JP3281445B2 - Fungicide composition - Google Patents
Fungicide compositionInfo
- Publication number
- JP3281445B2 JP3281445B2 JP10295793A JP10295793A JP3281445B2 JP 3281445 B2 JP3281445 B2 JP 3281445B2 JP 10295793 A JP10295793 A JP 10295793A JP 10295793 A JP10295793 A JP 10295793A JP 3281445 B2 JP3281445 B2 JP 3281445B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- ester
- component
- incomplete
- polyhydric alcohol
- 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.)
- Expired - Fee Related
Links
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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group; Thio analogues thereof
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/14—Boron; Compounds thereof
Description
【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION
【０００１】[0001]
【産業上の利用分野】本発明は、食品、製紙、繊維から
家庭まで幅広い分野で使用できる殺菌剤組成物に関し、
詳細には、水道水の水の浄化を目的とした殺菌・消毒、
食肉、魚貝類をはじめとする食品全般の殺菌・消毒、木
材の防腐、製紙工程での防腐、家庭のトイレ、風呂場、
台所の殺菌・消毒、その他の殺菌・消毒に用いることが
でき、殺菌効果及び保存安定性に優れる殺菌剤組成物に
関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a disinfectant composition which can be used in a wide range of fields from food, paper making, textile to household.
Specifically, sterilization and disinfection for the purpose of purifying tap water,
Sterilization and disinfection of meat, fish and shellfish and other foods in general, preservation of wood, preservation in the papermaking process, household toilets, bathrooms,
The present invention relates to a disinfectant composition which can be used for disinfection and disinfection of kitchens and other disinfections and disinfections, and has excellent disinfection effects and storage stability.
【０００２】[0002]
【従来の技術】過ホウ酸ナトリウム、過炭酸ナトリウ
ム、過硫酸ナトリウム等の過酸化物は、水中に溶解せし
めると、過酸化水素及び発生期の酸素を生じ、これによ
り洗浄、漂白、殺菌、消毒等の作用を示すことが知られ
ている。しかしながら、これらの過酸化物のみを用いる
と、短時間に酸素を一度に放出するため、酸素が大きな
気泡となり系外に放出されてしまい、発生期の酸素が短
時間で消失してしまうため、殺菌効果が不充分であると
いう欠点があった。2. Description of the Related Art Peroxides such as sodium perborate, sodium percarbonate and sodium persulfate produce hydrogen peroxide and nascent oxygen when dissolved in water, thereby washing, bleaching, sterilizing and disinfecting. It is known to exhibit such effects. However, when only these peroxides are used, oxygen is released at once in a short time, so that oxygen becomes large bubbles and is released out of the system, and oxygen in the nascent period disappears in a short time. There was a disadvantage that the bactericidal effect was insufficient.
【０００３】このような、欠点を解消し、安定に酸素を
発生する組成物として、有機過酸系の殺菌剤又は漂白剤
組成物（特開昭４８−１４８８６号公報、特開昭５５−
１３９５００号公報、特開昭６２−６３５０４号公報、
特開昭５１−９７６５５号公報）が開発された。[0003] As a composition for solving such disadvantages and stably generating oxygen, an organic peracid-based bactericide or bleaching composition (JP-A-48-14886, JP-A-55-14886).
139500, JP-A-62-63504,
JP-A-51-97655) has been developed.
【０００４】しかしながら、これらの内、多価アルコー
ルの有機過酸エステルを用いているもの（特開昭５１−
９７６５５号公報）は、そのエステルが置換度１００％
で飽和しているため、水に対しての溶解性が悪く、有機
過酸、次いでこれより酸素を安定に発生し、高い殺菌力
を発現させることが事実上困難である。However, among these, those using an organic peroxyester of a polyhydric alcohol (Japanese Patent Laid-Open No.
97655) discloses that the ester has a degree of substitution of 100%.
