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Patent 1064022 Summary

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Claims and Abstract availability

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(12) Patent: (11) CA 1064022
(21) Application Number: 1064022
(54) English Title: WATER-SOLUBLE DISAZO DYESTUFFS, A PROCESS FOR THEIR PREPARATION AND THEIR USE FOR DYEING SYNTHETIC AND NATURAL POLYAMIDES
(54) French Title: TEINTURE DISAZO SOLUBLES DANS L'EAU, PROCEDE POUR LEUR PREPARATION ET LEUR UTILISATION POUR TEINDRE DES POLYAMIDES SYNTHETIQUES ET NATURELS
Status: Term Expired - Post Grant Beyond Limit
Bibliographic Data
(51) International Patent Classification (IPC):
  • C9B 31/02 (2006.01)
  • C9B 31/065 (2006.01)
  • C9B 43/28 (2006.01)
  • D6P 1/06 (2006.01)
  • D6P 3/06 (2006.01)
(72) Inventors :
(73) Owners :
  • HOECHST AKTIENGESELLSCHAFT
(71) Applicants :
  • HOECHST AKTIENGESELLSCHAFT (Germany)
(74) Agent:
(74) Associate agent:
(45) Issued: 1979-10-09
(22) Filed Date:
Availability of licence: N/A
Dedicated to the Public: N/A
(25) Language of filing: English

Patent Cooperation Treaty (PCT): No

(30) Application Priority Data: None

Abstracts

English Abstract


Abstract of the Disclosure:
New water-soluble disazodyestuffs of the formula
<IMG>
in which R1 represents the methyl, ethyl, .beta.-hydroxyethyl or
.beta.-cyanoethyl group and R2 stands for a phenyl radical, whereby
the radical -OR1 stands in ring A in 2- or in 4- position to
the azo group, and their salts had been found which are very
well suitable for dyeing of synthetic and natural polyamides
and yield dyeings on these fibres with good to very good wet
fasteness and fastnesses to processing and to use. Furthermore
they possess a very good dyeing behaviour.


Claims

Note: Claims are shown in the official language in which they were submitted.


THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A water-soluble disazo dyestuff which corresponds in the form
of the free acid to the formula
<IMG>
in which R1 is methyl, ethyl, .beta.-hydroxyethyl or .beta.-cyano ethyl, R2 is phenyl
whereby -OR1 stands in ring A in 2- or 4-position to the azo group.
2. A process for colouring natural or synthetic polyamide fibres
which comprises applying to the fibres a dyestuff as claimed in claim 1 and
fixing the dyestuff.
3. A process as claimed in claim 2 wherein polyamide fibres are dyed
in a neutral or weakly acid aqueous bath at 90 - 105°C.
4. A process as claimed in claim 2 wherein polyamide fabric is
padded or printed with a dyestuff solution, thickened with a thickener, and
fixed by steaming after drying.
12

Description

Note: Descriptions are shown in the official language in which they were submitted.


HOE 74~F 381
L~ ,J ,~
The present invention concerns watsr-soluble di~azo-dye-
stu~f~, a proce~s for their preparation and their use ~or
dyei~g synthetic and natural polya~ides.
N~w water-soluble disazo dyestu~ were found, which, in
t~e ~or~ o~ 'he ree a~id, cor~espond tD ~ha general ~ormula
(1)
~03S~ =N~
OR1
in which R1 represents the ~ethyl, ethyl~ ~-hydroxyethyl ~
B-cya~oethyl group and R2 stands for a phenyl radicalv where-
by the radical -OR1 stands in ri~.g A in 2~ or in 4 positlo~.
to the azo group. These new dyestuffs of the formula (1) can
15 al50 be present as mixtures. Preference is given to thei.r
sodium9 potassium and ammonia salts.
The n~w dyestuffs are prepared, accordi~g to the inven-
tion9 by coupling the dia~o compound of 1 mol of 4~am~no-azo
ben~ene-4'-sul~o~$c acid of the ~ormula ~2
~03~ ~ -N~ NH~ (2)
with 1 mol of a coupling compo~ent of the fvr~ula ~4) or (5
.
25: EO
R2 R~
.
Z9 R2 hav~ng the above mentioned signifieatio~9 su~h $s for
,
.. ... . , , . , , . , ~ ................... . . . . .
.. ; . . . . .. . , -. , .. .- . . -

