GB1238868A - - Google Patents
Info
- Publication number
- GB1238868A GB1238868A GB1238868DA GB1238868A GB 1238868 A GB1238868 A GB 1238868A GB 1238868D A GB1238868D A GB 1238868DA GB 1238868 A GB1238868 A GB 1238868A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- aminopropane
- cyclohexyl
- compound
- betaine
- 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
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 abstract 8
- 229960003237 betaine Drugs 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000002252 acyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000002723 alicyclic group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 abstract 2
- -1 isopropyl - m - xylylene Chemical group 0.000 abstract 2
- 150000002897 organic nitrogen compounds Chemical class 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- ZMKGMRDHYTYLDH-UHFFFAOYSA-N (4-methylcyclohexyl)methanamine Chemical compound CC1CCC(CN)CC1 ZMKGMRDHYTYLDH-UHFFFAOYSA-N 0.000 abstract 1
- IWHLPMBLJZJCJK-UHFFFAOYSA-N 1-cyclohexyl-n-methylmethanamine Chemical compound CNCC1CCCCC1 IWHLPMBLJZJCJK-UHFFFAOYSA-N 0.000 abstract 1
- DVNDSHOBFJNZNP-UHFFFAOYSA-N 2,2-dipropylpentan-1-amine Chemical compound C(CC)C(CN)(CCC)CCC DVNDSHOBFJNZNP-UHFFFAOYSA-N 0.000 abstract 1
- PZRGOKSSPOFJKA-UHFFFAOYSA-N 2-(2-methylpropylamino)butanoic acid Chemical compound CCC(C(O)=O)NCC(C)C PZRGOKSSPOFJKA-UHFFFAOYSA-N 0.000 abstract 1
- HTFPTAKNJLIQHT-UHFFFAOYSA-N 2-(benzylamino)butanoic acid Chemical compound CCC(C(O)=O)NCC1=CC=CC=C1 HTFPTAKNJLIQHT-UHFFFAOYSA-N 0.000 abstract 1
- GSJHHYVLYJDKGO-UHFFFAOYSA-N 2-(cyclohexylamino)butanoic acid Chemical compound CCC(C(O)=O)NC1CCCCC1 GSJHHYVLYJDKGO-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229920002292 Nylon 6 Polymers 0.000 abstract 1
- 229920002302 Nylon 6,6 Polymers 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 229910010413 TiO 2 Inorganic materials 0.000 abstract 1
- IQOUVKKMFDZWOH-UHFFFAOYSA-N acetic acid N'-benzylpropane-1,3-diamine Chemical compound C(C)(=O)O.C(C1=CC=CC=C1)NCCCN IQOUVKKMFDZWOH-UHFFFAOYSA-N 0.000 abstract 1
- CGWVBPMMLKULCR-UHFFFAOYSA-N acetic acid;cyclohexylmethanamine Chemical compound CC(O)=O.NCC1CCCCC1 CGWVBPMMLKULCR-UHFFFAOYSA-N 0.000 abstract 1
- FAFRRWWYYOPZBO-UHFFFAOYSA-N acetic acid;n-methyl-1-phenylmethanamine Chemical compound CC(O)=O.CNCC1=CC=CC=C1 FAFRRWWYYOPZBO-UHFFFAOYSA-N 0.000 abstract 1
- MPPQYFREIJCHTB-UHFFFAOYSA-N acetic acid;phenylmethanamine Chemical compound CC([O-])=O.[NH3+]CC1=CC=CC=C1 MPPQYFREIJCHTB-UHFFFAOYSA-N 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- AVKNGPAMCBSNSO-UHFFFAOYSA-N cyclohexylmethanamine Chemical compound NCC1CCCCC1 AVKNGPAMCBSNSO-UHFFFAOYSA-N 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- AOPKHTALSHHYNJ-UHFFFAOYSA-N n'-(2,3-dimethylcyclohexyl)propane-1,3-diamine Chemical compound CC1CCCC(NCCCN)C1C AOPKHTALSHHYNJ-UHFFFAOYSA-N 0.000 abstract 1
- KZEVCRGCBNESNK-UHFFFAOYSA-N n'-(2-methylpropyl)hexane-1,6-diamine Chemical compound CC(C)CNCCCCCCN KZEVCRGCBNESNK-UHFFFAOYSA-N 0.000 abstract 1
- HUOLQRCLUIBWIH-UHFFFAOYSA-N n'-benzylhexane-1,6-diamine Chemical compound NCCCCCCNCC1=CC=CC=C1 HUOLQRCLUIBWIH-UHFFFAOYSA-N 0.000 abstract 1
- RFLHDXQRFPJPRR-UHFFFAOYSA-N n'-benzylpropane-1,3-diamine Chemical compound NCCCNCC1=CC=CC=C1 RFLHDXQRFPJPRR-UHFFFAOYSA-N 0.000 abstract 1
- ITZPOSYADVYECJ-UHFFFAOYSA-N n'-cyclohexylpropane-1,3-diamine Chemical compound NCCCNC1CCCCC1 ITZPOSYADVYECJ-UHFFFAOYSA-N 0.000 abstract 1
- FBJWOCSWSGEYRJ-UHFFFAOYSA-N n'-propan-2-ylbutane-1,4-diamine Chemical compound CC(C)NCCCCN FBJWOCSWSGEYRJ-UHFFFAOYSA-N 0.000 abstract 1
- LTGAVKFWROZLPO-UHFFFAOYSA-N n-(2-methylpropyl)pentanamide Chemical compound CCCCC(=O)NCC(C)C LTGAVKFWROZLPO-UHFFFAOYSA-N 0.000 abstract 1
- YXCRHNOACQLGPS-UHFFFAOYSA-N n-(3-phenylpropyl)acetamide Chemical compound CC(=O)NCCCC1=CC=CC=C1 YXCRHNOACQLGPS-UHFFFAOYSA-N 0.000 abstract 1
- SOGZMDYBQZTXIJ-UHFFFAOYSA-N n-(cyclohexylmethyl)propanamide Chemical compound CCC(=O)NCC1CCCCC1 SOGZMDYBQZTXIJ-UHFFFAOYSA-N 0.000 abstract 1
- VSKJCTSEACBXRC-UHFFFAOYSA-N n-[(4-methylphenyl)methyl]acetamide Chemical compound CC(=O)NCC1=CC=C(C)C=C1 VSKJCTSEACBXRC-UHFFFAOYSA-N 0.000 abstract 1
- UZJLYRRDVFWSGA-UHFFFAOYSA-N n-benzylacetamide Chemical compound CC(=O)NCC1=CC=CC=C1 UZJLYRRDVFWSGA-UHFFFAOYSA-N 0.000 abstract 1
- RIWRFSMVIUAEBX-UHFFFAOYSA-N n-methyl-1-phenylmethanamine Chemical compound CNCC1=CC=CC=C1 RIWRFSMVIUAEBX-UHFFFAOYSA-N 0.000 abstract 1
- SWKVQOVMQCHMDO-UHFFFAOYSA-N n-methyl-2,2-dipropylpentan-1-amine Chemical compound CCCC(CCC)(CCC)CNC SWKVQOVMQCHMDO-UHFFFAOYSA-N 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT810901 | 1967-08-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1238868A true GB1238868A (enrdf_load_stackoverflow) | 1971-07-14 |
Family
ID=11125833
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1238868D Expired GB1238868A (enrdf_load_stackoverflow) | 1967-08-08 | 1968-07-26 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1238868A (enrdf_load_stackoverflow) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4366306A (en) | 1980-02-01 | 1982-12-28 | The Dow Chemical Company | Melt polymerization of ε-caprolactam |
| WO2011048201A1 (en) | 2009-10-22 | 2011-04-28 | Grindeks, A Joint Stock Company | Use of 4-[ethyl(dimethyl)ammonio]butanoate in the treatment of cardiovascular disease |
| WO2012146736A1 (en) | 2011-04-27 | 2012-11-01 | Grindeks, A Joint Stock Company | Use of 3-carboxy-n-ethyl-n,n-dimethylpropan-1-aminium salts in the treatment of cardiovascular disease |
| WO2012146737A1 (en) | 2011-04-27 | 2012-11-01 | Grindeks, A Joint Stock Company | 4-[(haloalkyl)(dimethyl)ammonio]butanoates and use thereof in the treatment of cardiovascular disease |
-
1968
- 1968-07-26 GB GB1238868D patent/GB1238868A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4366306A (en) | 1980-02-01 | 1982-12-28 | The Dow Chemical Company | Melt polymerization of ε-caprolactam |
| WO2011048201A1 (en) | 2009-10-22 | 2011-04-28 | Grindeks, A Joint Stock Company | Use of 4-[ethyl(dimethyl)ammonio]butanoate in the treatment of cardiovascular disease |
| WO2012146736A1 (en) | 2011-04-27 | 2012-11-01 | Grindeks, A Joint Stock Company | Use of 3-carboxy-n-ethyl-n,n-dimethylpropan-1-aminium salts in the treatment of cardiovascular disease |
| WO2012146737A1 (en) | 2011-04-27 | 2012-11-01 | Grindeks, A Joint Stock Company | 4-[(haloalkyl)(dimethyl)ammonio]butanoates and use thereof in the treatment of cardiovascular disease |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 429H | Application (made) for amendment of specification now open to opposition (sect. 29/1949) | ||
| 429D | Case decided by the comptroller ** specification amended (sect. 29/1949) | ||
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |