SE461793B - Foerfarande foer frigoerande av steroler ur organiskt material - Google Patents

Foerfarande foer frigoerande av steroler ur organiskt material

Info

Publication number: SE461793B
Authority: SE; Sweden
Prior art keywords: sterols; organic material; release; amine; ammonia
Prior art date: 1986-09-12

Application number

SE8603846A

Other languages

English (en)

Swedish (sv)

Other versions

SE8603846L (sv

SE8603846D0 (sv

Inventor

B Aakermark

K Sjoeberg

Original Assignee

Triple Crown Ab

Priority date (The priority date 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 date listed.)

1986-09-12

Filing date

1986-09-12

Publication date

1990-03-26

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=20365570&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SE461793(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1986-09-12 Publication of SE8603846D0 publication Critical patent/SE8603846D0/xx

1986-09-12 Priority to SE8603846A priority Critical patent/SE461793B/sv

1986-09-12 Application filed by Triple Crown Ab filed Critical Triple Crown Ab

1987-09-09 Priority to ES87850275T priority patent/ES2021755B3/es

1987-09-09 Priority to EP87850275A priority patent/EP0260243B1/de

1987-09-09 Priority to AT87850275T priority patent/ATE61804T1/de

1987-09-09 Priority to DE8787850275T priority patent/DE3768743D1/de

1987-09-11 Priority to FI873962A priority patent/FI85865C/fi

1987-09-11 Priority to CA000546679A priority patent/CA1320947C/en

1987-09-11 Priority to NO873817A priority patent/NO167742C/no

1987-09-12 Priority to JP62227582A priority patent/JPS63101396A/ja

1988-03-13 Publication of SE8603846L publication Critical patent/SE8603846L/xx

1989-05-22 Priority to US07/356,579 priority patent/US4935168A/en

1990-03-26 Publication of SE461793B publication Critical patent/SE461793B/sv

Links

229930182558 Sterol Natural products 0.000 title claims abstract description 26
150000003432 sterols Chemical class 0.000 title claims abstract description 26
235000003702 sterols Nutrition 0.000 title claims abstract description 26
238000000034 method Methods 0.000 title claims abstract description 6
239000011368 organic material Substances 0.000 title claims abstract 4
150000001412 amines Chemical class 0.000 claims abstract description 12
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 10
229910021529 ammonia Inorganic materials 0.000 claims abstract description 5
150000002148 esters Chemical class 0.000 claims abstract description 4
238000004821 distillation Methods 0.000 claims abstract 2
239000002781 deodorant agent Substances 0.000 claims description 5
239000002253 acid Substances 0.000 claims description 4
150000007513 acids Chemical class 0.000 claims description 4
238000006243 chemical reaction Methods 0.000 claims description 3
150000001408 amides Chemical class 0.000 claims description 2
150000004985 diamines Chemical class 0.000 claims description 2
239000000463 material Substances 0.000 claims 2
201000006747 infectious mononucleosis Diseases 0.000 claims 1
150000003431 steroids Chemical class 0.000 claims 1
150000001875 compounds Chemical class 0.000 abstract 1
LGJMUZUPVCAVPU-UHFFFAOYSA-N beta-Sitostanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 LGJMUZUPVCAVPU-UHFFFAOYSA-N 0.000 description 9
238000000746 purification Methods 0.000 description 8
239000000203 mixture Substances 0.000 description 7
229950005143 sitosterol Drugs 0.000 description 7
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 6
239000000470 constituent Substances 0.000 description 6
