JPH06102604B2 - Disinfectant - Google Patents

Disinfectant

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Publication number
JPH06102604B2
JPH06102604B2 JP60189320A JP18932085A JPH06102604B2 JP H06102604 B2 JPH06102604 B2 JP H06102604B2 JP 60189320 A JP60189320 A JP 60189320A JP 18932085 A JP18932085 A JP 18932085A JP H06102604 B2 JPH06102604 B2 JP H06102604B2
Authority
JP
Japan
Prior art keywords
abdac
sterilizing
aqueous solution
amount
concentration
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 - Lifetime
Application number
JP60189320A
Other languages
Japanese (ja)
Other versions
JPS6248601A (en
Inventor
孫兵衛 山本
二郎 ▲高▼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.)
Takeda Pharmaceutical Co Ltd
Original Assignee
Takeda Pharmaceutical Co Ltd
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Application filed by Takeda Pharmaceutical Co Ltd filed Critical Takeda Pharmaceutical Co Ltd
Priority to JP60189320A priority Critical patent/JPH06102604B2/en
Publication of JPS6248601A publication Critical patent/JPS6248601A/en
Publication of JPH06102604B2 publication Critical patent/JPH06102604B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 産業上の利用分野 本発明はアルキルベンジルジメチルアンモニウム塩と、
ハロゲン化セチルトリメチルアンモニウムまたはハロゲ
ン化セチルピリジニウムとを含有してなる、アルキルベ
ンジルジメチルアンモニウム塩の高分子保持体への吸着
が抑制された殺菌消毒剤に関するものである。本剤は高
分子保持体の存在下で対象物に接触せしめても有効に殺
菌消毒力を発揮する。
TECHNICAL FIELD The present invention relates to an alkylbenzyldimethylammonium salt,
The present invention relates to a bactericidal disinfectant containing a cetyltrimethylammonium halide or a cetylpyridinium halide in which adsorption of an alkylbenzyldimethylammonium salt on a polymer support is suppressed. This agent effectively exhibits sterilizing power even when it is brought into contact with an object in the presence of a polymer support.

従来の技術 アルキルベンジルジメチルアンモニウムの、たとえば塩
化物(塩化ベンザルコニウムとも称される、以下「ABDA
C」と略称することがある)はその水溶液が無色、無臭
であり、グラム陽性菌および陰性菌のみならず、真菌類
に対しても抗菌性を有するので、殺菌消毒剤として有用
である(日本薬局方、第10改正,C−343,1981、広川書
店)。また、ハロゲン化セチルトリメチルアンモニウム
(例、臭化セチルトリメチルアンモニウム)およびハロ
ゲン化セチルピリジニウム(例、塩化セチルピリジニウ
ム)も殺菌消毒作用を有する化合物として知られている
(津田恭介、野上寿編;製剤設計法(2)、地人書館
(昭和46年)、第429頁)。
2. Description of the Related Art Alkylbenzyldimethylammonium, such as chloride (also called benzalkonium chloride, hereinafter referred to as “ABDA
C) is an aqueous solution that is colorless and odorless, and has antibacterial properties not only against Gram-positive and negative bacteria but also against fungi, so it is useful as a germicidal disinfectant (Japan Pharmacopoeia, 10th revision, C-343, 1981, Hirokawa Shoten). In addition, cetyltrimethylammonium halide (eg, cetyltrimethylammonium bromide) and cetylpyridinium halide (eg, cetylpyridinium chloride) are also known as compounds having a bactericidal action (Kyosuke Tsuda, Hisashi Nogami; formulation design) Law (2), Jishin Shokan (Showa 46), page 429).

発明が解決しようとする問題点 アルキルベンジルジメチルアンモニウム塩、たとえばAB
DAC水溶液は殺菌消毒剤として広範囲に用いられている
が、脱脂綿、ガーゼ等のセルロース系保持体を浸し、清
拭により殺菌消毒を行なう場合、その殺菌消毒力が低下
してくる現象が認められる。同じような殺菌消毒力の低
下はウールの他レイヨン,ポリウレタン系,シリコン系
などの合成高分子系材料から調製された保持体の場合に
も認められる。このために、上記高分子保持体を介する
場合においても、ABDACの殺菌消毒力を有効に発揮せし
める方法の開発が望まれている。
Problems to be Solved by the Invention Alkylbenzyldimethylammonium salts such as AB
Although the DAC aqueous solution is widely used as a sterilizing agent, when the cellulosic support such as absorbent cotton and gauze is soaked and sterilized by wiping, the sterilizing and disinfecting ability is reduced. A similar decrease in sterilization and disinfection ability is also observed in the case of a holder prepared from a synthetic polymer material such as rayon, polyurethane, silicone, etc. in addition to wool. Therefore, it is desired to develop a method for effectively exerting the bactericidal and disinfecting power of ABDAC even when the above-mentioned polymer support is used.

