[go: up one dir, main page]

KR101601279B1 - Composition for oil-based liquid cleansing - Google Patents

Composition for oil-based liquid cleansing Download PDF

Info

Publication number
KR101601279B1
KR101601279B1 KR1020090108355A KR20090108355A KR101601279B1 KR 101601279 B1 KR101601279 B1 KR 101601279B1 KR 1020090108355 A KR1020090108355 A KR 1020090108355A KR 20090108355 A KR20090108355 A KR 20090108355A KR 101601279 B1 KR101601279 B1 KR 101601279B1
Authority
KR
South Korea
Prior art keywords
acid
oil
cleansing
composition
liquid cleansing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
KR1020090108355A
Other languages
Korean (ko)
Other versions
KR20100061339A (en
Inventor
하나코 아키야마
Original Assignee
가부시키가이샤환케루
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
Priority claimed from JP2009216429A external-priority patent/JP5550873B2/en
Application filed by 가부시키가이샤환케루 filed Critical 가부시키가이샤환케루
Publication of KR20100061339A publication Critical patent/KR20100061339A/en
Application granted granted Critical
Publication of KR101601279B1 publication Critical patent/KR101601279B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cosmetics (AREA)

Abstract

본 발명은 사용시에 물이 부착된 상태에서도 클렌징 효과를 발휘하며, 또한, 증점성, 도포시의 사용성, 안정성이 우수한 유성 액상 클렌징료를 제공하는 것을 과제로 한다.It is an object of the present invention to provide a oily liquid cleansing preparation which exhibits a cleansing effect even in the state of attaching water at the time of use, and which is excellent in the viscosity, the usability at the time of application and the stability.

상기 과제를 해결하기 위해 본 발명은 25℃에서 액상 또는 페이스트상인 유제와 폴리글리세린 지방산 에스테르와 지방산 이눌린과 베헨산/에이코산이산 글리세릴을 포함하는 유성 액상 클렌징용 조성물을 제공한다.In order to solve the above problems, the present invention provides an oily liquid cleansing composition comprising an emulsion which is liquid or paste-like at 25 ° C, polyglycerin fatty acid ester, fatty acid inulin and behenic acid / eicosanic acid diacyl glyceryl.

Description

유성 액상 클렌징용 조성물{Composition for oil-based liquid cleansing}[0001] Composition for oil-based liquid cleansing [

본 발명은 유성 액상 클렌징용 조성물에 관한 것이다.The present invention relates to a composition for oily liquid cleansing.

피부의 오염이나 메이크업 화장료를 지울 목적으로, 유성 클렌징료가 시판되고 있다. 이것은 클렌징 효과를 발휘시키는 것을 주목적으로서 개발되며, 액상의 것이 다수 개발되어 있다. 종래의 유성 클렌징료는, 물에 젖은 피부에 사용하면, 유화물이나 현탁물이 되어 백탁하기 때문에, 클렌징력이 현저히 저하된다는 단점을 갖고 있었다. 그러나 최근, 유의한 양의 물이 혼입되어도 유화, 크게 증점되지 않는 유성 액상 클렌징용 조성물이 개발되어, 욕실이나 세면대 등 손이나 얼굴이 젖은 환경하에서 사용할 수 있는 제품으로서 시판되고 있다.For the purpose of cleansing skin contamination or make-up cosmetics, oily cleansing agents are commercially available. This has been developed primarily for the purpose of exerting a cleansing effect, and many liquid ones have been developed. Conventional oily cleansing agents have disadvantages in that their cleansing power is markedly lowered because they become opalescent as emulsions or suspensions when used in wet skin. In recent years, however, a composition for oily liquid cleansing that does not emulsify or significantly thicken even when a significant amount of water is mixed has been developed, and has been commercially available as a product that can be used in a wet environment such as a bathroom or wash basin.

상기 기능을 갖는 액상의 유성 클렌징용 조성물은, 사전에 물을 배합한 것이거나, 물을 다량으로 가용화할 수 있도록 설계되어 있어, 제제로서의 제약 상 모두가 저점도의 것이었다. 저점도의 유성 액상 클렌징용 조성물은 손에 덜기 어려운 것과 손가락으로부터 흘러내리는 것이 문제로, 사용시에 목적 부분으로 도포하는 것이 어렵다(특허문헌 1 일본국 특허공개 제2004-75566호 공보). 또한 저점도의 유성 액상 클렌징용 조성물은, 클렌징 중에 도포부에 남기 어렵기 때문에, 직접 피부 를 문지르는 행위가 되어, 그것이 피부로의 자극이나 사용 중의 불쾌감으로 이어지고 있었다.The liquid oily cleansing composition having the above function is designed so that water can be blended in advance or that a large amount of water can be solubilized, and all the pharmaceuticals as a formulation have low viscosity. A composition for oily liquid cleansing having a low viscosity has a problem that it is difficult to shake off hands and that it flows down from the fingers, and it is difficult to apply it as a target portion at the time of use (Japanese Patent Laid-Open No. 2004-75566). Further, since the composition for oily liquid cleansing having a low viscosity is difficult to leave in the coated portion during cleansing, the skin rubs directly on the skin, leading to irritation to the skin and discomfort during use.

유성 액상 클렌징용 조성물을 증점하는 기술로서는, (베헨산/에이코산이산) 글리세릴을 사용해서 증점하여, 사용 중에 손가락으로부터 흘러내리는 것을 방지하는 기술이 개시되어 있다(특허문헌 2 일본국 특허공개 제2003-267835호 공보).As a technique for thickening a composition for oily liquid cleansing, there has been disclosed a technique of thickening using (behenic acid / eicosanic acid) glyceryl to prevent it from flowing down from the finger during use (see Patent Document 2 2003-267835).

