GB927892A - Production of purified pyrethrum extract - Google Patents
Production of purified pyrethrum extractInfo
- Publication number
- GB927892A GB927892A GB7817/59A GB781759A GB927892A GB 927892 A GB927892 A GB 927892A GB 7817/59 A GB7817/59 A GB 7817/59A GB 781759 A GB781759 A GB 781759A GB 927892 A GB927892 A GB 927892A
- Authority
- GB
- United Kingdom
- Prior art keywords
- distillation
- hydrocarbons
- liquid paraffin
- oleoresin extract
- oils
- 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
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 229940048383 pyrethrum extract Drugs 0.000 title 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 5
- 150000002430 hydrocarbons Chemical class 0.000 abstract 5
- 238000004821 distillation Methods 0.000 abstract 4
- 239000000284 extract Substances 0.000 abstract 4
- 239000008601 oleoresin Substances 0.000 abstract 4
- 239000007788 liquid Substances 0.000 abstract 3
- 229940057995 liquid paraffin Drugs 0.000 abstract 3
- 239000003921 oil Substances 0.000 abstract 3
- 240000004460 Tanacetum coccineum Species 0.000 abstract 2
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 abstract 2
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 abstract 2
- 238000009835 boiling Methods 0.000 abstract 2
- 238000004040 coloring Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 abstract 2
- 229940070846 pyrethrins Drugs 0.000 abstract 2
- 239000002728 pyrethroid Substances 0.000 abstract 2
- 229940015367 pyrethrum Drugs 0.000 abstract 2
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 abstract 1
- VMORCWYWLVLMDG-YZGWKJHDSA-N Pyrethrin-II Natural products CC(=O)OC(=C[C@@H]1[C@H](C(=O)O[C@H]2CC(=O)C(=C2C)CC=CC=C)C1(C)C)C VMORCWYWLVLMDG-YZGWKJHDSA-N 0.000 abstract 1
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 238000004508 fractional distillation Methods 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
- 239000003350 kerosene Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- ROVGZAWFACYCSP-VUMXUWRFSA-N pyrethrin I Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-VUMXUWRFSA-N 0.000 abstract 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
- 238000005979 thermal decomposition reaction Methods 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
- A01N65/08—Magnoliopsida [dicotyledons]
- A01N65/16—Ericaceae [Heath or Blueberry family], e.g. rhododendron, arbutus, pieris, cranberry or bilberry
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Mycology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
A process for the production of a purified pyrethrum containing composition comprises distilling a solution of a pyrethrum oleoresin extract, in a fraction of normally liquid paraffinic hydrocarbons, which distils between 200 DEG C. and 500 DEG C. at atmospheric pressure the distillation being carried out at a pressure which is sufficiently low substantially to avoid thermal decomposition and degradation of the pyrethrins present. The paraffinic hydrocarbons are paraffins and cycloparaffins e.g. kerosenes distilling above 200 DEG C., technical oils or medicinal oils which have been treated to remove unsaturated, hydrocarbons, waxy materials and colouring matter, such as white oils, Deobase liquid paraffin or light liquid paraffin. The pressure is preferably not greater than 1 mm. of Hg. and more specifically 10-2-10-5 mm. of Hg. The oleoresin extract is dissolved in less than 12 and preferably 2-10 times its volume of liquid paraffin hydrocarbons before distillation and the distillation is desirably carried out as a short parth distillation, which results in the oleoresin extract being freed from colouring matter; and by carrying out the process in a flash still in a plurality of stages with short path evaporators, the oleoresin extract may be separated into fractions which predominate in pyrethrins I or II respectively or alternatively such fractions may be obtained by fractional distillation in a pot still. By variation of the boiling point ranges of the paraffinic hydrocarbons the component which is rich in Pyrethrin II may be left undistilled or distilled as a separate fraction of higher boiling point than the component rich in Pyrethrin I. The distillates are clear pale yellow mobile liquids, which may be diluted with kerosene or other miscible organic liquids to form insecticidal sprays or solutions.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7817/59A GB927892A (en) | 1959-03-06 | 1959-03-06 | Production of purified pyrethrum extract |
