There are many demanding performance requirements for dyes and inks used in IJP. For example they desirably provide sharp, non-feathered images having good water-fastness, light-fastness and optical density. The inks are often required to dry quickly when applied to a substrate to prevent smudging, but they should not form a crust over the tip of an ink jet nozzle because this will stop the printer from working. The inks should also be stable to storage over time without decomposing or forming a precipitate which could block the fine nozzle.

According to the present invention there is provided a compound of Formula (1) and salts thereof: Formula (1) wherein: B'and B2 are each independently-S03H,-COOH,-CF3, optionally substituted alkoxy, optionally substituted alkyl or-P03H2; Q is an organic linking group; R'and R2 are each independently H or optionally substituted alkyl; each A independently is N, C-CI, C-CN or C-N02; Z'and Z2 are each independently-SR3,-OR4,-NRSR6 or halogen;

R3, R4, R'& R'are each independently H, optionally substituted alkyl, optionally substituted aryl or optionally substituted aralkyl; or Rs and R6 together with the nitrogen to which they are attached form an optionally substituted five or six membered ring; provided that Q is not of the formula: B1 and B2 are preferably attached ortho to the azo group. It is also preferred that B2B1and are each -COOH,-CF3,optionallysubstitutedC1-4-alkoxy,-SO3H, optionally substituted C1-4-alkyl or -PO3H2, more preferably-S03H,-COOH or-CF3 and especially-S03H. When B'or B2 is substituted, the substituent (s) is/are preferably selected -SO3H,-COOH,-NH2,C1-4-hydroxyalkyl,C1-4-hydroxyalkoxyand-OH, C1-4-alkoxy.

Preferably each A is N.

Preferably R'and R2 are each independently H or optionally substituted C1 4-alkyl, more preferably H or C14-alkyl optionally substituted by hydroxy, carboxy, sulpho or cyano. It is especially preferred that R'and R2 are methyl or H, more especially H.

The organic linking group Q is preferably an optionally substituted piperazinylene group, or a group of the formula-X'-L-X2-wherein X'and X2 are each independently an optionally substituted piperazinylene group,-S-,-O-or-NR7-wherein R7 is H, optionally substituted alkyl or optionally substituted aryl, and L is a divalent organic linking group.

Preferably R'is H, C1-4-alkyl or -C1-4-hydroxyalkyl, more preferably H or methyl, especially H.

Preferred divalent organic linking groups represented by L are alkylene, preferably C120-alkylene, more preferably C2-10-alkylene, each of which is optionally interrupted; alkenylene, preferably C26-alkenylene; arylene, preferably arylene containing up to ten carbon atoms, more preferably phenylene or naphthylene, especially 1,3- or aralkylene, more preferably C7-10-aralkylene, especially phenylene-C1 6-alkylene more especially-phenylene-CH2- ; and two arylene groups joined together either directly or through a vinyl, oxygen, nitrogen or sulphur link; each of the above divalent organic linking groups may be substituted or unsubstituted.

The optional substituent (s) on L are preferably selected from alkyl optionally substituted by hydroxy, carboxy or sulpho, preferably hydroxy-C1-4-alkyl, carboxy-C1-4-alkyl or sulpho-C, 4-alkyl; alkoxy, preferably C,-4-alkoxy and especially methoxy; phenyl optionally substituted by C1-4 alkyl, carboxy, hydroxy, sulpho, amino or nitro; halo, preferably F or Cl;-S03H ;-COOH;-OH;-CN; or-N02.

When L is an alkylene group it is preferably C2_, o-alkylene optionally interrupted by -0- ;-S- ; optionally substituted arylene, especially optionally substituted phenylene ; -NR8-;

-C (O)- ;-CO (O)- ; or an optionally substituted piperazinylene group, wherein Rs is H, C14-alkyl, or-C14-hydroxyalkyl, more preferably H. When the interrupting group is a substituted piperazinylene group it is preferably substituted by C1 6-alkyl optionally substituted by hydroxy, carboxy or sulpho.

An especially preferred interrupted alkylene group is of the formula: R9 - (C-0-alkylene)-N N- (C-alkylene)- R1e R wherein: R9 and R'° each independently is H or C1 4-alkyl optionally substituted by hydroxy, sulpho or carboxy.

Preferably R9 and R'° are H.

Examples of optionally substituted alkylene and alkenylene groups represented by L include: ethylene; 1,2- & 1-, & 2-phenyl-1,3-propylene; 1,4-, 2,3- and 2-methyl-1,3-propylene; 2- (4'-sulphophenyl)-1, 3-propylene; 2-methyl-2,4-pentylene; ; 1-chloro-2,3-propylene; 1,6-& 1-carboxy-ethylene 1-carboxy-1,5-pentylene; 3-methyl-1, 6-hexylene ;-CH2CH=CHCH2-and 1- (methoxycarbonyl)-1, 5-pentylene.

Examples of optionally interrupted alkylene groups represented by L include -(CH2)3O(CH2)2O(CH2)2OCH2OCH2-;-CH2NHCH2-;-CH2CH2OCH2CH2-; -CH2CH2SCH2CH2-; o-, m-and p-xylylene and -C2H4-N # N-C2H4- A preferred aralkyl group represented by L is of the Formula (2): (C,. 6-alkylene)- L (R11) y Formula (2) wherein: each R"independentiy is H, C1-4-alkoxy, F, CI,-S03H,-COOH,-OH,-CN,-NO2 or C1 4-alkyl optionally substituted by-OH,-COOH or-SO3H; and

y is 1 to 4.

Preferably y is 1,2 or 3, more preferably 1.

We have found that compounds wherein L is of the Formula (2) exhibit a high solubility in aqueous media and when incorporated into an ink, the ink exhibits very good operability in ink jet printers.

Examples of preferred arylene and aralkylene groups include-C6H4-CH2-, -C6H4-CH2CH2-, 1,2-, 1,3- and 1,4-phenylene and 1,4-naphthylene.

When L is two arylene groups joined together directly it is preferably an optionally substituted biphenylene group, more preferably optionally substituted 4,4'-biphenylene.

When L is a two arylene groups joined by a divalent linking group it is preferably two of the hereinbefore defined arylene groups (especially optionally substituted phenylene) joined together by a linking group selected from-0-,-S-,-NR°-,-CH=CH-and C26-alkylene optionally interrupted by-O-,-S-or-NR8-, wherein R8 is as hereinbefore defined. Examples of two arylene groups joined by a divalent linking group include diphen-4,4'-ylene-methane,-C6H4-CH2CH2-C6H4-,-C6H4-CH=CH-C6H 4-,-C6H4-O-C6H4-, -C6H4-S-C6H4-and-C6H4-NHCH2-C6H4-.

When Q, X1 or X2 is an optionally substituted piperazinylene group it is preferably of the Formula (3): Formula (3) wherein R9 and R'° are each independently as hereinbefore defined.

Where one or both of X'and X2 is an optionally substituted piperazinylene group, Q (i. e. the group X'LX2-) is preferably one of the following formulae: /\N (C, 6-alkyleneF NR7 or -N N- (C alkylene- wherein R'is as hereinbefore defined.

In a preferred embodiment Q is an optionally substituted piperazinylene group or Q is a group of the formula-X'-L-X2-wherein X'and x2 are each independently selected from optionally substituted piperazinylene,-S-or-NR'-wherein R'is as hereinbefore defined; and L is a group of Formula (2), 1,3-phenylene, or C2 6-alkylene optionally interrupted by-O-,-S-, phenylene,-NR8-,-C (O)-,-CO (O)- or an optionally substituted

piperazinylene group, wherein R8 is as hereinbefore defined. In this embodiment preferred optionally substituted piperazinylene groups are of Formula (3).

When R3, R4, Rs, R6 or R7 is optionally substituted alkyl it is preferably optionally substituted C1 20-alkyl, more preferably optionally substituted C1-10-alkyl and especially optionally substituted C1-6-alkyl. Preferred optional substituents include hydroxy, carboxy, sulpho,-P03H2, cyano, a 5 or 6 membered heterocyclic group and optionally substituted amino. Preferred 5 or 6 membered heterocyclic groups are optionally substituted furanyl and tetrahydrofuranyl, more preferably furanyl and tetrahydrofuranyl optionally substituted byby-COOH -SO3H.

Preferred optionally substituted amino groups which may be present on the alkyl groups represented by R3, R4, Rs and Rs are of the formula-NRaRb wherein Ra and Rb are each independently H; alkyl, more preferably C1-6-alkyl, especially C1-4-alkyl, more especially methyl, ethyl, n-propyl or iso-propyl;-CO (alkyl), preferably-CO (C1-6-alkyl), more preferably-CO (C14-alkyl), especially-COCH3,-COCH2CH3 and-COCH2CH2CH3 ; -C1-6hydroxyalkyl ; or Ra and Rb together with the nitrogen to which they are attached form an optionally substituted morpholine, piperazine, pyrrolidine or piperidine ring.

When-NRaRb is a substituted morpholine or piperazine ring it preferably carries a substituent of the formula-M-NR'2R'3 wherein M is an alkylene linking group and R12 and R'3 each independently is H or C, 6-alkyl optionally substituted by hydroxy, C1-6-alkoxy or carboxy. M is preferably C1 6-alkylene, more preferably C2 6-alkylene and especially -(CH2)g-, where g is from 2 to 6.

A preferred substituted piperazinyl group represented by-NRaRb is of the formula: wherein M, R12 and R13 are as hereinbefore defined.

Especially preferred substituted piperazinyl groups represented by-NRaRb are of the formula: N N (c14-alkylene) NH2 N N (c14-alkylene) NH (C,-alkyl) ans A further preferred optionally substituted alkyl group represented by R3, R4, R R6 or R7 is of the Formula (4): -(CaH2aO)p(CbH2bO)qR14 Formula (4)

wherein: R'4 is H or alkyl; a and b are different and from 1 to 6; p is from 1 to 4; and q is from 0 to 3.

Preferably R'4 is H or C1 4-alkyl, more preferably H.

Preferably a and b are each independently 2 to 6, more preferably 2 or 3. p is preferably 1 or 2. Preferably q is 0.

Preferred groups of the Formula (4) are of the formula -(C2-6-alkylene)O(C2-6-alkylene)OH.Examples-(C1-6-alkylene)O (C1-6-alkylene)OC1-4alkylor of such groups include -C2H4OC2H4OH, -C2H4OC2H4OCH3, -CH2CH(CH3)CH2OC2H4OH and -C3H60C2H40H.

When R3, R4, RS, R6 or R'is optionally substituted aryl it is preferably optionally substituted phenyl or naphthyl, more preferably optionally substituted phenyl. Preferred optional substituents are C1 6-alkoxy, C, 6-alkyl, C, 6-alkyl substituted by hydroxy, carboxy or sulpho, halogen (preferably F or CI), hydroxy, cyano, carboxy, sulpho,-P03H2, nitro, -NHCOC1-4-alkyl,-SO2NH2and-SO2NHCOC1-4-alkyl.Moreamino,-COC1 -4-alkyl, preferably the optionally substituted aryl group is of the formula: wherein: R's is C14-alkyl, C, 4-alkoxy, halogen, carboxy, sulpho or -PO3H2 ; and t isOto5. t is preferably 0,1 or 2.

When R3, R4, Rs or R6 is optionally substituted aralkyl it is preferably of the formula: -- (C_6 alkylene) (Rl5), wherein R"and t are as hereinbefore defined.

When R'and R'together with the nitrogen to which they are attached form an optionally substituted 5 or 6 membered ring it is preferably an optionally substituted piperidine, piperazine, pyrrolidine or morpholine ring, more preferably optionally substituted piperazine or morpholine. The optional substituents are preferably selected from hydroxy, carboxy, sulpho, C1-6-alkoxy, C1-6-alkyl and C1 6-alkyl substituted by hydroxy, carboxy, sulpho and optionally substituted amino as hereinbefore defined. An especially preferred optional substituent is-M-NR'2R'3 wherein R12 and R'3 are as hereinbefore defined.

It is especially preferred that R7 is H or C1-4-alkyl optionally substituted by hydroxy, carboxy or sulpho.

R4 is preferably H or C1 4-alkyl.

The compound of Formula (1) preferably contains only two azo groups (-N=N-).

The preferred halogen represented by Z'and/or Z2 is chlorine. It is however, preferred that Z'and Z2 are, each independently,-SR3,-OR4 or-NR5R6, more preferably -SR3 or-NR5R6, and especially-SR3 or-NHR', wherein R3, R4, R5 and R6 are as hereinbefore defined.

In view of the foregoing preferences with respect to Formula (1), preferred compounds of the first aspect of the present invention are of Formula (5) and salts thereof: Formula (5) wherein: X3 and X4 are each independently an optionally substituted piperazinylene group,-S- or-NR'-;<BR> L2 is group of the Formula (2) as hereinbefore defined, or C210-alkylene optionally interrupted by-O-,-S-, phenylene, -NR8-, -C(O)-, -CO(O)- or by an optionally substituted piperazinylene group; or -X3L2X4-forms an optionally substituted piperazinylene group; and B', B2, z1, Z2, R7 and R8 are as hereinbefore defined.

The optionally substituted piperazinylene groups referred to in the definitions of X3,<BR> X4, L2 and-X3L2X4-are preferably of Formula (3), as hereinbefore defined.

In a preferred compound of Formula (5) Z'= Z'= halogen (especially CI), L'is C-2-6-alkylene (especially propylene), X3=X4= NH and B'= B2=-S03H.

The compounds of Formula (5) exhibit a high solubility in aqueous media and provide prints which exhibit high light-fastness and water-fastness when incorporated into inks for ink jet printing.

A particularly preferred embodiment of the present invention comprises a compound of Formula (5) and salts thereof wherein : X4areeachindependently-NR7-or-S-;X3and Z'and Z2 are each independently-SR's or-NR"R'e; R16 and R17 are each independently a group of the formula C1-6-alkyloptionallysubstiutedby-(C1-6-alkylene)O(C1-6-alkyl ene)OR19or C1-4-alkoxy, hydroxy, carboxy, sulpho, tetrahydrofuryl, morpholinyl or a group of the -NR19CO(C1-4-alkyl); R'9 is H or C1-4-alkyl ; R7 and R18 are independently H or C1 4-alkyl optionally substituted by hydroxy, carboxy or sulpho; B1 and B2 are sulpho; and <BR> <BR> <BR> L2 is as hereinbefore defined.<BR> <BR> <BR> <BR> <BR> <BR> <BR> <P> Preferably L2 is C210-alkylene optionally interrupted by-NR8-wherein R"is as hereinbefore defined, more preferably L2 is C2 4-alklene, and especially propylene.

For ease of synthesis B1 and B2 are preferably the same and Z'and Z2 are preferably the same.

An especially preferred embodiment of the present invention comprises a compound of the Formula (6) and salts thereof: Formula (6) wherein: a) both groups represented by Z are-NHCH2CH20H; or b) both groups represented by Z are Cl; or c) one group represented by Z is Cl and the other is -NHCH2CH2OH.

We have found that mixtures comprising two or more compounds of Formula (1), <BR> <BR> <BR> especially those in which the compounds contain different values for Z'and Z2 between the compounds of Formula (1), are particularly suitable for use in ink jet printing inks.

Accordingly, a second aspect of the present invention provides a composition comprising: (a) from 1 to 99 parts of a compound of the Formula (1) as defined in the first aspect of the present invention, provided that Z'and Z2 are each independently-SR3, -OR4 or-NRSR6; (b) from 0 to 50 parts of a compound of the Formula (1) as defined in the first aspect of the present invention, provided that one of Z'and Z2 is a labile atom or group and the other is-SR3,-OR4 or-NR5R6; and (c) from 1 to 99 parts of a compound of the Formula (1) as defined in the first aspect of the present invention, provided that Z'and Z2 are both a labile atom or group; wherein R3, R4, R'and R'are as hereinbefore defined and all parts are by weight and the total number of parts of (a) + (b) + (c) = 100.

The number of parts of component (a) is preferably from 20 to 80, more preferably 40 to 60. The number of parts of component (b) is preferably from 5 to 45 more preferably from 15 to 40. The number of parts of component (c) is preferably from 2 to 60, more preferably from 5 to 30 and especially from 10 to 30.

When Z'and/or Z2 is a labile atom or group, it is preferably an atom or group which is displaceable by a hydroxyl group of cellulose under mildly alkaline aqueous conditions to form a covalent bond between the compound of the Formula (1) and cellulose.

Preferred labile atoms and groups which may be represented by Z'and/or Z2 in the second aspect of the invention include halogen atoms, such as F or Cl; sulphonic acid groups; thiocyano groups; quaternary ammonium groups, for example trialkylammonium groups and optionally substituted pyridinium groups, for example 3-and 4-carboxy pyridinium groups. An especially preferred labile atom is Cl.

Preferably in component (a) Z'and Z2 are identical. In component (c) Z'and Z2 are preferably identical.

More preferably in component (a) Z'and Z2 are identical; in component (c) Z'and Z2 are identical (a); and in component (b) Z'is identical to Z'and Z2 in component (a) and Z2 is identical to Z'and Z2 in component (c).

In preferred compositions according to the second aspect of the invention the compounds of the Formula (1) are of the Formula (5), or more preferably Formula (6) as hereinbefore defined.

The compositions of this second aspect have the attractive shade good light-fastness, good freeze-thaw properties, high stability at elevated temperatures and

other properties of the compounds according to the first aspect of the invention, but they also benefit from greater solubility in ink media. This allows strongly coloured, storage stable inks to be prepared giving prints of high optical density. Surprisingly, wet-fastness is not adversely affected even though the compositions have high solubility in aqueous ink media.

An especially preferred composition comprises: (a) from 40 to 60 parts of a compound of the Formula (5) or a salt thereof wherein Z' and Z2 are the same and of the formula-NHR"wherein R"is as hereinbefore defined (preferably Cl-6-alkyl optionally substituted by-OH,-SO3H,-COOH or tetrahydrofuryl); (b) from 5 to 45 parts of a compound of the Formula (5) or a salt thereof wherein Z' is Cl and Z2 is the same as Z2 in component (a); and (c) from 10 to 30 parts of a compound of Formula (5) or a salt thereof wherein Z'and <BR> <BR> <BR> Z2 are Cl;<BR> <BR> <BR> <BR> <BR> <BR> wherein in Formula (5) B'and B2 are-SO3H; L2 ils the same in each of components (a), (b) and (c) and is C2 4-alkylene; X3 and X4 are NH; and all parts are by weight and the sum of the parts (a) + (b) + (c) = 100.

In this especially preferred composition the compound of the Formula (5) is preferably of the Formula (6) as hereinbefore defined.

The compounds of the invention may be in the free acid or salt form. Preferred salts are water-soluble, for example alkali metal salts, especially lithium, sodium and potassium salts, ammonium and substituted ammonium salts. Especially preferred salts are salts with sodium, ammonia and volatile amines. The dyes may be converted into a salt using known techniques. For example, an alkali metal salt of a dye may be converted into a salt with ammonia or an amine by dissolving an alkali metal salt of the dye in water, acidifying with a mineral acid and adjusting the pH of the solution to pH 9 to 9.5 with ammonia or the amine and removing the alkali metal cations by dialysis, reverse osmosis or ultrafiltration.

The compounds and composition according to the present invention may be, and preferably are, purified to remove undesirable impurities before they are incorporated into inks for ink jet printing. Conventional techniques may be employed for purifying the dyes, for example ultrafiltration, reverse osmosis and/or dialysis.

The compounds of the invention may be prepared using conventional techniques for the preparation of azo dyes. For example a suitable method comprises condensing a compound of the Formula HQH with approximately 2 molar equivalents of a compound of the Formula (7):

Formula (7) wherein Q, B, R'and Z'are as hereinbefore defined.

The compound HQH is preferably of the formula HX'LX2H wherein X', x2 and L are as hereinbefore defined.

The condensation is preferably performed in a liquid medium, more preferably an aqueous medium and especially water. Temperatures of 15°C to 100°C are preferred, more preferably from 30 to 40°C. The reaction time is preferably from 1 to 48 hours, more preferably from 3 to 24 hours.

The condensation is preferably performed in the presence of a base. The base may be any inorganic base for example, ammonia, an alkali metal or alkali earth metal hydroxide, carbonate or bicarbonate, or an organic base. Preferred organic bases are tertiary amines for example, N-alkylated heterocycles, for example <BR> <BR> <BR> <BR> N-(C14-alkyl)-morpholine, N-(C1 4-alkyl)(C14-alkyl)-morpholine, N-(C1 4-alkyl) piperidine, N, N'-di (C1 4-alkyl) piperazine; tri (C1 4-alkyl) amines, for example triethylamine, and optionally substituted pyridines, especially pyridine.

The amount of base used may be varied between wide limits but it is preferred to use less than 40, more preferably less than 10 and especially from 3 to 5 moles for each mole of the compound of Formula (7).

After the condensation the product may be isolated by precipitating the product as a salt from the reaction mixture for example by the addition of a suitable alkali metal salt, especially sodium chloride. Alternatively, the product may be isolated in its free acid form by acidifying the reaction mixture, preferably using a mineral acid, especially hydrochloric acid. Where the product precipitates as a solid it may be separated from the mixture by filtration.

If desired unwanted anions may be removed from the product of the above process by dialysis, osmosis, ultrafiltration or a combination thereof.

The product of the above process may be converted, if desired, to the NH4+, quaternary ammonium or organic amine salt by the addition of ammonia, ammonium hydroxide, primary, secondary, tertiary or quaternary amine. When the base used in the condensation process is an organic amine an excess may be used so that the compound of Formula (1) is formed as the organic amine salt.

The compound of the Formula (7) may be prepared using conventional techniques, for example by: (1) diazotising a compound of the Formula (8) to give the corresponding diazonium salt:

Formula (8) wherein R'and B'is as hereinbefore defined; (2) coupling the diazonium salt from stage (1) with 2-amino-8-naphthol-6-sulphonic acid at a pH < 7, preferably at a pH of from 3 to 5; Formula (9) (4) condensing the product from stage (3) with approximately 1 molar equivalent of the compound of the formula: wherein A is as hereinbefore defined; and (5) condensing the product from stage (4) with approximately 1 molar equivalent of the compound of the formula Z'H.

The diazotisation in stage (1) is preferably performed in an aqueous medium at a pH below 7 in the presence of a suitable diazotisation agent. Dilute mineral acid, e. g. HCI or H2SO4, is preferably used to achieve the desired acidic conditions. Conveniently the diazotisation agent is formed in-situ, for example by dissolving an alkali metal nitrite, preferably sodium nitrite, in a molar excess of mineral acid, preferably HCI. Normally at least one mole of diazotisation agent per mole of the compound of Formula (8), preferably from 1 to 1.25 moles will be used in the diazotisation.

The temperature of the diazotisation is not critical and may conveniently be carried out at from-5°C to 20°C, preferably from 0 to 10°C and especially from 0 to 5°C.

The hydrolysis in stage (3) is preferably performed at a pH of from 9 to 14. The temperature during hydrolysis is preferably 40 to 90°C.

When B'and B2, R'and R2 or Z'and Z2 are different, the compounds of Formula (1) are preferably prepared by condensing a compound of the Formula (7) with an approximately equimolar quantity of the compound of the formula HQH (preferably HX'LX2H). The product of this reaction is then further condensed with an approximately equimolar quantity of a compound of the Formula (7) wherein R'is Rz, B'is B2 and Z'is Z2 as hereinbefore defined.

Alternatively, a compound of Formula (1) or Formula (5) in which one or both of Z'and Z2 are other than halogen, may be prepared by condensing a compound of <BR> <BR> <BR> Formula (1) or Formula (5), in which Z'= Z2 = Ci, with sufficient of a compound or compounds Z'H and/or Z2 H, wherein Z'and Z2 are as hereinbefore defined except for Cl, under such conditions of temperature and/or time as to replace one or both Cl atoms.

The compositions according to the second aspect of the invention comprising components (a) and (c) can be prepared by mixing together the two components prepared as hereinbefore described. When the composition according to the second aspect of the invention comprises components (a), (b) and (c) it is preferably prepared by reacting the compound of Formula (7) in which both Z'and Z2 are Cl with insufficient of the compound Z'H (in which Z'is not Cl) and/or under such temperature and/or temperature conditions as not to replace all the Cl atoms in the compound of Formula (7) to give a mixture of non-reacted, mono-and di-reacted products.

