NO131329B - - Google Patents
Download PDFInfo
- Publication number
- NO131329B NO131329B NO4745/69A NO474569A NO131329B NO 131329 B NO131329 B NO 131329B NO 4745/69 A NO4745/69 A NO 4745/69A NO 474569 A NO474569 A NO 474569A NO 131329 B NO131329 B NO 131329B
- Authority
- NO
- Norway
- Prior art keywords
- water
- mixture
- trans
- acid
- isomers
- Prior art date
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 238000001640 fractional crystallisation Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 5
- 150000005075 thioxanthenes Chemical class 0.000 claims description 5
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 4
- 235000019253 formic acid Nutrition 0.000 claims description 4
- 239000012022 methylating agents Substances 0.000 claims description 4
- 230000011987 methylation Effects 0.000 claims description 4
- 238000007069 methylation reaction Methods 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 3
- 239000011541 reaction mixture Substances 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 34
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 22
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 238000002844 melting Methods 0.000 description 11
- 230000008018 melting Effects 0.000 description 11
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 150000003840 hydrochlorides Chemical class 0.000 description 7
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 7
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 7
- 238000001816 cooling Methods 0.000 description 6
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 6
- ZPEIMTDSQAKGNT-UHFFFAOYSA-N chlorpromazine Chemical compound C1=C(Cl)C=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 ZPEIMTDSQAKGNT-UHFFFAOYSA-N 0.000 description 5
- 229960001076 chlorpromazine Drugs 0.000 description 5
- -1 lithium aluminum hydride Chemical compound 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- WSPOMRSOLSGNFJ-UHFFFAOYSA-N chlorprothixene Chemical class C1=C(Cl)C=C2C(=CCCN(C)C)C3=CC=CC=C3SC2=C1 WSPOMRSOLSGNFJ-UHFFFAOYSA-N 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 238000001953 recrystallisation Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000012280 lithium aluminium hydride Substances 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- 230000004899 motility Effects 0.000 description 3
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229940095064 tartrate Drugs 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 229910000039 hydrogen halide Inorganic materials 0.000 description 2
- 239000012433 hydrogen halide Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
- 230000001035 methylating effect Effects 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 230000003285 pharmacodynamic effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 150000003892 tartrate salts Chemical class 0.000 description 2
- 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
- ISHNPOMLQRKDEC-UHFFFAOYSA-N 3-(2-methoxythioxanthen-9-ylidene)-n,n-dimethylpropan-1-amine Chemical compound C1=CC=C2C(=CCCN(C)C)C3=CC(OC)=CC=C3SC2=C1 ISHNPOMLQRKDEC-UHFFFAOYSA-N 0.000 description 1
- PQJUJGAVDBINPI-UHFFFAOYSA-N 9H-thioxanthene Chemical compound C1=CC=C2CC3=CC=CC=C3SC2=C1 PQJUJGAVDBINPI-UHFFFAOYSA-N 0.000 description 1
- 208000019901 Anxiety disease Diseases 0.000 description 1
- 208000000269 Hyperkinesis Diseases 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 206010029333 Neurosis Diseases 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 208000028017 Psychotic disease Diseases 0.000 description 1
- 238000003436 Schotten-Baumann reaction Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 230000003474 anti-emetic effect Effects 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229940125717 barbiturate Drugs 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 238000006480 benzoylation reaction Methods 0.000 description 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
