JPH0753643B2 - Microbicidal composition - Google Patents
Microbicidal compositionInfo
- Publication number
- JPH0753643B2 JPH0753643B2 JP5268694A JP26869493A JPH0753643B2 JP H0753643 B2 JPH0753643 B2 JP H0753643B2 JP 5268694 A JP5268694 A JP 5268694A JP 26869493 A JP26869493 A JP 26869493A JP H0753643 B2 JPH0753643 B2 JP H0753643B2
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Description
【0001】[0001]
【発明の目的】本発明は、木材、皮革、繊維、建材等を
侵かす変色菌、腐朽菌及び/又はカビ制禦、防除のため
に使用される殺微生物組成物に関する。OBJECT OF THE INVENTION The present invention relates to a microbicidal composition used for controlling and controlling discoloring bacteria, decaying fungi and / or mold which invade wood, leather, fibers, building materials and the like.
【0002】微生物による汚染や被害は、医薬品、食
品、農業分野のみならず、木材、繊維、皮革、建材、ゴ
ム、塗料、プラスチック等の分野も含まれ、多岐にわた
っている。[0002] Pollution and damage caused by microorganisms are not limited to the fields of medicine, food and agriculture, but include fields of wood, fibers, leather, building materials, rubber, paints, plastics, etc.
【0003】木材、繊維、皮革、塗料、建材、ゴム等の
分野で、特に被害をおよぼす微生物類は、オオウズラタ
ケ、ワタグサレタケ、カワラタケ、ヒイロタケ、ナミダ
タケ等の腐朽菌や、オフイオストマ(Ophiostoma)属、エ
ンドコニディオホラ(Endoconidiophora)属の変色菌及び
ペニシリウム(Penicillium) 属、アスペルギルス(Asper
gillus) 属、リゾプス(Rhizopus)属、トリコデルマ(Tri
choderma) 属等のカビ類で、一般に他分野で問題とされ
る細菌やその他の微生物類に比べ薬剤感受性が低い。In the fields of wood, textiles, leather, paints, building materials, rubbers, etc., microorganisms that are particularly damaging are rot fungi such as Pleurotus ostreatus, Pleurotus cornucopiae, Pleurotus cornucopiae, Pleurotus cornucopiae, Pleurotus cornucopiae, genus Ophiostoma, Endoconis A discoloring bacterium of the genus Endoconidiophora and the genus Penicillium, Aspergillus
gillus, Rhizopus, Trichoderma
Fungi, such as the genus choderma), have lower drug sensitivity than bacteria and other microorganisms that are generally problematic in other fields.
【0004】従って、これ等の微生物からの被害を防ぐ
為には、強力な殺微生物剤を、比較的高濃度で使用しな
ければならない。又、長期間にわたって高い効果が持続
するものが要求されるので、有効成分は揮散や溶脱がな
く、且つ、水、熱、紫外線などにより分解されない耐候
性を有していることが必要である。Therefore, in order to prevent damage from these microorganisms, powerful microbicides must be used in relatively high concentrations. Further, since it is required to have a high effect for a long period of time, it is necessary that the active ingredient has neither weathering nor leaching, and has weather resistance which is not decomposed by water, heat, ultraviolet rays or the like.
【0005】又、これ等の性能の外、安全衛生上又は、
環境汚染防止上の配慮も重要である。In addition to these performances, for safety and hygiene,
Consideration for preventing environmental pollution is also important.
【0006】本発明者等は、殺微生物組成物について、
長年に亘って鋭意検討を行い、微生物の酵素蛋白に作用
してそれを変化させることにより、微生物を致死せしめ
る殺微生物剤として知られている化合物(A群の化合
物)に、それ自体殺微生物力を殆ど有しないジオクチル
スルホコハク酸ナトリウム(B)を配合したことによ
り、協力作用により効力が増強され、殺微生物剤の処理
する成分量を減らすことができ、経済性、安全衛生上等
からも有利であること及び耐候性も改善されるため、長
期間にわたる残効性も期待できることを見出して、本発
明を完成した。[0006] The present inventors have found that the microbicidal composition is
After many years of diligent studies, by acting on the enzyme protein of the microorganism and changing it, the compound known as a microbicide that kills the microorganism (group A compound) is itself a microbicidal agent. By blending sodium dioctyl sulfosuccinate (B), which has almost no content, the efficacy is enhanced by the synergistic action, the amount of the components to be treated by the microbicide can be reduced, and it is advantageous from the economical and safety and hygiene viewpoints. Therefore, the present invention has been completed by finding out that there is a certain possibility and weather resistance is also improved, so that a residual effect over a long period can be expected.
