DE1961709A1 - Process for the production of a coloring paste for nail polish - Google Patents
Process for the production of a coloring paste for nail polishInfo
- Publication number
- DE1961709A1 DE1961709A1 DE19691961709 DE1961709A DE1961709A1 DE 1961709 A1 DE1961709 A1 DE 1961709A1 DE 19691961709 DE19691961709 DE 19691961709 DE 1961709 A DE1961709 A DE 1961709A DE 1961709 A1 DE1961709 A1 DE 1961709A1
- Authority
- DE
- Germany
- Prior art keywords
- water
- coloring
- production
- paste
- nail polish
- 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.)
- Granted
Links
- 238000004040 coloring Methods 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims description 11
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 19
- 239000004408 titanium dioxide Substances 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- -1 dunaiarablkun Polymers 0.000 claims description 4
- 229920000159 gelatin Polymers 0.000 claims description 4
- 235000019322 gelatine Nutrition 0.000 claims description 4
- 239000000725 suspension Substances 0.000 claims description 4
- 108010010803 Gelatin Proteins 0.000 claims description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- 239000008273 gelatin Substances 0.000 claims description 3
- 235000011852 gelatine desserts Nutrition 0.000 claims description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 239000000049 pigment Substances 0.000 description 8
- 239000002904 solvent Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000975 dye Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 102100026933 Myelin-associated neurite-outgrowth inhibitor Human genes 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000002036 drum drying Methods 0.000 description 1
- 230000037336 dry skin Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/29—Titanium; Compounds thereof
-
- 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
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
- A61K8/65—Collagen; Gelatin; Keratin; Derivatives or degradation products thereof
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8129—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers or esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers, e.g. polyvinylmethylether
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q3/00—Manicure or pedicure preparations
- A61Q3/02—Nail coatings
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
DR. E. WIEGAND DIPL.-ING. W. NIEMANN 1961709DR. E. WIEGAND DIPL.-ING. W. NIEMANN 1961709
DR. M. KOHiER DIPI-ING. C. GERNHARDTDR. M. KOHiER DIPI-ING. C. GERNHARDT
telefon, 55 54 7ί sooo MÜNCHEN is, 9.Do -!ember 1969phone, 55 54 7ί sooo MÜNCHEN is, 9th Thursday -! ember 1969
TELEGRAMME: KARPATENT N USSBAUMSTRAS 3E TuTELEGRAMS: CARPATENT N USSBAUMSTRAS 3E Tu
W. 14 599/69 - Kc/HW. 14 599/69 - Kc / H
lakaeago ierfaraery Ge., 1'okyOf Japanlakaeago ierfaraery Ge., 1'okyOf Japan
Verfahren 2ur Herstellung einer fäibepaste fürMethod 2 for the production of a fäibepaste for
ft&g&üackft & g & üack
wird die Jarbepa-sts ?ϋϊ üagellaok erhalten, indem ein. färbendes Material und fitandloxfd mit einen wasserlöslichen organiaohen Eoshpolymereßi das ia orgenieoheti LöBunganiitteln unlöslich ißt, Überzogen wird; nicrsu ein nicht flüchtiges orgaruachee lösungsmittel gegeben wird und dieses GteiBiech au einer iaote Terasaiilen wird«will the Jarbepa-sts? ϋϊ üagellaok received, by a. coloring material and one fitandloxfd water-soluble organic polymers ia orgenieoheti Eats solvent insoluble, becomes coated; nicrsu a non-volatile orgaruachee solvent is given and this part of an iaote terasaiile will "
Die Irrindang betrifft ein Verfahren aur Herstellung einer färbepaste für 3fagellaci£ und die Aafgab« besteht in einer JTärbtpatc«, die lor Heretellung von färbsndtsi Hiniküreitteln sit Ausgeseichneten Sigenechaften verwendet werden kann.The Irrindang relates to a process for producing a Coloring paste for 3fagellaci £ and the Aafgab «consists of one "Dye patch", the production of dye stuffs It can be used with approved characteristics.
jfiin färbende« ManücUrmittel ist im allgemeinen eine Suspension eines anorganischen oder organischen färbenden Materials und TitAndioxyds in elneia L^L-imgeaittel, das Nitrooellulof.o und Hare enthält.Any coloring agent is generally one Suspension of an inorganic or organic coloring agent Materials and titanium dioxide in elneia L ^ L-imgeaittel, the Nitrooellulof.o and contains hare.