| CH247860A CH393311A (en) | 1959-03-06 | 1960-03-04 | Process for the preparation of purified pyrethrin-containing compositions |
| BE588295A BE588295A (en) | 1959-03-06 | 1960-03-04 | Purified pyrethrum extract |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7817/59A GB927892A (en) | 1959-03-06 | 1959-03-06 | Production of purified pyrethrum extract |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB927892A true GB927892A (en) | 1963-06-06 |
Family
ID=9840335
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB7817/59A Expired GB927892A (en) | 1959-03-06 | 1959-03-06 | Production of purified pyrethrum extract |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE588295A (en) |
| CH (1) | CH393311A (en) |
| GB (1) | GB927892A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996039034A1 (en) * | 1995-06-06 | 1996-12-12 | Thermo Trilogy Corporation | Synergistic use of azadirachtin and pyrethrum |
-
1959
- 1959-03-06 GB GB7817/59A patent/GB927892A/en not_active Expired
-
1960
- 1960-03-04 CH CH247860A patent/CH393311A/en unknown
- 1960-03-04 BE BE588295A patent/BE588295A/en unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996039034A1 (en) * | 1995-06-06 | 1996-12-12 | Thermo Trilogy Corporation | Synergistic use of azadirachtin and pyrethrum |
| US5679662A (en) * | 1995-06-06 | 1997-10-21 | Thermo Trilogy Corporation | Synergistic use of azadirachtin and pyrethrum |
Also Published As
| Publication number | Publication date |
|---|---|
| CH393311A (en) | 1965-06-15 |
| BE588295A (en) | 1960-09-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Cheng et al. | The volatile oil of the leaves of Chamaecyparis nootkatensis | |
| GB948180A (en) | Process for the separation of an organic mixture containing hydrocarbons by means of extractive distillation | |
| GB927892A (en) | Production of purified pyrethrum extract | |
| GB1255570A (en) | Process for separating a mixture of c5 hydrocarbons into its constituents | |
| Gilby | Absence of natural volatile solvents in cockroach grease | |
| US2467903A (en) | Method of purifying and concentrating sesamin extracts | |
| JPS54160322A (en) | Separation of dichlorobenzene isomer | |
| US2463324A (en) | Sesame extract synergized insecticides | |
| GB668853A (en) | Separating alpha and beta methyl naphthalene by azeotropic distillation | |
| GB722390A (en) | Separating methyl acetate from other organic compounds by extractive distillation | |
| US1945235A (en) | Process of preparing a colorless household insecticide | |
| DE2354038C3 (en) | ||
| US2467859A (en) | Preparation of pyrethrin concentrate | |
| US2629750A (en) | Stabilized azulene oil | |
| Snajberk et al. | Chemical composition of volatiles from cortical oleoresin of Pseudotsuga menziesii | |
| US3133004A (en) | Production of purified pyrethrum extract | |
| GB851342A (en) | Improvements in the purification of acrylic esters | |
| SU394347A1 (en) | METHOD OF ISOLATION OF AROMATIC HYDROCARBONS OF SHEETS OF MIXTURES WITH NONAROMATIC HYDROCARBONS | |
| ES361112A1 (en) | Solvent extraction of aromatic hydrocarbons | |
| SU1689395A1 (en) | Method of extraction of biologically active substances from fur wood green | |
| GB588037A (en) | Process for the separation of c diolefins from mixtures thereof with other hydrocarbons | |
| SU105543A1 (en) | Extraction method from lavender product with fixator properties | |
| GB875760A (en) | Improvements in or relating to the purification of pyrethrum extract | |
| SU107275A1 (en) | The method of separation of mixtures of hydrocarbons and monohydric alcohols | |
| SU405926A1 (en) | ANTISTATIC PREPARATION |