-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MA | Patent expired | ||
| PC | Transfer of assignment of patent |
Owner name: KAO CORPORATION |
|
| MA | Patent expired |
Owner name: KAO CORPORATION |