FR2588264A1 - DISINFECTANT COMPOSITION FOR AIRWAY - Google Patents
DISINFECTANT COMPOSITION FOR AIRWAY Download PDFInfo
- Publication number
- FR2588264A1 FR2588264A1 FR8514906A FR8514906A FR2588264A1 FR 2588264 A1 FR2588264 A1 FR 2588264A1 FR 8514906 A FR8514906 A FR 8514906A FR 8514906 A FR8514906 A FR 8514906A FR 2588264 A1 FR2588264 A1 FR 2588264A1
- Authority
- FR
- France
- Prior art keywords
- composition
- butylglycol
- thymol
- water
- composition according
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/14—Disinfection, sterilisation or deodorisation of air using sprayed or atomised substances including air-liquid contact processes
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/22—Phase substances, e.g. smokes, aerosols or sprayed or atomised substances
Abstract
COMPOSITION POUR LA DESINFECTION DES SURFACES PAR VOIE AERIENNE, CARACTERISEE EN CE QU'ELLE CONTIENT COMME CONSTITUANTS ACTIFS, D'UNE PART, UN METHYL-ISOPROPYLPHENOL ET, D'AUTRE PART, UN ETHER ALKYLIQUE DE GLYCOL, ET EN CE QUE LESDITS CONSTITUANTS SONT EN SOLUTION DANS L'EAU.COMPOSITION FOR THE DISINFECTION OF SURFACES BY AIR, CHARACTERIZED IN THAT IT CONTAINS AS ACTIVE INGREDIENTS, ON THE ONE HAND, A METHYL-ISOPROPYLPHENOL AND, ON THE OTHER HAND, AN ALKYL ETHER OF GLYCOL, AND IN THAT SUCH CONSTITUENTS IN SOLUTION IN WATER.
Description
1 25882641 2588264
La présente invention concerne de nouvelles compositions destinées à être utilisées pour la désinfection des surfaces par The present invention relates to novel compositions intended to be used for disinfecting surfaces by
voie aérienne.airway.
De telles compositions sont connues dans leur principe et actuellement utilisées dans divers appareils générateurs d'aérosols tels que ceux décrits par la Déposante dans ses brevets français 1.568.295, 75.02188, 75.18474, 76.36270 et Such compositions are known in principle and currently used in various aerosol generating devices such as those described by the Applicant in its French patents 1,568,295, 75.02188, 75.18474, 76.36270 and
77.12479.77.12479.
Jusqu'à présent les compositions de ce genre contenaient essentiellement du formol comme constituant actif, les autres constituants figurant dans ces compositions n'ayant qu'un rôle subsidiaire, leur proportion étant insuffisante pour qu'ils Until now, the compositions of this kind essentially contained formaldehyde as active ingredient, the other constituents appearing in these compositions having only a subsidiary role, their proportion being insufficient for them
exercent une action propre, tout au moins à un degré appréciable. exercise their own action, at least to an appreciable degree.
Les récents développements des études sur les dangers présentés par le formol dans divers domaines médicaux ont incité la Déposante à rechercher une nouvelle composition dans laquelle le formol ne figurerait plus, mais qui exercerait cependant une The recent developments in studies on the dangers presented by formaldehyde in various medical fields have prompted the Applicant to seek a new composition in which formaldehyde would no longer appear, but which would however
activité désinfectante satisfaisante, sinon meilleure encore. satisfactory disinfecting activity, if not better still.
Les recherches de la Déposante l'ont donc conduite à la constatation surprenante qu'un tel résultat pouvait être atteint au moyen de la réunion, en proportions déterminées de plusieurs composants, connus en eux-mêmes, mais qui ne possédaient pas The Applicant's research therefore led her to the surprising observation that such a result could be achieved by means of the combination, in determined proportions of several components, known in themselves, but which did not have
individuellement les qualités requises pour cet emploi. individually the qualities required for this job.
