BE516349A - - Google Patents
Info
- Publication number
- BE516349A BE516349A BE516349DA BE516349A BE 516349 A BE516349 A BE 516349A BE 516349D A BE516349D A BE 516349DA BE 516349 A BE516349 A BE 516349A
- Authority
- BE
- Belgium
- Prior art keywords
- sep
- group
- alkyl
- benzene
- halogen atom
- Prior art date
Links
- 239000002253 acid Substances 0.000 claims description 25
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 125000005843 halogen group Chemical group 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 8
- 239000004952 Polyamide Substances 0.000 claims description 6
- 238000004043 dyeing Methods 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 229940081735 acetylcellulose Drugs 0.000 claims description 4
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 4
- 239000000975 dye Substances 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 230000000875 corresponding Effects 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 2
- 229920001098 polystyrene-block-poly(ethylene/propylene) Polymers 0.000 description 240
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- UZBQIPPOMKBLAS-UHFFFAOYSA-N diethylazanide Chemical compound CC[N-]CC UZBQIPPOMKBLAS-UHFFFAOYSA-N 0.000 description 4
- XRMLOZSMCSUBTL-UHFFFAOYSA-N phenylazanide Chemical compound [NH-]C1=CC=CC=C1 XRMLOZSMCSUBTL-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- DNSISZSEWVHGLH-UHFFFAOYSA-N Butyramide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 102100001249 ALB Human genes 0.000 description 2
- 101710027066 ALB Proteins 0.000 description 2
- SUSGHUIAEYFPLD-UHFFFAOYSA-N C=1C=CC=CC=1C[N-]C1=CC=CC=C1 Chemical compound C=1C=CC=CC=1C[N-]C1=CC=CC=C1 SUSGHUIAEYFPLD-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 230000002378 acidificating Effects 0.000 description 2
- 229940050528 albumin Drugs 0.000 description 2
- -1 atoms halogen Chemical class 0.000 description 2
- 239000000987 azo dye Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 239000007857 degradation product Substances 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- RYXDGHXYFOWAFV-UHFFFAOYSA-N dicyclohexylazanide Chemical compound C1CCCCC1[N-]C1CCCCC1 RYXDGHXYFOWAFV-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- OPVAJFQBSDUNQA-UHFFFAOYSA-N 3,4-dimethylbenzoic acid Chemical compound CC1=CC=C(C(O)=O)C=C1C OPVAJFQBSDUNQA-UHFFFAOYSA-N 0.000 description 1
- GEGAHISFTIPAPK-UHFFFAOYSA-N 3-amino-N-benzyl-4-methoxy-N-methylbenzamide Chemical compound C1=C(N)C(OC)=CC=C1C(=O)N(C)CC1=CC=CC=C1 GEGAHISFTIPAPK-UHFFFAOYSA-N 0.000 description 1
- VMNZNSDAIFNWHL-UHFFFAOYSA-N C(C)(=O)C1=C(C(=C(C(=C1)OC)Cl)NC(=O)C)OC Chemical compound C(C)(=O)C1=C(C(=C(C(=C1)OC)Cl)NC(=O)C)OC VMNZNSDAIFNWHL-UHFFFAOYSA-N 0.000 description 1
- KHBCLONCLYQEHQ-UHFFFAOYSA-N C1CCCCC1[N-]C1=CC=CC=C1 Chemical compound C1CCCCC1[N-]C1=CC=CC=C1 KHBCLONCLYQEHQ-UHFFFAOYSA-N 0.000 description 1
- ICCCZUHKMWQDKM-UHFFFAOYSA-N C=1C=CC=CC=1C[N-]CC1=CC=CC=C1 Chemical compound C=1C=CC=CC=1C[N-]CC1=CC=CC=C1 ICCCZUHKMWQDKM-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N Diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- ZEYHEAKUIGZSGI-UHFFFAOYSA-N P-Anisic acid Chemical compound COC1=CC=C(C(O)=O)C=C1 ZEYHEAKUIGZSGI-UHFFFAOYSA-N 0.000 description 1
- 229940098465 Tincture Drugs 0.000 description 1
- 210000002268 Wool Anatomy 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- WCYBYZBPWZTMDW-UHFFFAOYSA-N dibutylazanide Chemical compound CCCC[N-]CCCC WCYBYZBPWZTMDW-UHFFFAOYSA-N 0.000 description 1
- YCNWUPFZUVYVKV-UHFFFAOYSA-N diphenylazanide Chemical compound C=1C=CC=CC=1[N-]C1=CC=CC=C1 YCNWUPFZUVYVKV-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N ethanolamine Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- CKTNHGVJKUQEBM-UHFFFAOYSA-N ethylazanide Chemical compound CC[NH-] CKTNHGVJKUQEBM-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- FYVOPPWTSVAJIF-UHFFFAOYSA-N methyl(phenyl)azanide Chemical compound C[N-]C1=CC=CC=C1 FYVOPPWTSVAJIF-UHFFFAOYSA-N 0.000 description 1
- 239000011528 polyamide (building material) Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/23—Azo-compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE516349A true BE516349A (es) |
Family
ID=153569
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE516349D BE516349A (es) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE516349A (es) |
-
0
- BE BE516349D patent/BE516349A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3148178A (en) | Azo compounds containing a dicarboximido radical | |
| BE516349A (es) | ||
| FR2602251A1 (fr) | Utilisation de composes monoazoiques comme colorants | |
| FR2734274A1 (fr) | Nouveaux composes azoiques, leur preparation et leur utilisation comme colorants de dispersion | |
| BE518451A (es) | ||
| BE514050A (es) | ||
| BE518158A (es) | ||
| BE515346A (es) | ||
| BE517635A (es) | ||
| BE513854A (es) | ||
| BE521884A (es) | ||
| BE626752A (es) | ||
| CH367254A (de) | Verfahren zur Herstellung in Wasser schwer löslicher Monoazofarbstoffe | |
| BE626052A (es) | ||
| BE703200A (es) | ||
| BE566598A (es) | ||
| US4667023A (en) | 4-(2'-halo-4'-nitrophenylazo)-2-2[2'-(C1-2 alkoxy or 2"-methoxyethoxy)ethoxycarbonylamino --N,N-di-C2-3 alkylanilines | |
| BE523998A (es) | ||
| BE563861A (es) | ||
| BE538055A (es) | ||
| BE493406A (es) | ||
| BE557604A (es) | ||
| BE649242A (es) | ||
| BE623968A (es) | ||
| BE564621A (es) |