US1953438A - Process for coloring organic products - Google Patents
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- US1953438A US1953438A US572431A US57243131A US1953438A US 1953438 A US1953438 A US 1953438A US 572431 A US572431 A US 572431A US 57243131 A US57243131 A US 57243131A US 1953438 A US1953438 A US 1953438A
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- lecithin
- dye
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- fatty
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- 238000004040 coloring Methods 0.000 title description 12
- 238000000034 method Methods 0.000 title description 12
- 239000000975 dye Substances 0.000 description 26
- 239000000787 lecithin Substances 0.000 description 24
- 235000010445 lecithin Nutrition 0.000 description 24
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 23
- 229940067606 lecithin Drugs 0.000 description 23
- 239000000126 substance Substances 0.000 description 22
- 239000003921 oil Chemical class 0.000 description 17
- 235000019198 oils Nutrition 0.000 description 17
- 238000004043 dyeing Methods 0.000 description 14
- 239000001993 wax Chemical class 0.000 description 14
- 235000014113 dietary fatty acids Nutrition 0.000 description 12
- 239000000194 fatty acid Substances 0.000 description 12
- 229930195729 fatty acid Natural products 0.000 description 12
- 150000004665 fatty acids Chemical class 0.000 description 11
- 229930195733 hydrocarbon Natural products 0.000 description 11
- 239000003925 fat Chemical class 0.000 description 10
- 150000002430 hydrocarbons Chemical class 0.000 description 10
- -1 for instance Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 7
- 239000002966 varnish Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000004753 textile Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000000981 basic dye Substances 0.000 description 5
- 239000001913 cellulose Chemical class 0.000 description 5
- 229920002678 cellulose Chemical class 0.000 description 5
- 235000019197 fats Nutrition 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- KQSBZNJFKWOQQK-UHFFFAOYSA-N hystazarin Natural products O=C1C2=CC=CC=C2C(=O)C2=C1C=C(O)C(O)=C2 KQSBZNJFKWOQQK-UHFFFAOYSA-N 0.000 description 4
- 239000000983 mordant dye Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000000987 azo dye Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000011347 resin Chemical class 0.000 description 2
- 229920005989 resin Chemical class 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 229940117013 triethanolamine oleate Drugs 0.000 description 2
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 1
- FTJUZCBLWZLXFR-KTKRTIGZSA-N 2-[bis(2-hydroxyethyl)amino]ethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCN(CCO)CCO FTJUZCBLWZLXFR-KTKRTIGZSA-N 0.000 description 1
- WBBFBHOZKCHJHN-UHFFFAOYSA-N 2-amino-1-hydroxyanthracene-9,10-dione Chemical class C1=CC=C2C(=O)C3=C(O)C(N)=CC=C3C(=O)C2=C1 WBBFBHOZKCHJHN-UHFFFAOYSA-N 0.000 description 1
- 241000974482 Aricia saepiolus Species 0.000 description 1
- RTMBGDBBDQKNNZ-UHFFFAOYSA-L C.I. Acid Blue 3 Chemical compound [Ca+2].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=C(O)C=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1.C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=C(O)C=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 RTMBGDBBDQKNNZ-UHFFFAOYSA-L 0.000 description 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 206010021703 Indifference Diseases 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- IKCOOALACZVGLI-GNOQXXQHSA-K bis[[(z)-octadec-9-enoyl]oxy]alumanyl (z)-octadec-9-enoate Chemical compound [Al+3].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O IKCOOALACZVGLI-GNOQXXQHSA-K 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- QUQFTIVBFKLPCL-UHFFFAOYSA-L copper;2-amino-3-[(2-amino-2-carboxylatoethyl)disulfanyl]propanoate Chemical compound [Cu+2].[O-]C(=O)C(N)CSSCC(N)C([O-])=O QUQFTIVBFKLPCL-UHFFFAOYSA-L 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- SXQCTESRRZBPHJ-UHFFFAOYSA-M lissamine rhodamine Chemical compound [Na+].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=C(S([O-])(=O)=O)C=C1S([O-])(=O)=O SXQCTESRRZBPHJ-UHFFFAOYSA-M 0.000 description 1
- 125000005608 naphthenic acid group Chemical class 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000004177 patent blue V Substances 0.000 description 1
- 235000012736 patent blue V Nutrition 0.000 description 1
- IYDGMDWEHDFVQI-UHFFFAOYSA-N phosphoric acid;trioxotungsten Chemical compound O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.OP(O)(O)=O IYDGMDWEHDFVQI-UHFFFAOYSA-N 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- YEIGUXGHHKAURB-VAMGGRTRSA-N viridin Chemical compound O=C1C2=C3CCC(=O)C3=CC=C2[C@@]2(C)[C@H](O)[C@H](OC)C(=O)C3=COC1=C23 YEIGUXGHHKAURB-VAMGGRTRSA-N 0.000 description 1
- 108010086097 viridin Proteins 0.000 description 1
- YEIGUXGHHKAURB-UHFFFAOYSA-N viridine Natural products O=C1C2=C3CCC(=O)C3=CC=C2C2(C)C(O)C(OC)C(=O)C3=COC1=C23 YEIGUXGHHKAURB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/008—Preparations of disperse dyes or solvent dyes
Definitions
- My present invention relates to a process for dyeing organic products and more particularly to such a process in which organic dyes are used as a coloring matter which generally are not soluble in the products to be dyed.