, It is poorly soluble in water, and it is practically difficult to stably generate an organic peracid and then oxygen to exhibit high sterilizing power.
【０００５】また、直接有機過酸を配合した組成物は、
刺激臭があり、商品価値を低下させる。更に有機過酸単
体では長期保存すると分解してしまうという欠点があ
る。Further, a composition directly containing an organic peracid is:
It has an irritating odor and reduces the commercial value. Further, there is a disadvantage that the organic peracid alone decomposes when stored for a long time.
【０００６】[0006]
【発明が解決しようとする課題】従って、本発明の目的
は、安定に有機過酸を発生し、殺菌力が持続し、しかも
保存安定性のよい殺菌剤組成物を提供することにある。SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a bactericide composition which stably generates an organic peracid, maintains bactericidal activity, and has good storage stability.
【０００７】[0007]
【課題を解決するための手段】かかる実状に鑑み本発明
者らは鋭意研究を行った結果、無機過酸化物と、これの
活性化剤として多価アルコールの有機酸不完全エステ
ル、更にアルカリ土類金属塩を含有せしめることによ
り、水溶性が良好で、殺菌効果が高くしかも持続性が高
い殺菌剤組成物が得られ、更にこれは粉体により構成さ
れ、水和により有機過酸を発生させるため、保存安定性
に優れていることを見い出し本発明を完成した。Means for Solving the Problems In view of this situation, the present inventors have conducted intensive studies and have found that inorganic peroxides, organic acid incomplete esters of polyhydric alcohols as activators thereof, and alkaline earths. By containing a metal salt, a bactericide composition having good water solubility, high bactericidal effect and high persistence can be obtained, which is composed of powder and generates an organic peracid by hydration. Therefore, they found that they had excellent storage stability and completed the present invention.
【０００８】すなわち本発明は、次の成分（Ａ）、
（Ｂ）及び（Ｃ） （Ａ）無機過酸化物 （Ｂ）エステルの置換度が５〜９５％である、多価アル
コールの有機酸不完全エステル （Ｃ）アルカリ土類金属塩 を含有し、（Ｃ）成分の含有量は（Ｂ）成分に対して
０．１〜２０重量倍である、固形の殺菌剤組成物を提供
するものである。That is, the present invention provides the following component (A):
(B) and (C) (A) an inorganic peroxide, (B) an organic acid incomplete ester of a polyhydric alcohol having a degree of substitution of the ester of 5 to 95%, and (C) an alkaline earth metal salt, The present invention provides a solid germicidal composition in which the content of the component (C) is 0.1 to 20 times the weight of the component (B).
【０００９】本発明に用いられる（Ａ）成分の無機過酸
化物としては、例えば、過炭酸ナトリウム、過硼酸ナト
リウム、過酸化トリポリリン酸ナトリウム、過酸化ピロ
リン酸ナトリウム、過酸化ケイ酸ナトリウム等が挙げら
れる。The inorganic peroxide (A) used in the present invention includes, for example, sodium percarbonate, sodium perborate, sodium tripolyphosphate, sodium pyrophosphate, sodium peroxide and sodium silicate. Can be
【００１０】（Ｂ）成分の多価アルコールの有機酸不完
全エステルは、（Ａ）成分の無機過酸化物の活性化剤で
あり、（Ａ）成分と反応して有機過酸を生じるものであ
る。この多価アルコール部分としては、グリセリン、ジ
グリセリン、トリグリセリン、ポリグリセリン等のグリ
セリン類；ソルビトール、グルチトール、ペンタエリス
リトール、アルキルポリグリコシド、アルキルフラノシ
ド等のアルカリ変性糖類等又は、これらグリセリン類、
糖類のアルキレンオキサイド付加物等が例示される。ま
た有機酸としては、炭素数１〜８の飽和又は不飽和の脂
肪酸が好ましく、具体的には酢酸、プロピオン酸、酪
酸、吉草酸、カプロン酸、エナント酸、オクタン酸、ア
クリル酸、メタアクリル酸、クロトン酸、アリル酢酸、
ジメチルアクリル酸、モノカルボン酸が好ましいがシュ
ウ酸、マロン酸、コハク酸、マレイン酸、フマル酸等の
ジカルボン酸であってもよい。また不完全エステルと
は、エステル置換度が１００％でないことを言い、好ま
しくは、５〜９５％であり、測定法はＩＲの３５００cm
-1での吸光度の有無によった。また、（Ｃ）成分のアル
カリ土類金属塩としては、例えば、硫酸マグネシウム、
硫酸カルシウム、リン酸マグネシウム、リン酸カルシウ
ム、硝酸マグネシウム、硝酸カルシウム、塩化マグネシ
ウム、塩化カルシウム、塩基性炭酸マグネシウム、炭酸
カルシウム等又はこれらの無水塩が挙げられる。又これ
らのアルカリ土類金属は発生する過酸の安定性に必要で
ある。The incomplete organic acid ester of the polyhydric alcohol of the component (B) is an activator of the inorganic peroxide of the component (A), and reacts with the component (A) to generate an organic peracid. is there. Examples of the polyhydric alcohol moiety include glycerins such as glycerin, diglycerin, triglycerin, and polyglycerin; and alkali-modified sugars such as sorbitol, glutitol, pentaerythritol, alkylpolyglycoside, and alkylfuranoside; and these glycerins;
Examples thereof include an alkylene oxide adduct of a saccharide. As the organic acid, a saturated or unsaturated fatty acid having 1 to 8 carbon atoms is preferable. Specifically, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, enanthic acid, octanoic acid, acrylic acid, methacrylic acid , Crotonic acid, allyl acetic acid,
Dimethyl acrylic acid and monocarboxylic acid are preferred, but dicarboxylic acids such as oxalic acid, malonic acid, succinic acid, maleic acid and fumaric acid may be used. Incomplete ester means that the degree of ester substitution is not 100%, preferably 5 to 95%, and the measuring method was 3500 cm of IR.
It depends on the presence or absence of absorbance at -1 . Examples of the alkaline earth metal salt of the component (C) include magnesium sulfate,
Examples thereof include calcium sulfate, magnesium phosphate, calcium phosphate, magnesium nitrate, calcium nitrate, magnesium chloride, calcium chloride, basic magnesium carbonate, calcium carbonate and the like, and anhydrous salts thereof. These alkaline earth metals are necessary for the stability of the generated peracid.
【００１１】本発明の殺菌剤組成物は、上記の（Ａ）〜
（Ｃ）成分を目的に応じて適宜配合すればよいが、殺菌
効果、保存安定性、経済性等を考慮すると、（Ａ）成分
１重量部に対し（Ｂ）成分は０．０１〜１０重量部、
（Ｃ）成分は０．０１〜９０重量部とすることが好まし
く、特に（Ｃ）成分は（Ｂ）成分に対して０．１〜２０
重量倍の範囲とすることが好ましい。[0011] The fungicidal composition of the present invention comprises the above (A) to
The component (C) may be appropriately blended according to the purpose. However, considering the bactericidal effect, storage stability, economy, etc., the component (B) is used in an amount of 0.01 to 10 parts by weight with respect to 1 part by weight of the component (A). Department,
The component (C) is preferably used in an amount of 0.01 to 90 parts by weight, and particularly, the component (C) is used in an amount of 0.1 to 20 parts by weight based on the component (B).
It is preferable to set the weight range.