問題点を解決するための手段 上記のような状況に鑑み、本発明者らは上記の殺菌消毒
力の低下の原因について種々検討したところ、ABDACが
高分子材料に吸着され、殺菌消毒液中のABDAC遊離体量
が減少することに基づくものであることを見出した。
Means for Solving the Problems In view of the situation as described above, the present inventors have conducted various studies on the cause of the decrease in the above-mentioned sterilizing / disinfecting power, and ABDAC is adsorbed on the polymer material, and the sterilizing / disinfecting solution contains It was found that it was based on the decrease in the amount of ABDAC educt.

そこで、次に本発明者らはABDACの高分子保持体の吸着
を抑制する方法について種々研究した結果、ABDAC水溶
液中に臭化セチルトリメチルアンモニウムまたは塩化セ
チルピリジニウムを共存させておくことにより高分子保
持体に接触時のABDAC遊離体量が多くなることを見出
し、さらに研究して本発明を完成した。
Therefore, the present inventors next conducted various studies on methods for suppressing the adsorption of the polymer carrier of ABDAC, and as a result, the polymer retention was carried out by allowing coexistence of cetyltrimethylammonium bromide or cetylpyridinium chloride in the ABDAC aqueous solution. It was found that the amount of ABDAC educts on contact with the body was increased, and further research was conducted to complete the present invention.

すなわち、本発明はアルキルベンジルジメチルアンモニ
ウム塩と、ハロゲン化セチルトリメチルアンモニウムま
たはハロゲン化セチルピリジニウムとを含有してなる、
アルキルベンジルジメチルアンモニウム塩の高分子保持
体への吸着が抑制された殺菌消毒剤である。
That is, the present invention comprises an alkylbenzyldimethylammonium salt and cetyltrimethylammonium halide or cetylpyridinium halide,
It is a germicidal disinfectant in which the adsorption of alkylbenzyldimethylammonium salt on a polymer support is suppressed.

本発明の殺菌消毒剤において、アルキルベンジルジメチ
ルアンモニウム塩は常法で得たものが用いられ、特に塩
化物(ABDAC)が有利に用いられる。ABDACを構成するア
ルキル基としては、炭素数8〜18のものがあげられる。
これらは、いずれも高分子保持体に吸着するが、本発明
ではこれらの中でも、特に殺菌消毒力の強い炭素数12あ
るいは14のアルキル基を有する成分の吸着の阻害、また
は脱着に有効に使用し得る。
In the germicidal disinfectant of the present invention, the alkylbenzyl dimethyl ammonium salt obtained by a conventional method is used, and chloride (ABDAC) is particularly advantageously used. Examples of the alkyl group constituting ABDAC include those having 8 to 18 carbon atoms.
These are all adsorbed on the polymer support, but in the present invention, among them, particularly effective for inhibiting adsorption of components having an alkyl group having a carbon number of 12 or 14 having strong sterilizing / disinfecting power, or for desorption. obtain.

次に、ハロゲン化セチルトリメチルアンモニウムとして
は、臭化物、塩化物などがあげられ、特に臭化物が好ま
しい。また、ハロゲン化セチルピリジニウムとしては、
塩化物、臭化物があげられ、特に塩化物が好ましく用い
られる。
Next, examples of the cetyltrimethylammonium halide include bromide and chloride, and bromide is particularly preferable. Further, as cetylpyridinium halide,
Examples thereof include chloride and bromide, and chloride is particularly preferably used.

