BE628894A - - Google Patents
Info
- Publication number
- BE628894A BE628894A BE628894DA BE628894A BE 628894 A BE628894 A BE 628894A BE 628894D A BE628894D A BE 628894DA BE 628894 A BE628894 A BE 628894A
- Authority
- BE
- Belgium
- Prior art keywords
- water
- formula
- dye
- so2nhr
- group
- Prior art date
Links
- 239000000975 dye Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 229920000742 Cotton Polymers 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- PEYVWSJAZONVQK-UHFFFAOYSA-N hydroperoxy(oxo)borane Chemical compound OOB=O PEYVWSJAZONVQK-UHFFFAOYSA-N 0.000 claims 1
- 238000009938 salting Methods 0.000 claims 1
- 238000005185 salting out Methods 0.000 claims 1
- 238000000034 method Methods 0.000 description 6
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- -1 Ion sulfonamides Chemical class 0.000 description 1
- 241000220225 Malus Species 0.000 description 1
- 241001077660 Molo Species 0.000 description 1
- 101100409308 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) adv-1 gene Proteins 0.000 description 1
- 241000083869 Polyommatus dorylas Species 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- YXZRCLVVNRLPTP-UHFFFAOYSA-J turquoise blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Cu+2].NC1=NC(Cl)=NC(NC=2C=C(NS(=O)(=O)C3=CC=4C(=C5NC=4NC=4[N-]C(=C6C=CC(=CC6=4)S([O-])(=O)=O)NC=4NC(=C6C=C(C=CC6=4)S([O-])(=O)=O)NC=4[N-]C(=C6C=CC(=CC6=4)S([O-])(=O)=O)N5)C=C3)C(=CC=2)S([O-])(=O)=O)=N1 YXZRCLVVNRLPTP-UHFFFAOYSA-J 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 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
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/24—Obtaining compounds having —COOH or —SO3H radicals, or derivatives thereof, directly bound to the phthalocyanine radical
- C09B47/26—Amide radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE628894A true BE628894A (en)) |
Family
ID=198592
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE628894D BE628894A (en)) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE628894A (en)) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2404069A1 (de) * | 1973-02-01 | 1974-08-08 | Sandoz Ag | Phthalocyaninverbindungen, ihre herstellung und verwendung |
-
0
- BE BE628894D patent/BE628894A/fr unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2404069A1 (de) * | 1973-02-01 | 1974-08-08 | Sandoz Ag | Phthalocyaninverbindungen, ihre herstellung und verwendung |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN108358806B (zh) | 一种间乙酰胺基苯酚的连续化合成方法 | |
| BE628894A (en)) | ||
| JPS5955859A (ja) | フツ素化アクリレ−トと芳香族アミンとから誘導された化合物、それらの製造方法およびそれらを含有する汚れ防止剤 | |
| US483368A (en) | Senstiehl | |
| US563382A (en) | Friedrich krecke and ignaz rosenberg | |
| US1065440A (en) | Dyes of the anthraquinone series. | |
| KR100334466B1 (ko) | ｏ-클로로-ｐ-톨루이딘(ＯＣＰＴ)화합물의 신규한정제방법, 및 이를 이용한 ＯＣＰＴ-5-설폰산의 제조 방법 | |
| BE523495A (en)) | ||
| US525627A (en) | Jakob schmid and jacques bachelut | |
| US1280119A (en) | Arsenical compound. | |
| Shulman | New Compounds. Aminobenzene-(4-azo-1)-2-methyl-4-N-di-(β-hydroxyethyl)-aminobenzene | |
| JPH02246A (ja) | キラル・ジアチレン類 | |
| BE552843A (en)) | ||
| BE832269A (fr) | Pigments de benzidine et leur fabrication. | |
| CH355238A (fr) | Procédé de préparation de colorants monoazoïques | |
| BE516667A (en)) | ||
| BE539079A (en)) | ||
| BE460217A (en)) | ||
| BE440352A (en)) | ||
| CN1966486A (zh) | 硫酸甲基肼无溶剂法合成工艺 | |
| BE470179A (en)) | ||
| BE555800A (en)) | ||
| BE564944A (en)) | ||
| BE451168A (en)) | ||
| BE556059A (en)) |