- the phosphatides of the kind of lecithins have a surprisingly good capacity for dissolving numerous dyes which are insoluble or insufllciently soluble in organic substances, such as hydrocarbons and the halogen substitution products thereof, alcohols, ketones, esters, higher fatty acids, fats, oils, resins, waxes, cellulose derivatives and similar substances and that the dye solutions thus obtainable may be used for homogeneously dyeing any organic substance which is miscible with the dye preparationmade with, for instance, lecithin.
- organic substances such as hydrocarbons and the halogen substitution products thereof, alcohols, ketones, esters, higher fatty acids, fats, oils, resins, waxes, cellulose derivatives and similar substances and that the dye solutions thus obtainable may be used for homogeneously dyeing any organic substance which is miscible with the dye preparationmade with, for instance, lecithin.
- lecithin unobjectionably allows the dyeing of foods and any substances used to heighten the enjoyment of food, of products used in pharmacy, of cosmetics and other products which dare not be dyed with the aid of other well known assistants, such as, for instance, oil soluble soaps, organic amines or. soap-like compounds of the latter, such as, for instance, triethanolamine oleate.
- assistants such as, for instance, oil soluble soaps, organic amines or. soap-like compounds of the latter, such as, for instance, triethanolamine oleate.
- liquids or pastes as, for instance, oils or oily solutions dyed according to my invention show much less tendency to separate fast products even in' the presence of large proportions of water, such separations easily occurring when preparing the dye solution in oil with the aid of, for instance, triethanolamine oleate.
- solution for instance, stock solution containing a high amount of the dye.
- My new dyeing method is applicable for dyeing substances 40 of different kind.
- hydroaromatic and heterocyclic series natural and artificial resins, waxes, fats, fatty acids, cellulose derivatives and threads, bands, films or plastic masses made therefrom; varnishes from cellulose estersand ethers, fatty varnishes, spirit varnishes, and the like; oil emulsions as used, for instance, in the leather industry; candles, soaps,
- heavy metal salts of fatty acids or naphthenic acids may be carried out either during or after the dissolution of the dye.
- the addition of the compound forming the lake can be made at any desired stage of the operation.
- the solubility and the brightness of the coloration may be improved in some cases, especially when using mordant' dyes of the alizarine series, by addition of an oil-soluble amine such as, for instance, triethanolaminemonooleate, dibenzylamine and so on.
- an oil-soluble amine such as, for instance, triethanolaminemonooleate, dibenzylamine and so on.
- the solubility ' is only attained by the combination of the phosphatide and the oil-soluble base.
- the degree of purity of the phosphatide used as a solvent assistant such as, for instance, lecithin obtained from soy beans is in the most cases not of importance. Generally it is suillcient to use the second quality of products obtained when preparing the phosphatides from the raw materials.
- the products known on the market as textile lecithin, are very suitable for the proces in question. Impurities contained in the lecithin and remaining undissolved maybe easily removed by filtration.
- Example 1 -1 part of Kiton Fast Yellow 3 G (Schultz, Farbstofitabellen, 7th,edition, No. 748) is dissolved in 9 parts of textile lecithin while stirring the mixture warmed on the water bath.
- the solution obtained may be mixed with 390 parts of an oil varnish, whereby a clear transparent solution is obtained.
- Example 2.-1 part of Patent Blue V (Schultz, Farbstoiftabellen, 7th edition, No. 826? is dissolved as prescribed in Example 1 in 9 parts of textile lecithin.