本発明の殺菌消毒剤は、アルキルベンジルジメチルアン
モニウム塩の100重量部に対しハロゲン化セチルトリメ
チルアンモニウムまたはハロゲン化セチルピリジニウム
を約0.3重量部以上、好ましくは約3重量部以上、さら
に好ましくは約10重量部以上の割合で含有せしめること
により調製される。このような量比にすることにより、
アルキルベンジルジメチルアンモニウム塩の高分子保持
体への吸着抑制に効果がある。ハロゲン化セチルトリメ
チルアンモニウムまたはハロゲン化セチルピリジニウム
は上記の配合量より多くするほど前記吸着抑制効果は強
くなるが、通常、約4,000重量部で最大状態に達するの
で、一般にこの程度を最大配合量とすればよい。
The germicidal disinfectant of the present invention is about 0.3 parts by weight or more, preferably about 3 parts by weight or more, more preferably about 10 parts by weight of cetyltrimethylammonium halide or cetylpyridinium halide per 100 parts by weight of alkylbenzyldimethylammonium salt. It is prepared by containing the above components in a proportion of at least 1 part. By setting such an amount ratio,
It is effective in suppressing the adsorption of alkylbenzyldimethylammonium salt on the polymer support. When the amount of cetyltrimethylammonium halide or cetylpyridinium halide is greater than the above amount, the adsorption suppression effect becomes stronger, but usually the maximum state is reached at about 4,000 parts by weight, so this level is generally regarded as the maximum amount. Good.

本発明の殺菌消毒剤の剤型は、特に限定されず、たとえ
ば従来公知の方法により固形剤、液剤、スプレー剤等に
調製すればよい。液剤、スプレー剤の場合は、水、アル
コール等を溶媒として用いることができる。
The dosage form of the disinfectant of the present invention is not particularly limited, and may be prepared into a solid agent, a liquid agent, a spray agent or the like by a conventionally known method. In the case of a liquid agent or a spray agent, water, alcohol or the like can be used as a solvent.

次に、本殺菌消毒剤を使用するに際しては、アルキルベ
ンジルジメチルアンモニウム塩の濃度が約0.005〜1%
(重量/容量)で、ハロゲン化セチルトリメチルアンモ
ニウムまたはハロゲン化セチルピリジニウムの濃度が約
0.003〜0.4%(重量/容量)となるような溶液状態で殺
菌消毒の対象物に接触せしめればよい。このときの溶媒
としては、水、アルコール(例、エタノール)、アルコ
ール水溶液等を用いることができ、殺菌消毒の対象物の
種類を考慮し適宜に選択すればよい。
Next, when using this germicidal disinfectant, the concentration of alkylbenzyldimethylammonium salt should be about 0.005-1%.
(Weight / volume) the concentration of cetyltrimethylammonium halide or cetylpyridinium halide is about
It may be brought into contact with an object to be sterilized in a solution state such that the concentration becomes 0.003 to 0.4% (weight / volume). As the solvent at this time, water, alcohol (eg, ethanol), an aqueous alcohol solution, or the like can be used, and may be appropriately selected in consideration of the type of the sterilization object.

殺菌消毒対象物への接触方法は、従来公知の方法を採用
することができ、たとえば浸漬、スプレー、ふりかけ、
洗浄、清浄・清拭などにより実施できる。その対象物と
しては、微生物の汚染を排除する目的で各種用途に幅広
く適用できる。たとえば、人体、動物の患部あるいは各
種医療器具・施設などの医療用、手指の消毒、理容・美
容院、学校等の公共施設、家屋、乗物、食器、食品製造
工場あるいはその製造設備等の殺菌消毒に用いることが
できる。
The method of contacting the sterilization target can be a conventionally known method, for example, dipping, spraying, sprinkling,
It can be carried out by washing, cleaning and wiping. As the object, it can be widely applied to various uses for the purpose of eliminating microbial contamination. For example, medical treatment of affected parts of humans and animals or various medical instruments / facility, disinfection of fingers, barber / beauty salon, public facilities such as schools, houses, vehicles, tableware, food manufacturing factories or their manufacturing facilities. Can be used for.

