DD145022A3 - Verfahren zur herstellung von neue siliziumhaltigen nitrofarbstoffen - Google Patents
Verfahren zur herstellung von neue siliziumhaltigen nitrofarbstoffen Download PDFInfo
- Publication number
- DD145022A3 DD145022A3 DD78204587A DD20458778A DD145022A3 DD 145022 A3 DD145022 A3 DD 145022A3 DD 78204587 A DD78204587 A DD 78204587A DD 20458778 A DD20458778 A DD 20458778A DD 145022 A3 DD145022 A3 DD 145022A3
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- process according
- radical
- natural
- items
- general formula
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 7
- -1 siloxanes Chemical class 0.000 claims description 10
- 229910052710 silicon Inorganic materials 0.000 claims description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000000835 fiber Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 238000004043 dyeing Methods 0.000 claims description 5
- 150000004756 silanes Chemical class 0.000 claims description 5
- 239000010703 silicon Substances 0.000 claims description 5
- 229910000077 silane Inorganic materials 0.000 claims description 4
- 239000012209 synthetic fiber Substances 0.000 claims description 4
- 229920002994 synthetic fiber Polymers 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 3
- 150000003254 radicals Chemical class 0.000 claims description 3
- 239000000985 reactive dye Substances 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 239000006103 coloring component Substances 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 229910010272 inorganic material Inorganic materials 0.000 claims description 2
- 239000011147 inorganic material Substances 0.000 claims description 2
- 229920000620 organic polymer Polymers 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 2
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000005375 organosiloxane group Chemical group 0.000 claims 1
- 239000001005 nitro dye Substances 0.000 abstract description 7
- 239000000975 dye Substances 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229920001296 polysiloxane Polymers 0.000 description 6
- 229940024463 silicone emollient and protective product Drugs 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000987 azo dye Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- LXQOQPGNCGEELI-UHFFFAOYSA-N 2,4-dinitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O LXQOQPGNCGEELI-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- PBZHKWVYRQRZQC-UHFFFAOYSA-N [Si+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O Chemical compound [Si+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PBZHKWVYRQRZQC-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 239000001049 brown dye Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- QHOQHJPRIBSPCY-UHFFFAOYSA-N pirimiphos-methyl Chemical compound CCN(CC)C1=NC(C)=CC(OP(=S)(OC)OC)=N1 QHOQHJPRIBSPCY-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000012192 staining solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/008—Dyes containing a substituent, which contains a silicium atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Silicon Polymers (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD78204587A DD145022A3 (de) | 1978-04-05 | 1978-04-05 | Verfahren zur herstellung von neue siliziumhaltigen nitrofarbstoffen |
| DE19792908204 DE2908204A1 (de) | 1978-04-05 | 1979-03-02 | Siliziumhaltige nitrofarbstoffe |
| SU797770487A SU1013454A1 (ru) | 1978-04-05 | 1979-03-07 | Способ получени кремнийсодержащих нитрокрасителей |
| CS791668A CS248253B1 (en) | 1978-04-05 | 1979-03-12 | Method of organo-siliceous nitrodye stuffs production |
| GB7910303A GB2018799B (en) | 1978-04-05 | 1979-03-23 | Silicon-containing nitro dystuffs |
| BE0/194332A BE875230A (fr) | 1978-04-05 | 1979-03-30 | Colorants nitres contenant du silicium et leur procede de preparation |
| FR7908520A FR2421934A1 (fr) | 1978-04-05 | 1979-04-04 | Colorants nitres silicies |
| JP4152579A JPS54148022A (en) | 1978-04-05 | 1979-04-05 | Siliconncontaining nitro dye |
| US06/352,830 US4403099A (en) | 1978-04-05 | 1982-02-26 | Silicon-containing nitro dyes and process for making the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD78204587A DD145022A3 (de) | 1978-04-05 | 1978-04-05 | Verfahren zur herstellung von neue siliziumhaltigen nitrofarbstoffen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD145022A3 true DD145022A3 (de) | 1980-11-19 |
Family
ID=5512074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD78204587A DD145022A3 (de) | 1978-04-05 | 1978-04-05 | Verfahren zur herstellung von neue siliziumhaltigen nitrofarbstoffen |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4403099A (cs) |
| JP (1) | JPS54148022A (cs) |
| BE (1) | BE875230A (cs) |
| CS (1) | CS248253B1 (cs) |
| DD (1) | DD145022A3 (cs) |
| DE (1) | DE2908204A1 (cs) |
| FR (1) | FR2421934A1 (cs) |
| GB (1) | GB2018799B (cs) |
| SU (1) | SU1013454A1 (cs) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19710461A1 (de) | 1997-03-13 | 1998-09-17 | Wacker Chemie Gmbh | Farbstoffreste aufweisende Organopolysiloxane |
| US7354459B2 (en) | 2004-11-03 | 2008-04-08 | L'oreal S.A. | Use of organosilane compounds for dyeing keratin fibers |
| FR2877217B1 (fr) | 2004-11-03 | 2007-01-26 | Oreal | Utilisation de composes de type organosilane en teinture des fibres keratiniques |
| DE102006027533A1 (de) * | 2006-06-14 | 2007-12-20 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Farbige Organopolysiloxane |
| DE102006046465A1 (de) * | 2006-09-29 | 2008-04-03 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Farbige Organopolysiloxane |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2256246A (en) * | 1939-10-06 | 1941-09-16 | Master Metal Products Inc | Welding apparatus |
| US2985680A (en) * | 1959-08-03 | 1961-05-23 | Union Carbide Corp | Nitro and nitrito derivatives of organosilicon compounds |
| US2998406A (en) * | 1960-06-14 | 1961-08-29 | Union Carbide Corp | Aminoaralkyl silicon compounds and process for their production |
| US3131205A (en) * | 1962-03-09 | 1964-04-28 | Aerojet General Co | N-(silico-alkyl) polynitro-alkyl amines and their preparation |
| US4139403A (en) * | 1977-08-19 | 1979-02-13 | The United States Of America As Represented By The Secretary Of The Navy | Dinitroalkyl and fluorodinitroalkyl silicon compounds |
-
1978
- 1978-04-05 DD DD78204587A patent/DD145022A3/de not_active IP Right Cessation
-
1979
- 1979-03-02 DE DE19792908204 patent/DE2908204A1/de not_active Withdrawn
- 1979-03-07 SU SU797770487A patent/SU1013454A1/ru active
- 1979-03-12 CS CS791668A patent/CS248253B1/cs unknown
- 1979-03-23 GB GB7910303A patent/GB2018799B/en not_active Expired
- 1979-03-30 BE BE0/194332A patent/BE875230A/xx unknown
- 1979-04-04 FR FR7908520A patent/FR2421934A1/fr not_active Withdrawn
- 1979-04-05 JP JP4152579A patent/JPS54148022A/ja active Pending
-
1982
- 1982-02-26 US US06/352,830 patent/US4403099A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| GB2018799A (en) | 1979-10-24 |
| CS248253B1 (en) | 1987-02-12 |
| SU1013454A1 (ru) | 1983-04-23 |
| GB2018799B (en) | 1982-07-07 |
| US4403099A (en) | 1983-09-06 |
| JPS54148022A (en) | 1979-11-19 |
| FR2421934A1 (fr) | 1979-11-02 |
| DE2908204A1 (de) | 1979-10-18 |
| BE875230A (fr) | 1979-07-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |