JPH04503219A - コロホニウム―マレインイミドを基礎とする縮合生成物 - Google Patents

コロホニウム―マレインイミドを基礎とする縮合生成物

Info

Publication number: JPH04503219A
Authority: JP; Japan
Prior art keywords: colophonium; temperature; condensation product; maleimide; condensation products
Prior art date: 1988-11-04
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP1511555A

Other languages

English (en)

Japanese (ja)

Inventor

プラントル，ベルンハルト

フランク，エーリヒ

コッホ，ヴァルター

レベルト，ゲルト

Original Assignee

ベー・アー・エス・エフ、ラッケ、ウント、ファルベン、アクチェンゲゼルシャフト

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1988-11-04

Filing date

1989-10-31

Publication date

1992-06-11

1989-10-31 Application filed by ベー・アー・エス・エフ、ラッケ、ウント、ファルベン、アクチェンゲゼルシャフト filed Critical ベー・アー・エス・エフ、ラッケ、ウント、ファルベン、アクチェンゲゼルシャフト

1992-06-11 Publication of JPH04503219A publication Critical patent/JPH04503219A/ja

Status Pending legal-status Critical Current

Links

239000007859 condensation product Substances 0.000 title claims description 16
RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 claims description 19
239000000976 ink Substances 0.000 claims description 16
238000007639 printing Methods 0.000 claims description 15
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 13
150000005846 sugar alcohols Polymers 0.000 claims description 11
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
238000000034 method Methods 0.000 claims description 5
239000000203 mixture Substances 0.000 claims description 5
RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 claims description 4
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 3
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 3
125000001931 aliphatic group Chemical group 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 3
150000008064 anhydrides Chemical group 0.000 claims description 3
235000011187 glycerol Nutrition 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 3
239000000600 sorbitol Substances 0.000 claims description 3
TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 2
229940126062 Compound A Drugs 0.000 claims description 2
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
229920005989 resin Polymers 0.000 description 14
239000011347 resin Substances 0.000 description 14
238000006243 chemical reaction Methods 0.000 description 9
239000002480 mineral oil Substances 0.000 description 9
235000010446 mineral oil Nutrition 0.000 description 9
150000004985 diamines Chemical class 0.000 description 8
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 8
-1 That is Substances 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
239000002966 varnish Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 5
235000021388 linseed oil Nutrition 0.000 description 5
239000000944 linseed oil Substances 0.000 description 5
238000007645 offset printing Methods 0.000 description 5
150000001412 amines Chemical class 0.000 description 4
238000009835 boiling Methods 0.000 description 4
FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 4
239000012454 non-polar solvent Substances 0.000 description 4
238000009833 condensation Methods 0.000 description 3
230000005494 condensation Effects 0.000 description 3
150000001991 dicarboxylic acids Chemical class 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
229920000768 polyamine Polymers 0.000 description 3
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
150000003949 imides Chemical class 0.000 description 2
XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 1
YOOSAIJKYCBPFW-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)butoxy]propan-1-amine Chemical compound NCCCOCCCCOCCCN YOOSAIJKYCBPFW-UHFFFAOYSA-N 0.000 description 1
IGSBHTZEJMPDSZ-UHFFFAOYSA-N 4-[(4-amino-3-methylcyclohexyl)methyl]-2-methylcyclohexan-1-amine Chemical compound C1CC(N)C(C)CC1CC1CC(C)C(N)CC1 IGSBHTZEJMPDSZ-UHFFFAOYSA-N 0.000 description 1
DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 1
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
150000007824 aliphatic compounds Chemical class 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
229910002090 carbon oxide Inorganic materials 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
239000002274 desiccant Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000539 dimer Substances 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
230000006203 ethylation Effects 0.000 description 1
238000006200 ethylation reaction Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
239000002932 luster Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 description 1
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
230000002688 persistence Effects 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920003192 poly(bis maleimide) Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920000909 polytetrahydrofuran Polymers 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
239000012265 solid product Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/14—Polyamide-imides
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09F—NATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
- C09F1/00—Obtaining purification, or chemical modification of natural resins, e.g. oleo-resins
- C09F1/04—Chemical modification, e.g. esterification

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

JP1511555A 1988-11-04 1989-10-31 コロホニウム―マレインイミドを基礎とする縮合生成物 Pending JPH04503219A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3837520.6		1988-11-04
DE3837520A DE3837520A1 (de)	1988-11-04	1988-11-04	Kondensationsprodukte auf basis von kolophonium-maleinimiden

Publications (1)

Publication Number	Publication Date
JPH04503219A true JPH04503219A (ja)	1992-06-11

Family

ID=6366528

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP1511555A Pending JPH04503219A (ja)	1988-11-04	1989-10-31	コロホニウム―マレインイミドを基礎とする縮合生成物

Country Status (6)

Country	Link
EP (1)	EP0444065A1 (fr)
JP (1)	JPH04503219A (fr)
AU (1)	AU630126B2 (fr)
DE (1)	DE3837520A1 (fr)
ES (1)	ES2019495A6 (fr)
WO (1)	WO1990005158A1 (fr)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1232058A (fr) *	1967-10-10	1971-05-19

1988
- 1988-11-04 DE DE3837520A patent/DE3837520A1/de not_active Withdrawn
1989
- 1989-10-31 WO PCT/EP1989/001298 patent/WO1990005158A1/fr not_active Ceased
- 1989-10-31 EP EP19890912450 patent/EP0444065A1/fr not_active Withdrawn
- 1989-10-31 JP JP1511555A patent/JPH04503219A/ja active Pending
- 1989-10-31 AU AU45118/89A patent/AU630126B2/en not_active Ceased
- 1989-11-03 ES ES8903741A patent/ES2019495A6/es not_active Expired - Lifetime

Also Published As

Publication number	Publication date
EP0444065A1 (fr)	1991-09-04
DE3837520A1 (de)	1990-05-10
AU4511889A (en)	1990-05-28
ES2019495A6 (es)	1991-06-16
WO1990005158A1 (fr)	1990-05-17
AU630126B2 (en)	1992-10-22

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EP0490954B1 (fr)	1995-04-12	Composition de revetement comprenant un polyamide contenant du fluor
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US6172174B1 (en)	2001-01-09	Phenolic rosin resin compositions
EP0666281A2 (fr)	1995-08-09	Procédé de préparation de liants solubles dans l'eau à base d'ester de colophane modifiée pour encres stratifiables
US5154760A (en)	1992-10-13	Polyamide resin compositions for use as laminating ink resin binders
JPS60223823A (ja)	1985-11-08	ポリアミド樹脂
US4816549A (en)	1989-03-28	Toluene soluble polyamide resin from polymerized fatty acid and 1,2-diamino cyclohexane
JPH02175771A (ja)	1990-07-09	ロジンを基礎とする縮合生成物の製造法
US3639313A (en)	1972-02-01	Modified polyamide resins
EP0230014B1 (fr)	1994-02-02	Polyamides contenant des acides dicarboxyliques aromatiques
US4810747A (en)	1989-03-07	Water dispersible polyamide blend
US4873311A (en)	1989-10-10	Water dispersible polyamide ester
US3896064A (en)	1975-07-22	Vehicles for printing ink
US4894433A (en)	1990-01-16	Water dispersible polyamide diethanolamine ester
EP0214111B1 (fr)	1991-07-31	Agents thixotropes, compositions de peinture les contenant et leur procédé de préparation
JPH04503219A (ja)	1992-06-11	コロホニウム―マレインイミドを基礎とする縮合生成物
US3522270A (en)	1970-07-28	Polyamide-polyimide resin
JPS638998B2 (fr)	1988-02-25
US5085699A (en)	1992-02-04	Amniopolyester resins as dilution extenders for zinc-containing metal resinate inks
JP2902430B2 (ja)	1999-06-07	コロホニウム―マレインイミドを基礎とする縮合生成物
US4385166A (en)	1983-05-24	Printing inks based on poly(amide-ester) resins
US3786007A (en)	1974-01-15	Borax borated polymeric fat acid polyamides
JPS5817540B2 (ja)	1983-04-07	アルコ−ル可溶性ポリアミドの製造方法
JPS6146507B2 (fr)	1986-10-14
JPS5835611B2 (ja)	1983-08-03	アルコ−ル可溶性の変性ポリアミド樹脂の製造法