NO136595B - - Google Patents
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- Publication number
- NO136595B NO136595B NO741324A NO741324A NO136595B NO 136595 B NO136595 B NO 136595B NO 741324 A NO741324 A NO 741324A NO 741324 A NO741324 A NO 741324A NO 136595 B NO136595 B NO 136595B
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- general formula
- denotes
- group
- alkoxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 6
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 230000008095 long lasting therapeutic effect Effects 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- YAZSBRQTAHVVGE-UHFFFAOYSA-N 2-aminobenzenesulfonamide Chemical class NC1=CC=CC=C1S(N)(=O)=O YAZSBRQTAHVVGE-UHFFFAOYSA-N 0.000 claims description 2
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical class NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims description 2
- 150000001447 alkali salts Chemical class 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 238000006798 ring closing metathesis reaction Methods 0.000 claims 1
- 239000000243 solution Substances 0.000 description 17
- 238000002844 melting Methods 0.000 description 13
- 230000008018 melting Effects 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- -1 2-sulfanilamido-methoxy-pyrimidine Chemical compound 0.000 description 8
- 239000008280 blood Substances 0.000 description 7
- 210000004369 blood Anatomy 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- 229960000583 acetic acid Drugs 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229940124530 sulfonamide Drugs 0.000 description 5
- 150000003456 sulfonamides Chemical class 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000012362 glacial acetic acid Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 4
- KAHHAPNRIQLSFT-UHFFFAOYSA-N 5-methoxypyrimidin-2-amine Chemical compound COC1=CN=C(N)N=C1 KAHHAPNRIQLSFT-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 150000003230 pyrimidines Chemical class 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- XGOQVDSNQJJHTN-VRHVFUOLSA-N busam Chemical compound O1C(=O)\C=C/C=C\C(C(O)C)OCC(O)C(C)(OC(C)=O)CC(=O)OCC23CCC(C)=CC2OC2CC1C3(C)C21CO1 XGOQVDSNQJJHTN-VRHVFUOLSA-N 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- NCBOVAWEMBIIFK-UHFFFAOYSA-N (4-nitrophenyl) thiohypochlorite Chemical compound [O-][N+](=O)C1=CC=C(SCl)C=C1 NCBOVAWEMBIIFK-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-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
- GFGSMAWCAWBBPK-UHFFFAOYSA-N 2-amino-N-(5-propan-2-yloxypyrimidin-2-yl)benzenesulfonamide Chemical compound S(=O)(C=1C(=CC=CC=1)N)(=O)NC1=NC=C(C=N1)OC(C)C GFGSMAWCAWBBPK-UHFFFAOYSA-N 0.000 description 1
- RSUBGBZOMBTDTI-UHFFFAOYSA-N 2-chloro-5-methoxypyrimidine Chemical compound COC1=CN=C(Cl)N=C1 RSUBGBZOMBTDTI-UHFFFAOYSA-N 0.000 description 1
- ZAJAQTYSTDTMCU-UHFFFAOYSA-N 3-aminobenzenesulfonic acid Chemical compound NC1=CC=CC(S(O)(=O)=O)=C1 ZAJAQTYSTDTMCU-UHFFFAOYSA-N 0.000 description 1
- HJPXRPSGMWLORH-UHFFFAOYSA-N 4,6-dichloro-5-methoxypyrimidin-2-amine Chemical compound COC1=C(Cl)N=C(N)N=C1Cl HJPXRPSGMWLORH-UHFFFAOYSA-N 0.000 description 1
- IQIXOVZKIWONBZ-UHFFFAOYSA-N 4-aminobenzenesulfonamide;sodium Chemical compound [Na].NC1=CC=C(S(N)(=O)=O)C=C1 IQIXOVZKIWONBZ-UHFFFAOYSA-N 0.000 description 1
- NGWGYIGTWBAKAN-UHFFFAOYSA-N 5-ethoxypyrimidin-2-amine Chemical compound CCOC1=CN=C(N)N=C1 NGWGYIGTWBAKAN-UHFFFAOYSA-N 0.000 description 1
- OKESCPJZXOUZBO-UHFFFAOYSA-N 5-ethoxypyrimidine Chemical compound CCOC1=CN=CN=C1 OKESCPJZXOUZBO-UHFFFAOYSA-N 0.000 description 1
