WO2008029822A1 - Deodorant comprising deodorizing substance originating in sugarcane distillate as the active ingredient and method of improving odor originating in sugarcane - Google Patents

Deodorant comprising deodorizing substance originating in sugarcane distillate as the active ingredient and method of improving odor originating in sugarcane Download PDF

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Publication number
WO2008029822A1
WO2008029822A1 PCT/JP2007/067255 JP2007067255W WO2008029822A1 WO 2008029822 A1 WO2008029822 A1 WO 2008029822A1 JP 2007067255 W JP2007067255 W JP 2007067255W WO 2008029822 A1 WO2008029822 A1 WO 2008029822A1
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WIPO (PCT)
Prior art keywords
deodorant
odor
volume
water
sweet potato
Prior art date
Application number
PCT/JP2007/067255
Other languages
French (fr)
Japanese (ja)
Inventor
Masami Mizu
Hisanori Nakajima
Masahiro Okuno
Jun Kashimura
Original Assignee
Mitsui Sugar 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 Mitsui Sugar Co., Ltd. filed Critical Mitsui Sugar Co., Ltd.
Publication of WO2008029822A1 publication Critical patent/WO2008029822A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/01Deodorant compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9706Algae
    • A61K8/9717Rhodophycota or Rhodophyta [red algae], e.g. Porphyra
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9755Gymnosperms [Coniferophyta]
    • A61K8/9767Pinaceae [Pine family], e.g. pine or cedar
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9789Magnoliopsida [dicotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9794Liliopsida [monocotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00Anti-perspirants or body deodorants
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0068Deodorant compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/382Vegetable products, e.g. soya meal, wood flour, sawdust
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/04Preparations for permanent waving or straightening the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/06Preparations for styling the hair, e.g. by temporary shaping or colouring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners

Definitions

  • the present invention relates to a deodorant comprising a sweet potato-derived deodorant as an active ingredient, and more specifically, a sweet potato-derived odor derived from a sweet potato juice or a distillate obtained by distillation of a sweet potato solvent extract.
  • the present invention relates to a deodorant containing an improved deodorant substance as an active ingredient. Furthermore, this invention relates to the method of improving the odor derived from sweet potato.
  • the plant such as leaves, stems, and skins that are cultivated, is dried. After roasting, it is necessary to crush and extract with organic solvent and / or water, and there is a problem that its production cost is higher than that of chemically synthesized products that are mass-produced.
  • brown sugar is said to have a deodorizing effect on odors such as fishy odor when cooking.
  • brown sugar is a saccharide, and there is a problem that its own odor or taste (sweetness) is strong.
  • odors such as fishy odor
  • sweetness a problem that its own odor or taste (sweetness) is strong.
  • brown sugar is required, or it itself decays due to microorganisms, and on the contrary, it becomes a causative substance of bad odor.
  • There was a problem in using as a deodorant
  • the applicant of the present invention has proposed a deodorant substance obtained by treating a raw material selected from sweet potato juice and molasses derived from sweet potato with column chromatography, and an odor source containing a distillate derived from sweet potato as an active ingredient. Odorants were reported (Patent Documents 11 to 13).
  • the deodorizing substance and the deodorant are colorless or light yellow and do not have a strong odor per se.
  • the deodorizing substance and the deodorant have various and excellent effects.
  • the deodorant and deodorant have almost no odor when diluted to the use concentration, or have no strong odor! /, Odor! / As a result, there is a case where the user who is sensitive to the unique odor derived from sweet potato is uncomfortable.
  • the unique odor becomes a problem. A plan was desired.
  • Patent Document 14 As one of the measures for improving the unique odor, there has been reported a method for improving the odor of the deodorant by adding plant essential oil and / or essence to the deodorant (Patent Document). 14). Specifically, the addition of chamomile oil, citronella oil, bergamot oil, peppermint oil, melissa oil, lavender oil as essential oils, and orange fluff, chamomile, and melissa as essences are considered to be effective in improving the odor of the deodorant. ing.
  • the above improvement measures mask the odor derived from sweet potato by the plant essential oil and / or essence, and are limited to applications where the plant essential oil and / or essence can be added.
  • consumer interest is not limited to deodorization or deodorization, and there is a growing trend toward preference for odorless or fragrance-free products.
  • the use of essential oils or essences or fragrances is also a problem and tends to be avoided by consumers. Therefore, it is desired to develop a method for improving the unique odor derived from sweet potato without reducing the effective components such as the deodorizing effect of the deodorant and deodorant.
  • the active ingredient of a deodorant / deodorant is an odorous ingredient, and particularly, it is often seen as an active ingredient of a naturally-derived deodorant / deodorant. For this reason, odor cannot be eliminated or treated with ordinary distillation or various adsorbents such as activated carbon, activated clay, strong acid type, or anion type ion exchange resin, or the odor is reduced and deodorized. Deodorant's deodorant with no fragrance or odor It is difficult to manufacture!
  • Patent Document 1 Japanese Patent Application Laid-Open No. 62-211068
  • Patent Document 2 JP-A-60-7848
  • Patent Document 3 JP-A-60-185558
  • Patent Document 4 JP-A-60-207664
  • Patent Document 5 JP-A-61-106163
  • Patent Document 6 Japanese Unexamined Patent Publication No. 63-21060
  • Patent Document 7 Japanese Patent Laid-Open No. 60-214726
  • Patent Document 8 Japanese Patent Laid-Open No. 61-87562
  • Patent Document 9 JP-A-2-284997
  • Patent Document 10 Japanese Patent Laid-Open No. 7-33636
  • Patent Document 11 JP-A-10-151182
  • Patent Document 12 Japanese Patent Laid-Open No. 11-187825
  • Patent Document 13 Japanese Patent Laid-Open No. 2001-87365
  • Patent Document 14 Japanese Patent Laid-Open No. 2001-224673
  • the present invention is a deodorant substance with an improved odor derived from sweet potato, particularly derived from a distillate (sweet potato distillate) obtained by distilling a sweet potato juice or a sweet potato solvent extract.
  • the present invention provides a deodorant containing as an active ingredient. Furthermore, the present invention provides a method for improving the odor derived from sweet potato.
  • the present invention is a deodorant comprising a sweet potato-derived deodorant as an active ingredient, and the sweet potato-derived deodorant distilled a sweet potato juice or a sweet potato solvent extract (hereinafter referred to as the distillation).
  • the distillation With primary distillation
  • the distillate is referred to as a primary distillate
  • the fraction obtained by the treatment or the fraction Water in minutes Or when the mixture containing alcohol / water mixture is further distilled hereinafter referred to as secondary distillation
  • the alcohol concentration (volume / volume) in the kettle is 0% to 10%.
  • the present invention also provides a deodorant that is the residue of the kettle when the secondary distillation is completed (hereinafter sometimes referred to as the deodorizer of the present invention).
  • the deodorizer of the present invention has the original excellent deodorizing effect of the primary distillate, and the odor derived from sweet potato is improved.
  • the present invention also relates to a method for improving the sweet potato-derived odor of a distillate (primary distillate) obtained by distillation (primary distillation) of a sweet potato juice or a sweet potato solvent extract, wherein the primary distillate is fixed.
  • a distillate primary distillate obtained by distillation (primary distillation) of a sweet potato juice or a sweet potato solvent extract, wherein the primary distillate is fixed.
  • the method of the present invention surprisingly improves the sweet odor derived from sweet potato without reducing the original excellent deodorizing effect of the primary distillate.
  • the deodorant of the present invention and the deodorant obtained according to the method of the present invention are inherently excellent deodorants possessed by primary distillates. It has an effect, and the unique odor derived from sweet potato is improved. Therefore, even if the deodorant of the present invention is used for foods or cosmetics, it does not have a sweet odor derived from sweet potato, so it can be used as a fragrance-free or odorless deodorant-deodorant. The feeling can be satisfied. Furthermore, since the deodorant of the present invention can be produced using a sugar production or refined sugar process, the production cost is low.
  • FIG. 1 is a diagram showing the deodorizing effect of the deodorant of the present invention on hydrogen sulfide.
  • the odor derived from sweet potato is improved or the odor derived from sweet potato is improved.
  • the odor of the primary distillate in the present invention is reduced compared to the odor of the sweet potato, or the odor of the sweet potato is finally perceivable, or! I can't feel it.
  • the odor derived from sweet potato can be measured, for example, according to the odor intensity evaluation method described in Example 2 below. According to the evaluation method described in Example 2, the odor derived from sweet potato was improved when the intensity (2, 1, 0) was lower than the odor intensity of the primary distillate (determined to be 3). Evaluation 2 is weaker than the primary distillate, but the odor can be easily detected. Evaluation 1 is barely noticeable, and evaluation 0 is odorless.
  • the primary distillate in the present invention can be used as a stock solution for secondary distillation.
  • a primary distillate if it is a distillate obtained by distilling a sweet potato juice or a sweet potato solvent extract, it is a publicly known product having various forms obtained by various production methods with no particular restrictions on its production method, form, etc. Can be used (see, for example, Patent Document 13).
  • the sweet potato soup in the present invention is a squeezed juice obtained by squeezing sweet potato (sugar cane), a leached juice obtained by leaching sweet potato with water, or a lime-treated clean juice obtained from a raw sugar manufacturing plant. And concentrated juice.
  • the sweet potato solvent extract in the present invention means an extract obtained by extracting sweet potato with a general-purpose organic solvent. Examples of the organic solvent include alcohols such as methanol and ethanol, and these may be used alone or in combination. Furthermore, these solvents and water may be used in combination.
  • the primary distillate in the present invention can be obtained, for example, according to the following method or according to the method described in Patent Document 13 above.
  • the sweet potato soup or the sweet potato solvent extract is placed in a tank having a heating device and heated, and the resulting steam is recovered by cooling to obtain a liquid sweet potato-derived distillate.
  • a heating device any apparatus that has a heating device and can cool and recover the vapor as a liquid can be used.
  • the distillation conditions for obtaining the primary distillate may be 50 ° C to 120 ° C at a pressure at which the primary distillate boils. Preferably, it can be performed at a pressure of 70 ° C. to 120 ° C. at which the primary distillate boils.
  • the pressure is appropriately adjusted according to the solvent used for extraction and the apparatus used in the distillation step. For example, in the case of using water as an extraction solvent and distilling using a centrifugal thin film vacuum evaporator, a flask connected to a condenser, or a distillation machine, 70 to 105; At ° C, it is 240mmHg to normal pressure. It is also possible to carry out distillation at lower temperatures and pressures.
  • the primary distillate must be condensed in the trap below the distillation temperature. Is too expensive. Therefore, it is possible in the laboratory, but not industrially suitable.
  • high-temperature heating at 130 ° C or higher is not performed.
  • a distillation apparatus for example, a flask connected to a cooling pipe or the like is used in a laboratory, and a concentration can, a crystal can, a utility can, or the like is used in a factory. By adjusting these temperature and pressure conditions, the ratio of the sweet potato-derived deodorant substance to water (if water is included) can be changed to obtain a primary distillate with the desired concentration.
  • a fraction obtained by treating the above primary distillate by column chromatography using a fixed carrier, or a mixed solvent of water or alcohol-water is added to the fraction. Use the resulting mixture.
  • the components of the primary distillate can be concentrated.
  • a commercially available product can be used as the stock solution for secondary distillation in the present invention, and for example, an extract derived from sweet potato manufactured by Mitsui Sugar Co., Ltd. (corresponding to a primary distillate) is suitable.
  • an extract derived from sweet potato manufactured by Mitsui Sugar Co., Ltd. corresponding to a primary distillate
  • “sugar cane extract MSX_245” ethanol concentration 45% (volume / volume)) (manufactured by Mitsui Sugar Co., Ltd.), which is a sweet potato distillate.
  • Sugar cane extract MSX_245 is a product obtained by adjusting the alcohol concentration by adding a mixed solvent of alcohol and water to the fraction obtained by treating the primary distillate with column chromatography using a fixed carrier. It is.
  • the primary distillate can be passed through a column packed with a fixed carrier as it is or in order to adjust the alcohol concentration, the primary distillate is adjusted to an arbitrary concentration with water.
  • the water added to the primary distillate may be tap water, but pure water (that is, ion-exchanged water) or distilled water is more preferable for high-level distillation treatment for removing odor.
  • the alcohol concentration (volume / volume) of the primary distillate is the desired deodorant in the primary distillate.
  • the content is preferably adjusted to 10% or less 0% or more, more preferably 5% or less 0% or more.
  • the column chromatography treatment uses a column packed with a synthetic adsorbent as a fixed carrier.
  • the target sample is passed through the column, and the components adsorbed on the synthetic adsorbent are mixed with methanol. And eluting with a solvent selected from ethanol, and a mixture of water, methanol, and ethanol.
  • a synthetic adsorbent is preferable.
  • an organic resin can be preferably used.
  • an aromatic resin an acrylic acid-based methacrylic resin, an acrylonitrile fatty resin, or the like can be used.
  • such synthetic adsorbents are commercially available, for example, HP-10, HP-20, HP-21, HP-30, HP-40, HP-50 (and more, no substitution) Basic type aromatic resins, all trade names, manufactured by Mitsubishi Chemical Corporation); SP—825, SP—800, SP—850, SP—875, SP—70, SP—70 0 (or more, unsubstituted) SP-900 (Aromatic resin, trade name, manufactured by Mitsubishi Chemical Corporation); Amberlite (trademark) ), XAD-2, XAD-4, XAD-16, XAD-2000 (above, aromatic resins, all trade names, manufactured by Organo Corporation); Diaion (trademark) system, SP-205, SP — 206, SP— 207 (Aromatic resin having hydrophobic substituents, both trade names, manufactured by Mitsubishi Chemical Corporation); HP—2MG, EX—0021 (above Aromatic resins with hydrophobic substituents, all trade names, manufactured by Mitsubishi Chemical Corporation); Amberlite (trademark), XAD-7HP, XAD
  • the amount of the fixed carrier varies depending on the size of the column, the type of the solvent, the type of the fixed carrier, and the like.
  • primary distillate for example, 100 to 20,000 times distillation of fixed carrier
  • the substance is passed through and the active ingredient is adsorbed on the fixed carrier.
  • a primary distillate of 2,000 to 20,000 times that of the fixed carrier is passed through to adsorb the active ingredient onto the fixed carrier. Therefore, it is preferable to use a fixed carrier having a wet volume of 1/100 to 20,000 times that of the primary distillate to be passed. It is preferable to use a fixed carrier having a wet volume of 2,000 to 20,000 times that of the primary distillate to be passed.
  • the deodorizing substance in the primary distillate is adsorbed on the fixed carrier.
  • the flow rate and flow rate vary depending on the distillation method of the primary distillate. If the primary distillate contains alcohol, it is necessary to dilute this liquid with water and then pass it through the column chromatography. It is preferable to wash the column with water in order to remove impurities after removing the liquid-flowing object through the column, and remove components remaining in the column without being adsorbed by the resin.
  • the component adsorbed on the fixed carrier is eluted with a solvent.
  • the elution solvent is selected from methanol, ethanol, and a mixture of water, methanol, and ethanol.
  • the elution solvent is preferably a mixed solvent of water and alcohol, particularly an ethanol / water mixed solvent.
  • a 50/50 to 99.5 / 0.5 (volume / volume) ethanol / water mixed solvent is preferable.
  • the deodorizing component of the primary distillate is present in the fraction eluted with the solvent.
  • SV Space Velocity
  • SV Space Velocity
  • the column chromatography treatment of the primary distillate is not limited to this, but it can be preferably performed as follows. That is, after passing an object to be passed through a column packed with an unsubstituted aromatic resin or acrylic ester resin at a column temperature of 60 to 97 ° C, the inside of the column was washed with water, Next, the components adsorbed on the column are eluted with 50/50 to 99.5 / 0.5 (volume / volume) ethanol / water mixed solvent at a column temperature of 20 to 40 ° C. and mixed with ethanol / water mixed solvent. Collect the eluate that elutes within 6 times the wet volume of the resin from the elution start time at (5).
  • the eluate (including the elution solvent) obtained from the column is adjusted as it is, or adjusted to a suitable alcohol concentration with water or a mixed solvent of alcohol water, and the stock solution for secondary distillation in the present invention.
  • Alcohol may be any commercially available alcohol or food additive, but it has a high degree of distillation to remove odors. A special grade of JIS standard is preferable.
  • the alcohol may be any water-soluble alcohol such as methanol, ethanol, propanol, or a mixture thereof, but ethanol is optimal in view of food use and safety.
  • the alcohol concentration of the stock solution when starting the secondary distillation is preferably more than 0% to 60% or less, more preferably more than 0% to 20% or less, and still more preferably 0 % To 10% or less, or 5% to 60%, more preferably 5% to 20%, and still more preferably 5% to 10%.
  • the secondary distillation in the present invention refers to secondary distillation (or evaporation) of the above-mentioned secondary distillation raw material using a heating device or the like.
  • Heating devices, etc. can be used industrially, and can use a distillation column or distiller, concentrator, evaporator, container with heating device or kettle. It is preferable to use a centrifugal thin film vacuum evaporator in terms of manufacturing, quality and cost.
  • the treatment method of distillation (evaporation) may be either a batch method, a continuous method, or a combination thereof.
  • the distillation temperature (vapor temperature or product temperature) and pressure conditions are 90 ° C to 105 ° C under normal pressure, and 34 to 90 ° C under reduced pressure (vacuum). Any can be used, but preferably under reduced pressure (steam pressure 90mmHg The following should be distilled in the range of 34-40 ° C.
  • the alcohol concentration (volume / volume) of the residue in the kettle is 0 to 10%
  • the concentration rate of the primary distillate is 20% (volume) or more with respect to the liquid volume before distillation ( See Example 5 below, fraction 3 in Table 2), preferably 30% (volume) or more, more preferably 40% (volume) or more
  • the odor derived from sweet potato is distilled while the deodorant substance is Since it remains in the pot residue, it can remove the odor derived from sweet potato well.
  • the odor intensity of the residue (that is, the deodorant of the present invention) is 2 (weaker than the stock solution, but can be easily detected by following the method for evaluating the odor intensity derived from sweet potato described in Example 2 below. ) Or less, preferably 1 (finally perceptible) or less, more preferably 0 (odorless).
  • the alcohol concentration (volume / volume) of the residue in the kettle is 0 to 5%, and the concentration rate of the primary distillate is 40% (volume) or more with respect to the liquid volume before distillation (see below).
  • Example 5 see fraction 5 in Table 2), preferably more than 50% (volume), more preferably more than 60% (volume), the odor derived from sweet potato is almost completely distilled while deodorizing substances Since it remains in the pot residue, the odor derived from sweet potato can be removed even better.
  • the odor intensity of the residue (that is, the deodorant of the present invention) is 0 (odorless) according to the method for evaluating odor intensity derived from sweet potato described in Example 2 below.
  • the solvent of the primary distillate in the present invention has an alcohol concentration (volume / volume) of 10% or more, it is diluted with water, for example, in Example 2, the primary distillate (ethanol 59% by weight) is 20%. It may be used for secondary distillation after being diluted to% by weight or after being subjected to a concentration treatment.
  • the deodorant of the present invention has a unique odor component derived from sweet potato removed, and the deodorizing effect of the primary distillate is hardly reduced. Therefore, the deodorant substance of the present invention is considered to have no masking action. Neutralization, decomposition, oxidation and reduction of chemical deodorizing mechanism, adsorption of physical deodorizing mechanism, and offsetting effect of sensory deodorizing mechanism. It is thought that it has a deodorizing action by a complex mechanism.
  • the deodorant of the present invention can contain a deodorant other than the deodorant of the present invention (other deodorant) in addition to the deodorant of the present invention.
  • a deodorant other than the deodorant of the present invention other deodorant
  • Use the deodorant of the present invention in combination with other deodorants As a result, the deodorizing power of these components is enhanced, and a deodorant having both rapid efficacy and sustainability is obtained.
  • the type of the other deodorant is not particularly limited.
  • One or two or more types of deodorant components selected from plant extracts, organic compounds, inorganic compounds, etc. other than the deodorant of the present invention are used. More specifically, for example, sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, sodium bicarbonate, sulfuric acid, hydrochloric acid, phosphoric acid, sulfamic acid, oxalic acid, sorbic acid, Humic acid, Ascorbic acid, Malic acid, Methyl malic acid, Malonic acid, Succinic acid, Alkenyl succinic acid, Gnoretanolic acid, Adipic acid, Pimelic acid, Fumanoleic acid, Maleic acid, Methyl fumaric acid, Methyl maleic acid, Itaconic acid, Citracon Acid, mesaconic acid, acetylenic acid, succinic acid, iso-succinic acid, glycolic acid, tartaric
  • Zinc compounds such as zinc phosphate, zinc nitrate, zinc carbonate, zinc acetate, zinc oxalate, zinc citrate, zinc fumarate, zinc formate, zinc lactate, zinc gnoleconate and zinc ricinoleate. These can be used singly or in appropriate combination of two or more.
  • the deodorant of the present invention can contain any component other than the above essential components as needed, as long as the effects of the present invention are not hindered.
  • water and / or organic solvents for example, alcohols such as ethanol and isopropyl alcohol, hydrophilic organic solvents such as ketones such as acetone, various solvents such as hydrophobic organic solvents such as hexane and petroleum ether, Surfactant, lower alkylbenzene sulfonic acid or its salt formulated to maintain liquidity at low or high temperatures, hydrotropes such as ethylene glycol, bactericides, antiseptics and fungicides, fragrances, pigments , Antioxidants, thickeners, gelling agents, ultraviolet absorbers, and the like, and these can be formulated in ordinary doses in a range that does not interfere with the effects of the present invention.
  • the compounds used for these optional components are not particularly limited as long as they are usually used for deodorants.
  • the use of the deodorant of the present invention is not particularly limited.
  • Various dosage forms such as can be selected depending on the application, and the production method can also be produced using components commonly used depending on each application and dosage form.
  • the deodorant of the present invention is a food, etiquette deodorant, pet deodorant, environmental deodorant, deodorant cleaning agent, cosmetic, and other deodorant and fragrance as a raw material for the deodorant composition. , Alcohols, surfactants, fats and oils, fatty acids, esters, saccharides, zinc compounds, organic acids, inorganic acids, alkalis, and the like.
  • the use form of the deodorant of the present invention is not particularly limited, and for example, it can be used in the following form.
  • Deodorant with a deodorizing effect put the deodorant into a porous container such as ceramics, and the deodorant with a deodorizing effect by liquidizing the deodorant penetrated to the outside of the container, liquid Deodorant added directly to malodorous source, deodorant soaked in sheet 'film' filter, wallpaper containing deodorant on the surface or inside, building materials, diapers, sanitary products, insole of shoes, deodorant fiber Can be used for (cloth), deodorant leather, etc.
  • deodorizer of the present invention are commonly used additives and dispersions in each field. Agents, excipients, etc. can be included.
  • the deodorant of the present invention can be added to foods to remove unpleasant odors of the food material, for example, meat, seafood, vegetables such as Yura or garlic.
  • the deodorizer of this invention can be used as a raw material of an etiquette deodorizer.
  • the etiquette deodorant in the present invention is a deodorant used directly for humans, such as bad breath, body odor such as armpit (for body), foot odor, hair odor and the like.
  • This deodorant application is It is meant to be used directly on humans regardless of source. Specifically, underarm sweat odor spray lotion powder, mouth odor removal mouse spray 'capsule' mouthwash, hair spray to remove roasted meat or tobacco odor on hair 'shampoo' rinse 'hair one lotion Etc.
  • the deodorant of the present invention can also be used as a material for pet deodorants.
  • the pet deodorant of the present invention is a deodorant for unpleasant odors originating from pet animals, such as halitosis, body odor, and fecal odor of pet animals.
  • pet breath removal sprays' capsules, pet sprays that remove body odor from hair, shampoos, rinses, lotions, pet toilets, kennels or pet cages, pets themselves and pet supplies Can be mentioned.
  • the deodorizer of this invention can be used also as a raw material of an environmental deodorizer.
  • a mist spray type deodorant for domestic pet odor using the deodorant of the present invention more specifically, the following method can be used. Add the deodorant of the present invention to water at a concentration of 0.01 to 50% (volume / volume), and if necessary, add a surfactant, ethanol or antibacterial agent, and fill the mist spray bottle. To do.
  • the environmental deodorant of the present invention is a deodorant for an unpleasant odor attached to an object or space other than a human or a pet animal. Specifically, disposal of household waste or industrial waste storage site, household waste or industrial waste collection site, household waste or industrial waste collection site, waste collection site, household waste or industrial waste disposal site, etc. Offensive odors from sources, sewage treatment plants, human waste treatment plants, crematoriums, slaughterhouses, animal slaughterhouses, hospitals, clinics, inspection centers, toilets, bathrooms, bathrooms, etc.
  • the environmental deodorant of the present invention uses the environmental deodorant of the present invention to prepare a play type deodorant. Add the environmental deodorant of the present invention to water at a concentration of 0.01 to 50% (volume / volume). If necessary, add a surfactant, ethanol or antibacterial agent to the mist spray bottle. Fill.
  • the environmental deodorant of the present invention is diluted with water or an aqueous ethanol solution to a concentration of 0.2 to 70% (volume / volume) and filled into an aerosol container together with a propellant gas (for example, LPG and carbon dioxide).
  • a propellant gas for example, LPG and carbon dioxide
  • the active component of the deodorant is gradually volatilized, and a deodorant for space that maintains the deodorizing effect for a long period of time. More specifically, the following method can be used for the preparation.
  • the deodorant of the present invention at a concentration of 0.5 to 20% by weight, which is a gelling agent such as carrageenan, agar, locust bean gum, polyburu alcohol, gum arabic, dielan gum, gelatin, carboxymethylsenololose, chitin 'chitosan, Add sodium alginate, polyacrylamide, etc. alone or in combination to a solid gel.
  • the environmental deodorant of the present invention can be deodorized in a space by making it into a fine mist and scattering it in a space such as a building, a room, a car, or a factory. More specifically, the deodorizer of the present invention is added to a humidifier, a sprayer (for example, a device that sprays from a nozzle using a pressurizing device), etc. in an amount of 0.0;! To 20%, preferably 0.01 to 10%, more preferably 0.01-; 1% (volume / volume) concentration added to water, and if necessary, by adding a surfactant, ethanol, antibacterial agent, etc. The odor inside can be deodorized.
  • a humidifier for example, a device that sprays from a nozzle using a pressurizing device
  • a sprayer for example, a device that sprays from a nozzle using a pressurizing device
  • the deodorant of the present invention is in a concentration of 0.0 ;! to 20%, preferably 0.01 to 10%, more preferably 0.0;! To 1% (volume / volume) with water. It is preferable to dilute and use.
  • the environmental deodorant of the present invention is produced from pigs, dairy farms, poultry farms, etc. Odor can be reduced by spraying the mixture on a field or pasture with a vacuum car or the like. Odor can be suppressed by adding the environmental deodorant of the present invention to the urine in the tank at a concentration of 0.005-0. 5% (volume / volume) before spraying.
  • the excreta treating agent for pets is mainly bentonite, zeolite, wood powder, paper powder, etc., and sodium polyacrylate, other sodium compounds, magnesium compounds, etc. are added to this as necessary, and the present invention is added thereto.
  • 10% by weight of the deodorant of the main material is added to the main material, and an appropriate amount of water is added, followed by mixing and “molding” drying.
  • the deodorant cleaning agent of the present invention contains the deodorant of the present invention, has a deodorizing means for malodorous substances, and further contains a surfactant.
  • the surfactant used in the present invention is not particularly limited, but in consideration of safety to human bodies, pets, etc., monoglycerin esters, polyglycerin esterols and sonorebitans listed in the official food additive regulations. Estenole, propyleneglycoloneestre, sucrose esterole, saponin, and lecithin are preferred.
  • the blending amount of these surfactants is preferably 0.1% to 5.0%, more preferably 0.;! To 3.0%, based on the total amount of the deodorant cleaning agent. That's right. If the blending amount is less than 0.1%, the detergency is poor, and if it exceeds 5.0%, the stability of the product may be deteriorated.
  • the deodorant cleaning agent of the present invention is selected and added as desired from among additive components commonly used in ordinary cleaning agents as long as the object of the present invention is not impaired. May be.
  • additive components include a cosmetic raw material standard listed component such as a liquid stabilizer such as ethanol, ethylene glycol, propylene glycol, and sorbitol, and polyoxyethylene isostearyl ether having an average addition mole number of 5 to 10.
  • a cosmetic raw material standard listed component such as a liquid stabilizer such as ethanol, ethylene glycol, propylene glycol, and sorbitol, and polyoxyethylene isostearyl ether having an average addition mole number of 5 to 10.
  • foaming agents antibacterial agents, bactericides, fragrances, dyes, antioxidants, thickeners, gelling agents, ultraviolet absorbers, ion-exchanged water, and barley stone water, which have relatively secured properties.
  • the usage form of the deodorant cleaning agent of the present invention is not particularly limited, but it is preferable to use a spray type (trigger type, dispenser type, aerosol).
  • the foam form is provided with foaming means such as an aerosol type by mixing with LPG.
  • the foam form is a foam that is stable for a long time, specifically, a foam having good shape retention.
  • it is desirable that the foam is shaken once and foamed, and the stable foam is foamed again even if the aerosol can is left as it is for about 1 minute.
  • a soft brush with bristle feet it is desirable to use a soft brush with bristle feet.
  • the cosmetic of the present invention contains the deodorant of the present invention as a deodorant component and does not impair the effects of the present invention! /, Within the range, if necessary, a perfume and / or an inorganic ultraviolet scattering agent (for example, fatty acid soap, fatty acid, fatty acid ester, titanium oxide, zinc oxide), deodorants other than the deodorizer of the present invention, and ingredients used in cosmetics (for example, moisturizers, antioxidants, oil components, emulsifiers) , Surfactants, thickeners, alcohols, powder components, coloring materials, aqueous components, water, various skin nutrients, etc.) can be added as necessary.
  • a perfume and / or an inorganic ultraviolet scattering agent for example, fatty acid soap, fatty acid, fatty acid ester, titanium oxide, zinc oxide
  • deodorants other than the deodorizer of the present invention for example, moisturizers, antioxidants, oil components, emulsifiers
  • ingredients used in cosmetics for example, moisturizers,
  • edetate disodium, edetate trisodium, sodium citrate, sodium polyphosphate, sodium metaphosphate, darconic acid, malic acid and other metal sequestering agents caffeine, tannin, verapamil, tranexamic acid, And derivatives thereof, licorice extract, glabrizine, hot water extract of carin fruit, various herbal medicines, tocophenol acetate, glycyrrhizic acid, and derivatives thereof or salts thereof, retinoic acid, retinol, retinol acetate, pyroion Agents such as acid retinol, retinol normitate, and derivatives or salts thereof, whitening agents such as vitamin C, magnesium ascorbate phosphate, darcoside ascorbate, arbutin, kojic acid, funolectus, mannose, erythritole, trehalose, xylitol Sugars, arginine, amino acids such as
  • the cosmetic of the present invention can be widely applied to cosmetics, pharmaceuticals, and quasi-drugs applied to the outer skin.
  • the dosage form can be any drug formulation, including solution systems, solubilization systems, emulsification systems, powder dispersion systems, oil / oil two-layer systems, oil / oil powder three-layer systems, gels, aerosols, mists, and Can be provided in any form such as a capsule
  • the use form is also arbitrary, and conventional cosmetics such as sunscreens, foundations, emulsions, creams, lotions, sprays, mousses, jewels, hair shampoos, hair rinses, hair treatments, and lipsticks. It can be used in any form as long as it is used.
  • the ethanol concentration (volume / volume) of the obtained eluate (hereinafter also referred to as the primary distillate 2 stock solution) was 59%, and its color was transparent with a slight lemon color.
  • Primary distillate 2 had a unique odor derived from sweet potato.
  • the primary distillate 2 was diluted with water so as to have an ethanol concentration (volume / volume) force of 3 ⁇ 40% (stock solution).
  • 100 kg of the solution was supplied to a centrifugal thin film vacuum evaporator (trade name: Evapol CEP-5, Okawara Seisakusho Co., Ltd.) at a speed of 300 L / hour.
  • the pressure inside the can of the apparatus was controlled to 90 mmHg (reduced pressure) or less, and distillation was carried out at a temperature (product temperature) of 34 to 40 ° C.
  • the residue in the kettle reached approximately 37 kg, distillation was terminated and the residue was collected (referred to as the fraction obtained in Example 1).
  • the residue was a pale yellow liquid.
  • the ethanol concentration of the residue in the kettle was measured with an alcohol densitometer, it was 5.1% (volume / volume).
  • the ethanol concentration of the fraction was adjusted to 45% (volume / volume) with a mixed solution of ethanol and water, and the weight was 100 kg before distillation.
  • the solution was put into a tightly-sealed container (300 ml flask with a stopper), shaken gently, and immediately, the odor intensity in the container was sensory-evaluated according to the following evaluation criteria by 4 to 7 skilled panelists.
  • the primary distillate 2 (stock solution) obtained in Production Example 2 was adjusted to an ethanol concentration of 45% (volume / volume), and the odor intensity of the comparative control was set to 3.
  • Example 3 As a result of the sensory evaluation, the average value of the odor intensity of the fraction obtained in Example 1 was 0. Therefore, the odor of the fraction obtained in Example 1 was improved compared to the primary distillate 2.
  • Example 3
  • the pressure in the concentration can of the apparatus was controlled to 90 mmHg (reduced pressure) or less, and the temperature (product temperature) was distilled at 34 to 40 ° C.
  • the kettle residue reached approximately 113 kg, distillation was terminated and the kettle residue was recovered. The residue was almost colorless to light yellow liquid. Further, when the ethanol concentration of the residue was measured with an alcohol concentration meter, it was 3.5% (volume / volume).
  • the average value of odor intensity was 1. Therefore, the odor of the residue was improved compared to the stock solution.
  • the ethanol concentration was measured with an alcohol densitometer for each of the fractions !-11. Moreover, the odor derived from sweet potato was evaluated for each of fractions 1 to 11; The ethanol concentration of each of the fractions was adjusted to 45% (volume / volume) with a mixed solution of ethanol and water, and the weight was adjusted to be the same as the weight before distillation.
  • sugarcane extract MSX-245 raw material was adjusted to an ethanol concentration of 45% (volume / volume), and the odor intensity of the comparative control was set to 3.
  • the method of sensory evaluation is as described in Example 2. The results are shown in Table 1.
  • the distillation amount (concentration rate) of the residue in the kettle increased, and as the ethanol concentration in the residue in the kettle decreased, the odor intensity decreased and the odor derived from sweet potato decreased.
  • the odor was significantly improved in fractions 5 to 11 with an ethanol concentration of 5% or less (odor intensity 1 or 0).
  • Odor was improved in fraction 4 with an ethanol concentration of 10% or less (odor intensity 2).
  • the odor intensity is the same as that of the control, so the odor derived from sweet potato is not improved.
  • Example 5 Distillation by rotary evaporator (Method 4 for producing deodorant of the present invention)
  • the same sugarcane extract MSX-245 as in Example 4 was adjusted with water so that the ethanol concentration (volume / volume) was 10%.
  • a rotary evaporator Tokyo Rika Kikai Co., Ltd.
  • the ethanol concentration of each of fractions !! to 10 was measured with an alcohol densitometer.
  • the odor derived from sweet potato was evaluated for each of fractions 1 to 10; The evaluation method is as described in Example 4. The results are shown in Table 2.
  • the distillation amount (concentration rate) of the residue in the kettle increased, and as the ethanol concentration in the residue in the kettle decreased, the odor intensity decreased and the odor derived from sweet potato decreased.
  • the odor was significantly improved in fractions 3 to 10 with an ethanol concentration of 5% or less (odor intensity 1 or 0).
  • Odor was improved in fraction 2 with an ethanol concentration of 5.7% (odor intensity 2).
  • fraction 1 with an ethanol concentration of 10% was before the start of distillation and its odor intensity was the same as that of the comparative control, so the odor derived from sweet potato was not improved.
  • the ethanol concentration in the residue was 10%, unlike the case of Example 4, the ethanol concentration in the residue was low, so that the odor derived from sweet potato decreased soon after the start of distillation.
  • Example 4 The same sugarcane extract MSX-245 as in Example 4 was adjusted with water so that the ethanol concentration (volume / volume) was 40% (stock solution, fraction 1). 1000 ml of this solution was subjected to a rotary evaporator (Tokyo Rika Kikai Co., Ltd.) and distilled under the same conditions as in Example 4. At the same time, every time 100 ml of the residue was distilled, the residue was sampled (fractions 2 to 10), and the distillation was terminated when the amount of the residue was 100 ml. The ethanol concentration of each of fractions !! to 10 was measured with an alcohol densitometer. Moreover, the odor derived from sweet potato was evaluated for each of fractions 1 to 10; The evaluation method is as described in Example 4. The results are shown in Table 3.
  • the same sugarcane extract MSX_245 (stock solution, fraction 1) as in Example 4 was adjusted with water so that the ethanol concentration (volume / volume) was 20%. 1000 ml of the solution was subjected to a rotary evaporator (Tokyo Rika Instruments Co., Ltd.), controlled to 375 mmHg (decompression), and distilled at a steam temperature in the range of 70 to 84 ° C. At the same time, every time 100 ml of the residue was distilled, the residue was sampled (fractions 2 to 10), and the distillation was terminated when the amount of residue in the residue reached 100 ml. The ethanol concentration of each of fractions 1 to 10 was measured with an alcohol densitometer. The evaluation of the odor of the fractions is as described in Example 4. The results are shown in Table 4.
