IL92329A - Antiviral preparations for superficial purification containing aldehyde - Google Patents

Antiviral preparations for superficial purification containing aldehyde

Info

Publication number: IL92329A
Authority: IL; Israel
Prior art keywords: composition; glycol; accordance; weight; anionic surfactant
Prior art date: 1988-12-20

Application number

IL9232989A

Other languages

English (en)

Hebrew (he)

Other versions

IL92329A0 (en

Original Assignee

Wave Energy Systems

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.)

1988-12-20

Filing date

1989-11-16

Publication date

1995-03-30

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=23099954&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IL92329(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1989-11-16 Application filed by Wave Energy Systems filed Critical Wave Energy Systems

1990-07-26 Publication of IL92329A0 publication Critical patent/IL92329A0/xx

1995-03-30 Publication of IL92329A publication Critical patent/IL92329A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 85
230000003253 viricidal effect Effects 0.000 title claims abstract description 40
238000005202 decontamination Methods 0.000 title abstract description 4
230000003588 decontaminative effect Effects 0.000 title abstract description 4
125000002485 formyl group Chemical class [H]C(*)=O 0.000 title 1
SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims abstract description 74
241000700605 Viruses Species 0.000 claims abstract description 68
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 62
239000003945 anionic surfactant Substances 0.000 claims abstract description 36
239000000243 solution Substances 0.000 claims abstract description 36
150000001299 aldehydes Chemical class 0.000 claims abstract description 34
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 23
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims abstract description 14
150000008051 alkyl sulfates Chemical class 0.000 claims abstract description 10
150000008055 alkyl aryl sulfonates Chemical class 0.000 claims abstract description 7
150000008052 alkyl sulfonates Chemical class 0.000 claims abstract description 7
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 52
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 27
ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 claims description 23
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 16
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 14
239000002736 nonionic surfactant Substances 0.000 claims description 14
-1 alcohol sulfates Chemical class 0.000 claims description 11
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 7
239000003638 chemical reducing agent Substances 0.000 claims description 7
239000002904 solvent Substances 0.000 claims description 7
239000002202 Polyethylene glycol Substances 0.000 claims description 6
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims description 6
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
239000000337 buffer salt Substances 0.000 claims description 5
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229940075564 anhydrous dibasic sodium phosphate Drugs 0.000 claims description 4
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QZTKDVCDBIDYMD-UHFFFAOYSA-N 2,2'-[(2-amino-2-oxoethyl)imino]diacetic acid Chemical compound NC(=O)CN(CC(O)=O)CC(O)=O QZTKDVCDBIDYMD-UHFFFAOYSA-N 0.000 claims description 3
IHPYMWDTONKSCO-UHFFFAOYSA-N 2,2'-piperazine-1,4-diylbisethanesulfonic acid Chemical compound OS(=O)(=O)CCN1CCN(CCS(O)(=O)=O)CC1 IHPYMWDTONKSCO-UHFFFAOYSA-N 0.000 claims description 3
GHCZTIFQWKKGSB-UHFFFAOYSA-N 2-hydroxypropane-1,2,3-tricarboxylic acid;phosphoric acid Chemical compound OP(O)(O)=O.OC(=O)CC(O)(C(O)=O)CC(O)=O GHCZTIFQWKKGSB-UHFFFAOYSA-N 0.000 claims description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