OE 74/F 381
example
~ and - ~ ~
or with 1 mol o~ a mixture of the~e ~-oup].ing compo~ents, in a
temperature range o~ O - 30C a~d i~ a pEI ran~e 8 - 12~pre~er-
ably at a pH ~alue betwee~ 10 - i2; subsequently, the ~ree
hydroxy group is reacted optionally in presence o~ water, and
an acld binding agent with an alkylation agentS A~ a:L~ylat~n
agent~ there ca~ be cited :
dimethylsul~ate, diethylsul~ate, methylbro~ide~ eth~lbromide
or ethylchloride, ethylen~chlorhydrine or ethyle~ox~de,
B-chloro-propionitrile or acrylo~trile.
The present invention concerns furthermore the use o~
the dis~zo dyes of the invention and ~heir mixtures ~or the
dyelng of natural polyamide fibres, such a~ wvol and silk~ and
synthetlc polyam~des~ particularly those of caprolactam 5 of
hexamethglenediamine a~d adipic acid or o~ polycondensation pro-
ducts obtainable ~rom ~r-ami~o-undecan~ic acid.
The dyestu~fs are used as free acids or as salts. They
may alsc be used i~ mixture with other sultable dyestuf~s f'or
dyelng of the aboYementioned, pre~erably synthetic9 textile
materials. The dyebat~ contain 0.01 t~ 20 parts b~ weight of
dyestu~, O.Q5 to 10 parts by weigh~ o~ u~ual dye auxiliair~es
a~d 0.05 to 10 parts bg w~ight of usual dispersants per 1000
parts by weight of d~ebath. The admixture~ are chose~ in such
a way, so that the dyeing bath i~ ~eutr~l or acid. Also d~eing
can be carried out i~ a weak to strong acid bath by addition of
~ 3 --
-- .. . .
.. i,, . ,, " , ....... .. . ..... .. .. ... . . . ..

0~01 to 20 parts by weight of an acid, for example of form$c
acid or acetic acid or also of a mineral acl~ or of alkali
~lts of the formic or acetic acid, to that neutral dye-bath,
but preferably dyeing is carried out ln a we~ly acid or neu-
tr~l bath (r~ A - 7), and ad~a~'~g~^u~ly æt a tempe~at~e be-
tween 80 and 105C, preferably betwee~ 90 and 105C.
For local dyeing by printing 9 printiLng paste~ are used
which contain per 1000 parts by ~eight generally I to 50 part~
by wei~ht ~f dyestuff, 250 to 650 parts b~ weight of a usu~l
thickener such as, for 0xample, crystal gum, 1 to 50 parts by
weight of a usual printiIlg auxiliairy) 1 to 50 parts by weig~t
G~ a u.sual dispersa~t and 5 to 50 parts by weight o~ a salt
o~ a weak base and a strong mineral ac~d or o~ an organic, for
example, ammonium sulfate or a~mo~ium tartrate. For the ob-
tention o~ 1000 parts by weight o~ the prlnting pasteD water
or thickener~ are added adequately. The printed ~abrlrs are
dr~ed and treated for a short time wlth hot air or steam.
According to thi~ process applied on natural or syntheti~
polyamide fibres, golde~ yellow to ora~ge shades with good to
ver~ good ~astnesses to wet, for exampl~ ~astne~s to washl~g
at 40C and at 60C, generally called washing test 1 and 3
in DI~ 54 ~14 and DIN 54 010, to water uJlder severe con~itlons
~DIN 54 ~06), to alkaline and acid perspirationg to hypo-
chlorite ~each mild (DI~ 54 034) a~d to h~pochlorite bleach
severe (DIN 54 35)1 to chlorinated water to rubbin~ ln the
dry or wet state, to ~ullin~ in acid and alkaline med~um9 fas~--
ness to steaming, fastnes~ to alkali 9 to aold9 to decatlzing
and to dr~ cleani~g as well as with ~ery good to excelle~t
2~ .~as~ness propertie~ to light in xe~o-test a~d da~-light were
-- 4 --
.~ .
... : . . . , . ... - . -;, .: .. ,, : , .. .
.. : .. . : . .. .. . . . . . . - .
~ . .
: .. : . .. .. : , . - . ... , . , - . :
: ., ~ . ~ . .. . . . . -
. . : -: -,
: ~ . . . ... .. .

