JPH0215005A - Sterilizing composition for nonmedical treatment - Google Patents

Sterilizing composition for nonmedical treatment

Info

Publication number
JPH0215005A
JPH0215005A JP16271588A JP16271588A JPH0215005A JP H0215005 A JPH0215005 A JP H0215005A JP 16271588 A JP16271588 A JP 16271588A JP 16271588 A JP16271588 A JP 16271588A JP H0215005 A JPH0215005 A JP H0215005A
Authority
JP
Japan
Prior art keywords
salt
compound
composition
agent
salts
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
Application number
JP16271588A
Other languages
Japanese (ja)
Other versions
JP2592101B2 (en
Inventor
Hiroki Koma
寛紀 高麗
Koji Tsuchitani
槌谷 浩司
Yoshihiro Watanabe
義弘 渡辺
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Inui Corp
Original Assignee
Inui Corp
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.)
Filing date
Publication date
Application filed by Inui Corp filed Critical Inui Corp
Priority to JP16271588A priority Critical patent/JP2592101B2/en
Publication of JPH0215005A publication Critical patent/JPH0215005A/en
Application granted granted Critical
Publication of JP2592101B2 publication Critical patent/JP2592101B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain a composition for preventing harmful microorganism generating at paint, leather, wood or bamboo product, woven or knitted fabric or paper product, etc., containing bithionol, fenticlor or salt of said compound and trihalogenized phenol or salt of said phenol as active ingredients. CONSTITUTION:The subject composition containing a compound expressed by formula I [M is H, alkali (earth) metal; X is halogen; n is 1 or 2] or salt of said compound and a compound expressed by formula II [M' is H, alkali (earth) metal; Y is halogen] or salt of said compound in weight ratio of 5:1-1:20. Although said two components have respective weak points as single active ingredient preparation, an effect preventable of various molds or fungi with low dosage of 1/2-1/10 of the single active ingredient preparation is obtained by using in combination. Mixing other bactericide, insecticide and deterioration preventing agent, etc., in said composition is allowable and any formulation of hydration agent, powdery agent, tablet, emulsion and pasty agent is usable.

Description

【発明の詳細な説明】 本発明は塗料、木竹製品、皮革、糊料等の産業若しくは
日常生活に必要な産業用製品又はこれらの製造工程等で
発生する有害微生物を防除するための非医療用殺菌組成
物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to industrial products such as paints, wood and bamboo products, leather, pastes, etc. or industrial products necessary for daily life, or non-medical products for controlling harmful microorganisms generated in the manufacturing process of these products. The present invention relates to a disinfectant composition for use in disinfectants.

産業用製品又はこれらを製造する工程等に発生する微生
物を防除するための非医療用殺菌組成物としては従来よ
り、主として、有機溶剤、有機錫剤が広く使用されてい
た。しかしながら、この有機金属化合物を有効成分とす
る非医療用殺菌組成物は残留毒性及び薬剤使用時の安定
性に問題があるとされていた。これに代る薬剤として有
機塩素系化合物、第4級アンモニウム塩等が使用されて
きた。しかし、最近特に、細菌、黴類、酵母類による微
生物災害が多発しているが、これらに対してこれら従来
の薬剤では効果が充分でなく、新しい薬剤の開発が強く
要望されている。
Conventionally, organic solvents and organic tin agents have been widely used as non-medical sterilizing compositions for controlling microorganisms generated in industrial products or the processes for manufacturing them. However, non-medical sterilizing compositions containing this organometallic compound as an active ingredient have been thought to have problems with residual toxicity and stability during drug use. Organic chlorine compounds, quaternary ammonium salts, and the like have been used as alternative agents. However, recently, microbial disasters caused by bacteria, molds, and yeasts have been occurring frequently, and these conventional drugs are not sufficiently effective against these, and there is a strong demand for the development of new drugs.

本発明者らはかかる要望に鑑み、多くの細菌、黴に対し
て低薬量で活性を示す非医療用殺菌剤を開発するため鋭
意研究を重ねた結果、従来単独で殺菌剤として知られ、
また単独で殺菌剤として使用した場合充分満足し得なか
った特定の化合物を組合せて使用すると、それぞれ単独
の薬効からは全く予想し得ない種々の優れた相乗的効果
を有する非医療用殺菌組成物が見出された。
In view of this demand, the present inventors have conducted intensive research to develop a non-medical disinfectant that is active against many bacteria and molds at low dosages.
In addition, when specific compounds that were not fully satisfactory when used alone as bactericidal agents are used in combination, non-medical bactericidal compositions have various excellent synergistic effects that could not be expected from the medicinal effects of each of them alone. was discovered.

