WO2007145054A1 - フォーマー容器用液体洗浄剤組成物 - Google Patents
フォーマー容器用液体洗浄剤組成物 Download PDFInfo
- Publication number
- WO2007145054A1 WO2007145054A1 PCT/JP2007/060359 JP2007060359W WO2007145054A1 WO 2007145054 A1 WO2007145054 A1 WO 2007145054A1 JP 2007060359 W JP2007060359 W JP 2007060359W WO 2007145054 A1 WO2007145054 A1 WO 2007145054A1
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- WIPO (PCT)
- Prior art keywords
- acid
- fatty acid
- liquid detergent
- detergent composition
- hydrocarbon group
- Prior art date
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/835—Mixtures of non-ionic with cationic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/08—Liquid soap, e.g. for dispensers; capsuled
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/30—Organic compounds, e.g. vitamins containing nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5428—Polymers characterized by specific structures/properties characterized by the charge amphoteric or zwitterionic
Definitions
- Liquid detergent composition for former container Liquid detergent composition for former container
- the present invention relates to a liquid detergent composition, which is excellent in low-temperature storage stability of a composition having good foam quality and particularly low skin irritation at the time of washing, and clogging when filled in a former container.
- the present invention relates to a liquid detergent composition capable of discharging good foam without causing it.
- the detergent composition is excellent in the amount of foam and the quality of the foam at the time of washing, and that it does not become wet after rinsing. It is also important that people with weak skin have little skin irritation. Above all, liquid detergent compositions based on fatty acid salts are superior to general surfactants in foam tally, and they do not feel slippery and clean up. Used in soaps.
- a foam composition is filled by filling a liquid container with a liquid detergent composition, and the detergent composition and air are simultaneously passed through a mesh.
- liquid detergent compositions based on fatty acid salts can cause mesh clogging and foam formation when precipitates are formed immediately after storage due to low temperature or storage. There was a problem of being discharged.
- Patent Document 1 Japanese Patent Laid-Open No. 8-92064 contains a salt such as a triethanolamine salt of one or more higher fatty acids and other salts at low temperatures.
- a detergent composition has been proposed for the purpose of improving the usability.
- this proposal can suppress the increase in viscosity at low temperatures, but it is not sufficient to suppress precipitates when the pH decreases with time.
- Patent Document 2 Japanese Patent Laid-Open No. 8-143899 contains an amino acid surfactant and a higher fatty acid salt, and is a detergent composition intended to improve usability at low temperatures. Has been proposed. However, in this proposal, the refreshing rinse that is characteristic of fatty acid salts The feel is not obtained, and, as in Patent Document 1, it is not sufficient to suppress precipitates when the pH decreases with time.
- Patent Document 3 Japanese Patent Laid-Open No. 11 35972 contains a basic amino acid salt of a higher fatty acid, an amphoteric or semipolar surfactant, and a polyhydric alcohol, and has excellent foam quality and low-temperature stability.
- a cleaning composition has been proposed.
- the amphoteric or semipolar surfactant suppresses the precipitation of fatty acids at the beginning of compounding, but it is desirable to further suppress the precipitate when the pH decreases with time. It was.
- Patent Document 4 Japanese Unexamined Patent Application Publication No. 2005-154651 discloses a cleaning process that does not cause clogging of the mesh and has excellent low-temperature stability by mixing three kinds of higher fatty acid salts at a specific ratio. Agent compositions have been proposed. However, although this proposal is excellent in low-temperature stability at the initial stage of blending, it has been desired to further suppress precipitates when the pH decreases with time.
- Patent Document 5 Japanese Patent Laid-Open No. 2005-213230 discloses that a combination of a specific fatty acid composition, a neutralizing agent and a specific polymer compound does not use a synthetic surfactant, but only a fatty acid sarcophagus. A technology that can easily discharge bubbles from a pump former is proposed. However, only the fatty acid salt is used as the activator and no synthetic surfactant is used, and precipitates are easily generated at low temperatures. From the above, there has been a demand for a means for suppressing the occurrence of precipitates and improving clogging of the former container even when the pH of the cleaning composition is lowered.