【００１２】本発明の殺菌剤組成物には上記３成分以外
に必要に応じて各種界面活性剤、無機又は有機の塩類、
ビルダー、香料、顔料、染料、pH調整剤、金属キレート
剤等を添加配合することができる。界面活性剤として
は、非イオン性界面活性剤、陰イオン性界面活性剤及び
両性界面活性剤が用いられ、具体的には例えばポリオキ
シエチレン（以下ＰＯＥと記す）アルキル（炭素数６〜
２２）エーテル、ＰＯＥアルキル（炭素数４〜１８）フ
ェノールエーテル、ポリオキシプロピレンポリオキシエ
チレン（ブロック又はランダム）アルキルエーテル、Ｐ
ＯＥフェニルフェノールエーテル、ＰＯＥスチレン化フ
ェノールエーテル、ＰＯＥトリベンジルフェノールエー
テルなどの非イオン性界面活性剤；リグニンスルホン酸
塩、アルキルベンゼンスルホン酸塩、アルキルスルホン
酸塩、ＰＯＥアルキルスルホン酸塩、ＰＯＥアルキルフ
ェニルエーテルスルホン酸塩、ＰＯＥアルキルフェニル
エーテルリン酸エステル塩、ＰＯＥフェニルフェノール
エーテルスルホン酸塩、ＰＯＥフェニルフェノールエー
テルリン酸エステル塩、ナフタレンスルホン酸塩、ナフ
タレンスルホン酸ホルマリン縮合物、ＰＯＥトリベンジ
ルフェノールエーテルスルホン酸塩、ＰＯＥトリベンジ
ルフェニルフェノールエーテルリン酸エステル塩などの
陰イオン性界面活性剤；両性界面活性剤としては、アル
キルアミノトリメチルグリシン、アルキルジメチルアミ
ンオキシド、アルキルジアミノエチルグリシン塩酸塩等
が挙げられる。これらは単独又は組み合わせて用いるこ
とができる。その含有量は殺菌剤中０〜２０重量％、好
ましくは１〜１０重量％である。The fungicidal composition of the present invention may further contain various surfactants, inorganic or organic salts, if necessary, in addition to the above three components.
Builders, fragrances, pigments, dyes, pH adjusters, metal chelators and the like can be added and blended. As the surfactant, a nonionic surfactant, an anionic surfactant and an amphoteric surfactant are used, and specifically, for example, polyoxyethylene (hereinafter referred to as POE) alkyl (having 6 to 6 carbon atoms)
22) ether, POE alkyl (C4-18) phenol ether, polyoxypropylene polyoxyethylene (block or random) alkyl ether, P
Nonionic surfactants such as OE phenyl phenol ether, POE styrenated phenol ether, POE tribenzyl phenol ether; lignin sulfonate, alkyl benzene sulfonate, alkyl sulfonate, POE alkyl sulfonate, POE alkyl phenyl ether Sulfonate, POE alkyl phenyl ether phosphate, POE phenyl phenol ether sulfonate, POE phenyl phenol ether phosphate, naphthalene sulfonate, naphthalene sulfonic acid formalin condensate, POE tribenzyl phenol ether sulfonate And anionic surfactants such as POE tribenzyl phenyl phenol ether phosphate; and amphoteric surfactants include alkylaminotrime. Rugurishin, alkyl dimethyl amine oxides, alkyldiaminoethylglycine hydrochloride and the like. These can be used alone or in combination. Its content in the fungicide is 0 to 20% by weight, preferably 1 to 10% by weight.
