IL142590A - A preparation that contains cyclic peroxide concrete and a moisturizing substance - Google Patents

A preparation that contains cyclic peroxide concrete and a moisturizing substance

Info

Publication number: IL142590A
Authority: IL; Israel
Prior art keywords: phlegmatizer; composition; cyclic; cyclic ketone; composition according
Prior art date: 1998-10-16

Application number

IL14259099A

Other languages

English (en)

Hebrew (he)

Other versions

IL142590A0 (en

Original Assignee

Akzo Nobel Nv

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.)

1998-10-16

Filing date

1999-10-07

Publication date

2004-08-31

1999-10-07 Application filed by Akzo Nobel Nv filed Critical Akzo Nobel Nv

2002-03-10 Publication of IL142590A0 publication Critical patent/IL142590A0/xx

2004-08-31 Publication of IL142590A publication Critical patent/IL142590A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 86
-1 cyclic ketone peroxides Chemical class 0.000 title claims abstract description 50
239000001301 oxygen Substances 0.000 claims description 26
229910052760 oxygen Inorganic materials 0.000 claims description 26
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 25
150000002978 peroxides Chemical class 0.000 claims description 15
238000012986 modification Methods 0.000 claims description 7
230000004048 modification Effects 0.000 claims description 7
125000004122 cyclic group Chemical group 0.000 claims description 6
239000002904 solvent Substances 0.000 claims description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 5
239000000539 dimer Substances 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 5
150000002430 hydrocarbons Chemical class 0.000 claims description 5
239000013638 trimer Substances 0.000 claims description 5
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
229920001577 copolymer Polymers 0.000 claims 1
238000009472 formulation Methods 0.000 description 22
238000009835 boiling Methods 0.000 description 14
ZWEHNKRNPOVVGH-UHFFFAOYSA-N Methyl ethyl ketone Natural products CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 13
238000000034 method Methods 0.000 description 8
150000001875 compounds Chemical class 0.000 description 7
239000000243 solution Substances 0.000 description 7
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
238000010438 heat treatment Methods 0.000 description 6
150000002576 ketones Chemical class 0.000 description 6
229920000642 polymer Polymers 0.000 description 6
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 5
239000000654 additive Substances 0.000 description 5
238000004200 deflagration Methods 0.000 description 5
VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 5
238000006116 polymerization reaction Methods 0.000 description 5
GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
229910001873 dinitrogen Inorganic materials 0.000 description 4
239000007788 liquid Substances 0.000 description 4
YCOZIPAWZNQLMR-UHFFFAOYSA-N pentadecane Chemical compound CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 4
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 4
235000019345 sodium thiosulphate Nutrition 0.000 description 4
BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 4
238000004448 titration Methods 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000003921 oil Substances 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 2
PFCHFHIRKBAQGU-UHFFFAOYSA-N 3-hexanone Chemical compound CCCC(=O)CC PFCHFHIRKBAQGU-UHFFFAOYSA-N 0.000 description 2
FFWSICBKRCICMR-UHFFFAOYSA-N 5-methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
ZAJNGDIORYACQU-UHFFFAOYSA-N decan-2-one Chemical compound CCCCCCCCC(C)=O ZAJNGDIORYACQU-UHFFFAOYSA-N 0.000 description 2
125000005594 diketone group Chemical group 0.000 description 2
238000004880 explosion Methods 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000012362 glacial acetic acid Substances 0.000 description 2
239000005337 ground glass Substances 0.000 description 2
125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
239000003701 inert diluent Substances 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
VKCYHJWLYTUGCC-UHFFFAOYSA-N nonan-2-one Chemical compound CCCCCCCC(C)=O VKCYHJWLYTUGCC-UHFFFAOYSA-N 0.000 description 2
XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 description 2
RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 description 1
239000004604 Blowing Agent Substances 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-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
239000006001 Methyl nonyl ketone Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
KMPQYAYAQWNLME-UHFFFAOYSA-N Undecanal Natural products CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 description 1
239000000011 acetone peroxide Substances 0.000 description 1
235000019401 acetone peroxide Nutrition 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000007822 coupling agent Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
NIDHTBVIVPPBRJ-UHFFFAOYSA-N hexan-2-one;3-methylbutan-2-one Chemical compound CC(C)C(C)=O.CCCCC(C)=O NIDHTBVIVPPBRJ-UHFFFAOYSA-N 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
239000012535 impurity Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
QSOMFNQEXNFPNU-UHFFFAOYSA-L magnesium;hydrogen sulfate;hydroxide;hydrate Chemical compound O.O.[Mg+2].[O-]S([O-])(=O)=O QSOMFNQEXNFPNU-UHFFFAOYSA-L 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
239000010734 process oil Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
238000000518 rheometry Methods 0.000 description 1
238000011076 safety test Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 1
239000012855 volatile organic compound Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/06—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing oxygen
- 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
- C08K5/14—Peroxides
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/32—Hydrogen storage