- the deep bluish green mass thus obtained, may be used for dyeing a composition for candles consisting, for instance, of 60 parts-of stearic acid and 40 parts of ceresin. There is thus obtained an intensely greenish-blue candle wax; the wax colored under like conditions with triethanolamine is darker, more glazed and duller.
- Example 3.--'0.5 part-of Acid Red XB (Schultz, Farbstoiftabellen, 7th edition, No. 863) is heated to 90 C. together with 10 parts of lecithin until dissolved.
- the dye preparation may be applied for coloring an oil emulsion used for the treatment of leather. 7
- Example 4-1 part of Alizarine Viridin FF (powder) (Schultz, Farbstofftabellen, 7th edition, No. 1193) is dissolved in 15 parts of textile lecithin and the solution is mixed with a wax composition.
- a lake-forming compound thus as, for instance, chromium naphthenate, the coloration may be brightened.
- Example 5 1 part of Alizarine' Marron W (powder) (Schultz, Farbstofftabellen, 7th edition, No. 1159) is stirred on the water bath with 9 parts of textile lecithin until dissolved.
- the preparation may be used for coloring an oil varnish diluted with toluene.
- the intensity of the coloration may be increased by addition of aluminium oleate or chrome naphthenate.
- Example 6L part of Fanal Green LB (2. complex salt of a basic dye) Schultz, Farbstoiftabellen, 7th edition, No. 765) is dissolved while being warmed in 15 parts of lecithin.
- the intensely yellowish green colored dye preparation may be used for coloring a cellulose other varnish (containing, for instance, an aromatic hydrocarbon and an alcohol as solvents).
- Example 7 In a meltcontaining' 60 parts of stearic acid and 5 parts of lecithin there are dissolved on the water bath 0.2 part of the azo dye obtained by diazotizing 3.5-dichloro-2-amino-lhydroxybenzene and coupling with 1-phenyl-3- methyl-5-pyrazolone. The greenish yellow mass becomes reddish yellow on addition of aluminium chloride.
- the dye solution may be added, for instance, to a cellulose laurate varnish dissolved in toluene.
- an aluminium-, copper-, ironor nickel salt the shade of the color may be varied in known manner.
- linseed oil or paraifine oil are dissolved in the manner described in lecithin.
- fatty acid esters such as linseed oil, or'benzine hydrocarbons, such as parafline oil, may be homogeneously dyed without separation of the coloring matter.
- My invention is not limited to the foregoing examples or to the specific details given therein.
- I may use, for instance, a lecithin of another origin.
- dyes of the different groups may be used and generally I may apply as a coloring matter water-soluble salts of basic dyes, dye acids and .salts thereof, numerous difficulty soluble organic pigments, aminoanthraquinones and aminohydroxyanthraquinones, acid mordant dyes especially in form of the dye lakes, furthermore, complex compounds of basic dyes with heteropoly acids, such as phosphotungstic acid, or vat dyes.
- a process for dyeing liquid or fusible organic products with coloring substances which are insoluble or difficulty soluble in the products to be dyed which comprises adding a lecithin as a solvent assistant.
- waxes and hydrocarbons of the parafline series with organic dyes which are'insoluble' or difficulty'soluble in the products to be dyed which comprises adding a lec'thin as a solvent assistant.
- a process for dyeing fatty organic substances of the group consisting of fats, oils, fatty acids, waxes and hydrocarbons of the paraffine series with an acid azo dye which is insoluble or difficulty soluble in the products to be dyed which comprises adding a lecithin as a solvent assistant.
- a process for dyeing fatty organic substances of the group consisting of fats, oils. fatty acids, waxes and hydrocarbons of the parafiine series with a mordant' dye which is insoluble or difficulty soluble in the products to be dyed which comprises adding a lecithin as a solvent assistant.
- composition of matter comprising a liquidor fusible organic substance and dissolved therein a lecithin and an organic dye originally insoluble or difficulty soluble in said organic substance.
- a composition of matter comprising a fatty organic substance of the group consisting of fats, oil-s, fatty acids, waxes and hydrocarbons of the parafilne series and dissolved therein a lecithin and an organ'c dye originally insoluble or diificulty soluble in said fatty substance.
- a composition of matter comprising a fatty organic substance of the group consisting of fats, oils, fatty acids, waxes and hydrocarbons of the parafline series and dissolved therein a lecithin and a salt of a basic dye orig'nally insoluble or difiiculty soluble in said fatty substance.
