Organic compounds -- part of the class 532-570 series – Organic compounds – Azo
Patent
1997-07-17
1998-04-28
Powers, Fiona T.
Organic compounds -- part of the class 532-570 series
Organic compounds
Azo
534728, 534DIG4, 106496, C09B 6300, C09B 6720
Patent
active
057445907
DESCRIPTION:
BRIEF SUMMARY
This application is a 371 of PCT/GB95/02833, filed Dec. 5,1995 which was designated the U.S.
This invention relates to monoazo pigments and more particularly to orange pigments of the azo pyrazolone series.
J. of Chromatography, 665, 197 (1994) discloses certain sulphonated azopyrazolones and the corresponding sodium and potassium salts.
European patent EP 0 225 553 discloses certain isomeric azopyrazolones as the calcium salts.
The use of pigments for the colouring of plastics materials is well known. For the production of orange colorations, it has been traditional to employ inorganic pigments such as cadmiums, lead chromes and molybdate oranges but these are now being phased out because of environmental pressures. Organic pigments that have been proposed as replacements for these inorganic materials have not been found entirely satisfactory in all of the major polymer types, especially in respect of their heat stability.
It has now been found that certain organic pigments of the azo pyrazolone series are characterised by excellent heat stability, light stability, and bleed fastness when used in a wide range of plastics materials.
Accordingly, the invention provides an azo pyrazolone compound of the formula: ##STR2## in the form of a salt.
The salts of the compounds of Formula 1 may exhibit polyphormism and, where this is the case, the various polymorphic forms are regarded as within the scope of the invention.
Particularly advantageous compounds of Formula 1 in terms of superior heat and light stability are compounds in which the sulphonic acid group of the naphthalene nucleus is present in the 4- or 6-position relative to the azo link and the sulphonic acid group of the benzene ring is present in the 3- or 4-position relative to the pyrazolyl group.
The salt of the azo pyrazolone compound of Formula 1 may be a metal salt, for example, an alkali metal, alkaline earth metal or heavy metal salt, or a salt of a nitrogenous base, for example a primary, secondary or tertiary amine or quaternary ammonium salt, particularly useful pigments being the salts of barium, strontium, manganese, magnesium, sodium and, especially, calcium.
The most preferred compounds of the invention have the formula: ##STR3## wherein the sulphonate group of the naphthalene nucleus is in the 4- or 6-position relative to the azo group.
The azo pyrazolone compounds of the invention may be prepared by diazotising a naphthylamine sulphonic acid of the formula: ##STR4## and coupling the resulting diazo compound with a sulphonated 3-methyl-1-phenylpyrazol-5-one of the formula: ##STR5## and converting the resulting monoazo compound to the desired salt form.
The diazotisation and coupling reactions may be performed in a conventional manner appropriate to the classes of compound being used.
The preferred naphthylamine sulphonic acids for use in preparing the compounds of the invention are 1-naphthylamine-4-sulphonic acid and 1-naphthylamine-6-sulphonic acid whilst the preferred coupling components are 3-methyl-1-(4'-sulphophenyl)pyrazol-5-one and, especially 3-methyl-1-(3'-sulphophenyl)pyrazol-5-one.
It is often convenient to prepare the compound of Formula 1 in the form of a sodium salt and then convert the sodium salt to, for example, an alkaline earth or heavy metal lake by adding the required amount of a water-soluble alkaline earth metal or heavy metal salt, usually in the form of an aqueous solution.
Surface active agents and/or organic solvents may optionally be present during the synthesis of the compound of Formula 1 and/or during precipitation of the pigment.
The compounds of the invention, which may be subjected to conventional milling operations and/or thermal treatments in order to provide products of the desired particle size and/or crystal structure, are useful orange pigments which may be used in conventional manner. In particular, they may be used alone or in conjunction with other pigments for the coloration of plastics materials, for example polyvinyl chloride, polyolefins, polystyrene and ABS where they exhibit excellent pr
REFERENCES:
patent: 3802836 (1974-04-01), Speck
patent: 5457188 (1995-10-01), Zimmerman
Gasparic et al: "Effect of the number of sulpho group on the electrophoretic mobility of sulphonated azo dyes", Journal of Chromatography A, vol. 665, No. 1, 1994, pp. 197-202, XP002002367, see table 2.
Chorlton Alan Patrick
Mason James
Powers Fiona T.
Zeneca Limited
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