かくして、本発明によれば、(a)ビチオノール又はフ
ェンチクロル或いはそれらの塩類及び(b)トリハロゲ
ン化フェノール或いはその塩類を有効成分どする非医療
用殺菌剤が提供される。
Thus, according to the present invention, there is provided a non-medical disinfectant whose active ingredients are (a) bithionol or fentichlor or salts thereof and (b) trihalogenated phenol or salts thereof.

かかる本発明の組成物を使用すると、それぞれ単独で使
用する場合の効果から、全く予想し難い卓越した相乗的
な殺菌活性か得られる。
When such compositions of the present invention are used, an outstanding synergistic bactericidal activity is obtained which is completely unexpected from the effect when each is used alone.

本発明における(a)ヒチオノール又はフェンチクロル
は下記一般式(I)で表わされる化合物である。
(a) Hythionol or fentichlor in the present invention is a compound represented by the following general formula (I).

0M  M(( [但し式中、Mは水素原子、アルカリ金属及びアルカリ
土類金属からなる群から選ばれ、モしてXはハロゲン原
子を示し、nは1又は2の整数を示す。1 上記一般式(I)においてnが2の場合がビチオノール
であり、nが1の場合がフェンチクロルである。
0 MM In general formula (I), when n is 2, it is bithionol, and when n is 1, it is fentichlor.

上記ビチオノールは、細菌、真菌に対して抗菌作用がる
殺菌剤として開発されたものであり黄色ブドウ球菌の発
育阻止にはlO万分の1の濃度で効果があり、肺、肝、
腸のジストマや條虫駆除に内服するが化粧品や万両、シ
ャンプーに添加して常用することは、皮膚吸収により発
疹、黒革症が現われるため現在米国のFDAでは化粧品
(石ケン)に添加することは禁止されているが藻類の発
生防止やゴム製品、水溶性研磨液の防腐保存料としては
現在もなお使用されている。
The above-mentioned bitionol was developed as a bactericidal agent with antibacterial effects against bacteria and fungi, and is effective in inhibiting the growth of Staphylococcus aureus at a concentration of 1/1000 100,000 ml.
It is taken orally to treat intestinal dystomia and insect control, but regular use of it as an additive to cosmetics, soaps, and shampoos can cause rashes and melasma due to skin absorption, so the US FDA currently prohibits it from being added to cosmetics (soaps). Although it is prohibited, it is still used today to prevent the growth of algae and as a preservative for rubber products and water-soluble polishing fluids.

一方フェンチクロルは、外用抗感染抗カビ剤として開発
されたものである。本発明においてビチオノール及びフ
ェンチクロルは組合せて使用してもよい。
On the other hand, fentichlor was developed as a topical anti-infective and anti-fungal agent. Bithionol and fentichlor may be used in combination in the present invention.

力木発明において、前記ビチオノール又はフェンチクロ
ルと組合せて使用される(b)トリハロゲン化フェノー
ルは下記一般式(I[)で表わされる化合物である。
In the strength wood invention, the trihalogenated phenol (b) used in combination with bithionol or fentichlor is a compound represented by the following general formula (I[).