- UVVXVOXBBHGUIX-UHFFFAOYSA-N 5-propan-2-yloxypyrimidin-2-amine Chemical compound CC(C)OC1=CN=C(N)N=C1 UVVXVOXBBHGUIX-UHFFFAOYSA-N 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- PAHOLLKJXZDSIA-UHFFFAOYSA-N N-[4-[(4-hydroxy-5-methoxy-6-oxo-1H-pyrimidin-2-yl)sulfamoyl]phenyl]acetamide Chemical compound COc1c(O)nc(NS(=O)(=O)c2ccc(NC(C)=O)cc2)[nH]c1=O PAHOLLKJXZDSIA-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- XUOBDTNYHLQJCA-UHFFFAOYSA-N S(=O)(C=1C(=CC=CC=1)N)(=O)NC1=NC=C(C=N1)OCCCC Chemical compound S(=O)(C=1C(=CC=CC=1)N)(=O)NC1=NC=C(C=N1)OCCCC XUOBDTNYHLQJCA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 150000008331 benzenesulfonamides Chemical class 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- ORXJMBXYSGGCHG-UHFFFAOYSA-N dimethyl 2-methoxypropanedioate Chemical compound COC(=O)C(OC)C(=O)OC ORXJMBXYSGGCHG-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- CGRKCGWEOIQFRD-UHFFFAOYSA-N sodium;(4-aminophenyl)sulfonylazanide Chemical compound [Na+].NC1=CC=C(S([NH-])(=O)=O)C=C1 CGRKCGWEOIQFRD-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229960004306 sulfadiazine Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/02—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations
- G01N35/025—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations having a carousel or turntable for reaction cells or cuvettes
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/02—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations
- G01N35/04—Details of the conveyor system
- G01N2035/0439—Rotary sample carriers, i.e. carousels
- G01N2035/0446—Combinations of the above
- G01N2035/0448—Combinations of the above composed of interchangeable ring elements
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Optical Measuring Cells (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00350860A US3854508A (en) | 1973-04-13 | 1973-04-13 | Automated sample-reagent loader |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO741324L NO741324L (no) | 1974-10-15 |
| NO136595B true NO136595B (xx) | 1977-06-20 |
| NO136595C NO136595C (no) | 1977-09-28 |
Family
ID=23378508
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO741324A NO136595C (no) | 1973-04-13 | 1974-04-10 | Anordning for automatisk fylling av en rotor til en fotometeranalysator. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US3854508A (xx) |
| JP (1) | JPS5010181A (xx) |
| AT (1) | AT334116B (xx) |
| BE (1) | BE813661A (xx) |
| CA (1) | CA991885A (xx) |
| CH (1) | CH576136A5 (xx) |
| DE (1) | DE2416899A1 (xx) |
| ES (1) | ES425009A1 (xx) |
| FR (1) | FR2225745B1 (xx) |
| GB (1) | GB1428067A (xx) |
| IL (1) | IL44583A (xx) |
| IN (1) | IN141223B (xx) |
| IT (1) | IT1007912B (xx) |
| NL (1) | NL7404970A (xx) |
| NO (1) | NO136595C (xx) |
| SE (1) | SE388043B (xx) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4123173A (en) * | 1976-06-09 | 1978-10-31 | Electro-Nucleonics, Inc. | Rotatable flexible cuvette arrays |
| LU80809A1 (fr) * | 1979-01-19 | 1980-08-08 | C R T | Procede pour mesurer le temps de regeneration de plaquettes sanguines et dispsitif de dosage pouvant eventuellement etre utilise pour cette mesure |
| US4344768A (en) * | 1981-03-27 | 1982-08-17 | Baker Instruments Corp. | Automatic pipettor |
| DE3315868C2 (de) * | 1983-04-30 | 1985-09-26 | Kuiper Medische Instrumenten, Zwolle | Vorrichtung zum Reinigen von scheibenförmingen Analysencuvetten |
