JPS59212405A - Antimildew composition - Google Patents

Antimildew composition

Info

Publication number
JPS59212405A
JPS59212405A JP8578983A JP8578983A JPS59212405A JP S59212405 A JPS59212405 A JP S59212405A JP 8578983 A JP8578983 A JP 8578983A JP 8578983 A JP8578983 A JP 8578983A JP S59212405 A JPS59212405 A JP S59212405A
Authority
JP
Japan
Prior art keywords
long
composition
water
benzimidazole
chain
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
JP8578983A
Other languages
Japanese (ja)
Other versions
JPH0358324B2 (en
Inventor
Shoichi Miyano
宮野 正一
Takashi Nishino
西野 隆司
Koichi Yamada
幸一 山田
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.)
Lion Corp
Original Assignee
Lion 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 Lion Corp filed Critical Lion Corp
Priority to JP8578983A priority Critical patent/JPS59212405A/en
Publication of JPS59212405A publication Critical patent/JPS59212405A/en
Publication of JPH0358324B2 publication Critical patent/JPH0358324B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:The titled composition that is obtained by adding 2-(4-thiazolyl)-benzimidazole, a long-chain alkyl dimethyl benzyl ammonium salt and an N<alpha>-acyl basic aminoacid ester to a specific solvent, thus being suitable for use in moist places. CONSTITUTION:At least 0.01wt%, preferably more than 0.02wt% of 2-(4-thiazolyl)-benzimidazole, a long-chain alkyl dimethyl benzyl ammonium salt and a lower alkyl salt of an N<alpha>-long chain acyl basic aminoacid, respectively, are added to a solvent containing a water-insoluble high molecular weight compound, preferably a derivative of polyvinyl alcohol to give the objective composition. The solvent for preparing a solution of the water-insoluble high polymer is preferably ethanol. The weight ratio of 2-(4-thia-zolyl)-benzimidazole to the long- chain alkyl dimethyl benzyl ammonium salt is preferred to be 4:1-1:4 in particular.

Description

【発明の詳細な説明】 本発明は、水に濡れた場合においても長期間にわたって
強力な防かび効果を持続し、更に保存安定性に優れた新
規な防かび剤組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel antifungal composition that maintains a strong antifungal effect for a long period of time even when wet with water and has excellent storage stability.

近年、密閉性が高く冷暖房設備の完備した住居が増加す
るとともに、浴室や厨房など比較的湿度の高い場所だけ
でなく押入れ、大袋などにまで、かびの発生がみられる
ようになシ、衛生的、美観的見地からこれの抑制が大き
な課題となってきた。
In recent years, as the number of houses with highly airtight air conditioning and heating systems has increased, mold has begun to grow not only in relatively humid areas such as bathrooms and kitchens, but also in closets, large bags, etc. , suppression of this has become a major issue from an aesthetic standpoint.

ところで通常の生活環境の下で発生するかびの種類は多
種多様であり、これら全てを排しない限9かびの発生に
伴う被害を免れることはできないので、家庭用防かび剤
としては、広い範囲のかびに対して効果を萎しうるもの
でおって、かつ湿気の多い場所においても長期間にわた
って効力を持続しうるものが要求されている。そして、
これまで多くの家庭用防かび剤が知られているが、いず
れも広い範囲のかびに対する抑制効果が十分でなく、か
つ、その効力も長期間持続せず、且つ、非乳化タイプで
一般に用いられるアルコール系溶剤に溶解し、液状又は
噴射剤を使用してスプレー状この防かび剤の効力の喪失
は、特に湿気の多い場所において著しく認められ浴室、
厨房などの濡れる可能性の高い場所のかび発生を長期間
にわたって防止することは非常に困難でめった。
By the way, there are a wide variety of types of mold that occur in normal living environments, and unless all of these types are eliminated, it is impossible to avoid the damage caused by the outbreak of mold.As a household fungicide, it is recommended to use a wide range of molds. There is a need for a substance that can be effective against water and other diseases, and that can maintain its effectiveness for a long period of time even in humid places. and,
Many household fungicides have been known to date, but none of them have a sufficient inhibitory effect on a wide range of molds, their efficacy does not last for a long time, and they are generally used in non-emulsifying types. The loss of effectiveness of this fungicide, dissolved in alcoholic solvents and in liquid form or sprayed using a propellant, is particularly noticeable in humid areas, such as bathrooms,
It is extremely difficult and rare to prevent mold from growing in areas that are likely to get wet, such as kitchens, over a long period of time.

