US2070104A - Azodyestuffs insoluble in water - Google Patents
Azodyestuffs insoluble in water Download PDFInfo
- Publication number
- US2070104A US2070104A US725821A US72582134A US2070104A US 2070104 A US2070104 A US 2070104A US 725821 A US725821 A US 725821A US 72582134 A US72582134 A US 72582134A US 2070104 A US2070104 A US 2070104A
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- US
- United States
- Prior art keywords
- water
- insoluble
- azodyestuffs
- grams
- clear
- 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
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- 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
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Definitions
- the present invention relates to new azodyehot, rinsed again and dried. In this manner a clear golden-orange dyeing of excellent fastness qualities is obtained.
- the new products may be obtained by diazotizing an arylamine containing two sulfone groups of the aforesaid kind and combining the diazo-compound, in substance or on a substratum especially on the fiber, with an arylamide of 2- hydroXy-3-naphthoic acid.
- Eccample 1 40 grams of boiled cotton yarn are impregnated in the usual manner in the following impregnating bath (a) and then developed in the following dyeing bath (b) (a) Impaegnating bath.
- Dyeing bath 4 grams of 1-amino-2,4-di-(propylsulfone)- benzene are dissolved at about 40-50 C. in 40 cc. of concentrated sulfuric acid.
- the solution is cooled down to 5 C. and 1 gram of sodium nitrite is added.
- the solution is diluted with ice-water and the difiicultly soluble diazo-compound is sucked off. Then it is carefully stirred with about 1200 cc. of water.
- SO2C4H9 i NH 4-zggLoro-l-aminoben- Orange which dyestuff dyes when prepared on the fiber s 020E206]; 7 clear yellowish orange shades.
- the dyestuffs yield when produced per 'se and when mixed with the usual substrata clear lakes of similar shades and good fastness qualities.
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- Organic Chemistry (AREA)
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Description
Patented Feb. 9, 1937 AZODYESTUFFS INSOLUBLE IN vWVATER Werner Zerweck,
Frankfort-on-the-Main Fechenheirn, and Norbert Steiger, Frankforton-theMa1n, Germany, assignors to General Aniline Works, Inc., New York, N. Y., a corporation of Delaware No Drawing. Application May 15, 1934, Serial No. 725,821. In Germany May 23, 1933 8 Claims.
The present invention relates to new azodyehot, rinsed again and dried. In this manner a clear golden-orange dyeing of excellent fastness qualities is obtained.
stuffs insoluble in water more particularly to such corresponding to the general formula:
(wherein one of the Xs means hydrogen or alkyl or phenyl, the other X alkyl or phenyl and the benzene nucleus attached to the CONH-group may contain as substituents halogen, alkyl or alkoxy groups) The new products may be obtained by diazotizing an arylamine containing two sulfone groups of the aforesaid kind and combining the diazo-compound, in substance or on a substratum especially on the fiber, with an arylamide of 2- hydroXy-3-naphthoic acid.
They are distinguished by clear fast yellow to golden-orange shades being as yellowish as hitherto not obtainable by means of dyestuffs of this series.
In order to further illustrate our invention the following examples and table are given; but we wish it however to be understood that our invention is not limited to the particular products nor reacting conditions mentioned therein.
Eccample 1 40 grams of boiled cotton yarn are impregnated in the usual manner in the following impregnating bath (a) and then developed in the following dyeing bath (b) (a) Impaegnating bath.
2 grams of 1-(2'-hydroxy-3naphthoylam ino) -2-methyl-4-chloro-benzene, 4 cc. of Turkey red oil of 50%, 6 cc. of caustic soda lye of 34 B., 2 cc. of a solution of formaldehyde of 30%, 500 cc. of boiling water, made up with water to 1 liter.
(b) Dyeing bath 3.3 grams of 1-amino-2-benzylsulfone-4-methylsulfone-benzene are dissolved at room temperature in 10 cc. of concentrated sulfuric acid and at 0 C. 1 gram of sodium nitrite is added to the solution. After shortly standing at 5-10" C. the diazo-solution is diluted with ice-water to about 800 cc. and the sulfuric acid is neutralized by means of 40 grams of sodium acetate.
Then the dye goods are rinsed, seemed in the Example 2 In the same manner as described in the foregoing example 40 grams of cotton yarn are impregnated in an impregnating bath, containing 2 grams of 1-(2',3'-hydroxy-naphthoylamino) -4- chime-benzene, and then developed in the following dyeing bath:
Dyeing bath 4 grams of 1-amino-2,4-di-(propylsulfone)- benzene are dissolved at about 40-50 C. in 40 cc. of concentrated sulfuric acid. The solution is cooled down to 5 C. and 1 gram of sodium nitrite is added. After about hour's stirring the solution is diluted with ice-water and the difiicultly soluble diazo-compound is sucked off. Then it is carefully stirred with about 1200 cc. of water.
A clear golden-orange dyeing is obtained.
The following table shows the shades of some further dyestuffs obtained according to the present process:
Shade Diazocomponent ggg gg g l Shade NH: Ammobenzene yellowishomnge whlch y fi yes wh n pr pared on th fib r clear golden orange shades. gs 0,0113 3. The azodyestufi of the formula: s OzOHzCaHs elm-s mommy- NH 4 chloro 1 aminoben 2 zetnia ..fi i. l Yellowishorange 2- 2 5 4-c oro-2-met y I S 020411 aminobenzene Do.
SO2C4H9 i NH: 4-zggLoro-l-aminoben- Orange which dyestuff dyes when prepared on the fiber s 020E206]; 7 clear yellowish orange shades.
5 4. The azodyestuff of the formula:
S OzCHzCaHs CaHn-SO N=N SOg-CzHs OH In the same manner similar clear shades may be obtained according to one of the usual printing methods.
The dyestuffs yield when produced per 'se and when mixed with the usual substrata clear lakes of similar shades and good fastness qualities.
We claim:
1. The azodye'st'ufis insoluble in water corresponding to the general formula:
s oiomx CzHr-SO which dyestuff dyes when prepared on the fiber clear orange shades.
5. Fibers dyed with the dyestuffs claimed in claim 1.
'6. Fibers dyed with the dyestuif claimed in claim 2.
7. Fibers dyed with the dyestufi claimed in claim 3.
8. Fibers dyed with the d claim 4.
yestufi claimed in S Or-CaH1 OH WERNER ZERWECK. NORBERT STEIGER.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2070104X | 1933-05-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2070104A true US2070104A (en) | 1937-02-09 |
Family
ID=7983512
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US725821A Expired - Lifetime US2070104A (en) | 1933-05-23 | 1934-05-15 | Azodyestuffs insoluble in water |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2070104A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2811515A (en) * | 1955-02-02 | 1957-10-29 | Geigy Ag J R | Lakes and the production thereof |
-
1934
- 1934-05-15 US US725821A patent/US2070104A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2811515A (en) * | 1955-02-02 | 1957-10-29 | Geigy Ag J R | Lakes and the production thereof |
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