LUVOJBWJNHWVNG-UHFFFAOYSA-N [Na].[Na].[Na].OC(=O)CC(O)(C(O)=O)CC(O)=O Chemical compound [Na].[Na].[Na].OC(=O)CC(O)(C(O)=O)CC(O)=O LUVOJBWJNHWVNG-UHFFFAOYSA-N 0.000 claims description 3
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 3
239000007978 cacodylate buffer Substances 0.000 claims description 3
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
239000011976 maleic acid Substances 0.000 claims description 3
239000008363 phosphate buffer Substances 0.000 claims description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
229910000318 alkali metal phosphate Inorganic materials 0.000 claims 3
239000000872 buffer Substances 0.000 claims 2
CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 claims 2
CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical compound CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 claims 2
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims 1
229910019142 PO4 Inorganic materials 0.000 claims 1
229910000288 alkali metal carbonate Inorganic materials 0.000 claims 1
150000008041 alkali metal carbonates Chemical class 0.000 claims 1
150000001642 boronic acid derivatives Chemical class 0.000 claims 1
235000021317 phosphate Nutrition 0.000 claims 1
150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
150000003839 salts Chemical class 0.000 claims 1
239000000178 monomer Substances 0.000 abstract description 14
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LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 6
150000004677 hydrates Chemical class 0.000 abstract description 6
230000003389 potentiating effect Effects 0.000 abstract description 5
239000007864 aqueous solution Substances 0.000 abstract description 4
230000009965 odorless effect Effects 0.000 abstract description 4
230000002421 anti-septic effect Effects 0.000 abstract description 3
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QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract description 2
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239000004480 active ingredient Substances 0.000 abstract 2
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WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 17
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LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 8
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FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 6
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
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150000007523 nucleic acids Chemical class 0.000 description 4
235000010292 orthophenyl phenol Nutrition 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
108090001074 Nucleocapsid Proteins Proteins 0.000 description 3
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239000002253 acid Substances 0.000 description 3
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229960003333 chlorhexidine gluconate Drugs 0.000 description 2
YZIYKJHYYHPJIB-UUPCJSQJSA-N chlorhexidine gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.C1=CC(Cl)=CC=C1NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NC1=CC=C(Cl)C=C1 YZIYKJHYYHPJIB-UUPCJSQJSA-N 0.000 description 2
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
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SXGZJKUKBWWHRA-UHFFFAOYSA-N 2-(N-morpholiniumyl)ethanesulfonate Chemical compound [O-]S(=O)(=O)CC[NH+]1CCOCC1 SXGZJKUKBWWHRA-UHFFFAOYSA-N 0.000 description 1
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DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
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WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
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GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
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SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
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JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Compositions Of Macromolecular Compounds (AREA)

