JPS6058202B2 - Non-medical sterilizing composition - Google Patents

Non-medical sterilizing composition

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Publication number
JPS6058202B2
JPS6058202B2 JP12463479A JP12463479A JPS6058202B2 JP S6058202 B2 JPS6058202 B2 JP S6058202B2 JP 12463479 A JP12463479 A JP 12463479A JP 12463479 A JP12463479 A JP 12463479A JP S6058202 B2 JPS6058202 B2 JP S6058202B2
Authority
JP
Japan
Prior art keywords
salts
bacteria
medical sterilizing
sterilizing composition
parts
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
Application number
JP12463479A
Other languages
Japanese (ja)
Other versions
JPS5646801A (en
Inventor
健一 細井
芳広 小永井
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.)
Kumiai Chemical Industry Co Ltd
Original Assignee
Kumiai Chemical Industry Co Ltd
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 Kumiai Chemical Industry Co Ltd filed Critical Kumiai Chemical Industry Co Ltd
Priority to JP12463479A priority Critical patent/JPS6058202B2/en
Publication of JPS5646801A publication Critical patent/JPS5646801A/en
Publication of JPS6058202B2 publication Critical patent/JPS6058202B2/en
Expired legal-status Critical Current

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  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

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
は我々の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 our daily life, or non-medical products that control 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
生物の防除用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、有機錫剤が汎用されていた。しカ
ルながら、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が懸念
されるに至つた。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が
多発しているが、これらに対してこれらの薬剤では効果
が充分でなく、新しい薬剤の開発が強く要望されている
。 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殺菌剤を開発するため鋭意研
究を重ねた結果、既知の殺菌剤を混合して使用すること
によりこの目的に適合することを見出した。
Conventionally, non-medical sterilizing compositions for controlling microorganisms generated in industrial products or the process of manufacturing them include:
Mainly, organic solvents and organic tin agents were commonly used. However, concerns have arisen regarding the residual toxicity and stability of non-medical sterilizing compositions containing organometallic compounds as active ingredients 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 drugs are not sufficiently effective against these, and there is a strong demand for the development of new drugs. In view of this demand, the present inventors have conducted intensive research to develop a disinfectant that is active against many bacteria and molds at low dosages, and have found that by using a mixture of known disinfectants, We have found that it is suitable for this purpose.

本発明は、この知見に基づいてなされたものであり、
従来知られているそれぞれの薬剤を単独に用いる場合に
比べ予想し得ない卓越した活性を示すものである。
The present invention was made based on this knowledge,
It shows unexpected and excellent activity compared to when each of the conventionally known drugs is used alone.

テトラクロルイソフタロニトリル(以下πNと称する
Tetrachloroisophthalonitrile (hereinafter referred to as πN).

