NO135666B - - Google Patents
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- Publication number
- NO135666B NO135666B NO3609/71A NO360971A NO135666B NO 135666 B NO135666 B NO 135666B NO 3609/71 A NO3609/71 A NO 3609/71A NO 360971 A NO360971 A NO 360971A NO 135666 B NO135666 B NO 135666B
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- carbon atoms
- salts
- solution
- mixture
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 16
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- -1 monomethylamino compounds Chemical class 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000002872 contrast media Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 20
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 238000001816 cooling Methods 0.000 description 6
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- 238000000354 decomposition reaction Methods 0.000 description 5
- 239000005457 ice water Substances 0.000 description 5
- 235000011121 sodium hydroxide Nutrition 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000008098 formaldehyde solution Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 210000000941 bile Anatomy 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000008120 corn starch Substances 0.000 description 2
- 230000029142 excretion Effects 0.000 description 2
- 239000007903 gelatin capsule Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical class [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 230000007306 turnover Effects 0.000 description 2
- CUGDYSSBTWBKII-LXGUWJNJSA-N (2r,3r,4r,5s)-6-(dimethylamino)hexane-1,2,3,4,5-pentol Chemical compound CN(C)C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO CUGDYSSBTWBKII-LXGUWJNJSA-N 0.000 description 1
- OIRFJRBSRORBCM-YFKPBYRVSA-N (2s)-2-[(3-amino-2,4,6-triiodophenyl)methyl]butanoic acid Chemical compound CC[C@H](C(O)=O)CC1=C(I)C=C(I)C(N)=C1I OIRFJRBSRORBCM-YFKPBYRVSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- BVDHMFVGWNGIQE-UHFFFAOYSA-N 3-(3-amino-2,4,6-triiodophenyl)propanoic acid Chemical compound NC1=C(I)C=C(I)C(CCC(O)=O)=C1I BVDHMFVGWNGIQE-UHFFFAOYSA-N 0.000 description 1
- LCXACUQONAQZBR-UHFFFAOYSA-N 4-(3-amino-n-ethyl-2,4,6-triiodoanilino)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)N(CC)C1=C(I)C=C(I)C(N)=C1I LCXACUQONAQZBR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- ZFHZUGUCWJVEQC-FPUQOWELSA-M Ipodate Sodium Chemical compound [Na+].CN(C)\C=N\C1=C(I)C=C(I)C(CCC([O-])=O)=C1I ZFHZUGUCWJVEQC-FPUQOWELSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 description 1
- 206010058667 Oral toxicity Diseases 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000009606 cholecystography Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002497 iodine compounds Chemical class 0.000 description 1
- QIFJTEYRIMDFPK-UHFFFAOYSA-N iomeglamic acid Chemical compound OC(=O)CCCC(=O)N(C)C1=C(I)C=C(I)C(N)=C1I QIFJTEYRIMDFPK-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000012022 methylating agents Substances 0.000 description 1
- 230000011987 methylation Effects 0.000 description 1
- 238000007069 methylation reaction Methods 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- 238000009608 myelography Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 231100000418 oral toxicity Toxicity 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000020374 simple syrup Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229960003175 sodium iopodate Drugs 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
