GB1080907A

GB1080907A – Alkali-soluble cindensation products and their production
– Google Patents

GB1080907A – Alkali-soluble cindensation products and their production
– Google Patents
Alkali-soluble cindensation products and their production

Info

Publication number
GB1080907A

GB1080907A
GB51126/64A
GB5112664A
GB1080907A
GB 1080907 A
GB1080907 A
GB 1080907A
GB 51126/64 A
GB51126/64 A
GB 51126/64A
GB 5112664 A
GB5112664 A
GB 5112664A
GB 1080907 A
GB1080907 A
GB 1080907A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
acid
reacting
prepared
molar equivalents
Prior art date
1963-12-17
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.)

Expired

Application number
GB51126/64A
Inventor
Otto Hertel
Walter Hensel
Hans Burkhardt
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.)

BASF SE

Original Assignee
BASF SE
Badische Anilin and Sodafabrik 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.)
1963-12-17
Filing date
1964-12-16
Publication date
1967-08-31

1964-12-16
Application filed by BASF SE, Badische Anilin and Sodafabrik AG
filed
Critical
BASF SE

1967-08-31
Publication of GB1080907A
publication
Critical
patent/GB1080907A/en

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

Classifications

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

D06P1/52—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 using compositions containing synthetic macromolecular substances

D06P1/56—Condensation products or precondensation products prepared with aldehydes

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07G—COMPOUNDS OF UNKNOWN CONSTITUTION

C07G99/00—Subject matter not provided for in other groups of this subclass

Abstract

An alkali-soluble condensation product is prepared by reacting together in an acid aqueous medium (a) 1 to 5 molar equivalents of an aromatic hydroxy compound which is free from carboxyl groups (b) 0.1 to 0.5 molar equivalents of a lower alkyl (C1-C6) ether of dimethyolurea or a dimethyol compound of an aliphatic linear or cyclic urea derivative (c) 1 to 6 molar equivalents of an aromatic hydroxycarboxylic acid, an aliphatic dicarboxylic or hydroxy-dicarboxylic acid or an aryloxy fatty acid and (d) 5 to 11 molar equivalents of formaldehyde or a formaldehyde donor. The reaction is preferably carried out at 30 DEG C. to the boiling point of the composition. Many monohydric and polyhydric phenols are specified including monohydroxy and polyhydroxy compounds of diarylsulphones. Suitable compounds (b) are the dimethyl ether of dimethyolurea, dimethylolmethyl urea, dimethyol-N,N1-dimethylurea, dimethylolethyleneurea, dimethylolpropyleneurea, (di – N,N1 – methylol) 1 – 2 – ureylene-ethylene glycol and bis-(1,2-ureylene) ethanedimethylolate. Salicylic, gallic, malonic, malic, glutaric and phenoxyacetic acids are the specified acids (c) and the formaldehyde may be in the free form or in the form of formaldehyde donors such as 1,3,5-trioxane, paraformaldehyde and hexamethylenetetramine. The condensation product is prepared by first reacting the aromatic hydroxy compound with formaldehyde and then reacting this product with the acid and urea derivative or by reacting the components (a) to (d) together. The products are useful as laking agents for basic dyes. A flexographic printing ink is prepared by dissolving a copolymer of styrene and diethyl maleate in a mixture of ethanol and ethylene glycol to which is then added a basic dye such as Rhodamine B and a resin product prepared as above which is the reaction product of (1) p-tertiary – butylphenol, formaldehyde salicylic acid and dimethylolurea dimethyl ether (2) as (1) but using malic acid instead of salicylic acid and (3) as (1) but using 4,41-dihydroxydiphenyl sulphone instead of p-tertiary butyl phenol. Other dyes such as Rhodamine BA, auramine benzene sulphonate, Victoria Blue B and malachite green may also be used.

GB51126/64A
1963-12-17
1964-12-16
Alkali-soluble cindensation products and their production

Expired

GB1080907A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

DEB74696A

DE1236193B
(en)

1963-12-17
1963-12-17

Process for the production of nitrogen-containing condensation products

Publications (1)

Publication Number
Publication Date

GB1080907A
true

GB1080907A
(en)

1967-08-31

Family
ID=6978358
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB51126/64A
Expired

GB1080907A
(en)

1963-12-17
1964-12-16
Alkali-soluble cindensation products and their production

Country Status (9)

Country
Link

AT
(1)

AT246427B
(en)

BE
(1)

BE657203A
(en)

CH
(1)

CH479647A
(en)

DE
(1)

DE1236193B
(en)

DK
(1)

DK112773B
(en)

FR
(1)

FR1427122A
(en)

GB
(1)

GB1080907A
(en)

NL
(1)

NL6414544A
(en)

SE
(1)

SE309600B
(en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

DE827799C
(en)

*

1949-10-29
1952-01-14
Basf Ag

Process for the extraction of valuable tannins

1963

1963-12-17
DE
DEB74696A
patent/DE1236193B/en
active
Pending

1964

1964-12-10
CH
CH1593264A
patent/CH479647A/en
not_active
IP Right Cessation

1964-12-14
NL
NL6414544A
patent/NL6414544A/xx
unknown

1964-12-16
DK
DK618064AA
patent/DK112773B/en
unknown

1964-12-16
SE
SE15235/64A
patent/SE309600B/xx
unknown

1964-12-16
GB
GB51126/64A
patent/GB1080907A/en
not_active
Expired

1964-12-16
BE
BE657203D
patent/BE657203A/xx
unknown

1964-12-17
FR
FR999004A
patent/FR1427122A/en
not_active
Expired

1964-12-17
AT
AT1069564A
patent/AT246427B/en
active

Also Published As

Publication number
Publication date

AT246427B
(en)

1966-04-25

BE657203A
(en)

1965-06-16

SE309600B
(en)

1969-03-31

DE1236193B
(en)

1967-03-09

NL6414544A
(en)

1965-06-18

FR1427122A
(en)

1966-02-04

CH479647A
(en)

1969-10-15

DK112773B
(en)

1969-01-13

Similar Documents

Publication
Publication Date
Title

US4323667A
(en)

1982-04-06

Boric anhydride solutions and their use as hardeners of resols

ES426944A1
(en)

1976-07-16

Aqueous coating compositions

GB1080907A
(en)

1967-08-31

Alkali-soluble cindensation products and their production

GB726782A
(en)

1955-03-23

Cation exchange resins

DE1445535C3
(en)

1975-03-27

Process for the production of alkali-soluble condensation products

GB1055614A
(en)

1967-01-18

Colour lakes

GB1033700A
(en)

1966-06-22

Production of modified phenol-formaldehyde condensation products

US3296181A
(en)

1967-01-03

Phenolic-formaldehyde resins containing an alkyl phenol wherein the alkyl group contains 5-15 carbon atoms and ink compositions therefrom

ES353291A1
(en)

1969-08-16

Phenolic resin compositions and process

DE1495197C3
(en)

1974-07-11

Process for the production of condensation products

GB1356336A
(en)

1974-06-12

Stable varnishes lacquers and printing inks containing nitroce llulose

DE1235944B
(en)

1967-03-09

Process for the production of alkali-soluble condensation products

DE1246753B
(en)

1967-08-10

Process for the production of alkali-soluble condensation products

GB316700A
(en)

1929-08-08

Improvements in the manufacture of vulcanised fibre

ES268573A1
(en)

1961-12-16

Procedure for the preparation of inks for offset printing and appropriate formal resins for it (Machine-translation by Google Translate, not legally binding)

GB565472A
(en)

1944-11-13

Improved compositions of matter

US2014415A
(en)

1935-09-17

Process for the preparation of resinous condensation products from xylenol ethers and aldehydes

GB478988A
(en)

1938-01-28

Improvements in the process of treating phenol condensation products adapted for themanufacturing of phenol-aldehyde resins or products thereof

DE1247329B
(en)

1967-08-17

Process for the production of alkali-soluble condensation products

DE1224490B
(en)

1966-09-08

Process for the production of nitrogen-containing condensation products

ANDERSEN

1954

On the Quantitative Determination and Qualitative Charac-terization of Organic Compounds through their Salts or Addition Compounds with. Picric Acid.-

ES351117A1
(en)

1969-06-01

Procedure for the preparation of an emulgent composition based on an aliphatic amine. (Machine-translation by Google Translate, not legally binding)

DE1238483B
(en)

1967-04-13

Process for the production of alkali-soluble condensation products

ES385937A1
(en)

1973-11-16

Process for preparing barium-containing dispersion

DE1231711B
(en)

1967-01-05

Process for the production of alkali-soluble condensation products

Download PDF in English

None