CH647794A5 - Monoazo coloranti per la tintura e stampa di fibre sintetiche. - Google Patents

Monoazo coloranti per la tintura e stampa di fibre sintetiche. Download PDF

Info

Publication number: CH647794A5
Authority: CH; Switzerland
Prior art keywords: dyeing; parts; dye; printing; white
Prior art date: 1980-02-21

Application number

CH1138/81A

Other languages

English (en)

Italian (it)

Inventor

Pier Domenico Mattioli

Sisto Sergio Papa

Angelo Mazzocchi

Original Assignee

Acna

Priority date (The priority date 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 date listed.)

1980-02-21

Filing date

1981-02-20

Publication date

1985-02-15

1981-02-20 Application filed by Acna filed Critical Acna

1985-02-15 Publication of CH647794A5 publication Critical patent/CH647794A5/it

Links

238000004043 dyeing Methods 0.000 title claims description 17
238000007639 printing Methods 0.000 title claims description 9
NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 title 1
239000012209 synthetic fiber Substances 0.000 title 1
229920002994 synthetic fiber Polymers 0.000 title 1
239000000203 mixture Substances 0.000 claims description 17
238000005260 corrosion Methods 0.000 claims description 10
230000007797 corrosion Effects 0.000 claims description 10
239000000835 fiber Substances 0.000 claims description 4
230000000694 effects Effects 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
239000000987 azo dye Substances 0.000 claims 2
239000000126 substance Substances 0.000 claims 1
239000000975 dye Substances 0.000 description 33
229910021627 Tin(IV) chloride Inorganic materials 0.000 description 13
238000000034 method Methods 0.000 description 13
239000004744 fabric Substances 0.000 description 12
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 12
229920000728 polyester Polymers 0.000 description 10
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 7
XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 7
239000004952 Polyamide Substances 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
229920002647 polyamide Polymers 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
230000001419 dependent effect Effects 0.000 description 4
229910000916 rhodite Inorganic materials 0.000 description 4
229920002284 Cellulose triacetate Polymers 0.000 description 3
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229920002239 polyacrylonitrile Polymers 0.000 description 3
UIHYHADQHHUIOF-UHFFFAOYSA-N 2-[n-ethyl-3-methyl-4-[(5-nitro-1,3-thiazol-2-yl)diazenyl]anilino]ethanol Chemical compound CC1=CC(N(CCO)CC)=CC=C1N=NC1=NC=C([N+]([O-])=O)S1 UIHYHADQHHUIOF-UHFFFAOYSA-N 0.000 description 2
VGKYEIFFSOPYEW-UHFFFAOYSA-N 2-methyl-4-[(4-phenyldiazenylphenyl)diazenyl]phenol Chemical compound Cc1cc(ccc1O)N=Nc1ccc(cc1)N=Nc1ccccc1 VGKYEIFFSOPYEW-UHFFFAOYSA-N 0.000 description 2
241001584775 Tunga penetrans Species 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
238000004140 cleaning Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
235000011121 sodium hydroxide Nutrition 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
239000000243 solution Substances 0.000 description 2
238000000859 sublimation Methods 0.000 description 2
230000008022 sublimation Effects 0.000 description 2
MHXFWEJMQVIWDH-UHFFFAOYSA-N 1-amino-4-hydroxy-2-phenoxyanthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=CC=C1 MHXFWEJMQVIWDH-UHFFFAOYSA-N 0.000 description 1
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
QEORVDCGZONWCJ-UHFFFAOYSA-N 2-[[4-[2-cyanoethyl(ethyl)amino]phenyl]diazenyl]-5-nitrobenzonitrile Chemical compound C1=CC(N(CCC#N)CC)=CC=C1N=NC1=CC=C([N+]([O-])=O)C=C1C#N QEORVDCGZONWCJ-UHFFFAOYSA-N 0.000 description 1
BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 1
NPBDWXMKLFBNIW-UHFFFAOYSA-N 3-[4-[(2-chloro-4-nitrophenyl)diazenyl]-n-ethylanilino]propanenitrile Chemical compound C1=CC(N(CCC#N)CC)=CC=C1N=NC1=CC=C([N+]([O-])=O)C=C1Cl NPBDWXMKLFBNIW-UHFFFAOYSA-N 0.000 description 1
RXQNKKRGJJRMKD-UHFFFAOYSA-N 5-bromo-2-methylaniline Chemical compound CC1=CC=C(Br)C=C1N RXQNKKRGJJRMKD-UHFFFAOYSA-N 0.000 description 1
ZYHNHJAMVNINSY-UHFFFAOYSA-N 6-methylsulfonyl-1,3-benzothiazol-2-amine Chemical compound CS(=O)(=O)C1=CC=C2N=C(N)SC2=C1 ZYHNHJAMVNINSY-UHFFFAOYSA-N 0.000 description 1
235000013912 Ceratonia siliqua Nutrition 0.000 description 1
240000008886 Ceratonia siliqua Species 0.000 description 1
239000002253 acid Substances 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000012267 brine Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000027326 copulation Effects 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
150000001989 diazonium salts Chemical class 0.000 description 1
238000010017 direct printing Methods 0.000 description 1
229940117964 disperse blue 106 Drugs 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical class OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 1
238000001914 filtration Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
238000009998 heat setting Methods 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
LJFWQNJLLOFIJK-UHFFFAOYSA-N solvent violet 13 Chemical compound C1=CC(C)=CC=C1NC1=CC=C(O)C2=C1C(=O)C1=CC=CC=C1C2=O LJFWQNJLLOFIJK-UHFFFAOYSA-N 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
239000006200 vaporizer Substances 0.000 description 1
238000005406 washing Methods 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0074—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms
- C09B29/0077—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms containing a five-membered heterocyclic ring with one nitrogen and one sulfur as heteroatoms
- C09B29/0085—Thiazoles or condensed thiazoles
- C09B29/0088—Benzothiazoles
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
- C09B29/0805—Amino benzenes free of acid groups
- C09B29/0807—Amino benzenes free of acid groups characterised by the amino group
- C09B29/0809—Amino benzenes free of acid groups characterised by the amino group substituted amino group
- C09B29/081—Amino benzenes free of acid groups characterised by the amino group substituted amino group unsubstituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino, aralkylamino or arylamino