Le premier composant des compositions selon l'invention est choisi dans la classe des methyl-isopropylphénols, tels que The first component of the compositions according to the invention is chosen from the class of methyl-isopropylphenols, such as
le 5-méthyl-2-isopropyl-phénol, ou m-thymol, le 2-méthyl-5- 5-methyl-2-isopropyl-phenol, or m-thymol, 2-methyl-5-
isopropyl-phénol, ou carvacrol (ou iso-thymol), ou leurs dérivés chlorés. Le membre préféré de ce groupe est le m-thymol, et l'on isopropyl-phenol, or carvacrol (or iso-thymol), or their chlorinated derivatives. The preferred member of this group is m-thymol, and one
s'y réfèrera dans la suite sous le nom de "thymol". will be referred to in the following under the name of "thymol".
Le second composant des compositions selon l'invention est choisi dans la classe des ethers alkyliques de glycols, tels que l'ether mono-butylique de l'éthylène glycol ou l'éther éthylique du diéthylèneglycol. Le membre préféré de ce groupe est l'éther mono-butylique de l'éthylèneglycol, bien connu sous la marque commerciale "Butyl Cellosolve" et l'on s'y référera dans The second component of the compositions according to the invention is chosen from the class of alkyl ethers of glycols, such as mono-butyl ether of ethylene glycol or ethyl ether of diethylene glycol. The preferred member of this group is the mono-butyl ether of ethylene glycol, well known under the trademark "Butyl Cellosolve" and will be referred to in
la suite sous le nom simplifié de "butylglycol". hereinafter under the simplified name of "butylglycol".
Le troisième composant des compositions selon l'invention The third component of the compositions according to the invention
est l'eau.is water.
Si l'on considère maintenant chacun de ces trois composants, on est amené aux constatations suivantes: Le thymol est connu depuis très longtemps au titre de produit d'origine naturelle comme agent d'assinissement, pour son If we now consider each of these three components, we are led to the following observations: Thymol has been known for a very long time as a product of natural origin as a sanitizing agent, for its
action destructive sur les moisissures et les parasites végétaux. destructive action on molds and plant pests.
A cet égard il a été proposé en pharmacie en pommade et en solution alcoolique comme désinfectant de contact. Du fait qu'il n'est pas soluble dans l'eau, aucune préparation pour la désinfection par voie aérienne ne contenant que du thymol comme In this regard, it has been proposed in pharmacies as an ointment and in alcoholic solution as a contact disinfectant. Since it is not soluble in water, no preparation for disinfection by air contains only thymol as
ingrédient essentiel n'a été proposée jusqu'à aujourd'hui. essential ingredient has not been proposed until today.
Le butylglycol est également connu, mais uniquement comme dissolvant sans qu'aucune activité bactéricide n'en ait été signalée. Son rôle dans les compositions selon l'invention est multiple: - En premier lieu, il a pour effet de solubiliser le thymol; Butylglycol is also known, but only as a solvent, without any bactericidal activity being reported. Its role in the compositions according to the invention is multiple: - Firstly, it has the effect of dissolving thymol;
- En second lieu, l'expérience a montré qu'il possède en lui- - Second, experience has shown that it has in itself-
même une certaine activité bactéricide, d'ailleurs assez faible; - En troisième lieu, l'expérience montre de façon surprenante que cette activité bactéricide se trouve très notablement accrue even a certain bactericidal activity, moreover quite weak; - Third, experience has surprisingly shown that this bactericidal activity is very markedly increased
par la présence du thymol.by the presence of thymol.
Enfin l'eau est indispensable aux compositions selon l'invention, pour permettre à l'appareil de formation d'aérosol de diffuser une solution, sous forme de particules suffisamment fines pour se déposer extrêmement lentement, notamment sur les zones supérieures des cloisons, et pour traverser des obstacles Finally, water is essential for the compositions according to the invention, to allow the aerosol forming apparatus to diffuse a solution, in the form of particles sufficiently fine to be deposited extremely slowly, in particular on the upper zones of the partitions, and to cross obstacles
poreux, tels que des couvertures.porous, such as blankets.