손이나 얼굴이 젖은 환경하에서, 세정성을 유지하는 유성 액상 클렌징용 조성물로서, 상온 액상의 유분을 50 질량% 이상, HLB가 5~16인 비이온성 계면활성제를 20~40 질량% 함유하는 유성 액상 클렌징용 조성물(특허문헌 3 일본국 특허공개 제2006-225458호 공보), 모노글리세린 지방산 에스테르와 폴리글리세린 지방산 에스테르와 비이온성 계면활성제와 25℃에서 액상의 유분과 물을 함유하는 유성 액상 클렌징용 조성물(특허문헌 4 일본국 특허공개 제2004-75566호 공보)이 알려져 있다.A composition for oil-based liquid cleansing which maintains cleansing properties in a wet environment with hands or a face, comprising: a solvent-in-water emulsion containing at least 50 mass% of a liquid at room temperature in a liquid state and 20 to 40 mass% of a nonionic surfactant having an HLB of 5 to 16 A composition for cleansing (Patent Document 3: Japanese Unexamined Patent Application Publication No. 2006-225458), a composition for oily liquid cleansing containing a monoglycerin fatty acid ester, a polyglycerin fatty acid ester and a nonionic surfactant, and a liquid oil and water at 25 占 폚 (Patent Document 4: JP-A-2004-75566).

또한, 본 출원인은 먼저, 사용시에 손으로부터 흘러내리지 않아, 목적 부위에 도포하기 쉬운 우수한 사용성, 클렌징시에 잘 펴지고, 또한, 욕실이나 세면대 등 손이나 얼굴이 젖은 환경하에서 사용 가능한 유성 클렌징을 제안하였다(특허문헌 5 일본국 특허 제3729836호 공보).The applicant of the present invention first proposed an oil-based cleansing method which can be used in an environment in which hands and face such as a bathroom or a sink are not used, (Patent Document 5: Japanese Patent No. 3729836).

그러나, 요즘의 내구성이 향상된 메이크 화장료로의 대응으로서, 클렌징력이 우수한 유제를 처방 중에 배합하는 검토과정에서, 증점성과 분리의 문제가 발생하였다.However, as a response to make-up cosmetics with improved durability these days, problems of thickening and separation have arisen in the process of compounding the emulsions having excellent cleansing powers in prescription.

[선행기술문헌][Prior Art Literature]

[특허문헌][Patent Literature]

[특허문헌 1] 일본국 특허공개 제2004-75566호 공보[Patent Document 1] Japanese Patent Application Laid-Open No. 2004-75566

[특허문헌 2] 일본국 특허공개 제2003-267835호 공보[Patent Document 2] Japanese Patent Application Laid-Open No. 2003-267835

[특허문헌 3] 일본국 특허공개 제2006-225458호 공보[Patent Document 3] Japanese Patent Application Laid-Open No. 2006-225458

[특허문헌 4] 일본국 특허공개 제2004-75566호 공보[Patent Document 4] Japanese Patent Application Laid-Open No. 2004-75566

[특허문헌 5] 일본국 특허 제3729836호 공보[Patent Document 5] Japanese Patent No. 3729836

본원 발명은 내수성 메이크 화장료의 클렌징력이 우수하여, 사용시에 물이 부착된 상태에서도 클렌징 효과를 발휘하며, 또한, 증점성, 도포시의 사용성, 안정성이 우수한 유성 액상 클렌징료를 제공하는 것을 목적으로 한다.It is an object of the present invention to provide a oily liquid cleansing preparation which is excellent in cleansing power of a water-resistant make-up cosmetic, exhibits a cleansing effect even when water is used in use, and is excellent in viscosity, do.

내수성 메이크 화장료의 클렌징력을 향상시키기 위해 1가의 분지 지방산과 2가의 알코올의 디에스테르 오일과, 실리콘 오일을 함유시키는 것이 유효한 것을 발견하였으나, 증점성이 떨어지고, 도포시의 사용성이 떨어지는 동시에, 분리가 발생하여, 안정성이 떨어진다는 과제에 직면하였다.It has been found effective to improve the cleansing power of the water-resistant make-up cosmetic by adding a mono-valent branched aliphatic acid, a di-ester oil of a divalent alcohol and a silicone oil. However, it has been found that the viscosity is poor, And the stability is lowered.

이에, 본 연구자들은, 상기의 과제에 대해 연구를 거듭한 결과, 우수한 성능을 발휘하는 증점성분의 조합을 발견하여, 본 발명을 완성시켰다.Accordingly, the present inventors have repeatedly conducted studies on the above problems, and as a result, they found a combination of thickening components exhibiting excellent performance, and completed the present invention.

본 발명의 주된 구성은 다음과 같다.The main structure of the present invention is as follows.

(1) 25℃에서 액상 또는 페이스트상인 유제(A)와 폴리글리세린 지방산 에스테르(B)와 지방산 이눌린(C)과 베헨산/에이코산이산 글리세릴(D)을 포함하는 유성 액상 클렌징용 조성물.(1) A composition for oily liquid cleansing comprising an emulsion (A), a polyglycerin fatty acid ester (B), a fatty acid inulin (C) and a behenic acid / eicosanic acid disaccharide glyceryl (D) as liquid or paste at 25 占 폚.

(2) 점도가 450~700 mPa·s인 것을 특징으로 하는 (1) 기재의 유성 액상 클렌징용 조성물.(2) The oily liquid cleansing composition according to (1), wherein the viscosity is 450 to 700 mPa · s.

(3) 지방산 이눌린(C)의 배합량이 0.05~1.0 질량%이고, 베헨산/에이코산이산 글리세릴(D)의 배합량이 0.1~2.0 질량%인 것을 특징으로 하는 (2) 기재의 유성 액상 클 렌징용 조성물.(3) The liquid ointment according to (2), wherein the amount of the fatty acid inulin (C) is from 0.05 to 1.0% by mass and the amount of behenic acid / eicosanic acid diacyl glyceryl is from 0.1 to 2.0% A composition for lensing.

(4) 25℃에서 액상 또는 페이스트상인 유제(A)로서, 1가의 분지 지방산과 2가의 알코올의 디에스테르 오일(A1)과, 실리콘 오일(A2)을 포함하는 것을 특징으로 하는 (1) 기재의 유성 액상 클렌징용 조성물.(4) A lubricating oil composition as described in (1), characterized in that it contains a diester oil (A1) of a monovalent branched fatty acid and a dihydric alcohol and a silicone oil (A2) as an emulsion (A) Composition for oily liquid cleansing.

