NO124601B - - Google Patents
Download PDFInfo
- Publication number
- NO124601B NO124601B NO16687667A NO16687667A NO124601B NO 124601 B NO124601 B NO 124601B NO 16687667 A NO16687667 A NO 16687667A NO 16687667 A NO16687667 A NO 16687667A NO 124601 B NO124601 B NO 124601B
- Authority
- NO
- Norway
- Prior art keywords
- oil
- oils
- radicals
- denotes
- additives
- Prior art date
Links
- 239000003921 oil Substances 0.000 claims description 43
- 239000000654 additive Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000010687 lubricating oil Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 230000000996 additive effect Effects 0.000 claims description 4
- 229920000768 polyamine Polymers 0.000 claims description 4
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- XXAJVSYCSGAYCG-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethanol Chemical compound C1=CC=C2SC(SCO)=NC2=C1 XXAJVSYCSGAYCG-UHFFFAOYSA-N 0.000 claims description 2
- DQGBSPYYYCIELK-UHFFFAOYSA-N 1,1-bis(sulfanylidene)-1,3-benzothiazole Chemical compound C1=CC=C2S(=S)(=S)C=NC2=C1 DQGBSPYYYCIELK-UHFFFAOYSA-N 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 239000010723 turbine oil Substances 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000002480 mineral oil Substances 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 4
- -1 2-ethyl hexyl Chemical group 0.000 description 3
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 3
- 230000006698 induction Effects 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 240000005020 Acaciella glauca Species 0.000 description 2
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 235000003499 redwood Nutrition 0.000 description 2
- 150000003336 secondary aromatic amines Chemical class 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UTGQNNCQYDRXCH-UHFFFAOYSA-N N,N'-diphenyl-1,4-phenylenediamine Chemical compound C=1C=C(NC=2C=CC=CC=2)C=CC=1NC1=CC=CC=C1 UTGQNNCQYDRXCH-UHFFFAOYSA-N 0.000 description 1
- 241001061127 Thione Species 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000013556 antirust agent Substances 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000003863 metallic catalyst Substances 0.000 description 1
- 229910052752 metalloid Inorganic materials 0.000 description 1
- 150000002738 metalloids Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- AJTWXZCTAWXTLG-UHFFFAOYSA-N n-heptyl-n-phenylaniline Chemical compound C=1C=CC=CC=1N(CCCCCCC)C1=CC=CC=C1 AJTWXZCTAWXTLG-UHFFFAOYSA-N 0.000 description 1
- CVVFFUKULYKOJR-UHFFFAOYSA-N n-phenyl-4-propan-2-yloxyaniline Chemical compound C1=CC(OC(C)C)=CC=C1NC1=CC=CC=C1 CVVFFUKULYKOJR-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
- C07D239/49—Two nitrogen atoms with an aralkyl radical, or substituted aralkyl radical, attached in position 5, e.g. trimethoprim
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/50—Three nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Liquid Crystal Substances (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Lubricants (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO377771A NO133550C (fr) | 1966-02-19 | 1971-10-13 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB737666A GB1128234A (en) | 1966-02-19 | 1966-02-19 | 5-benzylpyrimidine derivatives and process for the preparation thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO124601B true NO124601B (fr) | 1972-05-08 |
Family
ID=9831956
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO16687667A NO124601B (fr) | 1966-02-19 | 1967-02-16 |
Country Status (16)
| Country | Link |
|---|---|
| AT (2) | AT275534B (fr) |
| BE (1) | BE694244A (fr) |
| CA (1) | CA977754A (fr) |
| CH (2) | CH513179A (fr) |
| DE (2) | DE1795635C3 (fr) |
| DK (2) | DK120344B (fr) |
| ES (1) | ES336945A1 (fr) |
| FI (1) | FI49714C (fr) |
| FR (1) | FR6595M (fr) |
| GB (1) | GB1128234A (fr) |
| GR (1) | GR33641B (fr) |
| IL (1) | IL27424A (fr) |
| MY (1) | MY7100226A (fr) |
| NL (1) | NL146811B (fr) |
| NO (1) | NO124601B (fr) |
| SE (2) | SE338998B (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE789904A (fr) * | 1971-10-12 | 1973-04-10 | Wellcome Found | Procedes de synthese organique |
