DE267815C - - Google Patents
Info
- Publication number
- DE267815C DE267815C DENDAT267815D DE267815DA DE267815C DE 267815 C DE267815 C DE 267815C DE NDAT267815 D DENDAT267815 D DE NDAT267815D DE 267815D A DE267815D A DE 267815DA DE 267815 C DE267815 C DE 267815C
- Authority
- DE
- Germany
- Prior art keywords
- saponins
- alcohol
- percent
- water
- saponin
- 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.)
- Active
Links
- 229930182490 saponin Natural products 0.000 claims description 13
- 150000007949 saponins Chemical class 0.000 claims description 13
- 235000017709 saponins Nutrition 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 8
- 150000007513 acids Chemical class 0.000 claims description 8
- 238000003776 cleavage reaction Methods 0.000 claims description 6
- 230000007017 scission Effects 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 3
- 239000008280 blood Substances 0.000 claims description 2
- 210000004369 blood Anatomy 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 230000002035 prolonged effect Effects 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 5
- INLFWQCRAJUDCR-IQVMEADQSA-N (1R,2S,4S,5'S,6R,7S,8R,9S,12S,13S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane] Chemical compound O([C@@H]1[C@@H]([C@]2(CC[C@@H]3[C@@]4(C)CCCCC4CC[C@H]3[C@@H]2C1)C)[C@@H]1C)[C@]11CC[C@H](C)CO1 INLFWQCRAJUDCR-IQVMEADQSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 241000580938 Sapindus Species 0.000 description 3
- 230000001476 alcoholic effect Effects 0.000 description 3
- WQLVFSAGQJTQCK-UHFFFAOYSA-N diosgenin Natural products CC1C(C2(CCC3C4(C)CCC(O)CC4=CCC3C2C2)C)C2OC11CCC(C)CO1 WQLVFSAGQJTQCK-UHFFFAOYSA-N 0.000 description 3
- 229930182470 glycoside Natural products 0.000 description 3
- 150000002338 glycosides Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- NWMIYTWHUDFRPL-UHFFFAOYSA-N sapogenin Natural products COC(=O)C1(CO)C(O)CCC2(C)C1CCC3(C)C2CC=C4C5C(C)(O)C(C)CCC5(CCC34C)C(=O)O NWMIYTWHUDFRPL-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241000157282 Aesculus Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002949 hemolytic effect Effects 0.000 description 1
- 235000010181 horse chestnut Nutrition 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 150000002972 pentoses Chemical class 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/24—Condensed ring systems having three or more rings
- C07H15/256—Polyterpene radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Steroid Compounds (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE267815C true DE267815C (enrdf_load_stackoverflow) |
Family
ID=524834
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT267815D Active DE267815C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE267815C (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1075278B (de) * | 1960-02-11 | National Research Development Corporation London | Ver fahren zur Gewinnung von Hecogenm |
-
0
- DE DENDAT267815D patent/DE267815C/de active Active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1075278B (de) * | 1960-02-11 | National Research Development Corporation London | Ver fahren zur Gewinnung von Hecogenm |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2430999C2 (de) | Neue Doppelsalze von S-Adenosyl-L-methionin mit Schwefel- und p-Toluolsulfonsäure, Verfahren zu ihrer Herstellung und Arzneimittel | |
DE2812041A1 (de) | Optisch aktive aminosaeure-mandelsaeure- komplexe, verfahren zu deren herstellung und verfahren zur herstellung optisch aktiver aminosaeuren oder mandelsaeure | |
DE1803978C2 (de) | Verfahren zur Gewinnung von S-Adenosyl-l-methionin und S-Adenosyl-l-ethionin | |
DE267815C (enrdf_load_stackoverflow) | ||
DE1040543B (de) | Verfahren zur Reinigung eines rohen, durch Hydrolyse von natuerlichem saponinhaltigenMaterial erhaltenen sapogeninhaltigen Materials | |
DE1243206B (de) | Verfahren zur Trennung von racemischem 1-Hydroxy-2-aminobutan in seine optisch aktiven Antipoden | |
DE697760C (de) | Verfahren zur Gewinnung der grossen Gesamtalkaloide des Mutterkorns | |
DE323135C (de) | Verfahren zur Herstellung von Tannin | |
DE148410C (enrdf_load_stackoverflow) | ||
DE282751C (enrdf_load_stackoverflow) | ||
DE2902755C2 (de) | Glycidyltrimethylammoniumchloridmonohydrat, stabile konzentrierte Lösungen von Glycidyltrimethylammoniumchlorid und Verfahren zur Herstellung derselben | |
DE10047444A1 (de) | Verfahren zur Trennung und hochreinen Isolierung von niedermolekularen, strukturell ähnlichen Verbindungen insbesondere von Tetrahydropyrimidinderivaten wie z.B. 1,4,5,6-Tetrahydro-2-methyl-4-pyrimidincarbonsäuren (Ectoine) und deren Spaltprodukte | |
DE637910C (de) | Verfahren zur Herstellung von schwefelhaltigeren Kondensationsprodukten aus Eiweissabbauprodukten | |
DE357272C (de) | Verfahren zur Gewinnung von Pflanzenalkaloiden | |
EP1537874B1 (de) | Verfahren zur Herstellung von Extrakten des Ginkgo Biloba | |
DE852122C (de) | Verfahren zur Gewinnung von hochprozentigen Vitamin-T-Praeparaten | |
DE252874C (enrdf_load_stackoverflow) | ||
AT403160B (de) | Verfahren zur herstellung von pyridoxin 5-oxo-2-pyrrolidoncarboxylat | |
DE843257C (de) | Verfahren zur Gewinnung neuer Glykoside aus Strophantus sarmentosus | |
DE103062C (enrdf_load_stackoverflow) | ||
DE2026626C3 (de) | 1 Isopropenyl 2 benzoylacetylen und Verfahren zu seiner Herstellung | |
DE276489C (enrdf_load_stackoverflow) | ||
DE240584C (enrdf_load_stackoverflow) | ||
DE1618492C (de) | Fruktosegewinnung aus Zucker | |
DE859514C (de) | Verfahren zur Gewinnung antianaemischer Wirkstoffe aus Leber |