PL194358B1 - Wodna jednofazowa kompozycja czyszcząca - Google Patents

Wodna jednofazowa kompozycja czyszcząca

Info

Publication number: PL194358B1
Authority: PL; Poland
Prior art keywords: composition; perfume; weight; surfactant; composition according
Prior art date: 2000-06-08

Application number

PL01360251A

Other languages

English (en)

Polish (pl)

Other versions

PL360251A1 (en

Inventor

Matthew James Leach

Franca Marianini

Der Scheur Frank Theodoor Van

Adriano Violante

Original Assignee

Unilever 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.)

2000-06-08

Filing date

2001-05-31

Publication date

2007-05-31

2001-05-31 Application filed by Unilever Nv filed Critical Unilever Nv

2004-09-06 Publication of PL360251A1 publication Critical patent/PL360251A1/xx

2007-05-31 Publication of PL194358B1 publication Critical patent/PL194358B1/pl

Links

239000000203 mixture Substances 0.000 title claims abstract description 78
238000004140 cleaning Methods 0.000 title claims abstract description 27
239000002304 perfume Substances 0.000 claims abstract description 31
-1 ester peracid Chemical class 0.000 claims abstract description 19
239000004094 surface-active agent Substances 0.000 claims abstract description 18
239000007800 oxidant agent Substances 0.000 claims abstract description 17
125000000217 alkyl group Chemical group 0.000 claims abstract description 7
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
239000003945 anionic surfactant Substances 0.000 claims description 9
239000002736 nonionic surfactant Substances 0.000 claims description 8
238000000034 method Methods 0.000 claims description 4
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 4
150000001335 aliphatic alkanes Chemical group 0.000 claims description 3
125000003158 alcohol group Chemical group 0.000 claims 1
239000008194 pharmaceutical composition Substances 0.000 claims 1
239000007788 liquid Substances 0.000 abstract description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
150000001298 alcohols Chemical group 0.000 description 7
239000003205 fragrance Substances 0.000 description 7
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
150000004965 peroxy acids Chemical class 0.000 description 6
150000001875 compounds Chemical class 0.000 description 5
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
239000000243 solution Substances 0.000 description 4
RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
150000002978 peroxides Chemical class 0.000 description 3
239000000126 substance Substances 0.000 description 3
229920001285 xanthan gum Polymers 0.000 description 3
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 2
XJMMNTGIMDZPMU-UHFFFAOYSA-N 3-methylglutaric acid Chemical compound OC(=O)CC(C)CC(O)=O XJMMNTGIMDZPMU-UHFFFAOYSA-N 0.000 description 2
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
KGEKLUUHTZCSIP-HOSYDEDBSA-N [(1s,4s,6r)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-HOSYDEDBSA-N 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 2
CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 2
239000002738 chelating agent Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000011010 flushing procedure Methods 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
229910021645 metal ion Inorganic materials 0.000 description 2
HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 2
SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 2
238000000926 separation method Methods 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
239000000341 volatile oil Substances 0.000 description 2
GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
BAERPNBPLZWCES-UHFFFAOYSA-N (2-hydroxy-1-phosphonoethyl)phosphonic acid Chemical compound OCC(P(O)(O)=O)P(O)(O)=O BAERPNBPLZWCES-UHFFFAOYSA-N 0.000 description 1
UGLFQJOXHCQGFQ-UHFFFAOYSA-N 1,3-dichloro-1,3,5-triazinane-2,4,6-trione;potassium Chemical compound [K].ClN1C(=O)NC(=O)N(Cl)C1=O UGLFQJOXHCQGFQ-UHFFFAOYSA-N 0.000 description 1
WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
WYMDDFRYORANCC-UHFFFAOYSA-N 2-[[3-[bis(carboxymethyl)amino]-2-hydroxypropyl]-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)CN(CC(O)=O)CC(O)=O WYMDDFRYORANCC-UHFFFAOYSA-N 0.000 description 1
239000005725 8-Hydroxyquinoline Substances 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229940120146 EDTMP Drugs 0.000 description 1
DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000013543 active substance Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
229940116229 borneol Drugs 0.000 description 1
229940115397 bornyl acetate Drugs 0.000 description 1
229930006739 camphene Natural products 0.000 description 1
ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 1
150000001735 carboxylic acids Chemical group 0.000 description 1
229960005233 cineole Drugs 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
239000008139 complexing agent Substances 0.000 description 1
230000006835 compression Effects 0.000 description 1
238000007906 compression Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
229940071118 cumenesulfonate Drugs 0.000 description 1
230000006837 decompression Effects 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
238000004332 deodorization Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
229940113120 dipropylene glycol Drugs 0.000 description 1
DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
238000004128 high performance liquid chromatography Methods 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000001165 hydrophobic group Chemical group 0.000 description 1
239000003752 hydrotrope Substances 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
238000003780 insertion Methods 0.000 description 1
230000037431 insertion Effects 0.000 description 1
239000002085 irritant Substances 0.000 description 1
231100000021 irritant Toxicity 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229940087305 limonene Drugs 0.000 description 1
235000001510 limonene Nutrition 0.000 description 1
238000004949 mass spectrometry Methods 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000003605 opacifier Substances 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
229960003540 oxyquinoline Drugs 0.000 description 1
230000002093 peripheral effect Effects 0.000 description 1
238000005502 peroxidation Methods 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical class [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229940081066 picolinic acid Drugs 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
238000011012 sanitization Methods 0.000 description 1
230000007017 scission Effects 0.000 description 1
238000012216 screening Methods 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
229940079842 sodium cumenesulfonate Drugs 0.000 description 1
QEKATQBVVAZOAY-UHFFFAOYSA-M sodium;4-propan-2-ylbenzenesulfonate Chemical group [Na+].CC(C)C1=CC=C(S([O-])(=O)=O)C=C1 QEKATQBVVAZOAY-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
230000008719 thickening Effects 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
229910001428 transition metal ion Inorganic materials 0.000 description 1
238000000870 ultraviolet spectroscopy Methods 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
GDJZZWYLFXAGFH-UHFFFAOYSA-M xylenesulfonate group Chemical class C1(C(C=CC=C1)C)(C)S(=O)(=O)[O-] GDJZZWYLFXAGFH-UHFFFAOYSA-M 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Detergent Compositions (AREA)