La présence de la proportion appropriée d'eau assure la création dans le local à désinfecter du taux d'humidité relative le plus favorable à I'action désinfectante, de l'ordre d'au moins The presence of the appropriate proportion of water ensures the creation in the room to be disinfected of the relative humidity rate most favorable to the disinfecting action, of the order of at least
-70% à 20 C.-70% at 20 C.
Les proportions relatives des trois composantes dans les compositions selon l'invention sont déterminées par le rôle respectif desdits composants: - le thymol devient inefficace au-dessous de 0-1% en The relative proportions of the three components in the compositions according to the invention are determined by the respective role of said components: - thymol becomes ineffective below 0-1% in
poids, et rend l'atmosphère difficilement respirable vers 5%. weight, and makes the atmosphere difficult to breathe at around 5%.
Dans la pratique sa proportion optimale est de l'ordre de 0,75 à In practice, its optimal proportion is around 0.75 to
1%.1%.
- le butylglycol n'assume plus son rôle solubilisant au- - butylglycol no longer assumes its solubilizing role at-
dessous d'environ 5 %, et il exerce une action décapante inacceptable audelà de 30%. Dans la pratique sa proportion below about 5%, and it has an unacceptable pickling action above 30%. In practice its proportion
optimale est de l'ordre de 20% environ. optimal is around 20%.
- l'eau représente normalement le complément à 100%. - water normally represents the complement to 100%.
3 25882643 2588264
- enfin, selon une variante rentrant dans le cadre de l'invention, une partie du butylglycol peut être remplacée par du 2-Méthyl-2,4-pentanediol (ou hexylèneglycol), jouant à la fois - finally, according to a variant coming within the framework of the invention, part of the butylglycol can be replaced by 2-methyl-2,4-pentanediol (or hexylene glycol), playing at the same time
le rôle de co-solvant et d'adjuvant stabilisateur. the role of co-solvent and stabilizing adjuvant.
A titre d'exemple non limitatif, une composition rentrant dans le cadre de l'invention contiendra, en % en poids: Thymol 0,75 Butylglycol 20 Hexylèneglycol 8 Eau (déminéralisée) 71,25 Une telle composition s'obtient par dissolution à froid du thymol dans le butylglycol, puis, après addition de l'hexylèneglycol, introduction de l'eau sous agitation. On obtient un liquide incolore légèrement opalescent, de densité By way of nonlimiting example, a composition coming within the scope of the invention will contain, in% by weight: Thymol 0.75 Butylglycol 20 Hexylene glycol 8 Water (demineralized) 71.25 Such a composition is obtained by cold dissolution thymol in butylglycol, then, after addition of hexylene glycol, introduction of water with stirring. A slightly opalescent colorless liquid of density is obtained
d20. = 0,9867-0,9877, d'indice de réfraction n200 = 1,3660 - d20. = 0.9867-0.9877, refractive index n200 = 1.3660 -
1,3670, se conservant sans perte d'activité pendant plusieurs années. Cette composition s'utilise telle quelle dans un appareil à génération d'aérosols tel que ceux mentionnés ci-dessus, à une dose de l'ordre de 20 mlIm3 de volume d'air à traiter, pendant environ 4 heures. Un avantage essentiel de cette composition est de permettre la réoccupation du local après seulement 30 minutes d'aération, au lieu des difficultés bien connues qui subsistent 1.3670, keeping without loss of activity for several years. This composition is used as it is in an aerosol generation device such as those mentioned above, at a dose of the order of 20 mlIm3 of air volume to be treated, for approximately 4 hours. An essential advantage of this composition is that it allows the room to be reoccupied after only 30 minutes of ventilation, instead of the well-known difficulties which remain
après usage des compositions à base de formol. after use of the formalin-based compositions.
