US3130193A

US3130193A - Mercurated melamine derivatives

Info

Publication number: US3130193A
Application number: US83368A
Authority: US
Inventors: John T Shaw; Frank J Gross; Richard K Madison
Original assignee: American Cyanamid Co
Current assignee: Wyeth Holdings LLC
Priority date: 1961-01-18
Filing date: 1961-01-18
Publication date: 1964-04-21
Anticipated expiration: 1981-04-21

Description

United States Patent O 3,139,193 MERCURATED NELAMINE DERIVATIVES John T. Shaw, Niiddlesex, Frank J. Gross, New Brunswick, and Richard K. Madison, Murray Hill, N..l.,

assignors to American (Iyanamid Company, New

York, N.Y., a corporation of Maine No Drawing. Filed Jan. 18, 1961, Ser. No. 83,363

8 Claims. (Cl. 260242) This invention relates to novel germicidal or bactericidal compounds, to their use on temile materials as durable germicidal finishes, to processes for applying such compounds as finishes to textile materials and to the textile materials so treated.

More particularly, this invention relates to novel mercurated allyltriazines as germicidal or bactericidal compounds, to their use on textile materials as durable germicidal finishes, to the processes of applying said compounds as finishes to textile materials, and to the materials so treated.

An object of the present invention is to provide a novel class of mercurial allyltriazines, their formaledehyde condensates, and their alkylated methylol derivatives.

A further object of this invention is to provide a durable antibacterial finish for textile materials and in particular a finish which is durable to laundering in the presence of'soaps and/ or chlorine, such as is normally employed as chlorine bleach.

A further object of this invention is to provide an antibacterial or germicidal finish which is also capable of contributing dimensional stability and wrinkle resistance to cellulosic materials.

A further object is to provide an antibacterial finishing composition which is compatible with known textile finishing agents or resins, which resins contribute dimensional stability and wrinkle resistance to cellulosic substrates.

A still further object of this invention is to provide a water soluble or water dispersible antibacterial finish which can be applied by standard textile finishing methods, i.e., those normally employed by the textile finishing industry to impart, in addition to a bactericidal finish, wrinkle resistance andshrinkage control to the cellulosic textile material.

These and other objects and advantages of the present invention will become more apparent from the detailed description thereof set forth hereinbelow.

According to the present invention, novel mercurial derivatives of amino-s-tn'azines are prepared of the formula:

Patented Apr. 21, 1964 or -CH2OR7, where n is a value of from 1 to 3, inelusive; R -R is hydrogen, -CH OR alkyl or phenyl; R R and R are hydrogen or lower alkyl; and X is a monovalent electronegative component or anionic radical such as CH COO, Cl, etc.

These compounds may be preformed and then applied to the textile substrates or materials or they may be formed in situ on such materials. The mercurial compounds are derivatives of allyl substituted amino-s-triazines with the allyl group attached to a nitrogen or to an oxygen atom which is attached to a ring carbon.

In general, these mercurated allyl substituted amino-striazines are prepared by reacting an appropriate allyl substituted amino-s-triazine with mercuric acetate or a similar mercuric salt in an alcohol or Water medium acidified with'a weak acid such as acetictacid. The reaction mixture is then stirred while being heated until tion is completed.

In an alternative procedure, the allyl derivative of an amino-s-triazine is first applied to the textile material and the material subsequently treated with a hot alcoholic solution of mercuric acetate or similar salt, acidified with a Weak acid such as acetic acid.

The values of A, R -R R and R in the general formulas will depend on the substituents in the corresponding positions of the starting compounds. However, the value for R is determined by the solvent medium in which the reaction is carried out. If the medium is an alcohol, R will be the alkyl radical of that alcohol. When the medium is water, R will be hydrogren.

The value of X, the anionic radical, will depend on the anion associated with mercury, of the salt'use'd. If mercuric acetate is employed, the anion willbeacetate, If mercuric-propionate is employed, the anion will be propionate. However, X may be changed to another electronegative component by reacting the original reaction product, such as the acetate, with a salt such as sodium chloride or silver nitrate, wherebylthe acetate will be con verted to a new salt such as the chloride or nitrate.