- 230000004531 blood pressure lowering effect Effects 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 1
- 230000000147 hypnotic effect Effects 0.000 description 1
- 230000002631 hypothermal effect Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- JJSMYTSEKDSFKK-UHFFFAOYSA-N n,n-dimethyl-3-thioxanthen-9-ylidenepropan-1-amine Chemical compound C1=CC=C2C(=CCCN(C)C)C3=CC=CC=C3SC2=C1 JJSMYTSEKDSFKK-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 230000002048 spasmolytic effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- GPTCOAHVPPDCNL-UHFFFAOYSA-N thioxanthylium Chemical compound C1=CC=CC2=CC3=CC=CC=C3[S+]=C21 GPTCOAHVPPDCNL-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K9/00—Arc welding or cutting
- B23K9/12—Automatic feeding or moving of electrodes or work for spot or seam welding or cutting
- B23K9/122—Devices for guiding electrodes, e.g. guide tubes
- B23K9/123—Serving also as contacting devices supplying welding current to an electrode
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K9/00—Arc welding or cutting
- B23K9/16—Arc welding or cutting making use of shielding gas
- B23K9/173—Arc welding or cutting making use of shielding gas and of a consumable electrode
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K9/00—Arc welding or cutting
- B23K9/24—Features related to electrodes
- B23K9/28—Supporting devices for electrodes
- B23K9/29—Supporting devices adapted for making use of shielding means
- B23K9/291—Supporting devices adapted for making use of shielding means the shielding means being a gas
- B23K9/295—Supporting devices adapted for making use of shielding means the shielding means being a gas using consumable electrode-wire
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T403/00—Joints and connections
- Y10T403/70—Interfitted members
- Y10T403/7009—Rotary binding cam or wedge
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Mechanical Engineering (AREA)
- Arc Welding In General (AREA)
- Clamps And Clips (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US78115168A | 1968-12-04 | 1968-12-04 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO131329B true NO131329B (fr) | 1975-02-03 |
| NO131329C NO131329C (fr) | 1975-05-14 |
Family
ID=25121852
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO4745/69A NO131329C (fr) | 1968-12-04 | 1969-12-01 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US3514570A (fr) |
| JP (1) | JPS5516755B1 (fr) |
| CH (1) | CH509127A (fr) |
| DE (1) | DE1960758C3 (fr) |
| ES (1) | ES374180A1 (fr) |
| FR (1) | FR2025200A1 (fr) |
| GB (1) | GB1291500A (fr) |
| NL (1) | NL164781C (fr) |
| NO (1) | NO131329C (fr) |
| SE (1) | SE367561B (fr) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3882643A (en) * | 1973-05-04 | 1975-05-13 | Sweco Inc | Locking mechanism for a vibratory mill |
| US3851846A (en) * | 1973-06-04 | 1974-12-03 | Westinghouse Electric Corp | Support and leveling arrangement |
| US4245781A (en) * | 1979-03-28 | 1981-01-20 | Robertshaw Controls Company | Engine cooling system thermostat and method of making the same |
| IT1121634B (it) * | 1979-12-21 | 1986-04-02 | Sartori Francesco | Dispositivo per l accoppiamento rigido tra un manico ed il relativo attrezzo manuale e attrezzo dotato di tale dispositivo |
| GB2118879A (en) * | 1982-03-18 | 1983-11-09 | Hee Chye Seat | Electrode holder for welding or gouging |
| US4560858A (en) * | 1984-08-28 | 1985-12-24 | Ashton Wray, Jr. | Long wearing contact tip for inert gas arc welding |
| US4554432A (en) * | 1984-10-05 | 1985-11-19 | Dover Corporation | Components for gas metal arc welding gun |
