SU655333A3 - Method of pigmenting high-molecular organic material - Google Patents

Method of pigmenting high-molecular organic material

Info

Publication number
SU655333A3
SU655333A3 SU731947364A SU1947364A SU655333A3 SU 655333 A3 SU655333 A3 SU 655333A3 SU 731947364 A SU731947364 A SU 731947364A SU 1947364 A SU1947364 A SU 1947364A SU 655333 A3 SU655333 A3 SU 655333A3
Authority
SU
USSR - Soviet Union
Prior art keywords
amino
organic material
acid
molecular organic
pigmenting high
Prior art date
Application number
SU731947364A
Other languages
Russian (ru)
Inventor
Мори Рудольф
Original Assignee
Циба Гейги Аг (Фирма)
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.)
Filing date
Publication date
Application filed by Циба Гейги Аг (Фирма) filed Critical Циба Гейги Аг (Фирма)
Application granted granted Critical
Publication of SU655333A3 publication Critical patent/SU655333A3/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/34Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3665Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic ring with two nitrogen atoms
    • C09B29/3669Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic ring with two nitrogen atoms from a pyrimidine ring

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

N-метилпирролидона до кипени . После повторного выделени  и -высушивани  получают 2,8 об. ч. пигмента в виде светлокрасного м гкого порошка. Пигмент окрашивает поливинилхлорид в очень интенсивный желто-красный оттенок превосходной прочностью к действию света и миграции .N-methylpyrrolidone before boiling. After re-isolation and drying, 2.8% v / v are obtained. including pigment in the form of a light red soft powder. Pigment paints polyvinyl chloride in a very intense yellow-red hue with excellent strength to light and migration.

Примеры 2-5. По примеру 1 получают пигменты, представленные в табл. 1.Examples 2-5. In example 1, get the pigments presented in table. one.

Таблица 1Table 1

ПримерExample

Диазосостав.ч Юща Diazosostav.ch guide

5-Ам Шо-6-этоксибензимидазолон5-Am Sho-6-ethoxybenzimidazolone

5-Амино-6-метоксибензимидазолон5-amino-6-methoxybenzimidazolone

5-Амино-6-мет11лбензимидазолон5-amino-6-met11lbenzimidazolone

7-Амино-6-мети.чфенморфолон-(3)7-amino-6-methi.chfenmorpholone- (3)

5-Амино-6-хлорбензимидазолон5-amino-6-chlorobenzimidazolone

5-Амино-6-этоксибензимидазолон5-amino-6-ethoxybenzimidazolone

7-Амино-6-метилфенморфолон-(3)7-amino-6-methylphenmorpholone- (3)

5-Амино-б-метоксибензим11дазолон5-Amino-b-methoxybenzim11dazolone

5-Амино-б-метилбенз11мидазолон5-Amino-b-methylbenz11midazolone

5-Амино-6-хлорбгнзимидазолон5-amino-6-chlorobgnimimazole

5-Амино-6-метоксибенз11мидазолон5-amino-6-methoxybenz11midazolone

5-Амино-6-метилбензимидазолон5-amino-6-methylbenzimidazolone

5-Амино-6-этоксибензимидазолон5-amino-6-ethoxybenzimidazolone

5-Амино-6-хлорбензимидазолон5-amino-6-chlorobenzimidazolone

7-Амино-б-метилфенморфолон-(3)7-Amino-b-methylfenmorpholone- (3)

5-Амино-6-метилбензнмидазолон5-amino-6-methylbenznmidazolone

7-Амино-6-метоксифенморфолон-(3)7-amino-6-methoxyfenmorpholone- (3)

Примеры 6-22. Процесс провод т по примеру 1. В табл. 2 представлены пигменты , полученные по примерам 6-22.Examples 6-22. The process is carried out according to example 1. In table. 2 shows the pigments obtained in examples 6-22.

Пример 23. 1,00 г полученного по примеру 9 пигмента тонко растирают с 4,00 г типографической олифы, состо шей из 29,4% лед ного масла-полимеризоваННого масла (300 Пз), 67,2% льн ного масла- полимеризованного масла (20 Пз), 2,1% октоата кобальта (8% Со) и 1,3% октоата свинца (24% РЬ) на растительной машине Энегльсманна и затем набивают с помоТаблица 2Example 23. 1.00 g of the pigment prepared according to Example 9 is finely ground with 4.00 g of a typographical drying oil, consisting of 29.4% icy oil-polymerized oil (300 Pz), 67.2% flax oil-polymerized oil (20 Pz), 2.1% cobalt octoate (8% Co) and 1.3% lead octoate (24% Pb) on an Eneglsmann plant machine and then packed with table 2