【００１３】塩類としては、コハク酸、マロン酸、クエ
ン酸、グルコン酸、グルタル酸等のカルボン酸金属塩、
トリポリリン酸、ヘキサメタリン酸、リン酸等のリン酸
化合物金属塩、Ｎａ2ＳＯ4、Ｋ2ＳＯ4、ＮａＨＳＯ4等
の無機塩等が挙げられる。これらは単独或いは組み合わ
せても用いることができる。pH調整剤としては、クエン
酸、マロン酸、コハク酸、グルコン酸等の有機酸が挙げ
られる。これらは単独或いは２種以上を組み合わせて用
いることができる。金属キレート剤としては、エチレン
ジアミン四酢酸、ニトリロトリ酢酸、トリポリリン酸、
ポリヒドロキシアクリル酸等又はこれらの塩が挙げられ
る。本発明の殺菌剤組成物は、常法により粉体、顆粒、
錠剤等の固形物として製造され、使用に当り、水に希釈
し施用される。その時の濃度は対象物によっても異なる
が、通常無機過酸物濃度で２５〜１０００ppmとするこ
とが好ましい。勿論、無機過酸化物、無機過酸化物の活
性化剤、アルカリ土類金属塩をそれぞれ別個に製剤し、
使用するに当り、それらを一緒に水に希釈して施用して
もよい。The salts include metal salts of carboxylic acids such as succinic acid, malonic acid, citric acid, gluconic acid and glutaric acid;
Metal salts of phosphoric acid compounds such as tripolyphosphoric acid, hexametaphosphoric acid and phosphoric acid, and inorganic salts such as Na 2 SO 4 , K 2 SO 4 and NaHSO 4 are mentioned. These can be used alone or in combination. Examples of the pH adjuster include organic acids such as citric acid, malonic acid, succinic acid, and gluconic acid. These can be used alone or in combination of two or more. Metal chelating agents include ethylenediaminetetraacetic acid, nitrilotriacetic acid, tripolyphosphoric acid,
Examples thereof include polyhydroxyacrylic acid and the like, and salts thereof. The fungicidal composition of the present invention, powder, granules, by a conventional method,
It is manufactured as a solid such as a tablet and diluted with water before use. Although the concentration at that time varies depending on the target, it is usually preferable to set the concentration of the inorganic peracid to 25 to 1000 ppm. Of course, the inorganic peroxide, the activator of the inorganic peroxide, the alkaline earth metal salt is separately formulated,
For use, they may be diluted together with water and applied.
【００１４】[0014]
【発明の効果】本発明の殺菌剤は、殺菌効果が高く、持
続性がよい。しかも、保存安定性に優れているので、工
場から家庭まで幅広い分野で用いることができる。The bactericide of the present invention has a high bactericidal effect and good persistence. Moreover, since it has excellent storage stability, it can be used in a wide range of fields from factories to homes.
【００１５】[0015]
【実施例】次に、種々の実施例を挙げて本発明を更に詳
細に説明するが、本発明はこれらに限定されるものでは
ない。EXAMPLES Next, the present invention will be described in more detail with reference to various examples, but the present invention is not limited to these examples.
【００１６】実施例１ 各分野に対応すべく、種々の殺菌剤組成物を表１〜４に
示す如く混合、調製した。このものを水和した後、発生
した有機過酢酸量を測定した。この結果を表１〜３に示
す。Example 1 Various fungicidal compositions were mixed and prepared as shown in Tables 1 to 4 in accordance with each field. After hydration, the amount of generated organic peracetic acid was measured. The results are shown in Tables 1 to 3.
【００１７】[0017]
【表１】 [Table 1]
【００１８】[0018]
【表２】 [Table 2]
【００１９】[0019]
【表３】 [Table 3]
【００２０】実施例２ 保存安定性試験：表４に示す
組成の殺菌剤組成物を混合し、４０℃、湿度７５％で１
ケ月間密閉保存し、夫々の有機酸臭を調べた。この結果
を表４に示す。Example 2 Storage stability test: A bactericide composition having the composition shown in Table 4 was mixed, and the mixture was added at 40 ° C. and 75% humidity for 1
It was stored tightly for a period of nine months, and the organic acid smell of each was examined. Table 4 shows the results.