[但し式中、M′は水素原子、アルカリ金属及びアルカ
リ土類金属からなる群から選ばれ、モしてYはハロゲン
原子を示すが、3個のYはそれぞれ同一もしくは相異な
っていてもよい。] 上記トリハロゲン化フェノールの具体例としては、 例
、tif、2. 4. 6− トリクロルフェノール(
以下”2,4.6−TCP’″と略称することがある)
、2.4.6−1−リブロムフェノール(以下”2.4
.6−TB P”と略称することがある)、2、5−ジ
クロル−4−ブロムフェノール(以下”2.5.4−D
CB”と略称することがある)、2.5−ジクロル−6
−ブロムフェノール(以下゛2,5.6−DCB”と略
称することがある)及びこれらの塩類が挙げられる。塩
類の例としては、ナトリウム塩、カリウム塩又はカルシ
ウム塩の如きアルカリ金属塩又はアルカリ土類金属塩を
示すことができる。これらのトリハロゲン化フェノール
又はその塩類は、水性ペイントの防黴、製紙ノスライム
・コントロールの如き産業用防黴剤、農業用土壌処理剤
、木材防腐などの殺菌防黴保存剤として使用されている
。しかしトリハロゲン化フェノール及びその塩類は、揮
発性が著しく高く、そのため予防効果が持続しないとい
う利用面の欠点があった。
[However, in the formula, M' is selected from the group consisting of a hydrogen atom, an alkali metal, and an alkaline earth metal, and Y represents a halogen atom, but each of the three Y's may be the same or different. . ] Specific examples of the above-mentioned trihalogenated phenol include, example, tif, 2. 4. 6- Trichlorophenol (
(Hereinafter, it may be abbreviated as "2,4.6-TCP'")
, 2.4.6-1-ribromophenol (hereinafter referred to as “2.4
.. (sometimes abbreviated as “6-TB P”), 2,5-dichloro-4-bromophenol (hereinafter “2.5.4-D
(sometimes abbreviated as "CB"), 2,5-dichloro-6
-bromophenol (hereinafter sometimes abbreviated as "2,5.6-DCB") and salts thereof. Examples of salts include alkali metal salts such as sodium salts, potassium salts, or calcium salts; These trihalogenated phenols or their salts can be used as fungicides in water-based paints, industrial fungicides such as NoSlime Control for papermaking, agricultural soil treatment agents, and wood preservatives. Trihalogenated phenols and their salts are used as anti-mold preservatives.However, trihalogenated phenols and their salts have a drawback in that their preventive effects do not last long because of their extremely high volatility.

本発明の非医療用殺菌組成物は、前述したそれぞれの単
剤としては欠点があり実用上の問題があったものを、組
合せて組成物とすることにより、それぞれの殺菌効果を
単に相加して対象徴生物の種類が拡大したに止らず、微
生物災害の起因菌であり従来防除が困難であった各種の
黴や細菌を低薬量の使用によって防除でき、殊にそれぞ
れ単剤の使用量と比べて’/2〜1/1゜以下で防除で
きるという優れた相乗効果が得られた。
The non-medical sterilizing composition of the present invention simply adds up the sterilizing effects of each of the above-mentioned single agents, which have drawbacks and practical problems, by combining them into a composition. Not only has the variety of symbolic organisms expanded, but various molds and bacteria that cause microbial disasters and were difficult to control in the past can be controlled by using low doses, especially when using a single agent. An excellent synergistic effect was obtained in that it was possible to control insects at a rate of 1/2 to 1/1 degree or less compared to that of the conventional method.

さらに本発明の組成物は、産業用製品の微生物災害起因
菌であるアスペルギウス属、トリコデルマ属の黴類に対
しても著しく低い濃度で活性を有しており経済的に安価
に且つ安全に防除できるという極めて優れた利点を有し
ている。
Furthermore, the composition of the present invention has activity at extremely low concentrations against molds of the genus Aspergius and genus Trichoderma, which are bacteria that cause microbial disasters in industrial products, and can be economically and safely controlled. It has extremely excellent advantages.

本発明の組成物において(a)ビチオノール又はフェン
チクロル或いはそれらの塩類と(b)トリハロゲン化フ
ェノール或いはその塩類とは、重量で10 : 1−1
 : tooの割合、好ましくは5: l−1: 20
の割合で配合するのが望ましい。
In the composition of the present invention, (a) bithionol or fentichlor or salts thereof and (b) trihalogenated phenol or salts thereof are 10:1-1 by weight.
: too ratio, preferably 5:l-1:20
It is desirable to mix in the ratio of .

本発明の組成物は、前記2種の組合せた有効成分を含有
していればよく、さらに−収約な殺菌・殺黴に使用され
ている担体に分散させるか或いは溶解させた形態であ・
〕てもよく、さらに固体担体に混合された形態であって
もよい。また必要に応じて、展着剤、安定剤、分散剤、
湿潤剤、浸透剤、懸濁向上剤などを加えることもできる
。組成物の剤型としては、水和剤、粉剤、錠剤、乳剤、
ペースト剤などのいずれであってもよい。
The composition of the present invention only needs to contain the above-mentioned two types of active ingredients in combination, and is further dispersed or dissolved in a carrier used for compact sterilization and fungicides.
] or may be in the form of a mixture in a solid carrier. In addition, spreading agents, stabilizers, dispersants,
Wetting agents, penetrants, suspension enhancers, etc. can also be added. The dosage forms of the composition include wettable powders, powders, tablets, emulsions,
It may be any paste agent or the like.

