JPH0417857A - Deodorant - Google Patents
DeodorantInfo
- Publication number
- JPH0417857A JPH0417857A JP2120477A JP12047790A JPH0417857A JP H0417857 A JPH0417857 A JP H0417857A JP 2120477 A JP2120477 A JP 2120477A JP 12047790 A JP12047790 A JP 12047790A JP H0417857 A JPH0417857 A JP H0417857A
- Authority
- JP
- Japan
- Prior art keywords
- glycine
- tea leaf
- formula
- glycine derivative
- deodorant
- 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.)
- Pending
Links
- 239000002781 deodorant agent Substances 0.000 title claims abstract description 19
- 150000002332 glycine derivatives Chemical class 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 150000003839 salts Chemical class 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
- 229940092665 tea leaf extract Drugs 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 6
- 238000000605 extraction Methods 0.000 abstract description 4
- 239000012046 mixed solvent Substances 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 3
- 241001122767 Theaceae Species 0.000 abstract 4
- FTJULAMXHCHGEP-UHFFFAOYSA-N 4-amino-2-(2-aminoethyl)-2-(octylamino)butanoic acid Chemical compound C(CCCCCCC)NC(C(=O)O)(CCN)CCN FTJULAMXHCHGEP-UHFFFAOYSA-N 0.000 abstract 1
- 235000019645 odor Nutrition 0.000 description 16
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 10
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 10
- 230000001877 deodorizing effect Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 8
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 8
- 238000004332 deodorization Methods 0.000 description 7
- 244000269722 Thea sinensis Species 0.000 description 6
- 235000013616 tea Nutrition 0.000 description 6
- 230000002195 synergetic effect Effects 0.000 description 5
- -1 Amine compounds Chemical class 0.000 description 4
- 239000004471 Glycine Substances 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- 229960002449 glycine Drugs 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 231100000676 disease causative agent Toxicity 0.000 description 3
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- RTIXKCRFFJGDFG-UHFFFAOYSA-N chrysin Chemical class C=1C(O)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=CC=C1 RTIXKCRFFJGDFG-UHFFFAOYSA-N 0.000 description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 235000009569 green tea Nutrition 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000005183 environmental health Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000002550 fecal effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229960001269 glycine hydrochloride Drugs 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
Description
【発明の詳細な説明】
:産業上の利用分野=
本発明は、環境上支障のある広範囲の不快臭に対して強
力な消臭作用を発揮する消臭剤に関する。DETAILED DESCRIPTION OF THE INVENTION: Industrial Application Field = The present invention relates to a deodorizing agent that exhibits a strong deodorizing effect against a wide range of unpleasant odors that cause environmental problems.
二従来の技術及びその解決すべき課題〕従来より、各種
産業分野で発生する臭い物質によって作業現場はもとよ
り、周囲の環境も汚染されることが多い。そのため、環
境衛生上、公衆衛生上の幾多の問題が発生している。2. Prior art and its problems to be solved] In the past, not only work sites but also the surrounding environment have often been contaminated by odorous substances generated in various industrial fields. As a result, numerous environmental and public health problems have arisen.
一般に、不快臭の原因物質として多くの物質が知られて
おり、例えば、アンモニア、トリメチルアミン、硫化水
素、メチルメルカプタンなどが有名である。In general, many substances are known to cause unpleasant odors, such as ammonia, trimethylamine, hydrogen sulfide, and methyl mercaptan.
また、不快臭としての汗臭、機具、家畜小屋の臭′7)
、糞便臭などは、単一の原因物質からなるのではなく、
いくつかの原因物質が複合した臭いである。In addition, unpleasant odors such as sweat odor, equipment, and livestock shed odor'7)
, fecal odor, etc. are not caused by a single causative substance;
The odor is a combination of several causative substances.
従来より、主に、原因物質を処理する消臭剤としては、
その原因物質を吸着して消臭する消臭剤と、原因物質に
直接作用してその臭いを破壊又は変化させる消臭剤とが
ある。前者の例としては、活性炭やシリカケルが知られ
ている。一方、後者の消臭剤としては、例えば、各種酸
化物、アルミニウム化合物、亜鉛化合物、金属石鹸、エ
チレングリコール、硼素化合物、フェノール系化合物、
アミン系化合物、サリチル酸系化合物、エステル系界面
活性剤、塩素化合物、アルデヒド系化合物、過酸化物な
どが知られている。Traditionally, deodorants that mainly treat causative substances include:
There are deodorants that deodorize by adsorbing the causative substances, and deodorizers that act directly on the causative substances to destroy or change their odors. Activated carbon and silica gel are known as examples of the former. On the other hand, the latter deodorants include, for example, various oxides, aluminum compounds, zinc compounds, metal soaps, ethylene glycol, boron compounds, phenolic compounds,
Amine compounds, salicylic acid compounds, ester surfactants, chlorine compounds, aldehyde compounds, peroxides, and the like are known.
ところで、原因物質に直接作用して臭いを破壊又は変性
する消臭剤は、一般に特定の原因物質との関係で消臭効
果を有するため、複合的な臭いに対しては、その臭いを
構成する原因物質を検討して、その原因物質に応した消
臭剤を併用することが行われている。By the way, deodorants that directly act on the causative substance to destroy or modify the odor generally have a deodorizing effect in relation to a specific causative substance. The causative agent is examined and a deodorant corresponding to the causative agent is used in conjunction with the causative agent.
しかしながら、併用された消臭剤は、一般に相互にその
消臭効果を相殺する場合が多く、そのため、個々の消臭
剤の量を単独の場合よりも多くしなければならないなど
問題となっていた。この結果、消臭剤のコストが掛かる
など経済面で不利となることが多かった。However, deodorants that are used together often cancel out their deodorizing effects, which has led to problems such as the need to use a larger amount of each deodorant than when used alone. . As a result, there were many economic disadvantages, such as the increased cost of deodorants.
従って、本発明は広範囲の不快臭↓こ対して相乗的シこ
作用し、個々の消臭剤の使用量を減少させても同等の効
果を発揮することのできる消臭剤を提供することを目的
とする。Therefore, the present invention aims to provide a deodorant that has a synergistic effect against a wide range of unpleasant odors and can exhibit the same effect even if the amount of each deodorant used is reduced. purpose.
本発明者は、上記目的を達成するため、鋭意検討した結
果、特定のグリシン誘導体と、茶葉抽出物とから消臭剤
を構成することにより、上記目的を達成できることを見
出し、本発明に到達したものである。In order to achieve the above object, the present inventors have made extensive studies and found that the above object can be achieved by constructing a deodorant from a specific glycine derivative and tea leaf extract, and have arrived at the present invention. It is something.
即ち、本発明は、
(1)一般式(I):
R+ (NHCHzCt(z) fi
(式中、
Roは炭素数8〜16個のアルキル基を示R2は水素原
子又は炭素数8〜16個のアルキル基を示し、
mは1〜4の整数を示し、
nは0.1又は2を示す。)
て表されるグリシン誘導体又はその塩と、(2)茶葉抽
出物と、
を有効成分として含有することを特徴とする消臭剤に関
するものである。That is, the present invention provides the following: (1) General formula (I): R+ (NHCHzCt(z) fi (wherein, Ro represents an alkyl group having 8 to 16 carbon atoms; R2 represents a hydrogen atom or a C 8 to 16 alkyl group; , m is an integer of 1 to 4, n is 0.1 or 2), and (2) a tea leaf extract, as active ingredients. The present invention relates to a deodorant characterized by containing:
以下、本発明について詳細に説明する。The present invention will be explained in detail below.
本発明で使用されるグリシン誘導体は、上記−般式(1
)に示される化合物である。The glycine derivative used in the present invention has the above general formula (1
).
上記式(I)において、R,又はR2としてのアルキル
基の好ましいものとしては、例えば、オクチル基、デシ
ル基、ドデシル基、テトラデシル基、ヘキサデシル基、
オクタデシル基などが挙げられる。In the above formula (I), preferred examples of the alkyl group as R or R2 include an octyl group, a decyl group, a dodecyl group, a tetradecyl group, a hexadecyl group,
Examples include octadecyl group.