| US5338917A (en) * | 1992-02-26 | 1994-08-16 | Tweco Products, Inc. | Ergonomic welding gun with quick disconnect cable assembly |
| US5440100A (en) * | 1992-02-26 | 1995-08-08 | Tweco Products, Inc. | Tips and diffusers for MIG welding guns |
| US5384444A (en) * | 1992-12-23 | 1995-01-24 | Basix Technologies Ltd. | Sleeve forming wire passageway around pickup |
| US5380973A (en) * | 1992-12-23 | 1995-01-10 | Basix Technologies Ltd. | Current pickup indexing apparatus |
| US5319175A (en) * | 1992-12-23 | 1994-06-07 | Basix Industries Ltd. | Apparatus for transferring electrical current to and from a moving wire |
| US5430268A (en) * | 1992-12-23 | 1995-07-04 | Basix Technologies Ltd. | Method and apparatus for adjusting and replacing EDM components from the guide assembly working end |
| US5384447A (en) * | 1993-01-06 | 1995-01-24 | Bernard Welding Equipment Company | Electric arc welding gun |
| US5366392A (en) * | 1993-01-21 | 1994-11-22 | Bernard Welding Company | Quick connect electrical cable connector |
| US5760373A (en) * | 1995-12-27 | 1998-06-02 | Miller Electric Manufacturing Company | Enhanced contact area quick release mig gun tip |
| US5841105A (en) * | 1996-01-16 | 1998-11-24 | Delaware Capital Formation, Inc. | Automatic mig welding torch and method of assembly |
| US5866874A (en) * | 1996-04-17 | 1999-02-02 | Delaware Capital Formation, Inc. | Robotic welding torch and method of assembly |
| FR2781171B1 (fr) * | 1998-07-20 | 2000-08-18 | Soudure Autogene Francaise | Buse de soudage a l'arc electrique de diametre et d'epaisseur controles |
| US6689987B2 (en) | 2001-02-16 | 2004-02-10 | Illinois Tool Works Inc. | Welding contact tip with rolled threads |
| US6525297B2 (en) | 2001-02-16 | 2003-02-25 | Illinois Tool Works Inc. | Mig gun nozzle with reduced cross-sectional area at the front |
| US6444950B1 (en) | 2001-02-16 | 2002-09-03 | Illinois Tool Works, Inc. | MIG gun nozzle with self centering, quick release screw and reduced cross-sectional area at the front |
| EP1450981B1 (fr) * | 2001-11-07 | 2011-04-27 | Commonwealth Scientific And Industrial Research Organisation | Pointe contact pour soudage à l'arc électrique employant un fil |
| US6847009B2 (en) * | 2002-05-10 | 2005-01-25 | Tweco Products, Inc. | Welding contact tip and diffuser |
| US20060076319A1 (en) * | 2004-10-07 | 2006-04-13 | Bechtel Bwxt Idaho, Llc | Arc welding apparatus |
| US9364915B2 (en) | 2013-03-15 | 2016-06-14 | Lincoln Global, Inc. | Welding diffuser insert |
| FR3015320B1 (fr) * | 2013-12-24 | 2016-06-10 | Gaztransport Et Technigaz | Machine de soudure a arc electrique |
| US20170080510A1 (en) * | 2015-09-18 | 2017-03-23 | Illinois Tool Works Inc. | Contact tip and coupling assembly of a welding torch |
| US10773332B2 (en) * | 2015-09-18 | 2020-09-15 | Illinois Tool Works Inc. | Contact tip and receiving assembly of a welding torch |
| US10583514B2 (en) * | 2015-09-18 | 2020-03-10 | Illinois Tool Works Inc. | Contact tip rotary lock of a welding torch |
| US10710189B2 (en) | 2017-01-31 | 2020-07-14 | Illinois Tool Works Inc. | Tip-retention device for use with a welding system |
| US10882133B2 (en) | 2017-01-31 | 2021-01-05 | Illinois Tool Works Inc. | Tip-retention device for use with a welding system |
| US11103949B2 (en) | 2017-04-03 | 2021-08-31 | Illinois Tool Works Inc. | Quick connect configurations for welding necks and gas diffusers |
| US11938573B2 (en) | 2017-04-19 | 2024-03-26 | Illlinois Tool Works Inc. | Welding systems for cooling welding contact tips |
| US11192202B2 (en) | 2018-02-06 | 2021-12-07 | Illinois Tool Works Inc. | Gas diffuser assemblies for nozzle assemblies having multiple attachment methods |