本発明の組成物中には、他の殺菌剤、殺虫剤、劣化防止
剤を配合しても差支えない。
Other bactericides, insecticides, and deterioration inhibitors may be added to the composition of the present invention.

本発明の組成物は、使用される対象物、目的、形態に応
じてそのまま直接施用するか、または適当な濃度に希釈
して使用することができる。
The composition of the present invention can be directly applied as it is or diluted to an appropriate concentration depending on the object, purpose, and form to which it is used.

かくして本発明の非医療用殺菌組成物は、塗料、皮革、
木竹製品、糊料、織編物、紙製品、壁材料、プラスチッ
ク製品などに混入させるか或いは表面処理せしめること
により、有害微生物の発生を防止しまた生育を阻止する
のでこれら製品の品質劣化を防止のために有利に使用さ
れる。
Thus, the non-medical sterilizing composition of the present invention can be applied to paints, leather,
By mixing it with wood and bamboo products, starch materials, woven and knitted fabrics, paper products, wall materials, plastic products, etc., or treating the surfaces thereof, it prevents the generation and growth of harmful microorganisms, thereby preventing quality deterioration of these products. advantageously used for.

以下実施例を示して本発明をさらに具体的に説明するが
、本発明はそれによって何等限定を受けるものではない
EXAMPLES The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited thereto in any way.

寒天希釈法による最低生育阻止濃度試験実験l 各薬剤は、それぞれエタノールで有効成分濃度ビチオノ
ールの場合は4,8,10.15,20゜25.30.
40ppm、2.4.6−TCPの場合は5,10.2
0,30,40.50.60ppmに希釈し9cmのベ
トリ皿1枚に2cm宛分注する。それに下記組成のサブ
ロー培地lOmQ加温溶解して加え、よく薬剤希釈液と
を混合せしめ固化平板とする。
Minimum inhibitory concentration test experiment using agar dilution method 1 The active ingredient concentration of each drug in ethanol was 4, 8, 10.15, 20°, 25.30° for bithionol.
40ppm, 5,10.2 for 2.4.6-TCP
Dilute to 0, 30, 40, 50, and 60 ppm and dispense 2 cm into a 9 cm veterinary dish. Sabouraud medium lOmQ having the following composition is added to the solution by heating and dissolved, and the mixture is thoroughly mixed with the drug dilution solution to form a solidified plate.

この上にJIS  Z−2911の方法により胞子液を
作り105w/rnQ含有する。それをマイクロプレー
ターで寒天上に0.01mQづつ胞子液を接種した。2
8°C1−週間培養後、菌の生育の有無を観察し、°最
低生育阻止濃度を求めた。その結果の一部を下記表1に
示した。
On top of this, a spore liquid was prepared according to the method of JIS Z-2911 and contained 105 w/rnQ. The spore liquid was inoculated onto agar using a microplate in an amount of 0.01 mQ. 2
After culturing at 8°C for 1 week, the presence or absence of bacterial growth was observed, and the minimum growth-inhibiting concentration was determined. Some of the results are shown in Table 1 below.

なおこの実験lからビチオノール及び2,4゜6−TC
Pの併用による相乗効果は上記表1から明らかであるが
、−層明瞭とするため実験lのデータを添付図1の(A
)〜(E)に示した。図1中の(A)〜(E)は、それ
ぞれ表1中に示した供試菌の欄に示したものと一致して
いる。図1中(A)〜(E)において、横軸は2,4.
6−TCPの濃度(ppm)であり、縦軸はビチオノー
ルの濃度である。図1中(A)〜(E)のいずれも点線
よりも下方に最低生育阻止濃度が示されており、このこ
とは、ビチオノール及び2,4.6−TCPの併用によ
って相乗効果があることを明らかに示している。
Furthermore, from this experiment 1, bithionol and 2,4゜6-TC
The synergistic effect of the combined use of P is clear from Table 1 above, but in order to clarify the - layer, the data of Experiment 1 is shown in attached Figure 1 (A
) to (E). (A) to (E) in FIG. 1 correspond to those shown in the column of test bacteria shown in Table 1, respectively. In (A) to (E) in FIG. 1, the horizontal axis represents 2, 4.
The concentration of 6-TCP (ppm) is shown, and the vertical axis is the concentration of bithionol. In all of (A) to (E) in Figure 1, the lowest growth inhibitory concentration is shown below the dotted line, which indicates that the combination of bitionol and 2,4.6-TCP has a synergistic effect. clearly shows.

実験2 実験方法は、前記実験1と同様に行った。但し、ビチオ
ノールの代りにビチオノール及びフェンチクロルをl:
lの配合率で混合して使用し、有効成分濃度で1,2,
5.to、20,50,100.200,400ppm
で実験を行った。また2、4.6−TCPについても同
様の濃度に希釈したものを使用した。
Experiment 2 The experimental method was the same as in Experiment 1 above. However, bithionol and fentichlor are used instead of bithionol:
It is used by mixing at a blending ratio of 1, 1, 2,
5. to, 20, 50, 100. 200, 400 ppm
I conducted an experiment. 2,4.6-TCP was also diluted to the same concentration and used.

その結果の一部を下記衣2に示した。A part of the results are shown in Figure 2 below.

また実験2における結果を添付図2の(A)〜(F)に
示した。図2の(A)〜(F)は表2中の供試菌の(A
)〜(F)にそれぞれ対応している。いずれも相乗効果
を有していることを示している。
Further, the results of Experiment 2 are shown in attached FIGS. 2 (A) to (F). (A) to (F) of Figure 2 are (A) of the test bacteria in Table 2.
) to (F), respectively. This shows that both have a synergistic effect.

実験3 各薬剤はそれぞれエタノールで有効成分濃度ビチオノー
ル+フェンチクロル(1: l)の混合比で1.2.5
.10.20.50.100.200.400ppm、
2,4.6−TCPも同じ濃度に希釈し、9cmのベト
リ皿1枚に2cm宛分注する。
Experiment 3 Each drug was mixed with ethanol at an active ingredient concentration of bithionol + fentichlor (1: l) at a mixing ratio of 1.2.5.
.. 10.20.50.100.200.400ppm,
2,4.6-TCP is also diluted to the same concentration and dispensed into 2 cm portions in a 9 cm veterinary dish.

それに下記標準培地10m12加温溶解して加え、よく
薬剤希釈液とを混合せしめ固化平板とする。
Add 10 ml of the standard medium shown below after heating and dissolving it, and mix well with the drug dilution solution to form a solidified plate.

この上に、全培養で1010個/mQを含有する細菌を
、マイクロプレーターで寒天上に0.OlmQづつ菌を
接種した。
On top of this, bacteria containing 1010 cells/mQ in total culture were plated on agar in a microplate. The bacteria were inoculated with OlmQ.

37°C148時間培養後菌の生育の有無を観察し、最
低生育阻止濃度を求めた。
After culturing at 37°C for 148 hours, the presence or absence of bacterial growth was observed, and the minimum growth-inhibiting concentration was determined.

上記実験の結果を下記表3に示した。The results of the above experiment are shown in Table 3 below.

その結果から菌に対しても本発明の効果が認められるこ
とが理解出来る。
From the results, it can be understood that the effect of the present invention is also recognized against bacteria.

【図面の簡単な説明】[Brief explanation of the drawing]

第1−(A)図〜第1−(E)図及び第2(A)図〜第
2−(F)図はいずれも本発明の実験l及び2において
得られた薬剤の組成と最低生育阻止濃度の関係を示した
ものである。 茅 −E図 隼 −A図 第1−C図 第 −B図 第 −り図 第2−A図 第2−C図 第2−8図 薯2−D図 第2−E図 第2−F図
Figures 1-(A) to 1-(E) and 2(A) to 2-(F) show the composition and minimum growth of the drugs obtained in Experiments 1 and 2 of the present invention. This shows the relationship between inhibitory concentrations. Kaya-E figure Hayabusa-A figure 1-C figure -B figure -ri figure 2-A figure 2-C figure 2-8 figure 2-D figure 2-E figure 2-F figure

Claims (1)

【特許請求の範囲】 1)(a)ビチオノール又はフェンチクロル或いはそれ
らの塩類、及び(b)トリハロゲン化フェノール或いは
その塩類を有効成分として含有することを特徴とする非
医療用殺菌組成物。 2)該有効成分が(a)ビチオノール又はその塩類、及
び(b)トリハロゲン化フェノール又はその塩類である
特許請求の範囲第1項記載の非医療用殺菌組成物。 3)該有効成分が(a)フェンチクロル又はその塩類、
及び(b)トリハロゲン化フェノール又はその塩類であ
る特許請求の範囲第1項記載の非医療用殺菌組成物。
[Scope of Claims] 1) A non-medical sterilizing composition characterized by containing (a) bithionol or fentichlor or salts thereof, and (b) trihalogenated phenol or salts thereof as active ingredients. 2) The non-medical sterilizing composition according to claim 1, wherein the active ingredients are (a) bithionol or its salts, and (b) trihalogenated phenol or its salts. 3) The active ingredient is (a) fentichlor or its salts,
and (b) the non-medical sterilizing composition according to claim 1, which is a trihalogenated phenol or a salt thereof.
JP16271588A 1988-07-01 1988-07-01 Non-medical bactericidal composition Expired - Fee Related JP2592101B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16271588A JP2592101B2 (en) 1988-07-01 1988-07-01 Non-medical bactericidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16271588A JP2592101B2 (en) 1988-07-01 1988-07-01 Non-medical bactericidal composition

