NO310421B1 - Blandinger av blokkoligomerer inneholdende 2,2,6,6-tetrametyl- 4-piperidyl-grupper som stabilisatorer for organiske materialer - Google Patents

Blandinger av blokkoligomerer inneholdende 2,2,6,6-tetrametyl- 4-piperidyl-grupper som stabilisatorer for organiske materialer Download PDF

Info

Publication number: NO310421B1
Authority: NO; Norway
Prior art keywords: formula; alkyl; substituted; unsubstituted; group
Prior art date: 1995-12-04

Application number

NO19965150A

Other languages

English (en)

Norwegian (no)

Other versions

NO965150D0 (no

NO965150L (no

Inventor

Valerio Borzatta

Fabrizio Guizzardi

Original Assignee

Ciba Sc Holding Ag

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.)

1995-12-04

Filing date

1996-12-03

Publication date

2001-07-02

1996-12-03 Application filed by Ciba Sc Holding Ag filed Critical Ciba Sc Holding Ag

1996-12-03 Publication of NO965150D0 publication Critical patent/NO965150D0/no

1997-06-05 Publication of NO965150L publication Critical patent/NO965150L/no

2001-07-02 Publication of NO310421B1 publication Critical patent/NO310421B1/no

Links

239000000203 mixture Substances 0.000 title claims description 190
-1 2,2,6,6-tetramethyl-4-piperidyl groups Chemical group 0.000 title claims description 144
239000011368 organic material Substances 0.000 title claims description 18
239000003381 stabilizer Substances 0.000 title description 17
150000001875 compounds Chemical class 0.000 claims description 156
229910052739 hydrogen Inorganic materials 0.000 claims description 46
239000001257 hydrogen Substances 0.000 claims description 45
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 38
125000000217 alkyl group Chemical group 0.000 claims description 33
239000004743 Polypropylene Substances 0.000 claims description 30
150000002431 hydrogen Chemical class 0.000 claims description 30
229920001155 polypropylene Polymers 0.000 claims description 26
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 24
238000006243 chemical reaction Methods 0.000 claims description 23
238000000034 method Methods 0.000 claims description 19
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
125000003884 phenylalkyl group Chemical group 0.000 claims description 15
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 14
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 14
125000002947 alkylene group Chemical group 0.000 claims description 13
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 12
239000004698 Polyethylene Substances 0.000 claims description 11
229920000573 polyethylene Polymers 0.000 claims description 11
125000000753 cycloalkyl group Chemical group 0.000 claims description 9
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 8
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 8
125000003342 alkenyl group Chemical group 0.000 claims description 8
150000007529 inorganic bases Chemical class 0.000 claims description 8
230000003647 oxidation Effects 0.000 claims description 8
238000007254 oxidation reaction Methods 0.000 claims description 8
230000015556 catabolic process Effects 0.000 claims description 7
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 7
238000006731 degradation reaction Methods 0.000 claims description 7
FDAKZQLBIFPGSV-UHFFFAOYSA-N n-butyl-2,2,6,6-tetramethylpiperidin-4-amine Chemical group CCCCNC1CC(C)(C)NC(C)(C)C1 FDAKZQLBIFPGSV-UHFFFAOYSA-N 0.000 claims description 7
239000003960 organic solvent Substances 0.000 claims description 7
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
229920001059 synthetic polymer Polymers 0.000 claims description 5
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
230000000087 stabilizing effect Effects 0.000 claims description 4
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
125000002252 acyl group Chemical group 0.000 claims description 3
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
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JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 claims 2
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239000003054 catalyst Substances 0.000 description 6
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238000005728 strengthening Methods 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
125000006488 t-butyl benzyl group Chemical group 0.000 description 1
MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
238000010998 test method Methods 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
235000010215 titanium dioxide Nutrition 0.000 description 1
YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
235000019149 tocopherols Nutrition 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
125000005591 trimellitate group Chemical group 0.000 description 1
AZSKHRTUXHLAHS-UHFFFAOYSA-N tris(2,4-di-tert-butylphenyl) phosphate Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(=O)(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C AZSKHRTUXHLAHS-UHFFFAOYSA-N 0.000 description 1
WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
125000005065 undecenyl group Chemical group C(=CCCCCCCCCC)* 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920006337 unsaturated polyester resin Polymers 0.000 description 1
125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
235000019154 vitamin C Nutrition 0.000 description 1
239000011718 vitamin C Substances 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000002023 wood Substances 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
- 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
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34926—Triazines also containing heterocyclic groups other than triazine groups

