US3392122A - Washing agents containing optical brightening agents - Google Patents

Washing agents containing optical brightening agents Download PDF

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Publication number
US3392122A
US3392122A US435021A US43502165A US3392122A US 3392122 A US3392122 A US 3392122A US 435021 A US435021 A US 435021A US 43502165 A US43502165 A US 43502165A US 3392122 A US3392122 A US 3392122A
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sodium
parts
agents
bis
washing
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Obayashi Kenro
Ishihara Koichiro
Mingawa Yuji
Noda Tomiro
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Sumitomo Chemical Co Ltd
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Sumitomo Chemical Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • C11D3/42Brightening agents ; Blueing agents
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06CFINISHING, DRESSING, TENTERING OR STRETCHING TEXTILE FABRICS
    • D06C2700/00Finishing or decoration of textile materials, except for bleaching, dyeing, printing, mercerising, washing or fulling
    • D06C2700/13Steaming or decatising of fabrics or yarns

Definitions

  • Patented July 9, 1968 3 392 122 pounds of them have such a defect as to decrease the de- WASHING AGENTS CNTAIN-ING OPTICAL gree of whiteness in appearance of soaps and synthetic BRIGHTENING AGENTS Washington agents by the effects of external conditions Kenro Obayashi, Toyonaka-shi, Koichiro Ishihara, Nishisuch as moisture.
  • the present inventors have solved these norniya-shi, Yuji Minagawa, Iked'a-shi, and Tomiro 5 problems.
  • One object of the present invention is to provide soaps g pf i Hlgashl'kib Osaka, p a 'P and synthetic washing agents which are extremely imion 0 apan N0 Drawing. Filed Feb. 24 1965, Ser. No 435,021 pror ed in their whiteness 1n the appearance.
  • Another ob ject is to provide soaps and synthetic washing agents hav- 4 4 Clams pnonty g f fg f Feb 2 196 mg high commercial value 1n their appearance.
  • the present invention relates to washing agents coning having P oPtical brightenmg abllity E taining optical brightening agents, more particularly it n as ullpmved Whlteness 111 appeijlrances- E f relates to Washing agents having improved White appear Ob ects will be apparent from the following descriptions.
  • ance 15 In order to accomplish these objects the present inven-
  • the washing agents according to the present invention tion provides Washing agents containing as a brightening include soaps and synthetic washing agents.
  • agent a 4,4-bis-triazinyl-stilbene-2,2-disulfonic acid de- Soaps and synthetic washing agents are colored in pale rivative having the general formula,
  • washing agents having improved white appearance have and M represents a member selected from the group conbeen desired. sisting of hydrogen atom and alkali metals.
  • Y and Y each represent a member strig the commercial point of view, because of their pale lected from the group consisting of amino radical, aliphayellow colorings.
  • tic cyclic amine residues, primary and secondary alkyl- For example, water soluble benzothiophene derivatives amine residues, primary and secondary hydroxyalkyldisclosed in the specification of Japanese Patent Publicaamine residues, primary and secondary aromatic amine tion Number SHO 27/4,339, fluorescent triazole comresidues including their nucleus substituted compounds, pounds disclosed in the specification of Japanese Patent and alkoxy radicals, in which examples of aliphatic cyclic Publication Number SHO 3 1/ 3,536 and others, and 4,4- amine include cyclohexylamine and morpholine, examples diaminostilbene-2,2-disulfonic acid derivatives containing of primary and secondary alkyl amine include monoacylamino group
  • nucleus substituted compound include aniline, toluidines,
  • 4,4-bis-triazinylamino stilbene-2,2-disulfonic chloroanilines aniline sulfonic acids such as sulfanilic acid derivatives are known to be used for the above menacid and metanilic acid, toluidine sulfonic acids, chlorotioned purposes, however, being added to soap and aniline sulfonic acids, paminobenzoic acid, anthranylic synthetic washing agents, most of these compounds acid, N-methylaniline, N-ethylaniline and N-phenyl rather color the appearances of soaps and synthetic washethanolamine, and examples of alkoxy radicals include ing agents in pale yellow shade, and even effective comrnethoxy and ethoxy radicals.