【0007】[0007]
【発明の構成】本発明の有効成分の1つであるA群の化
合物としては、例えば、N−シクロヘキシル−N−メト
キシ−2,5−ジメチル−3−フランカルボキサミド;
トリス−(N−シクロヘキシルジアゼニウムジオキシ)
−アルミニウム;N,N−ジメチル−N′−フェニル−
(N′−フルオロジクロロメチルチオ)−スルフアミ
ド;N−シクロヘキシル−ジアゼニウムジオキシ−カリ
ウム;ビス(ジメチルチオカルバモイル)ジスルフィ
ド;トリブチルスズフマレート;トリブチルスズオキサ
イド及びトリブチルスズフタレートをあげることがで
き、これらの化合物は、変色菌、腐朽菌、カビ等の防除
剤として公知である。又、これらの化合物は、有効成分
として1種又は2種以上使用できる。BEST MODE FOR CARRYING OUT THE INVENTION As the compound of Group A which is one of the active ingredients of the present invention, for example, N-cyclohexyl-N-methoxy-2,5-dimethyl-3-furancarboxamide;
Tris- (N-cyclohexyldiazenium dioxy)
-Aluminum; N, N-dimethyl-N'-phenyl-
(N'-fluorodichloromethylthio) -sulfamide; N-cyclohexyl-diazenium dioxy-potassium; bis (dimethylthiocarbamoyl) disulfide; tributyltin fumarate; tributyltin oxide and tributyltin phthalate. It is known as a control agent for discoloring bacteria, decaying fungi, mold and the like. Further, these compounds may be used alone or in combination of two or more as active ingredients.
【0008】本発明のもう一方の有効成分であるジオク
チルスルホコハク酸ナトリウム(B)は、次式で示さ
れ、The other active ingredient of the present invention, sodium dioctylsulfosuccinate (B), is represented by the following formula:
【0009】[0009]
【化1】 [Chemical 1]
【0010】医薬、化粧品、繊維、写真等の分野で、湿
潤剤、分散剤として公知であるが、それ自体殺微生物力
を殆ど有しない。又、毒性も低く、かつ前記のA群の化
合物に比し、安価で製造される為、本発明の殺微生物剤
は、安全衛生上又は環境汚染防止上から見ても有利であ
り、又、経済的でもある。It is known as a wetting agent and a dispersant in the fields of medicine, cosmetics, fibers, photography and the like, but it has almost no microbicidal activity. Further, since the toxicity is low and the compound is produced at a lower cost than the compounds of the group A, the microbicide of the present invention is advantageous from the viewpoint of safety and hygiene or prevention of environmental pollution. It is also economical.