In general, the allyl substituted amino-s-triazines employed as starting materials in the preparation of the compounds of this invention are Well known and may be readily prepared. The following are illustrative of the allyl amino-s-triazines which may be employed in the present invention: N-allyl substituted melamines such as N-allylmelainine, N,N-diallylmelamine, N-allyl-N'-methylmelamine, N-allyl-N-ethylmelamine, N-allyl-N-ethylmelamine, N,N-diallyl-N'-n-butylmelamine, 1 -allyl-N'- methyl N" n-propylmelamine, N-allyl-N',N -dimethylmelamine, N-allyl-N-phenylmelamine, N,N-diallyl-N phenylmelamine, and the 2,4-diamino-6-allyloxy-striazines, such as 2-allyloxy-4-amino-6-methylamino-s-tria- Zine, 2 allyloxy 4-ethylamino-6-methylamino-s-triazine and 2-allyloxy-4-amino-6-phenylarnino-s-triazine, and the like. It will be apparent that corresponding alkyl substituted allyl derivatives, such as methallyl derivatives, for example, N-methallylmelamine, N-methallyl-N'-methylmelamine and 2,4-diamino-6-methallyloxy-s-triazine are fully contemplated. p

The mercuric salts employable are preferably salts of aliphatic organic acids such as formic acid, acetic acid, propionic acid, butyric acid and the like.

The solvent medium in which the mercurated allyl-striazines of this invention are employed is preferably an alcohol such as methanol, ethanol, propanol, butanolor the like. However, Water and alcohol-water solutions may be employed.

Whether the mercurating medium is alcoholic, aqueous or a mixture, the medium is acidified with a weak, preferably organic acid, such as acetic acid, propionic acid, butyric acid, and the like in order to facilitate the mercuration and prevent hydrolysis of the mercury salt.

the reac- 1 While the allylamino-s-triazines of this invention may be mercurated prior to methylolation and alkylation if the latter is carried out, it is greatly preferred that the mercuration be effected on methylolated or alkylated methylolated allylamino-s-triazines. Mercuration of the formaldehyde condensed amino-s-triazines as noted above is carried out on the acid side in an alcoholic or aqueous medium, normally at a temperature of from 25 to 100 C. and preferably at a temperature of from 60 to 80 C. for from two to forty-eight and preferably from sixteen to twenty-four hours. The mercury compound is preferably employed in an amount equal. to one equivalent per double bond of the allylamino-s-triazine. While excesses may be employed, such usually presents recovery problems which are undesirable. Excesses of the allylamino-s-triazine may be employed usually up to about mole percent in terms of the number of double bonds present per mole of mercury compound.

The allylamino-s-triazines of this invention may be condensed with formaldehyde to introduce methylol groups on any of the amino-nitrogen atoms which bear a hydrogen atom. These formaldehyde condensates are prepared by reacting the allyl compound with formaldehyde, preferably under alkaline conditions, as for example at a pH of from about 8 to 11. In general, methylolation of the allyl amino-s-triazines of this invention is conducted in accordance with the procedures Well known to those skilled in the art for preparing the formaldehyde condensates of such materials as melamine, urea, ethylene urea, trimethylene urea and the like to prepare aminoplast derivatives thereof. Thus, a mole of formaldehyde for each amino-hydrogen sought to be methylolated is introduced into a reaction vessel and under alkaline conditions the reaction mixture would normally be maintained at a temperature of from between 25 C. and 80 C. until condensation is complete. Normally a slight excess of formaldehyde is employed to insure the degree of methylolation sought. Additionally, the methylol groups may be alkylated and formed into alkoxymethyl groups such as N-methoxymethyl by reacting a methylol compound with a suitable alcohol under acidic conditions, normally in the presence of a mineral acid. Suitable acids for such a condensation may be hydrochloric, sulfuric, nitric and the like. Suitable alcohols that may be employed in the process of this invention would include the saturated aliphatic monohydric alcohols and particularly those containing 1 to 4 carbon atoms, as for example methyl, ethyl, propyl, butyl and the like.

As examples of suitable methylol or formaldehyde condensates of the mercurated allylamino-s-triazines of this 7 invention, the following are illustrative: N,N-bis(3-acetoxymercuri-Z-methoxypropyl) N,N dimethylolmelamine; N (3-acetoxymercuri-2-methoxypropyl)-N-allyl- N,N"-dimethylolmelamine and the like.

As examples of the alkylated methylol derivatives of a the ,mercurated allylamino-s-triazines of this invention, the following are illustrative: N,N-bis(S-acetoxymercuri- Z-methoxypropyl) N',N,N" tris(methoxymethyl)meland a crease-resistant finish to cellulose textile materials. Preferably these compounds contain at least two methylol or alkylated methylol groups on difierent amino-nitrogens in order to insure cross-linking, and therefore the crease resistance and shrinkage control, in finished cellulosic textile material.

are the materials employed to provide both a germicidal 4 These formaldehyde condensates have the following general formula:

R: where A is selected from the group consisting of CR and in which R is 0 R3 CHr-JOH2HgX D and R is selected from the group consisting of hydrogen, alkyl, -CH CH=CH 0 Rs oH, J-oH,n x

and --CH OR and Where R R are selected from the group consisting of hydrogen, -CH OR alkyl and phenyl and at least two of the members R -R and R on different amino-nitrogens, are --CH OR where R R and R are selected from the group consisting of hydrogen and lower alkyl, and X is an anionic radical.

The N-methylol and N-alkoxymethyl derivatives are the preferred germicidal finishes of this invention where maximum durability is desired. These are particularly the preferred bactericidal finishes when the base textile material is of a cellulosic character, as for example, cotton, rayon and the like. Also, N-methylol and N-alkoxymethyl derivatives are preferred when the combination of bactericidal activity and dimensional stability and wrinkle resistance are desired on cellulosic textile materials.

As is well known, in order to cross link between two cellulosic molecules, which reaction is necessary to impart dimensional stability and wrinkle resistance to the cellulose material, it is essential that there be more than one and preferably at least two N-methylol or N-alkoxy methyl groups in each bactericidal molecule to obtain these eflects. When the antibacterial agents contain at least one methylol group, they are believed to be fiber reactive germicides. However, they normally will not produce a cross linking that will result in wrinkle resistance and shrinkproofing for cellulose textile materials.

The compounds of this invention are either water solule or water dispersible and are readily applied to textile materials from aqueous media by any of the well known methods for applying Water soluble textile resin finishes. Thus, for example, they may be padded, sprayed, applied by immersion, dipping or any of the other well known finishing techniques.

If desired, a thermosetting aminoplast resin, as for example, of the type well known to the textile finishing industry to be creaseproofing resins, may be applied with the antibacterial agents, either from the same bath or subsequently from a second treating bath or solution. As examples of suitable thermosetting aminoplast resins contemplated by this invention, the water soluble melamineformaldehyde resins prepared in accordance with US. Patent No. 2,197,357 and 2,529,856 are fully contemplated. Examples of such resins are tris-(methoxymethyl) melamine, tris(methoxymethyl) dimethylol melamine, hexakis(methoxymethyl) melamine, and the like. In addition to these melamine-formaldehyde resins, the urea and thiourea-formaldehyde condensates are contemplated,

l I 1 l l as are their alkylated derivatives. Thus, for example, dimethylol urea, methylated dimethylol urea and thiourea, dimethylol ethylene urea, dimethylol 1,2-propylene urea and thiourea, dimethylol 1,3-propylene urea and thiourea and other related homologous compounds are contemplated.

Additionally, the formaldehyde condensates of dicyandiamide, biuret and the like are contemplated, as are the water soluble formaldehyde condensates of thiobis amides of the type described in U.S. Patent No. 2,887,408.

Guanamine formaldehyde condensates, as for example, those described in U.S. Patent No. 2,887,409, including the formaldehyde condensates of methoxy acetoguanamine, ethoxy acetoguanamine, tertiary butoxy acetoguanamine, and the like are contemplated.

Urons may also be employed with the compounds of this invention as, for example, N,N'-bis(methoxymethyl) uron and various other and closely related compounds such as are described in U.S. Patent No. 2,373,135. Additionally, tetrahydro triazones such as tetrahydro-S-(B- hydroxyethyD-S-triazone and compounds of the type described in U.S. Patent No. 2,304,624 are also fully contemplated.

It has been our experience that when the antibacterial agents of this invention do not contain methylol groups, that greater durability of the germicidal finish is normally obtained by applying a textile resin, as for example, any of the water soluble potentially thermosetting aminoplast resins identified hereinabove in conjunction with the germicidal compounds.

When the germicidal compound contains methylol groups (including alkylated methylol groups) or when a thermosetting aminoplast textile finishing resin is employed in conjunction with the germicidal compounds of this invention, it is advantageous to employ a suitable acid-acting curing catalyst or accelerator such as ammonium sulfate for effecting the cure of these aminoplasts (mercurated methylol compound and thermosetting aminoplast textile finishing resin) on the textile material. It will be apparent that if the mercurated allylamino-s-tria- Zine does not contain methylol or alkylated methylol groups, a catalyst or curing accelerator is not required to fix it upon the textile material, and if a thermosetting arninoplast resin is not subsequently applied, all that is required is that the treated material be dried. Examples of such catalysts are free acids, acid salts, alkanolamine salts, metal salts and the like of the well known types. The concentration of catalyst employed may range from about 0.1 to about 25 or higher based on the weight of resin solids, depending upon the particular catalyst type employed. Thus, for example, from between about 0.1 and about of free acids, such as phosphoric, tartaric, oxalic and the like may be employed, while in the case of ammonium chloride amounts of from between 0.5 and about 10% are used. In the case of amine salts including alkanolamine salts such as diethanolamine hydrochloride, from about 1 to about 10% are most useful, while with respect to salts such as magnesium chloride, amounts of from between about 5 and have been successfully employed. In addition to magnesium chloride, zinc nitrate, zinc borate, aluminum chloride and other known conventional metal salts are normally employed in amounts corresponding to from between 5 and 25 based on the weight of the resin solids.