OE 74LF 381
obtained.
The dyestu~fs e~cell b~ a good built~up property and good
properties to migration, thus permitting to obtain deep clyeings
with good eve~ness. Particularly1 polyamide flbres oan well
e~ual be dyed in spite of their steady mvietie3.
Furthermore, together wlth well cho~en yellow, red and
blue acid dyes, the new d~estuffs are ~er~ suitable Xor the
dyeing of blended dye shades with very good fastness proper
ties to lighto
The ~ollowing examples illustrate th~ invention~ Parts
and percentages are by weight.
E X A M P ~ E 1:
, . .
a) 27.7 Parts of 4-aminoa~obenzene 4' sul~onic acld were
~tirred in form o~ the sodium salt into 150 parts of water,
6.9 parts o~ sodium nitrite were added alld the wh~le wa~
~lowly poured~ whilst stirr~g,i~to a mixture o~ 100 parts
o~ ice and 25 parts o~ a 31% hydrochloric acid. For the
deco~position of nitrous acid ~n ~xcess3 a small amount o~
amidosulfonie a id was added a~ter 3 hours 4 The suspen-
sion of the dia~o salt was the~ ad~usted with calcined so~
dium carbonate at a pH value o~ 6~5 to 7~0 a~d poured whils~
stirring, into a salution of 14.6 parts of 2-phenylphenol
and 13 parts o~ an aqueous 3~ by weight sodium hydroxide
~olution $n 250 parts of water a~d 250 parts of ice. The
coupling was effected ~ter 15 minutes. By a pH ad~ustmen~
at 6.0 with diluted hydrochloric ac~d, the d~estuff pre~l
pitated. It was then filtered off ~d washed with a ~% so~
diwm chloride solution,
29 b) 45.8 Parts of the dyestuf~ prepared accordin~ to a~ were
- 5 -
.. .
- ,.: . ... ~ , .: , ,. . . ~, ,

dissol~ed in a mixture of 400 parts o~ water and 350 part~
o~ aceto~e with an aqueous 33% by weight sodium hydroxide
solutlon at pH 12.0; a solution o~ 32 psrts of ethyleneoxide
in 150 parts o~ water were added, a~d the whole was stirred
a..;,0C. T~e et.heriîica~i~n was firlisned aI~er ~ hours at; .
p~ 12,0. The solvent was separated by distillation and tha
dyestuff was precipita~ed from the aqueous solution by adding
~odium chloride. A~ter filtration and dryi~g, a dyestuf~
was obtained, which corresponds as ~ree acid to the formula
. ; :
~OD S~N-==N~N==-~O-C~2 -CEI2 ~H
. ~ ', '' ~ ~ ,
Dn~lNG EXD~P5E:
100 Parts o~ a polycaprolactam fabric were put into a
bath ha~ng a temperature o~ 40C and co~taining 1.5 parts of
.
the d~estuff of Example 1b), 0O15 parts of an addition
product of 12 mol of ethylene oxid~ 1 mol of stearylamins,
0.40 parts of the condensation product o~ 1 mol of cyanurochloride
(trichloro-s-triazine3 with 3 mol o~ an~line-3 sul~o~ic acid9
2.0 parts o~ ammonium acetate and 1.Q part o~ a 60% acetic
acid in 3000 parts o~ water.
The temperature o~ the dye bath was raised within 15
minutss up to 98 - 100C, and dyeing was co~ti~ued for 50 ~inu- .
tes at 100&. After the usual finishing, a golden-~ellow dye-
~ng with good to very good fastness t~ wa~hing at 40C a~d
6~C9 to water (severe), to chlorlnate~ bath-water, to ~cid
a~d alkali~e perspiratio~J to mild a~d se~ere hypo~hlor~te
6 - :
... . . . . . . .... .., ., ~ . . . ~ . . .
., - .. . . , . , ,, .: .,, . .- ~ , ,. . . . . - . . . . . .. . ...

