DD279254A5 - Verwendung von ketogruppenhaltigen zyklischen verbindungen - Google Patents

Verwendung von ketogruppenhaltigen zyklischen verbindungen Download PDF

Info

Publication number: DD279254A5
Authority: DD; German Democratic Republic
Prior art keywords: integer; plasticizers; polymers; containing cyclic; cyclic compounds
Prior art date: 1988-03-18

Application number

DD89326621A

Other languages

German (de)

English (en)

Inventor

Hans-Rainer Hoffmann

Reinhart Von Kleinsorgen

Original Assignee

��@��@��`��@��@�K@��K@��k��

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.)

1988-03-18

Filing date

1989-03-15

Publication date

1990-05-30

1989-03-15 Application filed by ��@��@��`��@��@�K@��K@��k�� filed Critical ��@��@��`��@��@�K@��K@��k��

1990-05-30 Publication of DD279254A5 publication Critical patent/DD279254A5/de

Links

150000001923 cyclic compounds Chemical class 0.000 title claims abstract description 5
125000000468 ketone group Chemical group 0.000 claims abstract description 4
229930194542 Keto Natural products 0.000 claims description 3
239000004014 plasticizer Substances 0.000 abstract description 25
229920000642 polymer Polymers 0.000 abstract description 22
229920003023 plastic Polymers 0.000 abstract description 8
239000004033 plastic Substances 0.000 abstract description 8
125000000217 alkyl group Chemical group 0.000 abstract description 3
239000010408 film Substances 0.000 description 8
-1 fatty acid esters Chemical class 0.000 description 7
239000000126 substance Substances 0.000 description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
239000000203 mixture Substances 0.000 description 5
150000001875 compounds Chemical class 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
238000001704 evaporation Methods 0.000 description 4
239000011521 glass Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
229920001220 nitrocellulos Polymers 0.000 description 4
239000002904 solvent Substances 0.000 description 4
NVIPUOMWGQAOIT-RQOWECAXSA-N (Z)-7-Hexadecen-1,16-olide Chemical compound O=C1CCCCC\C=C/CCCCCCCCO1 NVIPUOMWGQAOIT-RQOWECAXSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
VHUGWUBIUBBUAF-UHFFFAOYSA-N cyclotridecanone Chemical compound O=C1CCCCCCCCCCCC1 VHUGWUBIUBBUAF-UHFFFAOYSA-N 0.000 description 3
UPOSSYJVWXLPTA-UHFFFAOYSA-N cycloundecanone Chemical compound O=C1CCCCCCCCCC1 UPOSSYJVWXLPTA-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
239000003205 fragrance Substances 0.000 description 3
229920000058 polyacrylate Polymers 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
XJDBBMWXVYBUTB-UHFFFAOYSA-N 2-methylcyclopentadecan-1-one Chemical compound CC1CCCCCCCCCCCCCC1=O XJDBBMWXVYBUTB-UHFFFAOYSA-N 0.000 description 2
ALHUZKCOMYUFRB-UHFFFAOYSA-N 3-methylcyclopentadecan-1-one Chemical compound CC1CCCCCCCCCCCCC(=O)C1 ALHUZKCOMYUFRB-UHFFFAOYSA-N 0.000 description 2
OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 description 2
SXVPOSFURRDKBO-UHFFFAOYSA-N Cyclododecanone Chemical compound O=C1CCCCCCCCCCC1 SXVPOSFURRDKBO-UHFFFAOYSA-N 0.000 description 2
FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
239000000020 Nitrocellulose Substances 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
OSOIQJGOYGSIMF-UHFFFAOYSA-N cyclopentadecanone Chemical compound O=C1CCCCCCCCCCCCCC1 OSOIQJGOYGSIMF-UHFFFAOYSA-N 0.000 description 2
238000009792 diffusion process Methods 0.000 description 2
239000003814 drug Substances 0.000 description 2
229940079593 drug Drugs 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
239000000463 material Substances 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
239000003973 paint Substances 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920000515 polycarbonate Polymers 0.000 description 2
239000004417 polycarbonate Substances 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
229920002689 polyvinyl acetate Polymers 0.000 description 2
239000011118 polyvinyl acetate Substances 0.000 description 2
239000005060 rubber Substances 0.000 description 2
PHXATPHONSXBIL-UHFFFAOYSA-N xi-gamma-Undecalactone Chemical compound CCCCCCCC1CCC(=O)O1 PHXATPHONSXBIL-UHFFFAOYSA-N 0.000 description 2
