CH619262A5 - - Google Patents

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Info

Publication number: CH619262A5
Authority: CH; Switzerland
Prior art keywords: carbon atoms; radicals; activator; per; compound
Prior art date: 1976-02-10

Application number

CH163477A

Other languages

English (en)

French (fr)

Inventor

Jean-Pierre Schirmann

Bernhard Dubreux

Michel Bakes

Serge Yvon Delavarenne

Marie-Christine Daude-Lagrave

Original Assignee

Ugine Kuhlmann

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.)

1976-02-10

Filing date

1977-02-10

Publication date

1980-09-15

1977-02-10 Application filed by Ugine Kuhlmann filed Critical Ugine Kuhlmann

1980-09-15 Publication of CH619262A5 publication Critical patent/CH619262A5/fr

Links

239000012190 activator Substances 0.000 claims description 21
125000004432 carbon atom Chemical group C* 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 12
-1 alkyl radicals Chemical class 0.000 claims description 11
238000004061 bleaching Methods 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 7
238000005406 washing Methods 0.000 claims description 6
239000000843 powder Substances 0.000 claims description 5
239000004215 Carbon black (E152) Substances 0.000 claims description 4
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 4
230000007547 defect Effects 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
150000001199 N-acyl amides Chemical class 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
150000003857 carboxamides Chemical class 0.000 claims description 2
150000002825 nitriles Chemical class 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
239000000126 substance Substances 0.000 claims description 2
238000004806 packaging method and process Methods 0.000 claims 2
150000003254 radicals Chemical class 0.000 claims 2
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims 1
239000004480 active ingredient Substances 0.000 claims 1
150000001555 benzenes Chemical class 0.000 claims 1
239000011248 coating agent Substances 0.000 claims 1
238000000576 coating method Methods 0.000 claims 1
239000002274 desiccant Substances 0.000 claims 1
125000004185 ester group Chemical group 0.000 claims 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
VPVSTMAPERLKKM-UHFFFAOYSA-N glycoluril Chemical compound N1C(=O)NC2NC(=O)NC21 VPVSTMAPERLKKM-UHFFFAOYSA-N 0.000 claims 1
125000000623 heterocyclic group Chemical group 0.000 claims 1
WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 claims 1
229940091173 hydantoin Drugs 0.000 claims 1
230000003301 hydrolyzing effect Effects 0.000 claims 1
239000004615 ingredient Substances 0.000 claims 1
BXRNXXXXHLBUKK-UHFFFAOYSA-N piperazine-2,5-dione Chemical compound O=C1CNC(=O)CN1 BXRNXXXXHLBUKK-UHFFFAOYSA-N 0.000 claims 1
239000007787 solid Substances 0.000 claims 1
125000001424 substituent group Chemical group 0.000 claims 1
230000002087 whitening effect Effects 0.000 description 7
230000001590 oxidative effect Effects 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 2
239000004744 fabric Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000011707 mineral Substances 0.000 description 2
ZSBDPRIWBYHIAF-UHFFFAOYSA-N n-acetylacetamide Chemical compound CC(=O)NC(C)=O ZSBDPRIWBYHIAF-UHFFFAOYSA-N 0.000 description 2
238000004659 sterilization and disinfection Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 1
XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
241001460678 Napo <wasp> Species 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
UOXZGINNWREKCS-UHFFFAOYSA-N [1-(acetylcarbamoyl)cyclohexyl] acetate Chemical compound CC(=O)NC(=O)C1(OC(C)=O)CCCCC1 UOXZGINNWREKCS-UHFFFAOYSA-N 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
WFKAJVHLWXSISD-UHFFFAOYSA-N anhydrous dimethyl-acetamide Natural products CC(C)C(N)=O WFKAJVHLWXSISD-UHFFFAOYSA-N 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910000397 disodium phosphate Inorganic materials 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical group 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
239000003925 fat Substances 0.000 description 1
239000000835 fiber Substances 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
229940047889 isobutyramide Drugs 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
239000003921 oil Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
238000002161 passivation Methods 0.000 description 1
125000005342 perphosphate group Chemical group 0.000 description 1
238000000746 purification Methods 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
239000000243 solution Substances 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
150000004685 tetrahydrates Chemical class 0.000 description 1
239000004753 textile Substances 0.000 description 1
238000011282 treatment Methods 0.000 description 1
239000001993 wax Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/88—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having the nitrogen atom of at least one of the carboxamide groups further acylated
- 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
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic compounds
- C11D3/3917—Nitrogen-containing compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/52—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the nitrogen atom of at least one of the carboxamide groups further acylated