- composition of matter comprising a fatty organic substance of the group consisting of fats,
- A'composition of matter comprising a fatty organic substance of the group consisting of fats, o Is, fatty acids, waxes and hydrocarbons of the parafiine series and dissolved therein a lecithin and a mordantdye originally insoluble or difli culty soluble in said fatty substance.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
Description
Patented Apr. 3, 1934 UNITED STATES PATENT OFFICE raocnss Foa COLORING ORGANIC Paoboors No Drawing. Application October 31, 1931, Serial No. 572,431. In Germany November 3, 1930 Claims.
My present invention relates to a process for dyeing organic products and more particularly to such a process in which organic dyes are used as a coloring matter which generally are not soluble in the products to be dyed.
I have found that the phosphatides of the kind of lecithins have a surprisingly good capacity for dissolving numerous dyes which are insoluble or insufllciently soluble in organic substances, such as hydrocarbons and the halogen substitution products thereof, alcohols, ketones, esters, higher fatty acids, fats, oils, resins, waxes, cellulose derivatives and similar substances and that the dye solutions thus obtainable may be used for homogeneously dyeing any organic substance which is miscible with the dye preparationmade with, for instance, lecithin.
My new dyeing method'has some essential advantages when compared with'the prior art.
Thus, the use of lecithin unobjectionably allows the dyeing of foods and any substances used to heighten the enjoyment of food, of products used in pharmacy, of cosmetics and other products which dare not be dyed with the aid of other well known assistants, such as, for instance, oil soluble soaps, organic amines or. soap-like compounds of the latter, such as, for instance, triethanolamine oleate.
Furthermore, I have found that the liquids or pastes as, for instance, oils or oily solutions dyed according to my invention show much less tendency to separate fast products even in' the presence of large proportions of water, such separations easily occurring when preparing the dye solution in oil with the aid of, for instance, triethanolamine oleate. Thus, it becomes possible to prepare solution, for instance, stock solution containing a high amount of the dye. -My new dyeing method is applicable for dyeing substances 40 of different kind. From among the large number of organic compounds and the products obtainable therefrom, to which the new dyeing and coloring process may be applied, may be named, without in any way limiting the invention thereto, hydrocarbons, alcohols, ethers, aldehydes, ketones, carboxylic acids, esters, nitro-compounds and amino compounds of the aliphatic. aromatic,
hydroaromatic and heterocyclic series, natural and artificial resins, waxes, fats, fatty acids, cellulose derivatives and threads, bands, films or plastic masses made therefrom; varnishes from cellulose estersand ethers, fatty varnishes, spirit varnishes, and the like; oil emulsions as used, for instance, in the leather industry; candles, soaps,
polishing waxes, shoe polishes, printing colors; cosmetics and galenic preparations. a
When carrying out my dyeing method, it is a matter of indifference whether the dye is dissolved first in the cold or, if necessary, in the warm lecithin and then this dye solution is added to the substance to be dyed, or whether the phosphatide is first incorporated into the goods to be dyed and then followed by treatment with the coloring matter.
In the case of mordant dyes which are soluble either in the lacithin or in the mixture containing the phosphatide, the formation of the lake with, v
for instance, heavy metal salts of fatty acids or naphthenic acids may be carried out either during or after the dissolution of the dye. The addition of the compound forming the lake, can be made at any desired stage of the operation. Thus, it may be advisable, for instance, to form the dye lake in the product,-. for instance, a film, already dyed according to my invention, by aftertreating it with a lake-forming substance.
The solubility and the brightness of the coloration may be improved in some cases, especially when using mordant' dyes of the alizarine series, by addition of an oil-soluble amine such as, for instance, triethanolaminemonooleate, dibenzylamine and so on. In the case of certain dyes as, for instance, mordant dyes of the alizarine series, the solubility 'is only attained by the combination of the phosphatide and the oil-soluble base.
The degree of purity of the phosphatide used as a solvent assistant such as, for instance, lecithin obtained from soy beans is in the most cases not of importance. Generally it is suillcient to use the second quality of products obtained when preparing the phosphatides from the raw materials. The products known on the market as textile lecithin, are very suitable for the proces in question. Impurities contained in the lecithin and remaining undissolved maybe easily removed by filtration.
My invention is illustrated in the examples following hereafter, the parts being by weight:-
Example 1.-1 part of Kiton Fast Yellow 3 G (Schultz, Farbstofitabellen, 7th,edition, No. 748) is dissolved in 9 parts of textile lecithin while stirring the mixture warmed on the water bath. The solution obtained may be mixed with 390 parts of an oil varnish, whereby a clear transparent solution is obtained.