又、アルコール系溶剤における低温時の安定性は防かび
効果を充分に発揮させるためにも不可欠の要件でめった
In addition, stability at low temperatures in alcoholic solvents is an essential requirement in order to fully exhibit the antifungal effect.

本発明者らは、このような従来の防かび剤の欠点を克服
し、生活環境下において発生する多種多様のかびに対し
て完全な発育抑制作用を示し、且つ、水に濡れやすい場
所においても長期間にわたり、その効果を持続しうるよ
う非水溶性高分子化合物を含有する防かび剤組成物を開
発したが、これらはアルコール系溶剤で用いる場合液体
の低温における保存安定性が悪いことが判明した。
The present inventors have overcome the shortcomings of conventional fungicides, have completely suppressed the growth of a wide variety of molds that occur in the living environment, and have long-lasting effects even in wet areas. We developed a fungicide composition containing a water-insoluble polymer compound to maintain its effectiveness over a period of time, but it was found that these had poor storage stability at low temperatures when used in alcohol-based solvents. .

そこで本発明者らは、かびに対して完全な発育抑制作用
を示し、且つ、水に濡れやすい場所においても長期間に
わたりその効果を持続し、さらに液安定性の優れた組成
物を得るために鋭意研究を重ねた結果、本発明をなすに
至ったO すなわち、本発明は非水溶性高分子化合物を含有する溶
媒中に、2−(4−チアゾリル)−ベンズイミダゾール
及び長鎖アルキルジメチルベンジルアンモニウム塩及び
N“−長鎖アシル塩基性アミノ酸の低級アルキルエステ
ル塩をそれぞれ少なくとも0,01重量%の濃度で含有
させてなる防かび剤組成物を提供するものである。
Therefore, the present inventors aimed to obtain a composition that exhibits a complete growth-inhibiting effect against mold, maintains its effect for a long period of time even in locations that are easily wetted with water, and has excellent liquid stability. As a result of extensive research, the present invention has been completed. That is, the present invention is based on the present invention, in which 2-(4-thiazolyl)-benzimidazole and long-chain alkyldimethylbenzylammonium are added to a solvent containing a water-insoluble polymer compound. The present invention provides a fungicidal composition comprising a salt and a lower alkyl ester salt of an N"-long chain acyl basic amino acid at a concentration of at least 0.01% by weight, respectively.

本発明組成物の一方の活性成分として用いられル2−(
4−−1F−アゾリル)−ベンズイミダゾールで表わさ
れる化合物で、多くのかびに対して生育阻止効果を示す
ことが知られているが、単独では家庭環境に発生するか
びを完全に抑制するのに十分な抗かび力を示さない。
Lu2-(
A compound represented by 4--1F-azolyl)-benzimidazole, which is known to exhibit a growth-inhibiting effect on many molds, but alone is not sufficient to completely suppress mold that grows in the home environment. Does not show strong anti-fungal properties.

もう一方の活性成分として用いられる長鎖アルキルジメ
チルベンジルアンモニウム塩は、一般式(式中)几は炭
素数8〜22のアルキル基、Xはハロゲン原子である) で表わされる化合物で、抗菌性、抗かび性を有すること
は知られているが、単独では家庭環境に発生する多種類
のかび全てに対しては、十分な防かび効果を示さない。
The long-chain alkyldimethylbenzyl ammonium salt used as the other active ingredient is a compound represented by the general formula (where 几 is an alkyl group having 8 to 22 carbon atoms, and X is a halogen atom), and has antibacterial properties. Although it is known to have anti-fungal properties, it does not show sufficient anti-fungal effects against all the various types of mold that occur in the home environment when used alone.

