SE448300B - Nya n-oxiranmetan-n,n,n-trialkylammoniumderivat, framstellningsforfarande och anvendning derav vid behandling av polyhydroxylerade och polyaminerade polymerer - Google Patents
Nya n-oxiranmetan-n,n,n-trialkylammoniumderivat, framstellningsforfarande och anvendning derav vid behandling av polyhydroxylerade och polyaminerade polymererInfo
- Publication number
- SE448300B SE448300B SE8301793A SE8301793A SE448300B SE 448300 B SE448300 B SE 448300B SE 8301793 A SE8301793 A SE 8301793A SE 8301793 A SE8301793 A SE 8301793A SE 448300 B SE448300 B SE 448300B
- Authority
- SE
- Sweden
- Prior art keywords
- formula
- med
- anion
- polyaminated
- preparation
- Prior art date
Links
- 229910052757 nitrogen Inorganic materials 0.000 title claims abstract description 17
- 238000011282 treatment Methods 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title claims description 5
- 229920000642 polymer Polymers 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 150000001450 anions Chemical class 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 230000001408 fungistatic effect Effects 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims description 2
- 241000233805 Phoenix Species 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract description 6
- -1 hydroxy ions Chemical class 0.000 abstract description 5
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract description 3
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 abstract description 2
- 238000001816 cooling Methods 0.000 abstract description 2
- 125000005265 dialkylamine group Chemical group 0.000 abstract description 2
- 239000011541 reaction mixture Substances 0.000 abstract description 2
- 150000002440 hydroxy compounds Chemical class 0.000 abstract 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 10
- 125000003118 aryl group Chemical group 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 229910052786 argon Inorganic materials 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000003385 bacteriostatic effect Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- OMEMQVZNTDHENJ-UHFFFAOYSA-N n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCNC OMEMQVZNTDHENJ-UHFFFAOYSA-N 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 125000006512 3,4-dichlorobenzyl group Chemical group [H]C1=C(Cl)C(Cl)=C([H])C(=C1[H])C([H])([H])* 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 101001053401 Arabidopsis thaliana Acid beta-fructofuranosidase 3, vacuolar Proteins 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-M Methanesulfonate Chemical compound CS([O-])(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 1
- 239000008896 Opium Substances 0.000 description 1
- 101100279541 Oryza sativa subsp. japonica EIN2 gene Proteins 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000277284 Salvelinus fontinalis Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 241000295644 Staphylococcaceae Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- SAQSTQBVENFSKT-UHFFFAOYSA-M TCA-sodium Chemical compound [Na+].[O-]C(=O)C(Cl)(Cl)Cl SAQSTQBVENFSKT-UHFFFAOYSA-M 0.000 description 1
- OJADDPKDAQXHHI-UHFFFAOYSA-N acetamide;hydron;bromide Chemical compound Br.CC(N)=O OJADDPKDAQXHHI-UHFFFAOYSA-N 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 244000000010 microbial pathogen Species 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- IHFXMTOFDQKABX-UHFFFAOYSA-N n-methylhexadecan-1-amine Chemical group CCCCCCCCCCCCCCCCNC IHFXMTOFDQKABX-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229960001027 opium Drugs 0.000 description 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 150000002924 oxiranes Chemical group 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 238000007781 pre-processing Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0058—Biocides