とりわけ、本発明の殺菌消毒剤はセルロース系材料、ポ
リエチレン、ポリエステル、ポリウレタンあるいはシリ
コン系の合成樹脂等の高分子保持体を介する適用方法に
特に有利に用いることができる。本適用方法の具体例と
しては、本殺菌消毒液中にガーゼ、精製脱脂綿、不織布
等を浸漬しておき手指、患部の消毒用、殺菌用皮膚もし
くは粘膜などの殺菌または消毒に医薬品として使用する
方法、脱脂綿、精製脱脂綿、不織布、おしぼり、紙綿、
紙布等に本殺菌消毒液を含浸させて乳児の皮膚、口腔の
清浄・清拭または授乳時の乳首乳房の清浄・清拭および
目、局部、肛門の清浄・清拭に医薬部外品として使用す
る方法があげられる。
In particular, the disinfectant of the present invention can be particularly advantageously used for an application method through a polymeric support such as a cellulosic material, polyethylene, polyester, polyurethane or silicone synthetic resin. As a specific example of the present application method, gauze, purified absorbent cotton, non-woven fabric, etc. are soaked in the sterilizing and disinfecting solution and used as a medicine for sterilizing or disinfecting fingers, disinfecting an affected area, sterilizing skin or mucous membrane, etc. , Absorbent cotton, purified absorbent cotton, non-woven fabric, towel, paper cotton,
As a quasi-drug for cleaning and cleaning the baby's skin and mouth, or cleaning and cleaning the nipple breast when breast-feeding and cleaning the eyes, local area and anus by impregnating a paper cloth etc. with this sterilizing solution The method used is given.

実施例 以下に実験例および実施例を挙げて本発明をさらに具体
的に説明する。
EXAMPLES The present invention will be described more specifically below with reference to experimental examples and examples.

実験例1 C12H25ABDAC,C14H29ABDACまたはC12H25ABDACとC14H29AB
DACの混合物(C12H25体とC14H29体のモル比1:0.54)を
それぞれ0.01%含有する各水溶液中に、精製脱脂綿をg/
10mlになるように浸漬し、25℃で1時間放置したとこ
ろ、これらABDACの精製脱脂綿への吸着量が平衡に達し
た。次に、この中へ臭化セチルトリメチルアンモニウム
(C16TMAB)を第1図に示すような種々の濃度で添加
し、水溶液中のABDACの濃度を高速液体クロマトグラフ
ィー(HPLC)で定量した。本定量法はMayer[ジャーナ
ル・オブ・ファーマシュウティカル・サイエンス(J.Ph
arm.Sci.69),1148(1980)]の方法を改良し、Radial
Pak 5CNカラム・検出波長λ254nm,0.1M,pH5.0酢酸緩
衝液−アセトニトリム(45:55),流速2ml/minの条件で
ABDACを定量する方法によった。
Experimental Example 1 C 12 H 25 ABDAC, C 14 H 29 AB DAC or C 12 H 25 AB DAC and C 14 H 29 AB
In each aqueous solution containing 0.01% of the mixture of DAC (molar ratio of C 12 H 25 form and C 14 H 29 form 1: 0.54), purified absorbent cotton was added in g /
When soaked to 10 ml and left at 25 ° C. for 1 hour, the amount of these ABDAC adsorbed on the purified absorbent cotton reached an equilibrium. Next, cetyltrimethylammonium bromide (C 16 TMAB) was added thereto at various concentrations as shown in FIG. 1, and the concentration of ABDAC in the aqueous solution was quantified by high performance liquid chromatography (HPLC). This quantitative method is based on Mayer [Journal of Pharmaceutical Sciences (J.Ph
arm.Sci. 69 ), 1148 (1980)] and improved Radial
Pak 5CN column ・ Detection wavelength λ254nm, 0.1M, pH5.0 Acetate buffer-acetonitrim (45:55), flow rate 2ml / min
By the method of quantifying ABDAC.

C16TMABの添加量と各ABDACの遊離体量の関係を第1図に
示す。この結果、C16TMABを0.1mmol/の添加ですでに
遊離ABDAC濃度が増加し、5mmol/の添加で95%のABDAC
が遊離した。
The relationship between the amount of C 16 TMAB added and the amount of free form of each ABDAC is shown in FIG. As a result, the concentration of free ABCAC was already increased by the addition of 0.1 mmol / C 16 TMAB, and the concentration of ABDAC was 95% by the addition of 5 mmol / AB.
Was released.