本発明においては、このようにそれぞれ単独では、家庭
用防かび剤として満足すべき効果を発揮できない、2−
(4−チアゾリル)−ベンズイミダシールド長鎖アルキ
ルジメチルベンジルアンモニウム塩及びN″−長鎖アシ
ル塩基性アミノ畝の低級アルキルエステル塩とを組み合
わせて使用することにより、個々のかびに対して抗かび
力を相乗的に高め、かつ抗かびスペクトルを拡大し、家
庭環境に発生する多種多様のかびのいずれに対してもす
ぐれた効果を示し、更に液安定性に優れた防かび剤を得
ることに成功したのである。
In the present invention, as described above, each of these alone cannot exhibit a satisfactory effect as a household fungicide.
(4-Thiazolyl)-Benzimidashield long-chain alkyldimethylbenzyl ammonium salt and N''-long chain acyl basic amino ridge lower alkyl ester salt are used in combination to provide anti-fungal properties against individual molds. We have succeeded in obtaining a fungicide that synergistically enhances the anti-fungal properties, expands the anti-fungal spectrum, shows excellent effects against a wide variety of molds that occur in the home environment, and has excellent liquid stability. That's what I did.

本発明において用いる長鎖アルキルジメチルベンジルア
ンモニウム塩は、単独で用いてもよいし、−1c2種以
上混合して用いてもよい。特に好適なのは塩化ベンザル
コニウムである。
The long-chain alkyldimethylbenzylammonium salts used in the present invention may be used alone or in combination of two or more -1c. Particularly preferred is benzalkonium chloride.

この2−(4−チアゾリル)−ベンズイミダゾ−#と&
fiフルキルジメチルベンジルアンモニウム塩の配合比
は、好ましくは重量比で9;1ないし1:9、特に好ま
しくは4:1ないし1:4の割合で使用される。また、
これら各成分の使用量は、全組成物に基づきそれぞれ少
なくとも0.01重量%とすることが必要である。これ
よシも少ない世では、十分な防かび効果が得られない。
This 2-(4-thiazolyl)-benzimidazo-# and &
The blending ratio of the fi-furkyldimethylbenzyl ammonium salt is preferably 9:1 to 1:9, particularly preferably 4:1 to 1:4 by weight. Also,
The amount of each of these components used should be at least 0.01% by weight, based on the total composition. In a world where there are so few insects, sufficient antifungal effects cannot be obtained.

次に非水溶性高分子化合物としては、例えばポリ酢酸ビ
ニル、部分けん化ポリ酢酸ビニル、ホルマール化ポリビ
ニルアルコール、ホルマール化部分けん化ポリ酢酸ビニ
ル、ブチラール化ポリビニルアルコール、ブチラール化
部分けん化ポリ酢酸ビニル、エチレン−酢酸ビニル共重
合体のけん化物、酢酸ビニル−アクリルアミド共重合体
、酢酸ビニル−メチルビニルエーテル共重合体、塩化ビ
ニル−酢酸ビニル共重合体のけん化物などを用いること
ができるが、好ましいのは酢酸ビニルの単独重合体、共
重合体、それらのけん化物及びそのアセタール化物であ
る。また、目的とする組成物を均一溶液にするために使
用される溶剤との関係から、アルコール町溶性のものが
有利である。本発明においては、この高分子化合物は、
濃度0.01重量%以上好ましくは0.1重量%以上の
溶液として用いられる。
Next, water-insoluble polymer compounds include, for example, polyvinyl acetate, partially saponified polyvinyl acetate, formalized polyvinyl alcohol, formalized partially saponified polyvinyl acetate, butyralized polyvinyl alcohol, butyralized partially saponified polyvinyl acetate, ethylene- Saponified products of vinyl acetate copolymer, vinyl acetate-acrylamide copolymer, vinyl acetate-methyl vinyl ether copolymer, saponified product of vinyl chloride-vinyl acetate copolymer, etc. can be used, but vinyl acetate is preferred. homopolymers, copolymers, their saponified products, and their acetalized products. In addition, in view of the relationship with the solvent used to make the target composition into a homogeneous solution, alcohol-soluble ones are advantageous. In the present invention, this polymer compound is
It is used as a solution with a concentration of 0.01% by weight or more, preferably 0.1% by weight or more.

