BG61860B2 - Синтетичен полиамид с подобрени багрилни свойства - Google Patents
Синтетичен полиамид с подобрени багрилни свойства Download PDFInfo
- Publication number
- BG61860B2 BG61860B2 BG098622A BG9862294A BG61860B2 BG 61860 B2 BG61860 B2 BG 61860B2 BG 098622 A BG098622 A BG 098622A BG 9862294 A BG9862294 A BG 9862294A BG 61860 B2 BG61860 B2 BG 61860B2
- Authority
- BG
- Bulgaria
- Prior art keywords
- compound
- synthetic polyamide
- synthetic
- acid
- compounds
- Prior art date
Links
- 239000004952 Polyamide Substances 0.000 title claims abstract description 29
- 229920002647 polyamide Polymers 0.000 title claims abstract description 29
- 238000004043 dyeing Methods 0.000 title claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims description 6
- 125000003277 amino group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 5
- 238000004040 coloring Methods 0.000 abstract description 2
- 239000000975 dye Substances 0.000 description 9
- 239000000835 fiber Substances 0.000 description 6
- 239000000985 reactive dye Substances 0.000 description 5
- 239000004744 fabric Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000980 acid dye Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- YNOSXQQLBPOTLB-UHFFFAOYSA-J [Na+].[Cr+3].Cc1[n-]n(-c2ccccc2)c(=O)c1\N=N\c1ccccc1C([O-])=O.Cc1[n-]n(-c2ccccc2)c(=O)c1\N=N/c1ccccc1C([O-])=O Chemical compound [Na+].[Cr+3].Cc1[n-]n(-c2ccccc2)c(=O)c1\N=N\c1ccccc1C([O-])=O.Cc1[n-]n(-c2ccccc2)c(=O)c1\N=N/c1ccccc1C([O-])=O YNOSXQQLBPOTLB-UHFFFAOYSA-J 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- UHXQPQCJDDSMCB-UHFFFAOYSA-L disodium;3-[[9,10-dioxo-4-(2,4,6-trimethyl-3-sulfonatoanilino)anthracen-1-yl]amino]-2,4,6-trimethylbenzenesulfonate Chemical compound [Na+].[Na+].CC1=CC(C)=C(S([O-])(=O)=O)C(C)=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=C(C)C=C(C)C(S([O-])(=O)=O)=C1C UHXQPQCJDDSMCB-UHFFFAOYSA-L 0.000 description 2
- GYGVRMLIQVFLPE-UHFFFAOYSA-L disodium;3-[[n-ethyl-4-[[4-[(3-sulfonatophenyl)diazenyl]naphthalen-1-yl]diazenyl]anilino]methyl]benzenesulfonate Chemical compound [Na+].[Na+].C=1C=C(N=NC=2C3=CC=CC=C3C(N=NC=3C=C(C=CC=3)S([O-])(=O)=O)=CC=2)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 GYGVRMLIQVFLPE-UHFFFAOYSA-L 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- BTLSLHNLDQCWKS-UHFFFAOYSA-N oxocan-2-one Chemical compound O=C1CCCCCCO1 BTLSLHNLDQCWKS-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- RRETZLLHOMHNNB-UHFFFAOYSA-M sodium;1-amino-9,10-dioxo-4-(2,4,6-trimethylanilino)anthracene-2-sulfonate Chemical compound [Na+].CC1=CC(C)=CC(C)=C1NC1=CC(S([O-])(=O)=O)=C(N)C2=C1C(=O)C1=CC=CC=C1C2=O RRETZLLHOMHNNB-UHFFFAOYSA-M 0.000 description 2
- AXMCIYLNKNGNOT-UHFFFAOYSA-N sodium;3-[[4-[(4-dimethylazaniumylidenecyclohexa-2,5-dien-1-ylidene)-[4-[ethyl-[(3-sulfophenyl)methyl]amino]phenyl]methyl]-n-ethylanilino]methyl]benzenesulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S(O)(=O)=O)=C1 AXMCIYLNKNGNOT-UHFFFAOYSA-N 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- YAXWOADCWUUUNX-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidine Chemical class CC1CCCN(C)C1(C)C YAXWOADCWUUUNX-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- WFGMRESWHYSOKC-UHFFFAOYSA-N 1,3,3,4-tetramethylpiperazin-2-one Chemical compound CN1CCN(C)C(C)(C)C1=O WFGMRESWHYSOKC-UHFFFAOYSA-N 0.000 description 1
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 1