- Patent Document 1 Japanese Patent Application Laid-Open No. 8-92064
- Patent Document 2 JP-A-8-143899
- Patent Document 3 Japanese Patent Application Laid-Open No. 11-35972
- Patent Document 4 Japanese Patent Laid-Open No. 2005-154651
- Patent Document 5 Japanese Unexamined Patent Application Publication No. 2005-213230
- Patent Document 6 Japanese Patent Laid-Open No. 7-315463
- Patent Document 7 Japanese Patent Laid-Open No. 8-230961
- Patent Document 8 Japanese Unexamined Patent Application Publication No. 2005-193972
- the present invention is excellent in low-temperature storage stability of a composition having good foam quality during washing and particularly low skin irritation, and discharges good foam without causing clogging when filled in a former container. It is an object of the present invention to provide a liquid detergent composition for a former container.
- the low temperature stability is to suppress the generation of precipitates and precipitates over time under low temperature storage even when the pH of the liquid detergent composition is lowered.
- the precipitate when the pH decreases with low temperature or with time is a fatty acid salt in which R 1 is a monovalent hydrocarbon group of 12 or more in the general formula (1). It was. Therefore, the ratio of the fatty acid salt having a specific carbon chain length is set to a specific ratio, and further, a liquid containing a fatty acid salt and an amphoteric surfactant or a semipolar surfactant.
- a compound having an acid dissociation index of 8.0 to 11.0 to the cleaning composition, the occurrence of precipitates is suppressed even at low temperatures and even when the pH of the cleaning composition is low. It was found that clogging of the former container was improved and it was possible to discharge as foam. Furthermore, the above-mentioned detergent composition has been found to have a particularly good foam quality at the time of washing and has little skin irritation, and has led to the present invention.
- R 1 represents a linear or branched monovalent hydrocarbon group having 5 to 25 carbon atoms, and a part of the hydrogen atoms may be substituted with a hydroxyl group.
- M represents an alkali metal.
- R 2 represents a linear or branched monovalent hydrocarbon group having 1 to 6 carbon atoms, and a part of the hydrogen atoms may be substituted with a hydroxyl group.
- liquid detergent composition for a former container according to [1] which is a compound represented by the following:
- a composition having good foam quality at the time of washing and particularly low skin irritation is excellent in low-temperature storage stability, and is excellent without causing clogging even when filled in a former container. It is possible to provide a liquid detergent composition for a foam container in which foam is discharged.
- Component (a) is a fatty acid salt represented by the following general formula (1), and can be used singly or in appropriate combination of two or more.
- R 1 represents a linear or branched monovalent hydrocarbon group having 5 to 25 carbon atoms, and a part of the hydrogen atoms may be substituted with a hydroxyl group.
- M represents an alkali metal.
- R 1 is a linear or branched monovalent hydrocarbon group having 5 to 25 carbon atoms, preferably 7 to 17 carbon atoms, more preferably 11 to 17 carbon atoms, and is saturated or unsaturated. Also good.
- caproic acid As the component (a), caproic acid, heptanoic acid, force prillic acid, pelargonic acid, force puric acid, undecanoic acid, lauric acid, force proleic acid, undecylenic acid, lauroleic acid, 2-ethylenobutanoic acid, A monovalent hydrocarbon group in which R 1 is 11 or less in the general formula (1) such as isopentanoic acid, 2-ethylpentanoic acid, 2-ethylhexanoic acid, isononanoic acid, 3,5,5-trimethylhexanoic acid, etc.
- Tridecanoic acid Tridecanoic acid, tetramethylnonanoic acid, myristic acid, pentadecanoic acid, palmitic acid, stearic acid, araquinic acid, behenic acid, lignoceric acid, serotic acid, myristoleic acid, panolemitreic acid, oleic acid, elaidic acid, gondonic acid , Enoleic acid, ceracoleic acid, linoleic acid, linoleic acid, linolenic acid, arachidonic acid, 2-hexyldecanoic acid, isostear
- Examples thereof include fatty acid salts in which R 1 in the general formula (1) such as phosphoric acid and 12-hydroxystearic acid is a monovalent hydrocarbon group having 5 to 25 carbon atoms.