実験例2 C12H25またはC14H29ABDACを0.005〜0.1%含有する水溶
液にC16TMABを0〜1mmol/となるように添加し、これ
らを種々の割合で含む水溶液を調製した。この水溶液中
に、精製脱脂綿をg/10mlになるように浸漬し、吸着平衡
後の各ABDACの遊離体量を実験例1と同様の方法により
測定した。
Experimental Example 2 C 16 TMAB was added to an aqueous solution containing C 12 H 25 or C 14 H 29 ABDAC in an amount of 0.005 to 0.1% so that the concentration of C 16 TMAB was 0 to 1 mmol / ml, to prepare an aqueous solution containing these at various ratios. Purified absorbent cotton was dipped in this aqueous solution so as to have a concentration of g / 10 ml, and the amount of the free form of each ABDAC after adsorption equilibrium was measured by the same method as in Experimental Example 1.

その結果をC14H29ABDACの場合については第2図に示
す。
The results are shown in Fig. 2 for the case of C 14 H 29 AB DAC.

第2図から明らかなように、C16TMAB濃度が高くなると
遊離ABDAC濃度が増加し、例えばC16TMAB 1mmol/では
ABDAC濃度0.005〜0.1%において遊離C14H29ABDACは45〜
59%を示した。
As is clear from FIG. 2, the higher the concentration of C 16 TMAB, the higher the concentration of free ABDAC. For example, C 16 TMAB 1 mmol /
Free C 14 H 29 ABDAC 45-at ABDAC concentration 0.005-0.1%
It showed 59%.

実験例3 C12H25ABDAC,C14H29ABDACまたはC12H25ABDACとC14H29AB
DACの混合物(C12H25体とC14H29体のモル比1:0.54)を
それぞれ0.01%含有する水溶液に塩化セチルピリジニウ
ム(C16PC)を0〜1mmol/となように添加し、これら
を種々の割合で含む水溶液を調製した。この水溶液中
に、精製脱脂綿をg/10mlになるように浸漬し、吸着平衡
後のABDACの遊離体量を実験例1と同様の方法により測
定した。その結果を第3図に示す。第3図から明らかな
ようにC16PC濃度が高くなると遊離ABDAC濃度が増加し、
例えばC16PC 1mmol/ではC12H25ABDAC濃度0.01%にお
いて遊離C12H25ABDACは70%、遊離C14H29ABDACは37%と
なり、両遊離体の合計量は59%を示した。
Experimental Example 3 C 12 H 25 ABDAC, C 14 H 29 AB DAC or C 12 H 25 AB DAC and C 14 H 29 AB
Cetylpyridinium chloride (C 16 PC) was added to an aqueous solution containing 0.01% of a mixture of DAC (molar ratio of C 12 H 25 form and C 14 H 29 form of 1: 0.54) at 0 to 1 mmol /, Aqueous solutions containing these in various ratios were prepared. Purified absorbent cotton was dipped in this aqueous solution so as to have a concentration of g / 10 ml, and the amount of the free form of ABDAC after adsorption equilibrium was measured by the same method as in Experimental Example 1. The results are shown in FIG. As is clear from FIG. 3, the higher the C 16 PC concentration, the higher the concentration of free ABDAC,
For example, with C 16 PC 1 mmol /, at a C 12 H 25 ABDAC concentration of 0.01%, free C 12 H 25 ABDAC was 70%, free C 14 H 29 ABDAC was 37%, and the total amount of both educts was 59%.

実施例1 縦10cm,横15cmの約0.7gの紙綿(布)にABDAC(C12H25AB
DAC:67%,C14H29ABDAC:29%,C16H33ABDAC:5%)0.1%,C
16TMAB 0.5mmol/を含有する殺菌、消毒水溶液を約1.
6g含浸させ、アルミニウム箔で密封し、手指用の殺菌、
消毒剤を製する。
Example 1 About 0.7 g of paper cotton (cloth) having a length of 10 cm and a width of 15 cm, ABDAC (C 12 H 25 AB
DAC: 67%, C 14 H 29 ABDAC: 29%, C 16 H 33 ABDAC: 5%) 0.1%, C
About 1 sterilizing and disinfecting aqueous solution containing 16 TMAB 0.5 mmol /.
Impregnated with 6g, sealed with aluminum foil, sterilized for fingers,
Make a disinfectant.