(5) 1가의 분지 지방산과 2가의 알코올의 디에스테르 오일(A1)로서 디이소노난산 1,3-부틸렌글리콜을 포함하는 것을 특징으로 하는 (4) 기재의 유성 액상 클렌징용 조성물.(5) A composition for oil-based liquid cleansing according to (4), which comprises 1,3-butylene glycol diisononanate as a diester oil (A1) of a monovalent branched fatty acid and a dihydric alcohol.

내수성 마스카라와 같은 제거하기 어려운 메이크 화장료의 클렌징력이 우수하고, 분리가 발생하지 않는 경시 안정성이 우수한 유성 액상 클렌징용 조성물을 제공할 수 있었다.It is possible to provide a composition for oily liquid cleansing which is excellent in cleansing power of make-up cosmetics which are difficult to remove such as water-resistant mascara and which has excellent stability over time without separation.

본 발명의 유성 액상 클렌징용 조성물은, 손이나 얼굴에 물방울이 묻은 상태에서도 립스틱이나 마스카라 등의 메이크 화장료를 제거하는 기능을 유지할 수 있다.The oily liquid cleansing composition of the present invention can retain the function of removing makeup cosmetics such as lipstick and mascara even in the state where water drops are stuck on the hands or face.

본 발명의 유성 액상 클렌징용 조성물은, 적절한 점성을 가져, 도포시에 피부와 손가락 사이에 클렌징료가 보유·유지(保持)되기 때문에 사용감이 우수하다.The oily liquid cleansing composition of the present invention has an appropriate viscosity and is excellent in feeling of use because a cleansing agent is held and held between the skin and fingers during application.

본 발명에 사용하는 25℃에서 액상 또는 페이스트상인 유제(A)로서는, 예를 들면 에스테르 오일, 동식물유, 탄화수소유, 실리콘 오일, 고급지방산, 고급알코올 등을 들 수 있다.Examples of the emulsions (A) which are liquid or paste-like at 25 占 폚 used in the present invention include ester oils, animal and vegetable oils, hydrocarbon oils, silicone oils, higher fatty acids and higher alcohols.

특히 에스테르 오일로서, 탄소수가 6~10인 분지 지방산과 2가의 알코올의 디에스테르를 사용하면, 메이크 화장료와의 상용성이 높아, 우수한 세정기능을 발휘한다. 탄소수가 6~10인 분지 지방산으로서는 2-에틸헥산산, 이소노난산 등을 들 수 있다. 2가의 알코올로서는 에틸렌글리콜, 프로필렌글리콜, 1,3-부틸렌글리콜, 디프로필렌글리콜, 네오펜틸글리콜, 1,2-펜탄디올 등을 들 수 있다. 2가의 알코올 중에서도 프로필렌글리콜, 1,3-부틸렌글리콜, 디프로필렌글리콜이 보다 높은 세정력을 얻기 때문에 바람직하다.In particular, when a diester of a branched fatty acid having 6 to 10 carbon atoms and a divalent alcohol is used as an ester oil, compatibility with a makeup cosmetic is high, and an excellent cleaning function is exhibited. Examples of branched fatty acids having 6 to 10 carbon atoms include 2-ethylhexanoic acid and isononanoic acid. Examples of divalent alcohols include ethylene glycol, propylene glycol, 1,3-butylene glycol, dipropylene glycol, neopentyl glycol, and 1,2-pentanediol. Of the dihydric alcohols, propylene glycol, 1,3-butylene glycol and dipropylene glycol are preferred because they give higher cleaning power.

탄소수가 6~10인 분지 지방산과 2가의 알코올의 디에스테르(A1)로서, 구체적으로는 디2-에틸헥산산 에틸렌글리콜, 디2-에틸헥산산 프로필렌글리콜, 디2-에틸헥산산 1,3-부틸렌글리콜, 디2-에틸헥산산 디프로필렌글리콜, 디2-에틸헥산산 네오펜틸글리콜, 디2-에틸헥산산 1,2-펜탄디올, 디이소노난산 에틸렌글리콜, 디이소노난산 프로필렌글리콜, 디이소노난산 1,3-부틸렌글리콜, 디이소노난산 디프로필렌글리콜, 디이소노난산 네오펜틸글리콜, 디이소노난산 1,2-펜탄디올 등을 들 수 있다.Specific examples of diesters (A1) of branched fatty acids and divalent alcohols having 6 to 10 carbon atoms include ethylene glycol di-2-ethylhexanoate, propylene glycol di-2-ethylhexanoate, Propylene glycol di-2-ethylhexanoate, 1,2-pentane diol di-2-ethylhexanoate, ethylene glycol diisononanoate, Diisononanic acid 1,3-butylene glycol, diisononanic acid dipropylene glycol, diisononanic acid neopentyl glycol, diisononanic acid 1,2-pentanediol, and the like.

또한, 실리콘 오일(A2)을 배합함으로써, 내수성 메이크 화장료와의 상용성을 높일 수 있다. 실리콘 오일로서는 디메틸폴리실록산, 메틸페닐폴리실록산, 시클로헥사실록산 등을 들 수 있다.Further, by blending the silicone oil (A2), compatibility with the water-resistant make cosmetic can be enhanced. Examples of the silicone oil include dimethylpolysiloxane, methylphenylpolysiloxane, and cyclohexasiloxane.

기타 에스테르 오일로서는, 1가의 지방산과 1가의 고급알코올의 에스테르 오일이 바람직하다. 1가의 지방산과 1가의 고급알코올의 에스테르 오일로서 예를 들면, 이소노난산 2-에틸헥실, 이소노난산 이소노닐, 이소노난산 이소데실, 팔미트산 옥틸, 2-에틸헥산산 세틸 등을 들 수 있다.As other ester oil, an ester oil of a monovalent fatty acid and a monovalent higher alcohol is preferable. Examples of ester oils of monovalent fatty acids and monovalent higher alcohols include 2-ethylhexyl isononanoate, isononyl isononanoate, isodecyl isononanoate, octyl palmitate and cetyl 2-ethylhexanoate. .

그 외에, 트리(카프릴산/카프르산) 글리세린, 트리-2-에틸헥산산 글리세린, 다이머디리놀산(피토스테릴/이소스테아릴/세틸/스테아릴/베헤닐), (디에틸렌글리콜/다이머디리놀산) 공중합체 등의 에스테르 오일, 올리브 오일, 호호바 오일, 메도우폼 오일, 로즈힙 오일, 밍크 오일 등의 동식물유, 유동 파라핀, 스쿠알란 등의 탄화수소유, 이소스테아르산, 올레산 등의 고급지방산, 옥틸도데칸올, 올레일알코올 등의 고급알코올을 사용할 수 있다.In addition, there may be mentioned glycerin tri (caprylic / capric acid), glycerin tri-2-ethylhexanoate, dimerdinoleic acid (phytosteryl / isostearyl / cetyl / stearyl / behenyl), (diethylene glycol / Dimerdinoleic acid) copolymer, higher fatty acids such as animal oils such as olive oil, jojoba oil, meadow foam oil, rose hip oil and mink oil, hydrocarbon oils such as liquid paraffin and squalane, isostearic acid and oleic acid, And higher alcohols such as octyldodecanol and oleyl alcohol.

본 발명에 사용하는 25℃에서 액상 또는 페이스트상인 유제의 배합량은 유성 액상 클렌징용 조성물의 전량에 대해, 40~95 질량%가 바람직하다. 40 질량% 미만에서는, 메이크 화장료를 피부로부터 들뜨게 하는 효과가 부족해지고, 95 질량%를 초과하면 메이크 화장료를 융합시킨 후의 씻어내기가 곤란해진다.The blending amount of the emulsion which is the liquid or paste phase at 25 캜 used in the present invention is preferably from 40 to 95% by mass relative to the total amount of the composition for oily liquid cleansing. If it is less than 40 mass%, the effect of making the makeup cosmetic from the skin becomes insufficient, and if it exceeds 95 mass%, it becomes difficult to wash the cosmetic cosmetic after the makeup cosmetic is fused.

본 발명에 사용하는 폴리글리세린 지방산 에스테르(B)로서는, 헥사카프릴산 폴리글리세릴-20, 옥타카프릴산 폴리글리세릴-25, 디이소스테아르산 폴리글리세릴-10, 디이소스테아르산 폴리글리세릴-15, 옥타이소노난산 폴리글리세릴-20, 헥사이소노난산 폴리글리세릴-15, 옥타이소노난산 폴리글리세릴-25, 모노이소스테아르산 폴리글리세릴-10, 트리이소스테아르산 폴리글리세릴-10, 카프르산 폴리글리세릴-10, 라우르산 폴리글리세릴-5, 카프르산 폴리글리세릴-2 등을 들 수 있다. 폴리글리세린 지방산 에스테르의 배합량은 유성 액상 클렌징용 조성물의 전량에 대해 1~40 질량%, 특히 4~25 질량%의 범위에서 배합하는 것이 바람직하다. 1 질량%보다 적은 경우에는 조성물의 세정성, 수세성이 불충분해지고, 40 질량%보다 많은 경우는, 유동성이 나빠지거나, 피부로의 자극성이 발생할 가능성이 있다. Examples of the polyglycerin fatty acid ester (B) used in the present invention include polyglyceryl hexaacrylate-20, polyglyceryl-25 octacaprylate, polyglyceryl-10 diisostearate, polyglyceryl diisostearate 15, octyisonananoic acid polyglyceryl-25, monoisostearic acid polyglyceryl-10, triisostearic acid polyglyceryl-10, polyglyceryl-10 , Caprylic acid polyglyceryl-10, lauric acid polyglyceryl-5, capric acid polyglyceryl-2, and the like. The blending amount of the polyglycerin fatty acid ester is preferably 1 to 40% by mass, more preferably 4 to 25% by mass, based on the total amount of the oily liquid cleansing composition. When the amount is less than 1% by mass, the cleaning property of the composition becomes insufficient, and when it is more than 40% by mass, fluidity may deteriorate or irritation to the skin may occur.

본 발명의 유성 액상 클렌징용 조성물에는, 폴리글리세린 지방산 에스테르 이외의 비이온 계면활성제를 배합할 수 있다. 예를 들면, 폴리옥시에틸렌알킬에테르류로서, 폴리옥시에틸렌(10) 이소스테아릴에테르, 폴리옥시에틸렌(10) 옥틸도데실에테르 등, 소르비탄지방산 에스테르류로서, 이소스테아르산 소르비탄, 라우르산 소르비탄, 야자 지방산 소르비탄 등, 지방산 폴리에틸렌글리콜류로서, 이소스테아르산 폴리에틸렌글리콜(8), 올레산 폴리에틸렌글리콜(10) 등, 폴리옥시에틸렌 피마자유류로서, 폴리에틸렌글리콜(30) 수소 첨가 피마자유 등, 폴리옥시에틸렌 소르비탄 지방산 에스테르류로서 야자유 지방산 폴리에틸렌글리콜(20) 소르비탄 등, 폴리옥시에틸렌글리세릴에테르 지방산 에스테르류로서, 이소스테아르산 폴리에틸렌글리콜(40) 글리세릴, 트리이소스테아르산 폴리에틸렌글리콜(30) 글리세릴 등을 들 수 있다.To the oily liquid cleansing composition of the present invention, a nonionic surfactant other than a polyglycerin fatty acid ester may be blended. Examples of the polyoxyethylene alkyl ethers include polyoxyethylene (10) isostearyl ether and polyoxyethylene (10) octyldodecyl ether. Examples of sorbitan fatty acid esters include sorbitan isostearate, lauryl (8), oleic acid polyethylene glycol (10), and the like, as polyoxyethylene castor oil, polyethylene glycol (30), hydrogenated castor oil, etc. as fatty acid polyethylene glycols such as sorbitan , Polyoxyethylene sorbitan fatty acid esters such as palm oil fatty acid polyethylene glycol (20) sorbitan and the like, polyoxyethylene glyceryl ether fatty acid esters such as polyethylene glycol (40) glyceryl isostearate, polyethylene glycol triisostearate 30) glyceryl and the like.