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
- D06M13/285—Phosphines; Phosphine oxides; Phosphine sulfides; Phosphinic or phosphinous acids or derivatives thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/385—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen containing epoxy groups
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Biodiversity & Conservation Biology (AREA)
- Epoxy Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8115888A FR2511001B1 (fr) | 1981-08-10 | 1981-08-10 | Produits de traitement des polymeres polyhydroxyles ou polyamines ainsi que procede utilisant ces produits |
Publications (3)
Publication Number | Publication Date |
---|---|
SE8301793L SE8301793L (sv) | 1983-03-30 |
SE8301793D0 SE8301793D0 (sv) | 1983-03-30 |
SE448300B true SE448300B (sv) | 1987-02-09 |
Family
ID=9261541
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE8301793A SE448300B (sv) | 1981-08-10 | 1983-03-30 | Nya n-oxiranmetan-n,n,n-trialkylammoniumderivat, framstellningsforfarande och anvendning derav vid behandling av polyhydroxylerade och polyaminerade polymerer |
SE8500362A SE459010B (sv) | 1981-08-10 | 1985-01-25 | Plana och tunna foeremaal,saasom textilfoeremaal, behandlade med n-oxiranmetan-n,n,n-trialkylammoniumderivat samt foerfarande foer framstaellning av foeremaalen |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE8500362A SE459010B (sv) | 1981-08-10 | 1985-01-25 | Plana och tunna foeremaal,saasom textilfoeremaal, behandlade med n-oxiranmetan-n,n,n-trialkylammoniumderivat samt foerfarande foer framstaellning av foeremaalen |
Country Status (16)
Country | Link |
---|---|
US (2) | US4652267A (nl) |
JP (1) | JPS58501431A (nl) |
AT (1) | AT380878B (nl) |
BE (1) | BE894063A (nl) |
BR (1) | BR8207818A (nl) |
CH (1) | CH669300GA3 (nl) |
DE (1) | DE3248947C2 (nl) |
DK (1) | DK142683A (nl) |
ES (1) | ES8308554A1 (nl) |
FR (1) | FR2511001B1 (nl) |
GB (1) | GB2116557B (nl) |
GR (1) | GR77215B (nl) |
IT (1) | IT1156483B (nl) |
NO (1) | NO159168C (nl) |
SE (2) | SE448300B (nl) |
WO (1) | WO1983000513A1 (nl) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2695800B1 (fr) * | 1992-09-23 | 1996-03-08 | Inst Textile De France | Compose antiseptique. |
FR2808022B1 (fr) * | 2000-04-19 | 2002-06-21 | Inst Textile Et Chimique De Ly | Sel de trialkylamonium epoxyde, procede de synthese et applications |
US7241453B2 (en) * | 2002-04-05 | 2007-07-10 | Long Island University | Antimicrobial surfaces |
DE102008007759B4 (de) * | 2007-12-04 | 2009-09-24 | Atlantichem Gmbh | Mittel zum Verhindern von Verfärbungen beim Waschen von Textilien |
DE102009052548B4 (de) | 2009-11-05 | 2012-11-08 | Atlantichem Gmbh | Rotationssymmetrische Formkörper, Verfahren zu deren Herstellung sowie deren Verwendung |
WO2012113360A1 (de) | 2011-02-21 | 2012-08-30 | Atlantichem Gmbh | Kompakter, entfaltbarer formkörper, verfahren zu dessen herstellung sowie dessen verwendung für säuberungszwecke und verteilen von wirkstoffen |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3091537A (en) * | 1959-05-04 | 1963-05-28 | Eastman Kodak Co | Hardening of photographic layers |
DE1469346A1 (de) * | 1964-05-23 | 1969-04-30 | Bayer Ag | Mittel zur Verhuetung der elektrostatischen Aufladung geformter Gebilde |
US3287375A (en) * | 1964-07-06 | 1966-11-22 | Bristol Myers Co | Nu, nu-dimethyl-nu-(2, 3-epoxypropyl)-omicron-substituted benzylammonium salts |