| PT69656A (en) * | 1978-05-24 | 1979-06-01 | Wellcome Found | Benzylpyrimidine compositions |
| DE2944145A1 (de) | 1979-11-02 | 1981-05-14 | Dynamit Nobel Ag, 5210 Troisdorf | Verfahren zur herstellung von 2,4-diaminopyrimidin |
-
1966
- 1966-02-19 GB GB737666A patent/GB1128234A/en not_active Expired
-
1967
- 1967-02-13 GR GR670133641A patent/GR33641B/el unknown
- 1967-02-13 IL IL2742467A patent/IL27424A/xx unknown
- 1967-02-15 CA CA983,015A patent/CA977754A/en not_active Expired
- 1967-02-16 AT AT409368A patent/AT275534B/de active
- 1967-02-16 NO NO16687667A patent/NO124601B/no unknown
- 1967-02-16 AT AT153867A patent/AT270653B/de active
- 1967-02-17 FI FI48067A patent/FI49714C/fi active
- 1967-02-17 CH CH191468A patent/CH513179A/de not_active IP Right Cessation
- 1967-02-17 DE DE19671795635 patent/DE1795635C3/de not_active Expired
- 1967-02-17 CH CH237967A patent/CH511239A/de not_active IP Right Cessation
- 1967-02-17 NL NL6702397A patent/NL146811B/xx not_active IP Right Cessation
- 1967-02-17 DE DE1967W0043385 patent/DE1720012B2/de active Granted
- 1967-02-17 BE BE694244D patent/BE694244A/xx not_active IP Right Cessation
- 1967-02-17 ES ES336945A patent/ES336945A1/es not_active Expired
- 1967-02-20 DK DK91167A patent/DK120344B/da not_active IP Right Cessation
- 1967-02-20 SE SE227867A patent/SE338998B/xx unknown
- 1967-02-20 SE SE796270A patent/SE390412B/xx unknown
- 1967-05-16 FR FR106573A patent/FR6595M/fr not_active Expired
-
1971
- 1971-02-10 DK DK59371A patent/DK128247B/da not_active IP Right Cessation
- 1971-12-31 MY MY7100226A patent/MY7100226A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK128247B (da) | 1974-03-25 |
| DE1720012B2 (de) | 1977-06-08 |
| ES336945A1 (es) | 1968-01-16 |
| DE1795635A1 (de) | 1972-10-19 |
| GB1128234A (en) | 1968-09-25 |
| AT270653B (de) | 1969-05-12 |
| DE1795635B2 (de) | 1977-09-22 |
| IL27424A (en) | 1971-02-25 |
| NL146811B (nl) | 1975-08-15 |
| AT275534B (de) | 1969-10-27 |
| NL6702397A (fr) | 1967-08-21 |
| CH511239A (de) | 1971-08-15 |
| SE338998B (fr) | 1971-09-27 |
| SE390412B (sv) | 1976-12-20 |
| CA977754A (en) | 1975-11-11 |
| GR33641B (el) | 1968-01-03 |
| FI49714B (fr) | 1975-06-02 |
| FI49714C (fi) | 1975-09-10 |
| BE694244A (fr) | 1967-08-17 |
| DE1720012A1 (de) | 1972-04-06 |
| DK120344B (da) | 1971-05-17 |
| DE1795635C3 (de) | 1978-05-11 |
| FR6595M (fr) | 1969-01-06 |
| CH513179A (de) | 1971-09-30 |
| MY7100226A (en) | 1971-12-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2699427A (en) | Mineral oil compositions containing amidic acids or salts thereof | |
| US2497521A (en) | Oil compositions containing amine salts of boro-diol complexes | |
| US2897152A (en) | Lubricating oils | |
| WO2009009293A1 (fr) | Compositions de lubrifiant stabilisées avec un antioxydant phénolique styréné | |
| US2372588A (en) | Compounded mineral oil | |
| US3536706A (en) | Phenothiazine compounds | |
| US2503401A (en) | Lubricants | |
| US2568472A (en) | Oil compositions containing amine salts of acid compounds of boric acid and hydroxy carboxylic acids | |
| US2181914A (en) | Oil composition containing arylated metallo-organic inhibitors | |
| US2841555A (en) | Metal nu-acyl sarcosinate thickened lubricating oils | |
| NO124601B (fr) | ||
| US2351657A (en) | Lubricant | |
| US3696851A (en) | Chemical compounds and compositions | |
| US4122021A (en) | Antioxidant stabilized lubricating oils | |
| US2999813A (en) | Lubricant comprising a sulfurized mineral oil and a polyvalent metal dithiocarbamate | |
| US2435655A (en) | Lubricant | |
| US2625511A (en) | Anticorrosion agents and compositions comprising the same | |
| US3781206A (en) | Lubricant compositions | |
| US2868730A (en) | Insulating oils | |
| US2491772A (en) | Extreme pressure lubricants | |
| US2662815A (en) | Oxidation inhibitors | |
| GB713423A (en) | Improvements in or relating to lubricating compositions | |
| US3359202A (en) | Lubricating compositions | |
| US3892670A (en) | Vapor space corrosion inhibited compositions | |
| GB810741A (en) | Improvements in or relating to lubricating oil compositions |