  • the compounds used in the present invention and represented by the above general formula are very much superior to the corresponding anilino compounds, i.e., the compounds of both X and X in the above general formula are hydrogen atom, concerning the effects of improving the appearances of the soaps or synthetic washing agents.
  • the compounds, the compounds having methyl radicals as X and X in the above general formula are rather superior to those having ethyl radicals as X and X in the above general formula concerning the improving effects of the appearances of the soaps or synthetic washing agents.
  • the appearances of the present soaps and synthetic washing agents are less changeable by the effects of external conditions, such as moisture, than those containing the corresponding anilino compounds. This is one of the characteristic properties of the present invention.
  • present soaps and synthetic washing agents are considerably stabler than those containing conventional optical brightening agents, when they are used together with chloric bleaching agents in the washing of articles, and possess higher optical brightening action towards articles to be washed than those containing the corresponding anilino compounds. This is another characteristic property of the present invention.
  • the soaps include Marseille soap and the synthetic washing agents include those containing, as the essential component, alkylaryl sulfonate, e.g., sodium dodecylbenzene sulfonate, and higher alcohol surfuric acid esters, e.g., sodium oleyl sulfate, and being solid type.
  • alkylaryl sulfonate e.g., sodium dodecylbenzene sulfonate
  • higher alcohol surfuric acid esters e.g., sodium oleyl sulfate
  • the shape of the washing agent product according to the present invention includes blocks, flakes, beads and powders. Especially beads and powders are preferred.
  • the soaps and synthetic washing agents according to the present invention are prepared as follows.
  • a solution of a slurry of a soap, a synthetic washing agent or a mixture of them is added with at least one of 4,4-bis-triazinylaminostilbene-2,2'-disulfonic acid sodium salt of the present invention in the form of powder, solution or suspension in an amount of 0.01 to 1% by weight based upon the weight of the washing agent, mixed homogeneously and dried, and then crushed.
  • the content of the 4,4-bis-triazinylaminostilbene-2,2'-disulfonic acid sodium salt of the present invention may improve the whiteness of the appearance of the soaps and synthetic washing agents, and 1% or more than 1% by weight may be chosen, if desired and possible, depending upon the compounds and the purposes such as improving of the whiteness of the appearances of the soaps and synthetic Washing agents and increasing of the effect of brightening articles to be washed.
  • the compound used in the present invention may be admixed to the solution or slurry of a soap, a synthetic washing agent or a mixture of them itselfor to the solution or slurry of a soap, a synthetic washing agent or a mixture of them containing preferred builder such as sodium sulfate, phosphoric acid salts, sulfonic acid salts of benzene series sodium carbonate, CMC and the like.
  • preferred builder such as sodium sulfate, phosphoric acid salts, sulfonic acid salts of benzene series sodium carbonate, CMC and the like.
  • powdery builders as mentioned above may be added thereto.
  • the solution or slurry may be dried with hot air, or may be dried by using vacuum dryer at room temperature, spray-dryer or dropping method in vacuum.
  • the compounds of the present invention may be applied to the mixture of more than one kind of soaps or synthetic washing agents.
  • the compounds of the present invention can improve the appearances of soaps or synthetic washing agents colored by the addition of other known compounds, and can be applied together with known compounds thereby to suppress or neutralize the coloring of soaps or synthetic washing agents which will be caused by the addition of such known compounds.
  • EXAMPLE 1 To a slurry obtained by mixing 100 parts of sodium dodecylbenzenesulfonate with 50 parts of water, a solution obtained by dissolving 1 part of sodium 4,4.-bis(2-N- methylanilino 4-monoisopropanolamino triazin 6 ylamino)stilbene-2,2-disulfonate in 10 parts of water with heating, was admixed and stirred to yield homogeneous slurry. The resulting slurry was dried with hot air at 60 C. and crushed, whereby the powdery washing agent, the appearance of which was much whiter than that of original material, was obtained.