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical class CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 1
- QEPXACTUQNGGHW-UHFFFAOYSA-N 2,4,6-trichloro-1h-triazine Chemical compound ClN1NC(Cl)=CC(Cl)=N1 QEPXACTUQNGGHW-UHFFFAOYSA-N 0.000 description 1
- JECOQZILBFQPFS-UHFFFAOYSA-N 2,4,6-trichlorothiazine Chemical compound ClN1SC(Cl)=CC(Cl)=C1 JECOQZILBFQPFS-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- VVMPKPRQECVYDV-UHFFFAOYSA-N 5-butyl-2-[[4-(4-butyl-2-sulfoanilino)-5,8-dihydroxy-9,10-dioxoanthracen-1-yl]amino]benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(CCCC)=CC=C1NC(C=1C(=O)C2=C(O)C=CC(O)=C2C(=O)C=11)=CC=C1NC1=CC=C(CCCC)C=C1S(O)(=O)=O VVMPKPRQECVYDV-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- TVZISJTYELEYPI-UHFFFAOYSA-N hypodiphosphoric acid Chemical class OP(O)(=O)P(O)(O)=O TVZISJTYELEYPI-UHFFFAOYSA-N 0.000 description 1
- -1 hypophosphoric acid alkali salts Chemical class 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229920000933 poly (ε-caprolactam) Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- QUBWRMVVDDDDBG-UHFFFAOYSA-M sodium;1-amino-4-(4-butylanilino)-9,10-dioxoanthracene-2-sulfonate Chemical compound [Na+].C1=CC(CCCC)=CC=C1NC1=CC(S([O-])(=O)=O)=C(N)C2=C1C(=O)C1=CC=CC=C1C2=O QUBWRMVVDDDDBG-UHFFFAOYSA-M 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/02—After-treatment
- D06P5/04—After-treatment with organic compounds
- D06P5/06—After-treatment with organic compounds containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
-
- 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
-
- 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
- C08K5/16—Nitrogen-containing compounds
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/6426—Heterocyclic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Polyamides (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Coloring (AREA)
- Artificial Filaments (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3901717A DE3901717A1 (de) | 1989-01-21 | 1989-01-21 | Synthetische polyamide mit verbesserter anfaerbbarkeit |
DE3901716A DE3901716A1 (de) | 1989-01-21 | 1989-01-21 | Synthetische polyamide mit verbesserter anfaerbbarkeit sowie in der masse gefaerbte synthetische polyamide |
DE3930089A DE3930089A1 (de) | 1989-09-09 | 1989-09-09 | Modifizierte synthetische polyamide |
Publications (1)
Publication Number | Publication Date |
---|---|
BG61860B2 true BG61860B2 (bg) | 1998-07-31 |
Family
ID=27198948
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BG098622A BG61860B2 (bg) | 1989-01-21 | 1994-02-28 | Синтетичен полиамид с подобрени багрилни свойства |
Country Status (11)
Country | Link |
---|---|
EP (2) | EP0379470B1 (es) |
JP (1) | JP3041819B2 (es) |
KR (1) | KR100199220B1 (es) |
BG (1) | BG61860B2 (es) |
BR (1) | BR9000241A (es) |
CZ (2) | CZ291961B6 (es) |
DE (2) | DE69025963T2 (es) |
ES (2) | ES2087141T3 (es) |
HK (1) | HK1012654A1 (es) |
SK (1) | SK30790A3 (es) |
TR (1) | TR28862A (es) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4131926A1 (de) * | 1990-10-04 | 1992-04-09 | Sandoz Ag | Verfahren zum nachbehandeln von mit anionischen farbstoffen gefaerbten substraten |
DE59502905D1 (de) * | 1994-04-15 | 1998-08-27 | Basf Ag | Inhärent licht- und hitzestabilisierte polyamide |
GB9609742D0 (en) * | 1996-05-10 | 1996-07-17 | Clariant Int Ltd | Improvements in or relating to organic compounds |
GB9800935D0 (en) | 1998-01-17 | 1998-03-11 | Clariant Int Ltd | Improvements in or relating to organic compounds |
