US1462613A - Wallace j - Google Patents
Wallace j Download PDFInfo
- Publication number
- US1462613A US1462613A US1462613DA US1462613A US 1462613 A US1462613 A US 1462613A US 1462613D A US1462613D A US 1462613DA US 1462613 A US1462613 A US 1462613A
- Authority
- US
- United States
- Prior art keywords
- acid
- solution
- developer
- colors
- amine
- 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 - Lifetime
Links
- 239000000987 azo dye Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 12
- 239000003921 oil Substances 0.000 description 10
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 8
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 8
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 7
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 7
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 7
- 239000005642 Oleic acid Substances 0.000 description 7
- 239000003125 aqueous solvent Substances 0.000 description 7
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 7
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 235000010288 sodium nitrite Nutrition 0.000 description 6
- JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 229950011260 betanaphthol Drugs 0.000 description 4
- 238000006193 diazotization reaction Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000003086 colorant Substances 0.000 description 3
- 150000008049 diazo compounds Chemical class 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 125000005456 glyceride group Chemical group 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KLBVIRPOVIVOLL-UHFFFAOYSA-N 3-hydroxy-4-[[4-[4-[[2-hydroxy-3-[(2-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-N-(2-methoxyphenyl)naphthalene-2-carboxamide Chemical compound COc1ccccc1NC(=O)c1cc2ccccc2c(N=Nc2ccc(cc2OC)-c2ccc(N=Nc3c(O)c(cc4ccccc34)C(=O)Nc3ccccc3OC)c(OC)c2)c1O KLBVIRPOVIVOLL-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 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 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- CSDTZUBPSYWZDX-UHFFFAOYSA-N n-pentyl nitrite Chemical class CCCCCON=O CSDTZUBPSYWZDX-UHFFFAOYSA-N 0.000 description 1
- GQPLMRYTRLFLPF-UHFFFAOYSA-N nitrous oxide Inorganic materials [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229940036248 turpentine Drugs 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
- C09B41/00—Special methods of performing the coupling reaction
Definitions
- the present invention relates to a method of producing azo colors in non-aqueous solvents, such as oils and materially increases the field of usefulness for such colors, as it enables their development in cases where the presence of water is undesirable.
- Azo colors are produced by treating an amine with nitrous acid in order to secure a diazo compound which is in turn treated with a developer to obtain the color, these azo colors having been invariably prepared in a water solution in the past,
- the preparation of the azo colors may be accomplished by treating a solution of the primary amine and developer in an oil, such as a liquid fatty acid, a glyceride, or hydro-carbon, containing a free acid, with sodium nitrite.
- an oil such as a liquid fatty acid, a glyceride, or hydro-carbon, containing a free acid
- this method produces colors directly in oil for use in inks and paints it has the decided advantage that the fatty acid or acidified oil will liberate nitrous acid from sodium nitrite and bring about diazotization without the use of water or mineral acids.
- the use of a mineral acid was necessary to liberate nitrous acid from sodium nitrite, it being necessary to neutralize this acid before couplin between the diazo compound and the deve oper could take place.
- these mineral acids have a corrosive action which is injurious to certain metals withwhich the solution may be in contact.
- One specific example of my new method consists in treating a solution of beta-naphthol and dianisidine in oleic acid with sodium nitrite.
- the oleic acid first liberates nitrous acidfrom the sodium nitrite which in turn diazotizes the dianisidine, the diazotized amine immediately reacting ,7 or coupling with the beta-naphthol or developer to precipitate the azo color, dianisidine blue, in the oil. Due to the red color of the oleic acid, the resulting combination may be purple or brown. This azo color may be made more resistant to treatment with chemicals, such as bleaching agents and acids by mordanting.
- metallic salts may be added to the mixture of oil, amine and developer; or they may be present in the material to be dyed, or they may be applied as an after-treatment.
- the oil solvent forming a part of the pres ent invention is intended to embrace all fatty acids and similar oils which are capa ble of liberating free nitrous acid from sodium or amyl nitrites to bring about diazotization. Included inthis classification are fatty acids such as oleic acid and glycerides and hydro-carbons containing free acids, such as a solution of rosin in turpentine. J
- a method of producing azo colors in non-aqueous solvents which consists in com bining a solution of an amine and a developer in oil with a nitrite.
- a method of producing azo colors in non-aqueous solvents whiclr consists in combining with a nitrite a solution of an amine and a developer in an oil capable of liberating freenitrous acid from the nitrite tocause diazotization of the amine by the nitrous acid.
- a method of producing a'zo colors in non-aqueous solvents which consists in combining a nitrite with a solution of an amine and a developer in a fatty acid.
- a method of producing azo colors in non-aqueous solvents which consists in combining a nitrite with a solution of a primary amine and a'developer in oleic acid.
- a method of producing azo colors in non-aqueous solvents which consists in combining a solution of dianisidine and betanaphthol in oleic acid with sodium nitrite to cause nitrous acid to be liberated by the oleic acid and diazotization of the dianisidine by the nitrous acid to take place, the
- a method of producing azo colors in non-aqueous solvents which consists in combining a nitrite with a solution of an amine and a developer in liquid organic acid capable of liberating free nitrous acid from the nitrite.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented July 24, 1923.
UNITED "STATES PA Er oer-loci,
WALLACE J. MURRAY, 01? BOSTON, MASSACHUSETTS, ASSIG-NOE' TO ARTHUR I). LITTIEQE,
INC OF CAMBRIDGE, MASSACHUSETTS, A CORPORATION OF 'JPIIASSACHUSE TTSQ METHOD or rnonucrno azo comes n nonaounous SOLVENTS.
1% D awin To all whom it may concern Be it known that I, WALLACE J. MURRAY, a citizen of the United States, residing at Boston, in the county of Sufiolk and State 5 of Massachusetts, have invented certain new and useful Improvements in Methods of Producing Azo Colors in Nonaqueous Solvents; and I do hereby declare the following to be a full, clear, and exact description of the invention, such as will enable others skilled in the art to which it appertains to make and use the same.
The present invention relates to a method of producing azo colors in non-aqueous solvents, such as oils and materially increases the field of usefulness for such colors, as it enables their development in cases where the presence of water is undesirable.
Azo colors are produced by treating an amine with nitrous acid in order to secure a diazo compound which is in turn treated with a developer to obtain the color, these azo colors having been invariably prepared in a water solution in the past,
I have discovered that the preparation of the azo colors may be accomplished by treating a solution of the primary amine and developer in an oil, such as a liquid fatty acid, a glyceride, or hydro-carbon, containing a free acid, with sodium nitrite. Aside from the fact that this method produces colors directly in oil for use in inks and paints it has the decided advantage that the fatty acid or acidified oil will liberate nitrous acid from sodium nitrite and bring about diazotization without the use of water or mineral acids. In previous methods the use of a mineral acid was necessary to liberate nitrous acid from sodium nitrite, it being necessary to neutralize this acid before couplin between the diazo compound and the deve oper could take place. In addition, these mineral acids have a corrosive action which is injurious to certain metals withwhich the solution may be in contact.
As one example of the increased field of Application filed June 9,
of the paper The use of a fatty acid as a vehicle causes a completepenetration of the paper, whereas the ordinary water solution of a primary amine and developer would not penetrate the sized paperduring the printing operation to any appreciable extent.
.One specific example of my new method consists in treating a solution of beta-naphthol and dianisidine in oleic acid with sodium nitrite. The oleic acid first liberates nitrous acidfrom the sodium nitrite which in turn diazotizes the dianisidine, the diazotized amine immediately reacting ,7 or coupling with the beta-naphthol or developer to precipitate the azo color, dianisidine blue, in the oil. Due to the red color of the oleic acid, the resulting combination may be purple or brown. This azo color may be made more resistant to treatment with chemicals, such as bleaching agents and acids by mordanting. Various substances arecknown to textile dyers for this purpose, the most impor tant being metallic salts. Thesemetallic salts may be added to the mixture of oil, amine and developer; or they may be present in the material to be dyed, or they may be applied as an after-treatment.
The oil solvent forming a part of the pres ent invention is intended to embrace all fatty acids and similar oils which are capa ble of liberating free nitrous acid from sodium or amyl nitrites to bring about diazotization. Included inthis classification are fatty acids such as oleic acid and glycerides and hydro-carbons containing free acids, such as a solution of rosin in turpentine. J
I claim:
1. A method of producing azo colors in non-aqueous solvents which consists in com bining a solution of an amine and a developer in oil with a nitrite.
2. A method of producing azo colors in non-aqueous solvents whiclr consists in combining with a nitrite a solution of an amine and a developer in an oil capable of liberating freenitrous acid from the nitrite tocause diazotization of the amine by the nitrous acid.
3. A method of producing a'zo colors in non-aqueous solvents which consists in combining a nitrite with a solution of an amine and a developer in a fatty acid.
4;. A method of producing azo colors in non-aqueous solvents which consists in combining a nitrite with a solution of a primary amine and a'developer in oleic acid.
5. A method of producing azo colors in non-aqueous solvents which consists in combining a solution of dianisidine and betanaphthol in oleic acid with sodium nitrite to cause nitrous acid to be liberated by the oleic acid and diazotization of the dianisidine by the nitrous acid to take place, the
diazo compound so produced coupling with the beta naphthol to produce a colored pigment.
6. A method of producing azo colors in non-aqueous solvents which consists in combining a nitrite with a solution of an amine and a developer in liquid organic acid capable of liberating free nitrous acid from the nitrite.
WALLACE J MURRAY.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1462613A true US1462613A (en) | 1923-07-24 |
Family
ID=3404616
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US1462613D Expired - Lifetime US1462613A (en) | Wallace j |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1462613A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2850493A (en) * | 1953-11-10 | 1958-09-02 | American Cyanamid Co | Oil soluble azo colors |
| JPS57131256A (en) * | 1980-12-23 | 1982-08-14 | Ciba Geigy Ag | Azo compound and manufacture |
-
0
- US US1462613D patent/US1462613A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2850493A (en) * | 1953-11-10 | 1958-09-02 | American Cyanamid Co | Oil soluble azo colors |
| JPS57131256A (en) * | 1980-12-23 | 1982-08-14 | Ciba Geigy Ag | Azo compound and manufacture |
| EP0055218A3 (en) * | 1980-12-23 | 1983-01-12 | Ciba-Geigy Ag | Manufacture of azoic compounds |
| US4496481A (en) * | 1980-12-23 | 1985-01-29 | Ciba-Geigy Corporation | Production of azo compounds |
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