Je:och seilen aahlr«ic&« iärbungsraataritlien eint Neigung zum Bluieraja in da» ,Lö^jungaiaittelj urul 2itandioxyd setsst οΙλλ in Verlauf dsr Zeit siufifroad seiaee girütimi sptii- tlL>M\ -'■ i-awichtes ab und bildet üin**i Hiöä^reohla^ a^ Boden de* A»'t'i'jwahranKSSöfilJiii^» Dtii*Gh dlof-üj f^sa-^.c-iniAagea wird nui- das 4uee»hen d«s i-ianiki'cKlbtela vsxaohleoütQX ei ouS beim aebxaajh au,-ti aus Aufbswahrimgsgefäu warden, us den vorstehendem Niederschlag homogen suJe: och ropes aahlr "ic &" iärungsraataritlien unites inclination to bluieraja in da ", Lö ^ jungaiaittelj urul 2itandioxyd setsst οΙλλ in the course of the time siufifroad seiaee girütimi later tiitlL> M \ - '■ i-awichtes and shows uin ** i Hiöä ^ reohla ^ a ^ Boden de * A »'t'i'jwahranKSSöfilJiii ^» Dtii * Gh dlof-üj f ^ sa - ^. C-iniAagea will nui- das 4uee »hen d« s i-ianiki'cKlbtela vsxaohleoütQX ei ouS at aebxaajh au, -ti from storage vessels, us the above precipitation homogeneously see below
BADBATH
00982 6/211200982 6/2112
Aufgrund Sahire Icher Untersuchungen.sos Herstellung von Mani'M-ürKltteln mit susgeseiehn$tem Eigeseohaftea wurde nun gefunden, daß» fall« die Oberflächen d*a färbenden Kateriala und dee Titandioxyds mit eines «.msssrluslichen organieohen Hoehpolymeren, da« in orgmnisehim XSsungestitteln unlöBlich ist» übersogen sind» da« ¥irlbs«aterial nicht in dae Lösungsmittel eluiert wird und sie ti das fitandioxyd nicht absetzt, worauf die Yorliegen&s Erfindung berufet.Due to Sahire Icher's investigations.sos manufacture by Mani'M-ürKltteln with susgeseiehn $ tem Eigeseohaftea now found that "fall" the surfaces of the Kateriala coloring and the titanium dioxide with a certain organic content High polymers, since they are dissolved in organic substances indelible is "oversaturated are" da "¥ irlbs" aterial not in The solvent is eluted and it causes the fitandioxyd does not set aside what the Yorhaben & s invention is based on.
Die vorliegende Erfindung btitAt mut tsr Basis dieses Sachverhaltes und betrifft ein Ter£abif®n mwc Herstellung einer. Färbepast@ für Nagtllack, das darin besteht, daß das färbende Material und Tit&ndioxyd ait »ines wasmerlösli&hen organischen Hoohpelymeren, das im organisonen Lösungsmitteln unlöslich igt, übersogen wirdt ein niöbt flüchtiges orgcnisohes Lösungen!tt#l hierin gugegebexi »ird und das erhaltene Hftterial su einer laste Teraahlen wM«The present invention btitAt mut tsr basis of these facts and concerns a Ter £ abif®n mwc production of a. Färbepast @ for Nagtllack, which consists in that the coloring material and Tit & ndioxyd ait "ines wasmerlösli & hen organic Hoohpelymeren, the IGT insoluble in organisonen solvents, is sucked t a niöbt volatile orgcnisohes solutions! Tt # l herein gugegebexi" ird and Hftterial obtained su one last Teraahlen wM «
Der Ausdruck ^färbendes Material* "sa^süichnet im Eahssn der Erfindung organische und anorganlseM' Pigmente und farbstoff, wie sie allgemein tür Eeraitelluas το» lfutlki!»itt«ln rerwendet werden« beisvielswelse S ft O Ee*. Kr. S (lariuasals des 1-(4-Chlor-0-<«alfe-5»tol^lASG}«>2-4Uiplithole}f B ft G Red Ir. 11 (CaloiöÄsals d€r? a-iS- In the context of the invention, the expression "coloring material" means organic and inorganic pigments and dyes, as they are generally used for Eeraitelluas το »lfutlki! des 1- (4-chloro-0 - <«alfe-5» tol ^ lASG} «> 2-4Uiplithole} f B ft G Red Ir. 11 (CaloiöÄsals d € r? a-iS-
napathalinsulfonsäure) usd D ft 0 Red Nr. 96 (1-(CKUhIor-pnitrophenylaso)-2-Kaphthol)· napathalinsulfonic acid) usd D ft 0 Red No. 96 (1- (CKUhIor-pnitrophenylaso) -2-kaphthol)
P* ν Auedruck * organisches Hos^fdlpags^sfi11 beseichnet Sm Rahüen i®r Irflmdung id» fsljissreü^ *; l^iaes In d^n.P * ν Auedruck * organic Hos ^ fdlpags ^ sfi 11 denotes Sm Rahüen i®r Irflmdung id »fsljissreü ^ *; l ^ iaes In d ^ n.