  • EXAMPLE 2 To a solution of 100 parts of Marseille soap in 200 parts of water, a solution obtained by dissolving 0.3 parts of sodium 4,4 bis(2 N methylanilino-4-m-sulfoanilinotriazin 6 ylamino)stilbene-2,2'-disulfonate in 10 parts of water, was admixed and stirred. The resulting mixture was spray-dried, whereby a powdery soap, the appearance of which was whiter than the original soap, was obtained.
  • EXAMPLE 5 To a slurry of parts of sodium oleyl sulfate in 30 parts of water, a hot solution obtained by dissolving 0.5 part of sodium 4,4 bis(2 N methylanilinot-monoethanolamino triazin 6 ylamino) stilbene-2,2'-disulfomate in 5 parts of water was added and mixed homogeneously. The resulting mixture was dried in vacuum at room temperature and crushed, whereby a powdery washing agent, the appearance of which was extremely improved, was obtained.
  • EXAMPLE 6 To a slurry obtained by mixing 100 parts of sodium oleyl sulfate, 200 parts 'of sodium sulfate, 50 parts of sodium pyrophosphateand 200 parts of water, a hot solution of 0.1 part of 4,4 bis(2 N methylanilino-4- morpholino triazin 6 ylamino) stilbene 2,2-disulfonate, 1 part of sodium p-toluenesulfonate in 5 parts of water, was added and mixed homogeneously. The resulting mixture was dried by dropping method in vacuum, whereby beads like powdery washing agent, the appearance of which was white in high degree, was obtained.
  • EXAMPLE 7 T o a slurry obtained by mixing 100 parts of sodium dodecylbenzenesulfonate, 30 parts of Marseille soap, 100 parts of sodium sulfate, 20 parts of sodium carbonate, 50 parts of sodium tripolyphosphate and 200 parts of water, a solution obtained by dissolving 1 part of sodium 4,4- bis(2 -N ethylanilino 4 methylethanolamino-triazin- 6-ylamino)stilbene-2,2-disulfonate and 20 parts of sodium benzenesulfonate in 50 parts of water with heating, was added and stirred homogeneously. The resulting mixture was spray-dried, whereby a powdery Washing agent, the appearance of which was extremely improved, was obtained.
  • EXAMPLE 9 To a slurry obtained by mixing 100 parts of sodium dodecylbenzene sulfonate, 100 parts of sodium sulfate, 100 parts of sodium tripolyphosphate and 200 parts of water, a hot solution of 1 part of the compound, prepared from the mixture of 1 mol portion :of 4,4-diaminostylbene-2,2-disulfonic acid, 2 mole portions of cyanuric chloride, 2 mole portions of N-methylaniline, 1 mole portion of methyl ethanolamine and 1 mole portion of monoisopropanolamine, in 10 parts of water, was added, homogeneously mixed and spray-dried, whereby a powdery washing agent, the appearance of which was extremely improved, was obtained.
  • washing agent was found to be improved as well as the washing agent obtained by employing the corresponding 4,4-bistriazinyl aminostylbene 2,2'-disulfonic acid derivatives obtained by synthesis without mixing the raw materials, i.e., that obtained by employing each 0.5 part of sodium 4,4 bis(2 N methylani'lino-44nethylethanolaminotriazin 6 ylamino) -stilbene-2,2-disulfon-ate and sodium 4,4 bis(2 N methylanilino-4-monoisopropanolaminotriazin-6-ylamino)stilbene-2,2-disulfonate respectively.
  • EXAMPLE 10 To a slurry obtained by mixing .100 parts of sodium dodecylbenzene sulfonate, 70 parts of sodium sulfate, 70 parts of sodium tripolyphosphate, 30 parts of sodium carbonate, 5 parts of CMC and 100 parts of water, a hot solution of 1 part of a compound, obtained by reacting -1 mole portion of 4,4-diaminostilbene-2,2'-disulfonic acid, 2 mole portions of cyanuric chloride, a mixture of 1 mole portion of N-methylaniline and 1 mole portion of N-ethylaniline and 2 mole portions of monoisopropanolamine, 5 parts of sodium p-toluenesulfonate and 10 parts of water, was added, mixed, and dried in vacuum, and then crushed, whereby a powdery washing agent, the appearance of which was very much improved, was obtained.
  • washing agent was found to be improved as well as the washing agent obtained by employing the corresponding 4,4 bis-triazinylaminostilbene-2,Z'-disulfonic acid derivatives obtained by synthesis without mixing the raw materials, i.e., that obtained by employing each 0.5 parts of sodium 4,4'-bis(2-N-methylanilino-4- monoisopropanolamino triazin 6-ylamino)stilbene-2,2- disulfonate, and sodium 4,4-bis(2-N-ethylanilino-4-monoisopropanolamino triazin 6 ylamino)stilbene 2,2- disulfonate respectively.