The compounds of Formula (1) may exist in tautomeric forms other than those shown in this specification. These tautomers are included within the scope of the present claims.

According to a third aspect of the present invention there is provided an ink comprising: (a) from 0.01 to 30 parts in total of one or more compounds of the Formula (1), as hereinbefore defined, with the proviso that Z'and/or Z2 may also be a labile atom or group; and (b) from 70 to 99.99 parts of a medium comprising a mixture of water and an organic solvent, an organic solvent free from water, or a low melting point solid; wherein all parts are by weight and the number of parts of (a) + (b) =100.

Preferred labile atoms and groups which may be represented by Z'and/or Z2 are as hereinbefore defined in the second aspect of the present invention, especially chloro.

When component (a) of the ink is a mixture of more than one compound of Formula (1) or (5) it is preferably from 2 to 8, more preferably 2 or 3, especially 3 compounds of Formula (1) as defined in the second aspect of the present invention, and

more especially is a two or three component mixture as hereinbefore defined in relation to the second aspect of the present invention.

In the inks according to the third aspect of the present invention component (a) of the ink is preferably a compound of the Formula (5), more preferably of the Formula (6), as hereinbefore defined in relation to the first aspect of the invention. It is especially preferred that component (a) of the ink is a composition according to the second aspect of the present invention.

The number of parts of component (a) is preferably from 0.1 to 20, more preferably from 0.5 to 15, and especially from 1 to 5 parts. The number of parts of component (b) is preferably from 99.9 to 80, more preferably from 99.5 to 85, especially from 99 to 95 parts.

When the medium is a mixture of water and an organic solvent or an organic solvent free from water, preferably component (a) is completely dissolved in component (b). Preferably component (a) has a solubility in component (b) at 20°C of at least 10%.

This allows the preparation of concentrates which may be used to prepare more dilute inks and reduces the chance of the dye precipitating if evaporation of the liquid medium occurs during storage.

When the medium comprises a mixture of water and an organic solvent, the weight ratio of water to organic solvent is preferably from 99: 1 to 1: 99, more preferably from 99: 1 to 50: 50 and especially from 95: 5 to 80: 20.

It is preferred that the organic solvent present in the mixture of water and organic solvent is a water-miscible organic solvent or a mixture of such solvents. Preferred water-miscible organic solvents include C1 6-alkanols, preferably methanol, ethanol, n-propanol, isopropanol, n-butanol, sec-butanol, tert-butanol, n-pentanol, cyclopentanol and cyclohexanol; linear amides, preferably dimethylformamide or dimethylacetamide; ketones and ketone-alcohols, preferably acetone, methyl ether ketone, cyclohexanone and diacetone alcohol; water-miscible ethers, preferably tetrahydrofuran and dioxane; diols, preferably diols having from 2 to 12 carbon atoms, for example pentane-1,5-diol, ethylene glycol, propylene glycol, butylene glycol, pentylene glycol, hexylene glycol and thiodiglycol and oligo-and poly-alkyleneglycols, preferably diethylene glycol, triethylene glycol, polyethylene glycol and polypropylene glycol; triols, preferably glycerol and mono-C14-alkyl ethers of diols, preferably mono-C14-alkyl ethers of diols having 2 to 12 carbon atoms, especially 2-methoxyethanol, 2- (2-methoxyethoxy) ethanol, 2- (2-ethoxyethoxy)-ethanol, 2- [2- (2-methoxyethoxy) ethoxy] ethanol, 2- [2- (2-ethoxyethoxy)-ethoxy]-ethanol and ethyleneglycol monoallylether; cyclic amides, preferably 2-pyrrolidone, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, caprolactam and cyclic esters, preferably caprolactone; sulphoxides, preferably dimethyl sulphoxide and sulpholane. Preferably the liquid medium comprises water and 2 or more, especially from 2 to 8, water-soluble organic solvents.

Especially preferred water-soluble organic solvents are cyclic amides, especially 2-pyrrolidone, N-methyl-pyrrolidone and N-ethyl-pyrrolidone; diols, especially 1,5-pentane diol, ethyleneglycol, thiodiglycol, diethyleneglycol and triethyleneglycol; and mono-C, <BR> <BR> <BR> and C14-alkyl ethers of diols, more preferably mono-C1 4-alkyl ethers of diols having 2 to 12 carbon atoms, especially 2-methoxy-2-ethoxy-2-ethoxyethanol.

A preferred medium comprises: (a) from 75 to 95 parts water; and (b) from 25 to 5 parts in total of one or more solvents selected from diethylene glycol, 2-pyrrolidone, thiodiglycol, N-methylpyrrolidone, cyclohexanol, caprolactone, caprolactam and pentane-1,5-diol; wherein the parts are by weight and the sum of the parts (a) and (b) = 100.

Examples of further suitable ink media comprising a mixture of water and one or more organic solvents are described in US 4,963,189, US 4,703,113, US 4,626,284, EP 425,150A and US 5,207,824.

When the liquid medium comprises an organic solvent free from water, (i. e. less than 1% water by weight) the solvent preferably has a boiling point of from 30° to 200°C, more preferably of from 40° to 150°C, especially from 50 to 125°C. The organic solvent may be water-immiscible, water-miscible or a mixture of such solvents. Preferred water-miscible organic solvents are any of the hereinbefore described water-miscible organic solvents and mixtures thereof. Preferred water-immiscible solvents include, for example, aliphatic hydrocarbons; esters, preferably ethyl acetate; chlorinated hydrocarbons, preferably CH2CI2; and ethers, preferably diethyl ether; and mixtures thereof.

When the liquid medium comprises a water-immiscible organic solvent, preferably a polar solvent is included because this enhances solubility of the dye in the liquid medium. Examples of polar solvents include C14-alcohols. In view of the foregoing preferences it is especially preferred that where the liquid medium is an organic solvent free from water it comprises a ketone (especially methyl ethyl ketone) &/or an alcohol (especially a C1 4-alkanol, for example ethanol or propanol).

The organic solvent free from water may be a single organic solvent or a mixture of two or more organic solvents. It is preferred that when the medium is an organic solvent free from water it is a mixture of 2 to 5 different organic solvents. This allows a medium to be selected which gives good control over the drying characteristics and storage stability of the ink.