본 발명에 사용하는 지방산 이눌린(C)은 지방산이 이눌린과 에스테르 결합한 화합물로 예를 들면, 스테아르산 이눌린, 팔미트산 이눌린, 미리스트산 이눌린, 라우르산 이눌린, 운데실렌산 이눌린을 들 수 있다. 시판품으로서 레오팔 ISL2(센바 제분(주)제 스테아르산 이눌린)를 사용할 수 있다. 지방산 이눌린의 배합량은 0.05~1.0 질량%가 바람직하다.The fatty acid inulin (C) used in the present invention is a compound in which a fatty acid is in ester bond with an inulin, for example, stearic acid inulin, palmitic acid inulin, myristic acid inulin, lauric acid inulin and undecylenic acid inulin . As a commercial product, Leofear ISL2 (manufactured by Senba Seiyaku Co., Ltd., stearic acid inulin) can be used. The blending amount of fatty acid inulin is preferably 0.05 to 1.0% by mass.

본 발명에 사용하는 베헨산/에이코산이산 글리세릴(D)은 유성 증점제로서 알려져 있으며, 시판품으로서 닛신 오일리오그룹(주)제 놈코트 HK-G를 사용할 수 있다. 베헨산/에이코산이산 글리세릴의 배합량은 0.1~2 질량%가 바람직하다.The behenic acid / eicosanic acid diacyl glyceryl (D) used in the present invention is known as an oil-based thickener, and NOMCOAT HK-G manufactured by Nissin Oil Group Co., Ltd. may be used as a commercially available product. The blending amount of behenic acid / eicosanic acid diacyl glyceryl is preferably 0.1 to 2% by mass.

그 외에, 화장품에 통상 사용되는 각종 원료를 본 발명의 효과를 손상시키지 않는 범위에서 배합할 수 있다.In addition, various raw materials commonly used in cosmetics can be compounded in such a range as not to impair the effects of the present invention.

실시예Example

이하에 실시예를 들어 구체적으로 설명하지만, 이것에 한정되지 않는다.Hereinafter, the present invention will be described in detail by way of examples, but the present invention is not limited thereto.

표 1에 나타내는 조성으로, 각 성분을 80℃에서 혼합하고, 실온까지 냉각하여 실시예 1~4, 비교예 1~6의 유성 액상 클렌징용 조성물을 조제하였다. 또한, 표 1 중 성분 E는 화장료에 통상 사용되는 원료를 표기하였다.The components shown in Table 1 were mixed at 80 캜 and cooled to room temperature to prepare compositions for oily liquid cleansing of Examples 1 to 4 and Comparative Examples 1 to 6. Component E in Table 1 indicates raw materials commonly used in cosmetics.

Figure 112009069118413-pat00001
Figure 112009069118413-pat00001

실시예 1~4, 비교예 1~6의 유성 액상 클렌징용 조성물에 대해, 이하의 조건으로, 점도, 안정성, 도포시의 사용성, 물을 첨가했을 때의 클렌징력, 내수성 마스카라의 클렌징력을 평가하였다. 결과를 표 1에 나타낸다.The oily liquid cleansing compositions of Examples 1 to 4 and Comparative Examples 1 to 6 were evaluated for viscosity, stability, usability at application, cleansing power when water was added, and cleansing power of water-resistant mascara under the following conditions Respectively. The results are shown in Table 1.

<점도><Viscosity>

조제 다음날에 B형 점도계를 사용하여 점도를 측정하였다. 로터는 No. 2를 사용하고, 회전수는 12 rpm으로 하였다.On the next day of preparation, the viscosity was measured using a B-type viscometer. The rotor is No. 2 was used, and the number of revolutions was set to 12 rpm.

<안정성><Stability>

40℃의 항온조에서 1개월 보관하고, 이하의 기준으로 안정성을 평가하였다.And stored for 1 month in a constant temperature bath at 40 DEG C, and the stability was evaluated based on the following criteria.

○: 외관이 균일하다.○: Appearance is uniform.

×: 상부에 투명층이 분리된다.X: The transparent layer is separated at the top.

<도포시의 사용성><Usability at application>

유성 액상 클렌징용 조성물을 볼에 도포하고, 이하의 기준으로 사용성을 평가하였다.The composition for oil-based liquid cleansing was applied to balls and the usability was evaluated according to the following criteria.

○: 흘러내리기 어려워, 도포시에 볼과 손가락 사이에 유성 액상 클렌징용 조성물이 보유·유지된다.O: It is difficult to flow down, and the oily liquid cleansing composition is held and held between the ball and the fingers during application.

△: 흘러내림은 발생하지 않으나, 도포시에 볼과 손가락 사이의 유성 액상 클렌징용 조성물이 적게 느껴진다.DELTA: No falling-off occurred, but the composition for oil-based liquid cleansing between the ball and the fingers felt less during application.

×: 흘러내림이 발생하기 쉽고, 도포시에 볼과 손가락 사이의 유성 액상 클렌징용 조성물이 적게 느껴진다.X: Flowing down easily occurs, and the composition for oil-based liquid cleansing between the ball and the fingers at the time of application is less felt.

<물을 80%량 첨가한 유성 액상 클렌징용 조성물의 클렌징력 시험>&Lt; Cleansing ability test of composition for oil-based liquid cleansing in which 80% of water is added >

(1) 바이오스킨(뷰락스사제)을 분광 측색계로 측색(입광각 45도, 측정각 0도)하였다.(1) Bioskin (manufactured by BUILLAX CO., LTD.) Was colorimetrically measured with a spectroscopic colorimeter (an angle of incidence of 45 degrees and a measurement angle of 0 degrees).

(2) 2 cm×2 cm 범위에 립스틱 0.01 g을 균일하게 도포하였다(n=3).(2) 0.01 g of lipstick was applied uniformly over 2 cm × 2 cm (n = 3).

(3) 10분 건조 후, 립스틱 도포 후의 바이오스킨을 분광 측색계로 측색(입광각 45도, 측정각 0도)하였다.(3) After drying for 10 minutes, the bio-skins after applying the lipstick were colorimetrically measured with a spectroscopic colorimetric system (an angle of incidence of 45 degrees and a measurement angle of 0 degrees).

(4) 유성 액상 클렌징용 조성물에, 유성 액상 클렌징용 조성물의 80%량(유성 액상 클렌징용 조성물의 질량×0.8)의 정제수를 첨가하고, 혼합하였다.(4) To the composition for oil-based liquid cleansing, purified water in an amount of 80% (mass of oil-based liquid cleansing composition x 0.8) of the oil-based liquid cleansing composition was added and mixed.

