SU668617A3 - Твердый красильный препарат - Google Patents

Твердый красильный препарат

Info

Publication number: SU668617A3
Authority: SU; USSR - Soviet Union
Prior art keywords: dye; aprotic polar; weight; cold water; preparation
Prior art date: 1974-07-04

Application number

SU752150558A

Other languages

English (en)

Russian (ru)

Inventor

К.Агарвал Суреш (Индия)

Зомло Тибор (Швейцария)

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.)

1974-07-04

Filing date

1975-07-03

Publication date

1979-06-15

1975-07-03 Application filed by Циба-Гейги Аг (Фирма) filed Critical Циба-Гейги Аг (Фирма)

1979-06-15 Application granted granted Critical

1979-06-15 Publication of SU668617A3 publication Critical patent/SU668617A3/ru

Links

238000002360 preparation method Methods 0.000 title claims description 16
239000007787 solid Substances 0.000 title claims description 8
238000004043 dyeing Methods 0.000 title description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
150000001875 compounds Chemical class 0.000 claims description 14
230000003287 optical effect Effects 0.000 claims description 14
239000007844 bleaching agent Substances 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 6
239000003814 drug Substances 0.000 claims description 4
229940079593 drug Drugs 0.000 claims description 4
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 3
GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 claims description 2
125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
239000000975 dye Substances 0.000 description 39
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
239000000243 solution Substances 0.000 description 7
QONGECDDDTYBGS-UHFFFAOYSA-N dimorpholin-4-ylmethanone Chemical group C1COCCN1C(=O)N1CCOCC1 QONGECDDDTYBGS-UHFFFAOYSA-N 0.000 description 6
238000001816 cooling Methods 0.000 description 4
239000000155 melt Substances 0.000 description 4
LGFRSWGKHVSPLU-UHFFFAOYSA-N 1,3-dimorpholin-4-ylurea Chemical compound C1COCCN1NC(=O)NN1CCOCC1 LGFRSWGKHVSPLU-UHFFFAOYSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
239000004202 carbamide Substances 0.000 description 3
239000000428 dust Substances 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
238000010410 dusting Methods 0.000 description 2
239000008187 granular material Substances 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
-1 tetramethyl hexamethylphosphoric triamide Chemical compound 0.000 description 2
AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
BBVIDBNAYOIXOE-UHFFFAOYSA-N 1,2,4-oxadiazole Chemical group C=1N=CON=1 BBVIDBNAYOIXOE-UHFFFAOYSA-N 0.000 description 1
GFJSEPREQTXWHA-UHFFFAOYSA-N 2,5-diphenyl-1,3-dihydropyrazole Chemical class C1C=C(C=2C=CC=CC=2)NN1C1=CC=CC=C1 GFJSEPREQTXWHA-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
ZGBGJBWBURQFMR-UHFFFAOYSA-N N=1N(N=CC1)C1(CC(C(C=C1)C=CC1=CC=CC=C1)(S(=O)(=O)O)S(=O)(=O)O)N1N=CC=N1 Chemical class N=1N(N=CC1)C1(CC(C(C=C1)C=CC1=CC=CC=C1)(S(=O)(=O)O)S(=O)(=O)O)N1N=CC=N1 ZGBGJBWBURQFMR-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
239000000956 alloy Substances 0.000 description 1
229910045601 alloy Inorganic materials 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000000010 aprotic solvent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000000981 basic dye Substances 0.000 description 1
XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical class C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000008139 complexing agent Substances 0.000 description 1
150000004696 coordination complex Chemical class 0.000 description 1
150000001907 coumarones Chemical class 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000000034 method Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
INAAIJLSXJJHOZ-UHFFFAOYSA-N pibenzimol Chemical class C1CN(C)CCN1C1=CC=C(N=C(N2)C=3C=C4NC(=NC4=CC=3)C=3C=CC(O)=CC=3)C2=C1 INAAIJLSXJJHOZ-UHFFFAOYSA-N 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
150000001629 stilbenes Chemical class 0.000 description 1
235000021286 stilbenes Nutrition 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1

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
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0092—Dyes in solid form
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
- D06L4/664—Preparations of optical brighteners; Optical brighteners in aerosol form; Physical treatment of optical brighteners
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/445—Use of auxiliary substances before, during or after dyeing or printing

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Detergent Compositions (AREA)
Plural Heterocyclic Compounds (AREA)
Paper (AREA)
Optical Filters (AREA)
Coloring (AREA)

SU752150558A 1974-07-04 1975-07-03 Твердый красильный препарат SU668617A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH919574A CH606359A5 (fr)	1974-07-04	1974-07-04

Publications (1)

Publication Number	Publication Date
SU668617A3 true SU668617A3 (ru)	1979-06-15

Family

ID=4349385

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU752150558A SU668617A3 (ru)	1974-07-04	1975-07-03	Твердый красильный препарат

Country Status (11)

Country	Link
JP (1)	JPS5130824A (fr)
BE (1)	BE830954A (fr)
BR (1)	BR7504219A (fr)
CH (1)	CH606359A5 (fr)
DD (1)	DD119603A5 (fr)
DE (1)	DE2529567A1 (fr)
ES (1)	ES439108A1 (fr)
FR (1)	FR2277129A1 (fr)
GB (1)	GB1516201A (fr)
IT (1)	IT1040796B (fr)
SU (1)	SU668617A3 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP4920029B2 (ja) *	2008-12-14	2012-04-18	日鐵住金溶接工業株式会社	インサートチップおよびプラズマトーチ

1974
- 1974-07-04 CH CH919574A patent/CH606359A5/xx not_active IP Right Cessation
1975
- 1975-07-02 DD DD187047A patent/DD119603A5/xx unknown
- 1975-07-02 FR FR7520772A patent/FR2277129A1/fr active Granted
- 1975-07-02 IT IT50321/75A patent/IT1040796B/it active
- 1975-07-02 DE DE19752529567 patent/DE2529567A1/de not_active Withdrawn
- 1975-07-03 GB GB28098/75A patent/GB1516201A/en not_active Expired
- 1975-07-03 ES ES439108A patent/ES439108A1/es not_active Expired
- 1975-07-03 SU SU752150558A patent/SU668617A3/ru active
- 1975-07-03 BE BE157937A patent/BE830954A/fr unknown
- 1975-07-04 JP JP50082005A patent/JPS5130824A/ja active Pending
- 1975-07-04 BR BR5400/75D patent/BR7504219A/pt unknown

Also Published As

Publication number	Publication date
CH606359A5 (fr)	1978-10-31
DE2529567A1 (de)	1976-01-22
ES439108A1 (es)	1977-03-01
IT1040796B (it)	1979-12-20
DD119603A5 (fr)	1976-05-05
GB1516201A (en)	1978-06-28
FR2277129A1 (fr)	1976-01-30
BE830954A (fr)	1976-01-05
BR7504219A (pt)	1976-07-06
JPS5130824A (fr)	1976-03-16
FR2277129B1 (fr)	1977-07-08

Publication	Publication Date	Title
SU668617A3 (ru)	1979-06-15	Твердый красильный препарат
US932290A (en)	1909-08-24	Compound of the anthracene series and process of making same.
JPS6058260B2 (ja)	1985-12-19	アントラキノン化合物、その製法および染色方法
BE634601A (fr)	1963-11-18	Colorants basiques, leurs procedes de fabrication et leurs applications
US3892734A (en)	1975-07-01	Novel anthraquino(3,2-d)oxazole dyes and coloring agents
US3959285A (en)	1976-05-25	Imides of 1,1'-dinaphthyl-4,4',5,5',8,8'-hexacarboxylic acid
Zolotukhin et al.	1992	A novel route to poly (triarylcarbinols)
US3860584A (en)	1975-01-14	4,4{40 -Bis-{8 benzoxazolyl-(2){9 -stilbenes
US2734901A (en)	1956-02-14	Process of preparing evdotlum
US3419563A (en)	1968-12-31	Process for producing 7-amino-carbostyrile derivatives
JPH0485366A (ja)	1992-03-18	ローダミン類の製造方法
US2980697A (en)	1961-04-18	Benzothiophene compounds
US3663539A (en)	1972-05-16	Process for the manufacture of basic oxazine dyestuffs
US2523528A (en)	1950-09-26	N' (4-hydroxy-4-isoimidazol-2-yl)sulfonamides and their production
US3600401A (en)	1971-08-17	Deketo-benzo-dipyrole polymers
US2447440A (en)	1948-08-17	Amino substituted aryl guanamines
JPS63233979A (ja)	1988-09-29	非対称型トリアジニル含有スチルベン誘導体の製法
US3960867A (en)	1976-06-01	Method of producing perylenetetracarboxylic acid derivatives
US3541107A (en)	1970-11-17	2,5-diaryl-1,2,3,4,5,6-hexaazapentalene synthesis
JPH0459874A (ja)	1992-02-26	ポリメチン化合物
DE2528698B2 (de)	1981-02-05	7-Sulfonylacetylamino-substituierte Cumarinverbindungen und ein Verfahren zu deren Herstellung sowie die Verwendung dieser Verbindungen zur Herstellung von optischen Cumarin-Aufhellern
US1251369A (en)	1917-12-25	Dyes and manufacture thereof.
SU919342A1 (ru)	1983-01-23	Производные 1,1-бинафтил-4,4,5,5,8,8-гексакарбоновой кислоты в качестве красителей дл хлопчатобумажных,льн ных и вискозных материалов и способ их получени
US1690775A (en)	1928-11-06	Vat dyestuffs derived from 1, 4, 5, 8-naphthalene tetracarboxylic acid and aromatic ortho-nitro-amines and process of preparing the same
SU1046264A1 (ru)	1983-10-07	Крас щий раствор дл бумаги