US6197060B1 (en) | 1999-01-19 | 2001-03-06 | Smith & Nephew, Inc. | Otologic prostheses |
KR100450381B1 (ko) * | 2002-04-09 | 2004-10-01 | 주식회사 효성 | 열, 자외선 안정성이 우수한 개질 폴리아미드6의 제조방법 |
US8007546B2 (en) | 2003-11-19 | 2011-08-30 | Huntsman International Llc | Method of increasing depth shade |
WO2011000772A1 (de) * | 2009-06-30 | 2011-01-06 | Basf Se | Polyamidfasern mit anfärbbaren partikeln und verfahren zu deren herstellung |
CN107835802B (zh) * | 2015-09-04 | 2022-04-22 | Dic株式会社 | 稳定剂化合物、液晶组合物和显示元件 |
KR20180052599A (ko) | 2015-09-04 | 2018-05-18 | 디아이씨 가부시끼가이샤 | 액정 조성물 및 그것을 사용한 액정 표시 소자 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1469633A1 (de) * | 1965-06-11 | 1969-04-30 | Basf Ag | Verfahren zur Herstellung von Farbstoffmischungen |
NL6509284A (es) * | 1965-07-17 | 1966-01-25 | ||
JPS5857444A (ja) * | 1981-09-29 | 1983-04-05 | Sumitomo Chem Co Ltd | 安定化された合成樹脂組成物 |
DE3233951A1 (de) * | 1982-09-14 | 1984-03-15 | Chemische Werke Hüls AG, 4370 Marl | Carbonamidgruppenhaltige formmassen oder formkoerper mit verbesserter bestaendigkeit gegen die einwirkung von licht |
DE3233953A1 (de) * | 1982-09-14 | 1984-03-15 | Chemische Werke Hüls AG, 4370 Marl | Carbonamidgruppenhaltige formmassen oder formkoerper mit verbesserter bestaendigkeit gegen die einwirkung von licht |
US4847333A (en) * | 1985-09-30 | 1989-07-11 | The Boeing Company | Blended polyamide oligomers |
-
1990
- 1990-01-17 EP EP90810040A patent/EP0379470B1/en not_active Expired - Lifetime
- 1990-01-17 ES ES90810040T patent/ES2087141T3/es not_active Expired - Lifetime
- 1990-01-17 ES ES94109533T patent/ES2120545T3/es not_active Expired - Lifetime
- 1990-01-17 EP EP94109533A patent/EP0618256B1/en not_active Expired - Lifetime
- 1990-01-17 DE DE69025963T patent/DE69025963T2/de not_active Expired - Fee Related
- 1990-01-17 DE DE69032665T patent/DE69032665T2/de not_active Expired - Fee Related
- 1990-01-20 KR KR1019900000737A patent/KR100199220B1/ko not_active IP Right Cessation
- 1990-01-22 JP JP2010780A patent/JP3041819B2/ja not_active Expired - Fee Related
- 1990-01-22 TR TR00106/90A patent/TR28862A/xx unknown
- 1990-01-22 SK SK307-90A patent/SK30790A3/sk unknown
- 1990-01-22 BR BR909000241A patent/BR9000241A/pt not_active IP Right Cessation
- 1990-01-22 CZ CZ1990307A patent/CZ291961B6/cs not_active IP Right Cessation
-
1994
- 1994-02-28 BG BG098622A patent/BG61860B2/bg unknown
-
1998
- 1998-12-17 HK HK98113845A patent/HK1012654A1/xx not_active IP Right Cessation
-
2002
- 2002-05-07 CZ CZ20021588A patent/CZ292091B6/cs not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CZ291961B6 (cs) | 2003-06-18 |
SK280042B6 (sk) | 1999-07-12 |
BR9000241A (pt) | 1990-11-20 |
EP0379470B1 (en) | 1996-03-20 |
TR28862A (tr) | 1997-09-23 |
DE69025963T2 (de) | 1996-11-21 |
EP0618256B1 (en) | 1998-09-16 |
DE69025963D1 (de) | 1996-04-25 |
KR900011825A (ko) | 1990-08-02 |
ES2120545T3 (es) | 1998-11-01 |
EP0618256A3 (en) | 1995-04-26 |
EP0618256A2 (en) | 1994-10-05 |
CZ292091B6 (cs) | 2003-07-16 |
EP0379470A3 (en) | 1992-03-18 |
DE69032665T2 (de) | 1999-02-25 |
JPH02265966A (ja) | 1990-10-30 |
KR100199220B1 (ko) | 1999-06-15 |
JP3041819B2 (ja) | 2000-05-15 |
HK1012654A1 (en) | 1999-08-06 |
SK30790A3 (en) | 1999-07-12 |
ES2087141T3 (es) | 1996-07-16 |
CZ30790A3 (cs) | 2000-08-16 |
EP0379470A2 (en) | 1990-07-25 |
DE69032665D1 (de) | 1998-10-22 |
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