After the application of the methylolated mercurated allylamino-s-triazzines, with or without the addition of a thermosetting aminoplast resin, the treated textile material is dried and subjected to temperatures normally considered to be the drying and curing temperatures employed for drying and curing for creaseproofing resins in the textile finishing industry. Thus, for example, the treated material may be subjected to temperatures of from between about 180 F. to about 450 F. or higher. Generally speaking, the time of drying and/ or curing operations is inversely proportional to the temperature employed and of course is influenced by whether or not separate or com bined drying and curing steps are employed. Generally, when drying and curing is carried out in a combined operation, a time of from about 1 minute to about 10 minutes may be employed at temperatures of from 450 to 250 F., respectively. When the fabric has been dried preliminary to curing, curing times of the order of about 5 minutes to about A minute at a temperature of from about 250 and 450 F., respectively, have been successfully employed.

The germicidal finish of this invention may be applied to textile materials or bases, usually in the form of fabric which may be knitted, woven, non-woven or otherwise formed, and which may be prepared from cellulosic or non-cellulosic fibers or mixtures of the two. Thus, the textile material may be a formed fabric of cellulosic fibers, as for example, cotton, linen or viscose rayon or mixtures thereof, or it may be a textile fabric prepared from acetate rayon, nylon, the polyester fibers and acrylic fibers, wool, silk and the like. Additionally, the textile material may be prepared from mixtures of these and other cellulosic and non-cellulosic fibers.

Preferably, the textile material is a cellulosic material formed principally from cellulosic fibers. In this regard, for purposes of this invention, the term cellulosic fabric shall mean to include fabrics containing te least 50% by weight of cellulosic fibers, whether they be cotton, viscose rayon, linen or the like.

The antibacterial compounds of this invention are normally applied in an amount of from between 0.0001% to 2.5% on the weight of the textile material. The prefer able amount is from between 01% to 1% based on the dry Weight of the textile material to which it is applied. In applications where the water soluble thermosetting amiuoplast resin is employed in conjunction with the allylamino-s triazines of this invention, these resins are normally applied in amounts of from between about 1 and about 25 and preferably in amounts of from 2.5 to 10% based on the dry weight of the textile material.

In order that the present invention may be more fully understood, the following examples are given primarily by way of illustration. No specific details or enumerations contained therein should be construed as limiting the present invention except insofar as they appear in the appended claims. All parts and percentages are by weight unless otherwise indicated.

EXAMPLE 1 N,N Bis(3-Acetoxymercuri-Z-Methoxypropyl)Melamine N N OCH:

A hot solution of 174.9 parts (0.55 mole) of mercuric acetate and '30 parts of glacial acetic acid in 320 parts of methanol is added to a solution consisting of 51.6 .parts (0.25 mole) of N,N-di-allylmelamine in 450 parts of methanol at 45 C. The reaction mixture is heated at the reflux for 24 hours, cooled and filtered. The filtrate is concentrated in vacuo, resulting in a thick syrup. The syrup is poured into 4000 parts of acetone, with stirring for several hours. The resultant precipitate is filtered ofi and then dried in vacuo over phosphoric anhydride.

The hygroscopic product obtained was 122 parts (60.6% yield); M.-P. C. to C. and had the following analysis.

Calculated 01 C 5H2 Hg N5O .H2OI C, H, Hg, 49.75; N, 10.4; 0, 13.9. Found: C, 22.1; H, 2.93; Hg, 50.2; N, 9.84; O, 13.0.

7 EXAMPLE 2 N (3 Acetoxymercuri-Z-Methoxyprpyl)-N-Allylmelamine OCH; Ifil' N CHg-CHCH;Hg-OCOOHa H2N-O C-N A hot solution of 79.5 parts (0.25 mole) of mercuric acetate and 15 parts of glacial acetic acid in 145 parts of methanol is added to a solution of 51.6 parts (0.25 mole) of N,N-diallylmelamine in 450 parts of methanol at 45 C. The procedure of Example 1 is then followed.

The hygroscopic product, amounting to 63 partsand melting at 152 C. to 160 C. had the following analysis.

Calculated for C H HgN O C, 29.1; H, 4.02; N, 17.0; Hg, 40.2. Found: C, 29.4; H, 3.54; N, 17.2; Hg, 39.4.