PL01360251A 2000-06-08 2001-05-31 Wodna jednofazowa kompozycja czyszcząca PL194358B1 (pl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP00304885		2000-06-08
PCT/EP2001/006296 WO2001094520A2 (en)	2000-06-08	2001-05-31	Hard surface cleaning compositions

Publications (2)

Publication Number	Publication Date
PL360251A1 PL360251A1 (en)	2004-09-06
PL194358B1 true PL194358B1 (pl)	2007-05-31

Family

ID=8173057

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL01360251A PL194358B1 (pl)	2000-06-08	2001-05-31	Wodna jednofazowa kompozycja czyszcząca

Country Status (9)

Country	Link
EP (1)	EP1290131B1 (de)
AR (1)	AR028688A1 (de)
AT (1)	ATE255629T1 (de)
AU (1)	AU2001285730A1 (de)
DE (1)	DE60101387T2 (de)
HU (1)	HUP0300968A3 (de)
PL (1)	PL194358B1 (de)
TR (1)	TR200302295T4 (de)
WO (1)	WO2001094520A2 (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1473355A1 (de)	2003-04-29	2004-11-03	The Procter & Gamble Company	Verfahren zur erhöhung der Hydrophobizität einer Toilettenbeckenoberfläche
US20080032912A1 (en)	2006-08-04	2008-02-07	Takasago International Corporation	Use of fragrance compositions for the prevention of the development of indole base malodours from fecal and urine based soils
EP2110118B1 (de)	2008-04-15	2014-11-19	Takasago International Corporation	Zusammensetzung zur Verringerung von schlechten Gerüchen und Verwendungen dafür
DE102010055742A1 (de) *	2010-12-22	2012-06-28	Clariant International Ltd.	Zusammensetzungen enthaltend sekundäres Paraffinsulfonat und Alkoholalkoxylat
EP3984599A1 (de)	2015-02-24	2022-04-20	Takasago International Corporation	Verbesserte parfümzusammensetzungen
US20190054200A1 (en)	2016-02-24	2019-02-21	Takasago International Corporation	Household product delivering warming and/or tingling sensations
US11851631B2 (en)	2016-02-24	2023-12-26	Takasago International Corporation	Household product delivering cooling sensations
ES2851677T3 (es)	2016-02-24	2021-09-08	Takasago Perfumery Co Ltd	Agente estimulante