- a palm that is a mixture of these Examples include oil fatty acid, hardened coconut oil fatty acid, palm oil fatty acid, hardened palm oil fatty acid, palm kernel oil fatty acid, hardened palm kernel oil fatty acid, beef tallow fatty acid, hardened tallow fatty acid and the like.
- lauric acid, myristic acid, normitic acid, stearic acid, isostearic acid, oleic acid, and coconut oil fatty acid are preferred, and lauric acid, myristic acid, and palm oil fatty acid are more preferred.
- the salt to be paired include alkali metals such as sodium and potassium, and potassium salt is preferable from the viewpoint of suppression of precipitation.
- Amino acid is also widely used as a fatty acid pair salt, but it is not included because there is concern about deterioration of color and fragrance during storage at high temperatures.
- fatty acid salt R 1 is 11 or less monovalent hydrocarbon group
- R 1 is 12 or more monovalent hydrocarbon one general formula (1)
- the mass ratio represented by the fatty acid salt which is a hydrogen group is from 1.5 to 10.0, preferably from ⁇ to 2.0 to 5.0, more preferably from f to 2.0 to 4.0.
- Fatty acid salts, which are monovalent hydrocarbon groups with an R 1 power of 12 or more, are the main cause of precipitation, and are particularly noticeable when the pH is lowered or at low temperatures. This is a new finding of the present inventors. If the above mass ratio is less than 1.5, the composition will be unsatisfactory in terms of low-temperature storage stability and foam ejection from the container. On the other hand, if it exceeds 10.0, there is a concern of skin irritation. The above figures are rounded to the first decimal place.
- the blending amount of the component (a) in the liquid detergent composition is preferably 8 to 20% by mass as a fatty acid salt, more preferably 8 to 15% by mass from the viewpoint of low temperature stability and foam quality. %. If it is less than 8% by mass, the foam quality may be poor, and if it exceeds 20% by mass, the viscosity of the composition may increase, and foam may not be easily discharged from the foam container.
- Component (b) is an amphoteric surfactant or a semipolar surfactant, and can be used singly or in appropriate combination of two or more.
- Amphoteric surfactants include carbobetaine amphoteric surfactants such as alkylbetaines and alkylamidobetaines, sulfobetaine amphoteric surfactants such as alkylsulfobetaines and alkylhydroxysulfobetaines, and phosphobetaine amphoteric interfaces.
- alkyl betaines include lauryl dimethylamino acetic acid betaine.
- aminoquinoleamide betaines include coconut oil fatty acid amidopropyl betaine.
- alkylsulfobetaine include coconut oil fatty acid dimethylsulfopropylbetaine, and examples of the aryloxyhydroxysulfobetaine include lauryldimethylaminohydroxysulfobetaine.
- phosphobetaine type amphoteric surfactant include lauryl hydroxyphosphobetaine.
- imidazoline type amphoteric surfactant include coconut oil alkynole-N-hydroxyethyl imidazolinum betaine.
- Examples of semipolar surfactants include acyl acyl tertiary amines, asinole tertiary phosphates and the like.
- Examples of the asinole tertiary amine oxide include lauryl dimethylamine oxide, POE coconut oil alkyldimethylamine oxide, and dihydroxyethyl lauryl amine oxide.
- Examples of the acyl tertiary phosphoxide include lauryl dimethyl phosphine oxide.
- laurinore dimethylaminoacetic acid betaine is preferable among carbobetaine types, which are preferred to carbobetaine type amphoteric surfactants and lauryl dimethylamine oxide, from the viewpoint of improving foaming properties and the like.
- lauryl dimethylamine oxide is preferred because the viscosity slightly increases at low temperatures and foam discharge from the former container is good.
- precipitation of fatty acids may be promoted by sodium chloride contained in the production process of the synthetic activator, and in the liquid detergent composition that is desalted from the viewpoint of improving low-temperature stability, it is more preferable.
- the sodium chloride concentration is preferably 0.001% by mass or less.
- the blending amount of the component (b) in the liquid detergent composition is preferably 0.5 to 3% by mass, more preferably 0.5 to 5% by mass. If it is less than 1% by mass, the stability at low temperatures may be insufficient, and if it exceeds 5% by mass, there is a concern that it may become wet during rinsing.
- the mass ratio represented by (a) / (b) is 50 / :! ⁇ 5/1 is preferable from the viewpoint of low temperature stability.
- Component (c) is a compound having an acid dissociation index of 8.0 to 11.0, and can be used alone or in appropriate combination of two or more.
- the acid dissociation index is _log [l / acid dissociation constant], and the acid dissociation constant is measured at 25 ° C.
- Compounds with an acid dissociation index of 8.0 to: 11.0 include monoethanolamine, diethanolamine, ethylamine, 2_amino-2_hydroxymethyl _ 1,3 _propanediol, 3-amino _ 1 _ Propanol, 2-amino-1, 2-methyl-1, 1-propanol, 2-amino-1, 2-methylol 1,3-propanediol, iso Examples include propanolamine and isopropylamine. Among these, the compound represented by the following general formula (2) is particularly preferable from the viewpoint of low-temperature stability.
- R 2 represents a linear or branched monovalent hydrocarbon group having 1 to 6 carbon atoms, preferably:! To 4 carbon atoms, and a part of hydrogen atoms may be substituted with a hydroxyl group.
- the monovalent hydrocarbon group may be saturated or unsaturated.
- the blending amount of the component (c) in the liquid detergent composition is preferably 0.3 to 3% by mass, more preferably 0.5 to:!% By mass. If it is less than 3%, it may be insufficient for improving the low-temperature stability, and if it exceeds 3% by mass, there is a concern about deterioration of color tone or odor.
- liquid detergent composition of the present invention other components can be blended alone or in combination of two or more as long as the object of the present invention is not impaired.
- Other components can be appropriately selected from those normally used in liquid detergent compositions, such as oils, silicones, lower or higher alcohols, lanolin derivatives, protein derivatives, acrylic resin dispersions.
- Medicines such as vitamins, bactericides, preservatives, pH adjusters, antioxidants, sequestering agents, UV absorbers, animal and plant extracts or their derivatives, dyes, fragrances, pigments, inorganic powders, clay minerals, nylon, Examples thereof include water-insoluble polymer powders such as polyethylene.
- perfume ingredients used as perfume ingredients can be found in various publications such as “Perfume and Flavor Chemicals”, Vol. I and II, Steffen Arctander, Allured Pu b. Co. (1994) and “Synthetic Perfumes”. “Chemistry and Product Knowledge”, Motoichi Into, Chemical Industry Daily (1 996) and “Perfume and Flavor Materials of Natural Origin”, Steffen
- Examples of the perfume solvent include ethanol, benzyl benzoate, acetin (triacetin), MMB acetate (3-methoxy_3_methylbutyl acetate), ethylene glycol dibutyrate, hexylene glycol nore, dibutinorecebacate, denoretino Re-extra (isopropyl myristate), methyl carbitol (diethylene glycol monomethyl ether), carbitol (diethylene glycol monoethyl ether), TEG (triethylene glycol), benzyl benzoate, propylene glycol, jetyl phthalate, tripropylene glycol , Carboline (dimethyl phthalate), deltyl prime (isopropyl palmitate), dipropylene glycol DPG—FC (dipropylene glycol), farnesene, dioctyl Dipetate, tributyrin (glycerinotributanoate), hydrolite 1-5 (1,2-
- fragrance solvents are blended in the fragrance composition in an amount of 0.:! To 99% by mass, and preferably in the range of 0.:! To 10% by mass.
- fragrance stabilizer examples include dibutylhydroxytoluene, butylhydroxyanisole, vitamin E and its derivatives, strength technic compounds, flavonoid compounds, polyphenol compounds and the like. ⁇ : 10% by mass of blending force Preferably, 0.00:! To 5% by mass of blending. Among these, a preferred stabilizer is dibutylhydroxytolenene.
- the fragrance composition is a mixture comprising the fragrance component, a solvent and a fragrance stabilizer.
- the fragrance composition power of the liquid detergent composition of the present invention is the power of blending 0.05 to 40% by mass in the liquid detergent composition, preferably 0.01 to 10% by mass.
- the liquid detergent composition of the present invention is used for a former container and for filling a former container to be filled in the former container. Moreover, it can be set as the liquid cleaning composition product provided with the liquid cleaning composition and the foamer container filled with this.
- the former container is a non-gas type foam discharge container.
- the non-gas type foam discharge container is not particularly limited as long as the liquid detergent composition can be mixed with air and discharged in a foamed state.
- the foam is discharged by manually squeezing the same part of the bottle month.
- examples include a squeeze foamer container that can be discharged, a pump foamer container that can discharge bubbles by pushing down the nozzle part, and the like, which can be appropriately selected according to the purpose.
- Yamato Seisakusho Co., Ltd., Yoshino Kogyo Co., Ltd., etc. can be used.
- a non-gas type foam discharge container usually has a porous film body for forming foam, and the liquid detergent composition passes through the porous film body to form bubbles.
- the mesh of the porous membrane is not particularly limited and can be appropriately selected depending on the purpose, but 100 mesh or more is preferable, 100 to 400 mesh is more preferable, and 150 to 350 is more preferable. It is a mesh.
- the material of the porous membrane is preferably a plastic material such as nylon, polyester or polyolefin.
- the number of porous membranes is not particularly limited, and can be appropriately selected according to the purpose. From the viewpoint of improving foam performance, 2 to 4 or more are preferable. More specifically, the former containers described in JP-A-7-315463, JP-A-8-230961, and JP-A-2005-193972 can be suitably used.
- liquid detergent composition When a liquid container is filled with a liquid detergent composition, it is important to accurately mix the liquid detergent composition and air on the mesh, and it is essential to keep the mesh normal. . If deposits formed in the composition are clogged in the mesh, or the liquid detergent composition filled is thickened and difficult to pass through the mesh, ejection failure and foam quality decrease. On the other hand, the liquid detergent composition of the present invention suppresses deposits, suppresses clogging of the mesh portion, and has excellent foam ejection properties.
- the liquid detergent composition of the present invention is filled in the container provided with the porous membrane, and the viscosity at 5 ° C normally assumed when used in winter is 0.1 to 15 mPa's. More preferably, it is less than lOmPa's, and it is a pump pump that can discharge bubbles by pushing down the nose part. Even when using two container containers and 200 mesh, 0.:! To 15 mPa's is preferable, and more preferably lOmPa's or less.
- the viscosity is measured using a viscometer (BL type viscometer, rotor Nol, 60 rpm, 60 seconds, manufactured by Tokyo Keiki).
- the liquid cleaning composition of the present invention is suitable as a skin cleaning agent, a hair cleaning agent and the like, and can be used in a usual amount and a cleaning method.
- the method for producing the liquid detergent composition of the present invention is not particularly limited, and can be obtained based on conventional methods. There are no particular restrictions on the device for preparing the liquid detergent composition, but it can be selected appropriately according to the purpose. A stirrer is preferred.
- the present invention will be specifically described with reference to Examples and Comparative Examples.
- the present invention is not limited to the following Examples.
- the “%” in the composition indicates mass%
- the ratio indicates the mass ratio
- the amount of each component in the table is the amount in terms of pure content. .
- Liquid detergent compositions having the compositions shown in Tables 1 to 4 were prepared by a conventional method. The following evaluation was performed about the obtained liquid detergent composition. The results are also shown in the table. The pH immediately after preparation of the liquid detergent composition was adjusted to 10.6. In addition, the pH was measured using a pH meter (HM-30V) manufactured by Toa DKK-I Co., Ltd., and the sample at 25 ° C. was stabilized for 2 minutes.
- HM-30V pH meter manufactured by Toa DKK-I Co., Ltd.
- Carbon dioxide was forcibly blown into the liquid detergent composition of initial ⁇ .6, and the pH was lowered over time during actual use (pH 9.5).