【００２１】[0021]
【表４】 [Table 4]
【００２２】実施例３ 本発明の殺菌効力を比較検定するため、Ｅｓｃｈｅｒｉ
ｃｈｉａ ＣｏｌｉＩＦＯ ３７９６を用い、田中の方
法〔田中徳満：薬剤感受性測定法（三橋進編）（１９８
０）講談社〕をモディファイして行った。すなわち、前
培養した菌（約１０8／ml）を約１００μｌ（±５％）
取り、滅菌蒸留水で所定の倍率に希釈した本発明の殺菌
剤液（水和１５分後）１０mlの入った試験管に接種し、
室温にて作用させた。接種後一定時間ごとに菌・殺菌液
を白金耳で取り、後培養の培地（３００μｌ）の入った
９６穴シャーレ（コーニング社製、１穴３７０μｌ）に
接種しその後３７℃、２日間培養し、菌の発育を判定し
た。この結果を表５〜７に示す。Example 3 To compare the bactericidal efficacy of the present invention, Escheri was used.
Using Tia Coli IFO 3796, the method of Tanaka [Tokumitsu Tanaka: Method for Measuring Drug Sensitivity (Susumu Mitsuhashi) (198)
0) Kodansha]. That is, about 100 μl (± 5%) of the pre-cultured bacteria (about 10 8 / ml)
Inoculated into a test tube containing 10 ml of the bactericide solution of the present invention (15 minutes after hydration) diluted with sterilized distilled water to a predetermined magnification,
Acted at room temperature. At regular intervals after the inoculation, the bacteria / bactericidal solution was taken with a platinum loop, inoculated into a 96-well petri dish (Corning Co., 1 well, 370 μl) containing a post-culture medium (300 μl), and then cultured at 37 ° C. for 2 days. The growth of the fungus was determined. The results are shown in Tables 5-7.
【００２３】[0023]
【表５】 [Table 5]
【００２４】[0024]
【表６】 [Table 6]
【００２５】[0025]
【表７】 [Table 7]
【００２６】[0026]
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7，ＤＢ名) A01N 59/00 A01N 25/22 ──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int.Cl. 7 , DB name) A01N 59/00 A01N 25/22
Claims (3)
コールの有機酸不完全エステル （Ｃ）アルカリ土類金属塩 を含有し、（Ｃ）成分の含有量は（Ｂ）成分に対して
０．１〜２０重量倍である、固形の殺菌剤組成物。An organic acid incomplete ester of a polyhydric alcohol, wherein the following components (A), (B) and (C): (A) an inorganic peroxide; and (B) an ester having a degree of substitution of 5 to 95%. A solid fungicide composition comprising (C) an alkaline earth metal salt, wherein the content of the component (C) is 0.1 to 20 times the weight of the component (B).
完全エステルの多価アルコール部分が、グリセリン類及
び／又は糖類である請求項１記載の殺菌剤組成物。2. The fungicidal composition according to claim 1, wherein the polyhydric alcohol moiety of the incomplete organic acid ester of the polyhydric alcohol (B) is a glycerin and / or a saccharide.