この胃分子化合物の溶液を調製するための溶媒は、有機
溶媒系、有機溶媒と水との混合系のいずれでもよい。こ
の有機溶媒としては、メタノール。
The solvent for preparing this gastric molecular compound solution may be an organic solvent or a mixture of an organic solvent and water. This organic solvent is methanol.

エタノール、プロパツール、イソプロパツールのような
低級アルコール類、エチレングリコール。
Lower alcohols such as ethanol, propatool, isopropanol, and ethylene glycol.

プロピレングリコールのような低級ジオール類。Lower diols such as propylene glycol.

アセトン、メチルエチルケトンのような低級ケトン類が
適当である。安全性及び乾燥性の点で特に好適なのは、
エタノール、プロパツール又はイソプロパツールであり
、これらは必要に応じて水と併用される。
Lower ketones such as acetone and methyl ethyl ketone are suitable. Particularly suitable in terms of safety and dryness are:
Ethanol, propatool or isopropatool, which are optionally used in combination with water.

さらに非水溶性高分子化合物の溶液に安定に防かび基材
を保持するために必要なNa−長鎖アシル塩基性アミノ
酸の低級アルキルエステル下記一般式2)は、長鎖アシ
ル基がラウロイル、ココイル。
Furthermore, the lower alkyl ester of Na-long chain acyl basic amino acid required to stably hold the fungicidal base material in a solution of a water-insoluble polymer compound has the following general formula 2), in which the long chain acyl group is lauroyl, cocoyl, etc. .

又はミリストイル基であり、特に好ましくはココイル基
である0 塩基性アミノ酸成分が、アルギニン又はリジンで特に好
ましいのはアルギニンである。
or a myristoyl group, particularly preferably a cocoyl group. The basic amino acid component is arginine or lysine, particularly preferably arginine.

本発明において配合量は0.01重量%以上、好ましく
は0.02重量%以上の溶液として用いられる。
In the present invention, the compounding amount is 0.01% by weight or more, preferably 0.02% by weight or more.

一般式・2) I RCO−は脂肪酸残基(C8+ 10+ 12y ta
l 16 )本発明の組成物を調製するには、適当な溶
媒に所定の高分子化合物を溶解し、さらに所定量の2−
(4−チアゾリル)−ベンズイミダゾールと長鎖アルキ
ルジメチルベンジルア7そニウム塩とを加え、均−力溶
液とする。
General formula 2) I RCO- is a fatty acid residue (C8+ 10+ 12y ta
l 16 ) To prepare the composition of the present invention, a given polymer compound is dissolved in a suitable solvent, and a given amount of 2-
Add (4-thiazolyl)-benzimidazole and long-chain alkyldimethylbenzyl-7sonium salt to form a homogeneous solution.

この際の高分子化合物と2種の活性成分及びN” −長
鎖アクル塩基性アミノ酸の低級アルキルエステルの添加
順序には、特に制限はなく、任意の順序で加えてもよい
しまた同時に加えることもできる。
In this case, there is no particular restriction on the order of addition of the polymer compound, the two active ingredients, and the lower alkyl ester of N''-long-chain acrylic basic amino acid, and they may be added in any order or at the same time. You can also do it.