  • the same sugarcane extract MSX_245 (stock solution, fraction 1) as in Example 4 was adjusted with water so that the ethanol concentration (volume / volume) was 20%. 1000 ml of the solution was supplied to a glass beaker (container), heated at a gas conical port installed in a draft chamber, and distilled under normal pressure at a liquid temperature of 85 to 105 ° C. At the same time, every time 100 ml of the residue was distilled, the residue was sampled (fractions 2 to 10), and the distillation was terminated when the remaining amount of the residue was 100 ml. The ethanol concentration of each of fractions !! to 10 was measured with an alcohol concentration meter. Moreover, the odor derived from sweet potato was evaluated for each of fractions 1 to 10; The evaluation method is as described in Example 4. The results are shown in Table 5.
  • Fraction 11 produced in Example 1 was adjusted to a concentration of 45% (volume / volume) of ethanol with a mixed solvent of ethanol and water so that it had the same weight as before distillation, and then 45% (Volume / volume) A 3-fold diluted solution was made with ethanol.
  • each of the fractions 10 produced in Examples 3 to 8 is adjusted to a concentration of 45% (volume / volume) ethanol with a mixed solvent of water or ethanol / water, and the same weight as before distillation. Then, the solution was further diluted 3 times with 45% (volume / volume) ethanol.
  • Each 3-fold diluted solution was adjusted to pH 6.5 to pH 8.5 with hydrochloric acid or sodium hydroxide, and allowed to stand at 4 ° C.
  • Example 1 Each was filtered with a membrane filter (model number C045A047A, manufactured by Advantech Toyo Co., Ltd.). Each of the filtrates was deodorized in Example 1, Deodorant in Example 3, Deodorant in Example 4, Deodorant in Example 5, Deodorant in Example 6, Example 7 The deodorant of Example 8 was used.
  • Preparation of hydrogen sulfide gas is as follows. In a 20 ml headspace vial, 0.1 ml of 360 mM sodium sulfide solution was added, and 0.1 ml of 720 mM hydrochloric acid was slowly added and mixed. This was placed in a 30 ° C. incubator for 30 minutes to volatilize the gas. This head space gas was used as a test hydrogen sulfide gas.
  • each lml of the deodorant was put into a new 20 ml headspace vial. Each was put, sealed, and used as a measurement sample.
  • a positive control sample the same sugarcane extract MSX_245 (manufactured by Mitsui Sugar Co., Ltd.) as in Example 4 was used instead of the deodorant.
  • control As a sample a deodorant-free! /, 45% (volume / volume) ethanol aqueous solution was used.
  • Deodorization rate (%) [(ji-3) / ji] 100
  • each deodorant prepared in Example 9 reduced the concentration of hydrogen sulfide to the same extent as the positive control sample.
  • the deodorizing mechanism for hydrogen sulfide of the deodorant prepared in Example 9 is probably due to chemical deodorization.
  • Example 9 100 ml of odorless water in which distilled water was passed through an activated carbon column and each of the deodorizers prepared in Example 9 (samples for measurement) were added to 0.1 ml each of a 300 ml conical stoppered flask (dark brown transparent flask). . 100% 1% (mass / volume) aqueous solution of isovaleric acid was injected into this, and after standing for 30 minutes, sensory evaluation was conducted by 7 skilled panelists to obtain an average.
  • As a positive control sample the same sugarcane extract MSX_245 (manufactured by Mitsui Sugar Co., Ltd.) as in Example 4 was used instead of the deodorant.
  • a 45% (volume / volume) ethanol aqueous solution containing no deodorant was used.
  • each of the deodorizers prepared in Example 9 showed a deodorizing effect on isovaleric acid that was equal to or higher than that of the positive control sample.
  • each deodorant prepared in Example 9 has the same level of tobacco odor as the positive control sample. Deodorizing effect on
  • Aspergillus nieer NBRC33023 was used as a test fungus.
  • Potato dextrose agar medium (PDA medium) was inoculated with the test fungus and cultured at 28 ° C for 5 days.
  • the grown mold for test was immersed in distilled water, filtered with a filter paper (model No. 2 Advantech Toyo Co., Ltd.), and the cells were further washed with distilled water.
  • the washed mold for test was suspended in distilled water to obtain a mold spore suspension.
  • the mold spore suspension was cultured at 28 ° C. for 10 days and then filtered through a filter paper (No. 2) to obtain a musty odor water.
  • the mold odor water (300 ml) was added to a lidded bottle (500 ml) containing a cloth (cotton towel) and immersed at 25 ° C. for 5 days.
  • the fabric was taken out from the bottle and air-dried in the shade, and then the fabric was cut into 10 cm ⁇ 10 cm squares to obtain a mold odor test fabric.
  • each deodorant prepared in Example 9 showed a deodorizing effect on the mold odor equivalent to or higher than that of the positive control sample.
  • a bath towel used for 6 months as a dog (indoor dog) rug at home was cut into a lcm x lcm test piece.
  • the test piece was mixed well and made uniform, and then about 6 g was spread on a glass petri dish so that the dough would not overlap, and this was used as a pet odor test piece.
  • dilute with water so that the concentration of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts is 1% (both volume / volume). And filled into mist spray bottles. After spraying about 1.5 g on the pet odor test piece, it was thoroughly stirred and homogenized.
  • the same sugarcane extract MSX-245 concentration as in Example 4 was diluted with water so that the concentration was 1% (both volume / volume).
  • about 1.5 g of distilled water was sprayed on a test piece by spraying, and then it was thoroughly stirred and homogenized.
  • the pet odor test piece was stored in a sealed container (sealed aluminum pack) at room temperature until evaluation.
  • each of the deodorizers prepared in Example 9 showed a deodorizing effect on the same level of pet cake as the positive control sample.
  • Example 9 Diluted with water so that the concentration of the deodorant sample prepared in Example 9 was equal to 20% and 0.1% (both volume / volume). Filled spray bottle. When these samples were sprayed on a large dog with animal odor and its kennel, the unpleasant odor due to animal odor disappeared in both the dog and kennel, and the effect lasted for 3 days.
  • the concentration of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts was 60% and 1% (both volume / volume), respectively, and the final ethanol concentration was 20% ( (Volume / volume) to dilute with ethanol and water.
  • Each of the resulting mixtures was filled into an aerosol container with a propellant gas (LPG and carbon dioxide). When these were sprayed onto malodorous garbage, the malodor derived from the garbage was suppressed, and the effect lasted for more than 24 hours.
  • a propellant gas LPG and carbon dioxide
  • Trimethylamine gas was injected into this desiccator to an initial concentration of about 20 ppm, and after 24 hours, the trimethylamine concentration was measured with a detector tube (model No. 180L, manufactured by Gastec Co., Ltd.) to determine the reduction rate of the trimethylamine concentration. It was.
  • the gel-type deodorant for which measurement was completed was individually placed in a 300 ml beaker and stored in a constant temperature and humidity chamber at 20 ° C and 60% humidity until the next measurement.
  • the deodorizing effect was measured on the day of preparation of the gel-type deodorant, 7 days after preparation, and 14 days after preparation, and the deodorization rate was determined from the residual concentration of trimethylamine.
  • the deodorization rate was obtained as follows, and the data for the three deodorants were averaged. The results are shown in Table 10.
  • Deodorization rate (%) [1 (Trimethylamine concentration at the end of measurement) / (Trimethylamine concentration at the start of measurement)] X 100
  • a room with a particularly strong odor was selected in a nursing home and used as a test control. About 1.5 liters of water was added so that the concentration of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts was 0.05% (volume / volume). The solution was set in a humidifier. humidifier The operation was intermittently operated at a rate of 1 minute per 15 minutes using an intermittent timer. As a result, odors were suppressed throughout the day.
  • An excrement treating agent for pets was prepared using a deodorant prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts.
  • a deodorant prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts.
  • 50 parts of bentonite, 50 parts of wood flour, 1 part of deodorant and 50 parts of water were used.
  • the raw materials were mixed with a ribbon mixer, and a disk-type pelleter with a diameter of 3 mm and a length of 8-20 mm was obtained. This was further dried with a rotary dryer as a sample.
  • As a positive control 1 part of the same sugarcane extract MSX-245 as in Example 4 was used instead of the deodorant.
  • 1 part of water was used in place of the deodorant in the above treatment agent.
  • control Since bentonite absorbs ammonia to some extent, the control also has a deodorizing effect compared to the blank, but the treatment using the above-mentioned deodorant of the present invention and the positive control deodorant is clearly more deodorant. Showed the effect.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 0.6% and trade name “TEGO DEO CW90” (manufactured by Goldschmidt) as zinc ricinoleate 2.0% (About 1% as zinc ricinoleate), dipropylene glycol (5.0%), industrial ethanol (35.0%), and water in the balance, prepare a spray-type deodorant by a conventional method. It was.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 1.0%, and trade name “TEGO SORB CONC. 50” (manufactured by Goldschmidt) as zinc ricinoleate 1 ⁇ 0% (approx.0.5% as zinc ricinoleate), dipropylene glycol 5.0%, ethanol for industrial use 20.0%, and water in the balance, mix the spray-type agent by a conventional method. Key
  • a spray type deodorant was prepared by a conventional method by mixing 0.6%, industrial ethanol 20.0% and the balance water.
  • a spray type deodorant was prepared by a conventional method by mixing 0.6%, industrial ethanol 20.0% and the balance water.
  • Example 20 In the formulation of the spray-type deodorant of Example 20, and sprayed in a conventional manner without using the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts. Type A deodorant was prepared.
  • Example 20 In addition to the spray type deodorant of Example 20 !, instead of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts, / 3-cyclodextrin 2 0% was blended and a spray was prepared by a conventional method to obtain a spray type deodorant.
  • An odor evaluation box was prepared in which the odor intensity of hydrogen odor, methyl mercabtan, and isovaleric acid, which are general malodors, was set to the odor intensity stage 3 shown in the following odor intensity standards.
  • the sensory test was conducted by skilled panelists on the deodorizing effect on the above three kinds of malodors according to the following evaluation method. Detailed test methods are shown below.
  • the spray-type deodorants of Examples 20 to 24 showed excellent deodorizing effect after 1 minute of spraying against hydrogen sulfide, methyl mercaptan and isovaleric acid, and the effect was 10 minutes after spraying. Lasted even after.
  • the spray type deodorizers of Comparative Examples 1 and 2 did not have a sufficient deodorizing effect after 1 minute of spraying and after 10 minutes of spraying.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.3%
  • the product name “Smeral LG” manufactured by Environmental Science Development Co., Ltd.
  • monoethanolamine 0.8% 1.0%
  • citrate 2.0% 1.0%
  • water in the balance are mixed with ammonia.
  • the pH was adjusted to 7.0 to obtain a deodorant composition.
  • a control sample was obtained by adding 1% 2% monoethanolamine, 2.0% citrate and water to the residue and adjusting to pH 7.0 with ammonia.
  • ⁇ Test method (1) Deodorization test of ammonia> Place 10 mL of sample (deodorant composition or control sample of Examples 25 to 28 above) into a 1 L glass bottle container, and inject 1 mL of 1% aqueous ammonia solution. After leaving for 10 minutes, sensory evaluation by 10 skilled panelists was performed and an average was taken. The evaluation criteria were in accordance with the 6-step odor intensity display method of the malodor control method described in Example 11.
  • ⁇ Test method (2) Deodorization test of methyl mercaptan> Place 10 mL of a sample in a 1 L glass bottle container, inject 1 mL of 0.1% methyl mercaptan ethanol solution, and let stand for 1 hour. Sensory evaluation was performed and the average was taken. The evaluation criteria were in accordance with the 6-step odor intensity display method of the malodor control method described in Example 11.
  • ⁇ Test method (3) Deodorization test of isovaleric acid> Place 10mL of sample in a 1L glass bottle container, inject 100% of 1% aqueous solution of isovaleric acid, leave it for 1 hour, and sensory evaluation by 10 skilled panelists And took the average. The evaluation criteria were in accordance with the 6-step odor intensity display method of the malodor control method described in Example 11.
  • ⁇ Test method (4) Deodorization test of rugs used by indoor dogs> The rug after the sample is sprayed three times (about 2.5 g) on the rug used by dogs kept at home and wiped off. The sensory evaluation was performed based on the remaining odor.
  • the evaluation criteria are as follows.
  • the deodorant compositions of Examples 25 to 28 showed excellent deodorizing effects on indoor dog rugs that are sources of ammonia, methyl mercaptan, isovaleric acid and offensive odor. .
  • the deodorant composition of Comparative Example 3 showed almost no deodorizing effect.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0% and the trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 1.0% And citrate 3 0%, polyglycerin esterol 0.5%, saponin 0.5%, industrial ethanol 10.0%, POE isostearyl ether 0.1% The pH was adjusted to 4.8 with sodium oxide to obtain a deodorant cleaning agent.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0% and the trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 1.0% And the product name “Super Piyurire A-10J (manufactured by Matsushita Electric Industrial Co., Ltd.) 1 ⁇ 0%, Chenic acid 2 ⁇ 5%, Propylene glycolenoestestole 1 ⁇ 0% and Saponin 0 ⁇ 5% In addition, 100% industrial ethanol and 100% ethanol and the balance water were adjusted to pH 4.8 with sodium hydroxide to obtain a deodorant cleaning agent.
  • the deodorant cleaning agent was obtained after adjusting to 4.8.
  • the trade name “Smeral LG” manufactured by Environmental Science Development Co., Ltd. 0.5%, citrate 2.5%, saponin 0.5%, POE isostearinoreethenore 0.1%, industrial Ethanol for use was mixed with 10.0% and the remaining water, and the pH was adjusted to 5.8 with sodium hydroxide to obtain a deodorant cleaning agent.
  • the residue was mixed with water and adjusted to pH 5.0 with sodium hydroxide to obtain a deodorant cleaning agent.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0% and the trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 1.0% And the product name "Super Piyurire A-10J (manufactured by Matsushita Electric Industrial Co., Ltd.) 1 ⁇ 0%, quenate 2 ⁇ 0%, sodium dihydrogen tate 2 ⁇ 5% and saponin 5 ⁇ 0% Then, 100% industrial ethanol and water were mixed with the residue and adjusted to pH 4.8 with sodium hydroxide to obtain a deodorant cleaning agent.
  • the product name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) 0. 01% and the product name “Super Pyrienore A-10J (manufactured by Matsushita Electric Industrial Co., Ltd.) 0. 01%, and citrate 3 ⁇ 0%, industrial ethanol 10.0%, and water in the remainder were adjusted to pH 6.0 with sodium hydroxide to obtain a deodorant cleaning agent.
  • Chenic acid 2.5%, industrial ethanol 10.0%, and the remainder were mixed with water and adjusted to pH 4.8 with sodium hydroxide to obtain a deodorant cleaning agent.
  • the deodorization test for ammonia, methyl mercabtan, and isovaleric acid was evaluated using the test methods (1) to (3) described in the above deodorization test 2. In addition, deodorization tests and washing tests using actual urine and model urine of dogs kept at home were evaluated by the following test methods.
  • ⁇ Test method (5) Deodorization test and washing test using actual urine and model urine of indoor dog> Indoor urine and model urine of indoor dog (0.003% bilirubin (urine pigment) ⁇ 1 1% NaCl) is applied to the carpet and lightly patted with a tissue, and then the sample is treated (foam the sample on the size of a golf ball, lift the dirt with a brush, and lightly wipe with a tissue). The remaining colors were subjected to sensory evaluation by 10 skilled panelists and averaged.
  • the evaluation standard for the deodorization test is in accordance with the 6-step odor intensity display method of the malodor control method described in Example 11. For the cleaning test, the untreated color is 5 points and the stain is completely removed. Was one point. The results are shown in Table 14.
  • Example 29 0 0 0 1 1 2 1
  • Example 30 0 0 1 2 2 1 1
  • Example 31 0 1 0 2 2 2 1
  • Example 32 0 0 0 1 1 1 1
  • Example 33 0 0 0 0 1 2 1
  • Example 34 0 1 1 0 1 2 1
  • Example 35 0 0 1 0 0 1 1
  • Example 36 0 0 1 1 1
  • the deodorant cleaners !! ⁇ 8 have better deodorant performance for ammonia, methylmerbutane and isovaleric acid compared to the deodorant cleaners AC, and In the deodorization test and cleaning test using real urine or model urine of dogs kept in Japan! /, It showed excellent deodorization and cleaning performance.
  • a hair essence was prepared by adding an appropriate amount of fragrance in the case of a hair essence containing a fragrance, and adding purified water to the remainder without adding a fragrance in the case of an unscented hair essence.
  • a hair mist was prepared by blending industrial ethanol with the residue.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 10.5%, dipropylene glycol 1.0%, monostearic acid POE (20) sorbitan 0.1%, ⁇ (2 5) POP (30) 0. 7%, ethylene glycol distearate 2 2.0% coconut oil fatty Monoe Tano one Honoré bromide 2 ⁇ 5 0/0, ⁇ La clinoptilolite les utility Honoré acid Natorikumu 5 2.0 o / o ⁇ Lacrinoreutere triethanolamine sulfate 10.0%, 2-alkyl ⁇ carboxymethyl ⁇ hydroxetyl imidazolinium betaine 2.0%, Marquat 550 (manufactured by Riki Norecon) 5.0.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 5.0%, glycerin 0.5%, ethylene glycol distearate 2.0%, coconut oil fatty acid monoethanolamide 1 0%, propylene glycol laurate 2.0%, sodium coconut oil fatty acid methyltaurine sodium 7.0%, coconut oil fatty acid amidopropyl betaine 6.0%, polymer JR400 OJC C) 1 ⁇ 0%, citrate 0 ⁇ 5%, phenoxyethanol 0.3%, sodium benzoate 0.2%, disodium edetate 0.1%, soybean lecithin 0.2%, cationized potato starch (Sensomer CI-50CALGON) 0 ⁇ Formulated with 5%.
  • an appropriate amount of fragrance is added. did.
  • hypoallergenic shampoos were tested for the deodorant effect against tobacco odor described in Example 12, the hypoallergenic shampoo of this example was superior in deodorant effect (sensory Evaluation: A).
  • Hair finish spray Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0%, methinorefinolole polysiloxane 0.5%, 1, 3 butylene glycolenole 0.5% Liquid lanolin 0.2%, 2-ethyl cetyl cetylate 0.5%, lauric acid diethanolamide 0.5%, pi-glutamic acid isostearic acid POE hydrogenated castor oil 0.2%, paraben 0.2%, paramethycin cinnamon 2% hexyl acid 2-0.5%, Yucaformer 104 (Mitsubishi Chemical Co., Ltd.) 8.0%, oil-soluble vegetable protein 0.02% were blended.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 3.0%, liquid paraffin 1.0%, methylpolysiloxane 3.0%, cetanol 1.0%, otatilde Decanol 3.0%, oil-soluble vegetable protein 0.1%, propylene glycol 5.0%, polyoxyethylene hydrogenated castor oil 0.5%, polyoxyethylene stearyl ether 0.5%, alkyltrimethylammonium chloride 1. 5%, 0.1% citrate, 0.5% potassium chloride, 0.3% phenoxyethanol, and 0.01% viricion zinc solution (50%) were mixed. Furthermore, in the case of rinsing containing a fragrance, an appropriate amount of fragrance was added, and in the case of an unscented rinsing, no fragrance was added and purified water was added to the residue to prepare a rinse.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.5%, glycerin 4.0%, monoethanolamine laurate 1.0%, polyoxyethylene oleyl Ether 0.5%, lauryltrimethylammonium chloride 0.2%, stearyltrimethyl ammonium monoxide 0.5%, ammonium carbonate 5.0%, urea 2.0%, ammonium thioglycolate solution (50%) 15.0% and hydroxyethane diphosphonic acid (60%) 0.2% were added.
  • a permanent wave agent containing a fragrance an appropriate amount of fragrance was added, and in the case of an unscented permanent wave agent, no fragrance was added, and purified water was added to the remainder to prepare a permanent tube 1 .
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.5%, methylsiloxane emulsion 5.0%, lauryl dimethylamino acetate betaine 0.5% , Sodium monohydrogen phosphate 0.1%, Sodium bromate solution (20%) 40.0%, Potassium dihydrogen phosphate 0.5%, Sodium benzoate 0.2%, and purified water Permanent tube agent 2 was prepared.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 1.0%
  • a body lotion was prepared by blending 0.8% OE (60) hydrogenated castor oil and 1.0% mugwort extract, and blending purified water with the remainder.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.1%, Vaseline 2.0%, Metinorepolysiloxane 3.0%, Cetanore 2.0%, Glycerin 3. 0%, 1, 3-propylene, styrene glycolol 5.0%, hard coconut oil 2.0%, stearic acid 2.0%, bis-2-ethanole glyceryl hexanoate 3.5%, isostearin Polyoxyethylene glyceryl acid 0.7%, glyceryl monostearate 2-3%, potassium hydroxide 0.15%, sodium hexametaphosphate 0.01% sodium hyaluronate, 0.1% sodium, ascorbic acid phosphate magnesium 2.0%, paraben 0.3%, carboxybule polymer 0.05%. Furthermore, in the case of a cream containing a fragrance, an appropriate amount of fragrance was added, and in the case of an unscented cream, a fragrance was not added, and purified water was added to the remainder to prepare a cream.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 1.0%, industrial ethanol 5.0%, glycerin 8.0%, polyoxyethylene methyldarcoside 4. 0%, ⁇ (12) Lauryl ether 1 ⁇ 0%, Lauryldimethylamine oxide 0 ⁇ 3%, Potassium hydroxide 0 ⁇ 5%, L-ascorbic acid-2-darcoside 2 ⁇ 0%, Paraben 0 ⁇ 3%, Carboxybule polymer 0.6% was blended. Furthermore, in the case of a jewel containing fragrance, an appropriate amount of fragrance was added. In the case of an unscented jewel, no fragrance was added, and purified water was added to the remainder to prepare a jewel.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 6.0%, liquid paraffin 5.0%, petrolatum 1.0%, methylpolysiloxane 2.0%, industrial use Etano one Norre 3.0 percent, Setanonore 0.5 0/0, glycerin 6.0%, 1, 3 off ,, Chile packaging Ricoh Norre 6.0%, polyethylene glycol Norre 1500 1.0%, Kati ⁇ 2.0%, cetylolehexanoic acid 4.0%, polyoxyethylene glyceryl isostearate 1.0%, polyoxyethylene glyceryl monostearate 1.0%, potassium hydroxide 0.1%, metalin Sodium acetate 0.02%, Arginine hydrochloride 0.1%, Acetic acid DL—a Tocopherol 0.1%, Oil-soluble plant protein Inn 0.
  • EXAMPLE 9 7 type of each deodorant deodorant was mixed with an equal volume of sample 6.0% was prepared in propylene glycol: .pi. Honoré 8 ⁇ 0 0/0, Sonorebi, Tsu preparative ⁇ night (70 o / o) 8 ⁇ 0 o / o, lauric acid 2-5 0/0, coconut derived fatty acid diethanolamide 4 ⁇ 0%, ⁇ Anorekinore (12, 13) ether sulfate Torietano Ruamin 2.
  • Deodorant sample prepared by mixing the 7 types of deodorants prepared in Example 9 in equal amounts 0.5%, Benzenore 7 "Nore Inore 10.0 ⁇ / ⁇ , ⁇ Metinorepyrrolidone 15.0% Hair manicure was prepared by blending 3.0% cunic acid, 1.0% xanthan gum, 0.8% acidic dye, and purified water in the remainder. [0201] When this hair manicure was tested for the deodorizing effect on the tobacco odor described in Example 12, the product of this Example showed an excellent deodorizing effect (sensory evaluation: ⁇ ) on the tobacco odor. .
  • Example 54
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.3%, cetanol 10.0%, POE (15) cetyl ether 2.0%, sodium lauryl sulfate 2 0%, liquid paraffin 5.0%, oil-soluble vegetable protein 0.3%, polymethylsiloxane 3.0. /.
  • Cetanol 10.0%, POE (15) cetyl ester 2.0%, sodium lauryl sulfate 2.0%, liquid paraffin 5.0%, polymethylsiloxane 3.0%, hydrogen peroxide (35%) 18 Purified water was blended in 0% and the remainder, and adjusted to pH 8.0 with citrate to prepare two parts of oxidative hair dye. Next, 1 part and 2 parts of oxidative hair dye were mixed in a ratio of 1 part / 2 parts 1 / 0.5-2 to obtain the oxidative hair dye of this example.
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.5%, industrial ethanol 90.0%, glyceryl tri-2-ethylhexylate 2.0%, POE Hydrogenated castor oil 0.5%, diglyceryl diisostearate 1.0%, lauryldimethylamine oxide 0.5%,? 0.1% acid Sodium oxalate 0.03%, assembly extract 0.5%, Hinokichi-no-re 0.1%, pantothruethyl ether 0.1%, / 3--glycyrrhetinic acid 0.1%, nicotinic acid benzil 0.
  • a hair restorer was prepared by blending 1%, 0.1% pyridoxine hydrochloride, 0.1% tocopherol acetate 0.1%, L-menthol 0.1%, and purified water. [0205] When this hair restorer was tested for the deodorant effect against the tobacco odor described in Example 12, the hair restorer of this example had an excellent deodorant effect (sensory evaluation: ⁇ ) against the tobacco odor. Indicated.
  • Example 56
  • Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.5%, industrial utannole 20.0%, glycerin 5.0%, dipropylene glycol: ⁇ -nore 5
  • industrial ethanol 15.0%
  • red alga extract 1.08% were blended.
  • hair colons containing fragrance add an appropriate amount of fragrance
  • unscented hair colons add no fragrance.
  • the residue was mixed with purified water to prepare a hair colon stock solution.
  • Example 9 Prepare a car deodorant by diluting it with water so that the concentration of the deodorant sample prepared in Example 9 was equal to 1% (both volume / volume). did.
  • the vehicle deodorant was set on the liquid side of a sprayer of a two-fluid nozzle (gas / liquid type). The sprayer is operated continuously by installing the sprayer in the rear seat of the vehicle under test and adjusting the pressure by the transformer (air side), for example, compressed air from a baby compressor (Hitachi Machine). Operated.
  • a car with a strong pet odor in the car (car A), a car with a strong tobacco odor in the car (car B), a car with a human odor in the car (car C), and a fragrance smell in the car
  • the car (car D) with! / was left as the test target.
  • the car deodorant was sprayed for 15 minutes in each vehicle under test. During the mist, the air conditioner was circulated at maximum airflow, and the deodorant was distributed throughout the car. After spraying, the car window was opened and dried outdoors for several hours (3-5 hours) at an outside temperature (20-30 ° C, fine weather-cloudy).
  • the evaluation was carried out by sensory evaluation by 10 skilled panelists before spraying the vehicle deodorant, after spraying (immediately), several hours after spraying (after drying), and 1 day after spraying, and taking the average.
  • the evaluation criteria were sensory evaluation according to the 6-step odor intensity display method of the malodor control method described in Example 11. So Table 15 shows the results.
  • the car deodorant in this example showed a high deodorizing effect on the car odor (pet odor, cigarette odor, human body odor, and fragrance smell).
  • the deodorant of the present invention is naturally derived, has high safety, and has a low production cost.
  • the deodorant of the present invention since the odor derived from sweet potato is improved, it can be used in a wide range of fields such as the food field, the environmental field, the industrial field, etc. Can be used.

Abstract

It is intended to provide a deodorant which is a deodorant containing a deodorizing substance originating in sugarcane as the active ingredient, wherein the above-described deodorizing substance originating in sugarcane is a pot residue that has been obtained by distilling sugarcane juice or a solvent extract of sugarcane, treating the resultant distillate with column chromatography using a fixed support, further distilling the fraction obtained by the above treatment or a mixture of the fraction with water or a solvent mixture consisting of water with an alcohol, and completing the distillation when the alcohol concentration (volume/volume) in the pot residue attains 0% or more but not more than 10%. It is also intended to provide a method of improving the odor originating in sugarcane of a distillate obtained by distilling sugarcane juice or a solvent extract of sugarcane, which comprises treating the distillate by column chromatography using a fixed support, further distilling the fraction obtained by the above treatment or a mixture of the fraction with water or a solvent mixture consisting of water with an alcohol, and collecting the pot residue after completing the distillation when the alcohol concentration (volume/volume) in the pot residue attains 0% or more but not more than 10%.

Description

明 細 書  Specification
甘蔗由来の消臭物質を有効成分とする消臭剤、及び甘蔗由来の臭いを 改善する方法  A deodorant containing a deodorant substance derived from sweet potato as an active ingredient, and a method for improving the odor derived from sweet potato
技術分野  Technical field
[0001] 本発明は甘蔗由来の消臭物質を有効成分とする消臭剤に関し、詳しくは甘蔗汁も しくは甘蔗の溶媒抽出物を蒸留して得られる蒸留物由来の、甘蔗由来の臭いが改善 された消臭物質を有効成分とする消臭剤に関する。さらに、本発明は、甘蔗由来の 臭いを改善する方法に関する。  TECHNICAL FIELD [0001] The present invention relates to a deodorant comprising a sweet potato-derived deodorant as an active ingredient, and more specifically, a sweet potato-derived odor derived from a sweet potato juice or a distillate obtained by distillation of a sweet potato solvent extract. The present invention relates to a deodorant containing an improved deodorant substance as an active ingredient. Furthermore, this invention relates to the method of improving the odor derived from sweet potato.
背景技術  Background art
[0002] 近年、生活水準の向上に伴い、消費者は商品の価格又は量だけでなぐ商品の質 又は多様性を重視し、さらに生活の質的向上に関連する商品への関心が高まってき た。また、社会環境および生活環境は、住居形態の洋風化、密閉化などが進み、快 適な生活空間を求める消費者の価値観またはニーズから、消臭および脱臭に対する 関心が年々高まっている。それに伴って、幅広いニーズに対応した芳香剤、消臭剤、 脱臭剤、マスキング剤等の製品が多数上市されている。製品例として、ヒトまたは動 物 (ペット、家畜など)の体臭用、環境用、食品分野用などの消臭剤、脱臭剤、予防 製品等が存在し、用途別では添加物、塗布剤、散布剤、練り込み剤等の様々な形態 の商品が存在する。  [0002] In recent years, with the improvement of living standards, consumers have emphasized the quality or diversity of products, not just the price or quantity of products, and have become more interested in products related to improving the quality of life. . In addition, the social environment and living environment have become increasingly westernized and sealed, and interest in deodorization and deodorization has been increasing year by year due to the values and needs of consumers seeking a comfortable living space. Along with this, many products such as fragrances, deodorants, deodorants, and masking agents that meet a wide range of needs are on the market. Examples of products include deodorants, deodorants, preventive products, etc. for body odors of humans or animals (pets, livestock, etc.), environment, foods, etc. There are various forms of products such as agents and kneading agents.
[0003] 従来、ヒトをはじめ様々な生物から発生する悪臭、室内、車内、冷蔵庫内、トイレ、 畜舎、工場またはタバコなどから発生する悪臭、家庭の生ごみ等の廃棄物または産 業廃棄物から発生する悪臭を、脱臭または消臭するための消臭'脱臭剤の製品が多 数上市されている力 その多くは大量生産される化学合成品であった。しかし、ヒトま たは動物が体内に摂取もしくは吸収する可能性のある消臭,脱臭剤に関しては高い 安全性が求められるため、天然の消臭 ·脱臭剤を使用することが望まれてきている。 また、ヒトまたは動物が直接的に摂取若しくは吸収することの無い製品では化学合成 品由来の消臭 ·脱臭剤(環境用途)が多数用いられるが、使用または廃棄後の環境 への影響、例えば汚染が懸念されるため、天然由来の消臭 ·脱臭剤を用いることが 望まれてきている。 [0003] Conventionally, from bad odors generated from various living organisms including humans, from bad odors generated from indoors, cars, refrigerators, toilets, barns, factories, tobacco, etc., from household waste or industrial waste Deodorant's ability to deodorize or deodorize the odors generated. Many of these products are chemically synthesized products that are mass-produced. However, since high safety is required for deodorants and deodorants that can be ingested or absorbed by humans or animals, it is desirable to use natural deodorants and deodorants. . In addition, many deodorants and deodorizers (environmental use) derived from chemically synthesized products are used in products that are not directly ingested or absorbed by humans or animals. Use natural deodorants and deodorants. It has been desired.
[0004] 従来から存在する天然由来の消臭 '脱臭剤としては、古くから使用されている脱臭 剤として活性炭、各種植物抽出物を利用する方法が開発されている。例えば、活性 炭とイオン交換樹脂、植物抽出物を混合した環境用消臭剤 (特許文献 1)、キキヨウ科 植物から抽出した消臭 ·脱臭剤 (特許文献 2)、緑茶エキスの消臭 '脱臭剤 (特許文献 3)、レッドビート、カカオ、コーヒー及びパセリ抽出物のうち 1種又は 2種以上の混合 物を含有する消臭 '脱臭剤(特許文献 4)、ツバキ科又はタスノキ科植物の抽出物を 有効成分として含有する消臭 ·脱臭剤 (特許文献 5)、マツ科植物の抽出液から消臭 成分を得る方法 (特許文献 6)、シソエキス (特許文献 7)、柿エキス (特許文献 8)、茶 葉タンニン画分 (特許文献 9)、ョモギエキス(特許文献 10)等が報告されて!/、る。  [0004] As a naturally occurring deodorant existing as a deodorant, a method using activated carbon and various plant extracts as a deodorant that has been used for a long time has been developed. For example, environmental deodorant mixed with activated charcoal, ion exchange resin, and plant extract (Patent Document 1), deodorant and deodorant extracted from asteraceae plant (Patent Document 2), deodorization of green tea extract 'deodorization' Deodorant containing one or a mixture of two or more of extracts (Patent Document 3), red beet, cacao, coffee and parsley extract (Patent Document 4), extraction of Camellia or Tasaceae plants Deodorant containing a product as an active ingredient (Patent Document 5), a method for obtaining a deodorant component from an extract of a pine family plant (Patent Document 6), perilla extract (Patent Document 7), persimmon extract (Patent Document 8) ), Tea leaf tannin fraction (Patent Document 9), mugwort extract (Patent Document 10), etc. have been reported!
[0005] 以上のような天然物由来の消臭 ·脱臭剤が報告されている力 活性炭は環境中に 固形で設置する必要があり、環境用途などに使用が限られる上、臭いの吸収、吸着 が飽和状態になると、逆にその悪臭物質の拡散または廃棄物処理の問題が生じる。 また、従来の植物由来の消臭剤では、植物または製造方法に由来する着色、味質ま たは風味を含む植物抽出物も多く存在しており、中でも食品分野においては消臭- 脱臭剤としての使用が敬遠される。環境用途等であれば使用可能である場合でも、 植物抽出物の消臭,脱臭剤の有効成分を得るためには、栽培した植物の葉、茎、皮 などの植物体を乾燥あるレ、は焙煎後、破砕し有機溶媒および/または水で抽出する ことが必要であり、大量生産される化学合成品と比較してその生産コストが高いと問 題がある。  [0005] Deodorant derived from natural products as described above · Deodorant has been reported. Activated carbon must be installed in the environment as a solid, and its use is limited to environmental applications, as well as odor absorption and adsorption. On the other hand, when saturates, problems of diffusion of the malodorous substance or waste disposal arise. In addition, many conventional plant-derived deodorants contain plant extracts containing coloring, taste, or flavor derived from plants or production methods, and in particular, in the food field, as deodorants and deodorants. The use of is avoided. Even if it can be used for environmental purposes, etc., in order to obtain an effective ingredient for the deodorant and deodorant of the plant extract, the plant, such as leaves, stems, and skins that are cultivated, is dried. After roasting, it is necessary to crush and extract with organic solvent and / or water, and there is a problem that its production cost is higher than that of chemically synthesized products that are mass-produced.
[0006] 次に、甘蔗由来のものとして、黒糖には調理を行う際には魚臭等の臭みに対して消 臭効果があるといわれている。しかし、黒糖の 90%前後は糖類であり、それ自体の臭 いまたは味 (甘味)が強ぐ問題がある。また、環境消臭用として消臭効果を発揮する ためには多量の黒糖を必要とすること、またはそれ自体が微生物により腐敗等し、逆 に悪臭の原因物質になること等のため、消臭 ·脱臭剤として用いるには問題があった  [0006] Next, as derived from sweet potato, brown sugar is said to have a deodorizing effect on odors such as fishy odor when cooking. However, around 90% of brown sugar is a saccharide, and there is a problem that its own odor or taste (sweetness) is strong. In addition, in order to exert the deodorizing effect for environmental deodorization, a large amount of brown sugar is required, or it itself decays due to microorganisms, and on the contrary, it becomes a causative substance of bad odor. · There was a problem in using as a deodorant
[0007] 本出願人は、甘蔗汁および甘蔗由来の製糖蜜から選ばれた原料をカラムクロマトグ ラフィ一で処理して得られる消臭物質、及び甘蔗由来の蒸留物を有効成分とする消 臭剤を報告した (特許文献 11〜特許文献 13)。該消臭物質及び該消臭剤は、無色 ないしは淡黄色であり、それ自身は強い臭いを持たない。しかも、植物由来のため安 全性が高ぐ固形分としての残存がほとんど無ぐ微量で高い消臭効果を有すること から、該消臭物質及び該消臭剤は多様で優れた効果を有する。 [0007] The applicant of the present invention has proposed a deodorant substance obtained by treating a raw material selected from sweet potato juice and molasses derived from sweet potato with column chromatography, and an odor source containing a distillate derived from sweet potato as an active ingredient. Odorants were reported (Patent Documents 11 to 13). The deodorizing substance and the deodorant are colorless or light yellow and do not have a strong odor per se. In addition, since it is derived from a plant and has a high deodorizing effect with a very small amount of solids that remain highly safe, the deodorizing substance and the deodorant have various and excellent effects.