【0011】本発明の殺微生物組成物が適用される微生
物としては、木材等に寄生して腐朽等させる微生物なら
特に制限されないが、好適には、オオウズラタケ、ワタ
グサレタケ、カワラタケ、ヒイロタケ、ナミダタケ等の
腐朽菌、オフィオストマ(Ophiostoma)属、エンドコニデ
ィオホラ(Endoconidiophora)属の変色菌及びペニシリウ
ム(Penicillium) 属、アスペルギルス(Aspergillus)
属、リゾプス(Rhizopus)属、トリコデルマ(Trichoderm
a) 属のカビ類である。The microorganism to which the microbicidal composition of the present invention is applied is not particularly limited as long as it is a microorganism which is parasitic on wood or the like and rots, but it is preferably rots such as Pleurotus ostreatus, Pleurotus cornucopiae, Pleurotus ostreatus, Pleurotus ostreatus, Pleurotus cornucopiae, etc. Fungi, Ophiostoma genus, Endoconidiophora genus discoloring bacteria and Penicillium (Penicillium) genus, Aspergillus (Aspergillus)
Genus, Rhizopus, Trichoderm
a) A genus of molds
【0012】本発明の有効成分は、担体及び必要に応じ
て他の補助剤と混合して、工業用防カビ・防腐として通
常用いられる製剤形態、例えば油溶性剤、乳剤、ペース
ト剤、粉剤、水和剤、エアゾール剤、塗料等に調製され
て使用される。The active ingredient of the present invention is mixed with a carrier and, if necessary, other auxiliary agents, and is in the form of a formulation usually used for industrial fungicides and preservatives, such as an oil-soluble agent, an emulsion, a paste agent, a powder agent, It is prepared and used as a wettable powder, an aerosol, a paint and the like.
【0013】適当な担体としてはクレー、タルク、ベン
トナイト、カオリン、無水硅酸、炭酸カルシウム、木粉
等の不活性固体担体;ケロシン、リグロイン、キシレ
ン、メチルナフタリン、ジメチルホルムアミド、ジメチ
ルスルホキシド等の液体担体;窒素ガス、ジメチルエー
テル、フロンガス、塩化ビニル単量体等の気体担体があ
げられる。製剤の性状を改善し、防腐・防カビ効果を高
めるために適宜使用される補助剤としては、例えば陰イ
オン性、陽イオン性、非イオン性の界面活性剤やメチル
セルロース、酢酸ピニル樹脂、アルギン酸ソーダ等の種
々の高分子化合物等があげられる。勿論、2−(4−チ
アゾリル)ベンツイミダゾール(サイアベンダゾー
ル)、N,N−ジメチル−N′−(ジクロロフルオロメ
チルチオ)−N′−フェニルスルファミド(ジクロフル
アニド)あるいはベンツアニリド系等の他の防腐・防カ
ビ剤と併用でき、それにより一層の効果向上をはかるこ
とも可能である。Suitable carriers include inert solid carriers such as clay, talc, bentonite, kaolin, silicic acid anhydride, calcium carbonate and wood flour; liquid carriers such as kerosene, ligroin, xylene, methylnaphthalene, dimethylformamide and dimethylsulfoxide. Gas carriers such as nitrogen gas, dimethyl ether, freon gas, vinyl chloride monomer and the like can be mentioned. Examples of the auxiliaries that are appropriately used to improve the properties of the preparation and enhance the antiseptic / antifungal effect include, for example, anionic, cationic and nonionic surfactants, methyl cellulose, pinyl acetate resin, sodium alginate. Various polymer compounds and the like are listed. Of course, such as 2- (4-thiazolyl) benzimidazole (thiabendazole), N, N-dimethyl-N '-(dichlorofluoromethylthio) -N'-phenylsulfamide (diclofluanide) or benzanilide series is used. It can be used in combination with other antiseptic / antifungal agents, which can further improve the effect.
【0014】実際の使用に際しての本発明の有効成分の
含量は、製剤の形態に従い広い範囲にわたって変化させ
得るが、一般には(A)群の化合物は、使用される木材
に対して0.2〜15重量%、好ましくは0.5〜5重
量%の範囲が適当であり、ジオクチルスルホコハク酸ナ
トリウム(B)は、(A)群の化合物に対して、重量比
で1:0.03〜10.0、好ましくは 1:0.5〜
5.0である。The content of the active ingredient of the present invention in actual use can be varied over a wide range depending on the form of the preparation, but in general, the compounds of the (A) group are contained in an amount of 0.2 to 10% based on the wood used. A suitable range is 15% by weight, preferably 0.5 to 5% by weight. Sodium dioctylsulfosuccinate (B) is used in a weight ratio of 1: 0.03 to 10. 0, preferably 1: 0.5-
It is 5.0.
【0015】[0015]
【発明の効果】次に本発明の殺微生物組成物の効果を試
験例によって説明する。The effect of the microbicidal composition of the present invention will be described below with reference to test examples.