~OE 74/F 381
bleach~ to ~ulllng ~n alkaline and ~cid medium, to decatizing
and steaming, to acid and alkali as wel:L as to xeno--test and
day-light were obtained.
When the caprolactam fabric was replaced by 100 parts
o~ woal, dyeings wlth simllar gOOd general ~ast~ess properties
to use and processing and an excellent fastness to light were
obtained.
E X A M P ~,E 2:
45.~ Parts o~ the dyestuf~ o~ Example la) were dissolved
in 500 parts of water together with an aqueous sodlum hydroxide
solution at p~ 12.0; whllst ~igourosly stirring~ 25 parts o~
dim~thylsulfate were added dropwise, while the pH was ~ept
at -11.5 - 12.0 with the aid o~ a~ aqueous 33% sodium hydroxide
solution. The methylation was finished after 4 hours. The
reaction product prec~pitated partially; precipitatio~ is
finally achieved by addition of sodium chloride~ A~ter ~ ra~
tion9 a dyestuff was obtained~ which, ln th~ ~orm o~ the fre~ :
~cld, correspond~ to the ~ollowing formula:
. , ~
~ ~OoS ~ N===N ~ N===~ ~ OCH3
.
~E!~C ~AIII'DI~
: ~ h polycaprolactam fabric was printed with a paste cDn
~ Qlstlng o~ 10 parts of the dyestuff o~ Example 2, 30 parts
: of dibutylglycol9 250 parts of water, 650 parts o~ a çry~tal
:: gum thickening, 30 parts o~ ~itrobenze~e-3-sul~onic ~cld and
: . 30 parts of ammonium sul~ate. The printed fabric was drled
: ~ u~id steamed at 100 - 10?~C during 3~ minutes. The ~ln{~h~ng
- 7 -
'
~ , , ,, , . . .: . . . -
:: - ., .... .. . . , . . i ... ~ : .

HOE ~
is ~ffected, ~s usual, after subsequent rin~ing and dr~ing.
The golden-yellow printing obtained, possesses a very good
fastness to light beside very good general fastness to use
and processing.
E X A M P ~ E ,3:
45.8 Parts of the d~estuff o~ Example 1a) were dissol~ed
in a m~xture o~ 300 parts of water and 350 parts of aoetone
with an ~queous 33% hydroxide solution at p~ 10.5; 12.5 parts
of acrylo~itrile were added dropwise, at room temperature.
The al~lation was finished after 5 hours. ~he solvent was
distilled off, the aque~us dyestuff solution was diluted w~th
200 parts of water and filtered until clear at 6G~C. The dye-
~tuff was salted out from the solution by addition of sodium
chloride. It corresponds in the f~rm o~ the free acid to
the following formula:
.
~03S ~ N~ ~ N~ ~ O CH2-CE2-C~
.' ' ' ~
`, ~ -'. .
D~n~o ~
100 Parts of a tufted carpet of polyamide ~ibres, pre~ :
heated in ~aturated steam to 100C) run during 5 minute~
through a hot aqueous solution of 10~ - 102C, containing
t5 parts of the dyestuf~ o~ Example 3~ 0.3 parts of an add~
tion product of 12 mol of ethylenoxide to 1 mol stearylaminet
, 2 parts of sodium acetate and 1 part of acetic acidr Subse~ :
quently the dyed carpe~ was ri~sed a~ dried~ An even gol~e~
yellowp even dyeing with ~xcellent fa~t~ess to lig~ and g~oo~
general fast~es~ to use was achieY~d.
:i - 8 -
'