)は近年農業用殺菌剤として開発されたものであり(特
公昭41−11358号)、毒性がほとんどなく安全な
薬剤として高い評価を受けている。しかし、TPNは治
療的効果、すなわち、既に生育しかかつた菌に対しては
ほとんど活性を示さないものである。また、トリハロゲ
ン化フェノール系化合物として、2・4・6−トリクロ
ルフェノール(以下2 ・ 4 ・ 6−TCPと称す
る。)、2・4・5−トリクロルフェノール(以下2・
4・ 5−TCPと称する。)、2・4・6−トリブロ
ムフェノール(以下2 ・ 4.6−TBPと称する。
)、2●5ージクロルー4−ブロムフェノール(以下2
・5・4−DCBと称する。)、2・5ージクロルー6
−ブロムフェノール(以下2●5●6一DCBと称する
。)及びこれらの塩類が知られているが、これらの化合
物は農業用土壌処理剤又は産業用防黴剤として使用され
たものである。しかし、このトリハロゲン化フェノール
及びこれらの塩類は揮発性が著しく高く、予防的効果が
劣り薬効の持続力の面で不満足な薬剤である。更に、オ
ルソフェニルフェノール(以下0PPと称する。)又は
その塩類は安全性が高く食品添加剤としても使用が認ら
れる柑橘類の保存剤として知られており、各種の黴に対
して全般的に活性を示すが、その効力は緩慢で産業用殺
菌剤としては劣り、実用化されていない。しかるに、本
発明の非医療用殺菌組成物はTPN又はトリハロゲン化
フェノール系化合物あるいはその塩類と0PPあるいは
その塩類とを有効成分として含有してなる。
) was recently developed as an agricultural fungicide (Japanese Patent Publication No. 11358/1973), and has received high praise as a safe drug with almost no toxicity. However, TPN shows little therapeutic effect, ie, activity against already grown bacteria. In addition, as trihalogenated phenol compounds, 2,4,6-trichlorophenol (hereinafter referred to as 2,4,6-TCP), 2,4,5-trichlorophenol (hereinafter referred to as 2,4,6-TCP),
It is called 4.5-TCP. ), 2,4,6-tribromophenol (hereinafter referred to as 2,4,6-TBP).
), 2●5-dichloro-4-bromophenol (hereinafter 2
・It is called 5.4-DCB. ), 2.5-dichlororu6
- Bromophenol (hereinafter referred to as 2●5●6-DCB) and salts thereof are known, and these compounds have been used as agricultural soil treatment agents or industrial fungicides. However, these trihalogenated phenols and their salts have extremely high volatility, have poor preventive effects, and are unsatisfactory in terms of the durability of their medicinal efficacy. Furthermore, orthophenylphenol (hereinafter referred to as 0PP) or its salts is known as a highly safe preservative for citrus fruits that can be used as a food additive, and is generally active against various molds. However, its efficacy is slow and it is inferior to an industrial disinfectant, so it has not been put to practical use. However, the non-medical sterilizing composition of the present invention contains TPN or a trihalogenated phenolic compound or a salt thereof and OPP or a salt thereof as active ingredients.

すなわち、本発明はTPNまたは一般式 (但し、式中、Mは水素原子、アルカリ金属原子又はア
ルカリ土類金属原子を示し、Xはハロゲン原子を示す。
That is, the present invention relates to TPN or the general formula (wherein M represents a hydrogen atom, an alkali metal atom, or an alkaline earth metal atom, and X represents a halogen atom).

)にて示されるトリハロゲン化フェノールの1種以上と
0PPあるいはそのアルカリ金属又はアルカリ土類金属
塩類とを有効成分として含有し、適当な担体に分散又は
溶解させるか、又は適当な固体担体と混合し、要すれは
更に、これらに分散剤、懸濁向上剤、展着剤、浸透剤、
湿潤剤、安定剤等を添加し、水和剤、粉剤、錠剤、ペー
スト剤、乳剤、液剤等の剤型としてなる。本発明の非医
療用殺菌組成物は使用目的によよつて一直接適用するか
、または適当な濃度に希釈して使用する。また、本発明
の非医療用殺菌組成物には他の殺菌剤、殺虫剤、劣化防
止剤等を配合して使用することも出来る。本発明で使用
するトリハロゲン化フェノールとしては前述の2・4・
6−・TCPl2●4・5−TCPl2●4●6−TB
Pl2・4・5−TBPl2・5・4−DCBl2・5
●6−DCB及びこれらのナトリウム塩、カリウム塩、
カルシウム塩等のアルカリ金属塩又はアルカリ土類金属
塩がある。本発明の非医療用殺菌組成物中の有効成分T
PN又はトリハロゲン化フェノールあるいはその塩類と
0PPあるいはその塩類の混合比率は目的により多少異
なるが、通常TPN.(50PP類の混合の場合、重量
比で、1:0.1〜10、好ましくは1:0.5〜3で
あり、トリハロゲン化フェノールあるいはその塩類と0
PP類との混合の場合、1:0.1〜5、好ましくは1
:0.2〜2である。
) and 0PP or its alkali metal or alkaline earth metal salts as active ingredients, and are dispersed or dissolved in an appropriate carrier, or mixed with an appropriate solid carrier. However, if necessary, in addition to these, dispersants, suspension improvers, spreading agents, penetrants,
By adding wetting agents, stabilizers, etc., it is made into dosage forms such as wettable powders, powders, tablets, pastes, emulsions, and liquids. The non-medical sterilizing composition of the present invention may be applied directly or diluted to an appropriate concentration depending on the purpose of use. Furthermore, the non-medical sterilizing composition of the present invention may be used by blending other sterilizing agents, insecticides, deterioration inhibitors, etc. The trihalogenated phenols used in the present invention include the above-mentioned 2.4.
6-・TCPl2●4・5-TCPl2●4●6-TB
Pl2・4・5-TBPl2・5・4-DCBl2・5
●6-DCB and their sodium salts, potassium salts,
There are alkali metal salts or alkaline earth metal salts such as calcium salts. Active ingredient T in the non-medical sterilizing composition of the present invention
The mixing ratio of PN or trihalogenated phenol or its salts and 0PP or its salts varies depending on the purpose, but is usually TPN. (In the case of mixing 50PPs, the weight ratio is 1:0.1 to 10, preferably 1:0.5 to 3, and the weight ratio is 1:0.1 to 10, preferably 1:0.5 to 3.
When mixed with PP, 1:0.1-5, preferably 1
:0.2-2.