実施例2 ABDAC(実施例1のものと同組成)0.02%,C16PCを1mmol
/を含有する殺菌、消毒水溶液を手動式スプレイ容器
に充てんしてスプレイ剤とし、この液約10.8gを縦7.5c
m,横8cmの約2.7gの脱脂綿にスプレイした後、包装用ラ
ミネートフィルム(ポリエチレン・ポリエステル複合フ
ィルム)に入れヒートシールする。これを121℃,20分の
高圧蒸気滅菌して皮膚清浄綿を製する。
Example 2 ABDAC (same composition as in Example 1) 0.02%, C 16 PC 1 mmol
A sterilizing and disinfecting aqueous solution containing / is filled in a manual spray container to make a spray agent, and about 10.8 g of this liquid is added to a vertical 7.5c
After spraying about 2.7 g of absorbent cotton with m and width of 8 cm, put it in a packaging laminate film (polyethylene / polyester composite film) and heat seal. This is sterilized by high-pressure steam for 20 minutes at 121 ° C to produce a skin cleansing cotton.

実施例3 縦17cm,横28.5cmの約4.2gのエンボス紙タオルにABDAC
(実施例1のものと同組成)0.05%,C16TMAB 0.2mmol/
を含有する殺菌、消毒水溶液を約7.1g含浸させ、セロ
ファン膜で密封し、殺菌、消毒用紙ナプキンを製する。
Example 3 ABDAC on an approximately 4.2 g embossed paper towel measuring 17 cm in length and 28.5 cm in width
(Same composition as that of Example 1) 0.05%, C 16 TMAB 0.2 mmol /
Approximately 7.1 g of a sterilizing and disinfecting aqueous solution containing is impregnated and sealed with a cellophane membrane to make a sterilizing and disinfecting paper napkin.

発明の効果 本発明の殺菌消毒剤は種々の対象物の殺菌消毒に幅広く
適用できる。特に、高分子保持体を介して殺菌消毒に用
いる場合であっても、アルキルベンジルジメチルアンモ
ニウム塩の殺菌消毒力を有効に発揮せしめることができ
る。すなわち、ハロゲン化セチルトリメチルアンモニウ
ムまたはハロゲン化セチルピリジニウムを共存させるこ
とにより、アルキルベンジルジメチルアンモニウム塩が
高分子保持体に吸着されるのを抑制することができ、こ
れによって溶液中のアルキルベンジルジメチルアンモニ
ウム塩の遊離体量が多くなり、殺菌消毒力の目的を十分
に達することができる。
Effect of the Invention The sterilizing agent of the present invention can be widely applied to sterilizing various objects. In particular, even when it is used for sterilization through a polymer support, the sterilization power of the alkylbenzyldimethylammonium salt can be effectively exerted. That is, the coexistence of cetyltrimethylammonium halide or cetylpyridinium halide can prevent the alkylbenzyldimethylammonium salt from being adsorbed on the polymer support, whereby the alkylbenzyldimethylammonium salt in the solution can be suppressed. The amount of free substance is increased, and the purpose of sterilizing power can be fully achieved.

【図面の簡単な説明】[Brief description of drawings]