(5) (4)에서 조제한 정제수를 첨가한 유성 액상 클렌징용 조성물을 립스틱 도포 후의 바이오스킨에 0.1 g 도포하고, 손가락으로 10 왕복 마찰하여, 립스틱과 융합시켰다.(5) 0.1 g of the oily liquid cleansing composition to which the purified water prepared in (4) was added, was applied to the liposome-applied bioskin, followed by 10 rounds of rubbing with fingers and fused with lipstick.

(6) 수세 후, 바이오스킨을 분광 측색계로 측색(입광각 45도, 측정각 0도)하였다.(6) After washing with water, the bioskin was colorimetrically measured with a spectroscopic colorimeter (an angle of incidence of 45 degrees and a measurement angle of 0 degrees).

(7) (1)의 측색값 L*(1), a*(1), b*(1), (3)의 측색값 L*(3), a*(3), b*(3), (6)의 측색값 L*(6), a*(6), b*(6)을 사용하여 이하의 식에 의해 립스틱의 잔존률을 산출하였다.(3), a * (3) and b * (3) of the colorimetric values L * (1), a * (1), b * (1) , The colorimetric values L * (6), a * (6) and b * (6) of (6) were used to calculate the residual ratio of lipstick by the following equation.

립스틱 도포 후의 바이오스킨과 립스틱 도포 전의 바이오스킨의 색차(R1)The color difference (R1) of the bioskin after applying lipstick and the bioskin before applying lipstick

Figure 112009069118413-pat00002
Figure 112009069118413-pat00002

세정 후의 바이오스킨과 립스틱 도포 전의 바이오스킨의 색차(R2)(R2) of the bioskin after cleaning and lipstick before application

Figure 112009069118413-pat00003
Figure 112009069118413-pat00003

Figure 112009069118413-pat00004
Figure 112009069118413-pat00004

<내수성 마스카라의 클렌징력 시험><Cleansing power test of water-resistant mascara>

(1) 바이오스킨(뷰락스사제)을 분광 측색계로 측색(입광각 45도, 측정각 0도)하였다.(1) Bioskin (manufactured by BUILLAX CO., LTD.) Was colorimetrically measured with a spectroscopic colorimeter (an angle of incidence of 45 degrees and a measurement angle of 0 degrees).

(2) 2 cm×2 cm 범위에 내수성 마스카라 0.005 g을 균일하게 도포하였다(n=3).(2) 0.005 g of water-resistant mascara was uniformly applied to the area of 2 cm x 2 cm (n = 3).

(3) 10분 건조 후, 내수성 마스카라 도포 후의 바이오스킨을 분광 측색계로 측색(입광각 45도, 측정각 0도)하였다.(3) After drying for 10 minutes, the bio-skins after water-resistant mascara application were colorimetrically measured with a spectroscopic colorimeter (an entrance angle of 45 degrees and a measurement angle of 0 degrees).

(4) 유성 액상 클렌징용 조성물을 내수성 마스카라 도포 후의 바이오스킨에 0.1 g 도포하고, 손가락으로 20 왕복 마찰하여, 내수성 마스카라와 융합시켰다.(4) 0.1 g of the composition for oil-based liquid cleansing was applied to the bio-skin after the application of the water-resistant mascara, followed by 20 rounds of rubbing with fingers to fuse with the water-resistant mascara.

(5) 수세 후, 바이오스킨을 분광 측색계로 측색(입광각 45도, 측정각 0도)하였다.(5) After washing with water, the bioskin was colorimetrically measured with a spectroscopic colorimeter (an angle of incidence of 45 degrees and a measurement angle of 0 degrees).

(6) (1)의 측색값 L*(1), a*(1), b*(1), (3)의 측색값 L*(3), a*(3), b*(3), (5)의 측색값 L*(5), a*(5), b*(5)를 사용하여 이하의 식에 의해 립스틱의 잔존률을 산출하였다.(3), a * (3), b * (3) of the colorimetric values L * (1), a * (1), b * (1) , The colorimetric values L * (5), a * (5), and b * (5) of (5) were used to calculate the remaining ratio of lipstick by the following equation.

내수성 마스카라 도포 후의 바이오스킨과 내수성 마스카라 도포 전의 바이오스킨의 색차(R1)Color difference (R1) between bio-skin after water-resistant mascara application and bio-skin before water-resistant mascara application

Figure 112009069118413-pat00005
Figure 112009069118413-pat00005

세정 후의 바이오스킨과 내수성 마스카라 도포 전의 바이오스킨의 색차(R2)(R2) of the bioskin after cleaning and the bioskin before water-resistant mascara application

Figure 112009069118413-pat00006
Figure 112009069118413-pat00006

Figure 112009069118413-pat00007
Figure 112009069118413-pat00007

유제로서 1가의 분지 지방산과 2가의 알코올의 디에스테르 오일과, 실리콘 오일을 포함하고, 베헨산/에이코산이산 글리세릴과 지방산 이눌린으로 증점시킨 실시예 1~4는 내수성 마스카라의 클렌징력이 우수한 동시에, 적절한 점성을 가져, 도포시의 사용성, 경시 안정성이 우수하고, 물을 함유시켰을 때에도 클렌징력이 우수하다.Examples 1 to 4 comprising a diester oil of a monovalent branched aliphatic acid and a dihydric alcohol as a tanning agent and a silicone oil and containing behenic acid / eicosanate diacylglyceryl and fatty acid inulin as the emulsifying agents were excellent in the cleansing power of the water-resistant mascara , Has an appropriate viscosity and is excellent in usability at the time of application and stability with time, and has excellent cleansing power even when water is contained.

한편, 1가의 분지 지방산과 2가의 알코올의 디에스테르 오일과, 실리콘 오일을 포함하지 않는 비교예 1, 2는 증점성, 경시 안정성이 우수하나, 내수성 마스카라의 클렌징력이 떨어졌다.On the other hand, the diester oil of monovalent branched aliphatic acid and divalent alcohol and Comparative Examples 1 and 2 which did not contain silicone oil showed excellent viscosity and aging stability, but the cleansing power of water-resistant mascara was lowered.