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polymerization Catalysts (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Cosmetics (AREA)
Anti-Oxidant Or Stabilizer Compositions (AREA)
Detergent Compositions (AREA)
Compositions Of Macromolecular Compounds (AREA)

IL14259099A 1998-10-16 1999-10-07 A preparation that contains cyclic peroxide concrete and a moisturizing substance IL142590A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP98203483		1998-10-16
PCT/EP1999/007767 WO2000023434A1 (en)	1998-10-16	1999-10-07	Improved phlegmatization of cyclic ketone peroxides

Publications (2)

Publication Number	Publication Date
IL142590A0 IL142590A0 (en)	2002-03-10
IL142590A true IL142590A (en)	2004-08-31

Family

ID=8234227

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL14259099A IL142590A (en)	1998-10-16	1999-10-07	A preparation that contains cyclic peroxide concrete and a moisturizing substance

Country Status (22)

Country	Link
US (1)	US6358435B1 (de)
EP (1)	EP1121352B1 (de)
JP (1)	JP2002527583A (de)
KR (1)	KR20010080185A (de)
CN (1)	CN1154643C (de)
AR (1)	AR020845A1 (de)
AT (1)	ATE237609T1 (de)
AU (1)	AU758234B2 (de)
BR (1)	BR9914581A (de)
CA (1)	CA2347077A1 (de)
CZ (1)	CZ20011345A3 (de)
DE (1)	DE69907007T2 (de)
ES (1)	ES2197687T3 (de)
HU (1)	HUP0103779A3 (de)
IL (1)	IL142590A (de)
MY (1)	MY120260A (de)
NO (1)	NO20011868L (de)
PL (1)	PL347265A1 (de)
RU (1)	RU2224756C2 (de)
TR (1)	TR200101809T2 (de)
WO (1)	WO2000023434A1 (de)
ZA (1)	ZA200103078B (de)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
PL347265A1 (en) *	1998-10-16	2002-03-25	Akzo Nobel Nv	Improved phlegmatization of cyclic ketone peroxides
EP1186618A1 (de) *	2000-09-08	2002-03-13	ATOFINA Research	Heterophasische Propylenpolymere mit kontrollierten rheologischen Werten
EP1312617A1 (de)	2001-11-14	2003-05-21	ATOFINA Research	Schlagzähes Polypropen
BR0317007A (pt) *	2002-12-06	2005-10-25	Akzo Nobel Nv	Formulações de peróxido de cetona cìclico aperfeiçoadas
US7252784B2 (en) *	2002-12-06	2007-08-07	Akzo Nobel N.V.	Cyclic ketone peroxide formulations
WO2006066984A1 (en) *	2004-12-23	2006-06-29	Akzo Nobel N.V.	Process for preparing trioxepane composition and use thereof in crosslinking polymers
RU2280042C1 (ru) *	2004-12-27	2006-07-20	Закрытое акционерное общество "Всероссийский научно-исследовательский институт органического синтеза в г. Новокуйбышевске" (ЗАО "ВНИИОС НК")	Способ приготовления порошкообразных товарных форм пероксидных инициаторов
WO2014086692A1 (en)	2012-12-05	2014-06-12	Akzo Nobel Chemicals International B.V.	Masterbatch comprising a cyclic ketone peroxide
KR20150091057A (ko)	2012-12-05	2015-08-07	아크조 노벨 케미칼즈 인터내셔널 비.브이.	바이오수지를 기재로 한 퍼옥사이드 마스터배치
SG11201607395QA (en)	2014-03-11	2016-10-28	Akzo Nobel Chemicals Int Bv	Cyclic ketone peroxide composition
CN108586802A (zh) *	2018-05-28	2018-09-28	广州印田新材料有限公司	含有酯类减敏剂的稳定环酮过氧化物组合物的制备方法

