BE507915A - - Google Patents
Info
- Publication number
- BE507915A BE507915A BE507915DA BE507915A BE 507915 A BE507915 A BE 507915A BE 507915D A BE507915D A BE 507915DA BE 507915 A BE507915 A BE 507915A
- Authority
- BE
- Belgium
- Prior art keywords
- esterifiable
- bifunctional
- hydroxyl
- proportion
- phosphoric acid
- Prior art date
Links
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
- 230000001588 bifunctional effect Effects 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 7
- 239000000470 constituent Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 238000006482 condensation reaction Methods 0.000 claims 1
- 239000003701 inert diluent Substances 0.000 claims 1
- 239000012442 inert solvent Substances 0.000 claims 1
- 238000006068 polycondensation reaction Methods 0.000 description 6
- 150000002894 organic compounds Chemical class 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- AFINAILKDBCXMX-PBHICJAKSA-N (2s,3r)-2-amino-3-hydroxy-n-(4-octylphenyl)butanamide Chemical compound CCCCCCCCC1=CC=C(NC(=O)[C@@H](N)[C@@H](C)O)C=C1 AFINAILKDBCXMX-PBHICJAKSA-N 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 235000011007 phosphoric acid Nutrition 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- -1 hydroxyl compound Chemical class 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- VJQGGZWPOMJLTP-UHFFFAOYSA-N octadecane-1,1-diol Chemical compound CCCCCCCCCCCCCCCCCC(O)O VJQGGZWPOMJLTP-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000002904 solvent Substances 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
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/02—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing phosphorus
- C08G79/04—Phosphorus linked to oxygen or to oxygen and carbon
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE507915A true BE507915A (enrdf_load_stackoverflow) |
Family
ID=147755
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE507915D BE507915A (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE507915A (enrdf_load_stackoverflow) |
-
0
- BE BE507915D patent/BE507915A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6127498A (en) | Modified hydrogenated polymers | |
| EP0259233A2 (fr) | Procédé de préparation de polyisocyanate à groupement biuret | |
| BE507915A (enrdf_load_stackoverflow) | ||
| JPH06293891A (ja) | 潤滑剤化合物用のエステルベースオイルおよび有機反応副生物からのエステルベースオイルの製造方法 | |
| DE69804607T2 (de) | Verfahren zur herstellung und reinigung von komplexestern | |
| WO2000066601A1 (fr) | Procede de preparation d'aloine par extraction | |
| EP0296935A1 (fr) | Composés polyfluorés, leur préparation et leur utilisation comme additifs pour lubrifiants | |
| EP0171307B1 (fr) | Procédé de fabrication de composés silylmétallocènes et composés obtenus par ce procédé | |
| JPH1017582A (ja) | 燐酸エステルの製造方法 | |
| JPH11506447A (ja) | アスコルビン酸の回収のための方法及び組成物 | |
| EP3569220B1 (fr) | Composition tensioactive a base d'esters d'oligomeres d'isosorbide et de 1,3-propanediol | |
| WO2003016263A1 (en) | A process for the preparation of methacrylamide (maa) from acetoncyanohydrin | |
| US2240437A (en) | Composition for hydraulic systems | |
| US5399730A (en) | Method of obtaining an purified wool fat and use as an additive to lubricants | |
| BE447087A (enrdf_load_stackoverflow) | ||
| BE562052A (enrdf_load_stackoverflow) | ||
| BE637442A (enrdf_load_stackoverflow) | ||
| US9695105B2 (en) | Process for the preparation of complex oligomeric structures | |
| BE498811A (enrdf_load_stackoverflow) | ||
| EP4031554A1 (fr) | Procede de coupure oxydante d'olefines utilisant comme catalyseur un halooxodiperoxometallate | |
| US2133080A (en) | Fluid composition | |
| EP0984916A1 (en) | Oligomers of fatty acids | |
| HK1025087B (en) | Process for preparing and purifying complex esters | |
| BE447389A (enrdf_load_stackoverflow) | ||
| BE404391A (enrdf_load_stackoverflow) |