第1図は、脱脂綿を含むABDAC水溶液中に、C16TMABを添
加したときのABDACの遊離体量を示し、図中、−●−はC
12H25ABDACの場合、−○−はC14H29ABDACの場合、−▲
−はC12H25ABDACとC14H29ABDACの混合物の場合をそれぞ
れ示す。第2図はC14H29ABDACとC16TMABの共存水溶液に
脱脂綿を浸漬したときの、遊離体の各ABDAC量を示し、
図において1,2,3,4および5の各番号で示される曲線はC
16TMABをそれぞれ0,0.1,0.2,0.5および1mmol/の濃度
で添加した場合を示す。 第3図は、ABDACとC16PCの共存水溶液に脱脂綿を浸漬し
たときの遊離体のABDAC量を示し、図中、−●−はC12H
25ABDACの場合、−○−はC14H29ABDACの場合、−▲−は
C12H25ABDACとC14H29ABDACの混合物の場合をそれぞれ示
す。
Fig. 1 shows the amount of free form of ABDAC when C 16 TMAB was added to the aqueous solution of ABDAC containing absorbent cotton. In the figure,-●-represents C
In the case of 12 H 25 ABDAC, − ○ − is C − in the case of 14 H 29 ABDAC − ▲
− Indicates the case of the mixture of C 12 H 25 ABDAC and C 14 H 29 ABDAC, respectively. Fig. 2 shows the amount of each ABDAC in the free form when absorbent cotton was immersed in a coexisting aqueous solution of C 14 H 29 ABDAC and C 16 TMAB.
In the figure, the curves indicated by the numbers 1, 2, 3, 4 and 5 are C
Shown is the case where 16 TMAB was added at concentrations of 0, 0.1, 0.2, 0.5 and 1 mmol /, respectively. Figure 3 shows the amount of ABDAC in the free form when absorbent cotton was dipped in a coexisting aqueous solution of ABDAC and C 16 PC. In the figure,-●-is C 12 H
In the case of 25 ABDAC, − ○ − is C 14 H 29 In the case of ABDAC, − ▲ − is
Shows the case of C 12 H 25 ABDAC and C 14 H 29 mixture of ABDAC respectively.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】アルキルジメチルアンモニウム塩と、ハロ
ゲン化セチルトリメチルアンモニウムまたはハロゲン化
セチルピリジニウムとを含有してなる、アルキルジメチ
ルアンモニウム塩の高分子保持体への吸着が抑制された
殺菌消毒剤。
1. A bactericidal disinfectant containing an alkyldimethylammonium salt and cetyltrimethylammonium halide or cetylpyridinium halide, in which adsorption of the alkyldimethylammonium salt to a polymer support is suppressed.
JP60189320A 1985-08-27 1985-08-27 Disinfectant Expired - Lifetime JPH06102604B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60189320A JPH06102604B2 (en) 1985-08-27 1985-08-27 Disinfectant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60189320A JPH06102604B2 (en) 1985-08-27 1985-08-27 Disinfectant

Publications (2)

Publication Number Publication Date
JPS6248601A JPS6248601A (en) 1987-03-03
JPH06102604B2 true JPH06102604B2 (en) 1994-12-14

Family

ID=16239384

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60189320A Expired - Lifetime JPH06102604B2 (en) 1985-08-27 1985-08-27 Disinfectant

Country Status (1)

Country Link
JP (1) JPH06102604B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010037295A (en) * 2008-08-07 2010-02-18 Kanae Technos:Kk Germicidal disinfectant solution and germicidal disinfectant

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05229904A (en) * 1992-02-25 1993-09-07 Tomoyuki Takahashi Disinfectant for pierced earring
KR19990054322A (en) * 1997-12-26 1999-07-15 성재갑 Liquid detergent composition
KR20030010788A (en) * 2001-07-27 2003-02-06 (주)지텍 바이오 메디컬 A composition comprising cetylpyridinium chloride for the prevention of bean sprout rot and improvement of brightness of bean sprout and the method of using the same
US20040033916A1 (en) * 2002-06-28 2004-02-19 Kuzmin Vladimir Semenovich Disinfecting composition
JP5337350B2 (en) * 2007-04-10 2013-11-06 ディバーシー株式会社 Disinfectant cleaning composition and disinfecting cleaning method using the same
JP5539661B2 (en) * 2008-03-24 2014-07-02 旭化成ケミカルズ株式会社 Wet wiper containing disinfectant
AU2009245152B2 (en) * 2008-05-09 2013-11-14 Hiroshima University Method of fixing antibacterial agent and article obtained by the method
JP5895478B2 (en) * 2011-11-29 2016-03-30 ライオン株式会社 Liquid-based sweat deodorant composition and liquid-based sweat deodorant product
WO2014069639A1 (en) * 2012-11-02 2014-05-08 ライオン株式会社 Deodorant composition and method for producing same

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1460279A (en) * 1973-05-10 1976-12-31 Ici Ltd Biocidal compositions
JPS5919921B2 (en) * 1976-07-08 1984-05-09 三菱瓦斯化学株式会社 Microbial growth inhibitor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010037295A (en) * 2008-08-07 2010-02-18 Kanae Technos:Kk Germicidal disinfectant solution and germicidal disinfectant

Also Published As

Publication number Publication date
JPS6248601A (en) 1987-03-03

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