Les essais d'efficacité bactéricide, menés conformément à la norme française T-72-281 sur les souches de micro-organismes suivantes: Bactericidal efficacy tests, conducted in accordance with French standard T-72-281 on the following strains of microorganisms:
SOUCHES BACTERIENNESBACTERIAL STRAINS
- Streptococcus faecalis CNCM 5855; - Staphylococcus aureus - Souche Oxford CNCM 53154 - Pseudomonas aeruginosa CNCM A 22; - Streptococcus faecalis CNCM 5855; - Staphylococcus aureus - Oxford strain CNCM 53154 - Pseudomonas aeruginosa CNCM A 22;
- Escherichia coli CNCM 54127.- Escherichia coli CNCM 54127.
SOUCHES DE MOISISSURESTRAINS OF MOLD
- Pénicilium verrucosum Var - Cyclopium CNCM 1186-79. - Penicilium verrucosum Var - Cyclopium CNCM 1186-79.
SOUCHES DE LEVUREYEAST STRAINS
- Candida albicans CNCM 1180-79.- Candida albicans CNCM 1180-79.
ont conduit à constater une activité bactéricide égale ou supu4ieure à 5 sur les souches bactériennes et les souches de levure, et égale ou supérieure à 4 sur les souches de moisissures have led to the observation of a bactericidal activity equal to or greater than 5 on the bacterial and yeast strains, and equal to or greater than 4 on the mold strains
(activité exprimée en Logs décimaux). (activity expressed in decimal Logs).
L'humidité relative du local d'essai qui devait être d'au moins 60-70 C en fin d'opération, était obtenue par la diffusion The relative humidity of the test room, which must have been at least 60-70 C at the end of the operation, was obtained by diffusion
du produit lui-même, grâce à sa teneur élevée en eau. of the product itself, thanks to its high water content.
L'expérience a montré que la diffusion de 17 glm3 de la composition selon l'invention fait passer l'humidité relative Experience has shown that the diffusion of 17 glm3 of the composition according to the invention causes the relative humidity to pass
d'un local de 45 à 82 %.from 45 to 82% local.
A titre d'illustration du phénomène de potentialisation de l'activité bactéricide du butylglycol par le thymol, on peut indiquer que, dans des conditions expérimentales identiques (10,7 glm3 - 4h de contact) une solution aqueuse à 40% de butylglycol seul et la composition selon l'invention exercent respectivement les effets suivants, exprimés en Logs décimaux: L Colibacilles Staphylocoques Streptocoques Composition selon l'invention > 5,0 5,0 5,0 Solution de butylglycol seul 1,21 0,33 0,42 Ces divers résultats démontrent clairement que les compositions selon l'invention possèdent une activité désinfectante des surfaces par voie aérienne au moins aussi satisfaisante que celle des anciennes compositions contenant du formol, tout en éliminant leurs inconvénients, et que cette activité doit être attribuée à une potentialisation d'effets, dont certains n'auraient d'ailleurs pas encore été observés en As an illustration of the phenomenon of potentiation of the bactericidal activity of butylglycol by thymol, it may be indicated that, under identical experimental conditions (10.7 glm3 - 4 h of contact) a 40% aqueous solution of butylglycol alone and the composition according to the invention exert respectively the following effects, expressed in decimal Logs: L Colibacilli Staphylococci Streptococci Composition according to the invention> 5.0 5.0 5.0 Butylglycol solution alone 1.21 0.33 0.42 These various results clearly demonstrate that the compositions according to the invention have an air disinfectant activity at least as satisfactory as that of the old formaldehyde-containing compositions, while eliminating their drawbacks, and that this activity must be attributed to a potentiation of effects, some of which have not yet been observed in
raison de leur faiblesse des constituants de ces compositions. because of their weakness of the constituents of these compositions.