- 239000012265 solid product Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/04—X-ray contrast preparations
- A61K49/0433—X-ray contrast preparations containing an organic halogenated X-ray contrast-enhancing agent
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Cephalosporin Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO763723A NO137638C (no) | 1970-10-02 | 1976-11-02 | Fremgangsmaate ved fremstilling av 3-methyl-amino-trijodbenzoesyreforbindelser |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19702050217 DE2050217A1 (de) | 1970-10-02 | 1970-10-02 | Monomethylamino Verbindungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO135666B true NO135666B (fr) | 1977-01-31 |
| NO135666C NO135666C (fr) | 1977-05-11 |
Family
ID=5784989
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO3609/71A NO135666C (fr) | 1970-10-02 | 1971-10-01 |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US3883578A (fr) |
| AT (2) | AT309670B (fr) |
| BE (1) | BE773417A (fr) |
| BR (1) | BR7106500D0 (fr) |
| CA (1) | CA955938A (fr) |
| CH (1) | CH582130A5 (fr) |
| CS (1) | CS170548B2 (fr) |
| DD (1) | DD96831A5 (fr) |
| DE (1) | DE2050217A1 (fr) |
| DK (1) | DK131990C (fr) |
| ES (2) | ES395601A1 (fr) |
| FI (1) | FI51766C (fr) |
| FR (1) | FR2110179B1 (fr) |
| GB (1) | GB1369999A (fr) |
| HU (1) | HU162899B (fr) |
| IL (1) | IL37829A (fr) |
| IT (1) | IT1019517B (fr) |
| NL (1) | NL7113557A (fr) |
| NO (1) | NO135666C (fr) |
| PL (2) | PL82567B1 (fr) |
| SE (1) | SE396073B (fr) |
| SU (1) | SU501667A3 (fr) |
| ZA (1) | ZA715707B (fr) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4025550A (en) * | 1972-07-21 | 1977-05-24 | Chemie Linz Aktiengesellschaft | Derivatives of triiodo-aminobenzenecarboxylic acids and the preparation thereof |
| US4175544A (en) * | 1974-08-28 | 1979-11-27 | Lafayette Pharmacal Inc. | Iodo-aryl carbonates for use in methods in radiography |
| US5250283A (en) * | 1990-03-28 | 1993-10-05 | Molecular Biosystems, Inc. | Organic contrast agent analog and method of making same |
| US5143715A (en) * | 1990-03-28 | 1992-09-01 | Molecular Biosystems, Inc. | Organic contrast agent analog and method of making same |
| US5463080A (en) * | 1992-08-27 | 1995-10-31 | Bracco International B.V. | 2,4,6-triiodo-1,3-benzenedicarboxylic acid compounds used as radiolabelling reagents |
| US5310538A (en) * | 1993-03-11 | 1994-05-10 | Sterling Winthrop Inc. | Compositions of iodophenoxy alkylene ethers in film-forming materials for visualization of the gastrointestinal tract |
| US5348727A (en) * | 1993-03-11 | 1994-09-20 | Sterling Winthrop Inc. | Compositions of iodophenoxy alkylene ethers for visualization of the gastrointestinal tract |
| US5492687A (en) * | 1993-03-11 | 1996-02-20 | Sterling Winthrop Inc. | Compositions of iodophenoxy alkylene ethers and pharmaceutically acceptable clays for visualization of the gastrointestinal tract |
| IT1316031B1 (it) * | 2000-12-19 | 2003-03-26 | Trelleborg Wheel Systems S P A | Procedimento per radiografare i tessuti di rinforzo tessili neipneumatici e nei manufatti in genere realizzati con detti tessuti. |
| BRPI0519754A2 (pt) | 2005-01-13 | 2009-03-10 | Cinv Ag | materiais compàsitos contendo nanopartÍculas de carbono |