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Detergent Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

CH163477A 1976-02-10 1977-02-10 CH619262A5 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR7603580A FR2340983A1 (fr)	1976-02-10	1976-02-10	Activateurs pour percomposes

Publications (1)

Publication Number	Publication Date
CH619262A5 true CH619262A5 (no)	1980-09-15

Family

ID=9168942

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH163477A CH619262A5 (no)	1976-02-10	1977-02-10

Country Status (16)

Country	Link
US (1)	US4221675A (no)
JP (1)	JPS5297912A (no)
BE (1)	BE850735A (no)
BR (1)	BR7700802A (no)
CA (1)	CA1094793A (no)
CH (1)	CH619262A5 (no)
DE (1)	DE2705047C3 (no)
DK (1)	DK53877A (no)
FR (1)	FR2340983A1 (no)
GB (1)	GB1565422A (no)
IE (1)	IE44222B1 (no)
IT (1)	IT1072747B (no)
LU (1)	LU76720A1 (no)
NL (1)	NL7701350A (no)
NO (1)	NO146670C (no)
SE (1)	SE7701451L (no)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4436726A (en)	1980-12-15	1984-03-13	Fujisawa Pharmaceutical Co., Ltd.	N-Acylpeptide compound, processes for the preparation thereof and the pharmaceutical compositions
AU9173582A (en) *	1982-01-05	1983-07-14	Fujisawa Pharmaceutical Co., Ltd.	N-acyl peptide
US4634551A (en) *	1985-06-03	1987-01-06	Procter & Gamble Company	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain
GB8415909D0 (en) *	1984-06-21	1984-07-25	Procter & Gamble Ltd	Peracid compounds
US4964870A (en) *	1984-12-14	1990-10-23	The Clorox Company	Bleaching with phenylene diester peracid precursors
US4959187A (en) *	1986-11-06	1990-09-25	The Clorox Company	Glycolate ester peracid precursors
US5112514A (en) *	1986-11-06	1992-05-12	The Clorox Company	Oxidant detergent containing stable bleach activator granules
US4778618A (en) *	1986-11-06	1988-10-18	The Clorox Company	Glycolate ester peracid precursors
US5002691A (en) *	1986-11-06	1991-03-26	The Clorox Company	Oxidant detergent containing stable bleach activator granules
US5269962A (en)	1988-10-14	1993-12-14	The Clorox Company	Oxidant composition containing stable bleach activator granules
DE4016980A1 (de) *	1990-05-25	1991-11-28	Hoechst Ag	Ureidoperoxicarbonsaeuren, verfahren zu deren herstellung und deren verwendung
US6117357A (en) *	1996-07-29	2000-09-12	The Procter & Gamble Company	Unsymmetrical acyclic imide bleach activators and compositions employing the same
US6291413B1 (en)	1997-11-10	2001-09-18	The Procter & Gamble Company	O-substituted N,N-diacylhydroxylamine bleach activators and compositions employing the same
IT201600070454A1 (it)	2016-07-06	2016-10-06	3V Sigma Spa	Attivatori di composti perossigenati

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2290881A (en) *	1940-07-22	1942-07-28	Emulsol Corp	Halogeno-carboxylic amides
US2477816A (en) *	1947-09-05	1949-08-02	Hoffmann La Roche	Benzil-acid derivative and process for the manufacture thereof