Publications (2)

Publication Number Publication Date
JPH0215005A true JPH0215005A (en) 1990-01-18
JP2592101B2 JP2592101B2 (en) 1997-03-19

Family

ID=15759918

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16271588A Expired - Fee Related JP2592101B2 (en) 1988-07-01 1988-07-01 Non-medical bactericidal composition

Country Status (1)

Country Link
JP (1) JP2592101B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2537511A (en) * 2013-12-10 2016-10-19 Dyson Technology Ltd A hand held appliance
US10004313B2 (en) 2013-12-10 2018-06-26 Dyson Technology Limited Hand held appliance
US10165843B2 (en) 2013-12-10 2019-01-01 Dyson Technology Limited Hand held appliance
US10441049B2 (en) 2014-12-16 2019-10-15 Dyson Technology Limited Hand held appliance

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2537511A (en) * 2013-12-10 2016-10-19 Dyson Technology Ltd A hand held appliance
GB2537511B (en) * 2013-12-10 2017-07-19 Dyson Technology Ltd A hand held appliance
US10004313B2 (en) 2013-12-10 2018-06-26 Dyson Technology Limited Hand held appliance
US10165843B2 (en) 2013-12-10 2019-01-01 Dyson Technology Limited Hand held appliance
US10441049B2 (en) 2014-12-16 2019-10-15 Dyson Technology Limited Hand held appliance

Also Published As

Publication number Publication date
JP2592101B2 (en) 1997-03-19

Similar Documents

Publication Publication Date Title
EP0611522B1 (en) Synergistic microbicidal combinations
JP5435475B2 (en) Liquid composition containing histidine silver complex, bactericidal composition, and method for stabilizing histidine silver complex
EP2227959B1 (en) Antimicrobial composition useful for preserving wood
HU203647B (en) Synergistic bactericidal and/or fungicidal compositions comprising isothiazolone derivatives
EP1139757A1 (en) Synergistic antimicrobial combination of 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one and a mixture of a chlorinated isocyanurate and a bromide compound and methods of using same
US5489588A (en) Synergistic microbicidal combinations containing 2-methyl-3-isothiazolone and certain commercial biocides
JP3584987B2 (en) Synergistic antimicrobial composition comprising methylene-bis (thiocyanate) and an organic acid
HUH3566A (en) Space-limiting structure particularly wall or ceiling and method for producing same
JPH0215005A (en) Sterilizing composition for nonmedical treatment
JP3524937B2 (en) Industrial fungicides
JPH0643285B2 (en) Microbial growth inhibitory composition
DE60213361T2 (en) LIQUID ANTIMICROBIAL COMPOSITIONS
EP1244358B1 (en) A stabilized isothiazolone composition and a method of stabilization of isothiazolone
HUT59566A (en) Microbicide compositions containing 4,5-dichloro-2-cyclohexyl-3-isothiazolone and known microbicide active component
JPH0341009A (en) Germicide composition
US5017592A (en) Stable biocide composition for industrial use
JPH02250805A (en) Industrial bactericide
US3856952A (en) Synergistic antimicrobial compositions employing certain n-(phenyl-carbamyl)amino-benzene sulfonyl flourides
JP2003192507A (en) Bactericidal composition for industrial use
JPS6058202B2 (en) Non-medical sterilizing composition
JP2001213707A (en) Sterilization composition and sterilization method for industry
EP0606985A1 (en) Synergistic microbicidal composition comprising 3-isothiazolones and 1-methyl-3,5-7-triaza-1-azoniatricyclo(3.3.1.1)decane chloride
JPH03161403A (en) Antibacterial and antifungal agent composition
JPH0853314A (en) Industrial fungicide and industrial sterilization
JP2001181113A (en) Industrial disinfectant/antiseptic and disinfecting/ antisepticizing method using the same

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees