GB910120A - - Google Patents

Info

Publication number

GB910120A

GB910120A GB910120DA GB910120A GB 910120 A GB910120 A GB 910120A GB 910120D A GB910120D A GB 910120DA GB 910120 A GB910120 A GB 910120A

Authority

GB

United Kingdom

Prior art keywords

aminophenol

dyes

benzene

residue

complexes

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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• 239000000975 dye Substances 0.000 abstract 5
• 239000002253 acid Substances 0.000 abstract 3
• 150000007513 acids Chemical class 0.000 abstract 3
• -1 cyclic primary Chemical class 0.000 abstract 3
• CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 abstract 2
• NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 abstract 2
• UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 2
• 210000002268 wool Anatomy 0.000 abstract 2
• RKPILPRSNWEZJV-UHFFFAOYSA-N 1-morpholin-4-ylbutane-1,3-dione Chemical compound CC(=O)CC(=O)N1CCOCC1 RKPILPRSNWEZJV-UHFFFAOYSA-N 0.000 abstract 1
• QINYBRXZAIWZBM-UHFFFAOYSA-N 2-(3-oxobutanoylamino)benzoic acid Chemical class CC(=O)CC(=O)NC1=CC=CC=C1C(O)=O QINYBRXZAIWZBM-UHFFFAOYSA-N 0.000 abstract 1
• FEDLEBCVFZMHBP-UHFFFAOYSA-N 2-amino-3-methylphenol Chemical compound CC1=CC=CC(O)=C1N FEDLEBCVFZMHBP-UHFFFAOYSA-N 0.000 abstract 1
• MHAFRUMLQZZSIN-UHFFFAOYSA-N 2-amino-4-chloro-6-nitrophenol Chemical compound NC1=CC(Cl)=CC([N+]([O-])=O)=C1O MHAFRUMLQZZSIN-UHFFFAOYSA-N 0.000 abstract 1
• ULUIMLJNTCECJU-UHFFFAOYSA-N 3-amino-4-hydroxybenzenesulfonate;hydron Chemical compound NC1=CC(S(O)(=O)=O)=CC=C1O ULUIMLJNTCECJU-UHFFFAOYSA-N 0.000 abstract 1
• ZBJVUXIVDBHNKW-UHFFFAOYSA-N 3-oxo-n-(3-sulfamoylphenyl)butanamide Chemical compound CC(=O)CC(=O)NC1=CC=CC(S(N)(=O)=O)=C1 ZBJVUXIVDBHNKW-UHFFFAOYSA-N 0.000 abstract 1
• ZNRACPWWAXITRC-UHFFFAOYSA-N N-(5-methoxy-2-methylphenyl)-3-oxobutanamide Chemical compound C(CC(=O)C)(=O)NC1=C(C=CC(=C1)OC)C ZNRACPWWAXITRC-UHFFFAOYSA-N 0.000 abstract 1
• 239000004952 Polyamide Substances 0.000 abstract 1
• GCPWJFKTWGFEHH-UHFFFAOYSA-N acetoacetamide Chemical class CC(=O)CC(N)=O GCPWJFKTWGFEHH-UHFFFAOYSA-N 0.000 abstract 1
• DYRDKSSFIWVSNM-UHFFFAOYSA-N acetoacetanilide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 abstract 1
• 229940051881 anilide analgesics and antipyretics Drugs 0.000 abstract 1
• 150000003931 anilides Chemical class 0.000 abstract 1
• PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 abstract 1
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 1
• 238000004043 dyeing Methods 0.000 abstract 1
• 239000002657 fibrous material Substances 0.000 abstract 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
• 239000010985 leather Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 125000001624 naphthyl group Chemical group 0.000 abstract 1
• 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
• 229920002647 polyamide Polymers 0.000 abstract 1
• 229920002635 polyurethane Polymers 0.000 abstract 1
• 239000004814 polyurethane Substances 0.000 abstract 1
• 150000003335 secondary amines Chemical class 0.000 abstract 1

Cited By (2)