GB1042891A - Bis-triazinylamino-stilbene derivatives and their use as optical brighteners - Google Patents
Bis-triazinylamino-stilbene derivatives and their use as optical brightenersInfo
- Publication number
- GB1042891A GB1042891A GB4333/63A GB433363A GB1042891A GB 1042891 A GB1042891 A GB 1042891A GB 4333/63 A GB4333/63 A GB 4333/63A GB 433363 A GB433363 A GB 433363A GB 1042891 A GB1042891 A GB 1042891A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radical
- primary
- aliphatic amine
- group
- secondary aliphatic
- Prior art date
- 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
Links
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/30—Luminescent or fluorescent substances, e.g. for optical bleaching
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Detergent Compositions (AREA)
- Paper (AREA)
Abstract
Detergent compositions comprise optical brightening agents of the general formula <FORM:1042891/C4-C5/1> wherein Z represents a hydrogen atom or a group imparting solubility in water, R1 represents a hydrogen atom or an alkyl or alkoxy radical, and X represents an -NH2 group or the radical of a primary or secondary aliphatic amine, with the proviso that when R1=H and Z=a sulphonic acid group then X=-NH2 or the radical of a primary or secondary aliphatic amine containing a sulphonic or carboxylic acid group. Other components specified in examples are (i) sodium silicate, sodium hydroxide solution, alkylaryl sulphonate and hydrogen peroxide solution, and (ii) the condensation product of oleyl alcohol and about 10 mols. of ethylene oxide, polyphosphate, soap powder, sodium metasilicate, sodium perborate, magnesium silicate, carboxymethylcellulose and a conventional filler, e.g. sodium or potassium sulphate or carbonate. Reference has been directed by the Comptroller to Specification 987,922.ALSO:The invention comprises compounds of the general formula <FORM:1042891/C2/1> in which Z represents a hydrogen atom or a group imparting solubility in water, R1 represents a hydrogen atom or an alkyl or alkoxy radical, and X represents an -NH2 group or the radical of a primary or secondary aliphatic amine, with the proviso that when R1 = H and Z = a sulphonic acid group then X = -NH2 or the radical of a primary or secondary aliphatic amine containing a sulphonic or carboxylic acid group. The compounds may be prepared by reacting together, in any desired sequence, cyanuric chloride, an amino-stilbene derivative, an aminoaryl-b -hydroxyethylsulphone or an aminoaryl-b -hydroxyethylsulphone containing substituents in the ring, and a primary or secondary aliphatic amine. Examples are given. Reference has been directed by the Comptroller to Specification 987,922.ALSO:Optical brightening agents of the general formula <FORM:1042891/D1-D2/1> which Z represents a hydrogen atom or a group imparting solubility in water, R1 represents a hydrogen atom or an alkyl or alkoxy radical, and X represents an -NH2 group or the radical of a primary or secondary aliphatic amine, with the proviso that when R1=H and Z=a sulphonic acid group then p X=-NH2 or the radical of a primary or secondary aliphatic amine containing a sulphonic or carboxylic acid group, may be employed for the optical brightening of foils, films, felts or textile materials for example fibres, filaments, flocks, fabrics or knit fabrics made of natural, regenerated or synthetic materials, as well as of leather and paper. Especially good effects are obtained with natural or regenerated cellulose. The brightening agents may be used in association with detergents or rinsing or finishing agents or they may be added to the materials to be brightened during the production of such materials, for example, they may be added to wash lyes, brightening baths, bleaching baths and paper pulp. Examples describe the use of the compounds to brighten (1) bleached cotton fabric, (2) desized crude cotton fabric, (3) paper, (4) polycaprolactam fabric, (5) white cotton poplin, (6) bleached nettle cloth, (7) bleached wool flannel, and (8) bleached cotton poplin impregnated with a urea-formaldehyde precondensation product and ammonium nitrate, the condensation of the resin being completed subsequently at 150 DEG C. to give a crease-resistant material. Reference has been directed by Comptroller to Specification 987,922.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF35895A DE1237525B (en) | 1962-02-01 | 1962-02-01 | Optical brightener |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1042891A true GB1042891A (en) | 1966-09-14 |
Family
ID=7096209
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4333/63A Expired GB1042891A (en) | 1962-02-01 | 1963-02-01 | Bis-triazinylamino-stilbene derivatives and their use as optical brighteners |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE627915A (en) |
CH (1) | CH441212A (en) |
DE (1) | DE1237525B (en) |
DK (1) | DK104782C (en) |
GB (1) | GB1042891A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1469218B1 (en) * | 1964-06-30 | 1971-09-08 | Hoechst Ag | 4,4'-bis-triazinylamino-stilbene compounds and their use as reactive optical brightening agents |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1098485B (en) * | 1957-06-05 | 1961-02-02 | Bayer Ag | Whitening agents |
NL230056A (en) * | 1957-07-30 |
-
1962
- 1962-02-01 DE DEF35895A patent/DE1237525B/en active Pending
-
1963
- 1963-01-29 CH CH107363A patent/CH441212A/en unknown
- 1963-01-31 DK DK46763AA patent/DK104782C/en active
- 1963-02-01 GB GB4333/63A patent/GB1042891A/en not_active Expired
- 1963-02-01 BE BE627915A patent/BE627915A/en unknown
Also Published As
Publication number | Publication date |
---|---|
CH441212A (en) | 1967-04-29 |
BE627915A (en) | 1963-08-01 |
DK104782C (en) | 1966-07-04 |
DE1237525B (en) | 1967-03-30 |
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