GB2031008A – Salt of a methine dy and process for pigmenting organic material of high molecular weight
– Google Patents
GB2031008A – Salt of a methine dy and process for pigmenting organic material of high molecular weight
– Google Patents
Salt of a methine dy and process for pigmenting organic material of high molecular weight
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Publication number
GB2031008A
GB2031008A
GB7930656A
GB7930656A
GB2031008A
GB 2031008 A
GB2031008 A
GB 2031008A
GB 7930656 A
GB7930656 A
GB 7930656A
GB 7930656 A
GB7930656 A
GB 7930656A
GB 2031008 A
GB2031008 A
GB 2031008A
Authority
GB
United Kingdom
Prior art keywords
formula
compound
parts
molecular weight
high molecular
Prior art date
1978-09-05
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB7930656A
Other versions
GB2031008B
(en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Ciba Geigy AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
1978-09-05
Filing date
1979-09-04
Publication date
1980-04-16
1979-09-04
Application filed by Ciba Geigy AG
filed
Critical
Ciba Geigy AG
1980-04-16
Publication of GB2031008A
publication
Critical
patent/GB2031008A/en
1982-09-08
Application granted
granted
Critical
1982-09-08
Publication of GB2031008B
publication
Critical
patent/GB2031008B/en
Status
Expired
legal-status
Critical
Current
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Classifications
C—CHEMISTRY; METALLURGY
C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
C09B23/04—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups one >CH- group, e.g. cyanines, isocyanines, pseudocyanines
Description
1
GB 2 031 008 A 1
15
SPECIFICATION
Salt of a Methine Dye and Process for Pigmenting Organic Material of High Molecular Weight
The present invention relates to a salt of a methine dye and process for pigmenting organic material of high molecular weight.
The present invention provides the sodium salt of the bis-methine-barbituric acid of the formula
10
This compound can also be in the form of an enol
OH H OH
(ID
The pigment is obtained preferably by condensation of the aldehyde of the formula
CHO
20
(III)
with thiobarbituric acid in the molar ratio 1:1 and subsequent salt formation by conventional methods.
The compound of the formula (I) is also obtained in good yield by condensing the metal salt of a compound of the formula
0
O^N^ONa H
(V)
25
30
35
40
with thiobarbituric acid.
The barbituric acid aldehyde is obtained by known methods. The condensation of the barbituric acid aldehyde and of its sodium salt with thiobarbituric acid is carried out by heating in a solvent at 20°—180°C, preferably at 70°— 150°C, resulting in many cases in an increase in the granular size of the pigment, which in turn has an advantageous influence on the fastness to light and migration of the pigment.
Particularly suitable solvents which can be employed in the above process are: water; ketones, such as acetone, methyl ethyl ketone or cyclohexanone; alcohols, such as methanol, ethanol, isopropanol, n-butanol, ethylene glycol monomethyl or monoethyl ether; benzenes, such as toluene, xylenes, chlorobenzene,
dichlorobenzenes or nitrobenzene; and also pyridine, picoline, quinoline, formamide, dimethyl formamide, N-methylpyrrolidone, dimethyl sulfoxide, formic acid or acitic acid. The reaction 45 can also be carried out in water in the presence of organic solvents. Instead of using pure solvents, it is also possible to use mixtures of different organic solvents with or without water.
The reaction proceeds preferably at elevated 50 temperature in the course of 30 minutes to 10 hours, preferably 2 to 4 hours. The sparingly soluble product is normally precipitated from the solution and can be isolated by filtration, washing and drying. To hasten the reaction, it is 55 furthermore possible to use catalytic amounts of piperidine.
The pigment of the formula (I) can be used for colouring organic material of high molecular weight, for example cellulose ethers and esters, 60 such as cellulose acetate, cellulose propionate, cellulose acetobutyrate, nitrocellulose, and also polyolefins, such as polyethylene, polypropylene, substituted polyolefins, such as polyvinyl chloride, polyvinyl acetate, copolymers of vinyl chloride 65 and vinyl acetate, polystyrene, polyacrylonitrile and polyacrylates, as well as aminoplasts, such as urea-formaldehyde and melamine-formaldehyde resins, and epoxy resins, alkyd resins, phenolic plastics and polycarbonates.
70 A particularly interesting utility is the colouring of lacquers, for example those based on alkyd-melamine-formaldehyde resins and alkyd-urea-formaldehyde resins, as well as on thermoplastic and thermohardening acrylic resins. The pigment 75 of the formula (I) is also of interest for use in printing inks.
The pigment of the formula (I) has good colour strength, dispersibility and thermostability, and the colourations obtained therewith are 80 distinguished by good fastness to migration, light and atmospheric influences.
The invention is illustrated by the following Examples, in which the parts and percentages are by weight, unless otherwise stated.
85 Example 1:
42.8 parts of the monosodium salt of 5-formylbarbituric acid (with 2 moles of water of crystallisation) are suspended in 280 parts of dimethyl formamide. A suspension of 28.8 parts 90 of thiobarbituric a.cid in 300 parts of glacial acetic acid are then added at room temperature to the above suspension in the course of 2 minutes.
Then 8 parts of piperidine are added. The suspension is stirred initially for 3 hours at 95 120°C, then for a further 3 hours at 145°C,
whereupon the pigment gradually begins to form. The resulting pigment suspension is cooled to 70°C and filtered by suction. The residue is washed with 70 parts of cold dimethyl 100 formamide, then with 300 parts of cold water and dried in vacuo at 90°C, affording 39.5 parts of the pigment of the formula
2
GB 2 031 008 A 2
HN
NH
‘ONa 0
H H
in the form of a yellow powder.
Analysis:
(with 1 mole of water of crystallisation)
5 Calculated
C 33.5 H 2.17 N 17.3 S 9.9 Na 7.1%
Found:
C 33.9 H 2.2 N 17.4 S 9.3 10 Na 7.0%
When rolled into polyvinyl chloride, this pigment gives reddish-yellow colourations which are fast to migration and light.
Example 2:
15 42.8 parts of the monosodium salt of 5-formylbarbituric acid (with 2 moles of water of crystallisation) and 28.8 parts of thiobarbituric acid are suspended at room temperature in 390 parts of o-dichlorobenzene, 150 parts of glacial 20 acetic acid and 0.25 part of pyridine. The suspension is stirred for 5 hours at 114°C, then cooled to room temperature and the yellow suspension is filtered by suction. The residue is washed with 500 parts of petroleum ether and 25 dried in vacuo at 90°C, affording 64 parts (92% of theory) of a yellow pigment of the same formula as in Example 1 and having the same good pigment properties.
Example 3:
30 67 g of polyvinyl chloride powder (suspension polymer), 33 g of dioctyl phthalate, 2 g of dibutyl tin dilaurate, 0.3 g of a phosphate stabiliser and 0.7 g of the pigment of Example 1 are mixed and the mixture is processed for 15 minutes on mixing 35 rolls at 160°C. A sheet having a thickness of 0.4 mm is produced on a calender. The sheet is coloured in a yellow shade which is heat-resistant and fast to migration.
Example 4:
40 0.2 g of the pigment obtained in Example 1, 1 g of titanium dioxide (rutile) and 100 g of LD polyethylene granules are mixed in a drum and the mixture is then processed on mixer rolls at 130°C. The plastic mass is then pressed 45 hot to sheets or moulded in an extruder. The sheets have a pleasing yellow shade of good lightfastness.
Example 5
0.1 g of the pigment obtained in Example 1, 50 0.5 g of titanium dioxide (rutile) and 1000 of polypropylene granules are mixed in a drum and the mixture is subsequently processed on mixer rolls until a homogeneously coloured mixture is obtained. The plastic mass is pressed to sheets of 1 mm thickness. The sheets are coloured in a pleasing yellow shade of good lightfastness.
Example 6:
100 g of a formaldehyde-urea resin powder suitable for moulding materials, 10 g of lithopone and 1 g of the pigment obtained in Example 1 are ground for 16 hours in a ball mill. The composition is then moulded at 140°C in moulds. The yellow samples obtained have good lightfastness and heat-resistance.
Example 7 :
(Alkyd-melamine stoving lacquer):
60 parts of a 60% solution of a nondrying alkyd resin in xylene