完全エステルが、炭素数１〜８の脂肪酸の不完全エステ
ルである請求項１又は２記載の殺菌剤組成物。3. The fungicidal composition according to claim 1, wherein the incomplete organic acid ester of the polyhydric alcohol (B) is an incomplete ester of a fatty acid having 1 to 8 carbon atoms.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10295793A JP3281445B2 (en) | 1993-04-28 | 1993-04-28 | Fungicide composition |
| TW83103723A TW252907B (en) | 1993-04-28 | 1994-04-26 | |
| PCT/JP1994/000710 WO1994024869A1 (en) | 1993-04-28 | 1994-04-27 | Germicidal composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10295793A JP3281445B2 (en) | 1993-04-28 | 1993-04-28 | Fungicide composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06305920A JPH06305920A (en) | 1994-11-01 |
| JP3281445B2 true JP3281445B2 (en) | 2002-05-13 |
Family
ID=14341285
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10295793A Expired - Fee Related JP3281445B2 (en) | 1993-04-28 | 1993-04-28 | Fungicide composition |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JP3281445B2 (en) |
| TW (1) | TW252907B (en) |
| WO (1) | WO1994024869A1 (en) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU1584495A (en) * | 1994-02-07 | 1995-08-21 | Warwick International Group Limited | Oxidising compositions |
| FR2728171B1 (en) * | 1994-12-14 | 1997-01-24 | Chemoxal Sa | PRODUCTION OF BIOCIDAL DISINFECTANT FORMULATIONS BASED ON PERACETIC IONS |
| SE9600663L (en) * | 1996-02-22 | 1997-08-23 | Jan Olof Eriksson | Procedures for controlling microorganisms |
| EP1064845B1 (en) * | 1999-06-30 | 2003-09-10 | Kao Corporation | Virucidal and sporicidal composition |
| PE20030729A1 (en) * | 2002-01-18 | 2003-10-21 | Novartis Ag | METHODS FOR PRESERVING OPHTHALMIC SOLUTIONS AND PRESERVED OPHTHALMIC SOLUTIONS |
| US7919122B2 (en) | 2003-04-02 | 2011-04-05 | Kao Corporation | Composition for production of a sterilizer and a process for producing organic peracid |
| JP5036962B2 (en) * | 2004-08-06 | 2012-09-26 | 花王株式会社 | Disinfectant composition for automatic washing machine |
| US8871807B2 (en) | 2008-03-28 | 2014-10-28 | Ecolab Usa Inc. | Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids |
| US8809392B2 (en) | 2008-03-28 | 2014-08-19 | Ecolab Usa Inc. | Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents |
| BRPI0907918B1 (en) | 2008-03-28 | 2018-07-24 | Ecolab Inc. | SULFOPEROXIC CARBOXYLIC ACIDS, THEIR PREPARATION AND METHODS OF USE AS AN ANTIMICROBYANES |
| US8034759B2 (en) * | 2008-10-31 | 2011-10-11 | Ecolab Usa Inc. | Enhanced stability peracid compositions |
| US8846107B2 (en) | 2010-12-29 | 2014-09-30 | Ecolab Usa Inc. | In situ generation of peroxycarboxylic acids at alkaline pH, and methods of use thereof |
| PL2687094T3 (en) | 2010-12-29 | 2018-09-28 | Ecolab Usa Inc. | Generation of peroxcarboxylic acids at alkaline pH, and their use as textile bleaching and antimicrobial agents |
| US8889900B2 (en) | 2010-12-29 | 2014-11-18 | Ecolab Usa Inc. | Sugar ester peracid on site generator and formulator |
| US9321664B2 (en) | 2011-12-20 | 2016-04-26 | Ecolab Usa Inc. | Stable percarboxylic acid compositions and uses thereof |
| CN106396037B (en) | 2012-03-30 | 2019-10-15 | 艺康美国股份有限公司 | Peracetic acid/hydrogen peroxide and peroxide reducing agent are used to handle drilling fluid, fracturing fluid, recirculation water and the purposes for discharging water |
| US10165774B2 (en) | 2013-03-05 | 2019-01-01 | Ecolab Usa Inc. | Defoamer useful in a peracid composition with anionic surfactants |
| US8822719B1 (en) | 2013-03-05 | 2014-09-02 | Ecolab Usa Inc. | Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring |
| US20140256811A1 (en) | 2013-03-05 | 2014-09-11 | Ecolab Usa Inc. | Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids |
| BR122018076176B1 (en) | 2014-12-18 | 2021-06-01 | Ecolab Usa Inc | METHOD TO FORM PEROXIFORMIC ACID, METHOD TO TREAT A SURFACE, METHOD TO TREAT A BIOFILM ON A SURFACE AND METHOD TO DISINFECT A SKIN SURFACE |