- This liquid detergent composition is filled into a non-gas type pump former container (200 mesh, 2 sheets, manufactured by Yoshino Kogyo Co., Ltd.), and 10 expert evaluation panels are used at low temperatures based on the following evaluation criteria: Evaluate the foam dischargeability at 0 ° C (overall evaluation of the appearance of the discharged foam and the absence of an increase in pressing pressure), and determine the average score of 10 panelists. Judgment was made based on the criteria for the average score.
- ⁇ 1. 5 points or more 2. less than 0 points
- a non-gas type pump former container made by Yoshino Kogyo Co., Ltd., 200 mesh, 2 sheets
- liquid detergent composition for skin
- 10 professional evaluation panels use the liquid detergent composition for skin.
- the hair was washed, and the foam performance (total evaluation of foam amount and foam quality) and skin irritation were evaluated based on the following evaluation criteria.
- the average score of 10 panelists was determined and judged based on the following criteria for the average score.
- liquid detergent compositions of the examples were excellent in low-temperature stability and foam ejection properties even when the pH was lowered over time during actual use (pH 9.5).
- As measures to improve the solubility of fatty acid salts increasing the amount of solvent (propylene glycol, sorbitol), nonionic surfactant-added caro, etc. were considered, but there was no effect.
- the following examples were also evaluated in the same manner. As a result, they were excellent in low-temperature stability and foam dischargeability, as well as excellent foam performance and no skin irritation. [Example 24]
- a liquid detergent composition for filling a former pump having the following composition was prepared based on a conventional method for each liquid detergent composition.
- Liquid detergent composition for filling a former container
- Amount part 1 ⁇ 1 Lauryldimethylamine oxide 0. Amount part ⁇ 1
- Ne 3 Propylene glycol (Asahi Glass Co., Ltd.)
- Ne 5 Oil-soluble sweetener extract P—T40N (Maruzen Pharmaceutical Co., Ltd.)
- Coconut oil fatty acid potassium is lauric acid: NAA-122 (manufactured by NOF Corporation), myristic acid: NAA-142 (manufactured by NOF Corporation), palmitic acid: NAA-171 (manufactured by NOF Corporation) ), Stearic acid: NAA-174 (manufactured by NOF Corporation), oleic acid: NAA-34 (manufactured by NOF Corporation), palm oil fatty acid: coconut fatty acid (manufactured by Nippon Oil & Chemical Co., Ltd.) It was.
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Abstract
Description
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008521126A JP5071687B2 (ja) | 2006-06-12 | 2007-05-21 | フォーマー容器用液体洗浄剤組成物 |
KR1020087029664A KR101355360B1 (ko) | 2006-06-12 | 2007-05-21 | 포머 용기용 액체 세정제 조성물 |
CN200780022017.5A CN101490234B (zh) | 2006-06-12 | 2007-05-21 | 包装在泡沫剂容器内的液体洗涤剂组合物 |
HK09112136.1A HK1135428A1 (en) | 2006-06-12 | 2009-12-24 | Liquid detergent composition to be packed into foamer containers |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006162389 | 2006-06-12 | ||
JP2006-162389 | 2006-06-12 |
Publications (1)
Publication Number | Publication Date |
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WO2007145054A1 true WO2007145054A1 (ja) | 2007-12-21 |
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ID=38831573
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP2007/060359 WO2007145054A1 (ja) | 2006-06-12 | 2007-05-21 | フォーマー容器用液体洗浄剤組成物 |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP5071687B2 (ja) |
KR (1) | KR101355360B1 (ja) |
CN (1) | CN101490234B (ja) |
HK (1) | HK1135428A1 (ja) |
WO (1) | WO2007145054A1 (ja) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
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Also Published As
Publication number | Publication date |
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JP5071687B2 (ja) | 2012-11-14 |
JPWO2007145054A1 (ja) | 2009-10-29 |
HK1135428A1 (en) | 2010-06-04 |
CN101490234B (zh) | 2014-03-12 |
CN101490234A (zh) | 2009-07-22 |
KR20090025225A (ko) | 2009-03-10 |
KR101355360B1 (ko) | 2014-01-23 |
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