  • EXAMPLE 11 To a slurry obtained by mixing a washing agent consisting of 0.5 part of sodium 4,4-bis(2-anilino-4-aminotriazin-6-ylamino) stilbene-2,2'-disulfonate which is known compound and parts of sodium dodecylbenzenesulfonate, the appearance of which washing agent was pale yellow shade, and 50 parts of water, a solution of 0.2 part of sodium 4,4 bis(2 N methylanilino-4-aminotriazin-6-ylamino)-sti-lbene-2,2'-disulfonate in 10 parts of water was added, homogeneously mixed and spray-dried, whereby a powdery washing agent, the appearance of which was whiter than that of original synthetic washing agent which was before admixing sodium 4,4-bis(2- anilino 4 amino triazin 6 ylamino)-stilbene-'2,2'- disulfonate, was obtained.
  • a washing agent consisting of
  • a washing agent which is referred to as A, which was obtained by admixing 0.2% by weight of sodium 4,4-bis (2 anilino-4-monoisopropanol-amino-triazin--ylamino)- stilbene-2,2'-disulfonate wit-h 99.8% by weight of sodium dodecylbenzenesulfonate which is known compound, was recognized to have improved whiteness in the appearance, however, a washing agent, which is referred to as B, which was obtained by admixing 0.2% by weight of the corresponding sodium 4,4-bis(Z-N-methylanilino-4-monoisopropanolamino triazin G-ylamino) stilbene-2,2'-disulfonate of the present invention with 99.8% by Weight of sodium dodecylbenzene-sulfonate was found to be far improved in the appearance with high degree of whiteness, as compared with A.
  • EXAMPLE 13' A washing agent, which is referred to as C, which was obtained by admixing 0.2% by weight of sodium 4,4 bis(2 anilino 4-ethanolamino-triazin-6-ylamino) stilbene-2,2-disulfonate with 99.8% by weight of sodium dodecylbenzenesulfonate which is known compound, was found to be very much decreased in the optical brightening effect of articles to be washed, when employed in the washing bath containing 100-500 p.p.m.
  • a composition consisting essentially of a member selected from the group consisting of marseille soap, dodecyl benzene sulfonate, a higher alcohol sulfate, or mixture thereof, and about 0.01 to 1% by weight, based on the weight of the composition, of a brightening agent, 4,4-bis-triazinylstilbene-2,2'-disulfonic acid derivative having the formula,
  • N l l 1 1 I l 2'1 som sOiM wherein X and X each represents methyl or ethyl radical; Y and Y each represents amino, cyclohexylamino, primary or secondary alkylamino having 1 to 4 carbon atoms, or primary or secondary hydroxyalkyl'amino, with each radical having 1 to 3 carbon atoms; and M represents hydrogen or alkali metal.
  • composition according to claim 1 wherein the disulfonic acid derivative is sodium 4,4-bis(2-N-methylanilino 4 monoisopropanolamino triazine-6-ylamino) stilbene-2,2'-disulfonate.
  • composition according to claim 1 wherein the disulfonic acid derivative is sodium 4,4-bis(2-N-methylanilino-4-methyl ethanolamino-triazin-6-ylamino stilbene- 2,2'-disulfonate.
  • composition according to claim 1 wherein the disulfonic acid derivative is sodium 4,4'-bis(2-N-methyl- :anilino 4 monoethanolamino triazin 6 ylamino)stilbene-2,2'-disulfonate.
  • composition according to claim 1 wherein the disulfonic acid derivative is sodium 4,4'-bis(2-N-ethylani- 1ino-4-methyl ethanolamino-triazin-6-ylamino)stilbene-2, 2-disulfonate.
  • composition according to claim 1 wherein the disulfonic acid derivative is sodium 4,4'-bis(2,4-bis-N- methylanilino-triazin-6-ylamino)stilbene-2,2'-disulfonate.
  • composition according to claim 1 wherein Y and Y each is a member selected from the group consisting of monomethylamino, monoethylamino, n-butylamino, dimethylamino, diethylamino and methylethylamino.
  • composition according to claim 1 wherein Y and Y each is a member selected from the group consisting of monoethanol amino, monoisopropanolamino, diethanolamino, methylethanolamino, ethyl ethanolamino and diisopropanolamino. .7
  • composition according to claim 1 further consisting essentially of an effective amount of at least one builder selected from the group consisting of sodium sulfate, sodium tripolyphosphate sodium pyrophosphate, and sodium carbonate.
  • at least one builder selected from the group consisting of sodium sulfate, sodium tripolyphosphate sodium pyrophosphate, and sodium carbonate.
  • composition according to claim 9 further consisting essentially of an eifective amount of sodiump-toluene sulfonate as a builder.
  • a composition according to claim 9 further consisting essentially of an elfective amount of carboxy methyl cellulose as a builder.