SGNBVLSWZMBQTH-FGAXOLDCSA-N Campesterol Natural products O[C@@H]1CC=2[C@@](C)([C@@H]3[C@H]([C@H]4[C@@](C)([C@H]([C@H](CC[C@H](C(C)C)C)C)CC4)CC3)CC=2)CC1 SGNBVLSWZMBQTH-FGAXOLDCSA-N 0.000 description 5
BTEISVKTSQLKST-UHFFFAOYSA-N Haliclonasterol Natural products CC(C=CC(C)C(C)(C)C)C1CCC2C3=CC=C4CC(O)CCC4(C)C3CCC12C BTEISVKTSQLKST-UHFFFAOYSA-N 0.000 description 5
SGNBVLSWZMBQTH-PODYLUTMSA-N campesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](C)C(C)C)[C@@]1(C)CC2 SGNBVLSWZMBQTH-PODYLUTMSA-N 0.000 description 5
235000000431 campesterol Nutrition 0.000 description 5
KZJWDPNRJALLNS-VPUBHVLGSA-N (-)-beta-Sitosterol Natural products O[C@@H]1CC=2[C@@](C)([C@@H]3[C@H]([C@H]4[C@@](C)([C@H]([C@H](CC[C@@H](C(C)C)CC)C)CC4)CC3)CC=2)CC1 KZJWDPNRJALLNS-VPUBHVLGSA-N 0.000 description 4
CSVWWLUMXNHWSU-UHFFFAOYSA-N (22E)-(24xi)-24-ethyl-5alpha-cholest-22-en-3beta-ol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(CC)C(C)C)C1(C)CC2 CSVWWLUMXNHWSU-UHFFFAOYSA-N 0.000 description 4
OILXMJHPFNGGTO-UHFFFAOYSA-N (22E)-(24xi)-24-methylcholesta-5,22-dien-3beta-ol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(C)C(C)C)C1(C)CC2 OILXMJHPFNGGTO-UHFFFAOYSA-N 0.000 description 4
KLEXDBGYSOIREE-UHFFFAOYSA-N 24xi-n-propylcholesterol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CCC)C(C)C)C1(C)CC2 KLEXDBGYSOIREE-UHFFFAOYSA-N 0.000 description 4
OQMZNAMGEHIHNN-UHFFFAOYSA-N 7-Dehydrostigmasterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)C=CC(CC)C(C)C)CCC33)C)C3=CC=C21 OQMZNAMGEHIHNN-UHFFFAOYSA-N 0.000 description 4
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
LPZCCMIISIBREI-MTFRKTCUSA-N Citrostadienol Natural products CC=C(CC[C@@H](C)[C@H]1CC[C@H]2C3=CC[C@H]4[C@H](C)[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C LPZCCMIISIBREI-MTFRKTCUSA-N 0.000 description 4
ARVGMISWLZPBCH-UHFFFAOYSA-N Dehydro-beta-sitosterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)CCC(CC)C(C)C)CCC33)C)C3=CC=C21 ARVGMISWLZPBCH-UHFFFAOYSA-N 0.000 description 4
HZYXFRGVBOPPNZ-UHFFFAOYSA-N UNPD88870 Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)=CCC(CC)C(C)C)C1(C)CC2 HZYXFRGVBOPPNZ-UHFFFAOYSA-N 0.000 description 4
MJVXAPPOFPTTCA-UHFFFAOYSA-N beta-Sistosterol Natural products CCC(CCC(C)C1CCC2C3CC=C4C(C)C(O)CCC4(C)C3CCC12C)C(C)C MJVXAPPOFPTTCA-UHFFFAOYSA-N 0.000 description 4
NJKOMDUNNDKEAI-UHFFFAOYSA-N beta-sitosterol Natural products CCC(CCC(C)C1CCC2(C)C3CC=C4CC(O)CCC4C3CCC12C)C(C)C NJKOMDUNNDKEAI-UHFFFAOYSA-N 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
-1 primary Chemical class 0.000 description 4
KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 description 4
235000015500 sitosterol Nutrition 0.000 description 4
NLQLSVXGSXCXFE-UHFFFAOYSA-N sitosterol Natural products CC=C(/CCC(C)C1CC2C3=CCC4C(C)C(O)CCC4(C)C3CCC2(C)C1)C(C)C NLQLSVXGSXCXFE-UHFFFAOYSA-N 0.000 description 4
HCXVJBMSMIARIN-PHZDYDNGSA-N stigmasterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)/C=C/[C@@H](CC)C(C)C)[C@@]1(C)CC2 HCXVJBMSMIARIN-PHZDYDNGSA-N 0.000 description 4
235000016831 stigmasterol Nutrition 0.000 description 4
229940032091 stigmasterol Drugs 0.000 description 4
BFDNMXAIBMJLBB-UHFFFAOYSA-N stigmasterol Natural products CCC(C=CC(C)C1CCCC2C3CC=C4CC(O)CCC4(C)C3CCC12C)C(C)C BFDNMXAIBMJLBB-UHFFFAOYSA-N 0.000 description 4
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
235000012000 cholesterol Nutrition 0.000 description 3
239000000047 product Substances 0.000 description 3
238000011084 recovery Methods 0.000 description 3
239000003760 tallow Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical class NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
229920000768 polyamine Polymers 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
VGSSUFQMXBFFTM-UHFFFAOYSA-N (24R)-24-ethyl-5alpha-cholestane-3beta,5,6beta-triol Natural products C1C(O)C2(O)CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 VGSSUFQMXBFFTM-UHFFFAOYSA-N 0.000 description 1
NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
RZYHXKLKJRGJGP-UHFFFAOYSA-N 2,2,2-trifluoro-n,n-bis(trimethylsilyl)acetamide Chemical compound C[Si](C)(C)N([Si](C)(C)C)C(=O)C(F)(F)F RZYHXKLKJRGJGP-UHFFFAOYSA-N 0.000 description 1
VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
SXAMGRAIZSSWIH-UHFFFAOYSA-N 2-[3-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,2,4-oxadiazol-5-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NOC(=N1)CC(=O)N1CC2=C(CC1)NN=N2 SXAMGRAIZSSWIH-UHFFFAOYSA-N 0.000 description 1
LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
QOLRLLFJMZLYQJ-LOBDNJQFSA-N Hecogenin Chemical compound O([C@@H]1[C@@H]([C@]2(C(=O)C[C@@H]3[C@@]4(C)CC[C@H](O)C[C@@H]4CC[C@H]3[C@@H]2C1)C)[C@@H]1C)[C@]11CC[C@@H](C)CO1 QOLRLLFJMZLYQJ-LOBDNJQFSA-N 0.000 description 1
OXLGJTRVVNGJRK-UHFFFAOYSA-N Hecogenin Natural products CC1CCC2(CC3CC4C5CCC6CC(O)CCC6(C)C5CC(=O)C4(C)C3C2C)OC1 OXLGJTRVVNGJRK-UHFFFAOYSA-N 0.000 description 1
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
UVLDESQWQRMYKD-UHFFFAOYSA-N Neobotogenin Natural products CC1C(C2(C(=O)CC3C4(C)CCC(O)CC4=CCC3C2C2)C)C2OC11CCC(C)CO1 UVLDESQWQRMYKD-UHFFFAOYSA-N 0.000 description 1
235000019482 Palm oil Nutrition 0.000 description 1
235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
235000011613 Pinus brutia Nutrition 0.000 description 1
241000018646 Pinus brutia Species 0.000 description 1
WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
LGJMUZUPVCAVPU-JFBKYFIKSA-N Sitostanol Natural products O[C@@H]1C[C@H]2[C@@](C)([C@@H]3[C@@H]([C@H]4[C@@](C)([C@@H]([C@@H](CC[C@H](C(C)C)CC)C)CC4)CC3)CC2)CC1 LGJMUZUPVCAVPU-JFBKYFIKSA-N 0.000 description 1
DWCSNWXARWMZTG-UHFFFAOYSA-N Trigonegenin A Natural products CC1C(C2(CCC3C4(C)CCC(O)C=C4CCC3C2C2)C)C2OC11CCC(C)CO1 DWCSNWXARWMZTG-UHFFFAOYSA-N 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000003613 bile acid Substances 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
WQLVFSAGQJTQCK-VKROHFNGSA-N diosgenin Chemical compound O([C@@H]1[C@@H]([C@]2(CC[C@@H]3[C@@]4(C)CC[C@H](O)CC4=CC[C@H]3[C@@H]2C1)C)[C@@H]1C)[C@]11CC[C@@H](C)CO1 WQLVFSAGQJTQCK-VKROHFNGSA-N 0.000 description 1
WQLVFSAGQJTQCK-UHFFFAOYSA-N diosgenin Natural products CC1C(C2(CCC3C4(C)CCC(O)CC4=CCC3C2C2)C)C2OC11CCC(C)CO1 WQLVFSAGQJTQCK-UHFFFAOYSA-N 0.000 description 1
LMXOWXVJZDTLAD-UHFFFAOYSA-N dodecan-1-amine Chemical compound CCCCCCCCCCCCN.CCCCCCCCCCCCN LMXOWXVJZDTLAD-UHFFFAOYSA-N 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002169 ethanolamines Chemical class 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000003925 fat Substances 0.000 description 1
235000019197 fats Nutrition 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
235000019388 lanolin Nutrition 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
230000008707 rearrangement Effects 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
239000002904 solvent Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
LGJMUZUPVCAVPU-HRJGVYIJSA-N stigmastanol Chemical compound C([C@@H]1CC2)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]2(C)CC1 LGJMUZUPVCAVPU-HRJGVYIJSA-N 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
230000007306 turnover Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Steroid Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Fats And Perfumes (AREA)

