GB1061022A – Salts of esters of sulpho-carboxylic acids and polymers thereof with acrylonitrile
– Google Patents
GB1061022A – Salts of esters of sulpho-carboxylic acids and polymers thereof with acrylonitrile
– Google Patents
Salts of esters of sulpho-carboxylic acids and polymers thereof with acrylonitrile
Info
Publication number
GB1061022A
GB1061022A
GB42012/63A
GB4201263A
GB1061022A
GB 1061022 A
GB1061022 A
GB 1061022A
GB 42012/63 A
GB42012/63 A
GB 42012/63A
GB 4201263 A
GB4201263 A
GB 4201263A
GB 1061022 A
GB1061022 A
GB 1061022A
Authority
GB
United Kingdom
Prior art keywords
compound
tertiary amine
formula
alkali metal
acrylonitrile
Prior art date
1962-10-24
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
Application number
GB42012/63A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
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.)
1962-10-24
Filing date
1963-10-24
Publication date
1967-03-08
1963-10-24
Application filed by Eastman Kodak Co
filed
Critical
Eastman Kodak Co
1967-03-08
Publication of GB1061022A
publication
Critical
patent/GB1061022A/en
Status
Expired
legal-status
Critical
Current
Links
Espacenet
Global Dossier
Discuss
NLHHRLWOUZZQLW-UHFFFAOYSA-N
Acrylonitrile
Chemical compound
C=CC#N
NLHHRLWOUZZQLW-UHFFFAOYSA-N
0.000
title
abstract
6
229920000642
polymer
Polymers
0.000
title
abstract
6
150000002148
esters
Chemical class
0.000
title
abstract
3
150000003839
salts
Chemical class
0.000
title
abstract
3
DIORMHZUUKOISG-UHFFFAOYSA-N
sulfoformic acid
Chemical class
OC(=O)S(O)(=O)=O
DIORMHZUUKOISG-UHFFFAOYSA-N
0.000
title
1
-1
aliphatic tertiary amine
Chemical class
0.000
abstract
16
150000001875
compounds
Chemical class
0.000
abstract
14
229910052783
alkali metal
Inorganic materials
0.000
abstract
8
150000001340
alkali metals
Chemical group
0.000
abstract
8
125000004432
carbon atom
Chemical group
C*
0.000
abstract
6
125000004435
hydrogen atom
Chemical group
[H]*
0.000
abstract
4
125000000217
alkyl group
Chemical group
0.000
abstract
3
150000001408
amides
Chemical class
0.000
abstract
3
229920001577
copolymer
Polymers
0.000
abstract
3
125000002496
methyl group
Chemical group
[H]C([H])([H])*
0.000
abstract
3
239000000203
mixture
Chemical class
0.000
abstract
3
239000000178
monomer
Substances
0.000
abstract
3
150000003512
tertiary amines
Chemical class
0.000
abstract
3
OZAIFHULBGXAKX-UHFFFAOYSA-N
2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile
Chemical class
N#CC(C)(C)N=NC(C)(C)C#N
OZAIFHULBGXAKX-UHFFFAOYSA-N
0.000
abstract
2
JUJWROOIHBZHMG-UHFFFAOYSA-N
Pyridine
Chemical compound
C1=CC=NC=C1
JUJWROOIHBZHMG-UHFFFAOYSA-N
0.000
abstract
2
KAESVJOAVNADME-UHFFFAOYSA-N
Pyrrole
Chemical compound
C=1C=CNC=1
KAESVJOAVNADME-UHFFFAOYSA-N
0.000
abstract
2
125000001931
aliphatic group
Chemical group
0.000
abstract
2
239000003054
catalyst
Substances
0.000
abstract
2
239000000975
dye
Substances
0.000
abstract
2
SNVLJLYUUXKWOJ-UHFFFAOYSA-N
methylidenecarbene
Chemical group
C=[C]
SNVLJLYUUXKWOJ-UHFFFAOYSA-N