~~OE 7$/F 381
.r ~
The same coloristic result was o~tained with tufted felt
carpets.
E X A M P ~ E 4:
a) 27~7 Parts ~f 4-aminoaæobenzene-4'-sulfonic ac~d were stirred
in the form of the sodium salt into 150 parts of water, 6.9
parts of sodium nitr~.te were added, and the whole was poured
slowl~, whilst stirring into a m~xtur~ of 100 parts of ice
and 25 parts of a ~ hydroohloric acidO After ~ hours,
a small am~unt of amidosulfonic acid was added in order to
'decompose th~ nitrous acid in excess. The suspe~sion o~ the
dia~o salt was ad~usted with sodium carbonate to a pll of 6,5
t~ 7.0 a~d the~ poured, whilst s~irri.~g9 into a solutlon of
14.6 part~ of 4-phenylphenol and 13 parts of an aqu~ous ~3%
sodlum hydroxide solution in 250 parts of water and 250
parts of ice. Coupling was complete after 15 minutes~ T~ ~
dyestuff precipitated after a pH ad~ustme~t at 6.0 with di~ -
luted hydrochloric acid. It was then filtered and washed
with a 1% sQdium chlor~de solution.
b) 45.8 Parts o~ the dyestu~f prepared accordi~g to ~xample a~
were dissolved in a mixture of 400 parts of water and 350
parts of acetone with an aqueous 33% ~odium hydroxide solu-
tion at pH 12,0; 20 parts of ethylenechlorhydri~e were added~
By a dropwi~e addition of said c~ncentrated sodi ~ hydrox~de
solution, the pH Yalue was kept at 11.5 to 12.~. The re-
~25 action was complete after 6 hour~. The sol~ent ~as ad,~usted
: . with hydrochloric aoid at 6:.0 9 and th~ dyestuf~ was salted
~:: out with ~he aid of sodium chloride. After ~iltration a~d
drying, a dyestuff was obtained which correspo~ds in the
29 f orm of free acld to the following form~la: -
: - _ g _
,. ., .. , .. . ~-~: .. :, . . . . . - -
,, - : , . ; ,: . . . ~ ., -
...... , . ".. .--. ~, .. ~ . , ... ,. - . ., ~ . .
- . .. . : . .i,. . . ~ .. . :. : . . . :, . .. .
- . ., -, ~ - , . . ,. ~ . , ~ .
. . . .. , ~ . , . ~ .

~L~
I~&~ f~
~0-H~C~ C-0
ROa S~3N~ N~63NGlG~sN~?
. ' ',J ~
n~ G E~ s:
~ pol~amide carpet garn was treated wi-th a padding li~uor
up to a li~uor plck-up of 100~ by wei~ht. The paddin~ liqour
cont~$ned per 1 litre 10 part~ of ~he dyestuff of Exa~ple 3
5 parts of a locust bean flour preparationg 4 parts of an addi-
tion product of 8 mnl o~ ethyl~noxide to 1 ~ol of lso~ritlecyl
alcohol and 15 parts o~ a 60% acetic a¢id. The padded.y~rn
was subsequently steamed duri~g 6 minutes at 100 - 120~C and
then rinsed with cold water~ The dyeing p:ossess~s ~ery good
general fastness to u~e and a very good to ex~elle~t fastnes~
to day-light. .
The following table contains further dyestu~s which were
prepared and dyed according to the abo~eme~tio~ed Examples9
presenting good general ~astnes~ to use and pr~cessing.
.~ . ' : .
Example Formula Shade on p ly~
~(~
~;o~s~3N=N~3N=N~ ~ golden-~el~ ow

. H~C20
~ 6~ ~ss ~ N=N ~ N=N ~ golden~yellow
:: :
.
10 -

OE 74lF 381
.
... .. . . ...
E~ample F'ormula Shade o:~ poly-
7 ~0~5~ N=N~3N~N~oc2~6 golden yellow
~ . . .
B lsl - Mixture composed of
~s S~N--N~N- aN~OC~3
~ .
-aDd ~ ~ golden~yello~ -
. ~1~0 -
.. ~ IIO"S~3~1=ll~ll_W~
J ~ .
1~1 - Mlxtur~ composed of
9 ' ~OoS~N~N~Ns N~OCH2-C~2-O~
and ~ 3 golde~-y~ll ow
o~ 2 c- q
{02~ S~_N~N=~
'
~ : ~
: ~ . :,
:
,, .': ` ' ' ' ' ' : . ': . . . ' . . ' . `. . ~ " . . I ' . . ' ' ' ' ' ' . ' .'.' '. . .' ' .' . . .'

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Event History

Description Date
Inactive: IPC from MCD 2006-03-11
Inactive: IPC from MCD 2006-03-11
Inactive: IPC from MCD 2006-03-11
Inactive: Expired (old Act Patent) latest possible expiry date 1996-10-09
Grant by Issuance 1979-10-09

Abandonment History

There is no abandonment history.

Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
HOECHST AKTIENGESELLSCHAFT
Past Owners on Record
None
Past Owners that do not appear in the "Owners on Record" listing will appear in other documentation within the application.
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Document
Description 
Date
(yyyy-mm-dd) 
Number of pages   Size of Image (KB) 
Cover Page 1994-04-27 1 33
Claims 1994-04-27 1 56
Abstract 1994-04-27 1 37
Drawings 1994-04-27 1 14
Descriptions 1994-04-27 10 505