GB522657A - - Google Patents

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Publication number

GB522657A

GB522657A GB522657DA GB522657A GB 522657 A GB522657 A GB 522657A GB 522657D A GB522657D A GB 522657DA GB 522657 A GB522657 A GB 522657A

Authority

GB

United Kingdom

Prior art keywords

amino

mols

mol

benzoylaminoanthraquinone

aminoanthraquinone

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.)

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• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 4
• 239000002253 acid Substances 0.000 abstract 4
• VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 4
• 239000003795 chemical substances by application Substances 0.000 abstract 4
• 150000001875 compounds Chemical class 0.000 abstract 4
• 239000000047 product Substances 0.000 abstract 4
• 235000011149 sulphuric acid Nutrition 0.000 abstract 4
• 239000001117 sulphuric acid Substances 0.000 abstract 4
• KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 abstract 3
• FWEQPMZEKHHFTB-UHFFFAOYSA-N n-(5-amino-9,10-dioxoanthracen-1-yl)benzamide Chemical compound C1=CC=C2C(=O)C=3C(N)=CC=CC=3C(=O)C2=C1NC(=O)C1=CC=CC=C1 FWEQPMZEKHHFTB-UHFFFAOYSA-N 0.000 abstract 3
• 229920000742 Cotton Polymers 0.000 abstract 2
• UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
• 150000001412 amines Chemical class 0.000 abstract 2
• 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 abstract 2
• 150000004056 anthraquinones Chemical class 0.000 abstract 2
• 239000007859 condensation product Substances 0.000 abstract 2
• GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical compound OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 abstract 2
• 238000004043 dyeing Methods 0.000 abstract 2
• WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 abstract 2
• 125000001841 imino group Chemical group [H]N=* 0.000 abstract 2
• KOJOUCAVSDKDPR-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)benzamide Chemical compound C=1C=CC=2C(=O)C3=CC=CC=C3C(=O)C=2C=1NC(=O)C1=CC=CC=C1 KOJOUCAVSDKDPR-UHFFFAOYSA-N 0.000 abstract 2
• 239000000126 substance Substances 0.000 abstract 2
• 239000000984 vat dye Substances 0.000 abstract 2
• AURPCSOOPBKTPM-UHFFFAOYSA-N 1-amino-N-(9,10-dioxoanthracen-1-yl)-9,10-dioxo-2H-anthracene-1-carboxamide Chemical class NC1(CC=CC=2C(C3=CC=CC=C3C(C1=2)=O)=O)C(=O)NC1=CC=CC=2C(C3=CC=CC=C3C(C1=2)=O)=O AURPCSOOPBKTPM-UHFFFAOYSA-N 0.000 abstract 1
• BYSUDJAFZYUOGY-UHFFFAOYSA-N 10h-acridin-9-one;anthracene-9,10-dione Chemical class C1=CC=C2C(=O)C3=CC=CC=C3NC2=C1.C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 BYSUDJAFZYUOGY-UHFFFAOYSA-N 0.000 abstract 1
• VZMULMSIWMLZLC-UHFFFAOYSA-N 2-aminoanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-dione Chemical compound C12=C3C4=CC=C2C2=CC=CC=C2C(=O)C1=CC=C3C1=CC=C2C(=O)C3=CC=C(N)C=C3C3=CC=C4C1=C32 VZMULMSIWMLZLC-UHFFFAOYSA-N 0.000 abstract 1
• KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 abstract 1
• CTSUDNDKRCPJGF-UHFFFAOYSA-N N-(5-amino-4-methoxy-9,10-dioxoanthracen-1-yl)benzamide Chemical compound NC1=CC=CC=2C(C3=C(C=CC(=C3C(C12)=O)OC)NC(C1=CC=CC=C1)=O)=O CTSUDNDKRCPJGF-UHFFFAOYSA-N 0.000 abstract 1
• IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 abstract 1
• WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 abstract 1
• 239000012346 acetyl chloride Substances 0.000 abstract 1
• 229920002678 cellulose Polymers 0.000 abstract 1
• 235000010980 cellulose Nutrition 0.000 abstract 1
• 230000005494 condensation Effects 0.000 abstract 1
• 238000009833 condensation Methods 0.000 abstract 1
• 239000000975 dye Substances 0.000 abstract 1
• 150000002148 esters Chemical class 0.000 abstract 1
• 125000005843 halogen group Chemical group 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 230000004048 modification Effects 0.000 abstract 1
• 238000012986 modification Methods 0.000 abstract 1
• FXYMBQQAXFHRGC-UHFFFAOYSA-N n-(5-amino-9,10-dioxoanthracen-1-yl)acetamide Chemical compound O=C1C2=C(N)C=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C FXYMBQQAXFHRGC-UHFFFAOYSA-N 0.000 abstract 1
• OBJNZHVOCNPSCS-UHFFFAOYSA-N naphtho[2,3-f]quinazoline Chemical class C1=NC=C2C3=CC4=CC=CC=C4C=C3C=CC2=N1 OBJNZHVOCNPSCS-UHFFFAOYSA-N 0.000 abstract 1
• 230000001590 oxidative effect Effects 0.000 abstract 1
• LLBIOIRWAYBCKK-UHFFFAOYSA-N pyranthrene-8,16-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1C=C4C=C5 LLBIOIRWAYBCKK-UHFFFAOYSA-N 0.000 abstract 1
• XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 abstract 1
• 210000002268 wool Anatomy 0.000 abstract 1

Cited By (1)