また、mとしては、2が好ましく、nとしてはOが好ま
しい。Further, m is preferably 2, and n is preferably O.
グリシン誘導体を塩の形で使用する場合には、塩酸や水
酸化ナトリウムなどとの塩が好ましく使用される。When using glycine derivatives in the form of salts, salts with hydrochloric acid, sodium hydroxide, etc. are preferably used.
上記一般式(I)で示される好ましい具体的化合物とし
ては、例えば、N−オクチルジ(アミノエチル)グリノ
ン、N−Fデシルアミノエチルグリニン、N−ドテシル
シ(アミノエチル)グリシン−NN−ジ(オクチJレア
ミノエチル)グリシン、N−オフタテシルアミノエチル
グリシン及びその塩酸塩、ナトリウム塩が挙げられる。Preferred specific compounds represented by the above general formula (I) include, for example, N-octyldi(aminoethyl)glinone, N-F decylaminoethylglinine, N-dodecylcy(aminoethyl)glycine-NN-di(octylaminoethyl)glycine, J rare aminoethyl) glycine, N-oftatecylaminoethylglycine, and its hydrochloride and sodium salt.
本発明で使用される茶葉抽出物は茶の葉を抽出したもの
からなる。茶葉抽出物は、その濃縮物の形態や、乾燥粉
末の形態なと種々の形態で使用することかできる。The tea leaf extract used in the present invention consists of tea leaves extracted. Tea leaf extracts can be used in various forms, including their concentrate form and dry powder form.
菜の葉としては、一般の茶の葉、例えば、緑茶なとが(
吏用できる。As rape leaves, common tea leaves, such as green tea (
Can be used as an official.
茶葉抽出物は、一般に茶の葉を水とエタノールとの混合
溶媒中に浸漬することにより得られる。Tea leaf extracts are generally obtained by soaking tea leaves in a mixed solvent of water and ethanol.
混合溶媒の割合は一般にエタノール濃度として20〜8
0%が好ましい。浸漬時間は5〜20時間か好ましい。The ratio of the mixed solvent is generally 20 to 8 in terms of ethanol concentration.
0% is preferred. The immersion time is preferably 5 to 20 hours.
浸漬温度は10〜50℃が好ましい。なお、浸漬中、攪
拌をするのが、効率的な抽出法として好ましい。The immersion temperature is preferably 10 to 50°C. Note that stirring during soaking is preferred as an efficient extraction method.
グリシン誘導体と茶葉抽出物との配合割合は一般にIl
l〜500:1、好ましくは10:1〜200 : 1
である。この範囲を外れると、両成分による相乗効果が
得られない。The blending ratio of glycine derivative and tea leaf extract is generally Il.
l~500:1, preferably 10:1~200:1
It is. Outside this range, the synergistic effect of both components cannot be obtained.
なお、上記両成分の他に、必要に応じて水やアルコール
などの溶媒を配合してもよい。In addition to the above-mentioned two components, a solvent such as water or alcohol may be added as necessary.
以下、実施例により更に本発明について詳細に説明する
。Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例 l
不快臭としてのトリメチルアミンに対する本発明の消臭
剤の消臭効果を実験した。Example 1 The deodorizing effect of the deodorant of the present invention on trimethylamine, which is an unpleasant odor, was tested.
グリシン誘導体として、以下の構造式で示すN−ドデシ
ルジ(アミノエチル)グリシン塩酸塩を使用した。As a glycine derivative, N-dodecyldi(aminoethyl)glycine hydrochloride shown by the following structural formula was used.
C1□Hzs(NHCHzCHz)z NHCHzCO
OH−HCl一方、茶葉抽出物として、緑茶(煎茶)2
5gを、水50−とエタノール50−との混合溶媒中に
浸漬し、20時間振盪した後、抽出液を濾過したものを
使用した。C1□Hzs(NHCHHzCHz)z NHCHzCO
OH-HCl On the other hand, as a tea leaf extract, green tea (Sencha) 2
5 g was immersed in a mixed solvent of 50 parts of water and 50 parts of ethanol, and after shaking for 20 hours, the extract was filtered and used.