[0008] しかし、上記消臭物質及び消臭剤は、使用濃度に希釈すればほとんど臭いが無い か或!/、は強!/、臭!/、を持たなレ、が、甘蔗由来の独特の臭レ、が残存して!/、ることから、 甘蔗由来の独特の臭いに対して敏感な使用者を不快にする場合があった。特に、密 閉度の高い空間で上記消臭物質及び消臭剤を使用する際、または化粧品として肌 に直接塗布する場合に、該独特の臭いが問題となることから、該独特の臭いの改善 策が望まれていた。 [0008] However, the deodorant and deodorant have almost no odor when diluted to the use concentration, or have no strong odor! /, Odor! / As a result, there is a case where the user who is sensitive to the unique odor derived from sweet potato is uncomfortable. In particular, when using the above deodorant and deodorant in a highly closed space, or when applied directly to the skin as cosmetics, the unique odor becomes a problem. A plan was desired.
[0009] 該独特の臭いの改善策の一つとして、上記消臭物質に、植物精油および/または エッセンスを添加することにより上記消臭物質の臭気を改善する方法が報告されてい る(特許文献 14)。具体的には、植物精油としてカモミール油、シトロネラ油、ベルガ モット油、ペパーミント油、メリッサ油、ラベンダー油、エッセンスとしてオレンジフラヮ 一、カモミール、メリッサの添加が上記消臭物質の臭気の改善に有効とされている。  [0009] As one of the measures for improving the unique odor, there has been reported a method for improving the odor of the deodorant by adding plant essential oil and / or essence to the deodorant (Patent Document). 14). Specifically, the addition of chamomile oil, citronella oil, bergamot oil, peppermint oil, melissa oil, lavender oil as essential oils, and orange fluff, chamomile, and melissa as essences are considered to be effective in improving the odor of the deodorant. ing.
[0010] しかしながら、上記改善策は植物精油および/またはエッセンスによる甘蔗由来の 臭気をマスキングするものであり、植物精油および/またはエッセンスを添加できる 用途に限定される。さらに、最近では化粧品を代表として、消費者の関心は消臭また は脱臭に留まらず、無臭または無香料の製品が好まれる傾向が年々高まっており、 甘蔗由来の臭気だけで無ぐ香料、植物精油若しくはエッセンスまたは香気物質の 使用も問題とされ、消費者に敬遠される傾向にある。従って、上記消臭物質及び消 臭剤が有する消臭効果等の有効成分を減じること無ぐ甘蔗由来の独特の臭いを改 善する方法の開発が望まれてレ、る。  [0010] However, the above improvement measures mask the odor derived from sweet potato by the plant essential oil and / or essence, and are limited to applications where the plant essential oil and / or essence can be added. Furthermore, recently, with cosmetics as a representative, consumer interest is not limited to deodorization or deodorization, and there is a growing trend toward preference for odorless or fragrance-free products. The use of essential oils or essences or fragrances is also a problem and tends to be avoided by consumers. Therefore, it is desired to develop a method for improving the unique odor derived from sweet potato without reducing the effective components such as the deodorizing effect of the deodorant and deodorant.
[0011] また、一般的に、消臭 ·脱臭剤の有効成分は臭いを持った成分であると考えられて おり、特に天然由来の消臭 ·脱臭剤の有効成分に多く見られる。そのため、通常の蒸 留または各種吸着剤、例えば活性炭、活性白土または強酸型、ァニオン型のイオン 交換樹脂を用いて処理をしても臭気を無くすことはできない、あるいは臭気を減少す ると共に脱臭'消臭効果等の有効成分も減少し、無香料または無臭の脱臭'消臭剤 を製造するのが難しレ、と考えられて!/、る。 [0011] In addition, it is generally considered that the active ingredient of a deodorant / deodorant is an odorous ingredient, and particularly, it is often seen as an active ingredient of a naturally-derived deodorant / deodorant. For this reason, odor cannot be eliminated or treated with ordinary distillation or various adsorbents such as activated carbon, activated clay, strong acid type, or anion type ion exchange resin, or the odor is reduced and deodorized. Deodorant's deodorant with no fragrance or odor It is difficult to manufacture!
[0012] 特許文献 1:特開昭 62-211068号公報 Patent Document 1: Japanese Patent Application Laid-Open No. 62-211068
特許文献 2:特開昭 60-7848号公報  Patent Document 2: JP-A-60-7848
特許文献 3:特開昭 60-185558号公報  Patent Document 3: JP-A-60-185558
特許文献 4:特開昭 60-207664号公報  Patent Document 4: JP-A-60-207664
特許文献 5:特開昭 61-106163号公報  Patent Document 5: JP-A-61-106163
特許文献 6:特開昭 63-21060号公報  Patent Document 6: Japanese Unexamined Patent Publication No. 63-21060
特許文献 7:特開昭 60-214726号公報  Patent Document 7: Japanese Patent Laid-Open No. 60-214726
特許文献 8:特開昭 61-87562号公報  Patent Document 8: Japanese Patent Laid-Open No. 61-87562
特許文献 9:特開平 2-284997号公報  Patent Document 9: JP-A-2-284997
特許文献 10:特開平 7-33636号公報  Patent Document 10: Japanese Patent Laid-Open No. 7-33636
特許文献 11 :特開平 10-151182号公報  Patent Document 11: JP-A-10-151182
特許文献 12:特開平 11-187825号公報  Patent Document 12: Japanese Patent Laid-Open No. 11-187825
特許文献 13:特開 2001-87365号公報  Patent Document 13: Japanese Patent Laid-Open No. 2001-87365
特許文献 14:特開 2001-224673号公報  Patent Document 14: Japanese Patent Laid-Open No. 2001-224673
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0013] 本発明は、上記の事情を鑑みて、特に甘蔗汁もしくは甘蔗の溶媒抽出物を蒸留し て得られる蒸留物 (甘蔗蒸留物)由来の、甘蔗由来の臭いが改善された消臭物質を 有効成分とする消臭剤を提供する。さらに、本発明は、甘蔗由来の臭いを改善する 方法を提供する。 [0013] In view of the above circumstances, the present invention is a deodorant substance with an improved odor derived from sweet potato, particularly derived from a distillate (sweet potato distillate) obtained by distilling a sweet potato juice or a sweet potato solvent extract. The present invention provides a deodorant containing as an active ingredient. Furthermore, the present invention provides a method for improving the odor derived from sweet potato.
課題を解決するための手段  Means for solving the problem
[0014] 本発明者は、上記目的を達成するために鋭意検討を重ねた結果、以下のことを見 出し、本発明を完成するに至った。 [0014] As a result of intensive studies in order to achieve the above object, the present inventor found the following and completed the present invention.
[0015] 本発明は、甘蔗由来の消臭物質を有効成分とする消臭剤であって、甘蔗由来の該 消臭物質が、甘蔗汁もしくは甘蔗の溶媒抽出物を蒸留 (以下、該蒸留を一次蒸留と[0015] The present invention is a deodorant comprising a sweet potato-derived deodorant as an active ingredient, and the sweet potato-derived deodorant distilled a sweet potato juice or a sweet potato solvent extract (hereinafter referred to as the distillation). With primary distillation
V、う)して得られる蒸留物(以下、該蒸留物を一次蒸留物とレ、う)を固定担体を用いた カラムクロマトグラフィーで処理し、該処理により得られる画分を、または該画分に水も しくはアルコール一水の混合溶媒を添加した混合物をさらに蒸留(以下、該蒸留を二 次蒸留という)し、釜残のアルコール濃度(体積/体積)が 0 %以上〜 10 %以下であ るときに該二次蒸留を終了した際の釜残であるところの消臭剤(以下、本発明の消臭 剤という場合がある)を提供する。本発明の消臭剤は、驚くべきことに、一次蒸留物が 有する本来の優れた消臭効果を有し、甘蔗由来の臭いが改善されている。 V, U)) (hereinafter, the distillate is referred to as a primary distillate) by column chromatography using a fixed carrier, and the fraction obtained by the treatment or the fraction Water in minutes Or when the mixture containing alcohol / water mixture is further distilled (hereinafter referred to as secondary distillation) and the alcohol concentration (volume / volume) in the kettle is 0% to 10%. The present invention also provides a deodorant that is the residue of the kettle when the secondary distillation is completed (hereinafter sometimes referred to as the deodorizer of the present invention). Surprisingly, the deodorizer of the present invention has the original excellent deodorizing effect of the primary distillate, and the odor derived from sweet potato is improved.
また、本発明は、甘蔗汁もしくは甘蔗の溶媒抽出物を蒸留 (一次蒸留)して得られる 蒸留物(一次蒸留物)の甘蔗由来の臭いを改善する方法であって、該一次蒸留物を 固定担体を用いたカラムクロマトグラフィーで処理すること、該処理により得られる画 分を、または該画分に水もしくはアルコール—水の混合溶媒を添加した混合物をさら に蒸留(二次蒸留)すること、釜残のアルコール濃度(体積/体積)が 0%以上〜 10 The present invention also relates to a method for improving the sweet potato-derived odor of a distillate (primary distillate) obtained by distillation (primary distillation) of a sweet potato juice or a sweet potato solvent extract, wherein the primary distillate is fixed. Treatment by column chromatography using a carrier, further distilling (secondary distillation) a fraction obtained by the treatment or a mixture obtained by adding water or an alcohol-water mixed solvent to the fraction; Alcohol concentration (volume / volume) of the remaining pot is 0% or more to 10
%以下であるときに該二次蒸留を終了した際の釜残を集めることを含むところの方法 (以下、本発明の方法という場合がある)を提供する。本発明の方法は、驚くべきこと に、一次蒸留物が有する本来の優れた消臭効果を減じることなぐ甘蔗由来の臭い を改善する。 Provided is a method including collecting the residue in the secondary distillation when it is less than or equal to% (hereinafter sometimes referred to as the method of the present invention). The method of the present invention surprisingly improves the sweet odor derived from sweet potato without reducing the original excellent deodorizing effect of the primary distillate.
発明の効果  The invention's effect
[0016] 本発明の消臭剤及び本発明の方法に従い得られた消臭剤(以下、まとめて本発明 の消臭剤という場合がある)は、一次蒸留物が有する本来の優れた消臭効果を有し、 しかも甘蔗由来の独特の臭いが改善されている。従って、本発明の消臭剤を食品ま たは化粧品等に利用しても甘蔗由来の臭いが無ぐそれ故に無香料または無臭の脱 臭-消臭剤として使用しても使用者にその使用感を満足させ得るものである。さらに、 本発明の消臭剤は製糖又は精製糖工程を利用して製造しうるため、生産コストが安 い。  [0016] The deodorant of the present invention and the deodorant obtained according to the method of the present invention (hereinafter sometimes collectively referred to as the "deodorant of the present invention") are inherently excellent deodorants possessed by primary distillates. It has an effect, and the unique odor derived from sweet potato is improved. Therefore, even if the deodorant of the present invention is used for foods or cosmetics, it does not have a sweet odor derived from sweet potato, so it can be used as a fragrance-free or odorless deodorant-deodorant. The feeling can be satisfied. Furthermore, since the deodorant of the present invention can be produced using a sugar production or refined sugar process, the production cost is low.
図面の簡単な説明  Brief Description of Drawings
[0017] [図 1]硫化水素に対する本発明の消臭剤の消臭効果を示す図である。 FIG. 1 is a diagram showing the deodorizing effect of the deodorant of the present invention on hydrogen sulfide.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0018] 以下、本発明を詳細に説明する。 [0018] Hereinafter, the present invention will be described in detail.
[0019] [甘蔗由来の臭いの改善] [0019] [Improved odor derived from sweet potato]
甘蔗由来の臭いが改善された又は甘蔗由来の臭いを改善するとは、甘蔗由来の臭 、が本発明における一次蒸留物の甘蔗由来の臭レ、と比べて低減されてレ、る、或い は甘蔗由来の臭レ、がやっと感知できる程度、或!、は甘蔗由来の臭レ、が感じられなレ、 ことをいう。甘蔗由来の臭いは、例えば下記実施例 2に記載の臭い強度の評価方法 に従い測定しうる。実施例 2に記載の評価方法によれば、一次蒸留物の臭い強度(3 と決める)よりも低い強度(2、 1、 0)になった場合に、甘蔗由来の臭いが改善されたと いう。評価 2は、一次蒸留物よりも弱いが、楽に臭いが感知でき、評価 1は、やっと感 知できる程度であり、評価 0は無臭である。 The odor derived from sweet potato is improved or the odor derived from sweet potato is improved. The odor of the primary distillate in the present invention is reduced compared to the odor of the sweet potato, or the odor of the sweet potato is finally perceivable, or! I can't feel it. The odor derived from sweet potato can be measured, for example, according to the odor intensity evaluation method described in Example 2 below. According to the evaluation method described in Example 2, the odor derived from sweet potato was improved when the intensity (2, 1, 0) was lower than the odor intensity of the primary distillate (determined to be 3). Evaluation 2 is weaker than the primary distillate, but the odor can be easily detected. Evaluation 1 is barely noticeable, and evaluation 0 is odorless.
[0020] [一次蒸留物]  [0020] [Primary distillate]
本発明における一次蒸留物は、二次蒸留の原液としうる。一次蒸留物として、甘蔗 汁もしくは甘蔗の溶媒抽出物を蒸留して得られる蒸留物であれば、その製造方法、 形態等に特に制限無ぐ各種の製造方法で得られる種々の形態を有する公知のもの を使用できる(例えば、特許文献 13を参照)。  The primary distillate in the present invention can be used as a stock solution for secondary distillation. As a primary distillate, if it is a distillate obtained by distilling a sweet potato juice or a sweet potato solvent extract, it is a publicly known product having various forms obtained by various production methods with no particular restrictions on its production method, form, etc. Can be used (see, for example, Patent Document 13).
[0021] ここで、本発明における甘蔗汁は、甘蔗 (サトウキビ)を圧搾して得られる圧搾汁、甘 蔗を水で浸出して得られる浸出汁、又は原糖製造工場における石灰処理した清浄 汁及び濃縮汁を包含する。本発明における甘蔗の溶媒抽出物とは、甘蔗を汎用の 有機溶媒で抽出した抽出液を意味する。該有機溶媒としては、例えばメタノール、ェ タノールなどのアルコール類が挙げられ、これらを単独でも組み合わせて使用しても 良い。さらに、これらの溶媒と水を組み合わせて使用しても良い。  [0021] Here, the sweet potato soup in the present invention is a squeezed juice obtained by squeezing sweet potato (sugar cane), a leached juice obtained by leaching sweet potato with water, or a lime-treated clean juice obtained from a raw sugar manufacturing plant. And concentrated juice. The sweet potato solvent extract in the present invention means an extract obtained by extracting sweet potato with a general-purpose organic solvent. Examples of the organic solvent include alcohols such as methanol and ethanol, and these may be used alone or in combination. Furthermore, these solvents and water may be used in combination.
[0022] 本発明における一次蒸留物は、具体的には例えば以下の方法に従い、或いは上 記特許文献 13に記載の方法に従い得られうる。  [0022] Specifically, the primary distillate in the present invention can be obtained, for example, according to the following method or according to the method described in Patent Document 13 above.
[0023] 甘蔗汁もしくは甘蔗の溶媒抽出物を、加熱装置を持つタンクに入れ加熱し、得られ る蒸気を冷却することにより回収し、液体の甘蔗由来の蒸留物を得る。この蒸留では 、加熱装置を持ち、蒸気を冷却し液体として回収できるあらゆる装置が使用できる。  [0023] The sweet potato soup or the sweet potato solvent extract is placed in a tank having a heating device and heated, and the resulting steam is recovered by cooling to obtain a liquid sweet potato-derived distillate. In this distillation, any apparatus that has a heating device and can cool and recover the vapor as a liquid can be used.
[0024] 一次蒸留物を得るための蒸留条件は、 50°C〜; 120°Cの、一次蒸留物が沸騰する 圧力で行うことができる。好ましくは、 70°C〜; 120°Cの、一次蒸留物が沸騰する圧力 で行うこと力 Sできる。圧力は、抽出に用いる溶媒、および蒸留工程で用いる装置等に 応じて適宜調整される。例えば、抽出溶媒に水を用いて、遠心式薄膜真空蒸発装置 、冷却管を接続したフラスコ、または蒸留機を用いて蒸留する場合には、 70〜; 105 °Cにおいて、 240mmHg〜常圧である。これより低い温度および圧力にて蒸留を行 うことも可能である。し力もながら、液体として蒸気を回収したい場合には、温度を低く するとそれだけ高い減圧条件にする必要があり、またトラップ内で蒸留温度以下で一 次蒸留物を凝縮させる必要があるので、装置等にコストがかかりすぎる。したがって、 実験室においては可能であるが、工業的には適さない。また、本発明における一次 蒸留では、 130°C以上での高温加熱は行わない。蒸留装置としては、例えば、実験 室内においては冷却管などに接続したフラスコが、工場においては濃縮缶、結晶缶 、効用缶等が用いられる。これら温度及び圧力条件を調節することにより、甘蔗由来 の消臭物質と水との割合 (水が含まれる場合)を変化させ、希望する濃度の一次蒸留 物を得ること力 Sでさる。 [0024] The distillation conditions for obtaining the primary distillate may be 50 ° C to 120 ° C at a pressure at which the primary distillate boils. Preferably, it can be performed at a pressure of 70 ° C. to 120 ° C. at which the primary distillate boils. The pressure is appropriately adjusted according to the solvent used for extraction and the apparatus used in the distillation step. For example, in the case of using water as an extraction solvent and distilling using a centrifugal thin film vacuum evaporator, a flask connected to a condenser, or a distillation machine, 70 to 105; At ° C, it is 240mmHg to normal pressure. It is also possible to carry out distillation at lower temperatures and pressures. However, if it is desired to recover the vapor as a liquid, the lower the temperature, the lower the pressure must be, and the primary distillate must be condensed in the trap below the distillation temperature. Is too expensive. Therefore, it is possible in the laboratory, but not industrially suitable. In the primary distillation in the present invention, high-temperature heating at 130 ° C or higher is not performed. As a distillation apparatus, for example, a flask connected to a cooling pipe or the like is used in a laboratory, and a concentration can, a crystal can, a utility can, or the like is used in a factory. By adjusting these temperature and pressure conditions, the ratio of the sweet potato-derived deodorant substance to water (if water is included) can be changed to obtain a primary distillate with the desired concentration.
[0025] [二次蒸留の原液] [0025] [Secondary distillation stock solution]
本発明における二次蒸留の原液として、上記一次蒸留物を固定担体を用いたカラ ムクロマトグラフィーで処理することにより得られる画分、または該画分に水もしくはァ ルコール—水の混合溶媒を添加した混合物を使用する。該カラムクロマトグラフィー 処理によって、一次蒸留物の成分が濃縮されうる。  As a stock solution for secondary distillation in the present invention, a fraction obtained by treating the above primary distillate by column chromatography using a fixed carrier, or a mixed solvent of water or alcohol-water is added to the fraction. Use the resulting mixture. By the column chromatography treatment, the components of the primary distillate can be concentrated.
さらなる実施態様において、本発明における二次蒸留の原液として、市販品を用い ることも可能であり、例えば三井製糖株式会社製の甘蔗由来の抽出物(一次蒸留物 に相当するもの)等を好適に用いることができ、例えば甘蔗蒸留物である「さとうきび 抽出物 MSX_245」(エタノール濃度 45% (体積/体積))(三井製糖株式会社製)が 挙げられる。 「さとうきび抽出物 MSX_245」は、一次蒸留物を固定担体を用いたカラム クロマトグラフィーで処理することにより得られる画分にアルコール一水の混合溶媒を 添加してアルコール濃度を調整して製品化したものである。  In a further embodiment, a commercially available product can be used as the stock solution for secondary distillation in the present invention, and for example, an extract derived from sweet potato manufactured by Mitsui Sugar Co., Ltd. (corresponding to a primary distillate) is suitable. For example, “sugar cane extract MSX_245” (ethanol concentration 45% (volume / volume)) (manufactured by Mitsui Sugar Co., Ltd.), which is a sweet potato distillate. Sugar cane extract MSX_245 is a product obtained by adjusting the alcohol concentration by adding a mixed solvent of alcohol and water to the fraction obtained by treating the primary distillate with column chromatography using a fixed carrier. It is.
[0026] 以下に、一次蒸留物のカラムクロマトグラフィー処理の方法を述べる。 [0026] A method of column chromatography treatment of the primary distillate will be described below.
[0027] 上記一次蒸留物は、そのまま又はアルコール濃度を調整するために該一次蒸留物 を水で任意の濃度に調整して、固定担体を充填したカラムに通液することができる。 一次蒸留物に添加する水は水道水でもよいが、臭気を除去する高度の蒸留処理上 、純水(すなわち、イオン交換水)または蒸留水がより好ましい。 [0027] The primary distillate can be passed through a column packed with a fixed carrier as it is or in order to adjust the alcohol concentration, the primary distillate is adjusted to an arbitrary concentration with water. The water added to the primary distillate may be tap water, but pure water (that is, ion-exchanged water) or distilled water is more preferable for high-level distillation treatment for removing odor.
[0028] 一次蒸留物のアルコール濃度(体積/体積)は、一次蒸留物中の目的とする消臭 物質を効率よく固定担体に吸着させるために、好ましくは 10%以下 0%以上、さらに 好ましくは 5 %以下 0 %以上に調整する。 [0028] The alcohol concentration (volume / volume) of the primary distillate is the desired deodorant in the primary distillate. In order to efficiently adsorb the substance on the fixed carrier, the content is preferably adjusted to 10% or less 0% or more, more preferably 5% or less 0% or more.
[0029] 上記カラムクロマトグラフィー処理は、さらに好ましくは、固定担体としての合成吸着 剤を充填したカラムを用い、該カラムに対象試料を通液し、該合成吸着剤に吸着され た成分を、メタノール、エタノール、及び水、メタノール、エタノールの混合物から選ば れる溶媒で溶出することによって行われる。 [0029] More preferably, the column chromatography treatment uses a column packed with a synthetic adsorbent as a fixed carrier. The target sample is passed through the column, and the components adsorbed on the synthetic adsorbent are mixed with methanol. And eluting with a solvent selected from ethanol, and a mixture of water, methanol, and ethanol.
[0030] 固定担体としては、合成吸着剤が好ましい。合成吸着剤としては、好ましくは有機 系樹脂を用いることができ、例えば、芳香族系樹脂、アクリル酸系メタクリル樹脂、ァク リロ二トリル脂肪族系樹脂等が使用できる。また、このような合成吸着剤は市販されて おり、例えばダイアイオン(商標)系として HP— 10、 HP— 20、 HP— 21、 HP— 30、 HP— 40、 HP— 50 (以上、無置換基型の芳香族系樹脂、いずれも商品名、三菱化 学株式会社製); SP— 825、 SP— 800、 SP— 850、 SP— 875、 SP— 70、 SP— 70 0 (以上、無置換基型に特殊処理を施した芳香族系樹脂、いずれも商品名、三菱化 学株式会社製); SP— 900 (芳香族系樹脂、商品名、三菱化学株式会社製);アンバ 一ライト(商標)として、 XAD— 2、 XAD— 4、 XAD— 16、 XAD— 2000 (以上、芳香 族系樹脂、いずれも商品名、株式会社オルガノ製);ダイアイオン (商標)系として、 S P— 205、 SP— 206、 SP— 207 (以上、疎水性置換基を有する芳香族系樹脂、いず れも商品名、三菱化学株式会社製); HP— 2MG、 EX— 0021 (以上、疎水性置換 基を有する芳香族系樹脂、いずれも商品名、三菱化学株式会社製);アンバーライト (商標)系として、 XAD— 7HP、 XAD— 8 (以上、アクリル酸系エステル樹脂、いずれ も商品名、株式会社オルガノ製);ダイアイオン(商標)系として、 HP1MG、 HP2MG (以上、アクリル酸系メタクリル樹脂、いずれも商品名、三菱化学株式会社製);セファ デッタス(商標)系として LH20、 LH60 (以上、架橋デキストランの誘導体、いずれも 商品名、フアルマシアバイオテク株式会社製)などが挙げられる。通液対象物の濃度 、溶媒、抽出法、共存物などにより適する合成吸着剤の種類は異なるため、適宜選 択を fiうこと力できる。 [0030] As the fixed carrier, a synthetic adsorbent is preferable. As the synthetic adsorbent, an organic resin can be preferably used. For example, an aromatic resin, an acrylic acid-based methacrylic resin, an acrylonitrile fatty resin, or the like can be used. In addition, such synthetic adsorbents are commercially available, for example, HP-10, HP-20, HP-21, HP-30, HP-40, HP-50 (and more, no substitution) Basic type aromatic resins, all trade names, manufactured by Mitsubishi Chemical Corporation); SP—825, SP—800, SP—850, SP—875, SP—70, SP—70 0 (or more, unsubstituted) SP-900 (Aromatic resin, trade name, manufactured by Mitsubishi Chemical Corporation); Amberlite (trademark) ), XAD-2, XAD-4, XAD-16, XAD-2000 (above, aromatic resins, all trade names, manufactured by Organo Corporation); Diaion (trademark) system, SP-205, SP — 206, SP— 207 (Aromatic resin having hydrophobic substituents, both trade names, manufactured by Mitsubishi Chemical Corporation); HP—2MG, EX—0021 (above Aromatic resins with hydrophobic substituents, all trade names, manufactured by Mitsubishi Chemical Corporation); Amberlite (trademark), XAD-7HP, XAD-8 (above, acrylic ester resins, both products Name: Organo Co., Ltd .; Diaion (trademark) system, HP1MG, HP2MG (Acrylic acid-based methacrylic resin, both trade names, manufactured by Mitsubishi Chemical Corporation); Sepha Dettas (trademark) system, LH20, LH60 (Derivatives of cross-linked dextran, all of which are trade names, manufactured by Falmasia Biotech Co., Ltd.). Since the types of synthetic adsorbents to be used vary depending on the concentration of the flow-through target, solvent, extraction method, coexisting substances, etc., it is possible to make appropriate selections.
[0031] 固定担体の量は、カラムの大きさ、溶媒の種類、固定担体の種類等によって変化 する。一次蒸留物を使用する場合には、例えば、固定担体の 100〜20,000倍の蒸留 物を通液し、有効成分を固定担体に吸着させる。好ましくは固定担体の 2,000〜20,0 00倍の一次蒸留物を通液し、有効成分を固定担体に吸着させる。したがって、通液 しょうとする一次蒸留物の 100〜20,000分の 1の湿潤体積量の固定担体を使用する のが好ましい。好ましくは通液しょうとする一次蒸留物の 2,000〜20,000分の 1の湿潤 体積量の固定担体を使用するのが好ましい。 [0031] The amount of the fixed carrier varies depending on the size of the column, the type of the solvent, the type of the fixed carrier, and the like. When primary distillate is used, for example, 100 to 20,000 times distillation of fixed carrier The substance is passed through and the active ingredient is adsorbed on the fixed carrier. Preferably, a primary distillate of 2,000 to 20,000 times that of the fixed carrier is passed through to adsorb the active ingredient onto the fixed carrier. Therefore, it is preferable to use a fixed carrier having a wet volume of 1/100 to 20,000 times that of the primary distillate to be passed. It is preferable to use a fixed carrier having a wet volume of 2,000 to 20,000 times that of the primary distillate to be passed.
[0032] 一次蒸留物を上記カラムに通すことにより、一次蒸留物中の消臭物質は固定担体 に吸着される。通液量及び通液速度は、一次蒸留物の蒸留方法によって異なる。ま た、一次蒸留物がアルコールを含む場合には、この液体を水で希釈してからカラムク 口マトグラフィ一に通液する必要がある。通液対象物をカラムに通液した後、不純物 除去のためカラムを水洗し、樹脂に吸着されずにカラム内に残存している成分を除 去することが好ましい。  [0032] By passing the primary distillate through the column, the deodorizing substance in the primary distillate is adsorbed on the fixed carrier. The flow rate and flow rate vary depending on the distillation method of the primary distillate. If the primary distillate contains alcohol, it is necessary to dilute this liquid with water and then pass it through the column chromatography. It is preferable to wash the column with water in order to remove impurities after removing the liquid-flowing object through the column, and remove components remaining in the column without being adsorbed by the resin.
[0033] 固定担体に吸着された成分は、溶媒により溶出する。溶出溶媒は、メタノール、エタ ノール、及び水、メタノール、エタノールの混合物から選ばれる。溶出溶媒は、水とァ ルコールの混合溶媒、特にエタノール一水混合溶媒が好ましい。更に、室温におい て効率よく目的の効果を有する成分を溶出できるので、 50/50〜99. 5/0. 5 (体 積/体積)エタノール一水混合溶媒が好ましい。このように、一次蒸留物の消臭成分 は、該溶媒で溶出される画分に存在する。溶出速度はカラムの大きさ、溶媒の種類、 固定担体の種類等によって変化するので特に限定されないが、 SV=0. ;!〜 10で溶 出し、樹脂の 6倍湿潤体積量以内に溶出する溶出液を回収するのが好ましい。なお 、 SV (Space Velocity,空間速度)は、 1時間あたり樹脂容積の何倍量の液体を通液 するかという単位である。  [0033] The component adsorbed on the fixed carrier is eluted with a solvent. The elution solvent is selected from methanol, ethanol, and a mixture of water, methanol, and ethanol. The elution solvent is preferably a mixed solvent of water and alcohol, particularly an ethanol / water mixed solvent. Furthermore, since a component having a desired effect can be efficiently eluted at room temperature, a 50/50 to 99.5 / 0.5 (volume / volume) ethanol / water mixed solvent is preferable. Thus, the deodorizing component of the primary distillate is present in the fraction eluted with the solvent. The elution rate varies depending on the column size, the type of solvent, the type of fixed carrier, etc., but is not particularly limited, but elution occurs at SV = 0.;! ~ 10 and elutes within 6 times wet volume of the resin. It is preferable to recover the liquid. Note that SV (Space Velocity) is a unit of how many times the volume of the resin is passed per hour.
[0034] 一次蒸留物のカラムクロマトグラフィー処理は、これに限定されるものではないが、 好ましくは次のようにして行うこと力 Sできる。すなわち、無置換基型の芳香族系樹脂あ るいはアクリル酸系エステル樹脂を充填したカラムに、カラム温度 60〜97°Cにて通 液対象物を通液した後、カラム内を水洗し、次いでカラムに吸着されている成分を、 カラム温度 20〜40°Cにて 50/50〜99. 5/0. 5 (体積/体積)エタノール一水混 合溶媒で溶出させ、エタノール一水混合溶媒での溶出開始時点から集めた溶出液 の量が該樹脂の 6倍湿潤体積量以内に溶出する溶出液を回収する。 [0035] 力、くしてカラムから得られた溶出液 (溶出溶媒を含む)をそのまま、又は水もしくはァ ルコール 水の混合溶媒で好適なアルコール濃度に調整して、本発明における二 次蒸留の原液として供することができる。アルコールは市販されている工業用アルコ ールまたは食品添加物用のものであれば何れでも良いが、臭気を除去する高度の 蒸留処理上、添加物が無く不純物の少ない JIS規格の 1級以上、好ましくは JIS規格 の特級が良い。アルコールとしては、例えばメタノール、エタノール、プロパノールま たはそれらの混合物等、水溶性のアルコールであれば何れでもよいが、食品用途及 び安全性を鑑みてエタノールが最適である。 [0034] The column chromatography treatment of the primary distillate is not limited to this, but it can be preferably performed as follows. That is, after passing an object to be passed through a column packed with an unsubstituted aromatic resin or acrylic ester resin at a column temperature of 60 to 97 ° C, the inside of the column was washed with water, Next, the components adsorbed on the column are eluted with 50/50 to 99.5 / 0.5 (volume / volume) ethanol / water mixed solvent at a column temperature of 20 to 40 ° C. and mixed with ethanol / water mixed solvent. Collect the eluate that elutes within 6 times the wet volume of the resin from the elution start time at (5). [0035] The eluate (including the elution solvent) obtained from the column is adjusted as it is, or adjusted to a suitable alcohol concentration with water or a mixed solvent of alcohol water, and the stock solution for secondary distillation in the present invention. Can serve as. Alcohol may be any commercially available alcohol or food additive, but it has a high degree of distillation to remove odors. A special grade of JIS standard is preferable. The alcohol may be any water-soluble alcohol such as methanol, ethanol, propanol, or a mixture thereof, but ethanol is optimal in view of food use and safety.
[0036] 二次蒸留を開始する際の原液のアルコール濃度は、好ましくは 0%より上〜 60% 以下であり、さらに好ましくは 0%より上〜 20%以下であり、よりさらに好ましくは、 0% より上〜 10%以下であり、或いは、 5%以上〜 60%以下であり、さらに好ましくは 5% 以上〜 20%以下であり、よりさらに好ましくは、 5%以上〜 10%以下である。  [0036] The alcohol concentration of the stock solution when starting the secondary distillation is preferably more than 0% to 60% or less, more preferably more than 0% to 20% or less, and still more preferably 0 % To 10% or less, or 5% to 60%, more preferably 5% to 20%, and still more preferably 5% to 10%.
[0037] 下記実施例 4、 5、 6の結果を示した表 1〜3より、二次蒸留を開始する際の釜残の エタノール濃度にかかわらず、釜残のエタノール濃度が 10%になったときに甘蔗由 来の臭いが除去されている。従って、エタノールを効率的に回収する目的からも、ェ タノール濃度を 10%またはそれに近い範囲に調整してから下記二次蒸留することが 好ましい。しかし、釜残のエタノール濃度が低い場合、例えば 5%、さらには 0%であ つても、二次蒸留によって甘蔗由来の臭いが釜残から除かれることから、必ずしもェ タノール濃度を 10%またはそれに近い濃度に調整する必要はない。  [0037] From Tables 1 to 3 showing the results of Examples 4, 5, and 6 below, the ethanol concentration in the residue was 10% regardless of the ethanol concentration in the residue when starting the secondary distillation. Sometimes the odor of Yasu Kanashi has been removed. Therefore, for the purpose of efficiently recovering ethanol, it is preferable to adjust the ethanol concentration to 10% or a range close thereto and then perform the following secondary distillation. However, if the ethanol concentration in the residue is low, for example 5% or even 0%, the odor derived from sweet potato is removed from the residue by secondary distillation. It is not necessary to adjust to a close concentration.
[0038] [二次蒸留]  [0038] [Secondary distillation]
本発明における二次蒸留とは、上記二次蒸留の原料を、加熱装置等を用いて二次 蒸留(或いは蒸発でもよレ、)することをレ、う。加熱装置等は工業的に利用されてレ、る 蒸留塔あるいは蒸留機、濃縮機、蒸発装置、加熱装置付き容器若しくは釜等を用い ること力 Sできる。好ましくは、製造、品質及びコスト面で、遠心式薄膜真空蒸発装置を 用いることが適当である。蒸留 (蒸発)の処理方法は回分式又は連続式、それらの組 み合わせた方式の何れでも良い。また、蒸留における温度 (蒸気温度若しくは品温) 及び圧力条件は常圧下であれば 90°C〜; 105°Cの範囲で、減圧(真空)下であれば 3 4〜90°Cの範囲であれば何れでも良いが、好ましくは減圧下(蒸気圧力 90mmHg 以下)で 34〜40°Cの範囲で蒸留するのが良い。 The secondary distillation in the present invention refers to secondary distillation (or evaporation) of the above-mentioned secondary distillation raw material using a heating device or the like. Heating devices, etc. can be used industrially, and can use a distillation column or distiller, concentrator, evaporator, container with heating device or kettle. It is preferable to use a centrifugal thin film vacuum evaporator in terms of manufacturing, quality and cost. The treatment method of distillation (evaporation) may be either a batch method, a continuous method, or a combination thereof. The distillation temperature (vapor temperature or product temperature) and pressure conditions are 90 ° C to 105 ° C under normal pressure, and 34 to 90 ° C under reduced pressure (vacuum). Any can be used, but preferably under reduced pressure (steam pressure 90mmHg The following should be distilled in the range of 34-40 ° C.
[0039] 二次蒸留において、釜残のアルコール濃度(体積/体積)が 0〜; 10%であり、且つ 一次蒸留物の濃縮率が蒸留前の液量に対して 20% (体積)以上(下記実施例 5、表 2の画分 3を参照)、好ましくは 30% (体積)以上、さらに好ましくは 40% (体積)以上 蒸留すれば、甘蔗由来の臭いが蒸留され、一方消臭物質は釜残に残るため、良好 に甘蔗由来の臭いを除去できる。該釜残 (すなわち、本発明の消臭剤)の臭い強度 は、下記実施例 2に記載した甘蔗由来の臭い強度評価の方法に従えば、 2 (原液より も弱いが、楽に臭いが感知できる)以下、好ましくは 1 (やっと感知できる程度)以下、 さらに好ましくは 0 (無臭)である。  [0039] In the secondary distillation, the alcohol concentration (volume / volume) of the residue in the kettle is 0 to 10%, and the concentration rate of the primary distillate is 20% (volume) or more with respect to the liquid volume before distillation ( See Example 5 below, fraction 3 in Table 2), preferably 30% (volume) or more, more preferably 40% (volume) or more, the odor derived from sweet potato is distilled while the deodorant substance is Since it remains in the pot residue, it can remove the odor derived from sweet potato well. The odor intensity of the residue (that is, the deodorant of the present invention) is 2 (weaker than the stock solution, but can be easily detected by following the method for evaluating the odor intensity derived from sweet potato described in Example 2 below. ) Or less, preferably 1 (finally perceptible) or less, more preferably 0 (odorless).