Азосостав.ч юща Azo composition

ЦветColour

2-Аминобарбнтурова  кислота 2-Иминобарбитурова  кислота 2-Иминобарбитурова  кислота 2-Имннобарбнтурова  кислота 2-Иминобарбитурова  кислота 2,4-Динминобарбитурова  кислот 2,4-ДиИдМинобарбитурова  кислот 2,4-Дииминобарбитурова  кислот 2,4-Дии.минобарбитурова  кислот 2,4-Дииминобарбитурова  кислот 2-Тиобарбитурова  кислота 2-Тиобарбитурова  кислота 2-Тиобарбитурова  кислота 2-Т110барбптурова  кислота 1-Фенилбарбитурова  кислота ЬФеиилбарбитурова  кислота Барбитурова  кислота2-Aminobarbnturian acid 2-Iminobarbituroic acid 2-Iminobarbiturova acid 2-Imnobarbnturova acid 2-Iminobarbiturova acid 2,4-Dinminobarbiturova acids 2,4-DiId Minobarbiturova acids 2,4-Diimobarbiturova acids 2,4-DiBarobobar Diimobarbiturova acids 2-Thiobarbituric acid 2-Thiobarbituric acid 2-Thiobarbituric acid 2-T110 barbrate acid 1-Phenylbarbituric acid FeFeiylbarbituric acid Barbituric acid

ш,ью клише способом книгопечатани  1 г/м на печатную бумагу дл  художественных изделий. Получают интенсивный, чистый желтый оттенок с хорошей прозрачностью и хорошим блеском.W, in a cliche way of printing 1 g / m on printed paper for art products. Get an intense, clear yellow tint with good transparency and good gloss.

Пример ы 24-35. В табл. 3 приведены другие высокомолекул рные органические материалы, которые можно пигментировать пигментами по предлагаемому способу с получением -светостойких и стойких к миграции крашений.Example s 24-35. In tab. 3 shows other high-molecular-weight organic materials that can be pigmented by the pigments according to the proposed method with obtaining light-resistant and migration-resistant dyeing.

Claims (1)

Формула изобретени Invention Formula Способ пигментировани  высокомолекул рного органического материала с использованием моноазопигмента, отличаюгде R1 - хлор, метил, окси.метил, окси R2 - водород или фснил; X - амино- или СН20-группы; Y - кислород, сера или иминогруппаThe method of pigmenting high molecular weight organic material using a monoazo pigment is different from R1 to chlorine, methyl, hydroxymethyl, hydroxy to R2 or hydrogen or phenyl; X is amino or CH20; Y - oxygen, sulfur or imino group Таблица 3Table 3 щи иС   тем, что, с целью повышени  светостойкости окраски, в качестве моноазопигмента используют соединение общей формулы 10 кислород или иминогруппа. Источники информации, прин тые во внимание при экспертизе 1. Патент Англии № 1136673, кл. С(4)Р, 1969.In order to improve the light fastness of the color, a compound of the general formula 10 is oxygen or an imino group as a monoazo pigment. Sources of information taken into account in the examination 1. Patent of England No. 1136673, cl. C (4) P, 1969.
SU731947364A 1972-07-13 1973-07-12 Method of pigmenting high-molecular organic material SU655333A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1052672A CH566371A5 (en) 1972-07-13 1972-07-13

Publications (1)

Publication Number Publication Date
SU655333A3 true SU655333A3 (en) 1979-03-30

Family

ID=4364159

Family Applications (1)

Application Number Title Priority Date Filing Date
SU731947364A SU655333A3 (en) 1972-07-13 1973-07-12 Method of pigmenting high-molecular organic material

Country Status (11)

Country Link
JP (1) JPS5735204B2 (en)
AR (1) AR198675A1 (en)
AU (1) AU465903B2 (en)
BE (1) BE802243A (en)
CA (1) CA1009650A (en)
CH (1) CH566371A5 (en)
ES (1) ES416814A1 (en)
FR (1) FR2193063B1 (en)
GB (1) GB1391883A (en)
NL (1) NL180676C (en)
SU (1) SU655333A3 (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1544394A1 (en) * 1966-02-03 1971-03-04 Basf Ag Water-insoluble azo dyes

Also Published As

Publication number Publication date
JPS5735204B2 (en) 1982-07-28
CH566371A5 (en) 1975-09-15
BE802243A (en) 1974-01-14
AR198675A1 (en) 1974-07-15
NL180676C (en) 1987-04-01
NL7309625A (en) 1974-01-15
GB1391883A (en) 1975-04-23
ES416814A1 (en) 1976-06-16
CA1009650A (en) 1977-05-03
JPS4959133A (en) 1974-06-08
DE2335121B2 (en) 1977-02-03
AU5803473A (en) 1975-01-16
FR2193063B1 (en) 1976-09-17
FR2193063A1 (en) 1974-02-15
AU465903B2 (en) 1975-10-09
DE2335121A1 (en) 1974-01-24

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