| US11268693B2 (en) | 2018-02-06 | 2022-03-08 | Illinois Tool Works Inc. | Nozzle assemblies having multiple attachment methods |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2949692A (en) * | 1958-02-24 | 1960-08-23 | Bromo Mint Company Inc | Construction toy |
| US3128370A (en) * | 1963-06-21 | 1964-04-07 | Machinery And Welder Corp | Gas cup assembly for welding gun |
| NL6411133A (fr) * | 1963-09-27 | 1965-03-29 | ||
| US3398231A (en) * | 1964-08-18 | 1968-08-20 | Air Reduction | Liquid cooling of oppositely charged conductive members with elongated insulated coollant passage between |
-
1968
- 1968-12-04 US US781151A patent/US3514570A/en not_active Expired - Lifetime
-
1969
- 1969-09-18 JP JP7432669A patent/JPS5516755B1/ja active Pending
- 1969-12-01 GB GB58650/69A patent/GB1291500A/en not_active Expired
- 1969-12-01 NO NO4745/69A patent/NO131329C/no unknown
- 1969-12-02 NL NL6918063.A patent/NL164781C/xx not_active IP Right Cessation
- 1969-12-03 SE SE16641/69A patent/SE367561B/xx unknown
- 1969-12-03 FR FR6941689A patent/FR2025200A1/fr not_active Withdrawn
- 1969-12-03 DE DE1960758A patent/DE1960758C3/de not_active Expired
- 1969-12-03 CH CH1802469A patent/CH509127A/de not_active IP Right Cessation
- 1969-12-03 ES ES374180A patent/ES374180A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL6918063A (fr) | 1970-06-08 |
| DE1960758C3 (de) | 1980-09-04 |
| DE1960758B2 (de) | 1979-12-13 |
| NL164781B (nl) | 1980-09-15 |
| US3514570A (en) | 1970-05-26 |
| SE367561B (fr) | 1974-06-04 |
| JPS5516755B1 (fr) | 1980-05-06 |
| CH509127A (de) | 1971-06-30 |
| ES374180A1 (es) | 1972-04-01 |
| DE1960758A1 (de) | 1970-07-16 |
| NO131329C (fr) | 1975-05-14 |
| GB1291500A (en) | 1972-10-04 |
| FR2025200A1 (fr) | 1970-09-04 |
| NL164781C (nl) | 1981-02-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO131329B (fr) | ||
| CZ292820B6 (cs) | Způsob přípravy clopidogrelu a jeho analogů | |
| NO153082B (no) | Apparat for stapping av en rynket roerformet omhylling | |
| DE2065636C3 (de) | Tricyclische Verbindungen, Verfahren zu ihrer Herstellung und diese enthaltende Arzneimittel | |
| DE1275069B (de) | 1-(3', 5'-Dihydroxyphenyl)-1-hydroxy-2-isopropylaminoalkane und Verfahren zu ihrer Herstellung | |
| NO131759B (fr) | ||
| US2185220A (en) | Medicinal agent | |
| US2229187A (en) | Amino-alcohol and a process for its production | |
| US3557127A (en) | Substituted cyclohexenes,derivatives thereof and processes for obtaining same | |
| NO140348B (no) | Analogifremgangsmaate til fremstilling av nye terapeutisk aktive 3-(amino-2-hydroksypropoksy)-isoindolin-1-on-forbindelser | |
| DE2623314C2 (de) | 1-Aryloxy-2-Hydroxy-3-aminopropane, Verfahren zu ihrer Herstellung und diese enthaltende Arzneimittel | |
| US4683245A (en) | Laevorotatory antipode of moprolol as an antihypertensive | |
| CH628346A5 (de) | Verfahren zur herstellung neuer xanthinderivate. | |
| US2625567A (en) | 1-benzyloxy-2-alkylaminoindanes | |
| Heymann et al. | Derivatives of p, p'-Diaminodiphenyl Sulfone1a | |
| US3086972A (en) | Aza-thiaxanthene derivatives | |
| US2265207A (en) | D-lysergic acid - d - l-bjtdroxybutyl | |
| DE1206437B (de) | Verfahren zur Herstellung von neuen 4-Aza-thioxanthenderivaten | |
| US2841609A (en) | Dextro-6-dimethylamino-4, 4-diphenyl-5-methyl-3-hexanone, salts thereof, and preparation thereof | |
| US2265217A (en) | D - lysergic acid - | |
| DE1165032B (de) | Verfahren zur Herstellung von Thioxanthenderivaten und deren Salzen | |
| US3345411A (en) | 2-alkyl-3, 3-diphenyl-propen-(2)-yl-amines and salts thereof | |
| US2773901A (en) | The resolution and optical isomers of 6-dimethylamino-4, 4-diphenyl-5-methyl-3-hexanone | |
| NO137964B (no) | Analogifremgangsm}te for fremstilling av terapeutisk virksomme norbornanderivater | |
| US3067247A (en) | Process for preparing l(+)-3, 5-diiodothyronine |