GB531316A - Improvements in cellulose derivate compositions, films, yarns, or the like containing organic ester amides - Google Patents
Improvements in cellulose derivate compositions, films, yarns, or the like containing organic ester amidesInfo
- Publication number
- GB531316A GB531316A GB12482/39A GB1248239A GB531316A GB 531316 A GB531316 A GB 531316A GB 12482/39 A GB12482/39 A GB 12482/39A GB 1248239 A GB1248239 A GB 1248239A GB 531316 A GB531316 A GB 531316A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acetate
- butyrate
- ethanolamine
- propionate
- diethanolamine
- 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
Links
- -1 organic ester amides Chemical class 0.000 title abstract 14
- 239000000203 mixture Substances 0.000 title abstract 8
- 229920002678 cellulose Polymers 0.000 title abstract 6
- 239000001913 cellulose Substances 0.000 title abstract 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- 239000003921 oil Substances 0.000 abstract 5
- 235000019198 oils Nutrition 0.000 abstract 5
- 239000007788 liquid Substances 0.000 abstract 4
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 229920002301 cellulose acetate Polymers 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- KMZHZAAOEWVPSE-UHFFFAOYSA-N 2,3-dihydroxypropyl acetate Chemical compound CC(=O)OCC(O)CO KMZHZAAOEWVPSE-UHFFFAOYSA-N 0.000 abstract 2
- UGZICOVULPINFH-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O UGZICOVULPINFH-UHFFFAOYSA-N 0.000 abstract 2
- AVMNFQHJOOYCAP-UHFFFAOYSA-N acetic acid;propanoic acid Chemical compound CC(O)=O.CCC(O)=O AVMNFQHJOOYCAP-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 abstract 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 abstract 2
- 238000001035 drying Methods 0.000 abstract 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 abstract 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 abstract 2
- 238000009940 knitting Methods 0.000 abstract 2
- 239000004006 olive oil Substances 0.000 abstract 2
- 235000008390 olive oil Nutrition 0.000 abstract 2
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 abstract 2
- 238000010992 reflux Methods 0.000 abstract 2
- VKVOGLJYUFZFFA-UHFFFAOYSA-N 1-aminobutan-2-ol propanoic acid Chemical compound C(CC)(=O)O.C(CC)(=O)O.C(C)C(O)CN VKVOGLJYUFZFFA-UHFFFAOYSA-N 0.000 abstract 1
- PHELOKYCCWVWFE-UHFFFAOYSA-N 2,2-dimethoxyacetic acid Chemical compound COC(OC)C(O)=O PHELOKYCCWVWFE-UHFFFAOYSA-N 0.000 abstract 1
- URKPRLOWLUURBJ-UHFFFAOYSA-N 2-(2-hydroxyethylamino)ethanol propanoic acid Chemical compound C(CC)(=O)O.C(CC)(=O)O.C(CC)(=O)O.N(CCO)CCO URKPRLOWLUURBJ-UHFFFAOYSA-N 0.000 abstract 1
- VJKVBYPPYRIGJH-UHFFFAOYSA-N 5-methyl-2-(1,2,3-trimethyl-6-oxabicyclo[3.1.0]hexan-3-yl)phenol Chemical compound CC1C2(C)OC2CC1(C)C1=CC=C(C)C=C1O VJKVBYPPYRIGJH-UHFFFAOYSA-N 0.000 abstract 1
- XMAXSKXWPAEUHP-UHFFFAOYSA-N C(C)(=O)O.C(C)(=O)O.C(C)(=O)N(CCCC)CC(O)CO Chemical compound C(C)(=O)O.C(C)(=O)O.C(C)(=O)N(CCCC)CC(O)CO XMAXSKXWPAEUHP-UHFFFAOYSA-N 0.000 abstract 1
- XLMLMOMFCIGMQD-UHFFFAOYSA-N C(C)(=O)OC(CNOCC)C(C)=O Chemical compound C(C)(=O)OC(CNOCC)C(C)=O XLMLMOMFCIGMQD-UHFFFAOYSA-N 0.000 abstract 1
- CLKWZQXGKAFADO-UHFFFAOYSA-N C(CC)(=O)O.C(C)(=O)O.C(C)(=O)O.N(CCO)CCO Chemical compound C(CC)(=O)O.C(C)(=O)O.C(C)(=O)O.N(CCO)CCO CLKWZQXGKAFADO-UHFFFAOYSA-N 0.000 abstract 1
- IXGJVXBXIWWJEX-UHFFFAOYSA-N C(CCC)(=O)O.C(C)(=O)O.C(=O)N(CCO)CCO Chemical compound C(CCC)(=O)O.C(C)(=O)O.C(=O)N(CCO)CCO IXGJVXBXIWWJEX-UHFFFAOYSA-N 0.000 abstract 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 abstract 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 abstract 1
- 239000001856 Ethyl cellulose Substances 0.000 abstract 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- LIHGIKBIBXNWIP-UHFFFAOYSA-N Laurol Natural products CC1C2(C)OC2CC1(C)c3ccc(C)cc3 LIHGIKBIBXNWIP-UHFFFAOYSA-N 0.000 abstract 1
- ZHVCLDYSFWXCBI-UHFFFAOYSA-N N-(2-hydroxyethyl)-N-[4-(hydroxymethyl)-3,5-dioxoheptan-4-yl]acetamide Chemical compound C(C)(=O)N(C(CO)(C(CC)=O)C(CC)=O)CCO ZHVCLDYSFWXCBI-UHFFFAOYSA-N 0.000 abstract 1
- 125000003047 N-acetyl group Chemical group 0.000 abstract 1
- 229910002651 NO3 Inorganic materials 0.000 abstract 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- HRDVBNIPOIUQNV-UHFFFAOYSA-N acetic acid N,N-bis(2-hydroxyethyl)cyclopentanecarboxamide Chemical compound C(C)(=O)O.C(C)(=O)O.C1(CCCC1)C(=O)N(CCO)CCO HRDVBNIPOIUQNV-UHFFFAOYSA-N 0.000 abstract 1
- WSAAJSFTLDZYJU-UHFFFAOYSA-N acetic acid N-cyclopentyl-N-(2,3-dihydroxypropyl)acetamide Chemical compound C(C)(=O)O.C(C)(=O)O.C(C)(=O)N(C1CCCC1)CC(O)CO WSAAJSFTLDZYJU-UHFFFAOYSA-N 0.000 abstract 1
- BTVGHQASHWCGHI-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O.CCCC(O)=O BTVGHQASHWCGHI-UHFFFAOYSA-N 0.000 abstract 1
- BTYMTWWNCHIQIZ-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CC(O)=O.CCCC(O)=O BTYMTWWNCHIQIZ-UHFFFAOYSA-N 0.000 abstract 1
- PNXNSVYZNGNYIN-UHFFFAOYSA-N acetic acid;butanoic acid;propanoic acid Chemical compound CC(O)=O.CCC(O)=O.CCCC(O)=O PNXNSVYZNGNYIN-UHFFFAOYSA-N 0.000 abstract 1
- GFGJNFKDZWVYRW-UHFFFAOYSA-N acetic acid;propanoic acid Chemical compound CC(O)=O.CCC(O)=O.CCC(O)=O GFGJNFKDZWVYRW-UHFFFAOYSA-N 0.000 abstract 1
- YUEZNSHWNXXYJG-UHFFFAOYSA-N acetic acid;propanoic acid Chemical compound CC(O)=O.CC(O)=O.CCC(O)=O YUEZNSHWNXXYJG-UHFFFAOYSA-N 0.000 abstract 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 abstract 1
- 239000012346 acetyl chloride Substances 0.000 abstract 1
- 239000010775 animal oil Substances 0.000 abstract 1
- PXGPQCBSBQOPLZ-UHFFFAOYSA-N butanoic acid;propanoic acid Chemical compound CCC(O)=O.CCCC(O)=O PXGPQCBSBQOPLZ-UHFFFAOYSA-N 0.000 abstract 1
- YHASWHZGWUONAO-UHFFFAOYSA-N butanoyl butanoate Chemical compound CCCC(=O)OC(=O)CCC YHASWHZGWUONAO-UHFFFAOYSA-N 0.000 abstract 1
- 239000010495 camellia oil Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 229920001727 cellulose butyrate Polymers 0.000 abstract 1
- 230000001143 conditioned effect Effects 0.000 abstract 1
- 230000003750 conditioning effect Effects 0.000 abstract 1
- 229960002380 dibutyl phthalate Drugs 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 229920001249 ethyl cellulose Polymers 0.000 abstract 1
- 235000019325 ethyl cellulose Nutrition 0.000 abstract 1
- 238000004508 fractional distillation Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- AINBEPHCZYXVTF-UHFFFAOYSA-N hexanoic acid 2-(2-hydroxyethylamino)ethanol Chemical compound C(CCCCC)(=O)O.C(CCCCC)(=O)O.C(CCCCC)(=O)O.N(CCO)CCO AINBEPHCZYXVTF-UHFFFAOYSA-N 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004922 lacquer Substances 0.000 abstract 1
- 229940059904 light mineral oil Drugs 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000002480 mineral oil Substances 0.000 abstract 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N monoethyl amine Natural products CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 abstract 1
- ZEPPOSLOJNPSPC-UHFFFAOYSA-N n-acetyl-n-(2-hydroxyethyl)acetamide Chemical compound CC(=O)N(C(C)=O)CCO ZEPPOSLOJNPSPC-UHFFFAOYSA-N 0.000 abstract 1
- FEOFWXBYTMJIBA-UHFFFAOYSA-N n-acetyl-n-butylacetamide Chemical compound CCCCN(C(C)=O)C(C)=O FEOFWXBYTMJIBA-UHFFFAOYSA-N 0.000 abstract 1
- 229920001220 nitrocellulos Polymers 0.000 abstract 1
- 239000004014 plasticizer Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000009987 spinning Methods 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 125000005156 substituted alkylene group Chemical group 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 abstract 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 abstract 1
- 239000008158 vegetable oil Substances 0.000 abstract 1
- 235000013311 vegetables Nutrition 0.000 abstract 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/06—Protein or carboxylic compound containing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2904—Staple length fiber
- Y10T428/2907—Staple length fiber with coating or impregnation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2965—Cellulosic
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US204374A US2143765A (en) | 1938-04-26 | 1938-04-26 | Yarn conditioning process and composition therefor |
Publications (1)
Publication Number | Publication Date |
---|---|
GB531316A true GB531316A (en) | 1941-01-02 |
Family
ID=22757645
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12482/39A Expired GB531316A (en) | 1938-04-26 | 1939-04-26 | Improvements in cellulose derivate compositions, films, yarns, or the like containing organic ester amides |
Country Status (3)
Country | Link |
---|---|
US (1) | US2143765A (enrdf_load_stackoverflow) |
GB (1) | GB531316A (enrdf_load_stackoverflow) |
NL (2) | NL49392C (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2576898A (en) * | 1945-04-09 | 1951-11-27 | Ciba Ltd | Semiesters of unsaturated dicarboxylic acids |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE472957A (enrdf_load_stackoverflow) * | 1946-05-01 | |||
US3340218A (en) * | 1963-01-22 | 1967-09-05 | Frank C Magne | Diesteramide plasticizers |
US3318837A (en) * | 1963-01-22 | 1967-05-09 | Frank C Magne | Diesteramide plasticizers for vinyl chloride and nitrile rubber compositions |
DE3842008A1 (de) * | 1988-12-14 | 1990-06-21 | Hoechst Ag | Verwendung von triacylierten ehtanolaminen als fluessige, wassermischbare peroxidaktivatoren |
-
0
- NL NL27399D patent/NL27399C/xx active
- NL NL49392D patent/NL49392C/xx active
-
1938
- 1938-04-26 US US204374A patent/US2143765A/en not_active Expired - Lifetime
-
1939
- 1939-04-26 GB GB12482/39A patent/GB531316A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2576898A (en) * | 1945-04-09 | 1951-11-27 | Ciba Ltd | Semiesters of unsaturated dicarboxylic acids |
Also Published As
Publication number | Publication date |
---|---|
NL49392C (enrdf_load_stackoverflow) | |
US2143765A (en) | 1939-01-10 |
NL27399C (enrdf_load_stackoverflow) |
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