【0016】[0016]
試験例1 トリス−(N−シクロヘキシルジアゼニウムジオキシ)
−アルミニウム(NCH-Al) とジオクチルスルホコハク酸
ナトリウム(N-290K)を使用し、表1に示す処方の薬液を
試製し、厚さ5mm、幅20mm、長さ40mmの木材片に、
各々110±10g/m2宛塗布した試験片を、(社)日本
木材保存協会規格第1号の防腐効力試験方法により試験
した。結果は表−2の通りであった。Test Example 1 Tris- (N-cyclohexyldiazenium dioxy)
-Aluminum (NCH-Al) and sodium dioctyl sulfosuccinate (N-290K) were used to trial-prepare the chemical solutions shown in Table 1, and a wood piece with a thickness of 5 mm, a width of 20 mm, and a length of 40 mm was prepared.
Each test piece applied to 110 ± 10 g / m 2 was tested by the preservative efficacy test method of Japan Wood Preservation Association Standard No. 1. The results are shown in Table-2.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【表2】 [Table 2]
【0019】試験例2 ビス(ジメチルチオカルバモイル)ジスルフィド(TMTD)
とジオクチルスルホコハク酸ナトリウム(N-290K)を使用
し、表3に示す処方の薬液を試製し、試験例1と同様の
方法で試験した。結果は表−4の通りであった。Test Example 2 Bis (dimethylthiocarbamoyl) disulfide (TMTD)
And sodium dioctyl sulfosuccinate (N-290K) were used to prepare chemical solutions having the formulations shown in Table 3 and tested in the same manner as in Test Example 1. The results are shown in Table-4.
【0020】[0020]
【表3】 [Table 3]
【0021】[0021]
【表4】 [Table 4]
【0022】試験例3 トリブチルスズオキサイド(TBTO)とジオクチルスルホコ
ハク酸ナトリウム(N-290K) を使用し、表5に示す処方
の薬液を試製し、試験例1と同様の方法で試験した。結
果は表−6の通りであった。Test Example 3 Tributyltin oxide (TBTO) and sodium dioctyl sulfosuccinate (N-290K) were used to prepare a chemical solution having the formulation shown in Table 5, and the same method as in Test Example 1 was tested. The results are shown in Table-6.
【0023】[0023]
【表5】 [Table 5]
【0024】[0024]
【表6】 [Table 6]
【0025】試験例4 N−シクロヘキシル−N−メトキシ−2,5−ジメチル
−3−フランカルボキサミド(キシラザン−B)とジオ
クチルスルホコハク酸ナトリウム(N-290K)を使用し、表
7に示す処方の薬液を試製し、厚さ3mm、幅20mm、長
さ50mmのブナ辺材、10〜20個を各薬液に3分間浸
漬処理し、各々試験片とし、(社)日本木材保存協会規
格第2号の木材用防カビ剤の防カビ効力試験方法により
試験した。結果は表−8の通りであった。Test Example 4 N-cyclohexyl-N-methoxy-2,5-dimethyl-3-furancarboxamide (xylazane-B) and sodium dioctylsulfosuccinate (N-290K) were used, and the formulations shown in Table 7 were used. The beech sapwood with a thickness of 3 mm, a width of 20 mm, and a length of 50 mm, and 10 to 20 pieces of the beech sapwood were immersed in each chemical solution for 3 minutes to make test pieces, respectively, according to the Japan Wood Preservation Association Standard No. 2 The antifungal agent for wood was tested by the antifungal efficacy test method. The results are shown in Table-8.