Example 2.-1 part of Patent Blue V (Schultz, Farbstoiftabellen, 7th edition, No. 826? is dissolved as prescribed in Example 1 in 9 parts of textile lecithin. The deep bluish green mass thus obtained, may be used for dyeing a composition for candles consisting, for instance, of 60 parts-of stearic acid and 40 parts of ceresin. There is thus obtained an intensely greenish-blue candle wax; the wax colored under like conditions with triethanolamine is darker, more glazed and duller. Example 3.--'0.5 part-of Acid Red XB (Schultz, Farbstoiftabellen, 7th edition, No. 863) is heated to 90 C. together with 10 parts of lecithin until dissolved. The dye preparation may be applied for coloring an oil emulsion used for the treatment of leather. 7
Example 4.-1 part of Alizarine Viridin FF (powder) (Schultz, Farbstofftabellen, 7th edition, No. 1193) is dissolved in 15 parts of textile lecithin and the solution is mixed with a wax composition. By addition of a lake-forming compound, thus as, for instance, chromium naphthenate, the coloration may be brightened.
Example 5.-- 1 part of Alizarine' Marron W (powder) (Schultz, Farbstofftabellen, 7th edition, No. 1159) is stirred on the water bath with 9 parts of textile lecithin until dissolved. The preparation may be used for coloring an oil varnish diluted with toluene. The intensity of the coloration may be increased by addition of aluminium oleate or chrome naphthenate.
Example 6.L part of Fanal Green LB (2. complex salt of a basic dye) Schultz, Farbstoiftabellen, 7th edition, No. 765) is dissolved while being warmed in 15 parts of lecithin. The intensely yellowish green colored dye preparation may be used for coloring a cellulose other varnish (containing, for instance, an aromatic hydrocarbon and an alcohol as solvents).
Example 7. -In a meltcontaining' 60 parts of stearic acid and 5 parts of lecithin there are dissolved on the water bath 0.2 part of the azo dye obtained by diazotizing 3.5-dichloro-2-amino-lhydroxybenzene and coupling with 1-phenyl-3- methyl-5-pyrazolone. The greenish yellow mass becomes reddish yellow on addition of aluminium chloride.
Example 8.0.5' part of AlizarineRG (Schultz, Farbstoiftabellen, 7th edition, No. 1154) and 10 parts of triethanolamino-mono-oleate are dissolved in 10 parts of textile lecithin. The dye solution may be added, for instance, to a cellulose laurate varnish dissolved in toluene. On addition of an aluminium-, copper-, ironor nickel salt, the shade of the color may be varied in known manner.
Example 9.--Dyes which are insoluble in oils,
such as linseed oil or paraifine oil, (for instance those mentioned in Examples 2:, 4 and 6) are dissolved in the manner described in lecithin. With the aid of the dye preparations thus obtainable, fatty acid esters, such as linseed oil, or'benzine hydrocarbons, such as parafline oil, may be homogeneously dyed without separation of the coloring matter.
In each case,'a clear and homogeneous solution of the dyes is obtainable in the products to be dyed and no separation of the coloring matter occurs even when storing them for a long time.
My invention is not limited to the foregoing examples or to the specific details given therein. Thus, I may use, for instance, a lecithin of another origin. Furthermore, dyes of the different groups may be used and generally I may apply as a coloring matter water-soluble salts of basic dyes, dye acids and .salts thereof, numerous difficulty soluble organic pigments, aminoanthraquinones and aminohydroxyanthraquinones, acid mordant dyes especially in form of the dye lakes, furthermore, complex compounds of basic dyes with heteropoly acids, such as phosphotungstic acid, or vat dyes.
A few simple comparative experiments should be made. to determine the best kind of dye and the most suitable amount of the phosphatideto employ with a particular product to be dyed.
What I claim is:
1. A process for dyeing liquid or fusible organic products with coloring substances which are insoluble or difficulty soluble in the products to be dyed which comprises adding a lecithin as a solvent assistant.
2. A process for dyeing fatty organic substances of the group consisting of fats, oils, fatty acids,
waxes and hydrocarbons of the parafline series with organic dyes which are'insoluble' or difficulty'soluble in the products to be dyed, which comprises adding a lec'thin as a solvent assistant.
3. A process for dyeing fatty organic substances of the group consistng of fats, oils, fatty acids, waxes and hydrocarbons of the parafiine series with a salt of a basic dye which is insoluble or difficulty soluble in the products to be dyed, which comprises adding alecithin as a solvent assistant.