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8716219D0 (en) *	1987-07-09	1987-08-12	Unilever Plc	Perfume compositions
DD292477B5 (de) *	1990-03-05	1994-12-08	Fit Chemische Produkte Gmbh	Parfuemierte, mit Riechstoffen versehene, fluessige Wasch-, Geschirrspuel-und Reinigungsmittel
US5248434A (en) *	1992-04-20	1993-09-28	The Proctor & Gamble Company	Liquid or gel bleaching composition containing amidoperoxyacid bleach and perfume
JP3197371B2 (ja) *	1992-11-04	2001-08-13	稲畑香料株式会社	芳香を有する過酢酸系殺菌剤組成物及び漂白剤組成物
GB9412051D0 (en) *	1994-06-16	1994-08-03	Solvay Interox Ltd	Novel peroxygen compounds
US6055679A (en) *	1995-03-03	2000-05-02	S. C. Johnson & Son, Inc.	Passive lavatory cleanser dispensing system
EP0784091A1 (de) *	1996-01-12	1997-07-16	The Procter & Gamble Company	Stabile parfümierte Bleichmittelzusammensetzung
US6010993A (en) *	1996-02-23	2000-01-04	The Procter & Gamble Company	Disinfecting compositions
EP0905227A1 (de) *	1997-09-30	1999-03-31	The Procter & Gamble Company	Persäure enthaltende wasserfreie Zusammensetzungen
EP1001012A1 (de) *	1998-11-10	2000-05-17	The Procter & Gamble Company	Desinfektions- und Reinigungszusammensetzungen
EP1072673A3 (de) *	1999-07-20	2001-03-21	The Procter & Gamble Company	Riechstoffkompositionen

2001
- 2001-05-31 AU AU2001285730A patent/AU2001285730A1/en not_active Abandoned
- 2001-05-31 PL PL01360251A patent/PL194358B1/pl not_active IP Right Cessation
- 2001-05-31 HU HU0300968A patent/HUP0300968A3/hu unknown
- 2001-05-31 AT AT01964957T patent/ATE255629T1/de not_active IP Right Cessation
- 2001-05-31 DE DE60101387T patent/DE60101387T2/de not_active Expired - Lifetime
- 2001-05-31 TR TR2003/02295T patent/TR200302295T4/xx unknown
- 2001-05-31 EP EP01964957A patent/EP1290131B1/de not_active Expired - Lifetime
- 2001-05-31 WO PCT/EP2001/006296 patent/WO2001094520A2/en not_active Ceased
- 2001-06-07 AR ARP010102721A patent/AR028688A1/es active IP Right Grant

Also Published As

Publication number	Publication date
TR200302295T4 (tr)	2004-01-21
WO2001094520A3 (en)	2002-03-07
EP1290131B1 (de)	2003-12-03
AU2001285730A1 (en)	2001-12-17
EP1290131A2 (de)	2003-03-12
HUP0300968A2 (hu)	2003-08-28
AR028688A1 (es)	2003-05-21
ATE255629T1 (de)	2003-12-15
DE60101387D1 (de)	2004-01-15
DE60101387T2 (de)	2004-06-09
WO2001094520A2 (en)	2001-12-13
HUP0300968A3 (en)	2006-06-28
PL360251A1 (en)	2004-09-06

Legal Events

Date	Code	Title	Description
2012-07-31	LAPS	Decisions on the lapse of the protection rights	Effective date: 20110531

Publication	Publication Date	Title
US4308625A (en)	1982-01-05	Article for sanitizing toilets
US4248827A (en)	1981-02-03	Method for sanitizing toilets
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