本発明の非医療用殺菌組成物は、塗料、木竹製品、皮革
、糊料、紙製品、織物類、壁材料、塩化ビニル製品等に
混入し又は表面処理することにより有害微生物の生育を
阻止し、品質劣化を防止するために用いられる。また、
これらの製品を製造する工程中の微生物汚染の防止のた
めにも使用することができる。本発明の非医療用殺菌組
成物は前述の如き欠点を有しており単剤としては実用上
問題があつた薬剤をある配合率で混合することによりそ
れぞれの殺菌効果を単に加算して対象徴生物の種類を拡
張すると止まらす相乗的効果により微生物災害の起因菌
であり、従来防除が困難であつた各種黴、細菌を低薬量
にて防除でき、単用の113乃至115以下にて防除す
ることができるものである。更に、特記すべきことは産
業用製品の微生物災害起因菌であるトリコデルマ属、ア
スペルギルス属、クラドスポリウム属の黴類、シュード
モナス属、アエロバクター属の細菌類に対しても著しく
低濃度で活性を示し、経済的にも安価に防除することも
可能となる点である。次に、試験例及び実施例を挙げて
本発明を更に詳しく説明するが、これらによつて本発明
の範囲を何ら限定するものではない。
The non-medical sterilizing composition of the present invention inhibits the growth of harmful microorganisms by mixing or surface-treating paints, wood and bamboo products, leather, pastes, paper products, textiles, wall materials, vinyl chloride products, etc. and is used to prevent quality deterioration. Also,
It can also be used to prevent microbial contamination during the manufacturing process of these products. The non-medical sterilizing composition of the present invention has the above-mentioned drawbacks, and by mixing the drugs at a certain blending ratio, the sterilizing effects of each drug can be simply added up. Due to the synergistic effect of increasing the number of types of organisms, various molds and bacteria that cause microbial disasters and which were difficult to control in the past can be controlled with a low dosage. It is something that can be done. Furthermore, it should be noted that it is active at extremely low concentrations against molds of the genus Trichoderma, genus Aspergillus, and genus Cladosporium, as well as bacteria of the genus Pseudomonas and Aerobacter, which are bacteria that cause microbial hazards in industrial products. This means that it can be controlled economically and at low cost. Next, the present invention will be explained in more detail with reference to test examples and examples, but the scope of the present invention is not limited by these in any way.

尚試験に用いた単剤TPN..OPPl2●4●6−T
CPl2●5●4−DCBl2・5・6−DCB,.C
PP−Ca塩は5%乳剤に製剤し、他は10%液剤に製
剤して使用した。実験例1 (寒天希釈法による最低生育阻止濃度試験)各薬剤をそ
れぞれ滅菌水で有効成分濃度6.25、12.\2\5
0、75、100ppmに希釈し、9C77!のペトリ
皿2枚に2cm宛分注する。
The single agent TPN used in the test. .. OPPl2●4●6-T
CPl2●5●4-DCBl2・5・6-DCB,. C
The PP-Ca salt was formulated into a 5% emulsion, and the others were formulated into a 10% solution. Experimental Example 1 (Minimum inhibitory concentration test using agar dilution method) Each drug was mixed with sterile water at an active ingredient concentration of 6.25, 12. \2\5
Diluted to 0, 75, 100 ppm, 9C77! Dispense 2 cm into two Petri dishes.