Ink media comprising an organic solvent free from water are particularly useful where fast drying times are required and particularly when printing onto hydrophobic and non-absorbent substrates, for example plastics, metal and glass.

Preferred low melting solid media have a melting point in the range from 60°C to 125°C. Suitable low melting point solids include long chain fatty acids or alcools, preferably those with Cil-24 chains, and sulphonamides. The dye of Formula (5) may be dissolved in the low melting point solid or may be finely dispersed in it.

The dyes according to the present invention exhibit a high solubility in aqueous media, accordingly it is preferred that the liquid medium is a mixture of water and one or more water miscible organic solvent (s).

The ink and composition may also contain addition components conventionally used in ink jet printing inks, for example viscosity and surface tension modifiers, corrosion inhibitors, biocides, kogation reducing additives, anti-cockle agents to reduce paper curling and surfactants which may be ionic or non-ionic.

When the inks according to the third aspect of the invention are used as ink jet printing inks, the ink preferably has a concentration of less than 100 parts per million, more preferably less than 50 parts per million, in total of halide ions and divalent and trivalent metals. This reduces nozzle blockage in ink jet printing heads, particularly in thermal ink jet printers.

A fourth aspect of the present invention provides a process for printing an image on a substrate comprising applying thereto an ink containing a compound or a composition according to the first or second aspect of the invention by means of an ink jet printer.

The ink used in this process is preferably as defined in the third aspect of the present invention, especially where component (a) is a composition according to the second aspect of the present invention.

The ink jet printer preferably applies the ink to the substrate in the form of droplets which are ejected through a small orifice onto the substrate. Preferred ink jet printers are piezoelectric ink jet printers and thermal ink jet printers. in thermal ink jet printers, programmed pulses of heat are applied to the ink in a reservoir by means of a resistor adjacent to the orifice, thereby causing the ink to be ejected in the form of small droplets directed towards the substrate during relative movement between the substrate and the orifice. In piezoelectric ink jet printers the oscillation of a small crystal causes ejection of the ink from the orifice.

The substrate is preferably paper, plastic, a textile, metal or glass, more preferably paper, an overhead projector slide or a textile material, especially paper.

Preferred papers are plain or treated papers which may have an acid, alkaline or neutral character. Examples of commercially available treated papers include HP Premium Coated Paper (available from Hewlett Packard Inc), HP Photopaper (available from Hewlett Packard Inc), Stylus Pro 720 dpi Coated Paper, Epson Photo Quality Glossy Film (available from Seiko Epson Corp.), Epson Photo Quality Glossy Paper (available from Seiko Epson Corp.), Canon HR 101 High Resolution Paper (available from Canon),

Canon GP 201 Glossy Paper (available from Canon), and Canon HG 101 High Gloss Film (available from Canon).

A fifth aspect of the present invention provides a substrate, preferably a paper, an overhead projector slide or a textile material, printed with an ink according to the third aspect of the present invention or by means of the process according to the fourth aspect of the present invention, or coated with a compound according to the first aspect of the present invention or a composition according to the second aspect of the present invention.

When the substrate is a textile material the ink according to the third aspect of the present invention preferably contains one or more compounds according to the first aspect or compositions according to the second aspect having at least one, and more preferably two, labile group or atom. Such an ink is preferably applied to the textile material by an ink jet printer followed by heating the printed textile material at a temperature of from 50°C to 250°C.

Preferred textile materials are natural, synthetic and semi-synthetic materials.

Examples of preferred natural textile materials include wool, silk, hair and cellulosic materials, particularly cotton, jute, hemp, flax and linen. Examples of preferred synthetic and semi-synthetic materials include polyamides, polyesters, polyacrylonitriles and polyurethanes.

The textile material is preferably pre-treated with an aqueous pre-treatment composition comprising a thickening agent and optionally a water-soluble base and a hydrotropic agent and dried prior to applying the ink. The pre-treatment composition preferably comprises a solution of the base and the hydrotropic agent in water containing the thickening agent. Particularly preferred pre-treatment compositions are described in EP 534,660A.

According to a sixth aspect of the present invention there is provided an ink jet printer cartridge containing an ink, characterised in that the ink contains a compound of the Formula (1) as defined in the first aspect of the invention, or a composition according to the second aspect of the invention.

Preferably the ink contained in the ink jet printer cartridge is an ink according to the third aspect of the present invention.

The invention is further illustrated by the following Examples in which all parts and percentages are by weight unless otherwise stated. Example 1 <BR> <BR> Dye (1)

Dye (1) Dye 1 was prepared in accordance with following process: Stage (1): Diazotisation and Couplina To N-acetyl p-phenylenediamine sulphonic acid (0.5moles) in water (400mut) was added concentrated hydrochloric acid (250ml) and the solution was cooled to 0-5°C. 2N sodium nitrite (250mut) was added dropwise over 5 minutes with stirring. After 15 minutes, excess nitrous acid was destroyed by the addition of sulphamic acid (0.2g). To the resulting suspension was added a solution of 2-amino-8-naphthol-6-sulphonic acid (0.5 moles in 600moi of water at pH6) and the pH was adjusted to 4 by the addition of sodium acetate. The mixture was stirred at 0-5°C for 4 hours before being allowed to warm to room temperature.

Stage (ii) Hydrolysis The acetyl group present on the product of stage (i) was removed by alkaline hydrolysis by adding concentrated sodium hydroxide (200moi) to the mixture resulting from stage 1 and heating at 70-80°C for 1.5 hours.

After cooling to room temperature, the pH was adjusted to 7 by the addition of concentrated hydrochloric acid. Sodium chloride (20% weight/volume) was added and the precipitated solid was collected by suction filtration, washed with 30% brine and dried at 70°C. Yield 132g (strength 45%).

Stage (iii) Condensation with Cyanuric Chloride The product from Stage (ii) (0.15 moles) was dissolved in water (500ml) at pH7.

Cyanuric chloride (0.17 moles) was dissolved in acetone (300ml) and added dropwise to the stirred solution at 0-5°C. The mixture was then stirred for 40 minutes.

Stage (iv) Condensations 1,3-diaminopropane (0.08 moles) was added. The temperature was raised to 30-40°C and the pH maintained at 8.5-9 for a period of 16 hours. Ethanolamine (0.45 moles) was added and the temperature of the mixture was elevated to 70-80°C. The pH

was maintained at 9-10 for a period of 6 hours. Methylated spirits was added to precipitate the product which was collecte by suction filtration and washed with further methylated spirits. The crude dye was redissolved in distille water and dialyse using visking tubing to a permeate conductivity of below 100pus. The solution was evaporated to dryness giving a yield of 185g of the title product.

Ink Ink 1 was prepared by dissolving 2 parts of Dye (1) in 98 parts of a mixture comprising 90 parts water and 10 parts 2-pyrrolidone.

Ink Jet Printing Ink 1 was loaded into a Hewlett Packard Deskjet 560c ink jet printer and was printed onto HP Premium Glossy Paper (available from Hewlett Packard Inc.). The resulting print was a bright magenta which had a good optical density and excellent light fastness.

The optical density of the print was 1.32, as measured using an X-Rite densitometer.

The print exhibited a DE value of 7.8, as measured using an X-Rite densitometer, and an optical density loss of just 9% after 64 hours irradiation in the Atlas Weatherometer.

Example 2 Dyes of the formula: were prepared by condensing the compound H-Q-H shown in Table 1 with approximately 2 molar equivalents of the product of stage (iii) in Example 1. The resulting product was then condensed with approximately 2 molar equivalents of the compound of the formula Z'H shown in Table 1. The reaction conditions used were analogous to those used in stage (iv) of Example 1. In Table 1 the symbol"-"indicates that the compound was not condensed with Z'H, i. e. Z'=-Cl. Table 1 Dye HQH Z'H 2 NH2 (CH2) 2NH2 NH2 (CH2) 2OH 82/\ NH2 (CH2) 20Hz NH2 (CH2) 2NuxN (CH2) 2NH2 HS (CH2) 3S03H NH2 NH2 NH2 (CH2) 3NH2 H2N-CH2ap 0 6 NH2 (CH2) 3NH2 H2N (CH2) 20 (CH2) 2OH 7 NH2 (CH2) 3NH2 HS (CH2) 3SO3H 8 NH2 (CH2) 3NH2 NH2 (CH2) 20H 9 NH2 (CH2) 3NH2 O NH 0 nu 10 NH2 (CH2) 3NH2 SH (CH2) 2COOH 11 NH2 (CH2) 3NH2 H2O 12 NH2 (CH2) 3NH2 13 NH2 (CH2) 2NH2 SH (CH2) 2COOH 14 NH2 (CH2) 3NH2 NH2 (CH2) 2SO3H 15 CH3 NH2 (CH2) 2OH HN NH H, C 16 NH2 (CH2) 3NH2 HOOC N H 17/C"'HZN (CH2) 20 (CH2) 2OH HN NH HIC HIC 18 NH2 (CH2) 3NH2 NH2 (CH2) 2COOH 19 NH2 (CH2) 4NH2 NH2 (CH2) 2OH 20 NH2 (CH2) 3NH2 NH2CH2COOH 21 NH2 (CH2) 4NH2 H2N (CH2) 20 (CH2) 20H 22 NHCHSOH 2 J Dye HQH Z'H 23 H2N (CH2) 3 (O (CH2) 2) 2 (OCH2) 2NH2 24 NH NH (CH2CH2OH) 2 4H2 NH 25 H2N (CH2) 3 (O (CH2) 2) 20 (CH2) 3NH2 NH2 (CH2) 2SO3H 26 H2NCH (COOH) SSCH2CH (COOH) NH2 NH2 (CH2) 2SO3H 27 H2NCH (COOH) CH2SH HN (CH3) (CH2CH2OH) 28 H2NCH (COOH) CH2SH HN (CH3) (CH2CH2SO3H) 29 H2NCH (COOH) CH2SH 30 H2N (CH2) 2 (0 (CH2) 2) 3NH2 NH2CH2CH (OH) CH20H 31 H (CH2CH20H) N (CH2) 2N (CH2CH20H) H NH2 (CH2) 20 (CH2) 2OH 32 H (CH2CH20H) N (CH2) 2N (CH2CH20H) H NH2 (CH2) 2SO3H 33 H (CH2CH2OH) N (CH2) 2N (CH2CH2OH) H NH2 (CH2) 2COOH 34 NH2 (CH2) 3NH2 NH2CH2CH (OH) CH20H 35 NH2 (CH2) 3NH2 HN (CH3) (CH2CH2SO3H) 36 NH2 (CH2) 3NH2 HN (CH3) (CH2CH2COOH) 37 NH2

Example 3 Inks and Ink Jet Printing Each dye shown in Table 1 was formulated into an ink by dissolving 2.5 parts of the relevant dye in 97.5 parts of an ink medium consisting of 88 parts water, 5 parts thiodiglycol, 5 parts 2-pyrrolidone and 2 parts Surfynol 465 (non-ionic surfactant).

Each ink was loaded into a Canon 4300 ink jet printer and printed onto Xerox Acid 4024TM"paper (available from Xerox Inc.) and SEC Glossy Film (available from Seiko Epson). The resulting prints exhibited a high reflected optical density, a high light fastness and good water-fastness.

The reflected optical density (ROD) and light-fastness (AE) were measured as described in Example 1.

The water-fastness (WF) was measured as follows. A print comprising a series of printed parallel bars was held at an angle of 45° with the parallel bars horizontal. A 3ml disposable bulb pipette (ex. Alpha Labs Ltd., Eastleigh, Hampshire-supplied by Orme Scientific), cut down to the 0.5ml mark (to give a 6mm aperture) was filled to the 0.1 ml mark with distille water. The distille water was then applied to the prints just above the top of the parallel printed bars, taking care to ensure that the rundown of the water occurred as a single'track'which was as vertical as possible through the horizontal printed bars.

The reflected optical density (ROD) in the area stained by the rundown of the water below the first four printed bars was measured and the mean ROD for each print calculated. The ROD values were measured using an X-RiteT""938 densitometer set to status T (Den T). The mean ROD was matched to a scale of 1 to 10 wherein 1 corresponds to a high mean ROD and hence a poor water fastness (i. e. high degree of staining between the printed bars) and 10 corresponds to a low mean ROD and a high water fastness (i. e. negligible staining between the printed bars).