0.000
abstract
2
239000002685
polymerization catalyst
Substances
0.000
abstract
2
238000006116
polymerization reaction
Methods
0.000
abstract
2
229920001897
terpolymer
Polymers
0.000
abstract
2
GETQZCLCWQTVFV-UHFFFAOYSA-N
trimethylamine
Chemical compound
CN(C)C
GETQZCLCWQTVFV-UHFFFAOYSA-N
0.000
abstract
2
229920002554
vinyl polymer
Polymers
0.000
abstract
2
SMZOUWXMTYCWNB-UHFFFAOYSA-N
2-(2-methoxy-5-methylphenyl)ethanamine
Chemical compound
COC1=CC=C(C)C=C1CCN
SMZOUWXMTYCWNB-UHFFFAOYSA-N
0.000
abstract
1
NIXOWILDQLNWCW-UHFFFAOYSA-N
2-Propenoic acid
Natural products
OC(=O)C=C
NIXOWILDQLNWCW-UHFFFAOYSA-N
0.000
abstract
1
FCYVWWWTHPPJII-UHFFFAOYSA-N
2-methylidenepropanedinitrile
Chemical compound
N#CC(=C)C#N
FCYVWWWTHPPJII-UHFFFAOYSA-N
0.000
abstract
1
NJIRSTSECXKPCO-UHFFFAOYSA-M
3-[n-methyl-4-[2-(1,3,3-trimethylindol-1-ium-2-yl)ethenyl]anilino]propanenitrile;chloride
Chemical compound
[Cl-].C1=CC(N(CCC#N)C)=CC=C1\C=C\C1=[N+](C)C2=CC=CC=C2C1(C)C
NJIRSTSECXKPCO-UHFFFAOYSA-M
0.000
abstract
1
125000002373
5 membered heterocyclic group
Chemical group
0.000
abstract
1
HRPVXLWXLXDGHG-UHFFFAOYSA-N
Acrylamide
Chemical compound
NC(=O)C=C
HRPVXLWXLXDGHG-UHFFFAOYSA-N
0.000
abstract
1
CERQOIWHTDAKMF-UHFFFAOYSA-N
Methacrylic acid
Chemical compound
CC(=C)C(O)=O
CERQOIWHTDAKMF-UHFFFAOYSA-N
0.000
abstract
1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M
Sodium bisulfite
Chemical compound
[Na+].OS([O-])=O
DWAQJAXMDSEUJJ-UHFFFAOYSA-M
0.000
abstract
1
WLKAMFOFXYCYDK-UHFFFAOYSA-N
[5-amino-4-[[3-[(2-amino-4-azaniumyl-5-methylphenyl)diazenyl]-4-methylphenyl]diazenyl]-2-methylphenyl]azanium;dichloride
Chemical compound
[Cl-].[Cl-].CC1=CC=C(N=NC=2C(=CC([NH3+])=C(C)C=2)N)C=C1N=NC1=CC(C)=C([NH3+])C=C1N
WLKAMFOFXYCYDK-UHFFFAOYSA-N
0.000
abstract
1
239000002253
acid
Substances
0.000
abstract
1
150000007513
acids
Chemical class
0.000
abstract
1
150000003926
acrylamides
Chemical class
0.000
abstract
1
230000003213
activating effect
Effects
0.000
abstract
1
125000005907
alkyl ester group
Chemical group
0.000
abstract
1
125000005037
alkyl phenyl group
Chemical group
0.000
abstract
1
KSCQDDRPFHTIRL-UHFFFAOYSA-N
auramine O
Chemical compound
[H+].[Cl-].C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1
KSCQDDRPFHTIRL-UHFFFAOYSA-N
0.000
abstract
1
239000000981
basic dye
Substances
0.000
abstract
1
125000001797
benzyl group
Chemical group
[H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])*
0.000
abstract
1
MMCOUVMKNAHQOY-UHFFFAOYSA-N
carbonoperoxoic acid
Chemical class
OOC(O)=O
MMCOUVMKNAHQOY-UHFFFAOYSA-N
0.000
abstract
1
125000003178
carboxy group
Chemical group
[H]OC(*)=O
0.000
abstract
1
150000001735
carboxylic acids
Chemical class
0.000
abstract
1
239000003153
chemical reaction reagent
Substances
0.000
abstract
1
239000003795
chemical substances by application
Substances
0.000
abstract
1
ZXJXZNDDNMQXFV-UHFFFAOYSA-M
crystal violet
Chemical compound
[Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1
ZXJXZNDDNMQXFV-UHFFFAOYSA-M
