NO128622B - - Google Patents
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- Publication number
- NO128622B NO128622B NO01477/69A NO147769A NO128622B NO 128622 B NO128622 B NO 128622B NO 01477/69 A NO01477/69 A NO 01477/69A NO 147769 A NO147769 A NO 147769A NO 128622 B NO128622 B NO 128622B
- Authority
- NO
- Norway
- Prior art keywords
- bath
- phthalimide
- dye
- acid
- hydroxy
- Prior art date
Links
- 239000000975 dye Substances 0.000 claims description 30
- -1 C 1 -C 4 alkoxy Chemical group 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 13
- 229920002678 cellulose Polymers 0.000 claims description 10
- 238000004043 dyeing Methods 0.000 claims description 10
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 10
- 239000006185 dispersion Substances 0.000 claims description 9
- 229920000728 polyester Polymers 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical group 0.000 claims description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000203 mixture Substances 0.000 description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 238000004040 coloring Methods 0.000 description 6
- 239000004753 textile Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- DLKDEVCJRCPTLN-UHFFFAOYSA-N 2-butylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCC)C(=O)C2=C1 DLKDEVCJRCPTLN-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 229940072395 n-butylphthalimide Drugs 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 3
- VPLDXHDOGVIETL-UHFFFAOYSA-N 2-propan-2-ylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C(C)C)C(=O)C2=C1 VPLDXHDOGVIETL-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- XXQHICUADUPMPL-UHFFFAOYSA-N 4-methoxycarbonylphthalic acid Chemical compound COC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 XXQHICUADUPMPL-UHFFFAOYSA-N 0.000 description 2
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 239000013505 freshwater Substances 0.000 description 2
- BWRCJLJJIXYLNV-UHFFFAOYSA-N methyl 2-hydroxy-3-methoxybenzoate Chemical compound COC(=O)C1=CC=CC(OC)=C1O BWRCJLJJIXYLNV-UHFFFAOYSA-N 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- MWAYRGBWOVHDDZ-UHFFFAOYSA-N vanillic acid ethyl ester Natural products CCOC(=O)C1=CC=C(O)C(OC)=C1 MWAYRGBWOVHDDZ-UHFFFAOYSA-N 0.000 description 2
- WXTMDXOMEHJXQO-UHFFFAOYSA-N 2,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC=C1O WXTMDXOMEHJXQO-UHFFFAOYSA-N 0.000 description 1
- FFWAFIBEOZWDJZ-UHFFFAOYSA-N 2-(1,3-dioxoisoindol-2-yl)ethyl acetate Chemical compound C1=CC=C2C(=O)N(CCOC(=O)C)C(=O)C2=C1 FFWAFIBEOZWDJZ-UHFFFAOYSA-N 0.000 description 1
- JDCMVWZZNHUBBR-UHFFFAOYSA-N 2-(2-ethylhexyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CC(CC)CCCC)C(=O)C2=C1 JDCMVWZZNHUBBR-UHFFFAOYSA-N 0.000 description 1
- DLGAPXQHTIJNJA-UHFFFAOYSA-N 2-(2-methylpropyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CC(C)C)C(=O)C2=C1 DLGAPXQHTIJNJA-UHFFFAOYSA-N 0.000 description 1
- HFQZKKICCDOQPD-UHFFFAOYSA-N 2-(3-methoxypropyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCOC)C(=O)C2=C1 HFQZKKICCDOQPD-UHFFFAOYSA-N 0.000 description 1
- IMOPXBPHKARACH-UHFFFAOYSA-N 2-(ethoxymethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(COCC)C(=O)C2=C1 IMOPXBPHKARACH-UHFFFAOYSA-N 0.000 description 1