2588264'2588264 '
Claims (7)
Priority Applications (16)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8514906A FR2588264B1 (en) | 1985-10-07 | 1985-10-07 | DISINFECTANT COMPOSITION FOR AIRWAY |
LU86166A LU86166A1 (en) | 1985-10-07 | 1985-11-14 | AERIAL DISINFECTANT COMPOSITION |
BE0/215881A BE903664A (en) | 1985-10-07 | 1985-11-18 | AERIAL DISINFECTANT COMPOSITION. |
IT22963/85A IT1186767B (en) | 1985-10-07 | 1985-11-22 | AIR DISINFECTANT COMPOSITION |
DE19853541814 DE3541814A1 (en) | 1985-10-07 | 1985-11-27 | DISINFECTING DRY COMPOSITION |
CH5299/85A CH667206A5 (en) | 1985-10-07 | 1985-12-12 | AERIAL DISINFECTANT COMPOSITION. |
NO860060A NO860060L (en) | 1985-10-07 | 1986-01-09 | Means for surface disinfection. |
DK009686A DK9686A (en) | 1985-10-07 | 1986-01-09 | MEDICINE FOR DISINFECTION OF AIRLINE SURFACES |
GB8600663A GB2181351B (en) | 1985-10-07 | 1986-01-13 | Disinfectant compositions |
GR860121A GR860121B (en) | 1985-10-07 | 1986-01-17 | Disifectant composition for spraying |
PT81864A PT81864B (en) | 1985-10-07 | 1986-01-17 | Process for the preparation of novel compounds containing butyl glycols suitable for surface disinfection by air |
MA20858A MA20633A1 (en) | 1985-10-07 | 1986-02-20 | AERIAL DISINFECTANT COMPOSITION |
TNTNSN86034A TNSN86034A1 (en) | 1985-10-07 | 1986-03-07 | AERIAL DISINFECTANT COMPOSITION |
MC861831A MC1745A1 (en) | 1985-10-07 | 1986-03-27 | AERIAL DISINFECTANT COMPOSITION |
SE8604230A SE8604230L (en) | 1985-10-07 | 1986-10-06 | disinfectant composition |
ES8602466A ES2002028A6 (en) | 1985-10-07 | 1986-10-07 | Disinfectant compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8514906A FR2588264B1 (en) | 1985-10-07 | 1985-10-07 | DISINFECTANT COMPOSITION FOR AIRWAY |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2588264A1 true FR2588264A1 (en) | 1987-04-10 |
FR2588264B1 FR2588264B1 (en) | 1987-11-27 |
Family
ID=9323641
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR8514906A Expired FR2588264B1 (en) | 1985-10-07 | 1985-10-07 | DISINFECTANT COMPOSITION FOR AIRWAY |
Country Status (16)
Country | Link |
---|---|
BE (1) | BE903664A (en) |
CH (1) | CH667206A5 (en) |
DE (1) | DE3541814A1 (en) |
DK (1) | DK9686A (en) |
ES (1) | ES2002028A6 (en) |
FR (1) | FR2588264B1 (en) |
GB (1) | GB2181351B (en) |
GR (1) | GR860121B (en) |
IT (1) | IT1186767B (en) |
LU (1) | LU86166A1 (en) |
MA (1) | MA20633A1 (en) |
MC (1) | MC1745A1 (en) |
NO (1) | NO860060L (en) |
PT (1) | PT81864B (en) |
SE (1) | SE8604230L (en) |
TN (1) | TNSN86034A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2818151B1 (en) | 2000-12-14 | 2004-04-02 | Prod Berger | ANTI-BACTERIAL COMPOSITION FOR DISSEMINATION TO FIGHT AGAINST BACTERIA CONTAINED IN AIR, METHOD FOR THE DISSEMINATION OF SUCH A COMPOSITION |
ITMI20010174A1 (en) * | 2001-01-31 | 2002-07-31 | B B & M T Italia S A S Di Berg | NEW FORMULATIONS FOR SANITIZATION AND SANITIZATION OF LIVING ENVIRONMENTS |
AU2003223183A1 (en) * | 2002-02-19 | 2003-09-09 | Eden Researach Plc | Improvement of indoor air quality and antiseptic composition for use therein |
US20100249166A1 (en) | 2007-09-19 | 2010-09-30 | Xy, Inc. | Differential evaporation potentiated disinfectant system |