NVIPUOMWGQAOIT-UHFFFAOYSA-N (E)-7-Hexadecen-16-olide Natural products O=C1CCCCCC=CCCCCCCCCO1 NVIPUOMWGQAOIT-UHFFFAOYSA-N 0.000 description 1
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
YAYNEUUHHLGGAH-UHFFFAOYSA-N 1-chlorododecane Chemical compound CCCCCCCCCCCCCl YAYNEUUHHLGGAH-UHFFFAOYSA-N 0.000 description 1
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical class CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
241000723346 Cinnamomum camphora Species 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
229920002292 Nylon 6 Polymers 0.000 description 1
229920002367 Polyisobutene Polymers 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
230000010933 acylation Effects 0.000 description 1
238000005917 acylation reaction Methods 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
150000001278 adipic acid derivatives Chemical class 0.000 description 1
150000001535 azelaic acid derivatives Chemical class 0.000 description 1
ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
150000001558 benzoic acid derivatives Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000001656 butanoic acid esters Chemical class 0.000 description 1
229960000846 camphor Drugs 0.000 description 1
229930008380 camphor Natural products 0.000 description 1
239000000969 carrier Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229920003086 cellulose ether Polymers 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
229920006018 co-polyamide Polymers 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
150000002168 ethanoic acid esters Chemical class 0.000 description 1
PUSKHXMZPOMNTQ-UHFFFAOYSA-N ethyl 2,1,3-benzoselenadiazole-5-carboxylate Chemical compound CCOC(=O)C1=CC=C2N=[Se]=NC2=C1 PUSKHXMZPOMNTQ-UHFFFAOYSA-N 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
OALYTRUKMRCXNH-QMMMGPOBSA-N gamma-Nonalactone Natural products CCCCC[C@H]1CCC(=O)O1 OALYTRUKMRCXNH-QMMMGPOBSA-N 0.000 description 1
PHXATPHONSXBIL-JTQLQIEISA-N gamma-Undecalactone Natural products CCCCCCC[C@H]1CCC(=O)O1 PHXATPHONSXBIL-JTQLQIEISA-N 0.000 description 1
229940020436 gamma-undecalactone Drugs 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000002466 imines Chemical class 0.000 description 1
239000007943 implant Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
235000021388 linseed oil Nutrition 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
229920002521 macromolecule Polymers 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
239000005445 natural material Substances 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
150000003021 phthalic acid derivatives Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
229920001610 polycaprolactone Polymers 0.000 description 1
239000004632 polycaprolactone Substances 0.000 description 1
229920006289 polycarbonate film Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920006254 polymer film Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
229920001289 polyvinyl ether Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003151 propanoic acid esters Chemical class 0.000 description 1
239000002994 raw material Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
150000003329 sebacic acid derivatives Chemical class 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003459 sulfonic acid esters Chemical class 0.000 description 1
239000010409 thin film Substances 0.000 description 1
239000003440 toxic substance Substances 0.000 description 1
231100000048 toxicity data Toxicity 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)

DD89326621A 1988-03-18 1989-03-15 Verwendung von ketogruppenhaltigen zyklischen verbindungen DD279254A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3809236A DE3809236A1 (de)	1988-03-18	1988-03-18	Verwendung von ketogruppenhaltigen zyklischen verbindungen

Publications (1)

Publication Number	Publication Date
DD279254A5 true DD279254A5 (de)	1990-05-30

Family

ID=6350151

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD89326621A DD279254A5 (de)	1988-03-18	1989-03-15	Verwendung von ketogruppenhaltigen zyklischen verbindungen

Country Status (10)