For Dye (5) the following results were obtained: Prints on Xerox 4024 Acid Paper Reflected optical density: 0.93 Water-fastness: 7 Light-fastness (after 50 hours fading): 6.8 Prints on SEC Glossy Film Reflected optical density: 1.79 Water-fastness: 10 Light-fastness (after 50 hours fading): 6.5 The dyes described in Examples 1 and 2 are preferably purified before incorporation into an ink, preferably using a combination of reverse osmosis and ultrafiltration, such that when the dye is incorporated into an ink, the ink contains less than 10 parts per million it total of halogen ions and divalent and trivalent metal ions.

Example 4-Preparation of a Mixture of Dyes (A), (B) and (C) In Dye (A) both groups represented by Z are-NH2CH2CH2OH.

In Dye (B) one group represented by Z is Cl and the other is-NH2CH2CH2OH.

In Dye (C) both groups represented by Z are Cl.

The method of Example 1 was repeated except that the condensation reaction with ethanolamine in stage (iv) was stopped after 2.5 hours. The product was a mixture of Dye (A), Dye (B) and Dye (C) in relative proportions 43: 35: 22 by weight. This dye

mixture has a solubility of 10% in water at 20°C compared to a solubility of 3% for Dye (A) alone under the same conditions. In spite of the significantly higher solubility of the mixture, the wet-fastness of the mixture on paper was the same as for Dye (A) alone.

Examples 5 to 9-Dve Compositions The ratio of Dyes (A), (B) and (C) in Example 4 may be varied by altering the time and temperature of the ethanolamine condensation step (Example 1, step (iv)). The solubility of a variety of dye compositions in water at 20°C and pH 9.5 is shown in Table 2 below together with optical density, light fastness (AE after 50 hours) and wet-fastness results of prints prepared from these compositions. The prints were prepared by printing an ink formed by dissolving 2.5 parts of each composition in 97.5 parts of a mixture consisting of 88 parts water, 5 parts thiodiglycol, 5 parts 2-pyrrolidone and 2 parts Surfynol 465 TM (a non-ionic surfactant) onto the substrate shown in the third column of Table 2 using a Canon 4300 ink jet printer.

The dye ratios in Table 2 are the relative proportions of Dye (A): (B): (C) by weight.

In Example 5 the dye used was Dye (1) as described in Example 1.

In Example 6 the dye was prepared using the process described in Example 1 except that the dye was isolated after the condensation with 1,3-diaminopropane in stage (iv) of the process.

In Example 7 the dye composition may be prepared as described in Example 1 except that the reaction with ethanolamine is stopped when all of the dichloro starting material has been consumed (i. e. once all the dichloro dye of Example 6 has reacted with ethanolamine).

In Example 8 the dye was prepared using an analogous process to that described in Example 1 except that in stage (iv) the condensation with diaminopropane was carried out at a temperature of 20°C for 5 hours; and the condensation with ethanolamine was stopped after 1.5 hours.

In Example 9 the dye was prepared by mixing in a 1: 1 ratio Dye (1) from example 1 and the dye used in Example 6.

Table 2 Ex Dye ratio Solubility Substrate OD Light-fastness Wet-fastness (%) (AE @ 50 hrs) 5 100: 0: 0 3 XA 0. 99 6. 2 7 SG 1. 84 6 10 6 0: 0 4.810SG1.7 7 50: 50: 0 4 XA-high good SG-high good 8 45 : 42: 13 7. 5 XA - high good SG-high good 9 50: 0: 50 - XA 0.97 7 7 SG 1. 76 4. 2 10 In Table 2 XA = Xerox 4024 Acid Paper

SG = Seiko Epson glossy film Example10 The inks described in Tables 3 and 4 may be prepared wherein the Dye described in the first column is the Dye described in Examples 1 and 2. Numbers quoted in the second column onwards refer to the number of parts of the relevant ingredient and all parts are by weight. The inks may be applied to paper by thermal or piezo ink jet printing.

The following abbreviations are used in Tables 3 and 4: PG = propylene glycol DEG = diethylene glycol NMP = N-methyl pyrrolidone DMK = dimethylketone IPA = isopropanol GLY = glycerol 2P = 2-pyrrolidone MIBK = methylisobutyl ketone P12 = propane-1,2-diol BDL = butane-2, 3-diol CET= cetyl ammonium bromide PHO = Na2HP04 and TBT = tertiary butanol TDG = thiodiglycol TABLE 3 Dye Dye Water PG DEG NMP DMK NaOH Na Stearate IPA GLY 2P MIBK Content 2 2.0 80 5 6 4 5 4 3.0 90 5 5 0.2 7 10.0 85 3 3 3 5 1 5 2.1 91 8 1 1 3.1 86 5 0.2 4 5 1 1.1 81 9 0.5 0.5 9 3 2.5 60 4 15 3 3 6 10 5 4 4 5 65 20 10 3 2.4 75 5 4 5 6 5 7 4.1 80 3 5 2 10 0.3 5 3.2 65 5 4 6 5 4 6 5 4 5.1 96 4 3 10.8 90 5 5 1 10.0 80 2 6 2 5 1 4 3 1.8 80 5 15 5 2.6 84 11 5 4 3.3 80 2 10 2 6 1 12.0 90 7 0.3 3 6 5.4 69 2 20 2 1 3 3 7 6.0 91 4 5 TABLE 4 Dye Dye Water PG DEG NMP CET TBT TDG BDL PHO 2P PI2 Content 2 3.0 80 15 0.2 5 3 9.0 90 5 1.2 5 5 1.5 85 5 5 0.15 5.0 0.2 7 2.5 90 6 4 0.12 6 3.1 82 4 8 0.3 6 1 0.9 85 10 5 0.2 2 8.0 90 5 5 0.3 6 4.0 70 10 4 1 4 11 12 2.2 75 4 10 3 2 6 5 10.0 91 6 3 7 9.0 76 9 7 3.0 0.95 5 3 5.0 78 5 11 6 1 5.4 86 7 7 3 2.1 70 5 5 5 0.1 0.2 0.1 5 0.1 5 4 2.0 90 10 2 2 88 10 5 5 78 5 12 5 3 8 70 2 8 15 5 7 10 80 8 12 6 10 80 10