| US4740472A (en) * | 1985-08-05 | 1988-04-26 | The United States Of America As Represented By The United States Department Of Energy | Method and apparatus for automated processing and aliquoting of whole blood samples for analysis in a centrifugal fast analyzer |
| US4847205A (en) * | 1987-04-08 | 1989-07-11 | Martin Marietta Energy Systems, Inc. | Device and method for automated separation of a sample of whole blood into aliquots |
| US4855110A (en) * | 1987-05-06 | 1989-08-08 | Abbott Laboratories | Sample ring for clinical analyzer network |
| US6436349B1 (en) | 1991-03-04 | 2002-08-20 | Bayer Corporation | Fluid handling apparatus for an automated analyzer |
| US5525304A (en) * | 1994-06-24 | 1996-06-11 | Pasteur Sanofi Diagnostics | Apparatus for automated chemical analysis with variable reagents |
| EP1493014A2 (en) | 2001-04-11 | 2005-01-05 | Burstein Technologies, Inc. | Multi-parameter assays including analysis discs and methods relating thereto |
| ES2398488T3 (es) | 2008-03-21 | 2013-03-19 | Abbott Point Of Care, Inc. | Método y aparato para determinar los índices de células sanguíneas rojas en una muestra de sangre utilizando la pigmentación intrínseca de la hemoglobina contenida en células sanguíneas rojas |
| CN105425715B (zh) * | 2015-12-11 | 2018-02-06 | 无锡职业技术学院 | 食品样品前处理仪器的控制电路及控制方法 |
| CN112857937B (zh) * | 2021-01-25 | 2022-07-01 | 吉林省吉科软信息技术有限公司 | 一种基于食品安全的自动化农残检测系统 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1051956A (xx) * | 1964-04-01 | |||
| SE313936B (xx) * | 1966-06-22 | 1969-08-25 | Autokemi Ab | |
| US3636777A (en) * | 1969-09-16 | 1972-01-25 | Vision Lab Inc | Laboratory beaker transporter and elevator |
| US3776700A (en) * | 1971-12-08 | 1973-12-04 | Linbro Chem Co Inc | Serial dilution apparatus |
-
1973
- 1973-04-13 US US00350860A patent/US3854508A/en not_active Expired - Lifetime
-
1974
- 1974-03-22 CA CA195,694A patent/CA991885A/en not_active Expired
- 1974-03-27 GB GB1350574A patent/GB1428067A/en not_active Expired
- 1974-03-28 IN IN692/CAL/1974A patent/IN141223B/en unknown
- 1974-04-02 CH CH462874A patent/CH576136A5/xx not_active IP Right Cessation
- 1974-04-05 ES ES425009A patent/ES425009A1/es not_active Expired
- 1974-04-05 IL IL44583A patent/IL44583A/en unknown
- 1974-04-06 DE DE2416899A patent/DE2416899A1/de active Pending
- 1974-04-08 SE SE7404747A patent/SE388043B/xx unknown
- 1974-04-10 NO NO741324A patent/NO136595C/no unknown
- 1974-04-11 NL NL7404970A patent/NL7404970A/xx unknown
- 1974-04-11 AT AT304174A patent/AT334116B/de not_active IP Right Cessation
- 1974-04-12 FR FR7412964A patent/FR2225745B1/fr not_active Expired
- 1974-04-12 BE BE143151A patent/BE813661A/xx unknown
- 1974-04-12 IT IT21381/74A patent/IT1007912B/it active
- 1974-04-13 JP JP49042105A patent/JPS5010181A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| IL44583A (en) | 1976-10-31 |
| FR2225745A1 (xx) | 1974-11-08 |
| BE813661A (fr) | 1974-07-31 |
| IL44583A0 (en) | 1974-06-30 |
| SE388043B (sv) | 1976-09-20 |
| NO136595C (no) | 1977-09-28 |
| US3854508A (en) | 1974-12-17 |
| IN141223B (xx) | 1977-02-05 |
| CH576136A5 (xx) | 1976-05-31 |
| NO741324L (no) | 1974-10-15 |
| IT1007912B (it) | 1976-10-30 |
| CA991885A (en) | 1976-06-29 |
| ES425009A1 (es) | 1977-07-01 |
| FR2225745B1 (xx) | 1978-01-20 |
| GB1428067A (en) | 1976-03-17 |
| DE2416899A1 (de) | 1974-11-28 |
| JPS5010181A (xx) | 1975-02-01 |
| ATA304174A (de) | 1976-04-15 |
| AT334116B (de) | 1976-12-27 |
| NL7404970A (xx) | 1974-10-15 |
| AU6774674A (en) | 1975-10-16 |
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