GB618406A - Improvements in or relating to processes of producing plant extracts and the products resulting therefrom - Google Patents
Improvements in or relating to processes of producing plant extracts and the products resulting therefromInfo
- Publication number
- GB618406A GB618406A GB8361/44A GB836144A GB618406A GB 618406 A GB618406 A GB 618406A GB 8361/44 A GB8361/44 A GB 8361/44A GB 836144 A GB836144 A GB 836144A GB 618406 A GB618406 A GB 618406A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ether
- sodium
- plant material
- solvent
- extract
- 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.)
- Expired
Links
- 238000000034 method Methods 0.000 title abstract 5
- 239000000419 plant extract Substances 0.000 title 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 32
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 17
- 241000196324 Embryophyta Species 0.000 abstract 15
- 239000000284 extract Substances 0.000 abstract 15
- HCZKYJDFEPMADG-TXEJJXNPSA-N masoprocol Chemical compound C([C@H](C)[C@H](C)CC=1C=C(O)C(O)=CC=1)C1=CC=C(O)C(O)=C1 HCZKYJDFEPMADG-TXEJJXNPSA-N 0.000 abstract 14
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 12
- 239000000463 material Substances 0.000 abstract 12
- 239000002904 solvent Substances 0.000 abstract 8
- 239000003513 alkali Substances 0.000 abstract 7
- HCZKYJDFEPMADG-UHFFFAOYSA-N erythro-nordihydroguaiaretic acid Natural products C=1C=C(O)C(O)=CC=1CC(C)C(C)CC1=CC=C(O)C(O)=C1 HCZKYJDFEPMADG-UHFFFAOYSA-N 0.000 abstract 7
- 229960003951 masoprocol Drugs 0.000 abstract 7
- 239000002244 precipitate Substances 0.000 abstract 7
- 239000000243 solution Substances 0.000 abstract 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 6
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 abstract 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 6
- 244000122992 Larrea divaricata Species 0.000 abstract 5
- 239000002253 acid Substances 0.000 abstract 5
- 239000007864 aqueous solution Substances 0.000 abstract 5
- 239000003638 chemical reducing agent Substances 0.000 abstract 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 abstract 4
- 238000000605 extraction Methods 0.000 abstract 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 4
- 238000011282 treatment Methods 0.000 abstract 4
- 230000003647 oxidation Effects 0.000 abstract 3
- 238000007254 oxidation reaction Methods 0.000 abstract 3
- 238000005406 washing Methods 0.000 abstract 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 abstract 2
- 235000002828 Larrea divaricata Nutrition 0.000 abstract 2
- 241001464837 Viridiplantae Species 0.000 abstract 2
- 239000003963 antioxidant agent Substances 0.000 abstract 2
- 230000003078 antioxidant effect Effects 0.000 abstract 2
- 235000006708 antioxidants Nutrition 0.000 abstract 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000001704 evaporation Methods 0.000 abstract 2
- 230000008020 evaporation Effects 0.000 abstract 2
- 230000002070 germicidal effect Effects 0.000 abstract 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 abstract 2
- 235000017557 sodium bicarbonate Nutrition 0.000 abstract 2
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 2
- 238000000638 solvent extraction Methods 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 abstract 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 241000935061 Larrea Species 0.000 abstract 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 abstract 1
- 239000000061 acid fraction Substances 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 235000012605 creosote bush Nutrition 0.000 abstract 1
- 239000000287 crude extract Substances 0.000 abstract 1
- 239000002178 crystalline material Substances 0.000 abstract 1
- -1 diethyl ether Chemical class 0.000 abstract 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 150000002366 halogen compounds Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 150000002896 organic halogen compounds Chemical class 0.000 abstract 1
- 150000002897 organic nitrogen compounds Chemical class 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 150000002927 oxygen compounds Chemical class 0.000 abstract 1
- 230000020477 pH reduction Effects 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 239000003755 preservative agent Substances 0.000 abstract 1
- 230000002335 preservative effect Effects 0.000 abstract 1
- YOSOSDBZAUWJJT-UHFFFAOYSA-L sodium dithionite monohydrate Chemical compound O.[Na+].[Na+].[O-]S(=O)S([O-])=O YOSOSDBZAUWJJT-UHFFFAOYSA-L 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
Landscapes
- Health & Medical Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Alternative & Traditional Medicine (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Medical Informatics (AREA)
- Medicinal Chemistry (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A crystalline compound comprising 85-90 per cent pure nordihydroguaiaretic acid obtained by extraction of plants of the species Larrea divaricata (creosote bush) is added to lard as an antioxidant and preservative in concentrations of about 0.01 per cent.ALSO:Extracts containing substantial proportions of nordihydroguaianetic acid <FORM:0618406/IV(b)/1> from plants of the species Larrea divaricata are prepared by treating the plant material with an organic solvent to form a primary or crude extract which may be purified by treating with an aqueous solution of an inorganic alkali; or by extracting the plant material with an aqueous solution of an alkali metal hydroxide, e.g. sodium hydroxide or potassium hydroxide, acidulating the resultant solution and separating the nordihydroguaianetic acid-containing precipitate. In the solvent extraction method powdered plant material is treated with a solvent capable of giving extracts showing a positive reaction for catechol when