本発明組成物は、液安定性が良好である為、塗布用、吹
き付は用、流展用など任意の使用形態に調製することが
できる。本発明組成物を所要の場所に施すと、乾燥後、
2種の活性成分が高分子化合物により固定された状態に
なる。そして、この高分子化合物は非水溶性であるため
、水に濡れても活性成分が除かれることはなく、長期間
にわたって強力な防かび効果を持続することができる。
Since the composition of the present invention has good liquid stability, it can be prepared in any form of use such as application, spraying, or spreading. When the composition of the present invention is applied to the desired location, after drying,
The two active ingredients are immobilized by the polymer compound. Since this polymer compound is water-insoluble, the active ingredient will not be removed even if it gets wet with water, and its strong antifungal effect can be maintained for a long period of time.

このように本発明の組成物は、2−(4−チアゾリル)
−ベンズイミダゾールと長鎖アルキルジメチルベンジル
アンモニウム塩及ヒN“−長鎖7 シル塩基性アミノ酸
の低級アルキルエステル塩とを併用したことによシ、使
用時の液安定性に優れ、かつ、低濃度で広い抗かびスペ
クトルを示し、かつ多種多様のかびに対して相乗的な生
育抑制効果を示す上に非水溶性高分子化合物により活性
成分の溶出が抑制されるので、家庭用特に湿気のある場
所に適用する防かび剤として好適である。
Thus, the composition of the present invention comprises 2-(4-thiazolyl)
- By using benzimidazole in combination with a long-chain alkyldimethylbenzyl ammonium salt and a lower alkyl ester salt of a long-chain 7-syl basic amino acid, it has excellent liquid stability during use and has a low concentration. It has a broad anti-fungal spectrum and has a synergistic growth-inhibiting effect against a wide variety of molds.The water-insoluble polymer compound suppresses the elution of active ingredients, making it suitable for household use, especially in humid areas. It is suitable as a fungicide to be applied.

次に実施例によυ本発明をさらに詳細に説明する。Next, the present invention will be explained in more detail with reference to Examples.

実施例1 2−(4−チアゾリル)−ベンズイミダゾール(以下T
BZと略記する)と塩化ベンザルコニウム(以下AMB
と略記する)及びNa−長鎖アシル塩基性アミノ酸の低
級アルキルエステル塩のそ、ILぞれ単独及び併用混合
物をエタノールに溶解し、JI8−Z−2911rかび
抵抗性試験法、7.塗料の試験」の項に率じて抗かび性
試験を行なった0すなわち、各試料のエタノール溶液に
濾紙(東洋濾紙、NO2,直径30燗)を浸して引き上
げ、室内に2時間放置したのち、ペトリざらに入れた所
定の培養基の培養部中央に配置し、試験用かび胞子懸濁
g、l ccをその上に均一に散布し、次いでペトリざ
らにふたをして、温度28℃において14日間培養した
。この際の培養基としては、水IQQQm、ブドウ糖4
09、ペプトン11及び寒天25りの組成のものを用い
た。
Example 1 2-(4-thiazolyl)-benzimidazole (hereinafter referred to as T
(abbreviated as BZ) and benzalkonium chloride (hereinafter referred to as AMB)
(abbreviated as ) and lower alkyl ester salt of Na-long chain acyl basic amino acid, IL alone or in combination were dissolved in ethanol and tested according to JI8-Z-2911r mold resistance test method, 7. An anti-mold test was carried out under the heading ``Testing of paint''. In other words, a filter paper (Toyo Roshi, NO2, 30 liters in diameter) was soaked in the ethanol solution of each sample, pulled out, and left indoors for 2 hours. Place the specified culture medium in a Petri colander at the center of the culture area, sprinkle the test mold spore suspension g, l cc evenly thereon, then cover the Petri colander for 14 days at a temperature of 28°C. Cultured. The culture medium at this time is water IQQQm, glucose 4
09, peptone 11 and agar 25.