유제로서 1가의 분지 지방산과 2가의 알코올의 디에스테르 오일과, 실리콘 오일을 포함하고, 스테아르산 이눌린을 함유하지 않으며, 베헨산/에이코산이산 글리세릴, 또는, 베헨산/에이코산이산 글리세릴과 이소스테아르산 트레할로오스 에스테르즈를 사용하여 증점을 시험해 본 비교예 3~5는, 40℃ 1개월 보관에서 분리되어, 점성이 낮은 경향이 있었다. 스테아르산 이눌린을 포함하고 베헨산/에이코산이산 글리세릴을 함유하지 않는 비교예 6에서는, 충분한 점성은 얻어지지 않고, 경시 안정성, 사용성도 떨어지는 것이었다.A diester oil of a monovalent branched fatty acid and a dihydric alcohol as a tanning agent and a silicone oil and a lubricant containing a stearic acid inulin-free and a behenic acid / eicosanic acid dianhydride glyceryl or a behenic acid / Comparative Examples 3 to 5, which were tested for thickening by using isostearic acid trehalose esters, were separated by storage at 40 ° C for one month, and the viscosity tended to be low. In Comparative Example 6, which contained stearic acid inulin and did not contain behenic acid / eicosanic acid diacid glyceryl, sufficient viscosity was not obtained, and stability with time and usability were also poor.

처방예 1Prescription Example 1

성분 배합량(질량%)Component amount (% by mass)

이소노난산 이소노닐 (A) 55.6Isononyl isononyl (A) 55.6

디이소노난산 1,3-부틸렌글리콜 (A1) 15Diisononanic acid 1,3-butylene glycol (A1) 15

디메틸폴리실록산 (A2) 5Dimethylpolysiloxane (A2) 5

헥사카프릴산 폴리글리세릴-20 (B) 10Hexacaprylate polyglyceryl-20 (B) 10

디이소스테아르산 폴리글리세릴-10 (B) 8Diisostearic acid polyglyceryl-10 (B) 8

옥타이소노난산 폴리글리세릴-20 (B) 5Octaisonanoic acid polyglyceryl-20 (B) 5

스테아르산 이눌린 (C) 0.2Stearic acid inulin (C) 0.2

(베헨산/에이코산이산) 글리세릴 (D) 1.2(Behenic acid / eicosanic acid) glyceryl (D) 1.2

처방예 2Prescription Example 2

성분 배합량(질량%)Component amount (% by mass)

팔미트산 옥틸 (A) 46.4Octyl palmitate (A) 46.4

디이소노난산 1,3-부틸렌글리콜 (A1) 20Diisononanic acid 1,3-butylene glycol (A1) 20

시클로헥사실록산 (A2) 5Cyclohexasiloxane (A2) 5

옥타카프릴산 폴리글리세릴-25 (B) 10Octacafrilate polyglyceryl-25 (B) 10

모노이소스테아르산 폴리글리세릴-10 (B) 810 (B) 8 monoisostearic acid polyglyceryl-10

헥사이소노난산 폴리글리세릴-15 (B) 1015 (B) hexaisononanic acid polyglyceryl-15

스테아르산 이눌린 (C) 0.1Stearic acid inulin (C) 0.1

(베헨산/에이코산이산) 글리세릴 (D) 0.5(Behenic acid / eicosanic acid) glyceryl (D) 0.5

처방예 3Prescription Example 3

성분 배합량(질량%)Component amount (% by mass)

2-에틸헥산산 세틸 (A) 46.4Cetyl 2-ethylhexanoate (A) 46.4

디이소노난산 1,3-부틸렌글리콜 (A1) 20Diisononanic acid 1,3-butylene glycol (A1) 20

메틸페닐폴리실록산 (A2) 5Methylphenylpolysiloxane (A2) 5

헥사카프릴산 폴리글리세릴-15 (B) 10Polyglyceryl hexaacrylate-15 (B) 10

디이소스테아르산 폴리글리세릴-15 (B) 8Diisostearic acid polyglyceryl-15 (B) 8

옥타이소노난산 폴리글리세릴-25 (B) 10Octaisononanic acid polyglyceryl-25 (B) 10

스테아르산 이눌린 (C) 0.05Stearic acid inulin (C) 0.05

(베헨산/에이코산이산) 글리세릴 (D) 1.2(Behenic acid / eicosanic acid) glyceryl (D) 1.2

처방예 4Prescription Example 4

성분 배합량(질량%)Component amount (% by mass)

2-에틸헥산산 세틸 (A) 48.15Cetyl 2-ethylhexanoate (A) 48.15

디이소노난산 1,3-부틸렌글리콜 (A1) 25Diisononanic acid 1,3-butylene glycol (A1) 25

메틸페닐폴리실록산 (A2) 5Methylphenylpolysiloxane (A2) 5

(디에틸렌글리콜/다이머디리놀산) 공중합체 (A) 1(Diethylene glycol / dimerdinoleic acid) copolymer (A) 1

헥사카프릴산 폴리글리세릴-20 (B) 2Hexacaprylate polyglyceryl-20 (B) 2

디이소스테아르산 폴리글리세릴-10 (B) 1010 (B) 10 diisostearic acid polyglyceryl-10

옥타이소노난산 폴리글리세릴-20 (B) 8Octaisonanoic acid polyglyceryl-20 (B) 8

스테아르산 이눌린 (C) 0.05Stearic acid inulin (C) 0.05

(베헨산/에이코산이산) 글리세릴 (D) 0.8(Behenic acid / eicosanic acid) glyceryl (D) 0.8

Claims (5)

25℃에서 액상 또는 페이스트상인 유제(A)와 폴리글리세린 지방산 에스테르(B)와 지방산 이눌린(C)과 베헨산/에이코산이산 글리세릴(D)을 포함하는 유성 액상 클렌징용 조성물로서,A composition for oily liquid cleansing comprising an emulsion (A), a polyglycerin fatty acid ester (B), a fatty acid inulin (C) and a behenic acid / eicosanic acid diacid glyceryl (D) 유제 (A)가 디이소노난산 1,3-부틸렌글리콜(A1)과 실리콘 오일(A2)을 포함하는 것을 특징으로 하는 유성 액상 클렌징용 조성물.Wherein the emulsion (A) comprises diisononanic acid 1,3-butylene glycol (A1) and a silicone oil (A2). 제1항에 있어서,The method according to claim 1, 지방산 이눌린(C)의 배합량이 0.05~1.0 질량%이고, 베헨산/에이코산이산 글리세릴(D)의 배합량이 0.1~2.0 질량%인 것을 특징으로 하는 유성 액상 클렌징용 조성물.Characterized in that the blending amount of fatty acid inulin (C) is 0.05 to 1.0 mass% and the blending amount of behenic acid / eicosanic acid diacyl glyceryl (D) is 0.1 to 2.0 mass%. 삭제delete 삭제delete 삭제delete
KR1020090108355A 2008-11-27 2009-11-11 Composition for oil-based liquid cleansing Active KR101601279B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JPJP-P-2008-302738 2008-11-27
JP2008302738 2008-11-27
JP2009216429A JP5550873B2 (en) 2008-11-27 2009-09-18 Oily liquid cleansing composition.
JPJP-P-2009-216429 2009-09-18

