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
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