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  • Engineering & Computer Science (AREA)
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US435021A 1964-02-24 1965-02-24 Washing agents containing optical brightening agents Expired - Lifetime US3392122A (en)

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BE (1) BE660137A (sv)
CH (1) CH451378A (sv)
DE (1) DE1301867B (sv)
ES (1) ES309699A1 (sv)
FR (1) FR1425151A (sv)
GB (1) GB1072867A (sv)
NL (2) NL6502303A (sv)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3716532A (en) * 1970-04-13 1973-02-13 C Tscharner Process for preparing crystalline forms of 4,4'-bis[(4-anilino-6-morpholino-1,3,5-triazin-2-yl)-amino]-stilbene-2,2'-disulfonic acid
US3895009A (en) * 1971-12-27 1975-07-15 Ciba Geigy Ag Stilbene compounds
US4058480A (en) * 1973-09-14 1977-11-15 Ciba-Geigy Corporation Non-dusting, readily free-flowing granules of optical brighteners
US5304462A (en) * 1992-07-20 1994-04-19 Anacomp, Inc. Composition for and method of cleaning continuous, nonreplenished film developers and replenished film developers

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1238833A (sv) * 1968-01-18 1971-07-14
GB2187749B (en) * 1986-03-11 1990-08-08 Procter & Gamble Stable liquid detergent composition hydrophobic brightener

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB930393A (sv) * 1959-11-20 1900-01-01
US2763650A (en) * 1956-09-18 Derivatives of x
AT224118B (de) * 1960-01-14 1962-11-12 Ciba Geigy Verfahren zur Herstellung neuer Bistriazinylaminostilbendisulfonsäuren
GB941993A (en) * 1960-01-14 1963-11-20 Ciba Ltd New bis-triazinylamino-stilbene disulphonic acids and process for their preparation
US3177207A (en) * 1965-04-06 Nh-chs

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH401074A (de) * 1960-03-04 1965-10-31 Ciba Geigy Verfahren zur Herstellung neuer Bistriazinylaminostilbendisulfonsäuren

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2763650A (en) * 1956-09-18 Derivatives of x
US3177207A (en) * 1965-04-06 Nh-chs
GB930393A (sv) * 1959-11-20 1900-01-01
AT224118B (de) * 1960-01-14 1962-11-12 Ciba Geigy Verfahren zur Herstellung neuer Bistriazinylaminostilbendisulfonsäuren
GB941993A (en) * 1960-01-14 1963-11-20 Ciba Ltd New bis-triazinylamino-stilbene disulphonic acids and process for their preparation

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3716532A (en) * 1970-04-13 1973-02-13 C Tscharner Process for preparing crystalline forms of 4,4'-bis[(4-anilino-6-morpholino-1,3,5-triazin-2-yl)-amino]-stilbene-2,2'-disulfonic acid
US3895009A (en) * 1971-12-27 1975-07-15 Ciba Geigy Ag Stilbene compounds
US4058480A (en) * 1973-09-14 1977-11-15 Ciba-Geigy Corporation Non-dusting, readily free-flowing granules of optical brighteners
US5304462A (en) * 1992-07-20 1994-04-19 Anacomp, Inc. Composition for and method of cleaning continuous, nonreplenished film developers and replenished film developers

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CH451378A (fr) 1968-05-15
NL6502303A (sv) 1965-08-25
BE660137A (sv) 1965-06-16
NL130816C (sv)
GB1072867A (en) 1967-06-21
FR1425151A (fr) 1966-01-14
DE1301867B (de) 1969-08-28
ES309699A1 (es) 1965-07-16

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