Publications (2)

Publication Number Publication Date
KR20100061339A KR20100061339A (en) 2010-06-07
KR101601279B1 true KR101601279B1 (en) 2016-03-08

Family

ID=42362103

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020090108355A Active KR101601279B1 (en) 2008-11-27 2009-11-11 Composition for oil-based liquid cleansing

Country Status (2)

Country Link
KR (1) KR101601279B1 (en)
CN (1) CN101744745B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5453556B1 (en) * 2013-01-31 2014-03-26 株式会社ファンケル Oily liquid cleansing composition
WO2017159249A1 (en) * 2016-03-15 2017-09-21 株式会社マンダム Warmth-imparting cleansing cosmetic
JP6684648B2 (en) * 2016-05-17 2020-04-22 株式会社ファンケル Oily cleansing cosmetics
JP7289492B2 (en) * 2018-09-12 2023-06-12 クラシエホームプロダクツ株式会社 Oily liquid skin cleanser composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003267835A (en) 2002-03-12 2003-09-25 Kose Corp Oil cleansing composition
JP2005314387A (en) 2004-03-29 2005-11-10 Kose Corp Foamy oil cleansing cosmetic
JP2006225403A (en) * 2005-06-17 2006-08-31 Asahi Kasei Chemicals Corp Oily gel cleansing

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2736486B2 (en) * 1992-07-03 1998-04-02 花王株式会社 Cleansing composition
JP3729836B1 (en) * 2004-07-06 2005-12-21 株式会社ファンケル Oily liquid cleansing composition
JP5248863B2 (en) * 2005-12-27 2013-07-31 株式会社ファンケル Oily liquid cleansing composition
JP4189886B1 (en) * 2008-03-28 2008-12-03 株式会社ファンケル Oily liquid cleansing composition.

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003267835A (en) 2002-03-12 2003-09-25 Kose Corp Oil cleansing composition
JP2005314387A (en) 2004-03-29 2005-11-10 Kose Corp Foamy oil cleansing cosmetic
JP2006225403A (en) * 2005-06-17 2006-08-31 Asahi Kasei Chemicals Corp Oily gel cleansing

Also Published As

Publication number Publication date
CN101744745A (en) 2010-06-23
KR20100061339A (en) 2010-06-07
CN101744745B (en) 2013-07-17

Similar Documents

Publication Publication Date Title
JP4189886B1 (en) Oily liquid cleansing composition.
JP7411709B2 (en) Oil-in-water emulsion composition
CN101330899B (en) Oil-based liquid cleansing composition
JP5550873B2 (en) Oily liquid cleansing composition.
JP6472981B2 (en) Cleansing cosmetics
KR101440161B1 (en) Gel composition
KR101521265B1 (en) Cleansing composition in the form of transparent or translucent gel
WO2003080004A1 (en) Cleansing preparation
KR20180115740A (en) Cleansing Cosmetic
KR101601279B1 (en) Composition for oil-based liquid cleansing
EP2932957B1 (en) Cleansing cosmetics
JP4429053B2 (en) Oily cleaning agent
TWI823851B (en) Water-in-oil emulsion composition
JP2010235514A (en) Liquid composition for cleansing
TW201334802A (en) Cosmetic composition
JP2022015058A (en) Cleansing agent
TW201900146A (en) Oil-type emulsified composition
JP2019196337A (en) Oil-based cleansing cosmetic
JP3881953B2 (en) Liquid oily skin cleanser
JP2007217302A (en) Oily skin cleanser
JP6536375B2 (en) Oil gel cosmetic
JP6487634B2 (en) Liquid oil composition
JP2020200259A (en) Cleansing cosmetic
HK1141463B (en) Composition for oil-based liquid cleansing
JP2014024788A (en) Oily cleansing composition

Legal Events

Date Code Title Description
PA0109 Patent application

Patent event code: PA01091R01D

Comment text: Patent Application

Patent event date: 20091111

PG1501 Laying open of application
A201 Request for examination
PA0201 Request for examination

Patent event code: PA02012R01D

Patent event date: 20140609

Comment text: Request for Examination of Application

Patent event code: PA02011R01I

Patent event date: 20091111

Comment text: Patent Application

E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

Comment text: Notification of reason for refusal

Patent event date: 20150731

Patent event code: PE09021S01D

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

Patent event code: PE07011S01D

Comment text: Decision to Grant Registration

Patent event date: 20160127

GRNT Written decision to grant
PR0701 Registration of establishment

Comment text: Registration of Establishment

Patent event date: 20160302

Patent event code: PR07011E01D

PR1002 Payment of registration fee

Payment date: 20160302

End annual number: 3

Start annual number: 1

PG1601 Publication of registration
FPAY Annual fee payment

Payment date: 20190219

Year of fee payment: 4

PR1001 Payment of annual fee

Payment date: 20190219

Start annual number: 4

End annual number: 4

FPAY Annual fee payment

Payment date: 20200219

Year of fee payment: 5

PR1001 Payment of annual fee

Payment date: 20200219

Start annual number: 5

End annual number: 5

PR1001 Payment of annual fee

Payment date: 20220222

Start annual number: 7

End annual number: 7

PR1001 Payment of annual fee

Payment date: 20230222

Start annual number: 8

End annual number: 8

PR1001 Payment of annual fee

Payment date: 20240220

Start annual number: 9

End annual number: 9

PR1001 Payment of annual fee

Payment date: 20250204

Start annual number: 10

End annual number: 10