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Hydrogenated Pyridines (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Plural Heterocyclic Compounds (AREA)
Dental Preparations (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

NO19965150A 1995-12-04 1996-12-03 Blandinger av blokkoligomerer inneholdende 2,2,6,6-tetrametyl- 4-piperidyl-grupper som stabilisatorer for organiske materialer NO310421B1 (no)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
EP95810756		1995-12-04
EP96810053		1996-01-29
EP96810458		1996-07-12

Publications (3)

Publication Number	Publication Date
NO965150D0 NO965150D0 (no)	1996-12-03
NO965150L NO965150L (no)	1997-06-05
NO310421B1 true NO310421B1 (no)	2001-07-02

Family

ID=27236983

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19965150A NO310421B1 (no)	1995-12-04	1996-12-03	Blandinger av blokkoligomerer inneholdende 2,2,6,6-tetrametyl- 4-piperidyl-grupper som stabilisatorer for organiske materialer

Country Status (17)

Country	Link
US (2)	US6046304A (fr)
JP (1)	JP3635317B2 (fr)
KR (1)	KR100449430B1 (fr)
CN (1)	CN1120165C (fr)
AT (1)	ATE232206T1 (fr)
AU (1)	AU718067B2 (fr)
BR (1)	BR9605826A (fr)
CA (1)	CA2191832C (fr)
CZ (1)	CZ294258B6 (fr)
DE (1)	DE69626095T2 (fr)
ES (1)	ES2189860T3 (fr)
MX (1)	MX9606006A (fr)
MY (1)	MY128982A (fr)
NO (1)	NO310421B1 (fr)
PT (1)	PT782994E (fr)
RU (1)	RU2175660C2 (fr)
SK (1)	SK283984B6 (fr)

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WO2015044785A2 (fr)	2013-09-27	2015-04-02	Basf Se	Compositions de polyoléfines pour matériaux de construction
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WO2016156328A1 (fr)	2015-03-31	2016-10-06	Shell Internationale Research Maatschappij B.V.	Utilisation d'une composition lubrifiante comprenant un photostabilisant de type amine encombrée pour une meilleure propreté d'un piston dans un moteur à combustion interne
CN104725361B (zh) *	2015-04-09	2017-05-31	江苏富比亚化学品有限公司	一种受阻胺类光稳定剂3346的制备方法
CN104818486B (zh) *	2015-05-08	2017-06-27	山东应天节能环保科技有限公司	一种黄铜专用缓蚀剂及其制备方法
WO2017006600A1 (fr) *	2015-07-09	2017-01-12	日本ゼオン株式会社	Composition de résine, article moulé en résine et élément optique
KR102580043B1 (ko)	2015-07-20	2023-09-20	바스프 에스이	난연성 폴리올레핀 물품
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1996
- 1996-11-25 US US08/756,225 patent/US6046304A/en not_active Expired - Lifetime
- 1996-11-26 ES ES96810823T patent/ES2189860T3/es not_active Expired - Lifetime
- 1996-11-26 AT AT96810823T patent/ATE232206T1/de active
- 1996-11-26 PT PT96810823T patent/PT782994E/pt unknown
- 1996-11-26 DE DE69626095T patent/DE69626095T2/de not_active Expired - Lifetime
- 1996-11-27 AU AU74142/96A patent/AU718067B2/en not_active Expired
- 1996-11-28 MY MYPI96004986A patent/MY128982A/en unknown
- 1996-11-28 RU RU96122845/04A patent/RU2175660C2/ru active
- 1996-12-02 SK SK1543-96A patent/SK283984B6/sk not_active IP Right Cessation
- 1996-12-02 MX MX9606006A patent/MX9606006A/es unknown
- 1996-12-02 CA CA002191832A patent/CA2191832C/fr not_active Expired - Lifetime
- 1996-12-02 CZ CZ19963523A patent/CZ294258B6/cs not_active IP Right Cessation
- 1996-12-03 CN CN96121514A patent/CN1120165C/zh not_active Expired - Lifetime
- 1996-12-03 BR BR9605826A patent/BR9605826A/pt not_active IP Right Cessation
- 1996-12-03 NO NO19965150A patent/NO310421B1/no not_active IP Right Cessation
- 1996-12-04 JP JP33898096A patent/JP3635317B2/ja not_active Expired - Lifetime
- 1996-12-04 KR KR1019960062958A patent/KR100449430B1/ko not_active Expired - Lifetime
1999
- 1999-11-04 US US09/433,468 patent/US6297299B1/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
JPH09216946A (ja)	1997-08-19
KR100449430B1 (ko)	2004-11-26
AU7414296A (en)	1997-06-12
AU718067B2 (en)	2000-04-06
ES2189860T3 (es)	2003-07-16
SK283984B6 (sk)	2004-06-08
DE69626095T2 (de)	2003-07-31
MX9606006A (es)	1997-08-30
RU2175660C2 (ru)	2001-11-10
NO965150D0 (no)	1996-12-03
US6297299B1 (en)	2001-10-02
CN1120165C (zh)	2003-09-03
BR9605826A (pt)	1998-09-01
CZ294258B6 (cs)	2004-11-10
CA2191832C (fr)	2006-01-24
CN1165138A (zh)	1997-11-19
DE69626095D1 (de)	2003-03-13
CA2191832A1 (fr)	1997-06-05
PT782994E (pt)	2003-06-30
MY128982A (en)	2007-03-30
ATE232206T1 (de)	2003-02-15
US6046304A (en)	2000-04-04
NO965150L (no)	1997-06-05
SK154396A3 (en)	1997-10-08
JP3635317B2 (ja)	2005-04-06
CZ352396A3 (en)	1997-06-11