| WO2008104588A1 (fr) * | 2007-02-28 | 2008-09-04 | Cinvention Ag | Système de culture à surface élevée |
| WO2008104599A1 (fr) * | 2007-02-28 | 2008-09-04 | Cinvention Ag | Sac à grande surface pour système de culture |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR6024559D0 (pt) * | 1959-12-08 | 1973-05-31 | Nyegaard & Co As | Processo para preparacao de novos derivados de acido 3 5-diamino-2 4 6-triiodo benzoico ou semi sais nao toxicos bem como de agentes ou meios de contraste para raios x baseados nos mesmos |
| US3721701A (en) * | 1970-06-19 | 1973-03-20 | Squibb & Sons Inc | Radiopaque triiodoalkylureido benzoic acids |
-
1970
- 1970-10-02 DE DE19702050217 patent/DE2050217A1/de active Pending
-
1971
- 1971-08-26 ZA ZA715707A patent/ZA715707B/xx unknown
- 1971-08-26 CS CS6127A patent/CS170548B2/cs unknown
- 1971-09-02 CH CH1295171A patent/CH582130A5/xx not_active IP Right Cessation
- 1971-09-06 DK DK436971A patent/DK131990C/da active
- 1971-09-06 FI FI712494A patent/FI51766C/fi active
- 1971-09-20 ES ES395601A patent/ES395601A1/es not_active Expired
- 1971-09-20 SU SU1698865A patent/SU501667A3/ru active
- 1971-09-20 GB GB4373371A patent/GB1369999A/en not_active Expired
- 1971-09-29 US US184941A patent/US3883578A/en not_active Expired - Lifetime
- 1971-09-30 ES ES395602A patent/ES395602A1/es not_active Expired
- 1971-09-30 DD DD161928A patent/DD96831A5/xx unknown
- 1971-09-30 BR BR006500/71A patent/BR7106500D0/pt unknown
- 1971-09-30 HU HUSC353A patent/HU162899B/hu unknown
- 1971-09-30 PL PL1971155404A patent/PL82567B1/pl unknown
- 1971-09-30 IT IT29316/71A patent/IT1019517B/it active
- 1971-09-30 PL PL1971150810A patent/PL81720B1/pl unknown
- 1971-10-01 SE SE7112468A patent/SE396073B/xx unknown
- 1971-10-01 BE BE773417A patent/BE773417A/fr unknown
- 1971-10-01 FR FR7135459A patent/FR2110179B1/fr not_active Expired
- 1971-10-01 IL IL37829A patent/IL37829A/en unknown
- 1971-10-01 AT AT850871A patent/AT309670B/de not_active IP Right Cessation
- 1971-10-01 AT AT797872A patent/AT319208B/de not_active IP Right Cessation
- 1971-10-01 CA CA124,211A patent/CA955938A/en not_active Expired
- 1971-10-01 NO NO3609/71A patent/NO135666C/no unknown
- 1971-10-01 NL NL7113557A patent/NL7113557A/xx not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU3302271A (en) | 1973-03-08 |
| CS170548B2 (fr) | 1976-08-27 |
| DE2050217A1 (de) | 1972-04-06 |
| FI51766C (fi) | 1977-04-12 |
| BR7106500D0 (pt) | 1973-08-16 |
| CH582130A5 (fr) | 1976-11-30 |
| SE396073B (sv) | 1977-09-05 |
| ZA715707B (en) | 1972-04-26 |
| IT1019517B (it) | 1977-11-30 |
| IL37829A0 (en) | 1971-12-29 |
| GB1369999A (en) | 1974-10-09 |
| FR2110179A1 (fr) | 1972-06-02 |
| DK131990C (da) | 1976-02-23 |
| CA955938A (en) | 1974-10-08 |
| AT309670B (de) | 1973-08-27 |
| ES395602A1 (es) | 1973-11-01 |
| NL7113557A (fr) | 1972-04-05 |
| ES395601A1 (es) | 1973-11-01 |
| SU501667A3 (ru) | 1976-01-30 |
| PL82567B1 (fr) | 1975-10-31 |
| FR2110179B1 (fr) | 1974-09-06 |
| US3883578A (en) | 1975-05-13 |
| DK131990B (da) | 1975-10-06 |
| NO135666C (fr) | 1977-05-11 |
| BE773417A (fr) | 1972-04-04 |
| AT319208B (de) | 1974-12-10 |
| HU162899B (fr) | 1973-04-28 |
| DD96831A5 (fr) | 1973-04-12 |
| FI51766B (fr) | 1976-12-31 |
| PL81720B1 (fr) | 1975-08-30 |
| IL37829A (en) | 1976-10-31 |
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