DE2839936C2 - Mischungen von optischen Aufhellern und deren Verwendung zum optischen Aufhellen - Google Patents
Mischungen von optischen Aufhellern und deren Verwendung zum optischen AufhellenInfo
- Publication number
- DE2839936C2 DE2839936C2 DE2839936A DE2839936A DE2839936C2 DE 2839936 C2 DE2839936 C2 DE 2839936C2 DE 2839936 A DE2839936 A DE 2839936A DE 2839936 A DE2839936 A DE 2839936A DE 2839936 C2 DE2839936 C2 DE 2839936C2
- Authority
- DE
- Germany
- Prior art keywords
- formula
- group
- alkyl
- compound
- hydrogen
- 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
- 239000000203 mixture Substances 0.000 title claims description 24
- 230000003287 optical effect Effects 0.000 title claims description 12
- 238000005282 brightening Methods 0.000 title claims 2
- 150000001875 compounds Chemical class 0.000 claims description 37
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 11
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 150000003254 radicals Chemical class 0.000 claims description 9
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- -1 alkylene radicals Chemical class 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000000835 fiber Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 4
- 125000004193 piperazinyl group Chemical group 0.000 claims description 4
- 239000004753 textile Substances 0.000 claims description 4
- 125000004965 chloroalkyl group Chemical group 0.000 claims description 3
- 239000004744 fabric Substances 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 229910052717 sulfur Chemical group 0.000 claims description 3
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 claims description 2
- 229940081735 acetylcellulose Drugs 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 125000005605 benzo group Chemical group 0.000 claims description 2
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 2
- 229920002301 cellulose acetate Polymers 0.000 claims description 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims description 2
- 125000000068 chlorophenyl group Chemical group 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000003106 haloaryl group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 235000021286 stilbenes Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- APFMPAFOMJHHBR-UHFFFAOYSA-N 2-[2-(1,3-benzothiazol-2-yl)-1,2-diphenylethenyl]-1,3-benzothiazole Chemical class C1=CC=CC=C1C(C=1SC2=CC=CC=C2N=1)=C(C=1C=CC=CC=1)C1=NC2=CC=CC=C2S1 APFMPAFOMJHHBR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 125000004188 dichlorophenyl group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 125000001326 naphthylalkyl group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical group C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005581 pyrene group Chemical group 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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
- D06L4/65—Optical bleaching or brightening with mixtures of optical brighteners
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paper (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2839936A DE2839936C2 (de) | 1978-09-14 | 1978-09-14 | Mischungen von optischen Aufhellern und deren Verwendung zum optischen Aufhellen |
| CH820879A CH660939GA3 (enrdf_load_stackoverflow) | 1978-09-14 | 1979-09-11 | |
| PH23025A PH15495A (en) | 1978-09-14 | 1979-09-12 | Mixtures of optical brighteners and their use for optical brightening |
| SE7907574A SE7907574L (sv) | 1978-09-14 | 1979-09-12 | Blandningar av optiska uppklarningsmedel och deras anvendning for optisk uppklarning |
| IT7925679A IT1165305B (it) | 1978-09-14 | 1979-09-12 | Miscele di sbiancanti ottici e loro impiego per la sbianca ottica |
| BR7905862A BR7905862A (pt) | 1978-09-14 | 1979-09-13 | Misturas de aclaradores oticos e sua aplicacao |
| JP11680279A JPS5540785A (en) | 1978-09-14 | 1979-09-13 | Optical whitener mixture |
| CA000335590A CA1136356A (en) | 1978-09-14 | 1979-09-13 | Mixtures of optical brighteners and their use for the optical brightening |
| FR7922868A FR2436212A1 (fr) | 1978-09-14 | 1979-09-13 | Melanges d'azureurs optiques et leur utilisation pour l'azurage optique |
| NLAANVRAGE7906854,A NL186588C (nl) | 1978-09-14 | 1979-09-13 | Mengsel van optische witmakers. |
| GB7931729A GB2032480B (en) | 1978-09-14 | 1979-09-13 | Mixtures of optical brighteners |
| BE0/19715A BE878795A (fr) | 1978-09-14 | 1979-09-14 | Melanges d'azureurs optiques et leur utilisation pour l'azurage optique |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2839936A DE2839936C2 (de) | 1978-09-14 | 1978-09-14 | Mischungen von optischen Aufhellern und deren Verwendung zum optischen Aufhellen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2839936A1 DE2839936A1 (de) | 1980-04-03 |
| DE2839936C2 true DE2839936C2 (de) | 1983-11-10 |
Family
ID=6049392
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2839936A Expired DE2839936C2 (de) | 1978-09-14 | 1978-09-14 | Mischungen von optischen Aufhellern und deren Verwendung zum optischen Aufhellen |
Country Status (12)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3104992A1 (de) * | 1981-02-12 | 1982-08-26 | Hoechst Ag, 6000 Frankfurt | "mischungen von optischen aufhellern" |
| DE19732109A1 (de) * | 1997-07-25 | 1999-01-28 | Clariant Gmbh | Mischungen von optischen Aufhellern |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2721084C3 (de) * | 1977-05-11 | 1981-02-26 | Hoechst Ag, 6000 Frankfurt | Mischungen von optischen Aufhellern |
-
1978
- 1978-09-14 DE DE2839936A patent/DE2839936C2/de not_active Expired
-
1979
- 1979-09-11 CH CH820879A patent/CH660939GA3/de unknown
- 1979-09-12 SE SE7907574A patent/SE7907574L/xx unknown
- 1979-09-12 PH PH23025A patent/PH15495A/en unknown
- 1979-09-12 IT IT7925679A patent/IT1165305B/it active
- 1979-09-13 JP JP11680279A patent/JPS5540785A/ja active Granted
- 1979-09-13 FR FR7922868A patent/FR2436212A1/fr active Granted
- 1979-09-13 NL NLAANVRAGE7906854,A patent/NL186588C/xx not_active IP Right Cessation
- 1979-09-13 BR BR7905862A patent/BR7905862A/pt unknown
- 1979-09-13 GB GB7931729A patent/GB2032480B/en not_active Expired
- 1979-09-13 CA CA000335590A patent/CA1136356A/en not_active Expired
- 1979-09-14 BE BE0/19715A patent/BE878795A/fr not_active IP Right Cessation
Non-Patent Citations (1)
| Title |
|---|
| NICHTS-ERMITTELT |
Also Published As
| Publication number | Publication date |
|---|---|
| CH660939GA3 (enrdf_load_stackoverflow) | 1987-06-30 |
| GB2032480A (en) | 1980-05-08 |
| BE878795A (fr) | 1980-03-14 |
| NL186588B (nl) | 1990-08-01 |
| PH15495A (en) | 1983-02-03 |
| NL7906854A (nl) | 1980-03-18 |
| DE2839936A1 (de) | 1980-04-03 |
| SE7907574L (sv) | 1980-03-15 |
| IT7925679A0 (it) | 1979-09-12 |
| CA1136356A (en) | 1982-11-30 |
| JPH0130868B2 (enrdf_load_stackoverflow) | 1989-06-22 |
| IT1165305B (it) | 1987-04-22 |
| NL186588C (nl) | 1991-01-02 |
| GB2032480B (en) | 1982-12-01 |
| BR7905862A (pt) | 1980-05-27 |
| FR2436212B1 (enrdf_load_stackoverflow) | 1982-04-16 |
| FR2436212A1 (fr) | 1980-04-11 |
| JPS5540785A (en) | 1980-03-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| AF | Is addition to no. |
Ref country code: DE Ref document number: 2759217 Format of ref document f/p: P |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8340 | Patent of addition ceased/non-payment of fee of main patent |