BE555327A - - Google Patents
Info
- Publication number
- BE555327A BE555327A BE555327DA BE555327A BE 555327 A BE555327 A BE 555327A BE 555327D A BE555327D A BE 555327DA BE 555327 A BE555327 A BE 555327A
- Authority
- BE
- Belgium
- Prior art keywords
- parts
- hydroxy
- dyes
- nitroso
- acid
- Prior art date
Links
- 239000000975 dye Substances 0.000 claims description 23
- 239000011780 sodium chloride Substances 0.000 claims description 9
- 238000004043 dyeing Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 claims description 4
- 230000002378 acidificating Effects 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- 150000004893 oxazines Chemical class 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- KYPOHTVBFVELTG-UHFFFAOYSA-N but-2-enedinitrile Chemical group N#CC=CC#N KYPOHTVBFVELTG-UHFFFAOYSA-N 0.000 claims description 2
- 238000004040 coloring Methods 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 19
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- 229960000583 Acetic Acid Drugs 0.000 description 11
- 239000000835 fiber Substances 0.000 description 9
- 229920002239 polyacrylonitrile Polymers 0.000 description 9
- 238000009835 boiling Methods 0.000 description 7
- 239000012362 glacial acetic acid Substances 0.000 description 7
- BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 239000005457 ice water Substances 0.000 description 6
- ZBIBQNVRTVLOHQ-UHFFFAOYSA-N 5-aminonaphthalen-1-ol Chemical class C1=CC=C2C(N)=CC=CC2=C1O ZBIBQNVRTVLOHQ-UHFFFAOYSA-N 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2H-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 235000011054 acetic acid Nutrition 0.000 description 4
- -1 4-nitroso-3-hydroxy- (ethyl-hydroxyethyl) - aniline Chemical compound 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-N propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
- OBESSQOKMPNJNS-UHFFFAOYSA-N 1,2,3,4-tetrahydrobenzo[h]quinolin-7-ol Chemical compound N1CCCC2=CC=C3C(O)=CC=CC3=C21 OBESSQOKMPNJNS-UHFFFAOYSA-N 0.000 description 2
- WRIZNEWVHJJMHU-UHFFFAOYSA-N 5-(dimethylamino)-2-nitrosophenol;hydrochloride Chemical compound Cl.CN(C)C1=CC=C(N=O)C(O)=C1 WRIZNEWVHJJMHU-UHFFFAOYSA-N 0.000 description 2
- LEPLYMVBUQERLB-UHFFFAOYSA-N 5-aminonaphthalen-1-ol;hydrochloride Chemical compound Cl.C1=CC=C2C(N)=CC=CC2=C1O LEPLYMVBUQERLB-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M Sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N Zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- WKJMQLMWPMZUQH-UHFFFAOYSA-N 1,2,3,4-tetrahydrobenzo[h]quinolin-3-ol Chemical compound C1=CC2=CC=CC=C2C2=C1CC(O)CN2 WKJMQLMWPMZUQH-UHFFFAOYSA-N 0.000 description 1
- FXYNGXZHZGJYPD-UHFFFAOYSA-N 1,2,3,4-tetrahydrobenzo[h]quinoline Chemical class C1=CC2=CC=CC=C2C2=C1CCCN2 FXYNGXZHZGJYPD-UHFFFAOYSA-N 0.000 description 1
- NXYYRSJPSPRDEO-UHFFFAOYSA-N 5-(diethylamino)-2-nitrosophenol Chemical compound CCN(CC)C1=CC=C(N=O)C(O)=C1 NXYYRSJPSPRDEO-UHFFFAOYSA-N 0.000 description 1
- JFOYWYLGEUIHOJ-UHFFFAOYSA-N 5-(diethylamino)-2-nitrosophenol;hydron;chloride Chemical compound Cl.CCN(CC)C1=CC=C(N=O)C(O)=C1 JFOYWYLGEUIHOJ-UHFFFAOYSA-N 0.000 description 1
- RXCPNLWXGCCTFR-UHFFFAOYSA-N 5-(dimethylamino)-2-nitrosophenol Chemical compound CN(C)C1=CC=C(N=O)C(O)=C1 RXCPNLWXGCCTFR-UHFFFAOYSA-N 0.000 description 1
- RAYQRDPSVGCFND-UHFFFAOYSA-N 5-amino-2-nitrosophenol Chemical class NC1=CC=C(N=O)C(O)=C1 RAYQRDPSVGCFND-UHFFFAOYSA-N 0.000 description 1
- 241000974482 Aricia saepiolus Species 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N Chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-Methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- CZTZIIXUGVMMID-UHFFFAOYSA-N N1CCCC2=CC=C3C(=C12)C=CC=C3S(=O)(=O)O Chemical compound N1CCCC2=CC=C3C(=C12)C=CC=C3S(=O)(=O)O CZTZIIXUGVMMID-UHFFFAOYSA-N 0.000 description 1
- GXKRDAUQHLPUCR-UHFFFAOYSA-N Nc1ccc(N=Nc2ccccc2)c(O)c1 Chemical class Nc1ccc(N=Nc2ccccc2)c(O)c1 GXKRDAUQHLPUCR-UHFFFAOYSA-N 0.000 description 1
- 229940116315 Oxalic Acid Drugs 0.000 description 1
- 229940095574 Propionic acid Drugs 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N Sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N Thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 229940013688 formic acid Drugs 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002562 thickening agent Substances 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
- C09B19/00—Oxazine dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE555327A true BE555327A (de) |
Family
ID=179491
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE555327D BE555327A (de) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE555327A (de) |
-
0
- BE BE555327D patent/BE555327A/fr unknown
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