IL9232989A 1988-12-20 1989-11-16 Antiviral preparations for superficial purification containing aldehyde IL92329A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/286,738 US5004757A (en)	1988-12-20	1988-12-20	Virucidal low toxicity compositions

Publications (2)

Publication Number	Publication Date
IL92329A0 IL92329A0 (en)	1990-07-26
IL92329A true IL92329A (en)	1995-03-30

Family

ID=23099954

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9232989A IL92329A (en)	1988-12-20	1989-11-16	Antiviral preparations for superficial purification containing aldehyde

Country Status (10)

Country	Link
US (1)	US5004757A (de)
EP (1)	EP0375149B1 (de)
JP (1)	JP2835180B2 (de)
AT (1)	ATE104111T1 (de)
CA (1)	CA2002856C (de)
DE (1)	DE68914622T2 (de)
ES (1)	ES2054026T3 (de)
FR (1)	FR2641447B1 (de)
IL (1)	IL92329A (de)
WO (1)	WO1990006677A1 (de)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA2052649A1 (en) *	1990-10-15	1992-04-16	Steris Inc.	Combined two stage method for cleaning and decontaminating surgical instruments
US5326492A (en) *	1991-11-18	1994-07-05	Medical Polymers, Inc.	Disinfectant mixture containing water soluble lubricating and cleaning agents and method
ES2050627B1 (es) *	1992-11-11	1994-12-16	Inibsa Lab	Nuevo glutaraldehido activado y sinergizado.
US5674829A (en) *	1993-01-29	1997-10-07	Antoinetta P. Martin	Stable aqueous glutaraldehyde solutions containing sodium acetate and a nonionic detergent
US5658560A (en) *	1994-01-18	1997-08-19	Serikov; Vladimir B.	Method of treating endotoxemia by administering tyloxapol
JP3515821B2 (ja) *	1994-10-21	2004-04-05	株式会社資生堂	消毒用組成物
DE19548880A1 (de) *	1995-12-28	1997-10-02	Herbert Dr Widulle	Verbesserung der Leistungsfähigkeit von Desinfektionsmittelwirkstoffen durch ungiftige Verbindungen
AUPO336796A0 (en) *	1996-11-01	1996-11-28	Whiteley Industries Pty Ltd	Ready-to-use glutaraldehyde concentrates
ES2191219T3 (es) *	1997-03-27	2003-09-01	Braun Medical Ag	Agente microbicida y su utilizacion.
ES2286852T3 (es)	1997-08-04	2007-12-01	Advanced Life Science Institute, Inc.	Metodos para detectar o analizar virus.
US6039921A (en) *	1997-11-25	2000-03-21	Boucher; Raymond M. G.	Liquid phase disinfection/sterilization with microwave energy
US6192887B1 (en)	1998-05-19	2001-02-27	The Pennsylvania State University	Broad spectrum microbicidal and spermicidal compositions and methods having activity against sexually transmitted agents including papillomaviruses
JP2004532286A (ja) *	2001-02-01	2004-10-21	ベクトン・ディキンソン・アンド・カンパニー	界面活性剤／酸化剤の溶液および使用法
US20040101881A1 (en) *	2002-02-01	2004-05-27	Gerard Durmowicz	Surfactant/oxidizing agent solution and methods of use
CA2533950C (en)	2005-01-28	2013-10-22	B. Braun Medical Ag	Virucidal disinfectant
CN101821224B (zh) *	2007-04-05	2015-08-19	马丁家族托拉斯	稳定醛的方法
US20090118352A1 (en) *	2007-11-07	2009-05-07	Esawtech, Ltd.	Broad spectrum microbicidal and spermicidal compositions and methods
CN117677292A (zh) *	2021-02-18	2024-03-08	安东尼埃塔·马丁	使用含有戊二醛的组合物灭活病毒的方法
JP2022164624A (ja) *	2021-04-15	2022-10-27	花王株式会社	液噴霧用ウイルス不活化組成物
WO2023009213A1 (en)	2021-07-28	2023-02-02	Grignard Pure Llc	Methods of inactivating pathogens

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2801216A (en) *	1956-04-05	1957-07-30	Union Carbide & Carbon Corp	Treatment of water with dialdehyde bactericides
US3079985A (en) *	1959-09-29	1963-03-05	Ethicon Inc	Process for preparing soluble, sporicidally active solid polyglyoxals
CH472354A (de) *	1966-01-25	1969-05-15	Lysoform Schweizerische Ges Fu	Verfahren zur Herstellung eines wasserlöslichen Desinfektionsmittels
US3968250A (en) *	1971-06-21	1976-07-06	Wave Energy Systems, Inc.	Method and sporicidal compositions for synergistic disinfection or sterilization
ZA724044B (en) *	1971-06-28	1973-03-28	West Laboratories Inc	Glutaraldehyde sporicidal compositions
US3886269A (en) *	1973-01-30	1975-05-27	Us Energy	Process for preparing odor and irritation free formaldehyde disinfectant
US3917850A (en) *	1973-06-05	1975-11-04	Wave Energy Systems	Biocidal synergistic compositions for surface and space disinfection
US3983252A (en) *	1973-10-26	1976-09-28	Gilbert Buchalter	Stable dialdehyde-containing disinfectant compositions and methods
US4048336A (en) *	1974-04-22	1977-09-13	West Chemical Products, Incorporated	Means for killing bacterial spores with glutaraldehyde sporicidal compositions
US4436754A (en) *	1980-08-14	1984-03-13	Surgikos, Inc.	Disinfecting and sterilizing composition
CA1158547A (en) *	1980-08-14	1983-12-13	Paul T. Jacobs	Disinfecting and sterilizing composition
EP0251743B1 (de) *	1986-06-27	1994-09-07	Reginald Keith Whiteley	Flüssige sterilisierende Zusammensetzung
US4859186A (en) *	1988-02-08	1989-08-22	Biomedical Development Corporation	Pulpotomy agent and method of use