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR862974A (fr)	1940-01-18	1941-03-20	Bataafsche Petroleum	Procédé pour la préparation de péroxydes de cétones aliphatiques et de combustibles liquides ayant une qualité d'ignition améliorée
GB1199722A (en) *	1966-08-16	1970-07-22	Laporte Chemical	Ketone Hydroperoxides
US3649548A (en) *	1967-05-15	1972-03-14	Norac Co	Non-hazardous ketone peroxide polymerization initiators
US3649546A (en) *	1967-05-15	1972-03-14	Norac Co	Non-hazardous ketone peroxide polymerization initiators
US3925417A (en) *	1970-06-29	1975-12-09	Story Chem Corp	Tricyclohexylidene peroxide and dicyclohexylidene peroxide and method of producing the same
US3833491A (en) *	1973-03-02	1974-09-03	C Kennedy	Production of macrocyclic compounds
AU666094B2 (en) *	1992-06-10	1996-01-25	Dow Chemical Company, The	Oligomers of styrene as flegmatizers for organic peroxides
WO1996003397A1 (en) *	1994-07-21	1996-02-08	Akzo Nobel N.V.	Cyclic ketone peroxide formulations
ATE177118T1 (de) *	1994-07-21	1999-03-15	Akzo Nobel Nv	Modifizierung von (co)polymeren mit cyclischen ketonperoxiden
AR001122A1 (es) *	1995-03-06	1997-09-24	Akzo Nobel Nv	Procedimiento de polímerizacion que utiliza una composición de peróxidos (co)polímero funcionalizadoobtenido por el proceso y uso de una composición de peróxidos
WO1998033770A1 (en) *	1997-02-03	1998-08-06	Akzo Nobel N.V.	Peroxide compositions with improved safety characteristics
PL347265A1 (en) *	1998-10-16	2002-03-25	Akzo Nobel Nv	Improved phlegmatization of cyclic ketone peroxides

1999
- 1999-10-07 PL PL99347265A patent/PL347265A1/xx unknown
- 1999-10-07 AT AT99953834T patent/ATE237609T1/de not_active IP Right Cessation
- 1999-10-07 TR TR2001/01809T patent/TR200101809T2/xx unknown
- 1999-10-07 RU RU2001113280/04A patent/RU2224756C2/ru not_active IP Right Cessation
- 1999-10-07 CA CA002347077A patent/CA2347077A1/en not_active Abandoned
- 1999-10-07 DE DE69907007T patent/DE69907007T2/de not_active Expired - Fee Related
- 1999-10-07 CZ CZ20011345A patent/CZ20011345A3/cs unknown
- 1999-10-07 CN CNB998133523A patent/CN1154643C/zh not_active Expired - Fee Related
- 1999-10-07 KR KR1020017004774A patent/KR20010080185A/ko not_active Withdrawn
- 1999-10-07 JP JP2000577162A patent/JP2002527583A/ja not_active Withdrawn
- 1999-10-07 BR BR9914581-2A patent/BR9914581A/pt not_active IP Right Cessation
- 1999-10-07 US US09/807,356 patent/US6358435B1/en not_active Expired - Fee Related
- 1999-10-07 AU AU10382/00A patent/AU758234B2/en not_active Ceased
- 1999-10-07 EP EP99953834A patent/EP1121352B1/de not_active Expired - Lifetime
- 1999-10-07 WO PCT/EP1999/007767 patent/WO2000023434A1/en not_active Ceased
- 1999-10-07 ES ES99953834T patent/ES2197687T3/es not_active Expired - Lifetime
- 1999-10-07 HU HU0103779A patent/HUP0103779A3/hu unknown
- 1999-10-07 IL IL14259099A patent/IL142590A/en not_active IP Right Cessation
- 1999-10-13 MY MYPI99004407A patent/MY120260A/en unknown
- 1999-10-15 AR ARP990105257A patent/AR020845A1/es unknown
2001
- 2001-04-11 NO NO20011868A patent/NO20011868L/no not_active Application Discontinuation
- 2001-04-12 ZA ZA200103078A patent/ZA200103078B/en unknown