tested with ferric chloride, e.g. organic halogen, nitrogen or oxygen compounds. Diethyl ether is preferred. The solvent is removed by evaporation and the extract is redissolved in a water immiscible solvent such as ether. The extract may be further purified by washing with alkaline bicarbonates or carbonates in the presence of a reducing agent, preferably sodium hydrosulphite, when the stronger alkali is used. In the extraction with aqueous alkali metal hydroxide the whole plant is leached with a 2-10 per cent solution of the alkali containing a reducing agent to prevent oxidation and the extract is neutralised with acid; a flocculent precipitate forms which is dissolved directly in an ether such as diethyl or isopropyl ether or is dissolved in an alcohol having not more than 3 carbon atoms, is washed with water to remove the alcohol and is then transferred to an ether solution. The extracts prepared by either of the above methods are finally purified by treating with aqueous alkali metal hydroxide either in one step or preferably in successive small portions and in the presence of a strong reducing agent, e.g. sodium hydrosulphite, to prevent oxidation of the phenolic compounds. Each extract fraction is acidified and where ether is used as a solvent, may be heated on a water bath to remove ether. On standing a solid residue separates out. The nordihydroguaianetic acid, as shown by testing with ferric chloride, is concentrated in the last fractions, from which it is ultimately obtained as a distinctly crystalline substance of 85-95 per cent purity. It is used as a germicide and anti-oxidant. In examples: (1) dried, powdered Larrea divaricata is extracted with ether and separated by successive treatment with aqueous solutions of sodium bicarbonate, sodium carbonate and sodium hydroxide, the latter two compounds being used in the presence of sodium hydrosulphite, giving on acidification of the later sodium hydroxide extracts, nordihydroguaianetic acid of 88 DEG C. purity; (2) and (3) the plant material is extracted with ethylene dichloride, sodium bicarbonate solution containing sodium hydrosulphite is added, the mixture is evaporated to near dryness, redissolved in ether and separated as in (1); (4) dried plant material is extracted with sodium hydroxide-sodium hydrosulphite and neutralised giving a flucculent precipitate which is separated, dissolved in methyl alcohol, acidified with hydrochloric acid, diluted with ether, washed with water and separated by successive treatments with aqueous potassium hydroxide; and (5) green plant material is subjected to the extraction process of (4).ALSO:Extracts of plants of the species Larrea divaricata containing substantial portions of nordihydroguaiaretic acid are prepared by treating the plant material with an organic solvent to form a primary extract which is purified by washing, with an aqueous solution of inorganic alkali; or by reacting the plant material with an aqueous solution of an alkali metal hydroxide, e.g. sodium or potassium hydroxide, acidulating and separating the nordihydroguaiaretic acid-containing precipitate. In the solvent extraction method powdered plant material is treated with a solvent for the nordihydroguaiaretic acid fractions, suitably an organic nitrogen, oxygen or halogen compound, such as diethyl ether, the solvent is removed by evaporation the extract is redissolved in a water immiscible solvent such as ether and, if desired, the solution is purified by washing with mild aqueous alkali. In the extraction with aqueous alkali metal hydroxide the plant is leached with a 2 - 10 per cent solution of the alkali containing a reducing agent such as sodium hydrosulphite to prevent oxidation, the extract is acidified to give a flocculent precipitate which is separated and dissolved in a water immiscible solvent such as ether. The extracts prepared by either of the above methods are purified by treating with aqueous alkali metal hydroxide in the presence of a reducing agent, either in one step, or preferably in successive small portions and the extract fractions are acidified to give a nordihydroguaiaretic acid containing precipitate. Where the final alkali treatment is carried out in successive small fractions the nordihydroguaiaretic acid is concentrated in the last fractions from which it may be obtained as a crystalline substance of 85 - 90 per cent purity. The crystalline material is a germicide. In examples (1) dried powdered Larrea divaricata is extracted with ether, washed with sodium bicarbonate and sodium carbonate and treated with successive portions of aqueous sodium hydroxide to give extracts which on acidifying yield nordihydroguaiaretic acid of 88 per cent purity; (2) and (3) the plant material is extracted with ethylene dichloride, evaporated to near dryness, redissolved in ether and treated as in (1); (4) the dried plant material is extracted with sodium hydroxide in the presence of sodium hydrosulphite, acidified to give a precipitate which is dissolved in methyl alcohol transferred to ether solution and separated by successive treatments with potassium hydroxide; and (5) green plant material is extracted as in (4).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US618406XA | 1943-03-06 | 1943-03-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB618406A true GB618406A (en) | 1949-02-22 |
Family
ID=22038470
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8361/44A Expired GB618406A (en) | 1943-03-06 | 1944-05-03 | Improvements in or relating to processes of producing plant extracts and the products resulting therefrom |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB618406A (en) |
-
1944
- 1944-05-03 GB GB8361/44A patent/GB618406A/en not_active Expired
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