GB928594A - Manufacture of perfumes - Google Patents
Manufacture of perfumesInfo
- Publication number
- GB928594A GB928594A GB3212259A GB3212259A GB928594A GB 928594 A GB928594 A GB 928594A GB 3212259 A GB3212259 A GB 3212259A GB 3212259 A GB3212259 A GB 3212259A GB 928594 A GB928594 A GB 928594A
- Authority
- GB
- United Kingdom
- Prior art keywords
- abs
- perfumery
- fluorinated hydrocarbon
- solvent
- materials
- 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 3
- 239000002304 perfume Substances 0.000 title abstract 3
- 239000000463 material Substances 0.000 abstract 12
- 239000002904 solvent Substances 0.000 abstract 11
- 229930195733 hydrocarbon Natural products 0.000 abstract 9
- 150000002430 hydrocarbons Chemical class 0.000 abstract 9
- 239000004215 Carbon black (E152) Substances 0.000 abstract 8
- 239000012141 concentrate Substances 0.000 abstract 6
- 239000003380 propellant Substances 0.000 abstract 5
- 239000000284 extract Substances 0.000 abstract 4
- 244000028419 Styrax benzoin Species 0.000 abstract 3
- 235000000126 Styrax benzoin Nutrition 0.000 abstract 3
- 239000004567 concrete Substances 0.000 abstract 3
- 238000000605 extraction Methods 0.000 abstract 3
- 239000011347 resin Substances 0.000 abstract 3
- 229920005989 resin Polymers 0.000 abstract 3
- 241001090476 Castoreum Species 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 244000111489 Gardenia augusta Species 0.000 abstract 2
- 235000015511 Liquidambar orientalis Nutrition 0.000 abstract 2
- 239000004870 Styrax Substances 0.000 abstract 2
- 235000004338 Syringa vulgaris Nutrition 0.000 abstract 2
- 244000297179 Syringa vulgaris Species 0.000 abstract 2
- 239000000443 aerosol Substances 0.000 abstract 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 abstract 2
- QPAXMPYBNSHKAK-UHFFFAOYSA-N chloro(difluoro)methane Chemical compound F[C](F)Cl QPAXMPYBNSHKAK-UHFFFAOYSA-N 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000006193 liquid solution Substances 0.000 abstract 2
- 239000011368 organic material Substances 0.000 abstract 2
- BAMUEXIPKSRTBS-UHFFFAOYSA-N 1,1-dichloro-1,2,2,2-tetrafluoroethane Chemical class FC(F)(F)C(F)(Cl)Cl BAMUEXIPKSRTBS-UHFFFAOYSA-N 0.000 abstract 1
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 abstract 1
- 241000205585 Aquilegia canadensis Species 0.000 abstract 1
- 244000025254 Cannabis sativa Species 0.000 abstract 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 abstract 1
- 240000008772 Cistus ladanifer Species 0.000 abstract 1
- 235000005241 Cistus ladanifer Nutrition 0.000 abstract 1
- 244000068485 Convallaria majalis Species 0.000 abstract 1
- 235000009046 Convallaria majalis Nutrition 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 abstract 1
- 235000018958 Gardenia augusta Nutrition 0.000 abstract 1
- 241000282375 Herpestidae Species 0.000 abstract 1
- 241001632576 Hyacinthus Species 0.000 abstract 1
- 239000004869 Labdanum Substances 0.000 abstract 1
- 244000178870 Lavandula angustifolia Species 0.000 abstract 1
- 235000010663 Lavandula angustifolia Nutrition 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 244000179970 Monarda didyma Species 0.000 abstract 1
- 235000010672 Monarda didyma Nutrition 0.000 abstract 1
- 235000014150 Myroxylon pereirae Nutrition 0.000 abstract 1
- 244000302151 Myroxylon pereirae Species 0.000 abstract 1
- 239000004341 Octafluorocyclobutane Substances 0.000 abstract 1
- 240000002505 Pogostemon cablin Species 0.000 abstract 1
- 235000011751 Pogostemon cablin Nutrition 0.000 abstract 1
- 241000220317 Rosa Species 0.000 abstract 1
- 240000000513 Santalum album Species 0.000 abstract 1
- 235000008632 Santalum album Nutrition 0.000 abstract 1
- 244000272264 Saussurea lappa Species 0.000 abstract 1
- 235000006784 Saussurea lappa Nutrition 0.000 abstract 1
- 235000008411 Sumatra benzointree Nutrition 0.000 abstract 1
- 244000284012 Vetiveria zizanioides Species 0.000 abstract 1
- 235000007769 Vetiveria zizanioides Nutrition 0.000 abstract 1
- 239000012675 alcoholic extract Substances 0.000 abstract 1
- 229960002130 benzoin Drugs 0.000 abstract 1
- 235000019406 chloropentafluoroethane Nutrition 0.000 abstract 1
- 239000001666 citrus aurantium l. flower Substances 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 239000000287 crude extract Substances 0.000 abstract 1
- BAPZCSMFCUVUHW-UHFFFAOYSA-N dichloro(fluoro)methane Chemical compound F[C](Cl)Cl BAPZCSMFCUVUHW-UHFFFAOYSA-N 0.000 abstract 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 abstract 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 abstract 1
- 239000000686 essence Substances 0.000 abstract 1
- 235000019441 ethanol Nutrition 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 230000008020 evaporation Effects 0.000 abstract 1
- 210000000416 exudates and transudate Anatomy 0.000 abstract 1
- 210000004907 gland Anatomy 0.000 abstract 1
- 235000019382 gum benzoic Nutrition 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000001102 lavandula vera Substances 0.000 abstract 1
- 235000018219 lavender Nutrition 0.000 abstract 1
- 238000012423 maintenance Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000001157 myroxylon pereirae klotzsch resin Substances 0.000 abstract 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 abstract 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 abstract 1
