BE452597A - - Google Patents
Info
- Publication number
- BE452597A BE452597A BE452597DA BE452597A BE 452597 A BE452597 A BE 452597A BE 452597D A BE452597D A BE 452597DA BE 452597 A BE452597 A BE 452597A
- Authority
- BE
- Belgium
- Prior art keywords
- reaction
- compounds
- amino
- group
- products
- Prior art date
Links
- 239000003381 stabilizer Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 6
- 150000001414 amino alcohols Chemical class 0.000 description 5
- 150000004985 diamines Chemical class 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 2
- XLJMAIOERFSOGZ-UHFFFAOYSA-N anhydrous cyanic acid Natural products OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000002648 azanetriyl group Chemical group *N(*)* 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000209761 Avena Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 241000195940 Bryophyta Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- -1 threads Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE452597A true BE452597A (enrdf_load_html_response) |
Family
ID=107178
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE452597D BE452597A (enrdf_load_html_response) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE452597A (enrdf_load_html_response) |
-
0
- BE BE452597D patent/BE452597A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE69316278T2 (de) | Verfahren zur Herstellung von Polysuccinimidpolymeren | |
EP0281461B1 (fr) | Polyesteramides et polyétheresteramides - leur procédé de fabrication | |
EP0783013A1 (de) | Copolymere Polyaminosäureester | |
DE69507001T2 (de) | Bisaminothiophenolverbindung, Verfahren zu ihrer Herstellung und diese Verbindung enthaltende Härter für Fluorelastomere | |
DE2708848A1 (de) | Mischpolyamide | |
BE452597A (enrdf_load_html_response) | ||
DE3022263A1 (de) | Dispergier-additive fuer schmiermittel | |
US4978756A (en) | Compound and use | |
Gupta et al. | L-tyrosine-based backbone-modified poly (amino acids) | |
DE1770336A1 (de) | Polyamide und Verfahren zu ihrer Herstellung | |
DE2735501A1 (de) | Polyaetherimid-zusammensetzungen | |
CA1049025A (en) | Ether-linked aryl tetracarboxylic dianhydrides | |
Wang et al. | Novel perfluorononenyloxy group containing aromatic polyamides | |
DE1274581B (de) | Verfahren zur Herstellung von halogenierten, gesaettigten, aliphatischen Carbonsaeuren, deren Salzen, Estern, Thioestern oder Amiden | |
JPS5811907B2 (ja) | 電線用塗料の製造法 | |
US2920086A (en) | Chemical compounds and methods for the preparation thereof | |
US5629448A (en) | Alcohol modified process for preparing bis-substituted phenolic amides | |
BE445791A (enrdf_load_html_response) | ||
US3492243A (en) | Organic solvent for prolamins | |
US3976669A (en) | Tertiary diamides | |
JP2540602B2 (ja) | 含フッ素アミド化合物 | |
BE451871A (enrdf_load_html_response) | ||
JPH0546369B2 (enrdf_load_html_response) | ||
BE442787A (enrdf_load_html_response) | ||
BE370232A (enrdf_load_html_response) |