[0040] さらに好ましくは、釜残のアルコール濃度(体積/体積)が 0〜5%であり、且つ一次 蒸留物の濃縮率が蒸留前の液量に対して 40% (体積)以上(下記実施例 5、表 2の 画分 5を参照)、好ましくは 50% (体積)以上、さらに好ましくは 60% (体積)以上蒸留 すれば、甘蔗由来の臭いがほぼ完全に蒸留され、一方消臭物質は釜残に残るため 、さらに良好に甘蔗由来の臭いを除去できる。該釜残 (すなわち、本発明の消臭剤) の臭い強度は、下記実施例 2に記載した甘蔗由来の臭い強度評価の方法に従えば 、 0 (無臭)である。  [0040] More preferably, the alcohol concentration (volume / volume) of the residue in the kettle is 0 to 5%, and the concentration rate of the primary distillate is 40% (volume) or more with respect to the liquid volume before distillation (see below). Example 5, see fraction 5 in Table 2), preferably more than 50% (volume), more preferably more than 60% (volume), the odor derived from sweet potato is almost completely distilled while deodorizing substances Since it remains in the pot residue, the odor derived from sweet potato can be removed even better. The odor intensity of the residue (that is, the deodorant of the present invention) is 0 (odorless) according to the method for evaluating odor intensity derived from sweet potato described in Example 2 below.
[0041] さらに、また、本発明における一次蒸留物の溶媒がアルコール濃度(体積/体積) 10%以上の場合、水で希釈、例えば実施例 2において一次蒸留物(エタノール 59重 量%)を 20重量%に希釈して、若しくは濃縮処理を行ってから、二次蒸留に用いても 良い。  [0041] Furthermore, when the solvent of the primary distillate in the present invention has an alcohol concentration (volume / volume) of 10% or more, it is diluted with water, for example, in Example 2, the primary distillate (ethanol 59% by weight) is 20%. It may be used for secondary distillation after being diluted to% by weight or after being subjected to a concentration treatment.
[0042] [本発明の消臭剤]  [0042] [Deodorizer of the present invention]
下記実施例 2乃至 12の結果から、本発明の消臭剤は甘蔗由来の独特の臭い成分 が除去されており、且つ一次蒸留物が有する消臭効果がほとんど低減していない。 従って、本発明の消臭物質はマスキング作用は無いと考えられる力 化学的脱臭機 構の中和、分解、酸化'還元および、物理的脱臭機構の吸着、および感覚的脱臭機 構の相殺作用の複合的なメカニズムによる消臭作用を持っていると考えられる。  From the results of Examples 2 to 12 below, the deodorant of the present invention has a unique odor component derived from sweet potato removed, and the deodorizing effect of the primary distillate is hardly reduced. Therefore, the deodorant substance of the present invention is considered to have no masking action. Neutralization, decomposition, oxidation and reduction of chemical deodorizing mechanism, adsorption of physical deodorizing mechanism, and offsetting effect of sensory deodorizing mechanism. It is thought that it has a deodorizing action by a complex mechanism.
[0043] 本発明の消臭剤は、本発明の消臭剤に加えて、本発明の消臭剤以外の消臭剤( 他の消臭剤)を含有すること力できる。本発明の消臭剤と他の消臭剤とを併用するこ とにより、これら成分の有する消臭力が互いに増強され、更に速効性及び持続性を 兼備する消臭剤が得られる。 [0043] The deodorant of the present invention can contain a deodorant other than the deodorant of the present invention (other deodorant) in addition to the deodorant of the present invention. Use the deodorant of the present invention in combination with other deodorants. As a result, the deodorizing power of these components is enhanced, and a deodorant having both rapid efficacy and sustainability is obtained.
他の消臭剤はその種類は特に限定されなるものではなぐ上記本発明の消臭剤以 外の植物抽出物、有機化合物、無機化合物などから選ばれる 1種又は 2種以上の消 臭成分を使用することができ、より具体的には、例えば水酸化ナトリウム、水酸化カリ ゥム、水酸化カルシウム、炭酸ナトリウム、炭酸水素ナトリウム、硫酸、塩酸、燐酸、ス ルファミン酸、シユウ酸、ソルビン酸、フミン酸、ァスコルビン酸、リンゴ酸、メチルリンゴ 酸、マロン酸、コハク酸、アルケニルコハク酸、グノレタノレ酸、アジピン酸、ピメリン酸、フ マノレ酸、マレイン酸、メチルフマル酸、メチルマレイン酸、ィタコン酸、シトラコン酸、メ サコン酸、アセチレン酸、クェン酸、イソクェン酸、グリコール酸、酒石酸、木酢、次亜 塩素酸塩、二酸化塩素、塩素、過酸化水素、過酸化物、過マンガン酸カリウム、ホル マリン、ダリオキサール、重亜硫酸ナトリウム、亜硫酸ナトリウム、硫酸第一鉄、塩化第 二鉄、ジヒドロキシ一アセトン、 3, 5, 5—トリメチルへキサノール、 β—エトキシプロピ オンアルデヒド、グルタ口アルデヒド、メタアクリル酸エステル、マレイン酸エステル、マ レイン酸モノエステル、マレイン酸モノアミド、マレイン酸イミド、フマル酸ジアルキル、 フマル酸エステル、 β ァシルアクリル酸、 β ァシルアクリル酸塩、セネシオン酸シ トロネリノレ、 1 , 3—ペンタジェン一 1—カルボン酸アルキルエステル、ピナンハイド口 パーオキサイド、 ρ サイメンバーオキサイド、 1 , 2—プロピレンオキサイド、 1 , 2—ブ チレンオキサイド、グリシジルエーテル、 —シクロデキストリン、ヒドロキシプロビルシ クロデキストリン、ォクタァセチルサッ力ロース、 Fe (III)—ォクタカルボキシフタロシア ニン、 Fe (III)—テトラカルボキシフタロシアニン、 5 メチル 2 イソプロピル一 2— へキセナ一ノレ、オイグノーノレ、 p ブトキシフエノーノレ、力テコーノレ、ハイドロキノン、 4 ーメチルカテコール、 1 , 2, 4 トリハイドロキシベンゼン、 3 メチルカテコーノレ、 3— メトキシカテコール、没食子酸、カルノソーノレ、ロズマノール、ブラジリン、へマトキシリ ン、シコニン、ミリセチン、ノ イカレイン、バイカリン、フラボノイド、タンニン、シトラーノレ 、バニリン、クマリン、カタバミの抽出物、ドクダミの抽出物、ッガの抽出物、イチヨウの 抽出物、クロマツの抽出物、カラマツの抽出物、ァカマツの抽出物、キリの抽出物、ヒ イラギモクセィの抽出物、ライラックの抽出物、キンモクセィの抽出物、フキの抽出物、 ッヮブキの抽出物、レンギヨウの抽出物、タリの抽出物、ハンノキの抽出物、コナラの 抽出物、ザクロの抽出物、イチジクの抽出物、ゼンマイの抽出物、タニゥツギの抽出 物、力キノキの抽出物、ォォバコの抽出物、ョモギの抽出物、ャマモミジの抽出物、サ ノレスベリの抽出物、シロバナハギの抽出物、ァセビの抽出物、シダの抽出物、ャマナ ラシの抽出物、コバノトネリコの抽出物、マツ科植物の抽出物、モクセィ科植物の抽 出物、シソエキス、お茶エキス、柿抽出エキス等の植物抽出物、より具体的にはこれ らを含有する植物抽出物消臭剤として市販されている「ピユリエール」(松下電工株式 会社製)、「スメラル」(環境科学開発株式会社製)、「パンシル」(リリース科学工業株 式会社製)等、酸化亜鉛、硫酸亜鉛、塩化亜鉛、リン酸亜鉛、硝酸亜鉛、炭酸亜鉛、 酢酸亜鉛、シユウ酸亜鉛、クェン酸亜鉛、フマル酸亜鉛、ギ酸亜鉛、乳酸亜鉛、グノレ コン酸亜鉛、リシノール酸亜鉛等の亜鉛化合物などを挙げることができ、これらは 1種 単独で又は 2種以上を適宜組み合わせて使用することができる。 The type of the other deodorant is not particularly limited. One or two or more types of deodorant components selected from plant extracts, organic compounds, inorganic compounds, etc. other than the deodorant of the present invention are used. More specifically, for example, sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, sodium bicarbonate, sulfuric acid, hydrochloric acid, phosphoric acid, sulfamic acid, oxalic acid, sorbic acid, Humic acid, Ascorbic acid, Malic acid, Methyl malic acid, Malonic acid, Succinic acid, Alkenyl succinic acid, Gnoretanolic acid, Adipic acid, Pimelic acid, Fumanoleic acid, Maleic acid, Methyl fumaric acid, Methyl maleic acid, Itaconic acid, Citracon Acid, mesaconic acid, acetylenic acid, succinic acid, iso-succinic acid, glycolic acid, tartaric acid, wood vinegar, hypochlorite, chlorine dioxide, chlorine Hydrogen peroxide, peroxide, potassium permanganate, formalin, dalyoxal, sodium bisulfite, sodium sulfite, ferrous sulfate, ferric chloride, dihydroxy monoacetone, 3, 5, 5-trimethylhexanol, β —Ethoxypropionaldehyde, glutaraldehyde, methacrylic acid ester, maleic acid ester, maleic acid monoester, maleic acid monoamide, maleic acid imide, dialkyl fumarate, fumaric acid ester, β-acylacrylic acid, β-acylacrylate, Citronellinole senesionate, 1,3-pentadiene 1-carboxylic acid alkyl ester, pinanhydride peroxide, ρ thimember oxide, 1,2-propylene oxide, 1,2-butylene oxide, glycidyl ether, —cyclodext , Hydroxypropyl cyclodextrin, octacetyl saccharose, Fe (III) -octacarboxyphthalocyanine, Fe (III) -tetracarboxyphthalocyanine, 5 methyl 2 isopropyl 1-2-hexena monoole, Eugnonor, p-Butoxyphenol, Power Teconole, Hydroquinone, 4-Methylcatechol, 1,2,4 Trihydroxybenzene, 3-Methylcatechol, 3-Methoxycatechol, Gallic Acid, Carnosanol, Rosmanol, Brazirin, Hematoxylin , Shikonin, myricetin, squid kalein, baicalin, flavonoid, tannin, citralanole, vanillin, coumarin, oxalis extract, wolfberry extract, clove extract, yew extract, black pine extract, larch extract , Akamatsu extract, Li of the extract, the extract of human Iragimokusi, lilac extract, extract of Kinmokusi, extract of butterbur, Extract of tsububuki, extract of forsythia, extract of tari, extract of alder, extract of quercus, extract of pomegranate, extract of fig, spring extract, extract of cypress, power extract of cypress , Leafhopper extract, mugwort extract, chrysanthemum extract, sanoresubi extract, white-bellied extract, asebi extract, fern extract, pomeliad extract, mosquito extract, pine family Plant extracts such as plant extracts, extracts of mossaceae plants, perilla extract, tea extract, strawberry extract, etc., and more specifically, “Piurière” marketed as a plant extract deodorant containing them. "(Matsushita Electric Works Co., Ltd.)," Smeral "(Environmental Science Development Co., Ltd.)," Pansil "(Release Science Industrial Co., Ltd.), etc., zinc oxide, zinc sulfate, chlorous acid Zinc compounds such as zinc phosphate, zinc nitrate, zinc carbonate, zinc acetate, zinc oxalate, zinc citrate, zinc fumarate, zinc formate, zinc lactate, zinc gnoleconate and zinc ricinoleate. These can be used singly or in appropriate combination of two or more.
[0045] 本発明の消臭剤は、本発明の効果を妨げない限り、必要に応じて上記必須成分以 外に任意の成分を適宜配合することができる。任意成分としては、水および/または 有機溶媒、例えばエタノール、イソプロピルアルコール等のアルコール類、アセトン等 のケトン類などの親水性有機溶媒、へキサン、石油エーテルなどの疎水性有機溶媒 などの各種溶媒、界面活性剤、低温下又は高温下での液性を保持するために配合 される低級アルキルベンゼンスルホン酸又はその塩、エチレングリコールなどのハイ ドロトロープ剤、殺菌剤、防腐剤及び防カビ剤、香料、色素、酸化防止剤、増粘剤、 ゲル化剤、紫外線吸収剤などを挙げることができ、これらは本発明の効果を妨げな!/ヽ 範囲で常用量配合することができる。なお、これら任意成分に用いられる化合物は、 通常消臭剤に使用されるものならば、どのようなものでもよく、特に限定されるもので はない。 [0045] The deodorant of the present invention can contain any component other than the above essential components as needed, as long as the effects of the present invention are not hindered. As optional components, water and / or organic solvents, for example, alcohols such as ethanol and isopropyl alcohol, hydrophilic organic solvents such as ketones such as acetone, various solvents such as hydrophobic organic solvents such as hexane and petroleum ether, Surfactant, lower alkylbenzene sulfonic acid or its salt formulated to maintain liquidity at low or high temperatures, hydrotropes such as ethylene glycol, bactericides, antiseptics and fungicides, fragrances, pigments , Antioxidants, thickeners, gelling agents, ultraviolet absorbers, and the like, and these can be formulated in ordinary doses in a range that does not interfere with the effects of the present invention. The compounds used for these optional components are not particularly limited as long as they are usually used for deodorants.
[0046] 本発明の消臭剤は、使用態様が特に限定されるものではなぐ例えば液剤、エアゾ ール等のスプレー剤、或いは担体への含浸、粉末、錠剤、顆粒剤、カプセル等への 成形などの各種剤型を用途に応じて多岐にわたって選択することができ、その製造 方法も各用途及び剤型に応じて常用される成分を用いて製造することができる。  The use of the deodorant of the present invention is not particularly limited. For example, liquids, sprays such as aerosols, or impregnation on carriers, molding into powders, tablets, granules, capsules, etc. Various dosage forms such as can be selected depending on the application, and the production method can also be produced using components commonly used depending on each application and dosage form.
[0047] [本発明の消臭剤の用途] 本発明の消臭剤は、食品、エチケット消臭剤、ペット用消臭剤、環境消臭剤、消臭 洗浄剤、化粧料、消臭剤組成物の素材として、他の消臭剤、香料、アルコール、界面 活性剤、油脂、脂肪酸、エステル類、糖類、亜鉛化合物、有機酸、無機酸、アルカリ 等と混ぜて使用することができる。 [Use of deodorant of the present invention] The deodorant of the present invention is a food, etiquette deodorant, pet deodorant, environmental deodorant, deodorant cleaning agent, cosmetic, and other deodorant and fragrance as a raw material for the deodorant composition. , Alcohols, surfactants, fats and oils, fatty acids, esters, saccharides, zinc compounds, organic acids, inorganic acids, alkalis, and the like.
[0048] また、本発明の消臭剤の使用形態は特に限定されず、例えば以下の様な形態で 使用すること力できる。噴霧用として、エアゾールスプレー、ミストスプレー、スプリンク ラー用液体品、塗布用として液状 ·ゲル状 ·ペースト状消臭剤およびこれらの消臭剤 を布 '紙'不織布にしみ込ませたシート状として使用できる。他にも、粉末'顆粒に吸 収させた消臭剤、粒状 ·ペレット状 ·ブロック状 ·タブレット状ゲルへ練り込み吸着させ た消臭剤、セラミック '活性炭 ·ベントナイト'珪藻土等の多孔質担体へ吸着させた消 臭剤、液状の消臭剤を容器に入れ、スポンジ '布*セラミックス等の液体を浸透させる ものを容器中の消臭剤に一部接触させ、浸透した消臭剤が気化することにより消臭 効果を持つ消臭剤、セラミックス等の多孔質性の容器に消臭剤を入れ、容器外部ま で浸透した消臭剤が気化することにより消臭効果を持つ消臭剤、液状でそのまま悪 臭源に添加する消臭剤、シート 'フィルム'フィルターにしみ込ませた消臭剤、消臭剤 を表面あるいは内部に含む壁紙、建材、おむつ、生理用品、靴の中敷き、消臭繊維( 布)、消臭皮革等に使用できる。  [0048] The use form of the deodorant of the present invention is not particularly limited, and for example, it can be used in the following form. Can be used for spraying, aerosol spray, mist spray, sprinkler liquid, liquid for application, gel, paste deodorant and sheet with these deodorants soaked in cloth 'paper' non-woven fabric . In addition, deodorant absorbed in powder 'granules', granular · pellet form · block form · deodorant mixed and adsorbed into tablet gel, ceramic 'activated carbon · bentonite' to porous carriers such as diatomaceous earth Place the adsorbed deodorant or liquid deodorant in the container and let the liquid that is infiltrated with sponge 'cloth * ceramics etc. partially contact the deodorant in the container, and the infiltrated deodorant vaporizes Deodorant with a deodorizing effect, put the deodorant into a porous container such as ceramics, and the deodorant with a deodorizing effect by liquidizing the deodorant penetrated to the outside of the container, liquid Deodorant added directly to malodorous source, deodorant soaked in sheet 'film' filter, wallpaper containing deodorant on the surface or inside, building materials, diapers, sanitary products, insole of shoes, deodorant fiber Can be used for (cloth), deodorant leather, etc.
[0049] また、本発明の消臭剤を含む食品、エチケット消臭剤、ペット用消臭剤、環境消臭 剤、消臭洗浄剤及び化粧料には、各分野で慣用の添加剤、分散剤、賦形剤などを 含むことができる。  [0049] In addition, foods, etiquette deodorants, pet deodorants, environmental deodorants, deodorants and cosmetics containing the deodorizer of the present invention are commonly used additives and dispersions in each field. Agents, excipients, etc. can be included.
[0050] [食品]  [0050] [Food]
具体的に本発明の消臭剤は、例えば肉類、魚介類、またはユラもしくはニンニクな どの野菜類に、該食品素材のもつ不快臭を除去するために食品に添加することがで きる。  Specifically, the deodorant of the present invention can be added to foods to remove unpleasant odors of the food material, for example, meat, seafood, vegetables such as Yura or garlic.
[0051] [エチケット消臭剤]  [0051] [Etiquette deodorant]
また、本発明の消臭剤は、エチケット消臭剤の素材として使用することができる。こ こで本発明におけるエチケット消臭剤とは、口臭、脇の下などの体臭(ボディー用)、 足臭、頭髪の臭い等、ヒトに直接使用する消臭剤である。この消臭用途は不快臭の 発生源は問わず、ヒトに直接使用することを意味する。具体的には、脇の下の汗臭用 スプレー.ローション.パウダー、口臭除去用マウススプレー'カプセル'洗口剤、頭髪 に付いた焼き肉またはタバコ臭を除去する頭髪用スプレー 'シャンプー'リンス'ヘア 一ローションなどが挙げられる。 Moreover, the deodorizer of this invention can be used as a raw material of an etiquette deodorizer. Here, the etiquette deodorant in the present invention is a deodorant used directly for humans, such as bad breath, body odor such as armpit (for body), foot odor, hair odor and the like. This deodorant application is It is meant to be used directly on humans regardless of source. Specifically, underarm sweat odor spray lotion powder, mouth odor removal mouse spray 'capsule' mouthwash, hair spray to remove roasted meat or tobacco odor on hair 'shampoo' rinse 'hair one lotion Etc.
[0052] [ペット用消臭剤]  [0052] [Deodorant for pets]
また、本発明の消臭剤はペット用消臭剤の素材としても用いることができる。本発明 のペット用消臭剤とは、愛玩動物の口臭、体臭、便臭など、愛玩動物が発生源である 不快な臭いに対する消臭剤である。具体的には、ペットの口臭除去用スプレー'カブ セル、毛に付いた体臭を除去するペット用スプレー、シャンプー、リンス、ローション、 ペット用トイレ、犬小屋またはペット用ケージ等、ペット自身およびペット用品が挙げら れる。また、本発明の消臭剤は、環境消臭剤の素材としても用いることができる。  The deodorant of the present invention can also be used as a material for pet deodorants. The pet deodorant of the present invention is a deodorant for unpleasant odors originating from pet animals, such as halitosis, body odor, and fecal odor of pet animals. Specifically, pet breath removal sprays' capsules, pet sprays that remove body odor from hair, shampoos, rinses, lotions, pet toilets, kennels or pet cages, pets themselves and pet supplies Can be mentioned. Moreover, the deodorizer of this invention can be used also as a raw material of an environmental deodorizer.
[0053] 本発明の消臭剤を用いて、家庭内のペット臭に対するミストスプレータイプ消臭剤 を調製するには、より具体的には以下のような方法をとることができる。本発明の消臭 剤を 0. 01〜50% (体積/体積)の濃度で水に添加し、必要が有れば、界面活性剤 、エタノールまたは抗菌剤などを添加し、ミストスプレーボトルに充填する。  [0053] To prepare a mist spray type deodorant for domestic pet odor using the deodorant of the present invention, more specifically, the following method can be used. Add the deodorant of the present invention to water at a concentration of 0.01 to 50% (volume / volume), and if necessary, add a surfactant, ethanol or antibacterial agent, and fill the mist spray bottle. To do.
[0054] [環境消臭剤]  [0054] [Environmental deodorant]
本発明の環境消臭剤とは、ヒトまたは愛玩動物以外の物体または空間に付いた不 快臭に対する消臭剤である。具体的には、家庭用ゴミ又は産業廃棄物置場、家庭用 ゴミ又は産業廃棄物収集所、家庭用ゴミ又は産業廃棄物集積場、廃品回収所、家庭 用ゴミ又は産業廃棄物処理場等の廃棄物が発生源の悪臭、下水処理場、し尿処理 場、火葬場、と畜場、へい獣処理場、病院 ·診療所 ·検査センター、トイレ、浴室、台 所等の水回り、一般の室内および室内の建材または壁紙 (ホルマリンなど加ェに使 用した処理剤の悪臭)、カーテン、塗装、家具(塗料または加工等の処理剤の悪臭) 、押入などのカビ臭、下駄箱、エアコン、衣類、自動車'トラックの車内、自動車'トラッ クが発生するガス、電車'航空機、工場、飲食店、写真屋'現像所、ガソリンスタンド、 プロパンガス詰め替え所、クリーニング店'洗濯工場、旅館'ホテル、美容院'理髪店 、 自動車修理工場、家畜用畜舎、建設作業現場等に使用できる。  The environmental deodorant of the present invention is a deodorant for an unpleasant odor attached to an object or space other than a human or a pet animal. Specifically, disposal of household waste or industrial waste storage site, household waste or industrial waste collection site, household waste or industrial waste collection site, waste collection site, household waste or industrial waste disposal site, etc. Offensive odors from sources, sewage treatment plants, human waste treatment plants, crematoriums, slaughterhouses, animal slaughterhouses, hospitals, clinics, inspection centers, toilets, bathrooms, bathrooms, etc. Building materials or wallpaper (bad odors of processing agents used in chemicals such as formalin), curtains, painting, furniture (bad odors of processing agents such as paint or processing), mold odors such as indentations, shoe boxes, air conditioners, clothing, automobiles Inside the truck, automobile 'truck-generating gas, train' aircraft, factory, restaurant, photo shop 'development shop, gas station, propane gas refilling place, laundry shop' laundry factory, ryokan 'hotel, beauty salon' hairdressing Store, car Can be used in repair shops, livestock barns, construction sites, etc.
[0055] 本発明の環境消臭剤を用いて、トイレ、台所の生ゴミ、調理器具等に対するミストス プレータイプ消臭剤を調製するには、より具体的には以下のような方法をとることがで きる。本発明の環境消臭剤を 0. 01〜50% (体積/体積)の濃度で水に添加し、必 要が有れば界面活性剤、エタノールまたは抗菌剤などを添加し、ミストスプレーボトル に充填する。 [0055] Using the environmental deodorant of the present invention, mist for toilets, kitchen garbage, cooking utensils, etc. More specifically, the following method can be used to prepare a play type deodorant. Add the environmental deodorant of the present invention to water at a concentration of 0.01 to 50% (volume / volume). If necessary, add a surfactant, ethanol or antibacterial agent to the mist spray bottle. Fill.
[0056] 本発明の環境消臭剤を用いて、家庭内の強い悪臭である生ゴミまたはトイレの悪臭 に対するエアゾールタイプ消臭剤を調製するには、より具体的には以下のような方法 をとること力 Sできる。本発明の環境消臭剤を 0. 2〜70% (体積/体積)の濃度に水又 はエタノール水溶液で希釈し、噴射ガス(例えば LPGおよび二酸化炭素など)と共に エアゾール容器に充填する。  [0056] In order to prepare an aerosol-type deodorant for household garbage or a bathroom odor, which is a strong odor in the home, using the environmental deodorant of the present invention, more specifically, the following method is used. Taking power S. The environmental deodorant of the present invention is diluted with water or an aqueous ethanol solution to a concentration of 0.2 to 70% (volume / volume) and filled into an aerosol container together with a propellant gas (for example, LPG and carbon dioxide).
[0057] 本発明の環境消臭剤をゲル又は適当な担体に吸着または練り込むことにより、消 臭の有効成分が徐々に揮散して、消臭効果を長期間持続する空間用消臭剤を調製 するには、より具体的には以下のような方法をとることができる。本発明の消臭剤を 0 . 5〜20重量%濃度で、ゲル化剤であるカラギーナン、寒天、ローカストビーンガム、 ポリビュルアルコール、アラビアガム、ジエランガム、ゼラチン、カルボキシメチルセノレ ロース、キチン'キトサン、アルギン酸ナトリウム、ポリアクリルアミド等を単独あるいは 組み合わせたゲルに添加し、固形化する。  [0057] By adsorbing or kneading the environmental deodorant of the present invention on a gel or a suitable carrier, the active component of the deodorant is gradually volatilized, and a deodorant for space that maintains the deodorizing effect for a long period of time. More specifically, the following method can be used for the preparation. The deodorant of the present invention at a concentration of 0.5 to 20% by weight, which is a gelling agent such as carrageenan, agar, locust bean gum, polyburu alcohol, gum arabic, dielan gum, gelatin, carboxymethylsenololose, chitin 'chitosan, Add sodium alginate, polyacrylamide, etc. alone or in combination to a solid gel.
[0058] 本発明の環境消臭剤は細かい霧状にして、建物内、室内、車内、工場内等の空間 内に飛散させることにより、空間内の消臭を行うことができる。より具体的には、加湿 器、噴霧器 (例えば、加圧装置を利用してノズルより噴霧する装置)等に本発明の消 臭剤を 0. 0;!〜 20%、好ましくは 0. 01〜; 10%、さらに好ましくは 0. 01〜; 1 % (体積 /体積)濃度で水に添加し、必要が有れば界面活性剤やエタノール、抗菌剤などを 添加して運転することにより、空間内の悪臭を消臭することができる。  [0058] The environmental deodorant of the present invention can be deodorized in a space by making it into a fine mist and scattering it in a space such as a building, a room, a car, or a factory. More specifically, the deodorizer of the present invention is added to a humidifier, a sprayer (for example, a device that sprays from a nozzle using a pressurizing device), etc. in an amount of 0.0;! To 20%, preferably 0.01 to 10%, more preferably 0.01-; 1% (volume / volume) concentration added to water, and if necessary, by adding a surfactant, ethanol, antibacterial agent, etc. The odor inside can be deodorized.
[0059] 本発明の環境消臭剤を断続的または連続的に空気中に噴霧、床面に散布すること により、養豚場、養鶏場、酪農畜舎、魚市場等の悪臭の発生しやすい場所の悪臭を 除去すること力 Sできる。このとき、本発明の消臭剤は 0. 0;!〜 20%、好ましくは 0. 01 〜; 10%、さらに好ましくは 0. 0;!〜 1 % (体積/体積)の濃度に水で希釈し使用するこ とが好ましい。  [0059] By spraying the environmental deodorant of the present invention intermittently or continuously into the air and spraying it on the floor surface, it is possible to avoid the occurrence of bad odors in pig farms, poultry farms, dairy farms, fish markets, etc. The ability to remove bad odors. At this time, the deodorant of the present invention is in a concentration of 0.0 ;! to 20%, preferably 0.01 to 10%, more preferably 0.0;! To 1% (volume / volume) with water. It is preferable to dilute and use.
[0060] また、本発明の環境消臭剤を養豚、酪農、養鶏場等から発生する粪、尿又は粪尿 混合物をバキュームカー等で畑または牧草地に散布して処理することによって悪臭 の低減を行うことができる。散布前に、本発明の環境消臭剤をタンク内の粪 '尿に対 して 0. 005-0. 5% (体積/体積)の濃度で添加することにより、悪臭を抑えることが できる。 [0060] Further, the environmental deodorant of the present invention is produced from pigs, dairy farms, poultry farms, etc. Odor can be reduced by spraying the mixture on a field or pasture with a vacuum car or the like. Odor can be suppressed by adding the environmental deodorant of the present invention to the urine in the tank at a concentration of 0.005-0. 5% (volume / volume) before spraying.
[0061] また、本発明の環境消臭剤を用いて、消臭効果の高いペット排泄物処理剤を製造 すること力 Sできる。ペット用排泄物処理剤は、ベントナイト、ゼォライト、木粉、紙粉等 を主材料とし、これに必要に応じてポリアクリル酸ナトリウム、他のナトリウム化合物、マ グネシゥム化合物等を加え、これに本発明の消臭剤を主材料に対して 0. 01〜; 10重 量%添加し、適当量の水を加え、混合 '成形'乾燥することにより製造できる。これを 犬、ネコ等のペット用トイレに入れ、犬またはネコがその処理剤の上に排泄することに より、消臭効果に優れた処理剤を得ることができる。  [0061] In addition, it is possible to produce a pet excrement treating agent having a high deodorizing effect using the environmental deodorant of the present invention. The excreta treating agent for pets is mainly bentonite, zeolite, wood powder, paper powder, etc., and sodium polyacrylate, other sodium compounds, magnesium compounds, etc. are added to this as necessary, and the present invention is added thereto. 10% by weight of the deodorant of the main material is added to the main material, and an appropriate amount of water is added, followed by mixing and “molding” drying. By putting this in a pet toilet such as a dog or cat and the dog or cat excreting it on the treatment agent, a treatment agent with an excellent deodorizing effect can be obtained.
[0062] この様に、他の材料と本発明の消臭剤を混合し、成形 ·乾燥する方法において、乾 燥中に消臭剤の有効成分が完全に揮発せず残存するため、消臭効果も残存する。 また、本発明の消臭剤以外の材料を先に混合し、成形'乾燥し、得られた成形品に 本発明の消臭剤を吸収させることによつても、消臭効果を有する物品を得ることがで きる。  [0062] In this way, in the method of mixing the other material and the deodorant of the present invention, molding and drying, the active ingredient of the deodorant remains without being completely volatilized during drying. The effect also remains. Further, by mixing materials other than the deodorant of the present invention first, molding and drying, and absorbing the deodorant of the present invention in the obtained molded article, an article having a deodorizing effect can also be obtained. Obtainable.
[0063] [消臭洗浄剤]  [0063] [Deodorant cleaning agent]
本発明の消臭洗浄剤は、本発明の消臭剤を配合しており、悪臭物質に対する消臭 手段を備え、更に界面活性剤を含有することを特徴とするものである。本発明に用い る界面活性剤としては、特に限定されるものでないが、人体、ペット等に対する安全 性を考慮して、食品添加物公定書に収載される、モノグリセリンエステル、ポリグリセリ ンエステノレ、ソノレビタンエステノレ、プロピレングリコーノレエステノレ、ショ糖エステノレ、サ ポニン、レシチンが好ましい。これらの界面活性剤の配合量は、消臭洗浄剤全量に 対して、 0. 1 %〜5. 0%が好ましぐ更に好ましくは、 0. ;!〜 3. 0%であることが望ま しい。この配合量が 0. 1 %未満では、洗浄力が劣り、また 5. 0%を越えると、製品の 安定性が悪くなる恐れがある。  The deodorant cleaning agent of the present invention contains the deodorant of the present invention, has a deodorizing means for malodorous substances, and further contains a surfactant. The surfactant used in the present invention is not particularly limited, but in consideration of safety to human bodies, pets, etc., monoglycerin esters, polyglycerin esterols and sonorebitans listed in the official food additive regulations. Estenole, propyleneglycoloneestre, sucrose esterole, saponin, and lecithin are preferred. The blending amount of these surfactants is preferably 0.1% to 5.0%, more preferably 0.;! To 3.0%, based on the total amount of the deodorant cleaning agent. That's right. If the blending amount is less than 0.1%, the detergency is poor, and if it exceeds 5.0%, the stability of the product may be deteriorated.
[0064] 本発明の消臭洗浄剤は、本発明の目的が損なわれない範囲で、所望に応じて通 常の洗浄剤に慣用される添加成分の中から任意のものを選択して添加しても良い。 このような添加成分としては、例えば、エタノール、エチレングリコール、プロピレンダリ コール、ソルビトールなどの液安定化剤、平均付加モル数 5〜10のポリオキシェチレ ンイソステアリルエーテルなどの化粧品原料基準収載成分である安全性が比較的確 保されている発泡剤、抗菌剤、殺菌剤、香料、色素、酸化防止剤、増粘剤、ゲル化剤 、紫外線吸収剤、イオン交換水、麦飯石水などが挙げられる。 [0064] The deodorant cleaning agent of the present invention is selected and added as desired from among additive components commonly used in ordinary cleaning agents as long as the object of the present invention is not impaired. May be. Examples of such an additive component include a cosmetic raw material standard listed component such as a liquid stabilizer such as ethanol, ethylene glycol, propylene glycol, and sorbitol, and polyoxyethylene isostearyl ether having an average addition mole number of 5 to 10. Examples thereof include foaming agents, antibacterial agents, bactericides, fragrances, dyes, antioxidants, thickeners, gelling agents, ultraviolet absorbers, ion-exchanged water, and barley stone water, which have relatively secured properties.
[0065] 本発明の消臭洗浄剤の使用形態は、特に制限されないが、スプレータイプ(トリガ 一タイプ、ディスペンサータイプ、エアゾール)を使用することが望ましい。特に、 LPG との混合によるエアゾールタイプなどの発泡手段を備えたフォーム状であることが好 ましぐ該フォーム状は長時間安定な泡、具体的には泡の保形性がよぐ液になりにく い、又 1度振って発泡させエアゾール缶をそのまま約 1分放置させておいても再度同 様に安定な泡が発泡させるものであるものが望ましい。更に、毛足の柔らかいブラシ を用いて洗浄することも望ましレ、。  [0065] The usage form of the deodorant cleaning agent of the present invention is not particularly limited, but it is preferable to use a spray type (trigger type, dispenser type, aerosol). In particular, it is preferable that the foam form is provided with foaming means such as an aerosol type by mixing with LPG. The foam form is a foam that is stable for a long time, specifically, a foam having good shape retention. In addition, it is desirable that the foam is shaken once and foamed, and the stable foam is foamed again even if the aerosol can is left as it is for about 1 minute. In addition, it is desirable to use a soft brush with bristle feet.
[0066] [化粧料]  [0066] [Cosmetics]
本発明の化粧料は、本発明の消臭剤を消臭成分として含有し、本発明の効果を損 なわな!/、範囲内で、必要に応じて香料および/または無機系紫外線散乱剤(例えば 、脂肪酸石けん、脂肪酸、脂肪酸エステル、酸化チタン、酸化亜鉛)、本発明の消臭 剤以外の消臭剤、化粧料に用いられる成分 (例えば、保湿剤、酸化防止剤、油性成 分、乳化剤、界面活性剤、増粘剤、アルコール類、粉末成分、色材、水性成分、水、 各種皮膚栄養剤等)を必要に応じて適宜配合することができる。  The cosmetic of the present invention contains the deodorant of the present invention as a deodorant component and does not impair the effects of the present invention! /, Within the range, if necessary, a perfume and / or an inorganic ultraviolet scattering agent ( For example, fatty acid soap, fatty acid, fatty acid ester, titanium oxide, zinc oxide), deodorants other than the deodorizer of the present invention, and ingredients used in cosmetics (for example, moisturizers, antioxidants, oil components, emulsifiers) , Surfactants, thickeners, alcohols, powder components, coloring materials, aqueous components, water, various skin nutrients, etc.) can be added as necessary.