以下の表−1に示す濃度になるように、グリシン誘導体
と茶葉抽出物とを水に希釈して、120mA容量のバイ
ヤルに3Qmlとなるように入れた。The glycine derivative and the tea leaf extract were diluted with water to the concentrations shown in Table 1 below, and placed in a vial with a capacity of 120 mA at a volume of 3 Qml.
次二二同表−1に示す濃度になるようにトリメチルアミ
ンを加えて、バイヤルを密閉した。Trimethylamine was added to the concentration shown in Table 1, and the vial was sealed.
バイヤルを30℃の水浴に入れて、10分間加温し、バ
イヤルの空間部分(ヘッドスペース)の気体をガスクロ
マトグラフィー(■柳本製作所製のG2800)又は検
知管(@ガスチック製直読式カス採取器)によって消臭
率を測定した。Place the vial in a 30°C water bath, warm it for 10 minutes, and collect the gas in the head space of the vial using gas chromatography (G2800 manufactured by Yanagimoto Seisakusho) or a detection tube (@Gastic direct reading dust collector). ) The deodorization rate was measured.
消臭率は式:
%式%()
て表される。ここて、Aは消臭剤を添加しない場合にお
けるヘットスペース中の臭気成分の量を示し、一方、B
は消臭剤を添加した場合のヘッドスペース中の臭気成分
の量を示す。The deodorization rate is expressed by the formula: % formula % (). Here, A indicates the amount of odor components in the head space when no deodorant is added, while B
indicates the amount of odor components in the headspace when a deodorant is added.
表−1
トリメチルアミン 300ppm
上記表−1より1−リメチルアミンに対してグリシ”a
B誘導体、茶葉抽出物とを単独で使用するよりも、併用
することにより消臭効果が相乗的に現れることか分かる
。Table-1 Trimethylamine 300ppm From the above Table-1, the amount of glycine “a” for 1-limethylamine
It can be seen that the deodorizing effect appears synergistically when the B derivative and tea leaf extract are used together rather than when used alone.
実施例 2
グリシン誘導体として、以下の式:
%式%
て示されるN−)デシル(アミノエチル)グリシンを使
用することを除いて、実施例1と同様にしてトリ、Jチ
ルアミンの消臭率を測定巳た。結果を以下の表−2に示
す。Example 2 The deodorization rate of tri- and J-thylamine was determined in the same manner as in Example 1, except that N-)decyl(aminoethyl)glycine, which is represented by the following formula: % formula %, was used as the glycine derivative. I took the measurements. The results are shown in Table 2 below.
トリメチルアミン
0 ppm
実施例1と同様にして、グリノン誘導体と茶葉抽出物と
も併用することにより、相乗的な消臭効果の得られるこ
とが分かる。Trimethylamine 0 ppm Similarly to Example 1, it can be seen that a synergistic deodorizing effect can be obtained by using the glinone derivative and tea leaf extract together.
実施例 3
不快臭としてメチルメルカプタンを使用し、グリシン誘
導体として以下の弐:
C8H,7NHCH□C112
で示されるN、N−ジ(オクチルアミノエチル)クリノ
ンナトリウムを使用することを除いて実施例1と同様に
しで、不快臭の消臭率を測定した。Example 3 Same as Example 1 except that methyl mercaptan was used as the unpleasant odor and N,N-di(octylaminoethyl)clinone sodium represented by the following 2: C8H,7NHCH□C112 was used as the glycine derivative. Similarly, the rate of deodorization of unpleasant odors was measured.
その結果を以下の1−3に示す。The results are shown in 1-3 below.
表−3
メチルメルカプタン
ppm
上記表−3より、実施例1と同様に、グリシン誘導体と
茶葉抽出物との併用の効果が得られた。Table 3 Methyl mercaptan ppm From Table 3 above, similar to Example 1, the effect of using the glycine derivative and tea leaf extract in combination was obtained.
実施例 4
クリ、/ン誘導体として、以下の弐:
C1o11z+(NHCllzCIMz NHCHzC
OO)I −HCj!て示されるN−デシル(アミノ
エチル)グリシン塩酸塩を使用することを除いて、実施
例3と同様Sこ巳てメチルメルカプタンの消臭率を測定
した。Example 4 The following two derivatives are C1o11z+(NHCllzCIMz NHCHzC
OO)I-HCj! The deodorization rate of methyl mercaptan was measured in the same manner as in Example 3 except that N-decyl (aminoethyl) glycine hydrochloride shown in Table 1 was used.
その端末を以下の表−4に示す。The terminals are shown in Table 4 below.
表−4
メチルメルカプタン
ppm
上記表−4より、実施例3と同様に、グリシン誘導体と
茶葉抽出物との併用効果の得られることが分かる。Table 4 Methyl mercaptan ppm From Table 4 above, it can be seen that similar to Example 3, the combined effect of the glycine derivative and tea leaf extract can be obtained.
実施例 5
不快臭として酪酸を使用し、グリシン誘導体とじて、以
下の式:
%式%
で示されるN−オクタデシルジ(アミノエチル)グリフ
゛ンを使用したことを除いて、実施例1と同様にして酪
酸の消臭率を測定した。その結果を以下の表−5に示す
。Example 5 The same procedure as in Example 1 was carried out, except that butyric acid was used as the unpleasant odor, and N-octadecyl di(aminoethyl)glyphin represented by the following formula: % formula % was used as the glycine derivative. The deodorization rate of butyric acid was measured. The results are shown in Table 5 below.
ppm
上記表−5より、酪酸に対する相乗的な消臭効果の得ら
れることが分かる。ppm From Table 5 above, it can be seen that a synergistic deodorizing effect with respect to butyric acid can be obtained.
実施例 6
クリシン誘導体として、以下の式:
%式%
で示されるN−オクタデシルジ(アミノエチル)り11
ノンナトリウムを使用することを除いて、実りト例5と
同様にして酪酸の消臭率を測定した。その結果を以下の
表−6に示す。Example 6 As a chrysin derivative, N-octadecyl di(aminoethyl) 11 represented by the following formula: % formula %
The deodorization rate of butyric acid was measured in the same manner as in Example 5 except that non-sodium was used. The results are shown in Table 6 below.
表 上記表 6より、 クリシン誘導体と茶葉抽出物 酪 酸 ppm とを併用することにより、 実施例5と同様に相乗 的な消臭効果の得られることか分かる。table Above table From 6, Chrysin derivatives and tea leaf extracts Dairy acid ppm By using in combination with Synergistic as in Example 5 You can see that it has a deodorizing effect.
平成 年 月 日Heisei Year Month Day
Claims (1)
は水素原子又は炭素数8〜16個のアルキル基を示し、 mは1〜4の整数を示し、 nは0、1又は2を示す。) で表されるグリシン誘導体又はその塩と、 (2)茶葉抽出物と、 を有効成分として含有することを特徴とする消臭剤。[Claims] The following components: (1) General formula (I): R_1(NHCH_2CH_2)_m > NCH_2COOH(I) R_2(NHCH_2CH_2)_n (wherein R_1 represents an alkyl group having 8 to 16 carbon atoms; Indicates, R_2
represents a hydrogen atom or an alkyl group having 8 to 16 carbon atoms, m represents an integer of 1 to 4, and n represents 0, 1 or 2. A deodorant characterized by containing as active ingredients a glycine derivative or its salt represented by (2) a tea leaf extract.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2120477A JPH0417857A (en) | 1990-05-10 | 1990-05-10 | Deodorant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2120477A JPH0417857A (en) | 1990-05-10 | 1990-05-10 | Deodorant |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0417857A true JPH0417857A (en) | 1992-01-22 |
Family
ID=14787148
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2120477A Pending JPH0417857A (en) | 1990-05-10 | 1990-05-10 | Deodorant |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0417857A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009263315A (en) * | 2008-04-30 | 2009-11-12 | Mandom Corp | Antibacterial composition and composition for deodorizer |
-
1990
- 1990-05-10 JP JP2120477A patent/JPH0417857A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009263315A (en) * | 2008-04-30 | 2009-11-12 | Mandom Corp | Antibacterial composition and composition for deodorizer |
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