1988
- 1988-12-20 US US07/286,738 patent/US5004757A/en not_active Expired - Lifetime
1989
- 1989-09-21 FR FR8912551A patent/FR2641447B1/fr not_active Expired - Lifetime
- 1989-11-14 CA CA002002856A patent/CA2002856C/en not_active Expired - Fee Related
- 1989-11-14 JP JP2501276A patent/JP2835180B2/ja not_active Expired - Fee Related
- 1989-11-14 WO PCT/US1989/005233 patent/WO1990006677A1/en not_active Ceased
- 1989-11-16 IL IL9232989A patent/IL92329A/en not_active IP Right Cessation
- 1989-11-16 AT AT89311852T patent/ATE104111T1/de not_active IP Right Cessation
- 1989-11-16 DE DE68914622T patent/DE68914622T2/de not_active Expired - Fee Related
- 1989-11-16 ES ES89311852T patent/ES2054026T3/es not_active Expired - Lifetime
- 1989-11-16 EP EP89311852A patent/EP0375149B1/de not_active Revoked

Also Published As

Publication number	Publication date
AU634193B2 (en)	1993-02-18
WO1990006677A1 (en)	1990-06-28
CA2002856A1 (en)	1990-06-20
DE68914622T2 (de)	1994-10-27
FR2641447B1 (fr)	1996-07-19
ATE104111T1 (de)	1994-04-15
DE68914622D1 (de)	1994-05-19
JPH04502616A (ja)	1992-05-14
IL92329A0 (en)	1990-07-26
AU4665089A (en)	1990-07-10
EP0375149A3 (de)	1992-04-08
US5004757A (en)	1991-04-02
ES2054026T3 (es)	1994-08-01
EP0375149B1 (de)	1994-04-13
EP0375149A2 (de)	1990-06-27
FR2641447A1 (fr)	1990-07-13
JP2835180B2 (ja)	1998-12-14
CA2002856C (en)	1997-07-01

Legal Events

Date	Code	Title
2000-06-29	KB	Patent renewed
2004-01-04	KB	Patent renewed
2008-01-06	KB	Patent renewed
2010-11-30	EXP	Patent expired

Publication	Publication Date	Title
EP0375149B1 (de)	1994-04-13	Viruzide Zusammensetzungen niedriger Giftigkeit
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US3282775A (en)	1966-11-01	Sporicidal compositions comprising a saturated dialdehyde and a cationic surfactant
US5403587A (en)	1995-04-04	Disinfectant and sanitizing compositions based on essential oils
US4975217A (en)	1990-12-04	Virucidal composition, the method of use and the product therefor
US20090061019A1 (en)	2009-03-05	Disinfectant compositions and methods of use thereof
Filipe et al.	2021	Antiviral and antibacterial activity of hand sanitizer and surface disinfectant formulations
US5145663A (en)	1992-09-08	Biodegradable disinfectant containing anhydrous alcohol and propylene glycol
US5322856A (en)	1994-06-21	Fortified glutaraldehyde chemical sterilant/disinfectant
NL2032962A (en)	2023-11-16	Foam type long-acting citric acid-containing compound disinfectant, preparation method and use thereof
Goddard et al.	2001	Phenolic compounds
JPS6322503A (ja)	1988-01-30	液体殺菌剤
US5219890A (en)	1993-06-15	Odorless Mycobactericidal compositions
AU634193C (en)	1993-12-23	Virucidal low toxicity compositions
WO1994022305A1 (en)	1994-10-13	Disinfectant compositions
EP0407672B1 (de)	1996-06-26	Geruchlose mykobakterizide Zusammensetzungen
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