weis* aus * setting out
lsilsi
indind
00932Π/211? BADOR1G1NAL00932Π / 211? BADOR 1 G 1 NAL
und Stärk·, sowie »ynthetiaebe organische Hochpolymere, «1· Polyvinylalkohol (der Poljaerleatioaegrad eollt· 900and starch ·, as well as »ynthetiaebe organic high polymers,« 1 · Polyvinyl alcohol (the polyleation degree eollt 900
OXY-OXY
1500 und d«r Terseifuagsgred 86 bis 89'Jt b*tr*g«n), ^vinylpyrrolidon (das Molekulargewicht seilt· «tu» 40 000 bis 760 000 betragen) und ähnliche «attrlmlien geeignet. Weiterhin können als nicht flüchtiges USsuagsmittel beiepieleweiee Leinöl«, Phthalsäureester, Trikresylpboephat and d«rgl· τ·ιν wendet werden, dl* stfatliohe üblicherweise sie Bestandteile Ton Nagellacken verwendet werden.1500 and the Terseifuagsgred 86 to 89'Jt b * tr * g «n), ^ vinylpyrrolidon (the molecular weight is 40,000 to 760,000) and similar attrlmlien are suitable. Furthermore, as a non-volatile US sweetener, for example Linseed oil, phthalic acid ester, tricresyl pboephate and d «rgl · τ · ιν are used, dl * stfatliohe usually constituents Clay nail polishes can be used.
Bei fer DtLPcnfCOiruag dee erfindongegeoseen Terfahrena wird das Toratehende organisch« Hoohpolyiaere aunächet in Wasser gelöst, vrotei das 7erbältniB ron organischem Bochpolyaeren «u Vass«r 0,05 I)Is 190 ι 25 fels 50 "beträgt. Das färbend· Material und das Titandioiyd werden darin auapendiert. Bas Verhältnis τοη färtendem Material and Titandioxyd su Wasser betragt 1ϊ5 bis 10 und das Terhältnia τοη färbenden Material su Titandioxyd beträgt «tv/a 1x9. SI« Aufgabe wird ausreichend ait Z bis 20 Qew.-^ dee Toretehend aufgeführten organ ie oben Hochpolyeeren, belogen auf färbendes Material und Titandloiyd, erreicht. Das Verfahren wird bei Rauntemperatur ausgeführt·When fer DtLPcnfCOiruag dee erfindongegeoseen Terfahrena, the organic Toratehende "Hoohpolyiaere aunächet dissolved in water, the organic 7erbältniB vrotei ron Bochpolyaeren" u Vass "r 0.05 I) Is 1 9 0 ι 25 rock 50" is. The coloring material and · Titandioiyd be auapendiert therein. Bas ratio τοη färtendem material and titanium dioxide su water amounts to 10 and the 1ϊ5 Terhältnia τοη coloring material su titanium dioxide is "tv / a 1x9. SI" object is sufficiently ait Z to 20 Qew .- ^ dee Toretehend listed organ The above high polyesters, lied about coloring material and titanium oxide, achieved. The process is carried out at room temperature.
Di· erhaltene Sospension wurdt dann getrocknet. Diese Trocknung kann mittels TakuusitroQknuns» Sprüh tr ocknting, aefriertrocknung oder Trotmeltrocknung durohgsfOhrt werden. Bei einer derartigen Arbeitsweise werflea die Teilcbenoberflachen des färbenden Materialn und des fItandioxyde mit dec organiaohsn Hoolipolyiatren in el.nar Htärke la Bereich von 100 bis 200 Mikron ttfcersogen*The suspension obtained was then dried. These Drying can be done using TakuusitroQknuns »Spray drying, Freeze drying or drum drying can be carried out. With such a method of operation, the partial surfaces are of coloring material and fItandioxyde with dec organiaohsn Hoolipolyiatren in el.nar Htärke la area from 100 to 200 microns ttfcerogenic *
dann au eines Pulver alt einer Feinheit entsprechend einer Sieböffnung von 0,3 bis 0,15 sm (50 ti,j 1o8 meshji, welches dann zu dem nicht flüchtigen Lösung ami tt«l sugesetst wurdethen a powder of a fineness corresponding to one Sieve opening from 0.3 to 0.15 nm (50 ti, j 1o8 meshji, which then to the non-volatile solution ami tt «l sugesetst became
0 0 9 i. ^w / 1 ■ ; ÖAD ORIGINAL0 0 9 i. ^ w / 1 ■; ÖAD ORIGINAL
•8 wurde gut su einer Past« vermählen. Das Verhältnis τοη getrocknetem Material su nicht flüchtigem Lösungsmittel beträgt 3t1 bis 5.• 8 was married well to a past «. The ratio τοη dried material su non-volatile solvent 3t1 to 5.