一方のペトリ皿には、酸性ワックスマン培地を他方のペ
トリ皿には、変法ワックスマン倍地をそれぞれ18m1
加温溶解して加え、よく薬剤希釈液と混和せしめ固化平
板とする。糸状菌は、予め増殖せしめた菌叢寒天を径8
TWLのゴルクボーラーで打抜いたものを酸性ワックス
マン培地にのせ、細菌は、斜面よソー白金耳をとり変性
ワックスマン培地上に画線し接種.した。28℃、48
I寺間培養後の菌の生育の有無を観察し、最低生育阻止
濃度を求めた。
One Petri dish contained 18 ml of acidic Waxmann's medium and the other Petri dish contained 18 ml of modified Waxmann's medium.
Dissolve and add by heating, mix thoroughly with drug dilution solution, and form a solidified plate. For filamentous fungi, pre-grown bacterial flora agar was prepared using
Place the punched pieces with a TWL Gork borer on acidic Waxman medium, and inoculate the bacteria by taking a platinum loop on the slant and streaking it onto the modified Waxman medium. did. 28℃, 48
After I Terama culture, the presence or absence of bacterial growth was observed, and the minimum growth-inhibiting concentration was determined.

(1)酸性ワックスマン培地組成 ペプトン 5Vグルコース
10y1KH2P041′Mg
SO4O.59 粉末寒天 15y水
1e使用直前に25%乳酸
でPH4.5に調整する。
(1) Acidic Waxman medium composition Peptone 5V glucose
10y1KH2P041'Mg
SO4O. 59 Powdered agar 15y water
1e Just before use, adjust the pH to 4.5 with 25% lactic acid.

1(2)変性ワックスマン培地組成ペプトン
10yグルコース
5yKH2P041yMgS040.5y2 粉末寒天 12f水
1e滅菌前にPH7.5に
1110NNa0Hで調整す3。
1 (2) Modified Waxman medium composition peptone
10y glucose
5yKH2P041yMgS040.5y2 Powder agar 12f water
1e Adjust the pH to 7.5 with 1110NNaOH before sterilization3.

供試菌 0アエロバクター・アエロゲネスIAM一1102(A
erObacteraerOgenes)()バチリス
・ズブチリスIAM−1069(Bacillussl
lbtilis)C) エスシリチア コリーNIHJ (EscherichiacOll) ))シュードモナス●エルギノサIAM−1054(P
aeudOmOnasaeruginOsa)ミ)アス
ペルギルス●ニガーATCC−6275(Asper?
11usni?r)・゛)ペニシリウム●シトリニウム
ATCC−9849(Penicilllurrlci
trinum);) リゾープス・ニグリンカスIAM
−6070(RhizOpusnigricansη
プルラリア・プルランスIAMF−24(Pullul
ariapullulans)1) トリコデルマT−
1ATCC−9645(TrichOderma)J)
ゲオトリクム アンデイデユム(GeOtrichum
lcandidum)試験例2(木材防黴試験)各薬剤
の希釈液に木片(赤松)を10分間浸漬し、軽く水切り
して2@間風乾した。
Test bacteria 0 Aerobacter aerogenes IAM-1102 (A
erObacteraerOgenes) () Bacillus subtilis IAM-1069 (Bacillus sl.
lbtilis)C) Escherichia coli NIHJ (EscherichiacOll))) Pseudomonas ●Aeruginosa IAM-1054(P
aeudOmOnasaeruginOsa) Mi) Aspergillus●niger ATCC-6275 (Asper?
11usni? r)・゛) Penicillium●Citrinium ATCC-9849
trinum) ;) Rhizopus nigrinchus IAM
-6070 (RhizOpusnigricansη
Pullularia pullulans IAMF-24 (Pullul
ariapullulans) 1) Trichoderma T-
1ATCC-9645(TrichOderma)J)
Geotrichum andeiduum
lcandidum) Test Example 2 (Wood Mildew Prevention Test) A piece of wood (red pine) was immersed in a diluted solution of each chemical for 10 minutes, lightly drained, and air-dried for 2 hours.