EXAMPLE 3 N (3-A cetoxymercuri-Z-M ethoxypropyl -N Ethylmelamine W C EXAMPLE 4 N,N-Bis(3-ACemxymercuri-Z Methoxypropyl)-N'- M ethylmelamine The procedure of Example 1 is followed substituting 55.1 parts of N,N-diallyl-N-methylmelamine for the 51.6 parts of N,N-diallylrnelamine.

EXAMPLE 5 N,N-Bis(3-Acetoxymercuri-Z-Meth0xypr0pyl) -N- Phenylmelamine F C The procedure of Example 1 is followed substituting 70.6 parts of N,N-diallyl-N'-phenylrnelamine for the 51.6 parts of N,N-diallylmelamine.

EXAMPLE 6 N ,N -Bis(3 -Acetoxymercuri-2Eth0xypr0pyl )M elamine N N 0 0 H,

N The procedure of Example 1 is followed substituting an equal amount of ethanol for the methanol.

8 EXAMPLE 7 Reaction Product of N,N-Diallyl-N',N',N"-Tris(Methoxymethyl)Melamine and Mercuric Acetate A reaction product of N,N-dia1lyl-N',N',N"-tris(methoxymethyhmelamine and mercuric acetate is accomplished in a three-step method.

1st step: N,N-dially1-N',N',N"-trimethylol melamine is prepared by mixing 103 parts (0.5 mole) of N,N- diallylmelamine and 202 parts (2.5 moles) of 37% formalin and heating to C. and the pH adjusted to 89 by adding 20% aqueous solution of caustic soda. After maintaining the temperature at 85 C. and the pH at 8-9 for 30 minutes, the resulting solution is cooled to room temperature, whereupon the liquid separates into two layers.

When cooled below 10 C., the lower layer slowly solidifies. The solid material is separated by filtration and dried in vacuo at 50-55 C. over phosphoric anhydride.

The product amounting to 132 parts (yield) had the following analysis.

Calculated for C H N O H O: C, 45.2; H, 7.00; N, 24.4. Found: C, 45.2; H, 6.30; N, 24.0.

2nd step: A mixture consisting of 132 parts (0.42 moles) of N,N diallyl N,N',N"-trimethylolmelamine, 158 parts (4.8 moles) of methanol and 0.45 part (.0032 mole) of oxalic acid dihydrate is prepared at room temperature and refluxed for 45 minutes. After cooling, the solution is neutralized to pH 9.6l0.0 with 1 N sodium hydroxide and then filtered and distilled in vacuo.

During distillation two layers are noticed. After removing all of the solvent, a pale yellow viscous syrup remains. The product, N,N-diallyl-N',N',N"-tris(methoxymethyDmelamine amounting to 114 parts (yield) had the following analysis.

Calculated for C H N O C, 53.2; H, 7.7; N, 24.8. Found: C, 52.2; H, 7.3; N, 24.2.

3rd step: Mercuration of product of Step No. 2 is accomplished by preparing two separate solutions.

EXAMPLE 8 N N NHakN NI-Ih To a solution of 10 parts (0.06 mole) of 2-allyloxy- 4,6-diamino-s-triazine in 162 parts of methanol at 33 C. is added (in small portions over hour period with stirring) 19.1 parts (.06 mole) of mercuric acetate. The resultant mixture is stirred for 24 hours and allowed to stand for 5 days. The milky product is evaporated in vacuo to a syrupy product which is stirred and saturated with 79.2 parts by weight of acetone for 3 hours. The

product is filtered and the filter cake washed with acetone and then dried over phosphoric anhydride.

The yield is 21.3 parts; MP. 320 C.; hygroscopic.

Analysis.Calculated for C H HgN O C, 22.9; H, 3.21; Hg, 42.4. Found: C, 22.8; H, 2.88; Hg, 43.4; N, 14.4.

EXAMPLE 9 Procedures of Application, Drying and Washing 0f Fabrics Treated With Product 0] Example 1 A pplication.All applications are made from aqueous solutions by padding through a two roll micro-set padder.

The product of Example 1 is applied at various concentrations and by several different methods, i.e.

Method A-Product applied alone Method BProduct plus creaseproofing resins Method CProduct applied alone and topped with creaseproofing resin Drying and curing.-The drying or curing of the Various treated fabrics is accomplished in hot, circulating air ovens.

Fabrics treated by method A are dried for 2 minutes at 225 F.

Fabrics treated by method B are predried for 2 minutes at 225 F. and then cured for 1.5 minutes at 350 F.

Fabrics treated by method C are predried for 2 minutes at 225 F., then repadded with the creaseproofing resin, dried for 2 minutes at 225 F. and then cured for 1.5 minutes at 350 F.