【0026】[0026]
【表7】 [Table 7]
【0027】[0027]
【表8】 [Table 8]
【0028】*) 供試菌 A1:Aspergillus niger van Tieghem IFO 6341=ATCC
6275 A2:Penicillium funiculosum Thom IFO 6345 =ATCC
9644 A3:Rhizopus javanicus Takeda IFO 6354 A4:Aureobasidium pullulans Arnaud IFO 6353 =IA
M A5:Gliocladium virens Miller,Giddens & Fosteb I
FO 6355 =ATCC 9645 試験例5 N,N−ジメチル−N′−フェニル−(N′−フルオル
ジクロメチルチオ)−スルファミド(ジクロフルアニ
ド)とジオクチルスルホコハク酸ナトリウム(N-290K)
を使用し、表9に示す処方の薬液を試製し、試験例4と
同様の方法で試験した。結果は表−10の通りであっ
た。*) Test bacteria A1: Aspergillus niger van Tieghem IFO 6341 = ATCC
6275 A2: Penicillium funiculosum Thom IFO 6345 = ATCC
9644 A3: Rhizopus javanicus Takeda IFO 6354 A4: Aureobasidium pullulans Arnaud IFO 6353 = IA
M A5: Gliocladium virens Miller, Giddens & Fosteb I
FO 6355 = ATCC 9645 Test Example 5 N, N-dimethyl-N'-phenyl- (N'-fluorodichloromethylthio) -sulfamide (diclofluanid) and sodium dioctylsulfosuccinate (N-290K)
Was used to prepare a drug solution having the formulation shown in Table 9, and the test was performed in the same manner as in Test Example 4. The results are shown in Table-10.
【0029】[0029]
【表9】 [Table 9]
【0030】尚、本試験に供した菌は試験例4と同様で
ある。The bacteria used in this test are the same as in Test Example 4.
【0031】[0031]
【表10】 [Table 10]
【0032】試験例6 トリブチルスズフタレートとジオクチルスルホコハク酸
ナトリウム(N-290K)を使用し、表11に示す処方の薬液
を試製し、試験例4と同様の方法で試験した。結果は表
−12の通りであった。Test Example 6 Tributyltin phthalate and sodium dioctyl sulfosuccinate (N-290K) were used, and a chemical solution having the formulation shown in Table 11 was prepared and tested in the same manner as in Test Example 4. The results are shown in Table-12.
【0033】[0033]
【表11】 [Table 11]
【0034】尚、本試験に供した菌は、試験例4と同様
である。The bacteria used in this test are the same as in Test Example 4.
【0035】[0035]
【表12】 [Table 12]
【0036】以上の試験例に示されるように、本発明の
組成物はすぐれた防腐・防カビ効力を示し、微生物の制
御及び/又は防除のために極めて有用である。As shown in the above test examples, the composition of the present invention exhibits excellent antiseptic / antifungal efficacy and is extremely useful for controlling and / or controlling microorganisms.
【0037】次に本発明の防カビ・防腐の若干の製剤例
をあげるが、配合量、補助剤の種類等は大幅に変え得る
ものであることは言うまでもない。(文中、単に部とあ
るのは全て重量部をあらわす。) 製剤例 1. 乳剤 NCH-Al10部及びN-290K10部をジメチルホルムアミド
40部に溶解させ、キシレン50部及びポリオキシエチ
レンノニルフェニルエーテル10部を加えて十分に混合
して乳剤を得る。この乳剤は用時適量の水で希釈して処
理すべき木質材料に塗布、浸漬もしくはスプレー等の方
法で使用される他、構造用合板、パーティクルボード等
の接着剤混入処理に適用できる。Next, some examples of the antifungal and antiseptic formulations of the present invention will be given, but it goes without saying that the compounding amount, the kind of the auxiliary agent, etc. can be greatly changed. (In the text, all parts are parts by weight.) Formulation example 1. Emulsion 10 parts of NCH-Al and 10 parts of N-290K were dissolved in 40 parts of dimethylformamide, 50 parts of xylene and 10 parts of polyoxyethylene nonyl phenyl ether were added and mixed sufficiently to obtain an emulsion. This emulsion is used by diluting it with an appropriate amount of water before use and applying it to a wood material to be treated by a method such as coating, dipping or spraying, and can also be applied to a treatment for mixing an adhesive agent such as structural plywood or particle board.
