PL76749B2 - - Google Patents

Info

Publication number

PL76749B2

PL76749B2 PL13967670A PL13967670A PL76749B2 PL 76749 B2 PL76749 B2 PL 76749B2 PL 13967670 A PL13967670 A PL 13967670A PL 13967670 A PL13967670 A PL 13967670A PL 76749 B2 PL76749 B2 PL 76749B2

Authority

PL

Poland

Prior art keywords

group

formula

hydroxynaphthalene

dye

wool

Prior art date

1970-03-28

Links

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• 239000000975 dye Substances 0.000 claims description 36
• 239000000835 fiber Substances 0.000 claims description 20
• 210000002268 wool Anatomy 0.000 claims description 15
• 229920000728 polyester Polymers 0.000 claims description 13
• 239000000203 mixture Substances 0.000 claims description 12
• 238000004043 dyeing Methods 0.000 claims description 10
• -1 hydroxyethyl group Chemical group 0.000 claims description 9
• 125000001424 substituent group Chemical group 0.000 claims description 5
• 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 2
• HGWQOFDAUWCQDA-UHFFFAOYSA-N 4-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(O)=CC=C(S(O)(=O)=O)C2=C1 HGWQOFDAUWCQDA-UHFFFAOYSA-N 0.000 claims description 2
• YLKCHWCYYNKADS-UHFFFAOYSA-N 5-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(O)=CC=CC2=C1S(O)(=O)=O YLKCHWCYYNKADS-UHFFFAOYSA-N 0.000 claims description 2
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
• 239000004480 active ingredient Substances 0.000 claims description 2
• 125000000217 alkyl group Chemical group 0.000 claims description 2
• 150000001555 benzenes Chemical class 0.000 claims description 2
• 229910052801 chlorine Inorganic materials 0.000 claims description 2
• 239000000460 chlorine Substances 0.000 claims description 2
• 239000002270 dispersing agent Substances 0.000 claims description 2
• 239000000945 filler Substances 0.000 claims description 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
• 150000002790 naphthalenes Chemical class 0.000 claims description 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
• RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 claims description 2
• 159000000000 sodium salts Chemical class 0.000 claims description 2
• 229940124530 sulfonamide Drugs 0.000 claims description 2
• 150000003456 sulfonamides Chemical class 0.000 claims description 2
• 239000000080 wetting agent Substances 0.000 claims description 2
• DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 1
• KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 1
• 125000004429 atom Chemical group 0.000 claims 1
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
• 229910052736 halogen Inorganic materials 0.000 claims 1
• 150000002367 halogens Chemical class 0.000 claims 1
• 229910052740 iodine Inorganic materials 0.000 claims 1
• RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical class CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 claims 1
• 125000000542 sulfonic acid group Chemical group 0.000 claims 1
• 238000009736 wetting Methods 0.000 claims 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
• WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
• 238000000034 method Methods 0.000 description 6
• 210000004243 sweat Anatomy 0.000 description 6
• 239000004753 textile Substances 0.000 description 5
• 238000005406 washing Methods 0.000 description 5
• 239000003795 chemical substances by application Substances 0.000 description 2
• 229960004279 formaldehyde Drugs 0.000 description 2
• 235000019256 formaldehyde Nutrition 0.000 description 2
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
• 229920001353 Dextrin Polymers 0.000 description 1
• 239000004375 Dextrin Substances 0.000 description 1
• SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
• 239000000980 acid dye Substances 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
• 229910052794 bromium Chemical group 0.000 description 1
• 235000019425 dextrin Nutrition 0.000 description 1
• 125000005843 halogen group Chemical group 0.000 description 1
• 229910052739 hydrogen Inorganic materials 0.000 description 1
• 239000001257 hydrogen Substances 0.000 description 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
• 239000000463 material Substances 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 238000012827 research and development Methods 0.000 description 1
• 239000011734 sodium Substances 0.000 description 1
• 229910052708 sodium Inorganic materials 0.000 description 1
• 235000015424 sodium Nutrition 0.000 description 1
• GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
• 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
• 239000000725 suspension Substances 0.000 description 1
• 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1