Laundering.The cotton fabrics treated with the product of Example 1 are laundered in a Laundromat washer as follows and are designated in the tables by code, i.e.

LW=0.1% neutral soap at 140 F.

at 140 F.

The synthetic or wool fabrics are laundered in a Najort reversing washer employing 0.1% neutral soap at 100 F. followed by rinsing and drying.

Agar difiujsz'on test method.Bacterial inhibition tests are made on treated fabrics by the following method.

Discs (11.5 mm.) of the treated fabrics are placed on an agar plate inoculated with bacteria culture. After several hours of contact, the discs are removed and the plate incubated overnight. The activity of the compound used on the fabric discs is recorded as the diameter (in mm.) of the clear area at the site of the discs. An effective agent will show a clear area with a diameter greater than that of the disc itself (11.5 mm.).

The larger the clear area, the greater is the compounds activity. The activity under the fabric disc is also noted where there is no zone outside the area covered by the fabric. The area under the disc of the fabric is rated as follows:

Completely clear area underneath disc PAt least clear area underneath disc S-VS-Less than 75% clear area underneath disc NNo clear area The results are shown in Tables I to V. The following is an explanation of the various treatments used in Example 12 (Tables I through V).

Table I-Applications by methods A and B on cotton percale at 0.0001, 0.001, 0.01, 0.1 and 1% solids (owf.).

Table IIApplications by methods A and B on cotton percale at 0.5% solids (owfi).

Table III-Applications by methods A and C on cotton percale at 1% solids (owf.).

Table IV-Applications by methods A and B on fabrics of synthetic fibers and also wool flannel at 1% solids (owf).

Table VApplications by method B on cotton percale at 1% solids (owf) with diglycidyl ether as a creaseproofing resin in the bath.

TABLE I.N,N-BIS(S-AGETOXYMERCURI-Z-h/IETHOXYPROPYDMELAMINE ON x 80 COTTONVARIATIONS OF CONCENTRATIONS Zones of inhibition (mm.)

Percent solids E. COZZ Staph. aureus (owt) Initial 25 LW 25 LWG Initial 25 LW 25 LWC 13.2; 27.0p C; (12.0p.

14.5. VS. 12.1. N. 12.0. N. C. N. O; (12.0p.

b 215% solids (owt) tris (methosymethyl)melamine+3.5% ammonium sulfate (based on resin solids) in treating TABLE II.N,N-BIS(3-ACETOXYMEROURLZ-MEIHOXYPBOPYL)MELAMINE ON 80 x 80 COTTON Zones of inhibition (mm.) Per cent solids E. coli Staph. aureus (owl) Initial 25 LW 25 LWG Initial 25 LW 25 LWG 19.2 C; l2.0p C; 12.0p 21.1; 26.5p 12.0; 2l.5p 12.0; 19.5p. 16.6 2 6 .4 20.2; 27.7p 13.9; 22.6p 17.1.

a 5% solids (owt) tris(methoxymethyl)melamine+5% ammonium sulfate (based on resin solids) in bath.

TABLE III.-N,N-BIS(3-AGETOXYMEROURI-2-METHOXYPROPYL)MELAMINE ON 80 x 80 COTTON Zones of inhibition (mm) Percent solids E. coli Staph. aureus (owt) Initial 5 LW 5 LWC 25 LW 25 LWO Initial 5 LW 5 LWO 25 LW 25 LWC 1.0 19.4; 20.6p 13.7 13. 7 12.7 12.1 24.7; 295p--- 16.3, 25.7p 15.6; 22.0p--- 14.5; 20.0p.-. 12.9 1.0 B 18.1 15. 1 14. 1 14.0 15.7 22.8; 27.0p-.- 18.8, 24.5p 15. 18.4; 22.7 17. 3

a Topped with 5% solids (owt) tris(methoxymethyl)melamine plus 12% magnesium chloride (based on resin solids).

TABLE IV.-N,N BIS(3ACETOXYMERCURI-2-METHOX- YPROPYL)NIELAMINE ON VARIOUS FABRICS (1.0% SOLIDS OWF.)

Zones of inhibition (mm.)

Fabric used E. coli Staph. aureus Initial 25 LW Initial 25 LW Spun nylon B 19.0 P-O 25.7; 32.91)--- C.

17.2 13.7 21.6; 27.2p 14.9; 20.71). Spun acrylic fiber e 19.9 VS-P 24.8;31.0p 5-1.

14. 3 l3. 7 l4.3 14.2; 22.91). Spun polyester fiber 20.1 VS-P 25.0; 31.5p VS.

13.1 12.6 13.6 12.6; 21.5 Taffeta fil. acetate 8 13. 5 S- 22.6; 26.71)- 19.8p.

