NO132631B - - Google Patents
Download PDFInfo
- Publication number
- NO132631B NO132631B NO71370A NO37071A NO132631B NO 132631 B NO132631 B NO 132631B NO 71370 A NO71370 A NO 71370A NO 37071 A NO37071 A NO 37071A NO 132631 B NO132631 B NO 132631B
- Authority
- NO
- Norway
- Prior art keywords
- propanetriamine
- bis
- methyl
- triamines
- approx
- Prior art date
Links
- -1 2-hydroxyalkyl Chemical group 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 238000005984 hydrogenation reaction Methods 0.000 claims description 4
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 230000000361 pesticidal effect Effects 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- DKYBVKMIZODYKL-UHFFFAOYSA-N 1,3-diazinane Chemical class C1CNCNC1 DKYBVKMIZODYKL-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 3
- 239000007868 Raney catalyst Substances 0.000 description 3
- 229910000564 Raney nickel Inorganic materials 0.000 description 3
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- DTOUUUZOYKYHEP-UHFFFAOYSA-N 1,3-bis(2-ethylhexyl)-5-methyl-1,3-diazinan-5-amine Chemical compound CCCCC(CC)CN1CN(CC(CC)CCCC)CC(C)(N)C1 DTOUUUZOYKYHEP-UHFFFAOYSA-N 0.000 description 1
- BKXBSQULLDQCLC-UHFFFAOYSA-N 1,3-diazinan-5-amine Chemical class NC1CNCNC1 BKXBSQULLDQCLC-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 description 1
- CMIUVKCNCRQWIG-UHFFFAOYSA-N 5-nitro-1,3-diazinane Chemical class [O-][N+](=O)C1CNCNC1 CMIUVKCNCRQWIG-UHFFFAOYSA-N 0.000 description 1
- 241000194032 Enterococcus faecalis Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 241000187488 Mycobacterium sp. Species 0.000 description 1
- 241000606860 Pasteurella Species 0.000 description 1
- 241000607764 Shigella dysenteriae Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 241000194017 Streptococcus Species 0.000 description 1
- 208000025087 Yersinia pseudotuberculosis infectious disease Diseases 0.000 description 1
- 238000002814 agar dilution Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- PZZICILSCNDOKK-UHFFFAOYSA-N propane-1,2,3-triamine Chemical compound NCC(N)CN PZZICILSCNDOKK-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 229940007046 shigella dysenteriae Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B13/00—Oxygen; Ozone; Oxides or hydroxides in general
- C01B13/14—Methods for preparing oxides or hydroxides in general
- C01B13/20—Methods for preparing oxides or hydroxides in general by oxidation of elements in the gaseous state; by oxidation or hydrolysis of compounds in the gaseous state
- C01B13/22—Methods for preparing oxides or hydroxides in general by oxidation of elements in the gaseous state; by oxidation or hydrolysis of compounds in the gaseous state of halides or oxyhalides
- C01B13/30—Removal and cooling of the oxide-containing suspension
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Oxygen, Ozone, And Oxides In General (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2005010A DE2005010B2 (de) | 1970-02-04 | 1970-02-04 | Vorrichtung zum Abkühlen und Naßabscheiden heißer metalloxidhaltiger Reaktionsgase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO132631B true NO132631B (fi) | 1975-09-01 |
| NO132631C NO132631C (fi) | 1975-12-10 |
Family
ID=5761391
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO71370A NO132631C (fi) | 1970-02-04 | 1971-02-02 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3681895A (fi) |
| JP (1) | JPS512078B1 (fi) |
| BE (1) | BE762515A (fi) |
| CA (1) | CA959411A (fi) |
| DE (1) | DE2005010B2 (fi) |
| ES (1) | ES387947A1 (fi) |
| FI (1) | FI54587C (fi) |
| FR (1) | FR2078211A5 (fi) |
| GB (1) | GB1339919A (fi) |
| NO (1) | NO132631C (fi) |
| ZA (1) | ZA71343B (fi) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2923182A1 (de) * | 1979-06-08 | 1980-12-18 | Degussa | Verfahren zur pyrogenen herstellung von feinstteiligem oxid eines matalls und/oder eines metalloids |
| US4578090A (en) * | 1984-10-15 | 1986-03-25 | Kerr-Mcgee Chemical Corporation | Method for processing gaseous effluent streams recovered from the vapor phase oxidation of metal halides |
| DE3939057A1 (de) * | 1989-11-25 | 1991-05-29 | Bayer Ag | Vorrichtung fuer den stoffaustausch zwischen einem heissen gasstrom und einer fluessigkeit |