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Date	Code	Title	Description
2016-12-12	MK1K	Patent expired

Publication	Publication Date	Title
NO310421B1 (no)	2001-07-02	Blandinger av blokkoligomerer inneholdende 2,2,6,6-tetrametyl- 4-piperidyl-grupper som stabilisatorer for organiske materialer
EP0782994B1 (fr)	2003-02-05	Oligomères en blocs contenant des groupes 2,2,6,6-tétraméthyle comme stabilisants pour des matériaux organiques
US6020406A (en)	2000-02-01	Synergistic stabilizer mixture
US5965643A (en)	1999-10-12	Synergistic stabilizer mixture
CA2167660C (fr)	2007-06-19	Melange stabilisateur synergiste
US6114420A (en)	2000-09-05	Triazine derivatives containing 2,2,6,6-tetramethyl-4-piperidyl groups
US5977221A (en)	1999-11-02	Synergistic stabilizer mixture
CA2287557C (fr)	2008-02-19	Oligomeres blocs contenant des groupes 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-pyperidyles comme agents stabilisants pour des materiaux organiques
AU2001262311B2 (en)	2006-08-31	Stabilizer mixtures
US5772921A (en)	1998-06-30	Synergistic mixture consisting of a 2,4-dimethyl-6-S-alkylphenol and a sterically hindered phenol
AU2001276341B2 (en)	2006-06-08	Stabilizer mixtures
US6005036A (en)	1999-12-21	Polysilanes
EP0984958B1 (fr)	2003-03-26	Blocs oligomeres contenant des groupes 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-piperidyl comme stabilisants pour des materiaux organiques
US6409941B1 (en)	2002-06-25	Block oligomers containing 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials
US5610211A (en)	1997-03-11	2,2,6,6-tetramethylpiperidine derivatives for use as stabilizing agents for organic materials
US5847132A (en)	1998-12-08	Polytriazine derivatives containing polyalkylpiperidinyloxy or polyalkylpiperidinylamino groups
US6403680B1 (en)	2002-06-11	Block oligomers containing 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials
US6492440B1 (en)	2002-12-10	Block oligomers containing 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials
EP0850938B1 (fr)	2003-02-12	Composés de triazine contenant des groupes 2,2,6,6-tetraméthyl-4-pipéridinyl comme stabilisateurs pour des matériaux organiques
EP0835873A1 (fr)	1998-04-15	Mélanges de composés de tétramines de polyalkylpiperidinylaminotriazine trisubstitués et tétrasubstitués
US6221937B1 (en)	2001-04-24	Triazine compounds containing 2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials
MXPA99010922A (en)	2000-09-04	Block oligomers containing 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials
MXPA99010923A (en)	2000-09-04	Block oligomers containing 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials
CA2217929A1 (fr)	1998-04-14	Melanges de composes de polyalkylpiperidinylaminotriazinetetramine trisubstitues et tetrasubstitues
MXPA99010921A (en)	2000-09-04	Block oligomers containing 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials