GB797383A - New anthraquinone dyestuffs - Google Patents
New anthraquinone dyestuffsInfo
- Publication number
- GB797383A GB797383A GB67656A GB67656A GB797383A GB 797383 A GB797383 A GB 797383A GB 67656 A GB67656 A GB 67656A GB 67656 A GB67656 A GB 67656A GB 797383 A GB797383 A GB 797383A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxy
- glycol
- ethylene
- glycols
- dyes
- 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
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 title 1
- 150000004056 anthraquinones Chemical class 0.000 title 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 11
- 239000000975 dye Substances 0.000 abstract 8
- -1 1 - ethoxy - ethoxy Chemical group 0.000 abstract 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 5
- 239000000203 mixture Substances 0.000 abstract 4
- 238000010438 heat treatment Methods 0.000 abstract 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 2
- 125000005907 alkyl ester group Chemical group 0.000 abstract 2
- 150000002334 glycols Chemical class 0.000 abstract 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 abstract 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 2
- 150000003568 thioethers Chemical class 0.000 abstract 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 2
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 abstract 1
- YHCIQYSVFONICB-UHFFFAOYSA-N 1-sulfanylanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2S YHCIQYSVFONICB-UHFFFAOYSA-N 0.000 abstract 1
- FBPWKAWGAXBMOI-UHFFFAOYSA-N 2-(4-anilino-1-hydroxy-9,10-dioxoanthracen-2-yl)sulfonylacetic acid Chemical compound N(C1=CC=CC=C1)C1=CC(=C(C=2C(C3=CC=CC=C3C(C12)=O)=O)O)S(=O)(=O)CC(=O)O FBPWKAWGAXBMOI-UHFFFAOYSA-N 0.000 abstract 1
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 abstract 1
- JUHXSFLHDUCNCZ-UHFFFAOYSA-N 2-hydroxyethyl 2-chloroacetate Chemical compound OCCOC(=O)CCl JUHXSFLHDUCNCZ-UHFFFAOYSA-N 0.000 abstract 1
- BCYJWJGAKPLFBT-UHFFFAOYSA-N 4-anilino-2-bromo-1-hydroxyanthracene-9,10-dione Chemical compound C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(O)=C(Br)C=C1NC1=CC=CC=C1 BCYJWJGAKPLFBT-UHFFFAOYSA-N 0.000 abstract 1
- DVIFYZOHMIWOIJ-UHFFFAOYSA-N C(CCC)OCCC1=C(C=2C(C3=CC=CC=C3C(C=2C=C1)=O)=O)S Chemical class C(CCC)OCCC1=C(C=2C(C3=CC=CC=C3C(C=2C=C1)=O)=O)S DVIFYZOHMIWOIJ-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 229920000297 Rayon Polymers 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- 229960000583 acetic acid Drugs 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229960003750 ethyl chloride Drugs 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 239000012362 glacial acetic acid Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002366 halogen compounds Chemical class 0.000 abstract 1
- 150000002431 hydrogen Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000007800 oxidant agent Substances 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920001021 polysulfide Polymers 0.000 abstract 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical class OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 abstract 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical class OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 abstract 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
- C09B1/51—N-substituted amino-hydroxy anthraquinone
- C09B1/514—N-aryl derivatives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE554049D BE554049A (enrdf_load_stackoverflow) | 1956-01-09 | ||
| GB67656A GB797383A (en) | 1956-01-09 | 1956-01-09 | New anthraquinone dyestuffs |
| FR1164107D FR1164107A (fr) | 1956-01-09 | 1957-01-09 | Colorants anthraquinoniques |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB67656A GB797383A (en) | 1956-01-09 | 1956-01-09 | New anthraquinone dyestuffs |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB797383A true GB797383A (en) | 1958-07-02 |
Family
ID=9708580
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB67656A Expired GB797383A (en) | 1956-01-09 | 1956-01-09 | New anthraquinone dyestuffs |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE554049A (enrdf_load_stackoverflow) |
| FR (1) | FR1164107A (enrdf_load_stackoverflow) |
| GB (1) | GB797383A (enrdf_load_stackoverflow) |
-
0
- BE BE554049D patent/BE554049A/xx unknown
-
1956
- 1956-01-09 GB GB67656A patent/GB797383A/en not_active Expired
-
1957
- 1957-01-09 FR FR1164107D patent/FR1164107A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1164107A (fr) | 1958-10-06 |
| BE554049A (enrdf_load_stackoverflow) |
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