シヤーレに平面固化させた培地(組成グルコース40y
1ペプトン10y1寒天25y1水1e)上に薬剤で処
理した木片を置き、この木片上に下記の供試菌胞子混合
懸濁液を噴霧接種した。28゜C±2℃で培養しながら
経時的に木片上の黴の生育の状況を調査した。
Medium solidified on a plate (composition: glucose 40y)
A piece of wood treated with a chemical was placed on 1 peptone, 10 y, 1 agar, 25 y, and 1 e) of water, and the following sample bacterial spore mixed suspension was spray inoculated onto this wood piece. While culturing at 28°C±2°C, the growth of mold on the wood chips was examined over time.

黴の生育状況は繁殖程度により次の5段階に分けた。The growth status of mold was divided into the following five stages depending on the degree of reproduction.

−ニ黴の生育の全く認められない。-No growth of mold was observed.

±:木片の側面及び表面に僅かに認められる。±: Slightly observed on the side and surface of the wood piece.

+:黴の生育が木片の側面及び表面の3分の1以下+:
3分の1以上に生育する。
+: Mildew growth is less than one-third of the sides and surface of the wood piece +:
Grows to more than one-third.

+FF:全面に生育する。+FF: Grows on the entire surface.

尚、1薬剤につき3区の試験を行なつた。In addition, three groups of tests were conducted for each drug.

供試菌 (4)アスペルギルス●ニガーATCC−6275(B
)ペニシリウム・シトリニヌムATCC−9849(C
)リゾープス●ニグリンカスS.Nl32(D)クラド
スポリウム●ヘルバルムIAM.F−517(Clad
OspOriunlherbarum)(E)ケトミウ
ム・グロポスムATCC−6205(ChaetOmi
umglObOsunl)試験例3(水性塗料の防腐防
徽効力試験) アクリル樹脂50%含有エマルジョン27部(重量部以
下同様)、チタン白8部、カオリン23部、重質炭酸カ
ルシウム18部、カルボキシメチルセルロース(2%溶
液)加部及び水4部よりなるアクリル系エマルジョン塗
料98gを錫メッキ塗料用缶に入れ、所定の濃度になる
様に薬剤を加え卓上型攪拌機を用いて3分間混合した。
Test bacteria (4) Aspergillus niger ATCC-6275 (B
) Penicillium citrininum ATCC-9849 (C
) Rhizopus ● Nigrinchus S. Nl32(D) Cladosporium ● Herbalum IAM. F-517 (Clad
OspOriunlherbarum) (E) Chaetomium gloposum ATCC-6205 (ChaetOmi
umglObOsunl) Test Example 3 (Test of antiseptic efficacy of water-based paint) 27 parts of emulsion containing 50% acrylic resin (same parts by weight), 8 parts of titanium white, 23 parts of kaolin, 18 parts of heavy calcium carbonate, carboxymethyl cellulose (2 % solution) 98 g of an acrylic emulsion paint consisting of 1 part and 4 parts of water was placed in a can for tin-plated paint, and the chemicals were added to a predetermined concentration and mixed for 3 minutes using a tabletop stirrer.

次に、塗料の微生物災害起因細菌であるシュードモナス
・エルギノサIAM−1054、アエロバクター・アエ
ロゲネスIAM−1102及び糸状菌であアスペルギル
ス●フラバスATCC−9643(.Aspergil
lusflavus)、クラドスポリウム・ヘルバルム
IAM,.F5l7の混合懸濁液を1mtづつ塗料に加
え接種した。接種菌は細菌の場合、1m1中1×1Cf
′個に、糸状菌の場合、1×103個になる様に希釈し
、1m1宛加えた。接種菌の希釈は微生物の生育を促進
するためブイヨン液体培地を用いた。接種後は、缶を密
封し、28℃の恒温器中に保ち、防腐効力は接種10日
及び30日後の塗料1m1中の細菌又は糸状菌数を、ま
た防黴効力は10日及び30日後における菌数測定のた
めの缶開封時に塗料表面の黴の生育状態を確認し判定し
た。
Next, we investigated Pseudomonas aeruginosa IAM-1054, Aerobacter aerogenes IAM-1102, which are bacteria that cause microbial hazards in paint, and Aspergillus flavus ATCC-9643 (.Aspergil), which is a filamentous fungus.
lusflavus), Cladosporium herbalum IAM, . A mixed suspension of F5l7 was added to the paint in an amount of 1 mt for inoculation. In the case of bacteria, the inoculum is 1 x 1 Cf per 1 m1.
In the case of filamentous fungi, the solution was diluted to 1 x 103 cells and added to 1 ml. A broth liquid medium was used to dilute the inoculum to promote the growth of microorganisms. After inoculation, the can is sealed and kept in a constant temperature chamber at 28°C. The antiseptic efficacy is determined by the number of bacteria or filamentous fungi in 1 ml of paint 10 and 30 days after inoculation, and the antifungal efficacy is determined by the number of bacteria or fungi in 1 ml of paint after 10 and 30 days of inoculation. When the can was opened to measure the number of bacteria, the state of mold growth on the surface of the paint was checked and judged.

尚、薬剤の持続的効力を判定するため10日後の菌数測
定時に新たに初回と同様菌の接種を行なつた。結果を第
3表に示す。
In addition, in order to determine the sustained efficacy of the drug, when measuring the number of bacteria 10 days later, a new inoculation of bacteria was performed in the same manner as the first time. The results are shown in Table 3.

実施例中部とあるのは重量部を示す。"Example Middle" indicates parts by weight.

実施例1 乳剤 TPN5部 0PP5部 ソルポール (東邦化学工業株式会社製界面活性剤)7部キシレン
(4)部ハイゾール#
100(日本石油化学株式会社製芳香族溶剤)33部以
上を混合して乳剤とする。
Example 1 Emulsion TPN 5 parts 0 PP 5 parts Solpol (surfactant manufactured by Toho Chemical Industry Co., Ltd.) 7 parts xylene
(4) Part Hysol#
100 (aromatic solvent manufactured by Nippon Petrochemical Co., Ltd.) and 33 parts or more are mixed to form an emulsion.

実施例2 水和剤 TPN3娼 0PP5部 ネオペレックスPExample 2 hydrating agent TPN3 prostitute 0PP5 parts Neoperex P

Claims (1)

【特許請求の範囲】 1 テトラクロルイソフタロニトリル又はトリハロゲン
化フェノールあるいはその塩類及びオルソフェニルフェ
ノールある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 有効成分がテトラクロルイソフタロニトリルとオル
ソフェニル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 有効成分がトリハロゲン化フェノール又はその塩類
とオルソフェニル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 tetrachloroisophthalonitrile or trihalogenated phenol or its salts, and orthophenylphenol or its salts as active ingredients. 2. The non-medical sterilizing composition according to claim 1, wherein the active ingredients are tetrachloroisophthalonitrile and orthophenylphenol or salts thereof. 3. The non-medical sterilizing composition according to claim 1, wherein the active ingredients are trihalogenated phenol or its salts and orthophenylphenol or its salts.
JP12463479A 1979-09-27 1979-09-27 Non-medical sterilizing composition Expired JPS6058202B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12463479A JPS6058202B2 (en) 1979-09-27 1979-09-27 Non-medical sterilizing composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12463479A JPS6058202B2 (en) 1979-09-27 1979-09-27 Non-medical sterilizing composition

Publications (2)

Publication Number Publication Date
JPS5646801A JPS5646801A (en) 1981-04-28
JPS6058202B2 true JPS6058202B2 (en) 1985-12-19

Family

ID=14890262

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12463479A Expired JPS6058202B2 (en) 1979-09-27 1979-09-27 Non-medical sterilizing composition

Country Status (1)

Country Link
JP (1) JPS6058202B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5920202A (en) * 1982-07-23 1984-02-01 Minolta Camera Co Ltd Evaporating antifungal material
JP4805432B2 (en) * 1998-12-28 2011-11-02 ランクセス・ドイチュランド・ゲーエムベーハー Chemicals for admixing adhesives used in manufacturing wood materials or wood composite materials
DE10046265A1 (en) * 2000-09-19 2002-03-28 Bayer Ag Synergistic mixtures protecting animal hides or leather against microbial attack comprise phenols and fungicides such as mercaptobenzothiazole or chlorthalonil
BR112014011903A2 (en) * 2011-12-01 2017-05-16 Rohm & Haas composition, and method for controlling microorganisms in an aqueous or water-containing system

Also Published As

Publication number Publication date
JPS5646801A (en) 1981-04-28

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