BtI den auf die rorstehend beschriebene Weise herge- . stellten Färbungspasten wird die Eluierung des iärbungsmaterials in das Lösungsmittel und das Absitzen von Titandioxid nicht beobachtet, selbst wenn das Maniküraittel durch Vermischen des Färbematerials mit einem Lösungsmittel, Nitrocellulose und Harzen entsprechend dem üblichen Verfahren hergestellt wurde« Das beruht darauf, daß die Teilchenoberflächen des färbenden Materials und des Titandloxyde mit dem organischen Hochpolymeren überzogen sind. Manikürmittel, die unter Anwendung der entsprechend dem vorliegenden Verfahren gestellten Pigmentpasten hergestellt wurden, sind im Vergleich su solchen mit üblichem Material in der folgenden Tabelle zusammengefaßt, wobei sämtliche Teile auf das Gewicht bezogen sind«BtI produced in the manner described below. The coloring pastes are used to elute the coloring material into the solvent and the settling of titanium dioxide not observed even when the manicure is mixed by mixing the coloring material with a solvent, nitrocellulose and resins were prepared according to the usual method «This is due to the fact that the particle surfaces of the coloring material and the titanium oxide are coated with the organic high polymer. Manicure products, which were produced using the pigment pastes prepared in accordance with the present process are im Compare those with common material in the following Table summarized, all parts being based on weight «
Arylsulf aoid-fonnaldehyd-Gopolymerea Arylsulf aoid-formaldehyde copolymerea
Toluoltoluene
Xylol - 13,0Xylene - 13.0
Nr. 9 und Titandloxyd im Verhältnis von 1:9No. 9 and titanium oxide in a ratio of 1: 9
0 0 9 r ' ■ .· -^ ι i .·0 0 9 r '■. · - ^ ι i. ·
Venn die durch Vermischen del? vorstehenden Bestandteil· hergestellten Manikürmittel bei R&ma temperatur während 1 Woche stehengelassen wurden» wurde keine Inder 1TIg bei den Präparaten (I), (II) und (III) beobachtet, während ein weißer Niederschlag τοη Titandioxyd bei» Präparat (IT) gebildet wurde«Venn the by mixing del? above component · manufactured manicure products were left to stand at R & ma temperature for 1 week »no Indian 1 TIg was observed with preparations (I), (II) and (III), while a white precipitate τοη titanium dioxide was formed with» preparation (IT) «
Die folgenden Beispiele dienen iur weiteren Erläuterung der Erfindung. The following examples serve to further illustrate the invention.
1 g Gelatine wurde in 50 ■! Wasser gelöst, 1Dg eines Pigmentgeeiechea aus 1 g D λ C Red Hr* 9 (Bariuseals des 1-(4-Chlor-0»ulffc-5-tolyla«o)-2-n*phthol») und 9g litandioxjd wurden hlersu sugegeben, homogen Termisoht und das Wasser unter reminder te« Druck unter lühren abdestilliert. Der erhaltene getrocknete RUoketand wurde nach Zugab· τοη 7,0 g leinöl und gründliche« Yermisohen Mittels 3-stufigen Waisen ausreichend Tarmahlea und eine lärbepaate für lagellack erhalten. .1 g gelatin was in 50 ■! Dissolved water, 1dg of one Pigment gelatine from 1 g of D λ C Red Hr * 9 (Bariuseal des 1- (4-chloro-0 »ulffc-5-tolyla« o) -2-n * phthol ») and 9g of litandioxide were suggested, homogeneous Termisoht and that Water is distilled off under reduced pressure while stirring. The dried RUoketand obtained was after addition · τοη 7.0 g of linseed oil and thorough «Yermishen means 3-stage Orphans have enough Tarmahlea and a paint paate for lagellack obtain. .