Country	Link
EP (1)	EP0332802A1 (fr)
AU (1)	AU2914289A (fr)
DD (1)	DD279254A5 (fr)
DE (1)	DE3809236A1 (fr)
IL (1)	IL89174A0 (fr)
PL (1)	PL278316A1 (fr)
PT (1)	PT89909A (fr)
WO (1)	WO1989008681A1 (fr)
YU (1)	YU53689A (fr)
ZA (1)	ZA89807B (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5288498A (en) *	1985-05-01	1994-02-22	University Of Utah Research Foundation	Compositions of oral nondissolvable matrixes for transmucosal administration of medicaments
US5171665A (en) *	1989-04-17	1992-12-15	Oncogen	Monoclonal antibody to novel antigen associated with human tumors
GB9023238D0 (en) *	1990-10-25	1990-12-05	Robinson Bros Ltd	Photodegradable compositions
IT1264608B1 (it) *	1993-06-15	1996-10-04	Caffaro Spa Ind Chim	Procedimento per la produzione di lattoni e lattoni ottenuti con il procedimento
US7622523B2 (en)	2002-08-12	2009-11-24	Exxonmobil Chemical Patents Inc.	Plasticized polyolefin compositions
CN100345896C (zh)	2002-08-12	2007-10-31	埃克森美孚化学专利公司	增塑聚烯烃组合物
US7531594B2 (en)	2002-08-12	2009-05-12	Exxonmobil Chemical Patents Inc.	Articles from plasticized polyolefin compositions
US8003725B2 (en)	2002-08-12	2011-08-23	Exxonmobil Chemical Patents Inc.	Plasticized hetero-phase polyolefin blends
US7998579B2 (en)	2002-08-12	2011-08-16	Exxonmobil Chemical Patents Inc.	Polypropylene based fibers and nonwovens
US7271209B2 (en)	2002-08-12	2007-09-18	Exxonmobil Chemical Patents Inc.	Fibers and nonwovens from plasticized polyolefin compositions
US8192813B2 (en)	2003-08-12	2012-06-05	Exxonmobil Chemical Patents, Inc.	Crosslinked polyethylene articles and processes to produce same
WO2007011530A2 (fr)	2005-07-15	2007-01-25	Exxonmobil Chemical Patents, Inc.	Compositions élastomères

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2214397A (en) *	1938-07-25	1940-09-10	Du Pont	Plasticized synthetic linear polyamide composition
US3219612A (en) *	1963-02-25	1965-11-23	Evald L Skau	Vinyl chloride resins and butadiene rubbers with n-acyl derivatives of cyclic imines
US3328329A (en) *	1964-12-07	1967-06-27	Celanese Corp	Emulsions of lactone plasticized polymers
DE2832055A1 (de) *	1978-07-21	1980-01-31	Gen Electric	Plastifizierte polycarbonat-zusammensetzung

1988
- 1988-03-18 DE DE3809236A patent/DE3809236A1/de not_active Withdrawn
1989
- 1989-01-11 WO PCT/DE1989/000013 patent/WO1989008681A1/fr not_active Ceased
- 1989-01-11 EP EP89100439A patent/EP0332802A1/fr not_active Withdrawn
- 1989-01-11 AU AU29142/89A patent/AU2914289A/en not_active Abandoned
- 1989-02-02 ZA ZA89807A patent/ZA89807B/xx unknown
- 1989-02-03 IL IL89174A patent/IL89174A0/xx unknown
- 1989-03-06 PT PT89909A patent/PT89909A/pt not_active Application Discontinuation
- 1989-03-15 YU YU00536/89A patent/YU53689A/xx unknown
- 1989-03-15 DD DD89326621A patent/DD279254A5/de not_active IP Right Cessation
- 1989-03-17 PL PL27831689A patent/PL278316A1/xx unknown

Also Published As

Publication number	Publication date
WO1989008681A1 (fr)	1989-09-21
AU2914289A (en)	1989-10-05
IL89174A0 (en)	1989-09-10
PT89909A (pt)	1989-11-10
YU53689A (en)	1990-12-31
EP0332802A1 (fr)	1989-09-20
DE3809236A1 (de)	1989-09-28
PL278316A1 (en)	1989-10-16
ZA89807B (en)	1989-10-25

Legal Events

Date	Code	Title	Description
1995-08-17	ENJ	Ceased due to non-payment of renewal fee

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