- SKRVQRQCLHCKBW-UHFFFAOYSA-N 2-(propoxymethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(COCCC)C(=O)C2=C1 SKRVQRQCLHCKBW-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical class NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- JZDSOQSUCWVBMV-UHFFFAOYSA-N 2-ethylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CC)C(=O)C2=C1 JZDSOQSUCWVBMV-UHFFFAOYSA-N 0.000 description 1
- AMEZJARRAUZZHY-UHFFFAOYSA-N 2-tert-butylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C(C)(C)C)C(=O)C2=C1 AMEZJARRAUZZHY-UHFFFAOYSA-N 0.000 description 1
- BKFXSOCDAQACQM-UHFFFAOYSA-N 3-chlorophthalic acid Chemical compound OC(=O)C1=CC=CC(Cl)=C1C(O)=O BKFXSOCDAQACQM-UHFFFAOYSA-N 0.000 description 1
- KFIRODWJCYBBHY-UHFFFAOYSA-N 3-nitrophthalic acid Chemical compound OC(=O)C1=CC=CC([N+]([O-])=O)=C1C(O)=O KFIRODWJCYBBHY-UHFFFAOYSA-N 0.000 description 1
- SELGXAAKRMIWMS-UHFFFAOYSA-N 4-butylisoindole-1,3-dione Chemical compound CCCCC1=CC=CC2=C1C(=O)NC2=O SELGXAAKRMIWMS-UHFFFAOYSA-N 0.000 description 1
- KHLNYSKHLDDQIZ-UHFFFAOYSA-N 4-ethoxyphthalic acid Chemical compound CCOC1=CC=C(C(O)=O)C(C(O)=O)=C1 KHLNYSKHLDDQIZ-UHFFFAOYSA-N 0.000 description 1
- MWRVRCAFWBBXTL-UHFFFAOYSA-N 4-hydroxyphthalic acid Chemical compound OC(=O)C1=CC=C(O)C=C1C(O)=O MWRVRCAFWBBXTL-UHFFFAOYSA-N 0.000 description 1
- ZCMKCGTYWKAYNK-UHFFFAOYSA-N 4-methyl-2-propoxyisoindole-1,3-dione Chemical compound C1=CC(C)=C2C(=O)N(OCCC)C(=O)C2=C1 ZCMKCGTYWKAYNK-UHFFFAOYSA-N 0.000 description 1
- YYEWRNLQOAIQDL-UHFFFAOYSA-N 4-phenylphthalic acid Chemical group C1=C(C(O)=O)C(C(=O)O)=CC=C1C1=CC=CC=C1 YYEWRNLQOAIQDL-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- NUQVHFYOQOWFMH-UHFFFAOYSA-N C(CC)(=O)OCCCN1C(C=2C(C1=O)=CC=CC2)=O Chemical compound C(CC)(=O)OCCCN1C(C=2C(C1=O)=CC=CC2)=O NUQVHFYOQOWFMH-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- BSMILTTURCQDGJ-UHFFFAOYSA-N N-(3-Hydroxypropyl)phthalimide Chemical compound C1=CC=C2C(=O)N(CCCO)C(=O)C2=C1 BSMILTTURCQDGJ-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000004744 butyloxycarbonyl group Chemical group 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- MNWFENBPJIWZOZ-UHFFFAOYSA-N methyl 3-hydroxy-5-methoxybenzoate Chemical compound COC(=O)C1=CC(O)=CC(OC)=C1 MNWFENBPJIWZOZ-UHFFFAOYSA-N 0.000 description 1
- XZGSPVJYILSEIY-UHFFFAOYSA-N methyl 4-(1,3-dioxoisoindol-2-yl)butanoate Chemical compound C1=CC=C2C(=O)N(CCCC(=O)OC)C(=O)C2=C1 XZGSPVJYILSEIY-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 125000005543 phthalimide group Chemical class 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 150000003870 salicylic acids Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002759 woven fabric Substances 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
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/34—Material containing ester groups
- D06P3/36—Material containing ester groups using dispersed dyestuffs
-
- 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
- D06P1/649—Compounds containing carbonamide, thiocarbonamide or guanyl groups
- D06P1/6495—Compounds containing carbonamide -RCON= (R=H or hydrocarbons)
- D06P1/6498—Compounds containing -CONCO-, e.g. phthalimides, hydantoine; Compounds containing RCONHSO2R (R=H or hydrocarbon)
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681769210 DE1769210A1 (de) | 1968-04-20 | 1968-04-20 | Druck- und Faerbeverfahren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO128622B true NO128622B (da) | 1973-12-17 |