10 g folrrlnylalkohel (Kolekulargewlcht etwa 4000, TerceifuBgsgrad 86 H) wurden Ia 500 el Wasser gelBst und 100 c eines Tigaentgeeiiaohes aus 25 S B ft O Red Vr. 56 (1-(0-Chlor-p-nitrophenylaeo)-2~naphthol) und 75 f Titandioxyd «lAgesilsoht OBd homogen rermisoht, so daB «la· luf-•oallasiaag erhalten wurde. Bann wurde dl· JLufsohlajnung sub Troeknen rersprilBt, wobei ein pulYerföraigee ^igmentgeeilsah aus »it Pelyriaylalkohol ttbereögene« Pigment umd Titandioxyd erhalten wurde, das dann aaoh linmisohen τοη 70 § Dibutylllithalat ausreiohewd mittels 5*stuflg·» Waisen rermablen wur«·, wobei ein färbendes Katerial für Magellaok erhalten wurde.10 g of vinyl alcohol (molecular weight about 4000, degree of TerceifuBgsgrad 86 H) were 500 tablespoons of water and 100 c of a Tigaentgeeiiaohes from 25 S B ft O Red Vr. 56 (1- (0-chloro-p-nitrophenylaeo) -2 ~ naphthol) and 75% titanium dioxide is completely dissociated so that it is homogeneous. Bann was sprayed under the dry skin, whereby a powdery gel pigment mixture was obtained from pigment and titanium dioxide, which was then made into a dye which could be colored by means of dibutyl alcohol Material for Magellaok was obtained.
BAD ORlGtNAL 00982 B/2112BAD ORlGtNAL 00982 B / 2112
10 g Gummiarabikum wurden in 250 ml Wasser gelöst und ein durchsichtig·« Gemisch erhalten, und 1OQ g eines Pigmentgemisehes aus 50 g D * C Red Sr. 1t (Oaleiuissals der 2-( 2-Hydroxy~1 -naphthylaao )-1 -naphthallnsulfonsäure } und 50 g Titandioxyd hi er au sugegeben and hoiaogen vermischt. Die Nasse wurde dann getrocknet unä ©ingeengt, wobei eine halbfest· Masse erhalten wurde« die nmoh der Irooknimg mittels eines froamteltrocioEiers in einer Iugelmlilile Terajahlea. wurde* Zu. diese» getrockneten Material wurde Dioctylphthalat zugegeben, ausreichend eingemischt und mittels Waisen, vermählen, so da* das ?ärbe»ateriai für nagellack erhalten de.10 g of gum arabic were dissolved in 250 ml of water and obtained a transparent mixture, and 10Q g of a pigment mixture from 50 g D * C Red Sr. 1t (Oaleiuissals der 2- (2-Hydroxy ~ 1 -naphthylaao) -1 -naphthalenesulfonic acid} and 50 g of titanium dioxide are added and mixed in a homogeneous way. The wet was then dried and concentrated, leaving a semisolid · mass was obtained «the nmoh of Irooknimg means of a froamteltrocio egg in an Iugelmlilile Terajahlea. became * to. this' dried material was dioctyl phthalate Admittedly, mixed in sufficiently and, by means of orphans, married, so that the? ärbe »ateriai for nail polish are preserved de.
009826/2112 baö a^ 009826/2112 baö a ^
Claims (4)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP9118168 | 1968-12-12 | ||
JP9118168 | 1968-12-12 |
Publications (3)
Publication Number | Publication Date |
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DE1961709A1 true DE1961709A1 (en) | 1970-06-25 |
DE1961709B2 DE1961709B2 (en) | 1976-12-09 |
DE1961709C3 DE1961709C3 (en) | 1977-07-21 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0479669A1 (en) * | 1990-10-01 | 1992-04-08 | L'oreal | Nail enamel containing oxidized polyethylene coated inorganic pigments |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0479669A1 (en) * | 1990-10-01 | 1992-04-08 | L'oreal | Nail enamel containing oxidized polyethylene coated inorganic pigments |
Also Published As
Publication number | Publication date |
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NL6918660A (en) | 1970-06-16 |
IT941531B (en) | 1973-03-10 |
CA923821A (en) | 1973-04-03 |
GB1242309A (en) | 1971-08-11 |
DE1961709B2 (en) | 1976-12-09 |
CH533449A (en) | 1973-02-15 |
FR2026023A1 (en) | 1970-09-11 |
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