【0038】製剤例2. 油溶性剤 NCH-Al1部及びN-290K1部をジメチルホルムアミド2部
に溶解し、ソルベントナフサ96部を加え油剤を得た。
この油剤は処理すべき木質材料にスプレー、塗布もしく
は浸漬、注入等の方法で使用される。Formulation Example 2. Oil-soluble agent 1 part of NCH-Al and 1 part of N-290K were dissolved in 2 parts of dimethylformamide, and 96 parts of solvent naphtha was added to obtain an oil solution.
This oil agent is used by a method such as spraying, coating or dipping, pouring, etc. on the wood material to be treated.
【0039】製剤例3. 粉剤 TMTD2部及びN-290K2部をアセトン10部に溶解し、ク
レー68部、タルク30部を加えて均一に混合した後ア
セトンを蒸発除去して粉剤を得た。Formulation Example 3. Dust agent 2 parts of TMTD and 2 parts of N-290K were dissolved in 10 parts of acetone, 68 parts of clay and 30 parts of talc were added and uniformly mixed, and then acetone was removed by evaporation to obtain a dust agent.
【0040】製剤例4. 水和剤 TBTO40部、N-290K20部、クレー56部、ラウリルア
ルコールスルホン酸ソーダ3部及びポリビニルアルコー
ル1部を混合機中で均一に混合し、ハンマーミルで粉砕
して水和剤を得た。Formulation Example 4. Wettable powder 40 parts of TBTO, 20 parts of N-290K, 56 parts of clay, 3 parts of sodium lauryl alcohol sulfonate and 1 part of polyvinyl alcohol were uniformly mixed in a mixer and ground by a hammer mill to obtain a wettable powder.
【0041】製剤例5. 塗料 キシラザンB10部、N-290K20部、パライト粉20
部、ビニール樹脂10部、松脂25部及びキシレン35
部を均一に混合して塗料を得た。Formulation Example 5. Paint Xylazane B 10 parts, N-290K 20 parts, perlite powder 20
Part, vinyl resin 10 parts, pine resin 25 parts and xylene 35
The parts were uniformly mixed to obtain a paint.
【0042】製剤例6. エアゾール ジクロフルアニド1部、N-290K1部及び香料0.5部を
脱臭灯油40部に溶解してエアゾール容器に充填し、バ
ルブを装着した後液化石油ガス58部を加圧充填してエ
アゾールを得た。Formulation Example 6. Aerosol 1 part of diclofluanid, 1 part of N-290K and 0.5 part of fragrance are dissolved in 40 parts of deodorizing kerosene and filled into an aerosol container, and after installing a valve, 58 parts of liquefied petroleum gas is pressurized to fill the aerosol. Obtained.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A01N 41:04) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display area A01N 41:04)
Claims (1)
ムジオキシ)−アルミニウム及びN−シクロヘキシルジ
アゼニウムジオキシ)−カリウムよりなる群(A)から
選ばれた1種又は2種以上の化合物に、ジオクチルスル
ホコハク酸ナトリウム(B)を配合したことを特徴とす
る腐朽菌防除剤。1. One or more compounds selected from the group (A) consisting of tris- (N-cyclohexyldiazeniumdioxy) -aluminum and N-cyclohexyldiazeniumdioxy) -potassium, A rot fungus control agent , characterized by containing sodium dioctyl sulfosuccinate (B).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5268694A JPH0753643B2 (en) | 1986-08-13 | 1993-10-27 | Microbicidal composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61190375A JPH0637369B2 (en) | 1986-08-13 | 1986-08-13 | Microbicidal composition |
| JP5268694A JPH0753643B2 (en) | 1986-08-13 | 1993-10-27 | Microbicidal composition |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61190375A Division JPH0637369B2 (en) | 1986-08-13 | 1986-08-13 | Microbicidal composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06199612A JPH06199612A (en) | 1994-07-19 |
| JPH0753643B2 true JPH0753643B2 (en) | 1995-06-07 |
Family
ID=26506045
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5268694A Expired - Lifetime JPH0753643B2 (en) | 1986-08-13 | 1993-10-27 | Microbicidal composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0753643B2 (en) |
-
1993
- 1993-10-27 JP JP5268694A patent/JPH0753643B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06199612A (en) | 1994-07-19 |
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