1976
- 1976-02-10 FR FR7603580A patent/FR2340983A1/fr active Granted
1977
- 1977-01-26 BE BE1007905A patent/BE850735A/xx not_active IP Right Cessation
- 1977-02-03 GB GB4496/77A patent/GB1565422A/en not_active Expired
- 1977-02-07 IT IT67269/77A patent/IT1072747B/it active
- 1977-02-08 JP JP1219977A patent/JPS5297912A/ja active Pending
- 1977-02-08 DE DE2705047A patent/DE2705047C3/de not_active Expired
- 1977-02-08 LU LU76720A patent/LU76720A1/xx unknown
- 1977-02-09 NL NL7701350A patent/NL7701350A/xx not_active Application Discontinuation
- 1977-02-09 DK DK53877A patent/DK53877A/da unknown
- 1977-02-09 NO NO770429A patent/NO146670C/no unknown
- 1977-02-09 BR BR7700802A patent/BR7700802A/pt unknown
- 1977-02-09 SE SE7701451A patent/SE7701451L/xx not_active Application Discontinuation
- 1977-02-09 CA CA271,422A patent/CA1094793A/fr not_active Expired
- 1977-02-10 CH CH163477A patent/CH619262A5/fr not_active IP Right Cessation
- 1977-02-10 IE IE281/77A patent/IE44222B1/en unknown
1978
- 1978-05-23 US US05/908,781 patent/US4221675A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
CA1094793A (fr)	1981-02-03
IT1072747B (it)	1985-04-10
US4221675A (en)	1980-09-09
DE2705047C3 (de)	1980-07-31
NO146670B (no)	1982-08-09
IE44222L (en)	1977-08-10
IE44222B1 (en)	1981-09-09
BR7700802A (pt)	1977-10-11
NL7701350A (nl)	1977-08-12
LU76720A1 (no)	1978-10-18
NO146670C (no)	1982-11-17
NO770429L (no)	1977-08-11
JPS5297912A (en)	1977-08-17
GB1565422A (en)	1980-04-23
FR2340983B1 (no)	1979-07-20
DK53877A (da)	1977-08-11
DE2705047A1 (de)	1977-08-18
SE7701451L (sv)	1977-08-11
BE850735A (fr)	1977-07-26
DE2705047B2 (de)	1979-11-29
FR2340983A1 (fr)	1977-09-09

Legal Events

Date	Code	Title	Description
1983-10-31	PL	Patent ceased

Publication	Publication Date	Title
US4128494A (en)	1978-12-05	Activators for percompounds
CH619262A5 (no)	1980-09-15
JP4837733B2 (ja)	2011-12-14	強化された酵素適合性を有する有機触媒
US5463115A (en)	1995-10-31	Sulfonimines as bleach catalysts
US5753599A (en)	1998-05-19	Thiadiazole dioxides as bleach enhancers
KR950003427B1 (ko)	1995-04-12	저온표백조성물
US3969257A (en)	1976-07-13	Washing and bleaching composition containing bleach, activator and a nitrilotricarboxylic acid compound
EP0186052A1 (fr)	1986-07-02	Procédé d'activation du peroxyde d'hydrogène dans des bains de lavage ou de désinfection
US5760222A (en)	1998-06-02	Thiadiazole dioxide derived oxaziridines as bleaching compounds
US5652207A (en)	1997-07-29	Phosphinoyl imines for use as oxygen transfer agents
EP0922090A2 (en)	1999-06-16	N-acylimines as bleach catalysts
JP2009516045A (ja)	2009-04-16	安定した放臭剤系
CA1088954A (fr)	1980-11-04	Activateurs pour percomposes
CA1084256A (fr)	1980-08-26	Activateurs phosphores pour percomposes
JP4813551B2 (ja)	2011-11-09	強化酵素適合性を有する有機触媒
EP0206959A2 (fr)	1986-12-30	Procédé de blanchiment de linge domestique dans un cycle de lavage
EP1038946A2 (en)	2000-09-27	N-acylimines as bleach catalysts
US3982891A (en)	1976-09-28	Bleaching and detergent compositions having imide activator and peroxygen bleach
EP0140799B1 (fr)	1986-12-03	Nouvelles compositions pour le blanchiment alcalin des textiles
BE897905A (fr)	1984-04-04	Composition de blanchiment et de lavage à base d'un peroxyacide
EP0182693B1 (fr)	1988-08-31	Perfectionnement aux procédés de blanchiment oxydant réalisés en milieu acide
GB1480405A (en)	1977-07-20	Activators for inorganic per-compounds
US5429768A (en)	1995-07-04	Grignard reaction intermediates as bleach catalysts
RU2413757C2 (ru)	2011-03-10	Чистящая композиция, содержащая органический катализатор с улучшенной совместимостью с ферментами
BE603768A (no)