, 4. A process for dyeing fatty organic substances of the group consisting of fats, oils, fatty acids, waxes and hydrocarbons of the paraffine series with an acid azo dye which is insoluble or difficulty soluble in the products to be dyed, which comprises adding a lecithin as a solvent assistant.
5. A process for dyeing fatty organic substances of the group consisting of fats, oils. fatty acids, waxes and hydrocarbons of the parafiine series with a mordant' dye which is insoluble or difficulty soluble in the products to be dyed, which comprises adding a lecithin as a solvent assistant.
6. A composition of matter comprising a liquidor fusible organic substance and dissolved therein a lecithin and an organic dye originally insoluble or difficulty soluble in said organic substance.
'7. A composition of matter comprising a fatty organic substance of the group consisting of fats, oil-s, fatty acids, waxes and hydrocarbons of the parafilne series and dissolved therein a lecithin and an organ'c dye originally insoluble or diificulty soluble in said fatty substance.
8. A composition of matter comprising a fatty organic substance of the group consisting of fats, oils, fatty acids, waxes and hydrocarbons of the parafline series and dissolved therein a lecithin and a salt of a basic dye orig'nally insoluble or difiiculty soluble in said fatty substance.
9. A composition of matter comprising a fatty organic substance of the group consisting of fats,
oils, fatty acids, waxes and hydrocarbons of the par-affine series and dissolved therein alecith'n and an acid azo dye originally insoluble or difficulty soluble in said fatty substance.
10. A'composition of matter comprising a fatty organic substance of the group consisting of fats, o Is, fatty acids, waxes and hydrocarbons of the parafiine series and dissolved therein a lecithin and a mordantdye originally insoluble or difli culty soluble in said fatty substance.
' PAUL SCHLACK.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1953438X | 1930-11-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1953438A true US1953438A (en) | 1934-04-03 |
Family
ID=7772352
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US572431A Expired - Lifetime US1953438A (en) | 1930-11-03 | 1931-10-31 | Process for coloring organic products |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1953438A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2432831A (en) * | 1945-01-04 | 1947-12-16 | Du Pont | Stable dispersions of aromatic amines |
| US2441172A (en) * | 1942-01-31 | 1948-05-11 | Shappirio Sol | Modified fuels and lubricants |
| US2524291A (en) * | 1948-01-19 | 1950-10-03 | Harold A Hoffman | Oil base coatings |
| US2535538A (en) * | 1949-03-17 | 1950-12-26 | Kohnstamm & Co Inc H | Gelatinous composition of matter and method of preparing same |
| US2546748A (en) * | 1942-06-02 | 1951-03-27 | Grindstedvaerket As | Agents for coloring emulsions and dispersions, especially those of the oil in water type |
| US3035923A (en) * | 1960-07-11 | 1962-05-22 | Atlas Chem Ind | Dye composition for edible fat and method of preparing the same |
| US3052552A (en) * | 1959-09-16 | 1962-09-04 | Beech Nut Life Savers Inc | Printing on confection items and the resulting product |
| US3272644A (en) * | 1963-07-31 | 1966-09-13 | Dennison Mfg Co | Development of latent electrostatic images with crystalline toners |
-
1931
- 1931-10-31 US US572431A patent/US1953438A/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2441172A (en) * | 1942-01-31 | 1948-05-11 | Shappirio Sol | Modified fuels and lubricants |
| US2546748A (en) * | 1942-06-02 | 1951-03-27 | Grindstedvaerket As | Agents for coloring emulsions and dispersions, especially those of the oil in water type |
| US2432831A (en) * | 1945-01-04 | 1947-12-16 | Du Pont | Stable dispersions of aromatic amines |
| US2524291A (en) * | 1948-01-19 | 1950-10-03 | Harold A Hoffman | Oil base coatings |
| US2535538A (en) * | 1949-03-17 | 1950-12-26 | Kohnstamm & Co Inc H | Gelatinous composition of matter and method of preparing same |
| US3052552A (en) * | 1959-09-16 | 1962-09-04 | Beech Nut Life Savers Inc | Printing on confection items and the resulting product |
| US3035923A (en) * | 1960-07-11 | 1962-05-22 | Atlas Chem Ind | Dye composition for edible fat and method of preparing the same |
| US3272644A (en) * | 1963-07-31 | 1966-09-13 | Dennison Mfg Co | Development of latent electrostatic images with crystalline toners |
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