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Coloring (AREA)

CH1138/81A 1980-02-21 1981-02-20 Monoazo coloranti per la tintura e stampa di fibre sintetiche. CH647794A5 (it)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT20069/80A IT1147323B (it)	1980-02-21	1980-02-21	Monoazocoloranti per la tintura e stampa di fibre sintetiche

Publications (1)

Publication Number	Publication Date
CH647794A5 true CH647794A5 (it)	1985-02-15

Family

ID=11163556

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1138/81A CH647794A5 (it)	1980-02-21	1981-02-20	Monoazo coloranti per la tintura e stampa di fibre sintetiche.

Country Status (10)

Country	Link
JP (1)	JPS56139560A (fr)
BE (1)	BE887619A (fr)
CA (1)	CA1168228A (fr)
CH (1)	CH647794A5 (fr)
DE (1)	DE3106126A1 (fr)
ES (1)	ES8300360A1 (fr)
FR (1)	FR2476664A1 (fr)
GB (1)	GB2070051A (fr)
IT (1)	IT1147323B (fr)
NL (1)	NL8100793A (fr)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS4935676A (fr) *	1972-08-15	1974-04-02
JPS6022112B2 (ja) *	1978-12-25	1985-05-31	住友化学工業株式会社	疎水性繊維を染色または捺染する方法

1980
- 1980-02-21 IT IT20069/80A patent/IT1147323B/it active
1981
- 1981-02-18 NL NL8100793A patent/NL8100793A/nl not_active Application Discontinuation
- 1981-02-19 DE DE19813106126 patent/DE3106126A1/de not_active Withdrawn
- 1981-02-19 FR FR8103286A patent/FR2476664A1/fr active Pending
- 1981-02-19 GB GB8105270A patent/GB2070051A/en not_active Withdrawn
- 1981-02-20 CH CH1138/81A patent/CH647794A5/it not_active IP Right Cessation
- 1981-02-20 CA CA000371431A patent/CA1168228A/fr not_active Expired
- 1981-02-20 ES ES499612A patent/ES8300360A1/es not_active Expired
- 1981-02-20 BE BE0/203870A patent/BE887619A/fr not_active IP Right Cessation
- 1981-02-20 JP JP2324881A patent/JPS56139560A/ja active Pending

Also Published As

Publication number	Publication date
NL8100793A (nl)	1981-09-16
CA1168228A (fr)	1984-05-29
DE3106126A1 (de)	1981-12-24
IT1147323B (it)	1986-11-19
ES499612A0 (es)	1982-11-01
GB2070051A (en)	1981-09-03
ES8300360A1 (es)	1982-11-01
BE887619A (fr)	1981-08-20
JPS56139560A (en)	1981-10-31
FR2476664A1 (fr)	1981-08-28
IT8020069A0 (it)	1980-02-21

Legal Events

Date	Code	Title	Description
1987-10-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

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CH699280A2 (it)	2010-02-15	Nuovo colorante bis-reattivo con gruppo ponte N,N-dialchilammino.
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