BE440267A - - Google Patents
Info
- Publication number
- BE440267A BE440267A BE440267DA BE440267A BE 440267 A BE440267 A BE 440267A BE 440267D A BE440267D A BE 440267DA BE 440267 A BE440267 A BE 440267A
- Authority
- BE
- Belgium
- Prior art keywords
- solutions
- materials
- solution
- acid
- water
- Prior art date
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 235000008994 Laurocerasus officinalis Nutrition 0.000 claims description 7
- 244000061600 Laurocerasus officinalis Species 0.000 claims description 7
- 235000004098 Prunus caroliniana Nutrition 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 244000144725 Amygdalus communis Species 0.000 claims description 2
- 235000003893 Prunus dulcis var amara Nutrition 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 17
- 239000000463 material Substances 0.000 description 12
- 230000003647 oxidation Effects 0.000 description 9
- 238000007254 oxidation reaction Methods 0.000 description 9
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 8
- UCTWMZQNUQWSLP-UHFFFAOYSA-N adrenaline Chemical compound CNCC(O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 description 3
- 229960004046 apomorphine Drugs 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 239000001096 (4-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol hydrochloride Substances 0.000 description 2
- NNKXWRRDHYTHFP-HZQSTTLBSA-N (r)-[(2s,4s,5r)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol;hydron;dichloride Chemical compound Cl.Cl.C([C@H]([C@H](C1)C=C)C2)CN1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 NNKXWRRDHYTHFP-HZQSTTLBSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 description 2
- ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 229960001811 quinine hydrochloride Drugs 0.000 description 2
- 229960004025 sodium salicylate Drugs 0.000 description 2
- 235000001258 Cinchona calisaya Nutrition 0.000 description 1
- MBYXEBXZARTUSS-QLWBXOBMSA-N Emetamine Natural products O(C)c1c(OC)cc2c(c(C[C@@H]3[C@H](CC)CN4[C@H](c5c(cc(OC)c(OC)c5)CC4)C3)ncc2)c1 MBYXEBXZARTUSS-QLWBXOBMSA-N 0.000 description 1
- AUVVAXYIELKVAI-UHFFFAOYSA-N SJ000285215 Natural products N1CCC2=CC(OC)=C(OC)C=C2C1CC1CC2C3=CC(OC)=C(OC)C=C3CCN2CC1CC AUVVAXYIELKVAI-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 description 1
- 229960002694 emetine Drugs 0.000 description 1
- AUVVAXYIELKVAI-CKBKHPSWSA-N emetine Chemical compound N1CCC2=CC(OC)=C(OC)C=C2[C@H]1C[C@H]1C[C@H]2C3=CC(OC)=C(OC)C=C3CCN2C[C@@H]1CC AUVVAXYIELKVAI-CKBKHPSWSA-N 0.000 description 1
- AUVVAXYIELKVAI-UWBTVBNJSA-N emetine Natural products N1CCC2=CC(OC)=C(OC)C=C2[C@H]1C[C@H]1C[C@H]2C3=CC(OC)=C(OC)C=C3CCN2C[C@H]1CC AUVVAXYIELKVAI-UWBTVBNJSA-N 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- 229960005181 morphine Drugs 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- -1 p-aminobenzoyldiethylamine-ethanol Chemical compound 0.000 description 1
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
- 239000004297 potassium metabisulphite Substances 0.000 description 1
- 229960000948 quinine Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE440267A true BE440267A (de) |
Family
ID=98085
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE440267D BE440267A (de) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE440267A (de) |
-
0
- BE BE440267D patent/BE440267A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0308278B1 (de) | Kosmetische Verwendung der N-acetylierten oder N-propionylierten Derivate von Prolin, Hydroxyprolin und/oder von der durch Hydrolyse von Kollagen erhaltenen Aminosäuremischung | |
| FR2832063A1 (fr) | Procede de production de solutions stables de substances phenoliques et les solutions en resultant | |
| Mawson | The influence of animal tissues on the oxidation of ascorbic acid | |
| CA1109798A (fr) | Compositions tinctoriales a base de colorants directs contenant un acide (2,5-dihydroxyphenyl) carboxylique ou l'un de ses sels | |
| US20080073291A1 (en) | Agents and methods for removing chloramine, chlorine, and other active chlorine compounds from water used for keeping water organisms | |
| CN106867736A (zh) | 一种山葡萄酒的澄清剂 | |
| Guthrie | A method for the determination of peroxidase activity | |
| Bernheim et al. | Studies on a new metabolite and its oxidation in the presence of ascorbic acid | |
| RU2129156C1 (ru) | Способ производства водки | |
| Pignatelli et al. | Modifying effects of polyphenols and other constituents of beer on the formation of N-nitroso compounds | |
| FR2483228A1 (fr) | Nouveau colorant capillaire extrait de pterocarpus indicus et procede pour sa preparation | |
| FR2555442A1 (fr) | Shampooing pour empecher la chute des cheveux et favoriser la croissance des cheveux | |
| FR2461463A1 (fr) | Procede de preparation d'eaux minerales ferrugineuses, eaux minerales obtenues par ce procede et leurs applications therapeutiques | |
| CH163070A (fr) | Procédé de durcissement en surface d'alliages d'acier inoxydables et alliage d'acier inoxydable, durci en surface par ce procédé. | |
| JPS6258343B2 (de) | ||
| DURHAM | THE practice of using preservatives in the process of making cider is very widely spread, and moreover is much encouraged by the makers | |
| CZ303556B6 (cs) | Použití smesi nasycených mastných kyselin pro inhibici alkoholové ci malolaktické fermentace a redukci dávkování oxidu siricitého pri technologii vína | |
| JP2003113139A (ja) | ヒドロキサム酸類および／またはカテキン類の使用方法 | |
| DE375302C (de) | Verfahren zum Verhueten des Nachfaerbens der Biere und Hopfenabsude | |
| BR102024019592A2 (pt) | Método para identificação de peróxido de hidrogênio em leite fluido | |
| Diehl Jr | Remarks On Some Chemical Processes | |
| US181651A (en) | Improvement in processes of treating wood | |
| SU207815A1 (ru) | Способ сохранения питьевой воды | |
| CH106774A (fr) | Procédé pour la préparation d'une solution de cyanamide à partir de la cyanamide calcique du commerce. | |
| BE428698A (de) |