Family
ID=5700048
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO01477/69A NO128622B (da) | 1968-04-20 | 1969-04-10 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3574513A (da) |
| AT (1) | AT291181B (da) |
| BE (1) | BE731752A (da) |
| CH (2) | CH500326A (da) |
| DE (1) | DE1769210A1 (da) |
| DK (1) | DK130799B (da) |
| FI (1) | FI45873C (da) |
| FR (1) | FR2006633A1 (da) |
| GB (1) | GB1193948A (da) |
| NL (1) | NL155064B (da) |
| NO (1) | NO128622B (da) |
| SE (1) | SE352119B (da) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3999942A (en) * | 1974-08-01 | 1976-12-28 | Cassella Farbwerke Mainkur Aktiengesellschaft | N-Acyloyl-N-alkyl-alkylenediamines as dye levelers |
| FR2503453A1 (fr) * | 1981-04-06 | 1982-10-08 | Cibie Projecteurs | Perfectionnements aux lampes halogenes et aux projecteurs equipes de telles lampes |
| DE3834737A1 (de) * | 1988-10-12 | 1990-04-19 | Bayer Ag | Carrier fuer das faerben von polyestermaterialien |
| DE3902052A1 (de) * | 1989-01-25 | 1990-07-26 | Bayer Ag | Carrier fuer das faerben von hydrophoben fasermaterialien |
| EP0414631A1 (de) * | 1989-02-22 | 1991-02-27 | Ciba-Geigy Ag | Hilfsmittelgemisch und seine Verwendung beim Färben von Polyesterfasermaterialien |
| ES2037597B1 (es) * | 1990-08-27 | 1994-03-16 | Sandoz Ag | Perfeccionamientos en o relacionados con compuestos organicos. |
| US5968203A (en) * | 1997-02-28 | 1999-10-19 | Sybron Chemicals Inc. | Clay-containing textile material treating composition and method |
| US5972049A (en) * | 1998-01-28 | 1999-10-26 | Sybron Chemicals Inc. | Clay-containing dispersing composition for carriers used in the disperse dyeing of hydrophobic textiles |
| CN112323518B (zh) * | 2020-11-16 | 2023-03-17 | 五邑大学 | 一种醋酯面料染色载体及其制备方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH324162A (de) * | 1953-06-18 | 1957-09-15 | Rohner Ag | Beständige Druckpaste |
-
1968
- 1968-04-20 DE DE19681769210 patent/DE1769210A1/de active Pending
-
1969
- 1969-03-24 FI FI690863A patent/FI45873C/fi active
- 1969-04-10 NO NO01477/69A patent/NO128622B/no unknown
- 1969-04-10 US US815191A patent/US3574513A/en not_active Expired - Lifetime
- 1969-04-16 GB GB09484/69A patent/GB1193948A/en not_active Expired
- 1969-04-16 NL NL696905878A patent/NL155064B/xx not_active IP Right Cessation
- 1969-04-17 AT AT369869A patent/AT291181B/de active
- 1969-04-18 FR FR6912310A patent/FR2006633A1/fr active Granted
- 1969-04-18 CH CH596169A patent/CH500326A/de not_active IP Right Cessation
- 1969-04-18 DK DK215269AA patent/DK130799B/da unknown
- 1969-04-18 CH CH596169D patent/CH596169A4/xx unknown
- 1969-04-18 BE BE731752D patent/BE731752A/xx not_active IP Right Cessation
- 1969-04-18 SE SE05512/69A patent/SE352119B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US3574513A (en) | 1971-04-13 |
| SE352119B (da) | 1972-12-18 |
| DK130799B (da) | 1975-04-14 |
| DE1769210A1 (de) | 1970-12-17 |
| FR2006633B1 (da) | 1973-08-10 |
| NL6905878A (da) | 1969-10-22 |
| FI45873C (fi) | 1972-10-10 |
| BE731752A (da) | 1969-10-01 |
| NL155064B (nl) | 1977-11-15 |
| FI45873B (da) | 1972-06-30 |
| CH500326A (de) | 1970-08-31 |
| DK130799C (da) | 1975-09-15 |
| FR2006633A1 (fr) | 1969-12-26 |
| AT291181B (de) | 1971-07-12 |
| CH596169A4 (da) | 1970-08-31 |
| GB1193948A (en) | 1970-06-03 |
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