Also Published As

Publication number	Publication date
ZA200103078B (en)	2002-07-12
EP1121352A1 (de)	2001-08-08
TR200101809T2 (tr)	2002-01-21
BR9914581A (pt)	2001-11-06
CZ20011345A3 (cs)	2001-10-17
HUP0103779A3 (en)	2004-06-28
NO20011868D0 (no)	2001-04-11
WO2000023434A1 (en)	2000-04-27
CN1154643C (zh)	2004-06-23
AU758234B2 (en)	2003-03-20
RU2224756C2 (ru)	2004-02-27
KR20010080185A (ko)	2001-08-22
HUP0103779A2 (hu)	2002-01-28
CA2347077A1 (en)	2000-04-27
AU1038200A (en)	2000-05-08
ATE237609T1 (de)	2003-05-15
DE69907007D1 (de)	2003-05-22
IL142590A0 (en)	2002-03-10
US6358435B1 (en)	2002-03-19
AR020845A1 (es)	2002-05-29
CN1326451A (zh)	2001-12-12
NO20011868L (no)	2001-06-11
ES2197687T3 (es)	2004-01-01
JP2002527583A (ja)	2002-08-27
PL347265A1 (en)	2002-03-25
MY120260A (en)	2005-09-30
DE69907007T2 (de)	2004-01-29
EP1121352B1 (de)	2003-04-16

Legal Events

Date	Code	Title
2005-01-24	FF	Patent granted
2005-02-20	KB	Patent renewed
2006-01-15	KB	Patent renewed
2010-11-30	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
AU686466B2 (en)	1998-02-05	Cyclic ketone peroxide formulations
EP1121352B1 (de)	2003-04-16	Verbesserte phlegmatisierung von zyklischer keton superoxyde
NO310419B1 (no)	2001-07-02	Fremgangsmåte for fremstilling av (ko)polymerer, den derved oppnådde funksjonaliserte (ko)polymer, samt anvendelse av enorganisk peroksyblanding
JP2011173895A (ja)	2011-09-08	貯蔵安定な環状ケトンパーオキサイド組成物
BR112020025725A2 (pt)	2021-03-16	Composição de monômero
EP0133514B1 (de)	1987-06-16	Diacylperoxydzusammensetzung
EP1592682B1 (de)	2010-01-27	Lagerungsstabile zusammensetzungen cyclischer ketonperoxide
JPH06340617A (ja)	1994-12-13	安全な過酢酸組成物
EP1585741A1 (de)	2005-10-19	Formulierungen cylischer ketonperoxide
MXPA01003838A (es)	2002-06-05	Flegmatizacion mejorada de peroxidos de cetona ciclicos
US9234087B2 (en)	2016-01-12	Preparation for initiating radical reactions
US5691462A (en)	1997-11-25	Stabilized vinyl ether composition
US7252784B2 (en)	2007-08-07	Cyclic ketone peroxide formulations
SA518390892B1 (ar)	2023-02-28	البلمرة الشقية لإيثيلين البادئة بواسطة زوج من مركبات بيروكسيد عضوية ذات إنتاجية عالية
PL243218B1 (pl)	2023-07-17	Bezbarwny kwas monochlorooctowy i sposób jego otrzymywania
JPH03210310A (ja)	1991-09-13	安定化されたトリアリルイソシアヌレート組成物