ES386268A1 - Stilbene compounds - Google Patents
Stilbene compoundsInfo
- Publication number
- ES386268A1 ES386268A1 ES386268A ES386268A ES386268A1 ES 386268 A1 ES386268 A1 ES 386268A1 ES 386268 A ES386268 A ES 386268A ES 386268 A ES386268 A ES 386268A ES 386268 A1 ES386268 A1 ES 386268A1
- Authority
- ES
- Spain
- Prior art keywords
- formula
- chosen
- moles
- mol
- substituted
- 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
-
- 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
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/14—Styryl dyes
- C09B23/148—Stilbene dyes containing the moiety -C6H5-CH=CH-C6H5
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Coloring (AREA)
- Detergent Compositions (AREA)
Abstract
Procedure for obtaining stilbene derivatives, of general formula **(See formula)** where X and Y, independent of each other, mean in each case a phenylemino residue, which can be substituted, and both a residue of the formula **(See formula)** how much formula **(See formula)** T and Z each signify both a residue of formula (II) and (III), R is chosen from hydrogen and low molecular weight alkyl, which may be substituted by hydroxy, alkoxy, cyano, aminocarbonyl, phenyl, phenoxy and cresoxy, R1 is chosen from hydrogen and a low molecular weight alkyl moiety, R2 means hydroxy, cyano, -CO-CmH2m + 1, (see formula) as well as -COOR7, R3 and R4, independent of each other, mean in each case both a low molecular weight alkyl moiety, and hydroxyalkyl as R3 and R4, together with the nitrogen atom, form a saturated heterocyclic moiety, R5 and R6, independent of each other, are chosen from a hydrogen atom, a low molecular weight alkyl moiety and a hydroxyalkyl group, since R5 and R6, together with the nitro-hay atom, form a saturated heterocyclic moiety, R7 stands for a low molecular weight alkyl moiety which may be substituted by hydroxy, alkoxy, phenoxy, cresoxy as well as phenyl, Me represents an equivalent of a metal chosen from an alkali and alkaline earth metal as well as an ammonium group. Anion is a colorless anion and m is a number from 1 to 3, n is chosen from 1 to 2 and p is a number from 2 to 6, with all residues being able **(See formula)** in the substituents T, X, Y and Z, they are the same as well as different from each other and all the residues R3 to R6, likewise, the same and also different from each other, the molecule presenting only two sulfonic radicals linked to the stilbene moiety, characterized in that in arbitrary sequence, both 2 moles of a cyanuric halide are reacted with a) 1 mole of 4,4'-diaminoestilben-2,2'-disulfonic acid, which may be in the form of a salt, b) 0 to 2 moles of an aminobenzene, which may be substituted and c) 2 to 4 moles of an amine of formula **(See formula)** both in the single state and in the form of a mixture of amines of formula (IV); the amines mentioned under b) and c) totaling 4 moles, the reaction product being reacted with a compound chosen from an acid and a quaternizing agent; as 1 mol of a cyanuric halide is reacted with a) 1 mol of acid chosen from 4-amino-4'-nitro- acid and 4-amino-4'-acylaminoestilben-2,2'-disulfonic acid, which may be in the form of a salt, b) 0 to 1 mol of an aminobenzene, which may be substituted, c) 1 to 2 mol of an amine of formula (IV) both in the single state and in the form of a mixture of amines of formula (IV), bringing the amines mentioned under b) and c) to a total of 2 moles, then the nitro group is reduced, just as the acylamino group is hydrolyzed and the amino group is reacted with 1 mole of a cyanuric halide and the compound Dihalogenotriazinioic acid is reacted in arbitrary sequence with d) 0 to 1 mol of an aminobenzene, which may be substituted, and e) 1 to 2 mol of an amine of formula (IV), both in the single state and in the form of a mixture of amines of formula (IV), the amines mentioned under d) and e) amounting to a total of 2 moles, being able to react the product reaction with a compound chosen from an acid and a quaternizing agent. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1842569A CH529770A (en) | 1969-12-11 | 1969-12-11 | Process for the preparation of new stilbene compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
ES386268A1 true ES386268A1 (en) | 1974-01-01 |
Family
ID=4432886
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES386268A Expired ES386268A1 (en) | 1969-12-11 | 1970-12-09 | Stilbene compounds |
Country Status (10)
Country | Link |
---|---|
US (1) | US3757010A (en) |
JP (2) | JPS527011B1 (en) |
BE (1) | BE760178A (en) |
CH (1) | CH529770A (en) |
DE (1) | DE2060085A1 (en) |
ES (1) | ES386268A1 (en) |
FR (1) | FR2073529A5 (en) |
GB (1) | GB1299120A (en) |
NL (1) | NL7018032A (en) |
ZA (1) | ZA708379B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH597204A5 (en) * | 1973-02-16 | 1978-03-31 | Sandoz Ag | |
CH583211A5 (en) * | 1973-05-22 | 1976-12-31 | Sandoz Ag | |
CH583212A5 (en) * | 1973-07-02 | 1976-12-31 | Sandoz Ag | |
CH603878B5 (en) * | 1973-09-21 | 1978-08-31 | Hoechst Ag | |
CH590965A5 (en) * | 1973-12-19 | 1977-08-31 | Ciba Geigy Ag | |
DE2712686C2 (en) * | 1977-03-23 | 1986-09-04 | Bayer Ag, 5090 Leverkusen | 4-Triazinyl-4'-benzoxazolyl or 4'-phenyl-stilbene derivatives |
US4478598A (en) * | 1981-02-26 | 1984-10-23 | Ciba-Geigy Corporation | Amphoteric styrene derivatives useful as fluorescent brighteners |
DE3922494A1 (en) * | 1989-07-08 | 1991-01-17 | Bayer Ag | FLUESSIGWASCHMITTEL |
US5319126A (en) * | 1993-01-29 | 1994-06-07 | Akzo N.V. | α-aminonitriles derived from fatty alkyl alkylene diamines |
GB9930247D0 (en) * | 1999-12-22 | 2000-02-09 | Clariant Int Ltd | Improvements in or relating to organic compounds |
GB9930177D0 (en) * | 1999-12-22 | 2000-02-09 | Clariant Int Ltd | Improvements in or relating to organic compounds |
JP2005529854A (en) * | 2002-03-19 | 2005-10-06 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | Amphoteric and cationic fluorescent whitening agents |
EP1511901B1 (en) * | 2002-06-11 | 2007-07-04 | Ciba SC Holding AG | Whitening pigments |
CN102898855B (en) * | 2012-09-29 | 2013-12-11 | 山东大学 | Synthesis and application of cetyl or octadecyl dimethyl tertiary amine quaternary ammonium salt high performance fluorescent whitening agent having amino acid structure |
-
1969
- 1969-12-11 CH CH1842569A patent/CH529770A/en not_active IP Right Cessation
-
1970
- 1970-12-07 DE DE19702060085 patent/DE2060085A1/en active Pending
- 1970-12-07 US US00095935A patent/US3757010A/en not_active Expired - Lifetime
- 1970-12-09 ES ES386268A patent/ES386268A1/en not_active Expired
- 1970-12-10 GB GB58647/70A patent/GB1299120A/en not_active Expired
- 1970-12-10 BE BE760178A patent/BE760178A/en unknown
- 1970-12-10 FR FR7044483A patent/FR2073529A5/en not_active Expired
- 1970-12-10 NL NL7018032A patent/NL7018032A/xx unknown
- 1970-12-10 JP JP45110044A patent/JPS527011B1/ja active Pending
- 1970-12-11 ZA ZA708379A patent/ZA708379B/en unknown
-
1972
- 1972-11-10 JP JP47112819A patent/JPS4924127B1/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
CH529770A (en) | 1972-10-31 |
JPS4924127B1 (en) | 1974-06-20 |
JPS527011B1 (en) | 1977-02-26 |
BE760178A (en) | 1971-05-17 |
FR2073529A5 (en) | 1971-10-01 |
GB1299120A (en) | 1972-12-06 |
ZA708379B (en) | 1972-07-26 |
NL7018032A (en) | 1971-06-15 |
DE2060085A1 (en) | 1971-06-16 |
US3757010A (en) | 1973-09-04 |
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