また、試験用かびとしては、以下に示すものを用いた。In addition, the molds shown below were used as test molds.

液体安定性は100−ガラスびんに入れ、−5”Cに保
存した後、所定の経時後目視による評価を行なったO 評価基準 O・・・・・・異常は認められない △・・・・・・極くわずかに不溶物あυ×・・・・・・
明らかに白濁もしくは不溶物を認めるこの結果を第1表
に示す。
Liquid stability was determined by putting it in a 100-glass bottle and storing it at -5"C, and then visually evaluating it after a predetermined period of time. O Evaluation criteria: O: No abnormalities observed △...・・Very slight insoluble matter Aυ×・・・・・・
The results, in which cloudiness or insoluble matter was clearly observed, are shown in Table 1.

表中の各記号は以下の意味をもつ。Each symbol in the table has the following meaning.

−:カどの発生は認められない + :カどの発生が若干認められる +十二カどの発生が著しく認められる 実施例2 x タ/ −ル中K TBZ O,2%、 AfvlB
 0.1% 及ヒN”−ココイル−L−アルギニンエチ
ルエステルD・Lピロリドンカルボン酸塩0,2%溶解
させたもの、およびTBZ 0.2 % 、 AMB 
O,1% 、 N”−ココイル−L−アルギニンエチル
エステルD−Lピロリドンカルボン酸塩0.2 ・%に
PVB (ブチラール化ポリビニルアルコール)1.0
%を加え溶解させたものに、さらに噴射剤フロン12を
259/100−の割合で加えてエアロゾルタイプの防
かび剤を調製した。この防かび剤を家庭内のかびが発生
しやすい場所にスプレーし、6ケ月間のかびの発生状況
を調べた。
−: No occurrence of mold is observed +: Slight occurrence of mold + Significant occurrence of mold is observed Example 2
0.1% and N''-cocoyl-L-arginine ethyl ester D.L pyrrolidone carboxylate 0.2% dissolved, and TBZ 0.2%, AMB
O, 1%, N”-cocoyl-L-arginine ethyl ester DL pyrrolidone carboxylate 0.2% to PVB (butyralized polyvinyl alcohol) 1.0
% was added and dissolved, and the propellant Freon 12 was further added in a ratio of 259/100 to prepare an aerosol type fungicide. This fungicide was sprayed on areas in the home where mold is likely to grow, and the mold growth status was investigated over a period of 6 months.

又、同時に内容液の液体安定性についても100f、/
ガラスびんに入れ、−5℃に保存し目視による評価を行
なったが経日30日後においても異常は認められなかっ
た。
At the same time, the stability of the liquid content is also 100f, /
It was placed in a glass bottle, stored at -5°C, and visually evaluated, but no abnormality was observed even after 30 days.

この結果は第2光に示す。This result is shown in the second light.

、手 続 補 正 書(方式) 昭和58年9月24日 特許庁長官若杉和夫殿 1、事件の表示  昭和58年特許願第85789号2
、発明の名称  防かび剤組成物 3、 1ffi正をする者 事件との関係 特許出願人 東京都墨田区本所−丁目3番7号 4、補正命令の日付  昭和58年8月10日(発送日
 昭和58年8月30日) 5、補正の対象 明細書全文の浄書(内容に変更なし) 6、補正の内容 別紙の通り
, Procedural amendment (method) September 24, 1980 Kazuo Wakasugi, Commissioner of the Patent Office 1, Indication of case Patent Application No. 85789, 1982 2
, Title of the invention: Fungicidal composition 3, Relationship to the 1ffi case Patent applicant: Honjo-chome-3-7-4, Sumida-ku, Tokyo Date of amendment order: August 10, 1982 (shipped) (August 30, 1982) 5. Engraving of the entire text of the specification subject to amendment (no change in content) 6. Contents of amendment as attached.

