NO134159B - - Google Patents
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- Publication number
- NO134159B NO134159B NO69154A NO15469A NO134159B NO 134159 B NO134159 B NO 134159B NO 69154 A NO69154 A NO 69154A NO 15469 A NO15469 A NO 15469A NO 134159 B NO134159 B NO 134159B
- Authority
- NO
- Norway
- Prior art keywords
- resin
- impregnating agent
- oil
- acid
- nitrogen
- Prior art date
Links
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 40
- 229920005989 resin Polymers 0.000 claims description 40
- 239000011347 resin Substances 0.000 claims description 40
- 229920000180 alkyd Polymers 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims description 20
- 239000003921 oil Substances 0.000 claims description 19
- 235000019198 oils Nutrition 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 17
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 12
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 238000001035 drying Methods 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 10
- 239000008096 xylene Substances 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 7
- 229920000877 Melamine resin Polymers 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 6
- 238000004804 winding Methods 0.000 claims description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 5
- 239000003849 aromatic solvent Substances 0.000 claims description 2
- 150000004668 long chain fatty acids Chemical class 0.000 claims description 2
- 239000002966 varnish Substances 0.000 claims description 2
- 238000009429 electrical wiring Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 27
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 238000005470 impregnation Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000005639 Lauric acid Substances 0.000 description 5
- 229920001807 Urea-formaldehyde Polymers 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- LFSAPCRASZRSKS-UHFFFAOYSA-N 2-methylcyclohexan-1-one Chemical compound CC1CCCCC1=O LFSAPCRASZRSKS-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000003679 aging effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 1
- 238000007922 dissolution test Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000009884 interesterification Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002531 isophthalic acids Chemical class 0.000 description 1
- 230000035800 maturation Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 150000003503 terephthalic acid derivatives Chemical class 0.000 description 1
- 150000003504 terephthalic acids Chemical class 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J73/00—Steroids in which the cyclopenta[a]hydrophenanthrene skeleton has been modified by substitution of one or two carbon atoms by hetero atoms
- C07J73/001—Steroids in which the cyclopenta[a]hydrophenanthrene skeleton has been modified by substitution of one or two carbon atoms by hetero atoms by one hetero atom
- C07J73/003—Steroids in which the cyclopenta[a]hydrophenanthrene skeleton has been modified by substitution of one or two carbon atoms by hetero atoms by one hetero atom by oxygen as hetero atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR90265A FR1526962A (fr) | 1967-01-06 | 1967-01-06 | Nouveau procédé de préparation d'un composé gonatriénique et produits en résultant |
FR90264A FR1526961A (fr) | 1967-01-06 | 1967-01-06 | Nouveaux 4-oxa stéroïdes et procédé de préparation |
Publications (2)
Publication Number | Publication Date |
---|---|
NO134159B true NO134159B (da) | 1976-05-18 |
NO134159C NO134159C (da) | 1976-08-25 |
Family
ID=26174488
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO6839A NO134214C (da) | 1967-01-06 | 1968-01-05 | |
NO69154A NO134159C (da) | 1967-01-06 | 1969-01-15 | |
NO69153A NO134213C (da) | 1967-01-06 | 1969-01-15 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO6839A NO134214C (da) | 1967-01-06 | 1968-01-05 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO69153A NO134213C (da) | 1967-01-06 | 1969-01-15 |
Country Status (13)
Country | Link |
---|---|
US (1) | US3499913A (da) |
AT (4) | AT281318B (da) |
BE (1) | BE708997A (da) |
CH (1) | CH483452A (da) |
DE (1) | DE1668641C3 (da) |
DK (3) | DK135630B (da) |
ES (2) | ES348970A1 (da) |
FR (2) | FR1526962A (da) |
GB (3) | GB1206818A (da) |
IL (3) | IL38246A (da) |
NL (1) | NL6800211A (da) |
NO (3) | NO134214C (da) |
SE (1) | SE328882B (da) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HU201091B (en) | 1985-12-26 | 1990-09-28 | Mitsubishi Chem Ind | Process for producing gonatriene derivatives and pharmaceutical compositions comprising same |
US5434274A (en) * | 1991-12-20 | 1995-07-18 | Washington University | Benz(epsilon)indene compounds |
US5206415A (en) * | 1991-12-20 | 1993-04-27 | Washington University | Tricyclic steroid analogs |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3138617A (en) * | 1959-08-27 | 1964-06-23 | Roussel Uclaf | Processes for the production of 19-nor-delta4-[9beta], [10alpha]-androstenes and intermediates |
FR1366725A (fr) * | 1961-01-31 | 1964-07-17 | Roussel Uclaf | Nouveaux oxa-stéroïdes, leur préparation et leur utilisation en synthèse stéroïdienne |
US3085098A (en) * | 1960-07-29 | 1963-04-09 | Roussel Uclaf | Process for the preparation of 17beta-oxy-genated-delta4, 9(10)-estradiene-3-one |
US3102145A (en) * | 1961-06-28 | 1963-08-27 | Roussel Uclaf | Intermediate in the preparation of 19-nor-progesterone |
FR1305992A (fr) * | 1961-07-21 | 1962-10-13 | Roussel Uclaf | Procédé de préparation de certains 19-nor stéroïdes et produits utilisés dans ce procédé |
BE657262A (da) * | 1962-03-06 | |||
US3422121A (en) * | 1965-08-13 | 1969-01-14 | Merck & Co Inc | Process for the preparation of 13-lower alkyl-gona-4,8(14),9-triene-3,17-dione |
-
1967
- 1967-01-06 FR FR90265A patent/FR1526962A/fr not_active Expired
- 1967-01-06 FR FR90264A patent/FR1526961A/fr not_active Expired
- 1967-12-18 IL IL38246A patent/IL38246A/xx unknown
- 1967-12-18 IL IL29150A patent/IL29150A/en unknown
- 1967-12-18 IL IL38446A patent/IL38446A/en unknown
- 1967-12-22 CH CH1810067A patent/CH483452A/fr not_active IP Right Cessation
-
1968
- 1968-01-03 US US695364A patent/US3499913A/en not_active Expired - Lifetime
- 1968-01-05 AT AT1123868A patent/AT281318B/de not_active IP Right Cessation
- 1968-01-05 DK DK3568AA patent/DK135630B/da not_active IP Right Cessation
- 1968-01-05 AT AT15168A patent/AT283610B/de not_active IP Right Cessation
- 1968-01-05 DE DE1668641A patent/DE1668641C3/de not_active Expired
- 1968-01-05 ES ES348970A patent/ES348970A1/es not_active Expired
- 1968-01-05 NL NL6800211A patent/NL6800211A/xx unknown
- 1968-01-05 AT AT1123768A patent/AT284353B/de not_active IP Right Cessation
- 1968-01-05 BE BE708997D patent/BE708997A/xx not_active IP Right Cessation
- 1968-01-05 ES ES348969A patent/ES348969A1/es not_active Expired
- 1968-01-05 NO NO6839A patent/NO134214C/no unknown
- 1968-01-05 SE SE00149/68A patent/SE328882B/xx unknown
- 1968-01-05 AT AT1123668A patent/AT287933B/de not_active IP Right Cessation
- 1968-01-08 GB GB6774/70A patent/GB1206818A/en not_active Expired
- 1968-01-08 GB GB995/68A patent/GB1206816A/en not_active Expired
- 1968-01-08 GB GB6773/70A patent/GB1206817A/en not_active Expired
-
1969
- 1969-01-15 NO NO69154A patent/NO134159C/no unknown
- 1969-01-15 NO NO69153A patent/NO134213C/no unknown
-
1970
- 1970-12-14 DK DK632870AA patent/DK126936B/da not_active IP Right Cessation
- 1970-12-14 DK DK632970AA patent/DK130307B/da not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
GB1206818A (en) | 1970-09-30 |
US3499913A (en) | 1970-03-10 |
DK130307B (da) | 1975-02-03 |
IL29150A (en) | 1972-09-28 |
NO134159C (da) | 1976-08-25 |
GB1206817A (en) | 1970-09-30 |
NL6800211A (da) | 1968-07-08 |
DK130307C (da) | 1975-06-30 |
DE1793691A1 (de) | 1972-07-27 |
NO134214B (da) | 1976-05-24 |
DK126936B (da) | 1973-09-03 |
ES348970A1 (es) | 1969-08-16 |
NO134213B (da) | 1976-05-24 |
DK135630C (da) | 1977-10-31 |
AT281318B (de) | 1970-05-11 |
DE1668641B2 (de) | 1974-08-08 |
BE708997A (da) | 1968-07-05 |
AT283610B (de) | 1970-08-10 |
CH483452A (fr) | 1969-12-31 |
ES348969A1 (es) | 1969-03-16 |
NO134213C (da) | 1976-09-01 |
DE1668641A1 (de) | 1972-03-02 |
AT284353B (de) | 1970-09-10 |
DE1793691B2 (de) | 1976-05-13 |
DE1668641C3 (de) | 1975-03-20 |
IL38246A (en) | 1972-10-29 |
NO134214C (da) | 1976-09-01 |
DK135630B (da) | 1977-05-31 |
GB1206816A (en) | 1970-09-30 |
IL38446A (en) | 1972-12-29 |
SE328882B (da) | 1970-09-28 |
FR1526962A (fr) | 1968-05-31 |
FR1526961A (fr) | 1968-05-31 |
AT287933B (de) | 1971-02-10 |
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