BE379193A - - Google Patents
Info
- Publication number
- BE379193A BE379193A BE379193DA BE379193A BE 379193 A BE379193 A BE 379193A BE 379193D A BE379193D A BE 379193DA BE 379193 A BE379193 A BE 379193A
- Authority
- BE
- Belgium
- Prior art keywords
- compound
- urine
- precipitate
- camphor
- lead
- Prior art date
Links
- 210000002700 urine Anatomy 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 11
- 229940097043 glucuronic acid Drugs 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- 239000002244 precipitate Substances 0.000 description 10
- IYRMWMYZSQPJKC-UHFFFAOYSA-N kaempferol Chemical compound C1=CC(O)=CC=C1C1=C(O)C(=O)C2=C(O)C=C(O)C=C2O1 IYRMWMYZSQPJKC-UHFFFAOYSA-N 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 241000723346 Cinnamomum camphora Species 0.000 description 8
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 8
- 229930008380 camphor Natural products 0.000 description 8
- 229960000846 camphor Drugs 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 159000000009 barium salts Chemical class 0.000 description 3
- -1 glucuronic acid compound Chemical class 0.000 description 3
- 229940046892 lead acetate Drugs 0.000 description 3
- 150000002611 lead compounds Chemical class 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 description 1
- AXMKZEOEXSKFJI-UHFFFAOYSA-N 2-hydroxy-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound C1CC2(C)C(=O)C(O)C1C2(C)C AXMKZEOEXSKFJI-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 229930008384 Oxocamphor Natural products 0.000 description 1
- DLKVHFJZTKTFRS-UHFFFAOYSA-N Oxocamphor Chemical compound C1CC2(C=O)C(=O)CC1C2(C)C DLKVHFJZTKTFRS-UHFFFAOYSA-N 0.000 description 1
- 229910000004 White lead Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/385—Saturated compounds containing a keto group being part of a ring
- C07C49/487—Saturated compounds containing a keto group being part of a ring containing hydroxy groups
- C07C49/507—Saturated compounds containing a keto group being part of a ring containing hydroxy groups polycyclic
- C07C49/513—Saturated compounds containing a keto group being part of a ring containing hydroxy groups polycyclic a keto group being part of a condensed ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE379193A true BE379193A (enrdf_load_html_response) |
Family
ID=49141
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE379193D BE379193A (enrdf_load_html_response) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE379193A (enrdf_load_html_response) |
-
0
- BE BE379193D patent/BE379193A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0178442B1 (fr) | Procédé d'enrichissement sélectif en acides gras polyinsaturés delta-6 d'un mélange contenant des acides gras delta-6 et delta-9, fractions enrichies obtenues et leur utilisation | |
| BE379193A (enrdf_load_html_response) | ||
| EP0678499B1 (fr) | Procédé de préparation d'acide L-aspartique à partir d'aspartate d'ammonium | |
| FR2589149A1 (fr) | Procede de separation et de purification de l'acide salicylique par precipitation a partir d'une solution aqueuse de son sel sodique | |
| FR2509322A1 (fr) | Huile, sa preparation et son utilisation | |
| CH154171A (fr) | Procédé de préparation de para-oxycamphre. | |
| EP0012640A1 (fr) | Procédé de purification de l'acide chénodésoxycholique et produits obtenus par ce procédé | |
| FR2472557A1 (fr) | Procede de resolution de l'acide d,1-2-(6-methoxy-2-naphtyl)-propionique et son application a un melange de sels des formes d et l de cet acide avec une n-alkyl-d-glucamine | |
| CH173727A (fr) | Procédé de purification de l'acide phosphorique. | |
| CH641149A5 (fr) | Procede de purification de l'isoleucine. | |
| BE426230A (enrdf_load_html_response) | ||
| BE435158A (enrdf_load_html_response) | ||
| Votocek et al. | sur l'acide 2-carboxyfurfuryl-5-glycolique (α-pyromucoglycolique) | |
| CH346891A (fr) | Procédé de préparation du chlorhydrate de l'ester méthylique de la cystéine | |
| BE663743A (enrdf_load_html_response) | ||
| BE416160A (enrdf_load_html_response) | ||
| BE522289A (enrdf_load_html_response) | ||
| BE524378A (enrdf_load_html_response) | ||
| BE480304A (enrdf_load_html_response) | ||
| BE434226A (enrdf_load_html_response) | ||
| BE445966A (enrdf_load_html_response) | ||
| BE440950A (enrdf_load_html_response) | ||
| BE425307A (enrdf_load_html_response) | ||
| CH157941A (fr) | Procédé de préparation de l'acide B-imidazolyl-propionique. | |
| BE506164A (enrdf_load_html_response) |