| US11040902B2 (en) | 2014-12-18 | 2021-06-22 | Ecolab Usa Inc. | Use of percarboxylic acids for scale prevention in treatment systems |
| US9845290B2 (en) | 2014-12-18 | 2017-12-19 | Ecolab Usa Inc. | Methods for forming peroxyformic acid and uses thereof |
| US10974211B1 (en) | 2016-02-17 | 2021-04-13 | Zee Company, Inc. | Peracetic acid concentration and monitoring and concentration-based dosing system |
| US11350640B1 (en) | 2016-08-12 | 2022-06-07 | Zee Company I, Llc | Methods and related apparatus for increasing antimicrobial efficacy in a poultry chiller tank |
| WO2019241635A1 (en) | 2018-06-15 | 2019-12-19 | Ecolab Usa Inc. | On site generated performic acid compositions for teat treatment |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7608265A (en) * | 1975-08-16 | 1977-02-18 | Henkel & Cie Gmbh | STABLE CONCENTRATES OF FUNCTIONAL RESOURCES IN STORAGE. |
| JPS5230795A (en) * | 1975-09-04 | 1977-03-08 | Kao Corp | Composition for bleaching agent |
| US4405482A (en) * | 1980-09-01 | 1983-09-20 | Richardson-Vicks Pty. Limited | Sanitizing formulation |
| JPH0617289B2 (en) * | 1985-12-27 | 1994-03-09 | エーザイ株式会社 | Fungicide composition for storage |
-
1993
- 1993-04-28 JP JP10295793A patent/JP3281445B2/en not_active Expired - Fee Related
-
1994
- 1994-04-26 TW TW83103723A patent/TW252907B/zh active
- 1994-04-27 WO PCT/JP1994/000710 patent/WO1994024869A1/en active Application Filing
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06305920A (en) | 1994-11-01 |
| WO1994024869A1 (en) | 1994-11-10 |
| TW252907B (en) | 1995-08-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3281445B2 (en) | Fungicide composition | |
| JP6943761B2 (en) | Activated hydrogen peroxide disinfectant composition | |
| AU676902B2 (en) | Peroxyacid antimicrobial composition | |
| US6479454B1 (en) | Antimicrobial compositions and methods containing hydrogen peroxide and octyl amine oxide | |
| AU652274B2 (en) | Peroxyacid antimicrobial composition | |
| US4404040A (en) | Short chain fatty acid sanitizing composition and methods | |
| JP3566454B2 (en) | Product disinfection and bleaching methods and compositions used therefor | |
| CA2475327C (en) | Enhanced activity hydrogen peroxide disinfectant | |
| JP2019502792A (en) | Amide-containing composition | |
| JP2018537479A (en) | Composition comprising ester and / or acid | |
| US11330819B2 (en) | Synergistic disinfectant compositions having enhanced antimicrobial efficacy and stability, and methods of using the same | |
| JP6704099B1 (en) | Sterilizing or virus inactivating agent composition, and method for enhancing efficacy of sterilizing or virus inactivating agent | |
| EP0096525B1 (en) | Sanitizer compositions | |
| JP2000109887A (en) | Detergent composition for sterilization of food | |
| JP2006045147A (en) | Detergent composition for sterilization of hard surface | |
| JPH07119436B2 (en) | Cleaning composition | |
| JP2956790B2 (en) | Foods with little skin irritation, dishwashing detergent, and disinfection method using the same | |
| JPH07197090A (en) | Liquid detergent composition | |
| WO1991003936A1 (en) | Effervescent compositions | |
| JPH06510536A (en) | Production of peroxyacids | |
| JPH11124597A (en) | Solid sterilizing detergent for hard object | |
| JP4137432B2 (en) | Disinfectant for medical equipment | |
| JP3607565B2 (en) | Disinfectant composition for fresh food | |
| JPH07119437B2 (en) | Cleaning composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20080222 Year of fee payment: 6 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090222 Year of fee payment: 7 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100222 Year of fee payment: 8 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100222 Year of fee payment: 8 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110222 Year of fee payment: 9 |
|
| LAPS | Cancellation because of no payment of annual fees |