CH534771A (de) * | 1968-04-30 | 1972-10-31 | Ciba Geigy Ag | Verfahren zur Erzeugung von gleichmässigen Färbungen auf textilem Fasermaterial aus polymerem oder copolymerem Acrylnitril |
FR1585665A (fr) * | 1968-08-30 | 1970-01-30 | Inst Textile De France | Nouveaux polymeres hydroxyles a caractere textile ayant des proprietes tinctorales ameliorees, procede de modification des proprietes tinctoriales des polymeres polyhydroxyles, et nouveau procede de teint |
FR2169001B1 (nl) * | 1972-01-26 | 1976-10-29 | Protex Manuf Prod Chimiq | |
FR2181448A2 (en) * | 1972-04-24 | 1973-12-07 | Inst Textile De France | Polyhydroxylic polymer fibres - treated with epoxypropylammonium salt to increase dye affinity |
JPS5045860A (nl) * | 1973-08-29 | 1975-04-24 | ||
DE2407147A1 (de) * | 1974-02-15 | 1975-08-28 | Bayer Ag | Quartaere n- (2,3-epoxyalkyl)-ammonium- verbindungen |
DE2527962A1 (de) * | 1975-06-24 | 1977-01-13 | Bayer Ag | Verfahren zur behandlung von cellulose-fasern |
AT358059B (de) * | 1977-03-09 | 1980-08-25 | Bayer Ag | Verfahren zur herstellung von neuen oxiranen |
JPS5912793B2 (ja) * | 1978-09-26 | 1984-03-26 | 東洋紡績株式会社 | 染色物の堅牢度向上法 |
US4380453A (en) * | 1980-02-06 | 1983-04-19 | Dixie Yarns, Inc. | Extraneous dye or colorant scavenging system in laundry |
US4447243A (en) * | 1981-08-17 | 1984-05-08 | Dixie Yarns, Inc. | Odor scavenging system |
-
1981
- 1981-08-10 FR FR8115888A patent/FR2511001B1/fr not_active Expired
-
1982
- 1982-08-02 IT IT67973/82A patent/IT1156483B/it active
- 1982-08-05 GB GB08309281A patent/GB2116557B/en not_active Expired
- 1982-08-05 WO PCT/FR1982/000131 patent/WO1983000513A1/en active Application Filing
- 1982-08-05 DE DE19823248947 patent/DE3248947C2/de not_active Expired
- 1982-08-05 US US06/493,560 patent/US4652267A/en not_active Expired - Fee Related
- 1982-08-05 AT AT0904282A patent/AT380878B/de active
- 1982-08-05 BR BR8207818A patent/BR8207818A/pt not_active IP Right Cessation
- 1982-08-05 JP JP57502422A patent/JPS58501431A/ja active Pending
- 1982-08-06 GR GR68973A patent/GR77215B/el unknown
- 1982-08-09 BE BE0/208775A patent/BE894063A/fr not_active IP Right Cessation
- 1982-08-09 ES ES514861A patent/ES8308554A1/es not_active Expired
-
1983
- 1983-03-29 NO NO83831153A patent/NO159168C/no unknown
- 1983-03-29 DK DK142683A patent/DK142683A/da not_active IP Right Cessation
- 1983-03-30 SE SE8301793A patent/SE448300B/sv not_active IP Right Cessation
- 1983-08-05 CH CH194883A patent/CH669300GA3/fr unknown
-
1984
- 1984-04-30 US US06/605,393 patent/US4582917A/en not_active Expired - Fee Related
-
1985
- 1985-01-25 SE SE8500362A patent/SE459010B/sv not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
US4582917A (en) | 1986-04-15 |
NO159168C (no) | 1988-12-07 |
GB2116557A (en) | 1983-09-28 |
DE3248947T1 (de) | 1983-12-01 |
US4652267A (en) | 1987-03-24 |
SE459010B (sv) | 1989-05-29 |
NO159168B (no) | 1988-08-29 |
CH669300GA3 (nl) | 1989-03-15 |
GB8309281D0 (en) | 1983-05-11 |
IT1156483B (it) | 1987-02-04 |
FR2511001A1 (fr) | 1983-02-11 |
GB2116557B (en) | 1986-03-12 |
JPS58501431A (ja) | 1983-08-25 |
BE894063A (fr) | 1983-02-09 |
DE3248947C2 (de) | 1986-10-23 |
FR2511001B1 (fr) | 1988-07-29 |
SE8500362L (sv) | 1985-01-25 |
DK142683D0 (da) | 1983-03-29 |
SE8301793L (sv) | 1983-03-30 |
AT380878B (de) | 1986-07-25 |
GR77215B (nl) | 1984-09-11 |
ES514861A0 (es) | 1983-10-01 |
ATA904282A (de) | 1985-12-15 |
ES8308554A1 (es) | 1983-10-01 |
DK142683A (da) | 1983-03-29 |
WO1983000513A1 (en) | 1983-02-17 |
IT8267973A0 (it) | 1982-08-02 |
NO831153L (no) | 1983-03-29 |
SE8500362D0 (sv) | 1985-01-25 |
BR8207818A (pt) | 1983-07-19 |
SE8301793D0 (sv) | 1983-03-30 |
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