- 239000002244 precipitate Substances 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/02—Recovery or refining of essential oils from raw materials
- C11B9/025—Recovery by solvent extraction
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
Abstract
A method of manufacturing concentrates from perfumery materials (which are chosen from raw naturally occurring organic materials and their concretes and absolutes) comprises treating the perfumery materials with a solvent which consists of at least one fluorinated hydrocarbon propellant, liquefied by the maintenance of sufficient pressure, and separating the resulting liquid solution from that portion of the perfumery material treated which does not dissolve in the solvent. The concretes referred to are crude extracts of the raw naturally occurring organic materials, while the absolutes are carefully prepared alcoholic extracts of the concretes. The fluorinated hydrocarbon propellants are fluorinated or chlorofluorinated hydrocarbons which may be used as propellants in aerosol packages, examples being CCl3F, CCl2F2, CHClF2, CCl2F.CClF2, C2ClF5, CH3.CClF2, dichloro-tetrafluoro-ethanes, octafluoro-cyclobutane and materials sold under the trade name "Isotron". It is stated that the fraction of the perfumery material which remains in solution in the propellant is characterized by the distinctive odour of the perfume oil and by an increased concentration of the active nerve-stimulating ingredient. The perfumery materials treated may be chosen from plant raw materials and their extracts, animal glands and their extracts and the exudates or resins and their extracts. The perfumery material may be agitated with the liquid solvent or the liquid solvent may be circulated through the perfumery material; the perfumery material may be given one, two or more extractions. If desired, a series of fluorinated hydrocarbon solvents may be used successively on any given perfumery material. Thus, (a) the perfumery material may be extracted with one fluorinated hydrocarbon solvent and then the concentrate from the extract may be treated with another fluorinated hydrocarbon solvent or (b) the perfumery material may be treated with one fluorinated hydrocarbon solvent and the residue treated with another fluorinated hydrocarbon solvent. The liquid solution obtained by the method of the invention may be cooled to separate wax or other precipitate and then filtered; the cooling may be effected by evaporation of the fluorinated hydrocarbon solvent. The concentrates obtained may be refined to very pure absolutes by extraction with ethyl alcohol. If desired the concentrates may be utilized in aerosol packages, either in the same solvent as was used for extraction or in a different propellant. In the examples, the manufacture of concentrates from flowers (hyacinth, lilac, lily of the valley, gardenia, rose or honeysuckle), leaves (grass or lilac), resins (Peru balsam, resinoid castoreum or styrax), essences (costus) and absolutes (abs. Resinoid Castoreum, abs. Summortelle, abs. Oak Moss, abs. Resin Styrax, abs. Orange Flowers, abs. Jasmin, abs. Civet, abs. Lavender or abs. Resinoid Benzoin) is described. In a further example, a concentrate is manufactured from a perfume oil made up of resinoid labdanum vetiver Bourbon, sandalwood, patchouly, coumarin, abs. Oak Moss and bergamot.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US76381358A | 1958-09-29 | 1958-09-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB928594A true GB928594A (en) | 1963-06-12 |
Family
ID=25068883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3212259A Expired GB928594A (en) | 1958-09-29 | 1959-09-21 | Manufacture of perfumes |
Country Status (2)
| Country | Link |
|---|---|
| CH (1) | CH386596A (en) |
| GB (1) | GB928594A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0752903A1 (en) | 1994-03-31 | 1997-01-15 | Imperial Chemical Industries Plc | Solvent extraction process |
| EP1055439A3 (en) * | 1993-02-22 | 2001-01-24 | Advanced Phytonics Limited | Fragrance extraction |
| US7250185B2 (en) | 2000-11-06 | 2007-07-31 | Ineos Fluor Holdings Limited | Process for reducing the concentration of undesired compounds in a composition |
| CN101851559A (en) * | 2010-06-11 | 2010-10-06 | 平阴县玫瑰研究所 | Method for extracting rose essential oil from rose dregs |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2617499B1 (en) * | 1987-07-03 | 1989-12-08 | Toulouse Inst Nat Polytech | PROCESS FOR EXTRACTING ESSENTIAL OILS FROM AROMATIC PLANTS AND PRODUCTS OBTAINED |
-
1959
- 1959-09-21 GB GB3212259A patent/GB928594A/en not_active Expired
- 1959-09-25 CH CH7865959A patent/CH386596A/en unknown
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1055439A3 (en) * | 1993-02-22 | 2001-01-24 | Advanced Phytonics Limited | Fragrance extraction |
| EP0752903A1 (en) | 1994-03-31 | 1997-01-15 | Imperial Chemical Industries Plc | Solvent extraction process |
| US7250185B2 (en) | 2000-11-06 | 2007-07-31 | Ineos Fluor Holdings Limited | Process for reducing the concentration of undesired compounds in a composition |
| CN101851559A (en) * | 2010-06-11 | 2010-10-06 | 平阴县玫瑰研究所 | Method for extracting rose essential oil from rose dregs |
Also Published As
| Publication number | Publication date |
|---|---|
| CH386596A (en) | 1965-01-15 |
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