US8119688B2 (en) * | 2007-09-19 | 2012-02-21 | Xy, Llc | Differential evaporation potentiated disinfectant system |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1134918A (en) * | 1954-09-01 | 1957-04-19 | Hoechst Ag | Disinfection of rooms with volatile substances in aerosol form |
US3287214A (en) * | 1964-07-20 | 1966-11-22 | Sterling Drug Inc | Surface disinfectant and space deodorant aerosol spray compositions |
GB1162770A (en) * | 1967-08-28 | 1969-08-27 | Vineland Lab Inc | Disinfectant Composition |
FR2181606A1 (en) * | 1972-04-27 | 1973-12-07 | Perrin Robert | |
US3787566A (en) * | 1969-07-29 | 1974-01-22 | Holliston Labor Inc | Disinfecting aerosol compositions |
-
1985
- 1985-10-07 FR FR8514906A patent/FR2588264B1/en not_active Expired
- 1985-11-14 LU LU86166A patent/LU86166A1/en unknown
- 1985-11-18 BE BE0/215881A patent/BE903664A/en not_active IP Right Cessation
- 1985-11-22 IT IT22963/85A patent/IT1186767B/en active
- 1985-11-27 DE DE19853541814 patent/DE3541814A1/en not_active Ceased
- 1985-12-12 CH CH5299/85A patent/CH667206A5/en not_active IP Right Cessation
-
1986
- 1986-01-09 NO NO860060A patent/NO860060L/en unknown
- 1986-01-09 DK DK009686A patent/DK9686A/en not_active Application Discontinuation
- 1986-01-13 GB GB8600663A patent/GB2181351B/en not_active Expired
- 1986-01-17 GR GR860121A patent/GR860121B/en unknown
- 1986-01-17 PT PT81864A patent/PT81864B/en not_active IP Right Cessation
- 1986-02-20 MA MA20858A patent/MA20633A1/en unknown
- 1986-03-07 TN TNTNSN86034A patent/TNSN86034A1/en unknown
- 1986-03-27 MC MC861831A patent/MC1745A1/en unknown
- 1986-10-06 SE SE8604230A patent/SE8604230L/en not_active Application Discontinuation
- 1986-10-07 ES ES8602466A patent/ES2002028A6/en not_active Expired
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1134918A (en) * | 1954-09-01 | 1957-04-19 | Hoechst Ag | Disinfection of rooms with volatile substances in aerosol form |
US3287214A (en) * | 1964-07-20 | 1966-11-22 | Sterling Drug Inc | Surface disinfectant and space deodorant aerosol spray compositions |
GB1162770A (en) * | 1967-08-28 | 1969-08-27 | Vineland Lab Inc | Disinfectant Composition |
US3787566A (en) * | 1969-07-29 | 1974-01-22 | Holliston Labor Inc | Disinfecting aerosol compositions |
FR2181606A1 (en) * | 1972-04-27 | 1973-12-07 | Perrin Robert |
Also Published As
Publication number | Publication date |
---|---|
LU86166A1 (en) | 1986-03-24 |
SE8604230L (en) | 1987-04-08 |
PT81864B (en) | 1988-05-27 |
ES2002028A6 (en) | 1988-07-01 |
GB2181351B (en) | 1989-10-11 |
GR860121B (en) | 1986-05-19 |
MC1745A1 (en) | 1987-02-26 |
DK9686D0 (en) | 1986-01-09 |
GB8600663D0 (en) | 1986-02-19 |
FR2588264B1 (en) | 1987-11-27 |
IT1186767B (en) | 1987-12-16 |
SE8604230D0 (en) | 1986-10-06 |
GB2181351A (en) | 1987-04-23 |
DK9686A (en) | 1987-04-08 |
MA20633A1 (en) | 1986-10-01 |
TNSN86034A1 (en) | 1990-01-01 |
CH667206A5 (en) | 1988-09-30 |
IT8522963A0 (en) | 1985-11-22 |
BE903664A (en) | 1986-03-14 |
PT81864A (en) | 1986-02-01 |
NO860060L (en) | 1987-04-08 |
DE3541814A1 (en) | 1987-04-09 |
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