Claims (1)

【特許請求の範囲】 1、非水溶性高分子化合物を含有する溶媒中に、2−(
4−チアゾリル)−ベンズイミダゾール及び長鎖アルキ
ルジメチルベンジルアンモニウム塩及びN”−長鎖アシ
ル塩基性アミノ酸の低級アルキルエステル塩をそれぞれ
少なくとも0.01重量慢の濃度で含有させてなる防か
び剤組成物02、非水溶性高分子化合物が、ポリビニル
アルコールの誘導体である特許請求の範囲第1項記載の
組成物0 3、  N”−長鎖アシル塩基性アミノ酸の低級アルキ
ルエステル塩の長鎖アシル部分がラウロイル基又はココ
イル基、又はミリストイル基で、1、塩基性アミノ酸部
分がアルギニン又はリジンである特許請求の範囲第1項
記載の組成物O
[Claims] 1. In a solvent containing a water-insoluble polymer compound, 2-(
A fungicidal composition comprising 4-thiazolyl)-benzimidazole and a long-chain alkyldimethylbenzylammonium salt and a lower alkyl ester salt of an N''-long-chain acyl basic amino acid, each at a concentration of at least 0.01% by weight. 02. The composition according to claim 1, wherein the water-insoluble polymer compound is a polyvinyl alcohol derivative. 3. The long-chain acyl moiety of the lower alkyl ester salt of a N''-long-chain acyl basic amino acid is Composition O according to claim 1, wherein the basic amino acid moiety is arginine or lysine in the lauroyl group, cocoyl group, or myristoyl group.
JP8578983A 1983-05-18 1983-05-18 Antimildew composition Granted JPS59212405A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8578983A JPS59212405A (en) 1983-05-18 1983-05-18 Antimildew composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8578983A JPS59212405A (en) 1983-05-18 1983-05-18 Antimildew composition

Publications (2)

Publication Number Publication Date
JPS59212405A true JPS59212405A (en) 1984-12-01
JPH0358324B2 JPH0358324B2 (en) 1991-09-05

Family

ID=13868651

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8578983A Granted JPS59212405A (en) 1983-05-18 1983-05-18 Antimildew composition

Country Status (1)

Country Link
JP (1) JPS59212405A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS624202A (en) * 1985-06-28 1987-01-10 Lion Corp Mildew proofing agent composition
US4859689A (en) * 1986-10-31 1989-08-22 Safer, Inc. Synergistic fungicidal composition comprise a benzimidazole compound, an alkyl pyridinium salt, and a carrier and the use thereof to combat fungi
WO2005072712A3 (en) * 2003-12-16 2005-09-09 Eastman Kodak Co Antimicrobial composition
JP2009531458A (en) * 2006-03-27 2009-09-03 エシコン・インコーポレイテッド Antibacterial composition

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2023149175A (en) 2022-03-30 2023-10-13 ウシオ電機株式会社 light source device
JP2023148403A (en) 2022-03-30 2023-10-13 ウシオ電機株式会社 light source device
JP2023149176A (en) 2022-03-30 2023-10-13 ウシオ電機株式会社 light source device

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS624202A (en) * 1985-06-28 1987-01-10 Lion Corp Mildew proofing agent composition
US4859689A (en) * 1986-10-31 1989-08-22 Safer, Inc. Synergistic fungicidal composition comprise a benzimidazole compound, an alkyl pyridinium salt, and a carrier and the use thereof to combat fungi
WO2005072712A3 (en) * 2003-12-16 2005-09-09 Eastman Kodak Co Antimicrobial composition
US7306777B2 (en) 2003-12-16 2007-12-11 Eastman Kodak Company Antimicrobial composition
JP2009531458A (en) * 2006-03-27 2009-09-03 エシコン・インコーポレイテッド Antibacterial composition
US8604073B2 (en) 2006-03-27 2013-12-10 Ethicon, Inc. Antimicrobial composition

Also Published As

Publication number Publication date
JPH0358324B2 (en) 1991-09-05

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