14. 13.0 14.5 12.2; 21.6p Taffeta Nylon til 1 20. 5 VS 25.6; 32.5p P.

13.0 5-0 13.0 PO; 18.7p Rayon challis B 19. 3 P-C 25.4; 30.1p C; 32.9p.

17. 9 12. 5 23.0; 28.1p 14.0; 23.61) Acrylic fiber 19. 9 O 25.5; .2 12.0; 22.7p l3. 1 12.0 13.9 12.9; 22.91) Wool 14. 2 N 18.0; 24.7 N. 14.5 N 18.0; 24.0 N.

B 5% solids (owt) tris (mcthoxymethyl)melamine+3.5% ammonium sulfate (based on resin solids) in treating bath. All fabrics washed wool/ rayon Wash=0.1% soap at 100 F.

b Uneven zone.

topping with, the creaseproofing resin imparts greater durability. Results on the various synthetic fabrics also show better durability when a creaseproofing resin is used in combination with the product of Example 1.

In a series of applications similar to those set forth in Example 9 employing the product of Example 2, good, durable zones of inhibition to E. coli are obtained by topping the fabric treated with the product of Example 2 with a creasep-roofing resin.

EXAMPLE 10 M ethylolation of N,N-Bis(3-Acetoxymercuri-Z-Methoxypropyl M elwmine A solution consisting of 7 .2 parts of N,N-bis(3-acetoxymercuri-2emethoxypropyl)melarnine (product of Example 1) in 10 0 parts of 37% aqueous formaldehyde is prepared by stirring for /2 hour at room temperature, then further diluted with water to give a final solution of 1% of the mercury compound.

Application of the 1% solution using zinc nitrate as a catalyst is made on 80 x 80 cotton fabric at 1% owf. by the previously described manner (method B, Example 12) The results are set forth below.

Zones of inhibition (mm.) Wrinkle Tensile recovery strength H E. coli S. aureus Initial 5 LW Initial 5 LW Initial 5 LW 5 LWO Initial 5 LW 5 LWO Treated 238 223 61 15. 3 12.2 12.3 19.9; 22.91) 12. 4 12. 1 Untreated 140 110 TABLE V.-N, N-Bis (3 acetoxymercuri- 2 methoxypropyDmelamine with 5% solids (owf.) diglycidyl ether on 80 x 80 cotton The results on 80 x 80 cotton percale show good durability after .25 LW or 25 LWC when 1% of product of Example 1 is used alone. However, addition of, or

TA BLE VI.MERCURATED N,ND

These results show good wrinkle recovery and durability of germicidal properties.

EXAMPLE '11 Aqueous solutions of the product of Example 7 at 5 or 15 solids (ow-f.) plus 12% solids zinc nitrate (based on resin solids) are applied to x 80 cotton percaile by padding as described in method A, Example 9.

The treated fabrics are chied for 2. minutes at 225 F. and cured for 1.5 minutes at 350 F., then washed and dried as previously described in Example 9.

Antibacterial, wrinkle resistance (Monsanto wrinkle recovery) and tensile strength (AA'ITCC) tests are obtained. Results are shown in Table VI.

I WITH ZINC NITRATE Wrinkle Zones of inhibition (mm.) Percent Percent Tensile Obs.) recovery,

solids Zn(NO3)1 degrees (owt) oi based on E. colt S. aureus compound resin solids Initial 5 LW Initial 5 LW Initial 5 LW 5 LWC Initial 5 LW 5 LWC 5 12 78 181 178 20.9 15.1 15.8 25. 6 17.9 17. 5 15 12 60 220 213 24. 2 17. 4 15. 0 29. 4 20. 5 16. 8 Untreated- 142 137 Washed in soap only. b Washed in soap plus a commercial sodium hypochlorite solution (02% available chlorine). No'rE.-Treated fabrics: dried for 2 at 225 F.; cured 1.5 at 350 F.

ALLYL-N',N,N"-TRIS(METHOXYMETHYDMELAMINE EXAMPLE 12 Polymethylol N,N-Diallylmelamine Pretreated 80 x 80 Cotton Percale A ftertreazed With Mercuric Acetate A swatch of 80 X 80 cotton percale is treated in an aqueous solution (at solids owf.) of poly-methylol N,N- diallylmelamine (approximately 3.3 moles of combined formaldehyde per mole of N,N-diallylmelamine) plus 12% (based on resin solids) of magnesium chloride. The treated fabric is dried at 225 F. for 3 minutes and cured at 350 F. for 1.5 minutes.

A portion of this fabric is then extracted with hot dimethylforrnamide for 4 hours, rinsed in water at 140 F. and air dried.

Percent N on fabric=1.17 (equivalent to 4.2% owf. of polymethylol compound).

The wrinkle recovery was 229 (W+F).

A 7.5 gram sample of the above treated fabric (containing 0.00 104 mole of compound durably fixed thereon) is heated at reflux with stirring in a solution of 264 parts of methyl alcohol, 1.05 parts of acetic acid and 1.33

parts (0.00416 mole) mercuric acetate for 27 hours.

The fabric is then Soxhlet extracted with methanol for 24 hours and air dried.

Percent N on tabric=1. 13.

The wrinkle recovery was 212 (W-i-F).

The treated fabric is washed for 25 cycles in a Laundromat washer and then dried.

(-An untreated swatch 80 x 80 cotton is also subjected to the mercuric acetate treatment only).

Test results are shown in Table VI-I.

TABLE VII.80 x 80 COTTON PERGALE PRETREATED WITH POLYMETHYLOL DIALLYLMELAMINE, THEN AFTERTREATED WITH MIERCURIC ACETATE Zones of inhibition (mm.) Percent Treatments Washes Hg on Fabric E. 0022' S. aureus Fabric pretreated with polymethylol None 16.9 21.6; 23.01)" 5 3. 21 diallyl melamine, 25 LW 14.6 18.9; 21.3p aftertreated with 25 LWO Not runmercuric acetate. Fabric treated Nonc 12.4 13.1 0. 04 with mercuric 25 LW 12.0 acetate only. 25 LWC Not run 1 Theory on basis of nitrogen analysis=5.28% Hg.

It will be apparent that the compositions of this invention may be employed in combination with other textile finishing agents, auxiliaries and assistants, as for example, lubricants, dyes, antistatic agents and the like insofar as these materials do not diminish the antibacterial effects sought to be achieved thereby.

We claim:

1. Mercurated allyl amino-s-triazines having the following formula:

14 in which R is (|)Rs OIL-([j-OHfilgX and R is selected from the group consisting of hydrogen, lower alkyl, -CH CH=CH 0 R5 CHg-?OH;HgX

and -CH OR and where R -R are selected from the group consisting of hydrogen, CH2OR7, lower alkyl and phenyl, and at least two of the members R R and R on difierent amino nitrogens, is CH OR R R and R are selected from the group consisting of hydrogen and lower alkyl, and X is an anionic radical.

2. A compound of the formula where R -R are selected from the group consisting of hydrogen and CH OR and where at least two of the members R 42 on different amino nitrogens are CH OR where R is selected from the group consisting of hydrogen and lower alkyl.

3. A compound of the formula where R R are selected from the group consisting of hydrogen and CH OR and where at least two of the members R R on diflerent amino nitrogens are CH OR where R is selected from the group consisting of hydrogen and lower alkyl.

4. A compound of the formula where il -R are selected from the group consisting of hydrogen and --CH OR and where at least two of the members R R on different amino nitrogens are CH OR where R is selected from the group consisting of hydrogen and lower alkyl.

5. A compound of the formula where R R are selected from the group consisting of hydrogen and CH OR and where at least two of the members R R on different amino nitrogens are -CH OR where R is selected from the group consisting of hydrogen and lower alkyl.

1 5 6. A compound of the formula OCH; ll 1 where R R are selected from the group consisting of 10 hydrogen and CH OR and where at least two of the members R R on different amino nitrogens are --CH OR where R-, is selected from the group consisting of hydrogen and lower alkyl.

7. A compound of the formula where R -R are selected from the group consisting of 5 hydrogen and -CH2OR7 and where at least two of the members Il -R on different amino nitrogens are 16 CH OR where R is selected from the group consisting of hydrogen and lower alkyl. 8. A compound of the formula where R -R are selected from the group consisting of hydrogen and CH OR and where at least two of the members R R on difierent amino nitrogens are CH OR where R, is selected from the group consisting of hydrogen and lower alkyl.

References Cited in the file of this patent UNITED STATES PATENTS UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No, 3,130,193 April 21, 1964 John T, Shaw et alo It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.

Column 9, line 5, for "Hg, 42,4," read Hg, 42,4; N, 14.9, columns 9 and 10, TABLE II in the footnote, for "5% ammonium sulfate" read 35% ammonium sulfate column 11, TABLE V, fourth column, for "20926.5" read 2l 9;26.5

Signed and sealed this 4th day of August 1964.

(SEAL) Attest:

ERNEST W. SWIDER EDWARD J. BRENNER Aitesting Officer Commissioner of Patents

Claims

1. MERCURATED ALLYL AMINO-S-TRIAZINES HAVING THE FOLLOWING FORMULA