0.000
abstract
1
JOXWSDNHLSQKCC-UHFFFAOYSA-N
ethenesulfonamide
Chemical class
NS(=O)(=O)C=C
JOXWSDNHLSQKCC-UHFFFAOYSA-N
0.000
abstract
1
125000005670
ethenylalkyl group
Chemical group
0.000
abstract
1
239000000945
filler
Substances
0.000
abstract
1
125000003187
heptyl group
Chemical group
[H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H]
0.000
abstract
1
SYGRIMFNUFCHJC-UHFFFAOYSA-N
hydron;4-methyl-6-phenyldiazenylbenzene-1,3-diamine;chloride
Chemical compound
Cl.C1=C(N)C(C)=CC(N=NC=2C=CC=CC=2)=C1N
SYGRIMFNUFCHJC-UHFFFAOYSA-N
0.000
abstract
1
150000003949
imides
Chemical class
0.000
abstract
1
150000002505
iron
Chemical class
0.000
abstract
1
125000000555
isopropenyl group
Chemical group
[H]\C([H])=C(\*)C([H])([H])[H]
0.000
abstract
1
239000000314
lubricant
Substances
0.000
abstract
1
150000002825
nitriles
Chemical class
0.000
abstract
1
150000002978
peroxides
Chemical class
0.000
abstract
1
JRKICGRDRMAZLK-UHFFFAOYSA-L
persulfate group
Chemical group
S(=O)(=O)([O-])OOS(=O)(=O)[O-]
JRKICGRDRMAZLK-UHFFFAOYSA-L
0.000
abstract
1
239000000049
pigment
Substances
0.000
abstract
1
239000004014
plasticizer
Substances
0.000
abstract
1
UMJSCPRVCHMLSP-UHFFFAOYSA-N
pyridine
Natural products
COC1=CC=CN=C1
UMJSCPRVCHMLSP-UHFFFAOYSA-N
0.000
abstract
1
150000003222
pyridines
Chemical class
0.000
abstract
1
PYWVYCXTNDRMGF-UHFFFAOYSA-N
rhodamine B
Chemical compound
[Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O
PYWVYCXTNDRMGF-UHFFFAOYSA-N
0.000
abstract
1
235000010267
sodium hydrogen sulphite
Nutrition
0.000
abstract
1
239000004289
sodium hydrogen sulphite
Substances
0.000
abstract
1
159000000000
sodium salts
Chemical class
0.000
abstract
1
239000002904
solvent
Substances
0.000
abstract
1
150000003440
styrenes
Chemical class
0.000
abstract
1
LSNNMFCWUKXFEE-UHFFFAOYSA-L
sulfite
Chemical compound
[O-]S([O-])=O
LSNNMFCWUKXFEE-UHFFFAOYSA-L
0.000
abstract
1
BDHFUVZGWQCTTF-UHFFFAOYSA-N
sulfonic acid
Chemical group
OS(=O)=O
BDHFUVZGWQCTTF-UHFFFAOYSA-N
0.000
abstract
1
239000004094
surface-active agent
Substances
0.000
abstract
1
IMFACGCPASFAPR-UHFFFAOYSA-N
tributylamine
Chemical compound
CCCCN(CCCC)CCCC
IMFACGCPASFAPR-UHFFFAOYSA-N
0.000
abstract
1
125000000391
vinyl group
Chemical group
[H]C([*])=C([H])[H]
0.000
abstract
1
XLYOFNOQVPJJNP-UHFFFAOYSA-N
water
Substances
O
XLYOFNOQVPJJNP-UHFFFAOYSA-N
0.000
abstract
1
Classifications
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
C08F220/42—Nitriles
C08F220/44—Acrylonitrile
C08F220/46—Acrylonitrile with carboxylic acids, sulfonic acids or salts thereof
C—CHEMISTRY; METALLURGY
C07—ORGANIC CHEMISTRY
C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
C07C309/01—Sulfonic acids
C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
C07C309/17—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing carboxyl groups bound to the carbon skeleton
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
C08F28/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur
Abstract