| US5354364A (en) * | 1993-06-23 | 1994-10-11 | The Babcock & Wilcox Company | High efficiency advanced dry scrubber |
| US5643344A (en) * | 1995-02-14 | 1997-07-01 | The Babcock & Wilcox Company | Dry scrubber with forced recirculation |
| DE19751851A1 (de) * | 1997-11-22 | 1999-05-27 | Babcock Anlagen Gmbh | Aerosolminderung |
| GB0005231D0 (en) * | 2000-03-03 | 2000-04-26 | Boc Group Plc | Abatement of semiconductor processing gases |
| US6699317B1 (en) * | 2003-03-27 | 2004-03-02 | Kerr-Mcgee Chemical, Llc | Titanium dioxide slurries |
| US7771514B1 (en) * | 2004-02-03 | 2010-08-10 | Airgard, Inc. | Apparatus and method for providing heated effluent gases to a scrubber |
| US7611684B2 (en) * | 2006-08-09 | 2009-11-03 | Airgard, Inc. | Effluent gas scrubber and method of scrubbing effluent gasses |
| US7854792B2 (en) * | 2008-09-17 | 2010-12-21 | Airgard, Inc. | Reactive gas control |
-
1970
- 1970-02-04 DE DE2005010A patent/DE2005010B2/de not_active Withdrawn
-
1971
- 1971-01-11 CA CA102,322A patent/CA959411A/en not_active Expired
- 1971-01-12 GB GB138871A patent/GB1339919A/en not_active Expired
- 1971-01-15 US US106755A patent/US3681895A/en not_active Expired - Lifetime
- 1971-01-19 ZA ZA710343A patent/ZA71343B/xx unknown
- 1971-01-28 FI FI225/71A patent/FI54587C/fi active
- 1971-02-02 NO NO71370A patent/NO132631C/no unknown
- 1971-02-04 FR FR7103823A patent/FR2078211A5/fr not_active Expired
- 1971-02-04 JP JP46004069A patent/JPS512078B1/ja active Pending
- 1971-02-04 BE BE762515A patent/BE762515A/xx unknown
- 1971-02-04 ES ES387947A patent/ES387947A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NO132631C (fi) | 1975-12-10 |
| DE2005010B2 (de) | 1979-08-02 |
| CA959411A (en) | 1974-12-17 |
| BE762515A (fr) | 1971-08-04 |
| JPS512078B1 (fi) | 1976-01-22 |
| ZA71343B (en) | 1972-04-26 |
| FI54587B (fi) | 1978-09-29 |
| DE2005010A1 (fi) | 1971-08-12 |
| FR2078211A5 (fi) | 1971-11-05 |
| FI54587C (fi) | 1979-01-10 |
| GB1339919A (en) | 1973-12-05 |
| ES387947A1 (es) | 1973-06-01 |
| US3681895A (en) | 1972-08-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO132631B (fi) | ||
| GB1071478A (en) | Dinitroaniline derivatives and herbicidal compositions containing them | |
| Badger et al. | Isolation of tetrahydroharman from Petalostyles labicheoides | |
| US2902514A (en) | Bis-iminodiacetamidoximes | |
| GB794395A (en) | Plant growth control and herbicidal composition and process of using the same | |
| US3359315A (en) | Reduction of aromatic nitro compounds to aromatic amines | |
| Brown et al. | Studies in Stereochemistry. VIII. The Effect of F-Strain on the Relative Base Strengths of the Isopropyl-and t-Butylamines | |
| CN108290825B (zh) | 烷醇胺组合物中减色的方法和由此制得的组合物 | |
| Fegley et al. | Chemistry of 1, 4-Diamino-1, 3-butadienes. II. A New Synthesis of N-Substituted Pyrroles1 | |
| US3072672A (en) | Certain oxazolidininone-2 and pyrrolidinone-2 derivatives of aromatic sulfonamides and process | |
| US3154561A (en) | Organic sulfide derivatives of decaborane | |
| US3049559A (en) | Ureas | |
| Strauss et al. | Condensation-cyclization reactions of electron-deficient aromatics. VII. Kinetics and mechanism of carbanionic. sigma.-complex formation and cyclization | |
| RU2478634C2 (ru) | СПОСОБ ПОЛУЧЕНИЯ α,ω-БИС-(1,5,3-ДИТИАЗЕПИНАН-3-ИЛ)АЛКАНОВ | |
| GB1000194A (en) | Aziridine compounds and method of preparing same | |
| US3068274A (en) | (2-cyano-3-amino)thio-2-alkenamides | |
| US3551490A (en) | Method for preparing tetramethyl-guanidine | |
| US3210420A (en) | Haloaromatic amides of propiolic acid | |
| US2615920A (en) | Conversion of nitroamines to lower amines | |
| Andrisano et al. | Elimination of the alkylamino group from diastereoisomeric 2-benzenesulphonyl-3-dimethylaminobutanes | |
| US3178465A (en) | Linear polyacetylenic isocyanato compounds | |
| US2868791A (en) | Process for the production of substituted piperazines | |
| Van Tilborg et al. | The chemistry of small ring compounds. Part 25. 1‐Acetoxycyclopropanol, a convenient precursor for cyclopropanone | |
| US2894034A (en) | Stabilized phenylene diamines | |
| US3038009A (en) | N-(beta, beta, beta-trinitroethyl)-4, 4, 4-trinitrobutyramide |