[0067] さらに、ェデト酸ニナトリウム、ェデト酸三ナトリウム、クェン酸ナトリウム、ポリリン酸ナ トリウム、メタリン酸ナトリウム、ダルコン酸、リンゴ酸等の金属封鎖剤、カフェイン、タン ニン、ベラパミル、トラネキサム酸、及びその誘導体、甘草抽出物、グラブリジン、カリ ン果実の熱水抽出物、各種生薬、酢酸トコフエノール、グリチルリチン酸、及びその誘 導体またはその塩等の薬剤、レチノイン酸、レチノール、酢酸レチノール、ピロオイォ ン酸レチノール、ノルミチン酸レチノール、及びその誘導体またはその塩等の薬剤、 ビタミン C、ァスコルビン酸リン酸マグネシウム、ァスコルビン酸ダルコシド、アルブチン 、コウジ酸等の美白剤、フノレクトース、マンノース、エリスリトーノレ、トレハロース、キシリ トール等の糖類、アルギニン、リジン等のアミノ酸、及びトリメチルグリシン等の誘導体 またはその塩等のアミノ酸等も適宜配合することができる。 [0067] Furthermore, edetate disodium, edetate trisodium, sodium citrate, sodium polyphosphate, sodium metaphosphate, darconic acid, malic acid and other metal sequestering agents, caffeine, tannin, verapamil, tranexamic acid, And derivatives thereof, licorice extract, glabrizine, hot water extract of carin fruit, various herbal medicines, tocophenol acetate, glycyrrhizic acid, and derivatives thereof or salts thereof, retinoic acid, retinol, retinol acetate, pyroion Agents such as acid retinol, retinol normitate, and derivatives or salts thereof, whitening agents such as vitamin C, magnesium ascorbate phosphate, darcoside ascorbate, arbutin, kojic acid, funolectus, mannose, erythritole, trehalose, xylitol Sugars, arginine, amino acids such as lysine, and trimethyl derivatives such as glycine Alternatively, amino acids such as salts thereof can be appropriately blended.
[0068] また、本発明の化粧料は、外皮に適用される化粧料、医薬品、及び医薬部外品に 広く適用することが可能である。その剤型はあらゆる薬剤処方形態とすることが可能 であり、溶液系、可溶化系、乳化系、粉末分散系、水 油 2層系、水 油 粉末 3層 系、ゲル、エアゾール、ミスト、及びカプセル等任意の形態で提供されることができる[0068] The cosmetic of the present invention can be widely applied to cosmetics, pharmaceuticals, and quasi-drugs applied to the outer skin. The dosage form can be any drug formulation, including solution systems, solubilization systems, emulsification systems, powder dispersion systems, oil / oil two-layer systems, oil / oil powder three-layer systems, gels, aerosols, mists, and Can be provided in any form such as a capsule
Yes
[0069] また、その使用形態も任意であり、例えばサンスクリーン、ファンデーション、乳液、 クリーム、化粧水、ローション、スプレー、ムース、ジエル、ヘアシャンプー、ヘアリンス 、ヘアトリートメント、及び口紅等、従来の化粧料に用いるものであれば何れの形態で あ使用すること力でさる。  [0069] The use form is also arbitrary, and conventional cosmetics such as sunscreens, foundations, emulsions, creams, lotions, sprays, mousses, jewels, hair shampoos, hair rinses, hair treatments, and lipsticks. It can be used in any form as long as it is used.
[0070] 実施例  [0070] Examples
以下に、実施例および比較例を挙げて本発明を更に詳細に説明する力 本発明は これらの実施例に限定されない。なお、以下の例において、%は特記ない限り、重量 %である。気体の濃度 ppmは、気体の濃度の通常の表示法に従い(モル/モル) pp mである。エタノール濃度は、アルコール濃度計(商品名: YSA— 200、矢崎計器株 式会社)で測定した。  The ability to explain the present invention in more detail with reference to the following examples and comparative examples The present invention is not limited to these examples. In the following examples,% is% by weight unless otherwise specified. Gas concentration ppm is pp m (mol / mol) according to the usual notation of gas concentration. The ethanol concentration was measured with an alcohol concentration meter (trade name: YSA-200, Yazaki Keiki Co., Ltd.).
[0071] [一次蒸留物の製造例]  [0071] [Production example of primary distillate]
原糖工場の製造工程にて得られた甘蔗の圧搾汁(Bx. 12.2) 2800Lを 250L/時 の速度で遠心式薄膜真空蒸発装置(商品名:エバポール CEP— 1、大川原製作所 株式会社)に供給し、 500〜630mmHgの減圧下、温度 90〜95°Cで留出する成分 を、冷却水温 25°C、冷却水量 15m3/時間、コンデンサ面積 2m2の条件でコンデン サにて冷却し、連続して集めた。原料圧搾汁が約 2400L、 Bx. 13.9になったときに、 蒸留を終了した。得られた蒸留液(以下、一次蒸留物 1という)は約 400Lであった。 一次蒸留物 1の色は、ほぼ無色透明であった。一次蒸留物 1は、甘蔗由来の特異な 臭いがあった。 Supply 2800L of sweet potato press (Bx. 12.2) obtained in the raw sugar factory manufacturing process to a centrifugal thin film vacuum evaporator (trade name: Evapor PEP-1, Okawara Seisakusho Co., Ltd.) at a speed of 250L / hr. The components distilled at a temperature of 90 to 95 ° C under a reduced pressure of 500 to 630 mmHg are continuously cooled by a condenser under the conditions of a cooling water temperature of 25 ° C, a cooling water amount of 15 m 3 / hour, and a capacitor area of 2 m 2. And collected. Distillation was terminated when the raw material juice reached about 2400L, Bx. 13.9. The obtained distillate (hereinafter referred to as primary distillate 1) was about 400 L. The color of the primary distillate 1 was almost colorless and transparent. Primary distillate 1 had a unique odor derived from sweet potato.
[0072] [二次蒸留物の原液の製造例]  [0072] [Production Example of Secondary Distillate Stock Solution]
一次蒸留物 1の約 400Lを、商品名 アンバーライト XAD7HP (オルガノ株式会社) 40mlを充填したカラム(カラムサイズ:内径 2· 6cm、高さ 20cm)に、 SV= 75の流速 で通液した。通液終了後、約 5分間、同じ流速で水洗した。吸着された成分を、 80% エタノール水溶液(エタノール/水 = 80/20 (体積/体積) )で溶出した。 SV= 2の 流速で通液し、はじめの 25mlの溶出液は捨て、溶出液の回収を開始した。 80%ェ タノール水溶液 80mlを通液した後は、成分の押し出しのため蒸留水を同じ速度で通 液し、回収溶出液の量が 100mlになった時点で溶出を終了した。得られた溶出液( 以下、一次蒸留物 2という、二次蒸留の原液でもある)のエタノール濃度(体積/体積 )は 59%であり、その色は、若干レモン色をした透明であった。一次蒸留物 2は、甘 蔗由来の特異な臭いがあった。 About 400L of the primary distillate 1 is packed into a column (column size: inner diameter 2.6cm, height 20cm) packed with 40ml of the trade name Amberlite XAD7HP (Organo Corporation). The liquid was passed through. After completion of the flow, the sample was washed with water at the same flow rate for about 5 minutes. The adsorbed components were eluted with an 80% aqueous ethanol solution (ethanol / water = 80/20 (volume / volume)). The solution was passed at a flow rate of SV = 2, and the first 25 ml of the eluate was discarded, and collection of the eluate was started. After passing 80 ml of 80% ethanol aqueous solution, distilled water was passed at the same speed to push out the components, and the elution was completed when the amount of the recovered eluate reached 100 ml. The ethanol concentration (volume / volume) of the obtained eluate (hereinafter also referred to as the primary distillate 2 stock solution) was 59%, and its color was transparent with a slight lemon color. Primary distillate 2 had a unique odor derived from sweet potato.
実施例 1  Example 1
[0073] 遠心式薄膜真空蒸発装置による蒸留 (本発明の消臭剤の製造方法 1)  [0073] Distillation by Centrifugal Thin Film Vacuum Evaporator (Production Method of Deodorant of the Present Invention 1)
一次蒸留物 2を、水で希釈してエタノール濃度(体積/体積)力 ¾0%になるように 希釈した (原液)。該溶液 100kgを 300L/時の速度で遠心式薄膜真空蒸発装置( 商品名:エバポール CEP— 5、大川原製作所株式会社)に供給した。該装置の濃縮 缶内圧力を 90mmHg (減圧)以下に制御し、温度(品温) 34〜40°Cで蒸留した。釜 残が約 37kgになったとき、蒸留を終了し、釜残を回収した(実施例 1で得られた画分 という)。該釜残は、淡黄色の液体であった。また、該釜残のエタノール濃度をアルコ ール濃度計で測定したところ、 5. 1 % (体積/体積)であった。  The primary distillate 2 was diluted with water so as to have an ethanol concentration (volume / volume) force of ¾0% (stock solution). 100 kg of the solution was supplied to a centrifugal thin film vacuum evaporator (trade name: Evapol CEP-5, Okawara Seisakusho Co., Ltd.) at a speed of 300 L / hour. The pressure inside the can of the apparatus was controlled to 90 mmHg (reduced pressure) or less, and distillation was carried out at a temperature (product temperature) of 34 to 40 ° C. When the residue in the kettle reached approximately 37 kg, distillation was terminated and the residue was collected (referred to as the fraction obtained in Example 1). The residue was a pale yellow liquid. Further, when the ethanol concentration of the residue in the kettle was measured with an alcohol densitometer, it was 5.1% (volume / volume).
実施例 2  Example 2
[0074] 実施例 1で得られた画分の甘蔗由来の臭いを評価した。  [0074] The sweet potato-derived odor of the fraction obtained in Example 1 was evaluated.
該画分のエタノール濃度をエタノール一水の混合溶液でエタノール濃度 45% (体 積/体積)とし、その重量を蒸留前の重量 100kgとした。該溶液を密栓容器(300ml 容の共栓付きフラスコ)に入れ、ゆるく振った後、速やかに容器内の臭い強度を 4〜7 人の熟練パネラーによって下記評価基準に従って官能評価をした。なお、比較対照 として、製造例 2で得られた一次蒸留物 2 (原液)をエタノール濃度 45% (体積/体積 )に調整し、該比較対照の臭い強度を 3とした。  The ethanol concentration of the fraction was adjusted to 45% (volume / volume) with a mixed solution of ethanol and water, and the weight was 100 kg before distillation. The solution was put into a tightly-sealed container (300 ml flask with a stopper), shaken gently, and immediately, the odor intensity in the container was sensory-evaluated according to the following evaluation criteria by 4 to 7 skilled panelists. As a comparative control, the primary distillate 2 (stock solution) obtained in Production Example 2 was adjusted to an ethanol concentration of 45% (volume / volume), and the odor intensity of the comparative control was set to 3.
[0075] 甘蔗由来の臭い強度 [0075] Odor intensity derived from sweet potato
0 : 無臭  0: Odorless
1 : やっと感知できる程度 2 : 一次蒸留物 2よりも弱いが、楽に臭いが感知できる 1: At last it can be perceived 2: It is weaker than primary distillate 2, but it can be easily detected.
3 : 一次蒸留物 2と同程度の臭い  3: Odor equivalent to primary distillate 2
4 : 一次蒸留物 2よりも強烈な臭い  4: Stronger smell than primary distillate 2
[0076] 官能評価の結果、実施例 1で得られた画分について臭い強度の平均値は 0であつ た。従って、実施例 1で得られた画分の臭気は、一次蒸留物 2に比べて改善された。 実施例 3 [0076] As a result of the sensory evaluation, the average value of the odor intensity of the fraction obtained in Example 1 was 0. Therefore, the odor of the fraction obtained in Example 1 was improved compared to the primary distillate 2. Example 3
[0077] 遠心式薄膜真空蒸発装置による蒸留 (本発明の消臭剤の製造方法 2)  [0077] Distillation by centrifugal thin film vacuum evaporator (Production method 2 of deodorant of the present invention)
甘蔗由来の一次蒸留物である [「さとうきび抽出物 MSX_245」(エタノール濃度 45% (体積/体積) )、三井製糖株式会社製]の溶液 600kg (原液)を 300L/時の速度で 遠心式薄膜真空蒸発装置 (商品名:エバポール CEP— 5、大川原製作所株式会社) に供給した。該装置の濃縮缶内圧力を 90mmHg (減圧)以下に制御し、温度(品温) 34〜40°Cで蒸留した。釜残が約 113kgになったとき、蒸留を終了し、釜残を回収し た。該釜残は、ほぼ無色〜淡黄色の液体であった。また、該釜残のエタノール濃度を アルコール濃度計で測定したところ、 3. 5% (体積/体積)であった。  Centrifugal thin film vacuum of 600 kg (stock solution) of [sugar cane extract MSX_245] (ethanol concentration 45% (volume / volume)), made by Mitsui Sugar Co., Ltd.] Evaporator (trade name: Evapole CEP-5, Okawara Seisakusho Co., Ltd.) was supplied. The pressure in the concentration can of the apparatus was controlled to 90 mmHg (reduced pressure) or less, and the temperature (product temperature) was distilled at 34 to 40 ° C. When the kettle residue reached approximately 113 kg, distillation was terminated and the kettle residue was recovered. The residue was almost colorless to light yellow liquid. Further, when the ethanol concentration of the residue was measured with an alcohol concentration meter, it was 3.5% (volume / volume).
[0078] 該釜残の甘蔗由来の臭いを評価した。該釜残のエタノール濃度をエタノール一水 の混合溶液でエタノール濃度 45% (体積/体積)に調整し、その重量を蒸留前と同 じ重量 600kgとした。なお、比較対照として、さとうきび抽出物 MSX_245 (原液)をエタ ノール濃度 45% (体積/体積)とし、該比較対照の臭い強度を 3とした。官能評価の 方法は、実施例 2に記載したとおりである。  [0078] The odor derived from the sweet potato of the residue was evaluated. The ethanol concentration in the kettle residue was adjusted to an ethanol concentration of 45% (volume / volume) with a mixed solution of ethanol and water, and the weight was 600 kg, the same as before distillation. As a comparative control, sugarcane extract MSX_245 (stock solution) had an ethanol concentration of 45% (volume / volume), and the odor intensity of the comparative control was 3. The method for sensory evaluation is as described in Example 2.
[0079] 官能評価の結果、臭い強度の平均値は 1であった。従って、該釜残の臭気は、原 液に比べて改善された。  As a result of sensory evaluation, the average value of odor intensity was 1. Therefore, the odor of the residue was improved compared to the stock solution.
実施例 4  Example 4
[0080] ロータリーエバポレーターによる蒸留(本発明の消臭剤の製造方法 3)  [0080] Distillation with a rotary evaporator (Method for producing deodorant of the present invention 3)
甘蔗由来の一次蒸留物である [「さとうきび抽出物 MSX_245」、三井製糖株式会社 製]の溶液を、水でエタノール濃度(体積/体積)力 ¾0%になるように調整した (原液 、画分 1)。該溶液 1000mlをロータリーエバポレーター(東京理化器械株式会社)に 供し、 90mmHg (減圧)以下、蒸気温が 30〜40°Cの範囲で蒸留した。同時に、釜残 力 SlOOml蒸留するごとに釜残についてサンプリングを行い(画分 2〜; 10)、釜残が乾 固するまで蒸留し画分 11を得た。画分;!〜 11の夫々につ!/、てエタノール濃度をアル コール濃度計で測定した。また、画分 1〜; 11の夫々について甘蔗由来の臭いを評価 した。該画分の夫々のエタノール濃度をエタノール一水の混合溶液でエタノール濃 度 45% (体積/体積)、その重量を蒸留前の重量と同じに調整した。なお、比較対照 として、さとうきび抽出物 MSX-245 (原料)をエタノール濃度 45% (体積/体積)に調 整し、該比較対照の臭い強度を 3とした。官能評価の方法は、実施例 2に記載したと おりである。その結果を表 1に示す。 A solution of [“sugar cane extract MSX_245”, manufactured by Mitsui Sugar Co., Ltd.], a primary distillate derived from sweet potato, was adjusted with water so that the ethanol concentration (volume / volume) force was ¾0% (stock solution, fraction 1 ). 1000 ml of the solution was supplied to a rotary evaporator (Tokyo Rika Kikai Co., Ltd.), and distilled at a temperature of 90 mmHg (decompression) or less and a vapor temperature of 30 to 40 ° C. At the same time, the residue is sampled every time SlOOml distillation is carried out (fractions 2 ~; 10). Distill until solid to obtain fraction 11. The ethanol concentration was measured with an alcohol densitometer for each of the fractions !!-11. Moreover, the odor derived from sweet potato was evaluated for each of fractions 1 to 11; The ethanol concentration of each of the fractions was adjusted to 45% (volume / volume) with a mixed solution of ethanol and water, and the weight was adjusted to be the same as the weight before distillation. As a comparative control, sugarcane extract MSX-245 (raw material) was adjusted to an ethanol concentration of 45% (volume / volume), and the odor intensity of the comparative control was set to 3. The method of sensory evaluation is as described in Example 2. The results are shown in Table 1.
[表 1] [table 1]
Figure imgf000024_0001
Figure imgf000024_0001
表 1より、釜残の蒸留量 (濃縮率)が多くなり、釜残のエタノール濃度が減少するほ ど、臭い強度が弱くなり、甘蔗由来の臭いが減少した。特に、エタノール濃度 5%以 下の画分 5〜; 11では著しく臭気が改善された(臭い強度 1又は 0)。エタノール濃度 1 0%以下の画分 4では臭気が改善された(臭い強度 2)。一方、エタノール濃度 10% より多い画分 1〜3では臭い強度が比較対照と同じであることから、甘蔗由来の臭い が改善されていない。 From Table 1, the distillation amount (concentration rate) of the residue in the kettle increased, and as the ethanol concentration in the residue in the kettle decreased, the odor intensity decreased and the odor derived from sweet potato decreased. In particular, the odor was significantly improved in fractions 5 to 11 with an ethanol concentration of 5% or less (odor intensity 1 or 0). Odor was improved in fraction 4 with an ethanol concentration of 10% or less (odor intensity 2). On the other hand, in fractions 1 to 3 with an ethanol concentration of more than 10%, the odor intensity is the same as that of the control, so the odor derived from sweet potato is not improved.
実施例 5 [0083] ロータリーエバポレーターによる蒸留(本発明の消臭剤の製造方法 4) 実施例 4と同じさとうきび抽出物 MSX-245を、水でエタノール濃度(体積/体積)が 10%になるように調整した(原液、画分 1)。該溶液 1000mlをロータリーエバポレー ター(東京理化器械株式会社)に供し、実施例 4と同条件にて蒸留した。同時に、釜 残が 100ml蒸留するごとに釜残についてサンプリングを行い(画分 2〜; 10)、釜残の 液量が 100mlになったときに蒸留を終了した。画分;!〜 10の夫々についてエタノー ル濃度をアルコール濃度計で測定した。また、画分 1〜; 10の夫々について甘蔗由来 の臭いを評価した。評価方法は、実施例 4に記載したとおりである。その結果を表 2に 示す。 Example 5 [0083] Distillation by rotary evaporator (Method 4 for producing deodorant of the present invention) The same sugarcane extract MSX-245 as in Example 4 was adjusted with water so that the ethanol concentration (volume / volume) was 10%. (Stock solution, fraction 1). 1000 ml of this solution was subjected to a rotary evaporator (Tokyo Rika Kikai Co., Ltd.) and distilled under the same conditions as in Example 4. At the same time, every time 100 ml of the residue was distilled, the residue was sampled (fractions 2 to 10), and the distillation was terminated when the amount of the residue was 100 ml. The ethanol concentration of each of fractions !! to 10 was measured with an alcohol densitometer. Moreover, the odor derived from sweet potato was evaluated for each of fractions 1 to 10; The evaluation method is as described in Example 4. The results are shown in Table 2.
[0084] [表 2]  [0084] [Table 2]
Figure imgf000025_0001
Figure imgf000025_0001
表 2より、釜残の蒸留量 (濃縮率)が多くなり、釜残のエタノール濃度が減少するほ ど、臭い強度が弱くなり、甘蔗由来の臭いが減少した。特に、エタノール濃度 5%以 下の画分 3〜; 10では著しく臭気が改善された(臭い強度 1又は 0)。エタノール濃度 5 . 7%の画分 2では臭気が改善された(臭い強度 2)。一方、エタノール濃度 10%の画 分 1は蒸留開始前でありその臭い強度が比較対照と同じであることから、甘蔗由来の 臭いが改善されていない。 また、釜残のエタノール濃度が 10%の場合、実施例 4の場合と異なり、釜残のエタ ノール濃度が低いことから蒸留開始後まもなく甘蔗由来の臭いが減少した。 According to Table 2, the distillation amount (concentration rate) of the residue in the kettle increased, and as the ethanol concentration in the residue in the kettle decreased, the odor intensity decreased and the odor derived from sweet potato decreased. In particular, the odor was significantly improved in fractions 3 to 10 with an ethanol concentration of 5% or less (odor intensity 1 or 0). Odor was improved in fraction 2 with an ethanol concentration of 5.7% (odor intensity 2). On the other hand, fraction 1 with an ethanol concentration of 10% was before the start of distillation and its odor intensity was the same as that of the comparative control, so the odor derived from sweet potato was not improved. When the ethanol concentration in the residue was 10%, unlike the case of Example 4, the ethanol concentration in the residue was low, so that the odor derived from sweet potato decreased soon after the start of distillation.
実施例 6  Example 6
[0086] ロータリーエバポレーターによる蒸留(本発明の消臭剤の製造方法 5)  [0086] Distillation with a rotary evaporator (Production method 5 of deodorant of the present invention)
実施例 4と同じさとうきび抽出物 MSX-245を、水でエタノール濃度(体積/体積)が 40%になるように調整した(原液、画分 1)。該溶液 1000mlをロータリーエバポレー ター(東京理化器械株式会社)に供し、実施例 4と同条件にて蒸留した。同時に、釜 残が 100ml蒸留するごとに釜残についてサンプリングを行い(画分 2〜; 10)、釜残の 液量が 100mlになったときに蒸留を終了した。画分;!〜 10の夫々についてエタノー ル濃度をアルコール濃度計で測定した。また、画分 1〜; 10の夫々について甘蔗由来 の臭いを評価した。評価方法は、実施例 4に記載したとおりである。その結果を表 3に 示す。  The same sugarcane extract MSX-245 as in Example 4 was adjusted with water so that the ethanol concentration (volume / volume) was 40% (stock solution, fraction 1). 1000 ml of this solution was subjected to a rotary evaporator (Tokyo Rika Kikai Co., Ltd.) and distilled under the same conditions as in Example 4. At the same time, every time 100 ml of the residue was distilled, the residue was sampled (fractions 2 to 10), and the distillation was terminated when the amount of the residue was 100 ml. The ethanol concentration of each of fractions !! to 10 was measured with an alcohol densitometer. Moreover, the odor derived from sweet potato was evaluated for each of fractions 1 to 10; The evaluation method is as described in Example 4. The results are shown in Table 3.
[0087] [表 3]  [0087] [Table 3]
Figure imgf000026_0001
表 3より、釜残の蒸留量 (濃縮率)が多くなり、釜残のエタノール濃度が減少するほ ど、臭い強度が弱くなり、甘蔗由来の臭いが減少した。特に、エタノール濃度 10%以 下の画分 7〜; 10では著しく臭気が改善された(臭い強度 1又は 0)。エタノール濃度 1 1. 5%の画分 6では臭気が改善された(臭い強度 2)。一方、エタノール濃度 12%以 上の画分 1〜5では臭い強度が比較対照と同じであることから、甘蔗由来の臭いが改 善されていない。
Figure imgf000026_0001
From Table 3, the distillation amount (concentration rate) of the residue in the kettle increased, and as the ethanol concentration in the residue in the kettle decreased, the odor intensity decreased and the odor derived from sweet potato decreased. In particular, the odor was remarkably improved in the fractions 7 to 10 where the ethanol concentration was 10% or less (odor intensity 1 or 0). Odor was improved in fraction 6 with an ethanol concentration of 11.5% (odor intensity 2). On the other hand, ethanol concentration of 12% or less In the above fractions 1-5, the odor intensity is the same as the control, so the odor derived from sweet potato is not improved.
[0089] 実施例 4〜6の結果から、蒸留前のエタノール濃度にかかわらず、釜残のエタノー ル濃度が 10%程度になったときに甘蔗由来の臭いが留去されている。従って、蒸留 前のエタノール濃度を 10%に調整することにより、短時間で甘蔗由来の臭いを留去 することが可能である。  [0089] From the results of Examples 4 to 6, the sweet potato-derived odor was distilled off when the ethanol concentration of the residue in the kettle reached about 10%, regardless of the ethanol concentration before distillation. Therefore, by adjusting the ethanol concentration before distillation to 10%, the odor derived from sweet potato can be distilled off in a short time.
実施例 7  Example 7
[0090] ロータリーエバポレーターによる蒸留(本発明の消臭剤の製造方法 6)  [0090] Distillation by rotary evaporator (Production method of deodorant of the present invention 6)
実施例 4と同じさとうきび抽出物 MSX_245 (原液、画分 1)を、水でエタノール濃度( 体積/体積)が 20%になるように調整した。該溶液 1000mlをロータリーエバポレー ター(東京理理化器械株式会社)に供し、 375mmHg (減圧)に制御し、蒸気温が 70 〜84°Cの範囲で蒸留した。同時に、釜残が 100ml蒸留するごとに釜残についてサ ンプリングを行い(画分 2〜; 10)、釜残の溶量が 100mlになったときに蒸留を終了し た。画分 1〜; 10の夫々についてエタノール濃度をアルコール濃度計で測定した。ま た、画分の臭いの評価を実施例 4に記載したとおりである。その結果を表 4に示す。  The same sugarcane extract MSX_245 (stock solution, fraction 1) as in Example 4 was adjusted with water so that the ethanol concentration (volume / volume) was 20%. 1000 ml of the solution was subjected to a rotary evaporator (Tokyo Rika Instruments Co., Ltd.), controlled to 375 mmHg (decompression), and distilled at a steam temperature in the range of 70 to 84 ° C. At the same time, every time 100 ml of the residue was distilled, the residue was sampled (fractions 2 to 10), and the distillation was terminated when the amount of residue in the residue reached 100 ml. The ethanol concentration of each of fractions 1 to 10 was measured with an alcohol densitometer. The evaluation of the odor of the fractions is as described in Example 4. The results are shown in Table 4.
[0091] [表 4]  [0091] [Table 4]
Figure imgf000027_0001
Figure imgf000027_0001
[0092] 表 4より、釜残の蒸留量 (濃縮率)が多くなり、釜残のエタノール濃度が減少するほ ど、臭い強度が弱くなり、甘蔗由来の臭いが減少した。特に、エタノール濃度 5% (体 積/体積)以下の画分 4〜; 10では著しく臭気が改善された(臭い強度 1又は 0)。エタ ノール濃度 10%以下の画分 3では臭気が改善された(臭い強度 2)。一方、エタノー ル濃度 12%以上の画分 1〜2では臭い強度が比較対照と同じであることから、甘蔗 由来の臭レ、が改善されて!/、なレ、。 [0092] From Table 4, the amount of distillation (concentration rate) of the residue in the kettle increases and the ethanol concentration in the residue in the kettle decreases. However, the odor intensity decreased and the odor derived from sweet potato decreased. In particular, the odor was remarkably improved (odor intensity 1 or 0) in fractions 4 to 10 with an ethanol concentration of 5% (volume / volume) or less. Odor was improved in fraction 3 with an ethanol concentration of 10% or less (odor intensity 2). On the other hand, in fractions 1 and 2 with an ethanol concentration of 12% or more, the odor intensity was the same as that of the comparative control, so the odor derived from sweet potato was improved!
実施例 8  Example 8
[0093] 開放容器 (釜)による蒸留 (本発明の消臭剤の製造方法 7)  [0093] Distillation in open container (kettle) (Production method of deodorant of the present invention 7)
実施例 4と同じさとうきび抽出物 MSX_245 (原液、画分 1)を、水でエタノール濃度( 体積/体積)が 20%になるように調整した。該溶液 1000mlをガラス製ビーカー(容 器)に供し、ドラフトチャンバ内に設置したガスコン口にて加熱し、常圧下、液温が 85 〜; 105°Cの範囲で蒸留した。同時に、釜残が 100ml蒸留するごとに釜残についてサ ンプリングを行い(画分 2〜10)、釜残の液量が 100mlになったとき蒸留を終了した。 画分;!〜 10の夫々についてエタノール濃度をアルコール濃度計で測定した。また、 画分 1〜; 10の夫々について甘蔗由来の臭いを評価した。評価方法は、実施例 4に記 載したとおりである。その結果を表 5に示す。  The same sugarcane extract MSX_245 (stock solution, fraction 1) as in Example 4 was adjusted with water so that the ethanol concentration (volume / volume) was 20%. 1000 ml of the solution was supplied to a glass beaker (container), heated at a gas conical port installed in a draft chamber, and distilled under normal pressure at a liquid temperature of 85 to 105 ° C. At the same time, every time 100 ml of the residue was distilled, the residue was sampled (fractions 2 to 10), and the distillation was terminated when the remaining amount of the residue was 100 ml. The ethanol concentration of each of fractions !! to 10 was measured with an alcohol concentration meter. Moreover, the odor derived from sweet potato was evaluated for each of fractions 1 to 10; The evaluation method is as described in Example 4. The results are shown in Table 5.
[0094] [表 5]  [0094] [Table 5]
Figure imgf000028_0001
Figure imgf000028_0001
[0095] 表 5より、釜残の蒸留量 (濃縮率)が多くなり、釜残のエタノール濃度が減少するほ ど、臭い強度が弱くなり、甘蔗由来の臭いが減少した。特に、エタノール濃度 8% (体 積/体積)以下の画分 4〜; 10では著しく臭気が改善された(臭い強度 1又は 0)。エタ ノール濃度 10. 5%の画分 3では臭気が改善された(臭い強度 2)。一方、エタノール 濃度 14%以上の画分 1〜2では臭い強度が比較対照と同じであることから、甘蔗由 来の臭!/、が改善されて!/、なレ、。 [0095] From Table 5, the distillation amount (concentration rate) of the residue in the kettle increases and the ethanol concentration in the residue in the kettle decreases. However, the odor intensity decreased and the odor derived from sweet potato decreased. In particular, the odor was remarkably improved (odor intensity 1 or 0) in fractions 4 to 10 with an ethanol concentration of 8% (volume / volume) or less. Odor was improved in fraction 3 with an ethanol concentration of 10.5% (odor intensity 2). On the other hand, in fractions 1 and 2 with an ethanol concentration of 14% or more, the odor intensity is the same as that of the control, so the odor derived from Gansu!
実施例 9  Example 9
[0096] 消臭剤の調製 [0096] Preparation of deodorant
実施例 1で製造した画分 11について、エタノール一水の混合溶媒でエタノール 45 % (体積/体積)濃度になるように且つ蒸留前と同じ重量になるように調整した後、さ らに 45% (体積/体積)エタノールで 3倍希釈溶液とした。同様に、実施例 3〜8で製 造した画分 10の夫々について、水若しくはエタノール一水の混合溶媒でエタノール 45% (体積/体積)濃度になるように且つ蒸留前と同じ重量になるように調整した後 、さらに 45% (体積/体積)エタノールで 3倍希釈溶液とした。各 3倍希釈溶液を塩酸 若しくは水酸化ナトリウムで pH 6.5〜pH 8.5の範囲内に調整後、 4°Cでー晚静置した 。夫々について、メンブレンフィルター(型番 C045A047A、アドバンテク東洋株式会社 製)でろ過した。該濾過液の夫々を、実施例 1の消臭剤、実施例 3の消臭剤、実施例 4の消臭剤、実施例 5の消臭剤、実施例 6の消臭剤、実施例 7の消臭剤、実施例 8の 消臭剤とした。  Fraction 11 produced in Example 1 was adjusted to a concentration of 45% (volume / volume) of ethanol with a mixed solvent of ethanol and water so that it had the same weight as before distillation, and then 45% (Volume / volume) A 3-fold diluted solution was made with ethanol. Similarly, each of the fractions 10 produced in Examples 3 to 8 is adjusted to a concentration of 45% (volume / volume) ethanol with a mixed solvent of water or ethanol / water, and the same weight as before distillation. Then, the solution was further diluted 3 times with 45% (volume / volume) ethanol. Each 3-fold diluted solution was adjusted to pH 6.5 to pH 8.5 with hydrochloric acid or sodium hydroxide, and allowed to stand at 4 ° C. Each was filtered with a membrane filter (model number C045A047A, manufactured by Advantech Toyo Co., Ltd.). Each of the filtrates was deodorized in Example 1, Deodorant in Example 3, Deodorant in Example 4, Deodorant in Example 5, Deodorant in Example 6, Example 7 The deodorant of Example 8 was used.
実施例 10  Example 10
[0097] 硫化水素に対する消臭効果 (ガスクロマトグラフィー分析)  [0097] Deodorizing effect on hydrogen sulfide (gas chromatography analysis)
硫化水素ガスの調製は、以下の通りである。 20ml容ヘッドスペースバイアルに 360 mM硫化ナトリウム溶液を 0. 1ml入れ、 720mM塩酸 0. 1mlをゆっくりと加えて混合 した。これを 30°Cのインキュベーターに 30分間入れ、ガスを揮発させた。このへッドス ペースガスを試験用硫化水素ガスとして用いた。  Preparation of hydrogen sulfide gas is as follows. In a 20 ml headspace vial, 0.1 ml of 360 mM sodium sulfide solution was added, and 0.1 ml of 720 mM hydrochloric acid was slowly added and mixed. This was placed in a 30 ° C. incubator for 30 minutes to volatilize the gas. This head space gas was used as a test hydrogen sulfide gas.
[0098] 実施例 9で調製した消臭剤(実施例 1、 3〜8の消臭剤)の夫々を pH 8.0に調整した 後、該消臭剤の lml夫々を新しい 20ml容ヘッドスペースバイアルに夫々入れ、密栓 し、測定用サンプルとした。陽性対照サンプルとして、上記消臭剤の代わりに、実施 例 4と同じさとうきび抽出物 MSX_245 (三井製糖株式会社製)を用いた。また、対照サ ンプルとして、消臭剤を含まな!/、45% (体積/体積)エタノール水溶液を用いた。 [0098] After adjusting each of the deodorants prepared in Example 9 (deodorants of Examples 1 and 3 to 8) to pH 8.0, each lml of the deodorant was put into a new 20 ml headspace vial. Each was put, sealed, and used as a measurement sample. As a positive control sample, the same sugarcane extract MSX_245 (manufactured by Mitsui Sugar Co., Ltd.) as in Example 4 was used instead of the deodorant. Also, control As a sample, a deodorant-free! /, 45% (volume / volume) ethanol aqueous solution was used.
[0099] 試験用硫化水素ガスの入ったバイアルから、ヘッドスペースガスをエアシリンジ(0. lml)で 0. 04ml取り、測定用サンプル、陽性対照サンプルおよび対照サンプルの夫 々に加えて、 30°Cでインキュベートした。インキュベーション開始から 30分後にその ヘッドスペースガスをエアシリンジ(lml)で 0· lml採取し、ガスクロマトグラフィー分 析(ガスクロマト装置: G— 3900 日立製作所製、カラム: CP- Silica Plot、検出器 F PD、試料注入口温度 200°C、検出器温度 230°C、カラム温度 220°C、キヤリャ 一ガス圧力 200kPa、 FPD用ガス圧力 O 60kPa、H 60kPa [0099] From the vial containing hydrogen sulfide gas for test, 0.04 ml of headspace gas was taken with an air syringe (0.1 ml) and added to each of the measurement sample, the positive control sample, and the control sample, 30 ° Incubated with C. 30 minutes after the start of incubation, 0 ml of the headspace gas was collected with an air syringe (lml) and analyzed by gas chromatography (gas chromatograph: G-3900, Hitachi, column: CP- Silica Plot, detector F PD, sample inlet temperature 200 ° C, detector temperature 230 ° C, column temperature 220 ° C, carrier single gas pressure 200 kPa, FPD gas pressure O 60 kPa, H 60 kPa
2 2 、 N 150kPa)  (2 2, N 150kPa)
2  2
を fiつた。  Fi.
[0100] 硫化水素に対する消臭率は、次の式により求めた。  [0100] The deodorization rate for hydrogen sulfide was determined by the following equation.
消臭率(%) = [ (じー3)/じ] 100  Deodorization rate (%) = [(ji-3) / ji] 100
c:対照サンプル容器内の硫化水素ガス濃度  c: Hydrogen sulfide gas concentration in the control sample container
s:測定用サンプル容器内または陽性対照容器内の硫化水素ガス濃度  s: Hydrogen sulfide gas concentration in the sample container for measurement or in the positive control container
[0101] その結果を図 1に示す。図 1より、実施例 9で調製した各消臭剤は、陽性対照サン プルと同程度に、硫化水素の濃度を減少させた。実施例 9で調製した消臭剤の硫化 水素に対する消臭メカニズムは、おそらく化学的消臭によるものと考えられる。 [0101] The results are shown in Figure 1. From FIG. 1, each deodorant prepared in Example 9 reduced the concentration of hydrogen sulfide to the same extent as the positive control sample. The deodorizing mechanism for hydrogen sulfide of the deodorant prepared in Example 9 is probably due to chemical deodorization.
実施例 11  Example 11
[0102] イソ吉草酸に対する消臭効果 (官能試験)  [0102] Deodorizing effect on isovaleric acid (sensory test)
蒸留水を活性炭カラムに通した 100ml無臭水、実施例 9で調製した消臭剤の夫々 (測定用サンプル)を、 300mlの共栓付き三角フラスコ(濃褐色透明フラスコ)に夫々 0. lml添加した。これに 1 % (質量/体積)のイソ吉草酸水溶液を 100 1注入し、 30 分間放置後に熟練パネラー 7名による官能評価を行って平均をとつた。陽性対照サ ンプルとして、上記消臭剤の代わりに、実施例 4と同じさとうきび抽出物 MSX_245 (三 井製糖株式会社製)を用いた。また、対照サンプルとして、消臭剤を含まない 45% ( 体積/体積)エタノール水溶液を用いた。  100 ml of odorless water in which distilled water was passed through an activated carbon column and each of the deodorizers prepared in Example 9 (samples for measurement) were added to 0.1 ml each of a 300 ml conical stoppered flask (dark brown transparent flask). . 100% 1% (mass / volume) aqueous solution of isovaleric acid was injected into this, and after standing for 30 minutes, sensory evaluation was conducted by 7 skilled panelists to obtain an average. As a positive control sample, the same sugarcane extract MSX_245 (manufactured by Mitsui Sugar Co., Ltd.) as in Example 4 was used instead of the deodorant. As a control sample, a 45% (volume / volume) ethanol aqueous solution containing no deodorant was used.
[0103] イソ吉草酸に対する消臭効果は、悪臭防止法の下記に示す 6段階臭気強度表示 法に準じた。その結果を下記表 6に示す。  [0103] The deodorizing effect on isovaleric acid was in accordance with the 6-step odor intensity labeling method shown below in the malodor control method. The results are shown in Table 6 below.
[0104] 6段階臭気強度表示法に評価基準 0 : 無臭 [0104] Evaluation criteria for 6-step odor intensity display method 0: Odorless
1 : やっと感知できる臭い  1: The smell you can finally detect
2: のにおいであるかわかる弱い臭い  2: A weak smell that tells you the smell
3 : 楽に感知できる臭い  3: Easily perceived odor
4 : 強い臭い  4: Strong smell
5 : 強烈な臭い  5: Strong smell
[0105] 表 6より、実施例 9で調製した各消臭剤は、陽性対照サンプルと同程度以上のイソ 吉草酸に対する消臭効果を示した。  [0105] From Table 6, each of the deodorizers prepared in Example 9 showed a deodorizing effect on isovaleric acid that was equal to or higher than that of the positive control sample.
[0106] [表 6] [0106] [Table 6]
Figure imgf000031_0001
実施例 12
Figure imgf000031_0001
Example 12
[0107] タバコ臭に対する消臭効果 (官能試験)  [0107] Deodorizing effect on tobacco odor (sensory test)
タバコ臭付着布地の調製は、 5L容三角フラスコを逆さにし、火のついたタバコを三 角フラスコの開口部から約 5cm入れ、タバコの煙を約 30〜40秒間捕集し、 lOcm X 10cmの布地 (綿タオル)に煙を捕集した三角フラスコに入れて素早く密栓し、フラス コを振盪しながら布地に煙を吸わせ、 5分後に布地を取り出し、試験用布地とした。そ して、測定用サンプルとして、実施例 9で調製した各消臭剤の 200倍希釈液を約 0.75 gスプレーした後、良く揉み、均一化にした。陽性対照として、上記消臭剤の代わりに 、実施例 4と同じさとうきび抽出物 MSX— 245の 200倍希釈液を用いた。また、対照 として、スプレーで蒸留水を試験用布地に 5回スプレー(0.15g X 5回 =約 0.75g)した 後、良く揉み、均一化にした。該試験用布地は評価に供するまで、室温で密封容器( 密封アルミパック)に保存した。  To prepare the tobacco odor-attached fabric, invert the 5 L Erlenmeyer flask, put a lit cigarette about 5 cm from the opening of the triangular flask, collect the cigarette smoke for about 30-40 seconds, and add lOcm x 10 cm. Placed in a Erlenmeyer flask that collected smoke on a cloth (cotton towel), quickly sealed, smoked into the cloth while shaking the flask, removed the cloth after 5 minutes, and used as a test cloth. Then, as a measurement sample, about 0.75 g of a 200-fold diluted solution of each deodorant prepared in Example 9 was sprayed, and then it was thoroughly stirred and homogenized. As a positive control, a 200-fold diluted solution of sugar cane extract MSX-245 as in Example 4 was used instead of the deodorant. In addition, as a control, distilled water was sprayed 5 times (0.15 g x 5 times = about 0.75 g) on the test fabric by spraying, and then it was thoroughly squeezed and homogenized. The test fabric was stored in a sealed container (sealed aluminum pack) at room temperature until evaluation.
[0108] 評価は各サンプルを噴霧後、 4〜5時間、 1日、 7日後に熟練パネラー 8名による官 能評価を行って平均をとつた。評価基準は以下の通りである。その結果を表 7に示す [0109] 官能評価基準 [0108] After the spraying of each sample, the evaluation was performed by evaluating the function by 8 skilled panelists 4 to 5 hours, 1 day and 7 days later and taking an average. The evaluation criteria are as follows. The results are shown in Table 7. [0109] Sensory evaluation criteria
◎: 完全に臭いが消えた  ◎: The smell disappeared completely
〇: かなり臭いが消えた  〇: The smell disappeared
Δ : わずかに臭いが消えた  Δ: Smell disappeared slightly
X: 消臭されていない  X: Not deodorized
[0110] [表 7]  [0110] [Table 7]
Figure imgf000032_0001
Figure imgf000032_0001
[0111] 表 7より、実施例 9で調製した各消臭剤は、陽性対照サンプルと同程度のタバコ臭 に対する消臭効果を示した。 [0111] From Table 7, each deodorant prepared in Example 9 has the same level of tobacco odor as the positive control sample. Deodorizing effect on
実施例 13  Example 13
[0112] カビ臭に対する消臭効果 (官能検査)  [0112] Deodorant effect against mold odor (Sensory test)
試験用カビとして、黒麹菌(Aspergillus nieer NBRC33023)を用いた。ポテトデキスト ロース寒天培地(PDA培地)に該試験用カビを接種し、 28°Cで 5日間培養した。生育 した該試験用カビを蒸留水に浸し、濾紙 (型番 No.2アドバンテック東洋株式会社製) で濾過後、さらに、蒸留水で菌体を洗浄した。洗浄した試験用カビを蒸留水に懸濁し 、カビ胞子懸濁液を得た。該カビ胞子懸濁液を 28°Cで 10日間培養後、濾紙 (No. 2 )で濾過して、力ビ臭水を得た。該カビ臭水(300ml)を布地 (綿タオル)を入れた蓋付 き瓶(500ml)に添加し、 25°Cで 5日間浸漬した。該布地を瓶より取り出し、 日陰で風 乾後、布地を 10cm X 10cm四方に切断し、これをカビ臭試験用布地とした。  As a test fungus, Aspergillus nieer NBRC33023 was used. Potato dextrose agar medium (PDA medium) was inoculated with the test fungus and cultured at 28 ° C for 5 days. The grown mold for test was immersed in distilled water, filtered with a filter paper (model No. 2 Advantech Toyo Co., Ltd.), and the cells were further washed with distilled water. The washed mold for test was suspended in distilled water to obtain a mold spore suspension. The mold spore suspension was cultured at 28 ° C. for 10 days and then filtered through a filter paper (No. 2) to obtain a musty odor water. The mold odor water (300 ml) was added to a lidded bottle (500 ml) containing a cloth (cotton towel) and immersed at 25 ° C. for 5 days. The fabric was taken out from the bottle and air-dried in the shade, and then the fabric was cut into 10 cm × 10 cm squares to obtain a mold odor test fabric.
[0113] 実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプルの濃度が  [0113] The concentration of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts was
1 % (共に体積/体積)になるように水で希釈し、ミストスプレーボトルに充填した。該 カビ臭試験用布地に約 1. Ogスプレーした後、良く揉み、均一化にした。陽性対照と して、上記消臭剤の代わりに、実施例 4と同じさとうきび抽出物 MSX— 245の濃度が 1 % (共に体積/体積)になるように水で希釈して用いた。また、対照として、スプレー で蒸留水を試験用布地に 6回スプレー(約 1. Og)した後、良く揉み、均一化にした。 該カビ臭試験用布地は評価に供するまで、室温で密封容器 (密封アルミパック)に保 存した。  Diluted with water to 1% (both volume / volume) and filled into mist spray bottles. After spraying about 1. Og on the mold odor test fabric, it was thoroughly squeezed and homogenized. As a positive control, instead of the above deodorant, the same sugarcane extract MSX-245 concentration as in Example 4 was diluted with water so that the concentration was 1% (both volume / volume). In addition, as a control, distilled water was sprayed 6 times (about 1. Og) on the test fabric by spraying, and then it was thoroughly stirred and homogenized. The mold odor test fabric was stored in a sealed container (sealed aluminum pack) at room temperature until evaluation.
[0114] 評価は各サンプルを噴霧後、 4〜5時間、 1日、 7日、 14日、 30日後に熟練パネラ 一 8名による官能評価を行って平均をとつた。なお、評価基準は実施例 11に記載し た悪臭防止法の 6段階臭気強度表示法に準じて官能評価した。その結果を表 8に示 す。  [0114] After spraying each sample, the sensory evaluation was performed by 8 skilled panelists 4 to 5 hours, 1 day, 7 days, 14 days, and 30 days, and an average was obtained. The evaluation criteria were sensory evaluation according to the 6-step odor intensity display method of the malodor control method described in Example 11. The results are shown in Table 8.
[0115] [表 8] 実施例 9の消臭剤を [0115] [Table 8] Deodorant of Example 9
カビ臭に対する  Against musty odor
対照サンプル 等量混合した 陽性対照  Control sample Equal volume mixed positive control
消臭効果  Deodorant effect
消臭剤  Deodorants
4〜6時間後 4.0 0.4 0.8  4-6 hours later 4.0 0.4 0.8
1曰後 4.1 0.5 0.5 After 1 hour 4.1 0.5 0.5
7曰後 4.3 0.8 0.77 days later 4.3 0.8 0.7
1 4曰後 4.1 0.7 1.01 4 days later 4.1 0.7 1.0
30曰後 4.5 1 .0 1.0 After 30 days 4.5 1 .0 1.0
[0116] 表 8より、実施例 9で調製した各消臭剤は、陽性対照サンプルと同程度以上のカビ 臭に対する消臭効果示した。 [0116] From Table 8, each deodorant prepared in Example 9 showed a deodorizing effect on the mold odor equivalent to or higher than that of the positive control sample.
実施例 14  Example 14
[0117] ペット臭に対する消臭効果 (官能検査)  [0117] Deodorizing effect on pet odor (sensory test)
家庭で犬(室内犬)の敷物として 6ヶ月間使用したバスタオルを切断して lcm X lc mの試験片とした。該試験片をよくかき混ぜ均一にした後、約 6gを生地が重ならない ようにガラスシャーレ上に広げ、これをペット臭試験用片とした。そして、測定用サン プルとして、実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプ ルの濃度が 1 % (共に体積/体積)になるように水で希釈し、ミストスプレーボトルに充 填した。該ペット臭試験用片に約 1. 5gスプレーした後、良く揉み、均一化にした。陽 性対照として、上記消臭剤の代わりに、実施例 4と同じさとうきび抽出物 MSX— 245 の濃度が 1 % (共に体積/体積)になるように水で希釈して用いた。また、対照として 、スプレーで蒸留水を試験用片に約 1. 5gスプレーした後、良く揉み、均一化にした 。該ペット臭試験用片は評価に供するまで、室温で密封容器 (密封アルミパック)に保 存した。  A bath towel used for 6 months as a dog (indoor dog) rug at home was cut into a lcm x lcm test piece. The test piece was mixed well and made uniform, and then about 6 g was spread on a glass petri dish so that the dough would not overlap, and this was used as a pet odor test piece. As a measurement sample, dilute with water so that the concentration of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts is 1% (both volume / volume). And filled into mist spray bottles. After spraying about 1.5 g on the pet odor test piece, it was thoroughly stirred and homogenized. As a positive control, instead of the above deodorant, the same sugarcane extract MSX-245 concentration as in Example 4 was diluted with water so that the concentration was 1% (both volume / volume). In addition, as a control, about 1.5 g of distilled water was sprayed on a test piece by spraying, and then it was thoroughly stirred and homogenized. The pet odor test piece was stored in a sealed container (sealed aluminum pack) at room temperature until evaluation.
[0118] 評価は各サンプルを噴霧後、 4〜5時間、 1日、 7日、 14日、 30日後に熟練パネラ 一 8名による官能評価を行って平均をとつた。なお、評価基準は実施例 11に記載し た悪臭防止法の 6段階臭気強度表示法に準じて官能評価した。その結果を表 9に示 す。 [0118] After spraying each sample, the sensory evaluation was performed by 8 skilled panelists 4 to 5 hours, 1 day, 7 days, 14 days, and 30 days, and an average was taken. The evaluation criteria were sensory evaluation according to the 6-step odor intensity display method of the malodor control method described in Example 11. The results are shown in Table 9. The
[0119] [表 9] [0119] [Table 9]
Figure imgf000035_0001
Figure imgf000035_0001
[0120] 表 9より、実施例 9で調製した各消臭剤は、陽性対照サンプルと同程度のペット昊に 対する消臭効果示した。 [0120] From Table 9, each of the deodorizers prepared in Example 9 showed a deodorizing effect on the same level of pet cake as the positive control sample.
実施例 15  Example 15
[0121] ミストスプレータイプ消臭剤  [0121] Mist spray type deodorant
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプルの濃度が 夫々 20%及び 0. 1 % (共に体積/体積)になるように水で希釈し、ミストスプレーボト ルに充填した。これらの試料を獣臭のある大型犬と、その犬小屋に噴霧したところ、 犬および犬小屋とも獣臭による不快臭が消え、その効果は 3日間持続した。  Diluted with water so that the concentration of the deodorant sample prepared in Example 9 was equal to 20% and 0.1% (both volume / volume). Filled spray bottle. When these samples were sprayed on a large dog with animal odor and its kennel, the unpleasant odor due to animal odor disappeared in both the dog and kennel, and the effect lasted for 3 days.
実施例 16  Example 16
[0122] エアゾールタイプ消臭剤 [0122] Aerosol type deodorant
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプルの濃度が 夫々 60%及び 1 % (共に体積/体積)になるように且つエタノール終濃度が 20% (体 積/体積)になるようにエタノールおよび水で希釈した。得られた混合物の夫々を噴 射ガス(LPGおよび二酸化炭素)と共にエアゾール容器に充填した。これらを悪臭の ある生ゴミに噴射したところ、生ゴミ由来の悪臭が抑えられ、その効果は 24時間以上 持続した。  The concentration of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts was 60% and 1% (both volume / volume), respectively, and the final ethanol concentration was 20% ( (Volume / volume) to dilute with ethanol and water. Each of the resulting mixtures was filled into an aerosol container with a propellant gas (LPG and carbon dioxide). When these were sprayed onto malodorous garbage, the malodor derived from the garbage was suppressed, and the effect lasted for more than 24 hours.
実施例 17 [0123] ゲル状消臭剤 Example 17 [0123] Gel deodorant
カラギーナン 2. 2g及び水 85gを 200mlのビーカーに添加し、良く攪拌しながら 70 °Cまで加熱し、完全に溶解させた。次に、この混合物を冷却して 50°Cになったとき、 実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 15gを添カロ 、混合し、全重量を 100gになるように水で調整し、冷却'固化させて、ゲル状消臭剤 を得た。同様にして、該ゲル状消臭剤を 3個調製した。該ゲル状消臭剤を夫々 2. 6リ ットル容量のデシケーターに入れ、密閉し、 20°Cで 3時間安定化させた。トリメチルァ ミンガスを初期濃度約 20ppmになるようにこのデシケーターに注入し、 24時間後にト リメチルァミン濃度を検知管(型番 No. 180L、株式会社ガステック製)で測定し、ト リメチルァミン濃度の減少率を求めた。測定が終了したゲル状消臭剤は次の測定ま での間、 300mlビーカーに個別に入れ、 20°C、湿度 60%の恒温恒湿槽内で保存し た。消臭効果の測定は、ゲル状消臭剤を調製した当日、調製 7日後、調製 14日後に 行い、トリメチルァミンの残存濃度から消臭率を求めた。消臭率は、次のようにして求 め、 3個の消臭剤のデータを平均して示した。その結果を表 10に示す。  2. 2 g of carrageenan and 85 g of water were added to a 200 ml beaker and heated to 70 ° C. with good stirring until completely dissolved. Next, when this mixture was cooled to 50 ° C., 15 g of a deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts was added and mixed to obtain the total weight. Was adjusted to 100 g with water, cooled and solidified to obtain a gel-like deodorant. Similarly, three gel-like deodorants were prepared. The gel-like deodorant was placed in a 2.6 liter desiccator, sealed, and stabilized at 20 ° C. for 3 hours. Trimethylamine gas was injected into this desiccator to an initial concentration of about 20 ppm, and after 24 hours, the trimethylamine concentration was measured with a detector tube (model No. 180L, manufactured by Gastec Co., Ltd.) to determine the reduction rate of the trimethylamine concentration. It was. The gel-type deodorant for which measurement was completed was individually placed in a 300 ml beaker and stored in a constant temperature and humidity chamber at 20 ° C and 60% humidity until the next measurement. The deodorizing effect was measured on the day of preparation of the gel-type deodorant, 7 days after preparation, and 14 days after preparation, and the deodorization rate was determined from the residual concentration of trimethylamine. The deodorization rate was obtained as follows, and the data for the three deodorants were averaged. The results are shown in Table 10.
[0124] 消臭率(%) = [1 (測定終了時のトリメチルァミン濃度)/ (測定開始時のトリメチ ルァミン濃度)] X 100  [0124] Deodorization rate (%) = [1 (Trimethylamine concentration at the end of measurement) / (Trimethylamine concentration at the start of measurement)] X 100
[0125] [表 10]
Figure imgf000036_0001
[0125] [Table 10]
Figure imgf000036_0001
[0126] 表 10より、本実施例におけるゲル状消臭剤は、トリメチルァミンの消臭に対して高い 消臭活性を示した。 [0126] From Table 10, the gel-like deodorant in this example showed high deodorizing activity against the deodorization of trimethylamine.
実施例 18  Example 18
[0127] 加湿器による室内消臭 [0127] Indoor deodorization by humidifier
老人ホームで特に悪臭の強い部屋を選び、試験対照とした。実施例 9で調製した 7 種類の各消臭剤を等量で混合した消臭剤サンプルの濃度が 0. 05% (体積/体積) になるように約 1. 5リットルの水を添加した。該溶液を、加湿器にセットした。加湿器 の運転は間欠タイマーを用いて 15分間に 1分間の割合で断続的に作動させた。そ の結果、一日中悪臭が抑えられた。 A room with a particularly strong odor was selected in a nursing home and used as a test control. About 1.5 liters of water was added so that the concentration of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts was 0.05% (volume / volume). The solution was set in a humidifier. humidifier The operation was intermittently operated at a rate of 1 minute per 15 minutes using an intermittent timer. As a result, odors were suppressed throughout the day.
実施例 19  Example 19
[0128] ペット用排泄物処理剤  [0128] Pet excreta treating agent
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤を用いて、ペット用 排泄物処理剤を調製した。処理剤の配合例は、ベントナイト 50部、木粉 50部、消臭 剤 1部、水 50部を用いた。原料はリボンミキサーで混合し、ディスク型のペレツターで 直径 3mm、長さ 8〜20mmのペレツターを得た。これをさらにロータリードライヤーで 乾燥させたものを試料とした。陽性対照として、上記消臭剤の代わりに、実施例 4と同 じさとうきび抽出物 MSX-245を 1部用いた。対照として、上記処理剤において消臭剤 の代わりに、水 1部を用いた。  An excrement treating agent for pets was prepared using a deodorant prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts. As a blending example of the treating agent, 50 parts of bentonite, 50 parts of wood flour, 1 part of deodorant and 50 parts of water were used. The raw materials were mixed with a ribbon mixer, and a disk-type pelleter with a diameter of 3 mm and a length of 8-20 mm was obtained. This was further dried with a rotary dryer as a sample. As a positive control, 1 part of the same sugarcane extract MSX-245 as in Example 4 was used instead of the deodorant. As a control, 1 part of water was used in place of the deodorant in the above treatment agent.
[0129] これら試料を 20gずつ 500ml容量の三角フラスコに入れ、 0· 5%アンモニア水 2ml を加えて密栓し、 30°C、 20分間インキュベートした。インキュベーション後、検知管( 型番 No. 3La、株式会社ガステック製)で気体部分のアンモニア濃度(ppm)を測 定した。ブランク値として、アンモニアだけを加えた場合のアンモニア濃度を測定し、 各消臭率(%)を算出した。その結果を下記表 11に示す。  [0129] 20 g of each sample was placed in a 500 ml Erlenmeyer flask, 2 ml of 0.5% aqueous ammonia was added and sealed, and incubated at 30 ° C for 20 minutes. After the incubation, the ammonia concentration (ppm) of the gas portion was measured with a detector tube (model No. 3La, manufactured by Gastec Co., Ltd.). As a blank value, the ammonia concentration when only ammonia was added was measured, and each deodorization rate (%) was calculated. The results are shown in Table 11 below.
[0130] [表 11]  [0130] [Table 11]
Figure imgf000037_0001
ベントナイトがアンモニアをある程度吸収するため、ブランクに比べて対照も消臭効 果を有するが、本発明の上記消臭剤および陽性対照の消臭剤を使用した処理剤は 明らかにそれ以上の消臭効果を示した。
Figure imgf000037_0001
Since bentonite absorbs ammonia to some extent, the control also has a deodorizing effect compared to the blank, but the treatment using the above-mentioned deodorant of the present invention and the positive control deodorant is clearly more deodorant. Showed the effect.
実施例 20 [0132] スプレータイプ消臭剤 1の調製 Example 20 [0132] Preparation of spray type deodorant 1
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 6%と 、リシノール酸亜鉛として商品名「TEGO DEO CW90」(ゴールドシュミット社製) 2. 0% (リシノール酸亜鉛として約 1 %)と、ジプロピレングリコール 5. 0%と、工業用エタ ノール 35. 0%と、残部に水とを配合して、常法によりスプレータイプ消臭剤を調製し た。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 0.6% and trade name “TEGO DEO CW90” (manufactured by Goldschmidt) as zinc ricinoleate 2.0% (About 1% as zinc ricinoleate), dipropylene glycol (5.0%), industrial ethanol (35.0%), and water in the balance, prepare a spray-type deodorant by a conventional method. It was.
実施例 21  Example 21
[0133] スプレータイプ消臭剤 2の調製 [0133] Preparation of spray type deodorant 2
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と 、リシノール酸亜鉛として商品名「TEGO SORB CONC. 50」(ゴールドシュミット社 製) 1 · 0% (リシノール酸亜鉛として約 0· 5%)と、ジプロピレングリコール 5· 0%と、ェ 業用エタノール 20. 0%と、残部に水とを配合して、常法によりスプレータイプ剤を調 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 1.0%, and trade name “TEGO SORB CONC. 50” (manufactured by Goldschmidt) as zinc ricinoleate 1 · 0% (approx.0.5% as zinc ricinoleate), dipropylene glycol 5.0%, ethanol for industrial use 20.0%, and water in the balance, mix the spray-type agent by a conventional method. Key
; ^^し/ ; ^^
実施例 22  Example 22
[0134] スプレータイプ消臭剤 3の調製 [0134] Preparation of spray type deodorant 3
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 6%と Deodorant sample prepared by mixing the same amount of the seven types of deodorants prepared in Example 9 and 0.6%
、甘蔗抽出物以外の植物抽出物として商品名「ピユリエール」(松下電工株式会社製As a plant extract other than the sweet potato extract, the trade name “Pyurière” (Matsushita Electric Works, Ltd.)
) 0. 6%と、工業用エタノール 20. 0%と、残部に水とを配合して、常法によりスプレー タイプ消臭剤を調製した。 ) A spray type deodorant was prepared by a conventional method by mixing 0.6%, industrial ethanol 20.0% and the balance water.
実施例 23  Example 23
[0135] スプレータイプ消臭剤 4の調製 [0135] Preparation of spray type deodorant 4
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 6%と Deodorant sample prepared by mixing the same amount of the seven types of deodorants prepared in Example 9 and 0.6%
、甘蔗抽出物以外の植物抽出物として商品名「スメラル」(環境科学開発株式会社製The product name “Smeral” (produced by Environmental Science Development Co., Ltd.)
) 0. 6%と、工業用エタノール 20. 0%と、残部に水とを配合して、常法によりスプレー タイプ消臭剤を調製した。 ) A spray type deodorant was prepared by a conventional method by mixing 0.6%, industrial ethanol 20.0% and the balance water.
実施例 24  Example 24
[0136] スプレータイプ消臭剤 5の調製 実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 6%と 、甘蔗抽出物以外の植物抽出物として商品名「パンシル」(リリース科学工業株式会 社製) 0. 6%と、工業用エタノール 20. 0%と、残部に水とを配合して、常法によりス プレータイプ消臭剤を調製した。 [0136] Preparation of spray type deodorant 5 Deodorant sample prepared in Example 9 with the same amount of 7 kinds of deodorants mixed with 0.6%, and the plant name “Pancil” (Release Kagaku Kogyo Co., Ltd.) as a plant extract other than sweet potato extract A spray type deodorant was prepared by a conventional method by mixing 0.6%, industrial ethanol 20.0%, and the balance water.
[0137] [比較例 1] [0137] [Comparative Example 1]
スプレータイプ消臭剤 Aの調製  Preparation of spray type deodorant A
実施例 20のスプレータイプ消臭剤の配合にお!/、て、実施例 9で調製した 7種類の 各消臭剤を等量で混合した消臭剤サンプルを用いずに、常法によりスプレータイプ 消臭剤を調製した。  In the formulation of the spray-type deodorant of Example 20, and sprayed in a conventional manner without using the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts. Type A deodorant was prepared.
[0138] [比較例 2] [Comparative Example 2]
スプレータイプ消臭剤 Bの調製  Preparation of spray type deodorant B
実施例 20のスプレータイプ消臭剤の配合にお!/、て、実施例 9で調製した 7種類の 各消臭剤を等量で混合した消臭剤サンプルの代わりに /3—シクロデキストリン 2. 0% を配合して、常法によりスプレー剤を調製し、スプレータイプ消臭剤を得た。  In addition to the spray type deodorant of Example 20 !, instead of the deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts, / 3-cyclodextrin 2 0% was blended and a spray was prepared by a conventional method to obtain a spray type deodorant.
[0139] [消臭試験 1]  [0139] [Deodorization test 1]
上記実施例 20〜24のスプレータイプ消臭剤 1〜5および比較例 1〜2のスプレータ イブ消臭剤 A〜Bにつ!/、て以下の試験を行ない、それらの消臭効果を評価した。  Spray type deodorant 1 to 5 of Examples 20 to 24 and spray type deodorant A to B of Comparative Examples 1 to 2! The following tests were conducted to evaluate their deodorizing effects. .
[0140] 一般的な悪臭である硫化水素、メチルメルカブタン、イソ吉草酸の臭気強度を下記 臭気強度の基準に示した臭気強度の段階 3に設定した臭気評価ボックスを用意した 。上記 3種類の悪臭に対する消臭効果を下記評価方法に従って熟練パネラーにより 官能試験した。詳細な試験方法を以下に示す。  [0140] An odor evaluation box was prepared in which the odor intensity of hydrogen odor, methyl mercabtan, and isovaleric acid, which are general malodors, was set to the odor intensity stage 3 shown in the following odor intensity standards. The sensory test was conducted by skilled panelists on the deodorizing effect on the above three kinds of malodors according to the following evaluation method. Detailed test methods are shown below.
[0141] 庫内が臭気強度 3になるように上記 3種類の悪臭を夫々入れた 2000L容の上記臭 気評価ボックスに上記スプレータイプ消臭剤を噴霧した(1回の噴霧量は 0. 3g)。 10 名の熟練パネラーが、噴霧 1分後と 10分後の悪臭に対する消臭効果を実施例 11に 記載した悪臭防止法の 6段階臭気強度表示法に準じて官能評価し、各スプレータイ プ消臭剤について各パネラーの評価値の平均点を求めた。その結果を表 12に示す [0141] The above-mentioned spray-type deodorant was sprayed into the 2000-liter odor evaluation box containing the above three kinds of bad odors so that the inside of the chamber had an odor intensity of 3 (the amount of spray per spray was 0.3 g) ). Ten skilled panelists sensory-evaluated the deodorizing effect against bad odor after 1 minute and 10 minutes after spraying according to the 6-step odor intensity display method of the malodor control method described in Example 11, and each spray type was turned off. The average score of the evaluation values of each panel was determined for the odorant. The results are shown in Table 12.
Yes
[0142] [表 12] スプレータ 硫化水素 メチルメルカブタン イソ吉草酸 イブ消臭剤 1分後 1 0分後 1分後 1 0分後 1分後 1 0分後 実施例 20 0. 4 0. 6 0. 4 0. 4 0. 5 0. 5 実施例 21 0. 7 0. 8 0. 2 0. 2 0. 3 0. 5 実施例 22 0. 3 0. 5 0. 4 0. 3 0. 5 0. 4 実施例 23 0. 8 0. 8 0. 9 0. 7 0. 9 1 . 1 実施例 24 0. 4 0. 5 1 . 0 1 . 0 0. 5 0. 8 比較例 1 3. 0 3. 2 2. 7 3. 0 3. 1 3. 3 比較例 2 2. 9 3. 1 2. 8 2. 8 2. 9 3. 0 [0142] [Table 12] Sprayer Hydrogen sulfide Methyl mercabtan Isovaleric acid Eve deodorant 1 minute later 1 0 minute later 1 minute later 1 0 minute later 1 minute later 1 0 minute later Example 20 0. 4 0. 6 0. 4 0. 4 0 5 0. 5 Example 21 0. 7 0. 8 0. 2 0. 2 0. 3 0. 5 Example 22 0. 3 0. 5 0. 4 0. 3 0. 5 0. 4 Example 23 0. 8 0. 8 0. 9 0. 7 0. 9 1.1 Example 24 0. 4 0. 5 1. 0 1. 0 0. 5 0. 8 Comparative Example 1 3. 0 3. 2 2. 7 3. 0 3. 1 3. 3 Comparative Example 2 2. 9 3. 1 2. 8 2. 8 2. 9 3. 0
[0143] 表 12より、実施例 20〜24のスプレータイプ消臭剤は、硫化水素、メチルメルカプタ ン、イソ吉草酸に対して噴霧 1分後に優れた消臭効果を示し、その効果は噴霧 10分 後であっても持続した。一方、比較例 1〜2のスプレータイプ消臭剤は噴霧 1分後、噴 霧 10分後のいずれにおいても充分な消臭効果が得られなかった。 [0143] From Table 12, the spray-type deodorants of Examples 20 to 24 showed excellent deodorizing effect after 1 minute of spraying against hydrogen sulfide, methyl mercaptan and isovaleric acid, and the effect was 10 minutes after spraying. Lasted even after. On the other hand, the spray type deodorizers of Comparative Examples 1 and 2 did not have a sufficient deodorizing effect after 1 minute of spraying and after 10 minutes of spraying.
実施例 25  Example 25
[0144] 消臭剤組成物 1の調製 [0144] Preparation of Deodorant Composition 1
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 3%と 、植物抽出液として商品名「スーパーピユリエール A-10」(松下電工化研社製) 1. 0 %と、トリエタノールァミン 4. 0%と、クェン酸 2· 0%と、残分に水とを配合してアンモ ユアで pH 7.0に調整し、消臭剤組成物を得た。  A deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 0.3%, and a product name “Super Piurier A-10” (Matsushita Electric Industrial Chemical Co., Ltd.) as a plant extract. 1) 1.0%, triethanolamine 4.0%, quenic acid 2.0%, and water in the remainder, adjusted to pH 7.0 with ammonia and deodorant composition Obtained.
実施例 26  Example 26
[0145] 消臭剤組成物 2の調製 [0145] Preparation of Deodorant Composition 2
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 0. 5%と、トリェタノ ールァミン 0. 6%と、クェン酸 2水素ナトリウム 2. 0%と、残分に水とを配合してアンモ ユアで pH 7.0に調整し、消臭剤組成物を得た。  A deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0%, and a trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 0.5% Then, trihetanolamine 0.6%, sodium dihydrogen citrate 2.0%, and the remainder were mixed with water and adjusted to pH 7.0 with ammonia to obtain a deodorant composition.
実施例 27  Example 27
[0146] 消臭剤組成物 3の調製 [0146] Preparation of Deodorant Composition 3
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 3%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 1. 0%と、モノエタノ ールァミン 0. 8%と、クェン酸 2. 0%と、残分に水とを配合してアンモニアで pH 7.0に 調整し、消臭剤組成物を得た。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.3% As a plant extract, the product name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) 1.0%, monoethanolamine 0.8%, citrate 2.0%, and water in the balance are mixed with ammonia. The pH was adjusted to 7.0 to obtain a deodorant composition.
実施例 28  Example 28
[0147] 消臭剤組成物 4の調製 [0147] Preparation of Deodorant Composition 4
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 3%と Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.3%
、植物抽出液として商品名「スーパーピユリエール A-10」(松下電工化研社製) 3. 0As a plant extract, the trade name “Super Piyurire A-10” (manufactured by Matsushita Electric Industrial Co., Ltd.) 3.0
%と、モノエタノールァミン 2· 3%と、クェン酸 3. 0%と、残分に水とを配合してアンモ ユアで pH 7.0に調整し、消臭剤組成物を得た。 %, Monoethanolamine 2.3%, quenic acid 3.0%, and water in the remainder were adjusted to pH 7.0 with ammonia to obtain a deodorant composition.
[0148] [比較例 3] [0148] [Comparative Example 3]
消臭剤組成物の調製  Preparation of deodorant composition
モノエタノールァミン 1 · 2%と、クェン酸 2· 0%と残分に水とを配合してアンモニア で pH 7.0に調整し、対照サンプルを得た。  A control sample was obtained by adding 1% 2% monoethanolamine, 2.0% citrate and water to the residue and adjusting to pH 7.0 with ammonia.
[0149] [消臭試験 2]  [0149] [Deodorization test 2]
実施例 25〜28の消臭剤組成物;!〜 4及び比較例 3の消臭剤組成物の消臭効果を 確認するために、アンモニア、メチルメルカブタン、イソ吉草酸に対する消臭試験、及 び家庭で飼ってレ、る犬が使用して!/、る敷物(カーペット)を用いた消臭試験を行った 。その結果を表 13に示す。  In order to confirm the deodorizing effect of the deodorant compositions of Examples 25 to 28;! To 4 and Comparative Example 3, a deodorization test for ammonia, methyl mercabtan and isovaleric acid, and A deodorizing test was conducted using rugs (carpets) used by ru dogs kept at home. The results are shown in Table 13.
[0150] 試験方法の詳細は次の通りである。  [0150] Details of the test method are as follows.
<試験方法(1):アンモニアの消臭試験〉 1Lのガラス瓶容器に試料(上記実施例 25〜28の消臭剤組成物又は対照サンプル) 10mLを入れ、 1 %のアンモニア水溶 液を lmL注入し、 10分間放置後に熟練パネラー 10名による官能評価を行って平均 をとつた。なお、評価基準は実施例 11に記載した悪臭防止法の 6段階臭気強度表 示法に準じた。  <Test method (1): Deodorization test of ammonia> Place 10 mL of sample (deodorant composition or control sample of Examples 25 to 28 above) into a 1 L glass bottle container, and inject 1 mL of 1% aqueous ammonia solution. After leaving for 10 minutes, sensory evaluation by 10 skilled panelists was performed and an average was taken. The evaluation criteria were in accordance with the 6-step odor intensity display method of the malodor control method described in Example 11.
<試験方法(2):メチルメルカブタンの消臭試験〉 1Lのガラス瓶容器に試料 10m Lを入れ、 0. 1 %のメチルメルカプタンエタノール溶液を lmL注入し、 1時間放置後 に熟練パネラー 10名による官能評価を行って平均をとつた。なお、評価基準は実施 例 11に記載した悪臭防止法の 6段階臭気強度表示法に準じた。 <試験方法(3):イソ吉草酸の消臭試験〉 1Lのガラス瓶容器に試料 10mLを入れ 、 1 %のイソ吉草酸水溶液を 100 注入し、 1時間放置後に熟練パネラー 10名によ る官能評価を行って平均をとつた。なお、評価基準は実施例 11に記載した悪臭防止 法の 6段階臭気強度表示法に準じた。 <Test method (2): Deodorization test of methyl mercaptan> Place 10 mL of a sample in a 1 L glass bottle container, inject 1 mL of 0.1% methyl mercaptan ethanol solution, and let stand for 1 hour. Sensory evaluation was performed and the average was taken. The evaluation criteria were in accordance with the 6-step odor intensity display method of the malodor control method described in Example 11. <Test method (3): Deodorization test of isovaleric acid> Place 10mL of sample in a 1L glass bottle container, inject 100% of 1% aqueous solution of isovaleric acid, leave it for 1 hour, and sensory evaluation by 10 skilled panelists And took the average. The evaluation criteria were in accordance with the 6-step odor intensity display method of the malodor control method described in Example 11.
<試験方法 (4):室内犬が使用した敷物の消臭試験〉 家庭で飼っている犬が使用 している敷物に、試料を 3回噴霧 (約 2. 5g)し、拭き取った後の敷物に残った臭いに っレ、て官能評価を行った。評価基準は下記の通りである。  <Test method (4): Deodorization test of rugs used by indoor dogs> The rug after the sample is sprayed three times (about 2.5 g) on the rug used by dogs kept at home and wiped off. The sensory evaluation was performed based on the remaining odor. The evaluation criteria are as follows.
[0151] 官能評価基準 [0151] Sensory evaluation criteria
◎: 完全に臭いが消えた  ◎: The smell disappeared completely
〇: かなり臭いが消えた  〇: The smell disappeared
Δ : わずかに臭いが消えた  Δ: Smell disappeared slightly
X: 消臭されていない  X: Not deodorized
[表 13]  [Table 13]
Figure imgf000042_0001
Figure imgf000042_0001
[0152] 表 13より、実施例 25〜28の消臭剤組成物では、アンモニア、メチルメルカプタン、 イソ吉草酸及び悪臭の発生源となる室内犬の敷物に対して優れた消臭効果を示した 。一方、比較例 3の消臭剤組成物では、消臭効果をほとんど示さな力 た。 [0152] From Table 13, the deodorant compositions of Examples 25 to 28 showed excellent deodorizing effects on indoor dog rugs that are sources of ammonia, methyl mercaptan, isovaleric acid and offensive odor. . On the other hand, the deodorant composition of Comparative Example 3 showed almost no deodorizing effect.
実施例 29  Example 29
[0153] 消臭洗浄剤 1の調製 [0153] Preparation of Deodorant Cleaning Agent 1
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 1. 0%と、クェン酸 3 . 0%と、ポリグリセリンエステノレ 0. 5%と、サポニン 0. 5%と、工業用エタノーノレ 10. 0 %と、 POEイソステアリルエーテル 0. 1 %と、残分に水を配合して水酸化ナトリウムで p H 4.8に調整し、消臭洗浄剤を得た。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0% and the trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 1.0% And citrate 3 0%, polyglycerin esterol 0.5%, saponin 0.5%, industrial ethanol 10.0%, POE isostearyl ether 0.1% The pH was adjusted to 4.8 with sodium oxide to obtain a deodorant cleaning agent.
実施例 30  Example 30
[0154] 消臭洗浄剤 2の調製  [0154] Preparation of Deodorant Cleaning Agent 2
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 1. 0%および商品名 「スーパーピユリエール A-10J (松下電工化研社製) 1 · 0%と、クェン酸 2· 5%と、プロ ピレングリコーノレエステノレ 1 · 0%と、サポニン 0· 5%と、工業用エタノーノレ 10· 0%と、 残分に水とを配合して、水酸化ナトリウムで pH 4.8に調整し、消臭洗浄剤を得た。 実施例 31  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0% and the trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 1.0% And the product name “Super Piyurire A-10J (manufactured by Matsushita Electric Industrial Co., Ltd.) 1 · 0%, Chenic acid 2 · 5%, Propylene glycolenoestestole 1 · 0% and Saponin 0 · 5% In addition, 100% industrial ethanol and 100% ethanol and the balance water were adjusted to pH 4.8 with sodium hydroxide to obtain a deodorant cleaning agent.
[0155] 消臭洗浄剤 3の調製  [0155] Preparation of Deodorant Cleaning Agent 3
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 0. 5%と、クェン酸 2 . 5%と、サポニン 0. 5%、 POEイソステアリノレエーテノレ 0. 1 %、工業用エタノーノレ 10 . 0%と、残分に水とを配合して水酸化ナトリウムで pH 4.8に調整し、消臭洗浄剤を得 た。  A deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0%, and a trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 0.5% Chenic acid 2.5%, saponin 0.5%, POE isostearinoleethenore 0.1%, industrial ethanol 10.0%, and water in the remainder and pH with sodium hydroxide The deodorant cleaning agent was obtained after adjusting to 4.8.
実施例 32  Example 32
[0156] 消臭洗浄剤 4の調製 [0156] Preparation of Deodorant Cleaning Agent 4
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 1. 0%および商品名 「スーパーピユリエール A-10」(松下電工化研社製) 0· 3%と、クェン酸 2· 5%と、レシ チン 0. 1 %と、サポニン 0. 5%と、工業用エタノール 10. 0%と、残分に水とを配合し て水酸化ナトリウムで pH 5.0に調整し、消臭洗浄剤を得た。  A deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 0.5%, and a trade name “Smeral LG” (produced by Environmental Science Development Co., Ltd.) as a plant extract 1.0% And the product name "Super Piyurire A-10" (Matsushita Electric Works), 0.3%, Chenic acid 2.5%, Lecithin 0.1%, Saponin 0.5% Ethanol for commercial use was mixed with 10.0% and water in the residue, and the pH was adjusted to 5.0 with sodium hydroxide to obtain a deodorant cleaning agent.
実施例 33  Example 33
[0157] 消臭洗浄剤 5の調製 [0157] Preparation of Deodorant Cleaning Agent 5
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 0. 5%と、クェン酸 2 . 5%と、サポニン 0. 5%、 POEイソステアリノレエーテノレ 0. 1 %、工業用エタノーノレ 10 . 0%と、残分に水とを配合して水酸化ナトリウムで pH 5.8に調整し、消臭洗浄剤を得 た。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 1.0% As a plant extract, the trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) 0.5%, citrate 2.5%, saponin 0.5%, POE isostearinoreethenore 0.1%, industrial Ethanol for use was mixed with 10.0% and the remaining water, and the pH was adjusted to 5.8 with sodium hydroxide to obtain a deodorant cleaning agent.
実施例 34  Example 34
[0158] 消臭洗浄剤 6の調製 [0158] Preparation of Deodorant Cleaning Agent 6
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 1. 0%および商品名 「スーパーピユリエール A-10」(松下電工化研社製) 0· 3%と、クェン酸 2· 5%と、レシ チン 0. 5%と、工業用エタノール 10. 0%と、残分に水とを配合して水酸化ナトリウム で pH 5.0に調整し、消臭洗浄剤を得た。  A deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 0.5%, and a trade name “Smeral LG” (produced by Environmental Science Development Co., Ltd.) as a plant extract 1.0% And the product name "Super Piyurire A-10" (manufactured by Matsushita Electric Industrial Co., Ltd.) 0.3%, citrate 2.5%, lecithin 0.5%, and industrial ethanol 10.0% The residue was mixed with water and adjusted to pH 5.0 with sodium hydroxide to obtain a deodorant cleaning agent.
実施例 35  Example 35
[0159] 消臭洗浄剤 7の調製 [0159] Preparation of Deodorant Cleaning Agent 7
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 0. 5%および商品名 「スーパーピユリエール A-10J (松下電工化研社製) 0· 5%と、クェン酸 2· 0%と、サ ポニン 0. 1 %と、工業用エタノール 10. 0%と、残分に水とを配合して水酸化ナトリウ ムで pH 4.5に調整し、消臭洗浄剤を得た。  A deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 0.5%, and a trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 0.5% And the product name "Super Piyurire A-10J (manufactured by Matsushita Electric Industrial Co., Ltd.)" 0.5%, Chenic acid 2.0%, Saponin 0.1%, Industrial ethanol 10.0%, The residue was mixed with water and adjusted to pH 4.5 with sodium hydroxide to obtain a deodorant cleaning agent.
実施例 36  Example 36
[0160] 消臭洗浄剤 8の調製 [0160] Preparation of Deodorant Cleaning Agent 8
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と 、植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 1. 0%および商品名 「スーパーピユリエール A-10J (松下電工化研社製) 1 · 0%と、クェン酸 2· 0%と、タエ ン酸ニ水素ナトリウム 2· 5%と、サポニン 5· 0%と、工業用エタノール 10· 0%と、残 分に水とを配合して水酸化ナトリウムで pH 4.8に調整し、消臭洗浄剤を得た。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0% and the trade name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) as a plant extract 1.0% And the product name "Super Piyurire A-10J (manufactured by Matsushita Electric Industrial Co., Ltd.) 1 · 0%, quenate 2 · 0%, sodium dihydrogen tate 2 · 5% and saponin 5 · 0% Then, 100% industrial ethanol and water were mixed with the residue and adjusted to pH 4.8 with sodium hydroxide to obtain a deodorant cleaning agent.
[0161] [比較例 4] [0161] [Comparative Example 4]
消臭洗浄剤 Aの調製  Preparation of deodorant cleaning agent A
クェン酸 1. 0%と、レシチン 10. 0%、工業用エタノール 10. 0%と、残分に水とを 配合して水酸化ナトリウムで PH3.5に調整し、消臭洗浄剤を得た。 Chenic acid 1.0%, lecithin 10.0%, industrial ethanol 10.0%, and water in the balance Blended and adjusted to pH 3.5 with sodium hydroxide to obtain a deodorant cleaning agent.
[0162] [比較例 5] [0162] [Comparative Example 5]
消臭洗浄剤 Bの調製  Preparation of deodorant cleaner B
植物抽出液として商品名「スメラル L-G」(環境科学開発社製) 0. 01 %および商品 名「スーパーピユリエーノレ A-10J (松下電工化研社製) 0· 01 %と、クェン酸 3· 0%と、 工業用エタノール 10. 0%と、残分に水とを配合して、水酸化ナトリウムで pH 6.0に調 整し、消臭洗浄剤を得た。  As a plant extract, the product name “Smeral LG” (manufactured by Environmental Science Development Co., Ltd.) 0. 01% and the product name “Super Pyrienore A-10J (manufactured by Matsushita Electric Industrial Co., Ltd.) 0. 01%, and citrate 3 · 0%, industrial ethanol 10.0%, and water in the remainder were adjusted to pH 6.0 with sodium hydroxide to obtain a deodorant cleaning agent.
[0163] [比較例 6] [0163] [Comparative Example 6]
消臭洗浄剤 Cの調製  Preparation of deodorant cleaner C
クェン酸 2. 5%と、工業用エタノール 10. 0%と、残分に水とを配合して水酸化ナト リウムで pH 4.8に調整し、消臭洗浄剤を得た。  Chenic acid 2.5%, industrial ethanol 10.0%, and the remainder were mixed with water and adjusted to pH 4.8 with sodium hydroxide to obtain a deodorant cleaning agent.
[0164] [消臭試験 3]  [0164] [Deodorization test 3]
実施例 29〜36の消臭洗浄剤;!〜 8及び比較例 4〜6の消臭洗浄剤 A〜Cの消臭 効果を確認するために、アンモニア、メチルメルカブタン、イソ吉草酸に対する消臭試 験、室内犬の実尿及びモデル尿に対する消臭試験を行った。さらに、室内犬の実尿 、モデル尿に対する洗浄効果を確認した。アンモニア、メチルメルカブタン、イソ吉草 酸に対する消臭試験は、上記消臭試験 2に記載の試験方法(1)〜(3)を用いて評価 した。また、家庭で飼っている犬の実尿及びモデル尿を用いた消臭試験及び洗浄試 験は、下記試験方法により評価を行った。  Deodorant cleaning agents of Examples 29 to 36;! To 8 and deodorant cleaning agents of Comparative Examples 4 to 6 To confirm the deodorizing effect of A to C, deodorization to ammonia, methyl mercabtan, isovaleric acid A deodorization test was conducted on the test, actual urine of model dogs, and model urine. Furthermore, the cleaning effect on the actual urine and model urine of indoor dogs was confirmed. The deodorization test for ammonia, methyl mercabtan, and isovaleric acid was evaluated using the test methods (1) to (3) described in the above deodorization test 2. In addition, deodorization tests and washing tests using actual urine and model urine of dogs kept at home were evaluated by the following test methods.
[0165] <試験方法(5) :室内犬の実尿およびモデル尿を用いた消臭試験と洗浄試験〉 室 内犬の実尿およびモデル尿(0. 003%ビリルビン(尿の色素) · 1 %アンモニア · 1 % NaCl)をカーペットに lmr塗布し、ティッシュで軽くたたいた後、試料を処理(ゴルフ ボール大に試料を発泡させ、ブラシで汚れを浮かせ、ティッシュで軽く拭き処理)し、 臭いと残った色について、熟練パネラー 10名による官能評価を行って平均をとつた。 なお、消臭試験の評価基準は実施例 11に記載した悪臭防止法の 6段階臭気強度表 示法に準じ、洗浄試験については、色は無処理を 5点とし、汚れが完全に落ちたもの を 1点とした。その結果を表 14に示す。  [0165] <Test method (5): Deodorization test and washing test using actual urine and model urine of indoor dog> Indoor urine and model urine of indoor dog (0.003% bilirubin (urine pigment) · 1 1% NaCl) is applied to the carpet and lightly patted with a tissue, and then the sample is treated (foam the sample on the size of a golf ball, lift the dirt with a brush, and lightly wipe with a tissue). The remaining colors were subjected to sensory evaluation by 10 skilled panelists and averaged. The evaluation standard for the deodorization test is in accordance with the 6-step odor intensity display method of the malodor control method described in Example 11. For the cleaning test, the untreated color is 5 points and the stain is completely removed. Was one point. The results are shown in Table 14.
[0166] [表 14] 消臭洗浄 消臭効果 洗浄効果 剤組成物 メチル 室内犬の 室内犬の [0166] [Table 14] Deodorizing cleaning Deodorizing effect Cleaning effect Agent composition Methyl Indoor dog Indoor dog
アンモニア イソ吉草酸 モデル尿 モデル尿 メルカブタン 実尿 実尿  Ammonia Isovaleric acid Model urine Model urine Mercabtan Actual urine Actual urine
実施例 29 0 0 0 1 1 2 1 実施例 30 0 0 1 2 2 1 1 実施例 31 0 1 0 2 2 2 1 実施例 32 0 0 0 1 1 1 1 実施例 33 0 0 0 0 1 2 1 実施例 34 0 1 1 0 1 2 1 実施例 35 0 0 1 0 0 1 1 実施例 36 0 0 1 1 0 1 1 比較例 4 2 5 5 5 5 3 2 比較例 5 4 5 4 5 5 5 4 比較例 6 3 5 5 5 5 5 5  Example 29 0 0 0 1 1 2 1 Example 30 0 0 1 2 2 1 1 Example 31 0 1 0 2 2 2 1 Example 32 0 0 0 1 1 1 1 Example 33 0 0 0 0 1 2 1 Example 34 0 1 1 0 1 2 1 Example 35 0 0 1 0 0 1 1 Example 36 0 0 1 1 0 1 1 Comparative Example 4 2 5 5 5 5 3 2 Comparative Example 5 4 5 4 5 5 5 4 Comparative Example 6 3 5 5 5 5 5 5
[0167] 表 14より、消臭洗浄剤;!〜 8は、消臭洗浄剤 A〜Cに比べて、アンモニア、メチルメ ルカブタン、イソ吉草酸に対して優れた消臭性能を有し、さらに家庭で飼っている犬 の実尿またはモデル尿を用いた消臭試験と洗浄試験にお!/、ても優れた消臭及び洗 浄性能を示した。 [0167] From Table 14, the deodorant cleaners !! ~ 8 have better deodorant performance for ammonia, methylmerbutane and isovaleric acid compared to the deodorant cleaners AC, and In the deodorization test and cleaning test using real urine or model urine of dogs kept in Japan! /, It showed excellent deodorization and cleaning performance.
実施例 37  Example 37
[0168] ヘアエッセンス [0168] Hair Essence
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 3. 2%、 揮発性イソパラフィン 5. 0%、メチルポリシロキサン 1. 5%、グリセリン 1. 5%、 1、 3- ブチレングリコール 2· 5%、ソルビット溶液(70%) 1 · 0%、ポリエチレングリコール 60 00 0. 5%、ジォレイン酸ポリエチレングリコール 0. 05%、ジイソステアリン酸ポリダリ セリノレ 0. 5%、水酸ィ匕ナトリウム 0. 05%、ノ ラベン 0. 2%、フエノキシエタノーノレ 0. 2 %、ェデト酸 3ナトリウム 0· 1 %、カラギーナン 0· 5%、ジメチルジステアリルアンモニ ゥムヘクトライト 0· 5%、パルミチン酸デキストリン 0· 8%、カルボキシビュルポリマー 0 . 4%、及び高分子量メチルポリシロキサン(重合度 = 3000) 1. 5%を配合した。さら に、香料を含むヘアエッセンスの場合は適量の香料を加え、無香料のヘアエッセン スの場合は香料を加えずに、残分に精製水を配合して、ヘアエッセンスを調製した。 [0169] これらヘアエッセンスについて実施例 12に記載のタバコ臭に対する消臭効果の試 験を行ったところ、本実施例のヘアエッセンスは、タバコ臭に対して優れた消臭効果( 官能評価:◎)を示した。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 3.2%, volatile isoparaffin 5.0%, methylpolysiloxane 1.5%, glycerin 1.5%, 1, 3-butylene glycol 2.5%, sorbite solution (70%) 1 0%, polyethylene glycol 60 00 0.5%, polyethylene glycol dioleate 0.05%, polyisodiole diisostearate 0.5%, water Sodium oxalate 0.05%, Noraben 0.2%, Phenoxyethanolate 0.2%, Trisodium edetate 0.1%, Carrageenan 0.5%, Dimethyldistearyl ammonium hectorite 0.5% And 0.8% of dextrin palmitate, 0.4% of carboxybule polymer, and 1.5% of high molecular weight methylpolysiloxane (degree of polymerization = 3000). Furthermore, a hair essence was prepared by adding an appropriate amount of fragrance in the case of a hair essence containing a fragrance, and adding purified water to the remainder without adding a fragrance in the case of an unscented hair essence. [0169] When these hair essences were tested for the deodorizing effect on the tobacco odor described in Example 12, the hair essence of this example had an excellent deodorizing effect on the tobacco odor (sensory evaluation: ◎ )showed that.
実施例 38  Example 38
[0170] ヘアミスト(ディスペンサー) [0170] Hair mist (dispenser)
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 6. 0%、 P Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 6.0%, P
VP/VA S-630 (GAF社製) 5· 0%、ユカフォーマー AM-75 (三菱化学社製) 5· 0%VP / VA S-630 (GAF) 5.0%, Yuka Former AM-75 (Mitsubishi Chemical) 5.0%
、及び残分に工業用エタノールを配合してヘアミストを調製した。 A hair mist was prepared by blending industrial ethanol with the residue.
[0171] このへアミストについて実施例 12に記載のタバコ臭に対する消臭効果の試験を行 つたところ、本実施例のヘアミストは、タバコ臭に対して優れた消臭効果(官能評価:[0171] When the deodorizing effect on the tobacco odor described in Example 12 was tested for this hair mist, the hair mist of the present example had an excellent deodorizing effect on the tobacco odor (sensory evaluation:
◎)を示した。 ◎).
実施例 39  Example 39
[0172] シャンプー [0172] Shampoo
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 10. 5%、 ジプロピレングリコール 1 · 0%、モノステアリン酸 POE (20)ソルビタン 0. 1 %、 ΡΟΕ (2 5) POP (30) 0. 7%、ジステアリン酸エチレングリコール 2· 0%、ヤシ油脂肪酸モノェ タノ一ノレ ミド 2· 50/0、 ΡΟΕラクリノレユーテノレ 酸ナトリクム 5· 0ο/ο、 ΡΟΕラクリノレユー テル硫酸トリエタノーノレアミン 10. 0%、 2—アルキル一 Ν カルボキシメチル一 Ν ヒ ドロキシェチルイミダゾリニゥムベタイン 2· 0%、 マーコート 550 (力ノレコン社製) 5. 0 。/。、クェン酸 0· 5%、クェン酸ナトリウム 1 · 0%、塩化ナトリウム 0· 8%、酢酸 DL— a トコフエロール 0· 2%、フエノキシエタノール 0· 3%、安息香酸ナトリウム 0· 2%、レ シチン 0. 3%を配合した。さらに、香料を含むシャンプーの場合は適量の香料を加え 、無香料のシャンプーの場合は香料を加えずに、残分に精製水を配合して、シャン ブーを調製した。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 10.5%, dipropylene glycol 1.0%, monostearic acid POE (20) sorbitan 0.1%, ΡΟΕ (2 5) POP (30) 0. 7%, ethylene glycol distearate 2 2.0% coconut oil fatty Monoe Tano one Honoré bromide 2 · 5 0/0, ΡΟΕ La clinoptilolite les utility Honoré acid Natorikumu 5 2.0 o / o ΡΟΕ Lacrinoreutere triethanolamine sulfate 10.0%, 2-alkyl Ν carboxymethyl Ν hydroxetyl imidazolinium betaine 2.0%, Marquat 550 (manufactured by Riki Norecon) 5.0. /. , Citrate 0.5%, sodium citrate 1.0%, sodium chloride 0.8%, acetic acid DL—a tocopherol 0.2%, phenoxyethanol 0.3%, sodium benzoate 0.2%, Lecithin 0.3% was added. Further, in the case of a shampoo containing a fragrance, an appropriate amount of fragrance was added, and in the case of an unscented shampoo, no fragrance was added, and purified water was added to the residue to prepare a shampoo.
[0173] これらシャンプーについて実施例 12に記載のタバコ臭に対する消臭効果の試験を 行ったところ、本実施例のシャンプーは、タバコ臭に対して優れた消臭効果(官能評 価:◎)を示した。  [0173] When these shampoos were tested for the deodorizing effect on the tobacco odor described in Example 12, the shampoo of this example had an excellent deodorizing effect (sensory evaluation: ◎) on the tobacco odor. Indicated.
実施例 40 [0174] 低刺激性シャンプー Example 40 [0174] Hypoallergenic shampoo
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 5. 0%、 グリセリン 0. 5%、ジステアリン酸エチレングリコール 2. 0%、ヤシ油脂肪酸モノエタノ ールアミド 1 · 0%、ラウリン酸プロピレングリコール 2· 0%、ヤシ油脂肪酸メチルタウリ ンナトリウム 7. 0%、ヤシ油脂肪酸アミドプロピルべタイン 6. 0%、ポリマー JR400 OJC C社製) 1 · 0%、クェン酸 0· 5%、フエノキシエタノール 0· 3%、安息香酸ナトリウム 0 . 2%、ェデト酸 2ナトリウム 0· 1 %、大豆レシチン 0· 2%、カチオン化馬鈴薯デンプン (Sensomer CI-50CALGON社製) 0· 5%を配合した。さらに、香料を含む低刺激性シ ヤンブーの場合は適量の香料を加え、無香料の低刺激性シャンプーの場合は香料 を加えずに、残分に精製水を配合して、低刺激性シャンプーとした。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 5.0%, glycerin 0.5%, ethylene glycol distearate 2.0%, coconut oil fatty acid monoethanolamide 1 0%, propylene glycol laurate 2.0%, sodium coconut oil fatty acid methyltaurine sodium 7.0%, coconut oil fatty acid amidopropyl betaine 6.0%, polymer JR400 OJC C) 1 · 0%, citrate 0 · 5%, phenoxyethanol 0.3%, sodium benzoate 0.2%, disodium edetate 0.1%, soybean lecithin 0.2%, cationized potato starch (Sensomer CI-50CALGON) 0 · Formulated with 5%. In addition, in the case of a hypoallergenic shampoo containing fragrance, an appropriate amount of fragrance is added. did.
[0175] これら低刺激性シャンプーについて実施例 12に記載のタバコ臭に対する消臭効果 の試験を行ったところ、本実施例の低刺激性シャンプーは、タバコ臭に対して優れた 消臭効果 (官能評価:◎)を示した。  [0175] When these hypoallergenic shampoos were tested for the deodorant effect against tobacco odor described in Example 12, the hypoallergenic shampoo of this example was superior in deodorant effect (sensory Evaluation: A).
実施例 41  Example 41
[0176] 化粧料  [0176] Cosmetics
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 2. 0%、メ チルポリシロキサン 2· 0%、セタノーノレ 3. 0%、ベへニルアルコール 3· 0%、グリセリ ン 4· 0%、ジグリセリン 2· 0%、 2—ェチルへキサン酸セチル 1 · 0%、モノステアリン 酸グリセリノレ 1. 0%、塩化ステアリルトリメチルアンモニゥム 2. 0%、クェン酸 0. 1 %、 油溶性植物プロテイン 0. 05%、ァミノ変性ポリシロキサン(東レダウ SM8702C) 1. 0 %、高分子量ポリシロキサン(重合度 = 4000) 0. 5%、パラペン 0. 2%を配合した。 さらに、香料を含む化粧料の場合は適量の香料を加え、無香料の化粧料の場合は 香料を加えずに、残分に精製水を配合して、化粧料を調製した。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 2.0%, methylpolysiloxane 2.0%, cetanolol 3.0%, behenyl alcohol 3.0 %, Glycerin 4.0%, diglycerin 2.0%, cetyl 2-ethylhexanoate 1.0%, glycerinole monostearate 1.0%, stearyltrimethylammonium chloride 2.0%, citrate 0.1%, Oil-soluble plant protein 0.05%, Amino-modified polysiloxane (Toray Dou SM8702C) 1.0%, High molecular weight polysiloxane (Polymerization degree = 4000) 0.5%, Parapen 0.2% did. Furthermore, in the case of cosmetics containing a fragrance, an appropriate amount of fragrance was added, and in the case of an unscented cosmetic, no fragrance was added and purified water was added to the remainder to prepare a cosmetic.
[0177] これら化粧料について実施例 12に記載のタバコ臭に対する消臭効果の試験を行 つたところ、本実施例の化粧料は、タバコ臭に対して優れた消臭効果 (官能評価:◎) を示した。 [0177] When these cosmetics were tested for the deodorizing effect on the tobacco odor described in Example 12, the cosmetic of the present example had an excellent deodorizing effect on the tobacco odor (sensory evaluation: ◎) showed that.
実施例 42  Example 42
[0178] 毛髪仕上げ用スプレー 実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%、メ チノレフェニノレポリシロキサン 0· 5%、 1、 3 ブチレングリコーノレ 0· 5%、液状ラノリン 0 . 2%、 2 ェチルへキサン酸セチル 0· 5%、ラウリン酸ジエタノールアミド 0· 5%、ピ 口グルタミン酸イソステアリン酸 POE硬化ヒマシ油 0· 2%、パラベン 0· 2%、パラメトキ シ桂皮酸 2 ェチルへキシル 0. 5%、ユカフォーマー 104 (三菱化学社製) 8. 0%、 油溶性植物プロテイン 0. 02%を配合した。さらに、香料を含む化粧料の場合は適量 の香料を加え、無香料の化粧料の場合は香料を添加せずに、残分に工業用ェタノ ールを配合して毛髪仕上げ用スプレーの原液を得た。この原液と LPGを、原液/ LP G = 55/45で混合して常法により毛髪仕上げ用スプレーを調製した。 [0178] Hair finish spray Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.0%, methinorefinolole polysiloxane 0.5%, 1, 3 butylene glycolenole 0.5% Liquid lanolin 0.2%, 2-ethyl cetyl cetylate 0.5%, lauric acid diethanolamide 0.5%, pi-glutamic acid isostearic acid POE hydrogenated castor oil 0.2%, paraben 0.2%, paramethycin cinnamon 2% hexyl acid 2-0.5%, Yucaformer 104 (Mitsubishi Chemical Co., Ltd.) 8.0%, oil-soluble vegetable protein 0.02% were blended. In addition, in the case of cosmetics containing fragrances, an appropriate amount of fragrance is added, and in the case of unscented cosmetics, no fragrance is added, and industrial ethanol is added to the remainder to prepare a stock solution for hair finish spray. Obtained. This stock solution and LPG were mixed at a stock solution / LPG = 55/45 to prepare a hair finishing spray by a conventional method.
[0179] これら毛髪仕上げ用スプレーについて実施例 12に記載のタバコ臭に対する消臭 効果の試験を行ったところ、本実施例の毛髪仕上げ用スプレーは、タバコ臭に対して 優れた消臭効果 (官能評価:◎)を示した。  [0179] When these hair-finishing sprays were tested for the deodorizing effect against tobacco odor described in Example 12, the hair-finishing spray of this example had an excellent deodorizing effect (sensory Evaluation: A).
実施例 43  Example 43
[0180] ヘアスプレー 1  [0180] Hairspray 1
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%、 2 ーェチルへキサン酸セチル 0· 5%、ポリオキシエチレンォレイルエーテル 0· 3%、油 溶性植物プロテイン 0· 1 %、プラスサイズ L 53 (互応化学社製) 12· 0%、及び残 分に工業用エタノールを配合してヘアスプレー 1の原液を得た。この原液と LPG、 D MEを、原液/ LPG/DME = 40/10/50で混合して常法によりヘアスプレー 1を 調製した。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 0.5%, cetyl hexylate 0.5%, polyoxyethylene glycol ether 0.3%, A stock solution of hair spray 1 was obtained by blending oil-soluble plant protein 0.1%, plus size L 53 (manufactured by Reciprocal Chemical Co., Ltd.) 12% and industrial ethanol. This stock solution was mixed with LPG and DME at a stock solution / LPG / DME = 40/10/50 to prepare hair spray 1 by a conventional method.
[0181] このヘアスプレー 1について実施例 12に記載のタバコ臭に対する消臭効果の試験 を行ったところ、本実施例のヘアスプレー 1は、タバコ臭に対して優れた消臭効果(官 能評価:◎)を示した。  [0181] When this hair spray 1 was tested for the deodorizing effect against tobacco odor described in Example 12, the hair spray 1 of this example had an excellent deodorizing effect on the tobacco odor (evaluation of function). : ◎).
実施例 44  Example 44
[0182] ヘアスプレー 2  [0182] Hairspray 2
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 2. 0%、 流動パラフィン 6· 0%、メチルポリシロキサン 3· 0%、メチルフエ二ルポリシロキサン 2 . 0%、デシルテトラデカノール 6. 0%、 2 ェチルへキサン酸セチル 3. 0%、及び残 分に工業用エタノールを配合してヘアスプレー 2の原液を得た。この原液と LPGを、 原液/ LPG = 50/50で混合して常法によりヘアスプレー 2を調製した。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 2.0%, liquid paraffin 6.0%, methylpolysiloxane 3.0%, methylphenylpolysiloxane 2. 0%, decyltetradecanol 6.0%, cetyl hexyl hexanoate 3.0%, and the balance Ingredients were mixed with industrial ethanol to obtain a hairspray 2 stock solution. This stock solution and LPG were mixed at stock solution / LPG = 50/50 to prepare hair spray 2 by a conventional method.
[0183] このヘアスプレー 2について実施例 12に記載のタバコ臭に対する消臭効果の試験 を行ったところ、本実施例のヘアスプレー 2は、タバコ臭に対して優れた消臭効果(官 能評価:◎)を示した。 [0183] When this hair spray 2 was tested for the deodorizing effect against tobacco odor described in Example 12, the hair spray 2 of this example had an excellent deodorizing effect against cigarette odor (evaluation of the function). : ◎).
実施例 45  Example 45
[0184] リンス [0184] Rinse
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 3. 0%、 流動パラフィン 1 · 0%、メチルポリシロキサン 3· 0%、セタノール 1 · 0%、オタチルド デカノール 3. 0%、油溶性植物プロテイン 0. 1 %、プロピレングリコール 5. 0%、ポリ ォキシエチレン硬化ヒマシ油 0. 5%、ポリオキシエチレンステアリルエーテル 0. 5%、 塩化アルキルトリメチルアンモニゥム 1. 5%、クェン酸 0. 1 %、塩化カリウム 0. 5%、 フエノキシエタノール 0· 3%、ビリチオン亜鉛液(50%) 0· 01 %を配合した。さらに、 香料を含むリンスの場合は適量の香料を加え、無香料のリンスの場合は香料を加え ずに、残分に精製水を配合して、リンスを調製した。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 3.0%, liquid paraffin 1.0%, methylpolysiloxane 3.0%, cetanol 1.0%, otatilde Decanol 3.0%, oil-soluble vegetable protein 0.1%, propylene glycol 5.0%, polyoxyethylene hydrogenated castor oil 0.5%, polyoxyethylene stearyl ether 0.5%, alkyltrimethylammonium chloride 1. 5%, 0.1% citrate, 0.5% potassium chloride, 0.3% phenoxyethanol, and 0.01% viricion zinc solution (50%) were mixed. Furthermore, in the case of rinsing containing a fragrance, an appropriate amount of fragrance was added, and in the case of an unscented rinsing, no fragrance was added and purified water was added to the residue to prepare a rinse.
[0185] これらリンスを実施例 12に記載のタバコ臭に対する消臭効果の試験を行ったところ 、本実施例のリンスは、タバコ臭に対して優れた消臭効果(官能評価:◎)を示した。 実施例 46  [0185] When these rinses were tested for the deodorant effect against the tobacco odor described in Example 12, the rinse of this example showed an excellent deodorant effect (sensory evaluation:)) against the tobacco odor. It was. Example 46
[0186] パーマネントウエーブ剤 1  [0186] Permanent wave agent 1
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%、 グリセリン 4. 0%、ラウリン酸モノエタノールァミン 1. 0%、ポリオキシエチレンォレイル エーテル 0· 5%、塩化ラウリルトリメチルアンモニゥム 0· 2%、塩化ステアリルトリメチ ノレアンモニゥム 0. 5%、炭酸アンモニゥム 5. 0%、尿素 2. 0%、チォグリコール酸ァ ンモニゥム液(50%) 15· 0%、ヒドロキシエタンジホスホン酸(60%) 0· 2%を配合し た。さらに、香料を含むパーマネントウエーブ剤の場合は適量の香料を加え、無香料 のパーマネントウエーブ剤の場合は香料を加えずに、残分に精製水を配合して、パ 一マネントゥエーブ剤 1を調製した。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.5%, glycerin 4.0%, monoethanolamine laurate 1.0%, polyoxyethylene oleyl Ether 0.5%, lauryltrimethylammonium chloride 0.2%, stearyltrimethyl ammonium monoxide 0.5%, ammonium carbonate 5.0%, urea 2.0%, ammonium thioglycolate solution (50%) 15.0% and hydroxyethane diphosphonic acid (60%) 0.2% were added. In addition, in the case of a permanent wave agent containing a fragrance, an appropriate amount of fragrance was added, and in the case of an unscented permanent wave agent, no fragrance was added, and purified water was added to the remainder to prepare a permanent tube 1 .
[0187] これらパーマネントウエーブ剤 1について実施例 12に記載のタバコ臭に対する消 臭効果の試験を行ったところ、本実施例のパーマネントウエーブ剤 1は、タバコ臭に 対して優れた消臭効果 (官能評価:◎)を示した。 [0187] With respect to these permanent wave agents 1, the effects on tobacco odor described in Example 12 were eliminated. When the odor effect was tested, the permanent wave agent 1 of this example showed an excellent deodorizing effect (sensory evaluation: ◎) against tobacco odor.
実施例 47  Example 47
[0188] パーマネントウエーブ剤 2 [0188] Permanent wave agent 2
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%、メ チルシロキサンェマルジヨン 5· 0%、ラウリルジメチルァミノ酢酸べタイン 0· 5%、リン 酸 1水素ナトリウム 0. 1 %、臭素酸ナトリウム液(20%) 40. 0%、リン酸 2水素カリウム 0. 5%、安息香酸ナトリウム 0. 2%、及び残分に精製水を配合してパーマネントゥェ ーブ剤 2を調製した。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.5%, methylsiloxane emulsion 5.0%, lauryl dimethylamino acetate betaine 0.5% , Sodium monohydrogen phosphate 0.1%, Sodium bromate solution (20%) 40.0%, Potassium dihydrogen phosphate 0.5%, Sodium benzoate 0.2%, and purified water Permanent tube agent 2 was prepared.
[0189] このパーマネントウエーブ剤 2について実施例 12に記載のタバコ臭に対する消臭 効果の試験を行ったところ、本実施例のパーマネントウエーブ剤は、タバコ臭に対し て優れた消臭効果 (官能評価:◎)を示した。  [0189] When this permanent wave agent 2 was tested for the deodorizing effect against the tobacco odor described in Example 12, the permanent wave agent of this example had an excellent deodorizing effect on the tobacco odor (sensory evaluation). : ◎).
実施例 48  Example 48
[0190] ボディー用化粧水(ディスペンサー) [0190] Body lotion (dispenser)
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 1.0%
、工業用エタノーノレ 20· 0%,グリセリン 6· 0%, 1、 3—フ、、チレングリコーノレ 3· 0%, P, Industrial Ethanol Nole 20 · 0%, Glycerin 6 · 0%, 1, 3—F, Tylene Glycolanol 3 · 0%, P
OE (60)硬化ヒマシ油 0. 8%、ョモギエキス 1. 0%を配合し、残分に精製水を配合し てボディー用化粧水を調製した。 A body lotion was prepared by blending 0.8% OE (60) hydrogenated castor oil and 1.0% mugwort extract, and blending purified water with the remainder.
[0191] このボディー用化粧水について実施例 12に記載のタバコ臭に対する消臭効果の 試験を行ったところ、本実施例のボディー用化粧水は、タバコ臭に対して優れた消臭 効果 (官能評価:◎)を示した。 [0191] When this body lotion was tested for the deodorant effect against tobacco odor described in Example 12, the body lotion of this example had an excellent deodorant effect (sensory Evaluation: A).
実施例 49  Example 49
[0192] クリーム [0192] cream
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 1 %、 ワセリン 2. 0%,メチノレポリシロキサン 3. 0%,セタノーノレ 2. 0%,グリセリン 3. 0%, 1 、 3—プ、チレングリコーノレ 5. 0%、硬ィ匕油 2. 0%、ステアリン酸 2. 0%、卜リ 2—ェチノレ へキサン酸グリセリル 3. 5%、イソステアリン酸ポリオキシエチレングリセリル 0. 7%、 モノステアリン酸グリセリン 2· 3%、水酸化カリウム 0· 15%、へキサメタリン酸ナトリウ ム 0. 01 %、ヒアノレロン酸ナトリウム 0. 1 %、ァスコルビン酸リン酸エステルマグネシゥ ム 2· 0%、パラベン 0. 3%、カルボキシビュルポリマー 0. 05%を配合した。さらに、 香料を含むクリームの場合は適量の香料を加え、無香料のクリームの場合は香料を 加えずに、残分に精製水を配合して、クリームを調製した。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.1%, Vaseline 2.0%, Metinorepolysiloxane 3.0%, Cetanore 2.0%, Glycerin 3. 0%, 1, 3-propylene, styrene glycolol 5.0%, hard coconut oil 2.0%, stearic acid 2.0%, bis-2-ethanole glyceryl hexanoate 3.5%, isostearin Polyoxyethylene glyceryl acid 0.7%, glyceryl monostearate 2-3%, potassium hydroxide 0.15%, sodium hexametaphosphate 0.01% sodium hyaluronate, 0.1% sodium, ascorbic acid phosphate magnesium 2.0%, paraben 0.3%, carboxybule polymer 0.05%. Furthermore, in the case of a cream containing a fragrance, an appropriate amount of fragrance was added, and in the case of an unscented cream, a fragrance was not added, and purified water was added to the remainder to prepare a cream.
[0193] これらクリームを水で適宜希釈して実施例 12に記載のタバコ臭に対する消臭効果 の試験を行ったところ、本実施例のクリームは、タバコ臭に対して優れた消臭効果(官 能評価:◎)を示した。 [0193] When these creams were appropriately diluted with water and tested for the deodorizing effect against tobacco odor described in Example 12, the cream of this example had an excellent deodorizing effect (governmental) against tobacco odor. Performance evaluation: ◎).
実施例 50  Example 50
[0194] ジェノレ [0194] Genore
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%、 工業用エタノール 5· 0%、グリセリン 8· 0%、ポリオキシエチレンメチルダルコシド 4· 0%、 ΡΟΕ (12)ラウリルエーテル 1 · 0%、ラウリルジメチルアミンォキシド 0· 3%、水 酸化カリウム 0· 5%、 Lーァスコルピン酸ー2—ダルコシド 2· 0%、パラベン 0· 3%、 カルボキシビュルポリマー 0. 6%を配合した。さらに、香料を含むジエルの場合は適 量の香料を加え、無香料のジエルの場合は香料を加えずに、残分に精製水を配合し て、ジエルを調製した。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 1.0%, industrial ethanol 5.0%, glycerin 8.0%, polyoxyethylene methyldarcoside 4. 0%, ΡΟΕ (12) Lauryl ether 1 · 0%, Lauryldimethylamine oxide 0 · 3%, Potassium hydroxide 0 · 5%, L-ascorbic acid-2-darcoside 2 · 0%, Paraben 0 · 3%, Carboxybule polymer 0.6% was blended. Furthermore, in the case of a jewel containing fragrance, an appropriate amount of fragrance was added. In the case of an unscented jewel, no fragrance was added, and purified water was added to the remainder to prepare a jewel.
[0195] これらジエルを水で適宜希釈して実施例 12に記載のタバコ臭に対する消臭効果の 試験を行ったところ、本実施例のジエルは、タバコ臭に対して優れた消臭効果 (官能 評価:◎)を示した。  [0195] When these jewels were appropriately diluted with water and tested for the deodorant effect against tobacco odor described in Example 12, the jewel of this example had an excellent deodorant effect (sensory Evaluation: A).
実施例 51  Example 51
[0196] 美白用クリーム [0196] Cream for whitening
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 6. 0%、 流動パラフィン 5· 0%、ワセリン 1 · 0%、メチルポリシロキサン 2· 0%、工業用ェタノ 一ノレ 3. 0%,セタノーノレ 0. 50/0、グリセリン 6. 0%, 1、 3 フ、、チレングリコーノレ 6. 0% 、ポリエチレングリコーノレ 1500 1. 0%、硬ィ匕油 2. 0%、 2 ェチノレへキサン酸セチ ル 4. 0%、イソステアリン酸ポリオキシエチレングリセリル 1. 0%、モノステアリン酸ポリ ォキシエチレングリセリン 1. 0%、水酸化カリウム 0. 1 %、メタリン酸ナトリウム 0. 02% 、塩酸アルギニン 0. 1 %、酢酸 DL— a トコフエロール 0. 1 %、油溶性植物プロテ イン 0. 50/o、ローズマリーエキス 1. 0ο/ο、ヒアノレロン酸ナトリウム 0. 2%,ァノレフ、、チン 5 . 0%、フエノキシエタノール 0· 3%、ェデト酸 3ナトリウム 0· 05%、パラメトキシ桂皮 酸 2—ェチルへキシル 1. 0%、キサンタンガム 0. 1 %、カルボキシビュルポリマー 0. 1 %を配合した。さらに、香料を含む美白用クリームの場合は適量の香料を加え、無 香料の美白用クリームの場合は香料を加えずに、残分に精製水を配合して、美白用 クリーム 1を調製した。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 6.0%, liquid paraffin 5.0%, petrolatum 1.0%, methylpolysiloxane 2.0%, industrial use Etano one Norre 3.0 percent, Setanonore 0.5 0/0, glycerin 6.0%, 1, 3 off ,, Chile packaging Ricoh Norre 6.0%, polyethylene glycol Norre 1500 1.0%, Kati匕油2.0%, cetylolehexanoic acid 4.0%, polyoxyethylene glyceryl isostearate 1.0%, polyoxyethylene glyceryl monostearate 1.0%, potassium hydroxide 0.1%, metalin Sodium acetate 0.02%, Arginine hydrochloride 0.1%, Acetic acid DL—a Tocopherol 0.1%, Oil-soluble plant protein Inn 0. 5 0 / o, rosemary extract 1. 0 ο / ο, sodium Hianoreron acid 0.2%, Anorefu ,, Chin 5.0%, phenoxyethanol 0, 3%, Edeto acid trisodium 0 - 05%, paramethoxycinnamate 2-ethylhexyl 1.0%, xanthan gum 0.1%, carboxybule polymer 0.1% were blended. Further, in the case of a whitening cream containing a fragrance, an appropriate amount of fragrance was added, and in the case of an unscented whitening cream, no fragrance was added, and purified water was added to the residue to prepare a whitening cream 1.
[0197] これら美白用クリームを水で適宜希釈して実施例 12に記載のタバコ臭に対する消 臭効果の試験を行ったところ、本実施例の美白用クリームは、タバコ臭に対して優れ た消臭効果 (官能評価:◎)を示した。  [0197] When these whitening creams were appropriately diluted with water and tested for the deodorizing effect on tobacco odor as described in Example 12, the whitening cream of this example was excellent in eliminating tobacco odor. Odor effect (sensory evaluation: ◎) was shown.
実施例 52  Example 52
[0198] デォドライントボディークレンジング  [0198] Deodorant Body Cleansing
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 6. 0%、 プロピレングリ: π—ノレ 8· 00/0、ソノレビ、ット ί夜(70ο/ο) 8· 0ο/ο、ラウリン酸 2· 50/0、ヤシ由 脂肪酸ジエタノールアミド 4· 0%、 ΡΟΕァノレキノレ(12、 13)エーテル硫酸トリエタノー ルァミン 2. 0%、 Ν ヤシ油脂肪酸ァシル L グルタミン酸トリエタノールァミン 3· 0%、 Ν ヤシ油脂肪酸アシノレー L グノレタミン酸ナトリウム 3· 0%、 2 アミノー 2— メチル 1—プロパノール 2· 5%、メタリン酸ナトリウム 0. 1 %、 α—トコフェローノレ 0. 02%,ユリエキス 0. 5%,パラペン 0· 2%,カノレポキシヒ、、ニノレポリマー 1. 0%,及び 残分に精製水を配合してデォドライントボディークレンジングを調製した。 EXAMPLE 9 7 type of each deodorant deodorant was mixed with an equal volume of sample 6.0% was prepared in propylene glycol: .pi. Honoré 8 · 0 0/0, Sonorebi, Tsu preparative ί night (70 o / o) 8 · 0 o / o, lauric acid 2-5 0/0, coconut derived fatty acid diethanolamide 4 · 0%, ΡΟΕ Anorekinore (12, 13) ether sulfate Torietano Ruamin 2. 0%, New coconut oil fatty Ashiru L Triethanolamine glutamate 3.0%, 、 Palm oil fatty acid asinole L Sodium gnoretamine 3.0%, 2-amino-2-methyl 2-propanol 2.5%, sodium metaphosphate 0.1%, alpha-tocophero Nodole body cleansing was prepared by blending Nore 0.02%, Lily extract 0.5%, Parapen 0.2%, Canolepoxyhi, Ninore polymer 1.0%, and the remaining purified water.
[0199] このデォドライントボディークレンジングについて実施例 12に記載のタバコ臭に対 する消臭効果の試験を行ったところ、本実施例のデォドライントボディークレンジング は、タバコ臭に対して優れた消臭効果 (官能評価:◎)を示した。  [0199] When this deodorant body cleansing was tested for the deodorizing effect on the tobacco odor described in Example 12, the deodorant body cleansing of this example was superior to the tobacco odor. Deodorizing effect (sensory evaluation: ◎) was shown.
実施例 53  Example 53
[0200] ヘアマニキュア [0200] Hair manicure
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%と 、ベンジノレ 7 "ノレ 一ノレ 10. 0ο/ο、 Ν メチノレピロリドン 15. 0%,クユン酸 3. 0%,キサ ンタンガム 1. 0%、酸性染料 0. 8%、及び残分に精製水を配合して、ヘアマニキュア を調製した。 [0201] このヘアマニキュアを実施例 12記載のタバコ臭に対する消臭効果の試験を行った ところ、本実施例品は、タバコ臭に対して優れた消臭効果 (官能評価:◎)を示した。 実施例 54 Deodorant sample prepared by mixing the 7 types of deodorants prepared in Example 9 in equal amounts 0.5%, Benzenore 7 "Nore Inore 10.0 ο / ο , Ν Metinorepyrrolidone 15.0% Hair manicure was prepared by blending 3.0% cunic acid, 1.0% xanthan gum, 0.8% acidic dye, and purified water in the remainder. [0201] When this hair manicure was tested for the deodorizing effect on the tobacco odor described in Example 12, the product of this Example showed an excellent deodorizing effect (sensory evaluation: ◎) on the tobacco odor. . Example 54
[0202] 酸化染毛料  [0202] Oxidative hair dye
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 3%、 セタノール 10· 0%、 POE (15)セチルエーテル 2· 0%、ラウリル硫酸ナトリウム 2· 0 %、流動パラフィン 5. 0%、油溶性植物プロテイン 0. 3%、ポリメチルシロキサン 3. 0 。/。、モノエタノールァミン 3. 0%、プロピレングリコール 8. 0%、炭酸水素アンモニゥ ム 2· 0%、チォグリコール酸アンモニゥム 0· 5%、メタアミノフエノーノレ 0. 5%パラアミ ノフエノーノレ 0. 50/0、レゾノレシン 0. 5%,トノレェンー 2、 5—ジァミン 0. 50/0、ノ ラァミノ オタトクレゾール 0· 5%、ポリマー JR4000JCC社製) 0. 2%、及び残分に精製水を 配合して、酸化染毛料の 1剤を調製した。セタノール 10. 0%と、 POE (15)セチルェ 一テル 2· 0%、ラウリル硫酸ナトリウム 2· 0%、流動パラフィン 5· 0%、ポリメチルシロ キサン 3. 0%、過酸化水素水(35%) 18. 0%、及び残分に精製水を配合し、クェン 酸で pH 8.0に調整して、酸化染毛料の 2剤を調製した。次に、酸化染毛料の 1剤と 2 剤を、 1剤 /2剤 = 1/0. 5〜2の比率で混合し、本実施例の酸化染毛料を得た。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.3%, cetanol 10.0%, POE (15) cetyl ether 2.0%, sodium lauryl sulfate 2 0%, liquid paraffin 5.0%, oil-soluble vegetable protein 0.3%, polymethylsiloxane 3.0. /. , Monoethanolamine § Min 3.0%, propylene glycol 8.0%, bicarbonate Anmoniu arm 2 · 0% Chio glycolic acid Anmoniumu 0 - 5%, meta-amino Hue no Honoré 0.5% Paraami Nofuenonore 0.5 0 / 0, Rezonoreshin 0.5% Tonoreen 2, 5-Jiamin 0.5 0/0, Bruno Raamino OTA preparative cresol 0 - 5%, manufactured by polymer JR4000JCC Co.) 0.2%, and blended with purified water residue Thus, one preparation of oxidative hair dye was prepared. Cetanol 10.0%, POE (15) cetyl ester 2.0%, sodium lauryl sulfate 2.0%, liquid paraffin 5.0%, polymethylsiloxane 3.0%, hydrogen peroxide (35%) 18 Purified water was blended in 0% and the remainder, and adjusted to pH 8.0 with citrate to prepare two parts of oxidative hair dye. Next, 1 part and 2 parts of oxidative hair dye were mixed in a ratio of 1 part / 2 parts = 1 / 0.5-2 to obtain the oxidative hair dye of this example.
[0203] この酸化染毛料を水で適宜希釈して実施例 12記載のタバコ臭に対する消臭効果 の試験を行ったところ、本実施例の酸化染毛料は、タバコ臭に対して優れた消臭効 果 (官能評価:◎)を示した。  [0203] When this oxidative hair dye was appropriately diluted with water and tested for its deodorizing effect on tobacco odor as described in Example 12, the oxidative hair dye of this example was excellent in deodorizing tobacco odor. The effect (sensory evaluation: ◎) was shown.
実施例 55  Example 55
[0204] 育毛料  [0204] Hair restorer
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%、 工業用エタノール 90. 0%、トリ 2—ェチルへキサン酸グリセリル 2· 0%、 POE硬化ヒ マシ油 0. 5%、ジイソステアリン酸ジグリセリル 1. 0%、ラウリルジメチルアミンォキシド 0. 5%、?し酸0. 1 %、?し酸ナトリウム 0· 03%、センブリエキス 0· 5%、ヒノキチ才ーノレ 0. 1 %、パントテュルェチルエーテル 0. 1 %、 /3—グリチルレチン酸 0. 1 %、ニコチ ン酸べンジル 0. 1 %、塩酸ピリドキシン 0. 1 %、酢酸トコフェローノレ 0. 1 %、L—メント ール 0. 1 %、及び残分に精製水を配合して、育毛料を調製した。 [0205] この育毛料を実施例 12記載のタバコ臭に対する消臭効果の試験を行ったところ、 本実施例の育毛料は、タバコ臭に対して優れた消臭効果(官能評価:◎)を示した。 実施例 56 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.5%, industrial ethanol 90.0%, glyceryl tri-2-ethylhexylate 2.0%, POE Hydrogenated castor oil 0.5%, diglyceryl diisostearate 1.0%, lauryldimethylamine oxide 0.5%,? 0.1% acid Sodium oxalate 0.03%, assembly extract 0.5%, Hinokichi-no-re 0.1%, pantothruethyl ether 0.1%, / 3--glycyrrhetinic acid 0.1%, nicotinic acid benzil 0. A hair restorer was prepared by blending 1%, 0.1% pyridoxine hydrochloride, 0.1% tocopherol acetate 0.1%, L-menthol 0.1%, and purified water. [0205] When this hair restorer was tested for the deodorant effect against the tobacco odor described in Example 12, the hair restorer of this example had an excellent deodorant effect (sensory evaluation: ◎) against the tobacco odor. Indicated. Example 56
[0206] 制汗ローション  [0206] Antiperspirant lotion
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 0%と 、工業用エタノーノレ 45· 00/0、イソプロノ ノーノレ 0· 50/0、 1、 3—フ、、チレングリコーノレ 0· 5%、クェン酸トリェチル 0. 7%、ポリオキシエチレンポリオキシプロピレンデシルテト ラデシルエーテル 0· 2%、微粒子酸化亜鉛被覆ナイロン末 0· 2%、アルミニウムハイ ドロォキシクロライド液(50%) 20· 0%、へキサメタリン酸ナトリウム 0· 1 %、塩化ベン ザノレコニゥム夜(50ο/ο) 0· 20/0、メチノレセノレロース 0. 10/0、ポリビニノレピロリドン 0. 1 % 、及び残分に精製水を配合して、制汗ローションを調製した。 A deodorant samples 1.0% were mixed in equal amounts was seven each deodorant prepared in Example 9, industrial Etanonore 45 - 0 0/0, Isopurono Nonore 0 - 5 0/0, 1, 3-F, Tyleneglycolol 0.5%, Triethyl citrate 0.7%, Polyoxyethylene polyoxypropylene decyltetradecyl ether 0.2%, Fine zinc oxide coated nylon powder 0.2%, Aluminum high mud o · the cyclo ride solution (50%) 20 - 0% to Kisametarin sodium 0/1% chloride Ben Zanorekoniumu night (50 o / o) 0 - 2 0/0, methylcarbamoyl Roh receptacle Honoré loin 0.1 0/0 Antibiotic lotion was prepared by adding 0.1% of polyvinylino pyrrolidone and purified water to the residue.
[0207] この制汗ローションについて実施例 12に記載のタバコ臭に対する消臭効果の試験 を行ったところ、本実施例の制汗ローションは、タバコ臭に対して優れた消臭効果(官 能評価:◎)を示した。  [0207] When this antiperspirant lotion was tested for the deodorant effect against the tobacco odor described in Example 12, the antiperspirant lotion of this example had an excellent deodorant effect against the tobacco odor (evaluation of the function). : ◎).
実施例 57  Example 57
[0208] ボディー用消臭スプレー  [0208] Deodorant spray for body
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 1. 5%、 工業用ユタノーノレ 20. 0%,グリセリン 5. 0%,ジプロピレングリ: π—ノレ 5. 0%, ΡΟΕ· POPデシノレテトラデシノレエーテル 1 · 0%、及び残分に精製水を配合して、ボディー 用消臭スプレーの原液を調製した。この原液と窒素ガスを、原液/窒素ガス = 99. 3 / . 7で混合して、常法によりボディー用消臭スプレーを調製した。  Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in an equal amount 1.5%, industrial utannole 20.0%, glycerin 5.0%, dipropylene glycol: π-nore 5 A stock solution of a deodorizing spray for body was prepared by blending 0%, ΡΟΕ · POP decenoretetradecenoleether 1 · 0%, and purified water into the residue. This undiluted solution and nitrogen gas were mixed at undiluted solution / nitrogen gas = 99.3 / 3. 7 to prepare a deodorizing spray for body by a conventional method.
[0209] このボディー用消臭スプレーについて実施例 12に記載のタバコ臭に対する消臭効 果の試験を行ったところ、本実施例のボディー用消臭スプレーは、タバコ臭に対して 優れた消臭効果 (官能評価:◎)を示した。  [0209] This body deodorant spray was tested for the deodorant effect on the tobacco odor described in Example 12. As a result, the body deodorant spray of the present example was excellent in deodorizing the tobacco odor. The effect (sensory evaluation: ◎) was shown.
実施例 58  Example 58
[0210] タバコ臭消臭へアミスト  [0210] Amist to tobacco deodorant
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 2. 0%と 、工業用エタノール 50. 0%、揮発性イソパラフィン 0. 5%、メチルポリシロキサン 2· 0 %、高分子量ァミノ変性ジメチルポリシロキサン 0· 5%、プロピレングリコール 2· 0% 、 ΡΟΕ硬ィ匕ヒマシ油 0. 5%、ヒドロキシプロピノレー βーシクロデキストリン 1 · 0%、及 び残分に精製水を配合してタバコ臭消臭へアミストの原液を調製した。この原液と窒 素ガスを、原液/窒素ガス = 99. 2/0. 8で混合して、常法によりタバコ臭消臭ヘア ミストを調製した。 Deodorant sample prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 2.0%, industrial ethanol 50.0%, volatile isoparaffin 0.5%, methylpolysiloxane 2 · 0 %, High molecular weight amino-modified dimethylpolysiloxane 0.5%, propylene glycol 2.0%, hard-hardened castor oil 0.5%, hydroxypropinole β-cyclodextrin 1.0%, and the remainder Purified water was added to prepare a stock solution of amist to deodorize tobacco. This stock solution and nitrogen gas were mixed at stock solution / nitrogen gas = 99.2 / 0.8, and tobacco odor deodorizing hair mist was prepared by a conventional method.
[0211] このタバコ臭消臭へアミストについて実施例 12に記載のタバコ臭に対する消臭効 果の試験を行ったところ、本実施例のタバコ臭消臭へアミストは、タバコ臭に対して優 れた消臭効果 (官能評価:◎)を示した。  [0211] The test of the deodorizing effect on the tobacco odor described in Example 12 was conducted on this odor and deodorant of cigarette odor. Deodorizing effect (sensory evaluation: ◎) was shown.
実施例 59  Example 59
[0212] ヘアコロン  [0212] Hair colon
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 5. 0%と 、工業用エタノール 15· 0%、紅藻エキス 1 · 0%、を配合した。さらに、香料を含むへ アコロンの場合は適量の香料を加え、無香料のへアコロンの場合は香料を加えずに A deodorant sample (5.0%) prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts, industrial ethanol (15.0%), and red alga extract (1.0%) were blended. In addition, in the case of hair colons containing fragrance, add an appropriate amount of fragrance, and in the case of unscented hair colons, add no fragrance.
、残分に精製水を配合して、ヘアコロンの原液を調製した。この原液とジメチルエー テルを、原液/ジメチルエーテル = 60/40で混合して、ヘアコロンを調製した。 The residue was mixed with purified water to prepare a hair colon stock solution. This stock solution and dimethyl ether were mixed at a stock solution / dimethyl ether = 60/40 to prepare a hair colon.
[0213] このへアコロンについて実施例 12に記載のタバコ臭に対する消臭効果の試験を行 つたところ、本実施例品は、タバコ臭に対して優れた消臭効果 (官能評価:◎)を示し た。 [0213] When this hair colon was tested for the deodorizing effect on the tobacco odor described in Example 12, the product of this example showed an excellent deodorizing effect (sensory evaluation: ◎) on the tobacco odor. It was.
実施例 60  Example 60
[0214] 室内用消臭スプレー [0214] Deodorant spray for indoor use
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 3. 5%と Deodorant sample prepared by mixing the same amount of the seven types of deodorants prepared in Example 9 and 3.5%
、工業用エタノール 5. 0%、緑茶エキス 2. 0%、 ΡΟΕ (60)硬化ヒマシ油 0. 1 %、ジ イソステアリン酸ジグリセリル 0. 2%、及び残分に精製水を配合して室内用消臭スプ レーの原液を調製した。この原液と窒素ガスを、原液/窒素ガス = 99. 4/0. 6で混 合して、常法により室内用消臭スプレーを調製した。 , Industrial ethanol 5.0%, green tea extract 2.0%, persimmon (60) hydrogenated castor oil 0.1%, diglyceryl diisostearate 0.2%, and the balance containing purified water for indoor use A stock solution of deodorant spray was prepared. This undiluted solution and nitrogen gas were mixed at undiluted solution / nitrogen gas = 99.4 / 0.6 to prepare a deodorizing spray for indoor use by a conventional method.
[0215] この室内用消臭スプレーについて実施例 12に記載のタバコ臭に対する消臭効果 の試験を行ったところ、本実施例の室内用消臭スプレーは、タバコ臭に対して優れた 消臭効果 (官能評価:◎)を示した。 実施例 61 [0215] When this indoor deodorant spray was tested for the deodorant effect against the tobacco odor described in Example 12, the indoor deodorant spray of this example was superior in the deodorant effect against the tobacco odor. (Sensory evaluation: A). Example 61
[0216] 泡状ボディーデオドラント  [0216] Foam body deodorant
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプル 0. 5%と 、工業用エタノーノレ 30. 0%,シリコーン由 0. 5%, 1、 3 フ、、チレングリコーノレ 1. 00/0 、酸ィ匕亜 ロ、2. 0%、セリサイ卜 1. 0%、 POP · POPセチノレエーテノレ 0. 8%、クェン酸 0 . 2%、L メントール 0· 1 %、及び残分に精製水を配合して、泡状ボディーデォドラ ントの原液を調製した。この原液と LPGを、原液/ LPG = 92/8で混合して、常法に より泡状ボディーデオドラントを調製した。 Deodorant samples prepared by mixing the seven types of deodorants prepared in Example 9 in equal amounts 0.5%, industrial ethanol 30.0%, silicone-based 0.5%, 1, 3 Chile ring Ricoh Honoré 1.0 0/0, Sani匕亜Russia, 2.0%, Serisai Bok 1.0% POP · POP isethionate Honoré ether Honoré 0.8%, Kuen acid 0. 2% L-menthol 0 · Prepared a stock solution of foam body detergent by adding 1% and purified water to the residue. This stock solution and LPG were mixed at a stock solution / LPG = 92/8 to prepare a foam body deodorant by a conventional method.
[0217] この泡状ボディーデオドラントについて実施例 12に記載のタバコ臭に対する消臭 効果の試験を行ったところ、本実施例の泡状ボディーデオドラントは、タバコ臭に対し て優れた消臭効果 (官能評価:◎)を示した。  [0217] When this foam body deodorant was tested for the deodorant effect against tobacco odor described in Example 12, the foam body deodorant of this example had an excellent deodorant effect (sensory Evaluation: A).
実施例 62  Example 62
[0218] 車用消臭剤  [0218] Car deodorant
実施例 9で調製した 7種類の各消臭剤を等量で混合した消臭剤サンプルの濃度が 1 % (共に体積/体積)になるように水で希釈し、車用消臭剤を調製した。該車用消 臭剤を、二流体ノズル (気/液型)の噴霧器の液側にセットした。噴霧器の運転は、 噴霧器を試験対象の車内後部座席に設置し、変圧機にて圧力調整された圧縮空気 (気側)、例えばべビーコンプレッサー(日立機械)からの圧縮空気にて、連続的に作 動させた。  Prepare a car deodorant by diluting it with water so that the concentration of the deodorant sample prepared in Example 9 was equal to 1% (both volume / volume). did. The vehicle deodorant was set on the liquid side of a sprayer of a two-fluid nozzle (gas / liquid type). The sprayer is operated continuously by installing the sprayer in the rear seat of the vehicle under test and adjusting the pressure by the transformer (air side), for example, compressed air from a baby compressor (Hitachi Machine). Operated.
[0219] 車内にペットの体臭が強く残る車(車 A)、車内にタバコ臭が強く残る車(車 B)、車 内にヒトの体臭が残る車(車 C)、車内に芳香剤の臭!/、が残る車(車 D)を試験対象と した。試験対象、夫々の車内に上記車用消臭剤を噴霧器力も 15分間噴霧した。噴 霧中はエアコンを最大風量にて内気循環させ、車内に満遍なく消臭剤を行き渡らせ た。噴霧後、車の窓を開けて屋外にて外気温(20〜30°C、晴天〜曇天)で数時間(3 〜5時間)乾燥させた。  [0219] A car with a strong pet odor in the car (car A), a car with a strong tobacco odor in the car (car B), a car with a human odor in the car (car C), and a fragrance smell in the car The car (car D) with! / Was left as the test target. The car deodorant was sprayed for 15 minutes in each vehicle under test. During the mist, the air conditioner was circulated at maximum airflow, and the deodorant was distributed throughout the car. After spraying, the car window was opened and dried outdoors for several hours (3-5 hours) at an outside temperature (20-30 ° C, fine weather-cloudy).
[0220] 評価は車用消臭剤の噴霧前、噴霧 (直後)後、噴霧数時間後(乾燥後)、噴霧 1日 後に熟練パネラー 10名による官能評価を行って平均をとつた。なお、評価基準は実 施例 11に記載した悪臭防止法の 6段階臭気強度表示法に準じて官能評価した。そ の結果を表 15に示す。 [0220] The evaluation was carried out by sensory evaluation by 10 skilled panelists before spraying the vehicle deodorant, after spraying (immediately), several hours after spraying (after drying), and 1 day after spraying, and taking the average. The evaluation criteria were sensory evaluation according to the 6-step odor intensity display method of the malodor control method described in Example 11. So Table 15 shows the results.
[0221] [表 15] [0221] [Table 15]
Figure imgf000058_0001
Figure imgf000058_0001
[0222] 表 15より、本実施例における車用消臭剤は、車内の臭気 (ペット臭、タバコ臭、ヒト の体臭及び芳香剤の臭い)に対して高い消臭効果を示した。 [0222] From Table 15, the car deodorant in this example showed a high deodorizing effect on the car odor (pet odor, cigarette odor, human body odor, and fragrance smell).
産業上の利用可能性  Industrial applicability
[0223] 本発明の消臭剤は、天然由来で高い安全性を持ち、且つ生産コストが安い。さらに[0223] The deodorant of the present invention is naturally derived, has high safety, and has a low production cost. further
、本発明の消臭剤では、甘蔗由来の臭いが改善されていることから、無香料の消臭' 脱臭剤、及び化粧品、飲食品等として、食品分野、環境分野、工業分野等の幅広い 分野で利用されうる。 In the deodorant of the present invention, since the odor derived from sweet potato is improved, it can be used in a wide range of fields such as the food field, the environmental field, the industrial field, etc. Can be used.

Claims

請求の範囲 The scope of the claims
甘蔗由来の消臭物質を有効成分とする消臭剤であって、甘蔗由来の該消臭物質 が、甘蔗汁もしくは甘蔗の溶媒抽出物を蒸留して得られる蒸留物を固定担体を用い たカラムクロマトグラフィーで処理し、該処理により得られる画分を、または該画分に 水もしくはアルコール一水の混合溶媒を添加した混合物をさらに蒸留し、釜残のアル コール濃度(体積/体積)が 0 %以上〜 10 %以下であるときに該蒸留を終了した際 の釜残である、消臭剤。  A column using a deodorizing agent comprising a deodorant derived from sweet potato as an active ingredient, wherein the deodorant derived from sweet potato is obtained by distilling a sweet potato juice or a sweet potato solvent extract. The fraction obtained by the chromatography and the fraction obtained by the treatment or a mixture obtained by adding a mixed solvent of water or alcohol to water to the fraction are further distilled, and the alcohol concentration (volume / volume) in the kettle remains 0. A deodorant which is a residue of the kettle when the distillation is completed when the content is not less than 10% and not more than 10%.
該カラムクロマトグラフィー処理力 s、固定担体としての合成吸着剤を充填したカラム に、前記原料を通液し、該合成吸着剤に吸着させた成分を、メタノール、エタノール、 及び水、メタノール、エタノールの二以上の混合物から選ばれる溶媒で溶出する処 理である、請求項 1に記載の消臭剤。  The column chromatographic treatment power s, the raw material is passed through a column packed with a synthetic adsorbent as a fixed carrier, and the components adsorbed on the synthetic adsorbent are mixed with methanol, ethanol, water, methanol, and ethanol. 2. The deodorant according to claim 1, which is a process of eluting with a solvent selected from two or more mixtures.
甘蔗由来の該消臭物質力 釜残のアルコール濃度(体積/体積)が 0%以上〜 5 %以下であるときに該蒸留を終了した際の釜残である、請求項 1または 2に記載の消 臭剤。  The deodorizing substance power derived from sweet potato is the residue when the distillation is terminated when the alcohol concentration (volume / volume) of the residue is 0% to 5%. Deodorants.
アルコール力 Sメタノール、エタノール、プロパノール及びこれらの混合物から選ばれ る、請求項;!〜 3のいずれか一項に記載の消臭剤。  Alcohol power S The deodorizer according to any one of claims 1 to 3, which is selected from methanol, ethanol, propanol and mixtures thereof.
請求項 1 〜4のいずれか-一項に記載の消臭剤を含む食品。  A food comprising the deodorant according to any one of claims 1 to 4.
請求項 1 〜4のいずれか-一項に記載の消臭剤を含むエチケット消臭剤  Etiquette deodorant comprising the deodorant according to any one of claims 1 to 4
請求項 1 〜4のいずれか-一項に記載の消臭剤を含むペット用消臭剤。  A pet deodorant comprising the deodorant according to any one of claims 1 to 4.
請求項 1 〜4のいずれか-一項に記載の消臭剤を含む環境消臭剤。  An environmental deodorant comprising the deodorant according to any one of claims 1 to 4.
請求項 1 〜4のいずれか-一項に記載の消臭剤を含む消臭洗浄剤。  A deodorant cleaning agent comprising the deodorant according to any one of claims 1 to 4.
請求項 1 〜4のいずれか-一項に記載の消臭剤を含む化粧料。  A cosmetic comprising the deodorant according to any one of claims 1 to 4.
甘蔗汁もしくは甘蔗の溶媒抽出物を蒸留して得られる蒸留物の甘蔗由来の臭いを 改善する方法であって、該蒸留物を固定担体を用いたカラムクロマトグラフィーで処 理すること、該処理により得られる画分を、または該画分に水もしくはアルコール一水 の混合溶媒を添加した混合物をさらに蒸留すること、釜残のアルコール濃度(体積/ 体積)が 0%以上〜 10%以下であるときに該蒸留を終了した際の釜残を集めることを 含む、方法。 [12] 該カラムクロマトグラフィー処理力 S、固定担体としての合成吸着剤を充填したカラム に、前記原料を通液し、該合成吸着剤に吸着させた成分を、メタノール、エタノール、 及び水、メタノール、エタノールの二以上の混合物から選ばれる溶媒で溶出する処 理である、請求項 1 1記載の方法。 A method for improving a sweet potato-derived odor of a distillate obtained by distilling a sweet potato juice or a sweet potato solvent extract, wherein the distillate is treated by column chromatography using a fixed carrier, When the obtained fraction or a mixture obtained by adding water or a mixed solvent of alcohol and water to the fraction is further distilled, and the alcohol concentration (volume / volume) in the kettle is 0% to 10% Collecting the residue of the kettle at the end of the distillation. [12] The column chromatographic treatment power S, and the raw material is passed through a column packed with a synthetic adsorbent as a fixed carrier, and the components adsorbed on the synthetic adsorbent are methanol, ethanol, water, methanol The method according to claim 11, which is a process of eluting with a solvent selected from a mixture of two or more of ethanol.
[13] 釜残のアルコール濃度(体積/体積)が 0%以上〜 5%以下であるときに該蒸留を 終了した際の釜残を集めることを含む、請求項 1 1または 12に記載の方法。  [13] The method according to claim 11 or 12, comprising collecting the residue when the distillation is completed when the alcohol concentration (volume / volume) of the residue is 0% to 5%. .
[14] アルコール力 Sメタノール、エタノール、プロパノール及びこれらの混合物から選ばれ る、請求項 1 1〜; 13の!/、ずれか一項に記載の方法。  [14] Alcohol strength S The method according to any one of claims 11 to 13; selected from S methanol, ethanol, propanol and mixtures thereof.
[15] 請求項;!〜 4のいずれか一項に記載の消臭剤を用いて対象を消臭する方法。  [15] A method for deodorizing an object using the deodorizer according to any one of claims;! To 4.
PCT/JP2007/067255 2006-09-07 2007-09-05 Deodorant comprising deodorizing substance originating in sugarcane distillate as the active ingredient and method of improving odor originating in sugarcane WO2008029822A1 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009067712A (en) * 2007-09-12 2009-04-02 Arimino Kagaku Kk Deodorizer for hair deformation
JP2009067711A (en) * 2007-09-12 2009-04-02 Arimino Kagaku Kk Treatment agent for hair deformation
WO2015152271A1 (en) * 2014-03-31 2015-10-08 三井製糖株式会社 Flavor improver, flavoring agent composition, and beverage or food containing said flavor improver or said flavoring agent composition
JP2020062199A (en) * 2018-10-17 2020-04-23 アルケア株式会社 Ostomy prosthesis lubricating deodorant composition

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001087365A (en) * 1999-06-24 2001-04-03 Mitsui Sugar Co Ltd Deodorant
JP2001224673A (en) * 2000-02-17 2001-08-21 Lion Corp Method for improving offensive smell of sugarcane extract
JP2002143285A (en) * 2000-11-06 2002-05-21 Takasago Internatl Corp Cigaret odor deodorizer
JP2002238455A (en) * 2001-02-15 2002-08-27 Oriza Yuka Kk Rice bran oil and method for producing the same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001087365A (en) * 1999-06-24 2001-04-03 Mitsui Sugar Co Ltd Deodorant
JP2001224673A (en) * 2000-02-17 2001-08-21 Lion Corp Method for improving offensive smell of sugarcane extract
JP2002143285A (en) * 2000-11-06 2002-05-21 Takasago Internatl Corp Cigaret odor deodorizer
JP2002238455A (en) * 2001-02-15 2002-08-27 Oriza Yuka Kk Rice bran oil and method for producing the same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009067712A (en) * 2007-09-12 2009-04-02 Arimino Kagaku Kk Deodorizer for hair deformation
JP2009067711A (en) * 2007-09-12 2009-04-02 Arimino Kagaku Kk Treatment agent for hair deformation
WO2015152271A1 (en) * 2014-03-31 2015-10-08 三井製糖株式会社 Flavor improver, flavoring agent composition, and beverage or food containing said flavor improver or said flavoring agent composition
JP2015192610A (en) * 2014-03-31 2015-11-05 三井製糖株式会社 Flavor improver, aromatic composition, and beverage and food product including them
JP2020062199A (en) * 2018-10-17 2020-04-23 アルケア株式会社 Ostomy prosthesis lubricating deodorant composition

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