The invention comprises compounds of the general formula
GB42012/63A
1962-10-24
1963-10-24
Salts of esters of sulpho-carboxylic acids and polymers thereof with acrylonitrile
Expired
GB1061022A
(en)
Applications Claiming Priority (1)
Application Number
Priority Date
Filing Date
Title
US232900A
US3260707A
(en)
1962-10-24
1962-10-24
Allyl and methallyl esters of sulfoaliphatic acids, and interpolymers thereof with acrylonitrile
Publications (1)
Publication Number
Publication Date
GB1061022A
true
GB1061022A
(en)
1967-03-08
Family
ID=22875055
Family Applications (1)
Application Number
Title
Priority Date
Filing Date
GB42012/63A
Expired
GB1061022A
(en)
1962-10-24
1963-10-24
Salts of esters of sulpho-carboxylic acids and polymers thereof with acrylonitrile
Country Status (2)
Country
Link
US
(1)
US3260707A
(en)
GB
(1)
GB1061022A
(en)
Families Citing this family (11)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
DE1595590A1
(en)
*
1966-02-02
1970-05-21
Bayer Ag
Process for the production of acrylonitrile copolymers
DE1595589A1
(en)
*
1966-02-02
1970-04-30
Bayer Ag
Process for the production of acrylonitrile copolymers
US3475364A
(en)
*
1966-10-17
1969-10-28
Celanese Corp
Art of producing dyeable acrylonitrile copolymer compositions and articles
US3666722A
(en)
*
1971-03-25
1972-05-30
Bayer Ag
Acrylonitrile copolymers containing sulfonic acid groups
US4136078A
(en)
*
1971-05-21
1979-01-23
The Lubrizol Corporation
Compositions comprising a plasticizer and an n-sulfohydrocarbon-substituted acrylamide polymer
US3923755A
(en)
*
1972-03-01
1975-12-02
Firestone Tire & Rubber Co
Amine sulfonates as dye sites in suspension polymers
CS170387B1
(en)
*
1973-08-15
1976-08-27
US4698413A
(en)
*
1979-08-01
1987-10-06
E. I. Du Pont De Nemours And Company
Acrylic fiber suitable for preparing carbon or graphite fibers
US4336022A
(en)
*
1979-08-01
1982-06-22
E. I. Du Pont De Nemours And Company
Acrylic precursor fibers suitable for preparing carbon or graphite fibers
US5273750A
(en)
*
1988-05-02
1993-12-28
Institute National De La Sante Et De La Recherche Medicale- Inserm
Uncrosslinked hydrogel, process for its preparation and its uses as an article for medical and/or surgical purposes such as tubes, films, joints, implants and the like, particularly in ophthalmology
DE102006055397B3
(en)
*
2006-11-22
2008-05-15
Heraeus Quarzglas Gmbh & Co. Kg
Method and device for the production of a cylindrical profile element made of quartz glass and use thereof
Family Cites Families (2)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
US2496275A
(en)
*
1945-08-17
1950-02-07
Eastman Kodak Co
Polymers and copolymers of unsaturated amides
BE523059A
(en)
*
1950-10-27
1953-10-15
1962
1962-10-24
US
US232900A
patent/US3260707A/en
not_active
Expired – Lifetime
1963
1963-10-24
GB
GB42012/63A
patent/GB1061022A/en
not_active
Expired
Also Published As
Publication number
Publication date
US3260707A
(en)
1966-07-12
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Hcxcxn-
None