SE8603846A 1986-09-12 1986-09-12 Foerfarande foer frigoerande av steroler ur organiskt material SE461793B (sv)

Priority Applications (10)

Application Number	Priority Date	Filing Date	Title
SE8603846A SE461793B (sv)	1986-09-12	1986-09-12	Foerfarande foer frigoerande av steroler ur organiskt material
ES87850275T ES2021755B3 (es)	1986-09-12	1987-09-09	Proceso para la preparacion de alcoholes.
EP87850275A EP0260243B1 (de)	1986-09-12	1987-09-09	Verfahren zur Aminolyse von Sterolestern
AT87850275T ATE61804T1 (de)	1986-09-12	1987-09-09	Verfahren zur aminolyse von sterolestern.
DE8787850275T DE3768743D1 (de)	1986-09-12	1987-09-09	Verfahren zur aminolyse von sterolestern.
FI873962A FI85865C (fi)	1986-09-12	1987-09-11	Foerfarande foer frigoerande av steroler ur organiska material.
NO873817A NO167742C (no)	1986-09-12	1987-09-11	Fremgangsmaate ved frisetting av steroler.
CA000546679A CA1320947C (en)	1986-09-12	1987-09-11	Process for the preparation of alcohols
JP62227582A JPS63101396A (ja)	1986-09-12	1987-09-12	アルコール製剤法
US07/356,579 US4935168A (en)	1986-09-12	1989-05-22	Process for the preparation of alcohols

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE8603846A SE461793B (sv)	1986-09-12	1986-09-12	Foerfarande foer frigoerande av steroler ur organiskt material

Publications (3)

Publication Number	Publication Date
SE8603846D0 SE8603846D0 (sv)	1986-09-12
SE8603846L SE8603846L (sv)	1988-03-13
SE461793B true SE461793B (sv)	1990-03-26

Family

ID=20365570

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8603846A SE461793B (sv)	1986-09-12	1986-09-12	Foerfarande foer frigoerande av steroler ur organiskt material

Country Status (10)

Country	Link
US (1)	US4935168A (de)
EP (1)	EP0260243B1 (de)
JP (1)	JPS63101396A (de)
AT (1)	ATE61804T1 (de)
CA (1)	CA1320947C (de)
DE (1)	DE3768743D1 (de)
ES (1)	ES2021755B3 (de)
FI (1)	FI85865C (de)
NO (1)	NO167742C (de)
SE (1)	SE461793B (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SE9202305L (sv) *	1992-08-06	1994-02-07	Triple Crown Ab	Kvalitativ styrning vid isolering av steroler
US20080262251A1 (en) *	2004-05-31	2008-10-23	Setsuo Sato	Process For the Recovery of Sterols From Organic Material

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2410590A (en) *	1944-01-21	1946-11-05	Distillation Products Inc	Concentration of fat-soluble vitamins
GB638393A (en) *	1947-01-09	1950-06-07	Veenendaalsche Sajet En Vijfsc	Improvements in and relating to the production of sterols and their addition products from material containing sterols
CH274237A (fr) *	1947-01-09	1951-03-31	Veenendaalsche Sajet En Vijfsc	Procédé pour isoler les stérols des mélanges qui les contiennent.
US2866739A (en) *	1955-05-18	1958-12-30	American Cyanamid Co	Recovery of beta-sitosterol from tall oil pitch by steam distillation
US2835682A (en) *	1955-08-08	1958-05-20	Swift & Co	Sterol recovery process
US3840570A (en) *	1970-12-07	1974-10-08	Procter & Gamble	Process for preparing sterols from tall oil pitch
SE417107B (sv) *	1973-06-29	1981-02-23	Bjarne Holmbom	Forfarande for foredling av sapor
US3879431A (en) *	1973-10-05	1975-04-22	Gen Mills Chem Inc	Purification of sterols by distillation
DE2936125A1 (de) *	1979-09-07	1981-03-26	Henkel KGaA, 40589 Düsseldorf	Neue sterinkonzentrate, verfahren zu ihrer gewinnung und ihre verwendung in der fermentativen sterintransformation
FI65440C (fi) *	1981-07-21	1984-05-10	Kaukas Ab Oy	Foerfarande foer separering av beta-sitosterol med en laog alfa-sitosterolhalt

1986
- 1986-09-12 SE SE8603846A patent/SE461793B/sv not_active IP Right Cessation
1987
- 1987-09-09 EP EP87850275A patent/EP0260243B1/de not_active Expired - Lifetime
- 1987-09-09 DE DE8787850275T patent/DE3768743D1/de not_active Expired - Lifetime
- 1987-09-09 ES ES87850275T patent/ES2021755B3/es not_active Expired - Lifetime
- 1987-09-09 AT AT87850275T patent/ATE61804T1/de not_active IP Right Cessation
- 1987-09-11 NO NO873817A patent/NO167742C/no unknown
- 1987-09-11 FI FI873962A patent/FI85865C/fi not_active IP Right Cessation
- 1987-09-11 CA CA000546679A patent/CA1320947C/en not_active Expired - Fee Related
- 1987-09-12 JP JP62227582A patent/JPS63101396A/ja active Pending
1989
- 1989-05-22 US US07/356,579 patent/US4935168A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
FI85865C (fi)	1992-06-10
NO167742C (no)	1991-12-04
EP0260243B1 (de)	1991-03-20
FI873962L (fi)	1988-03-13
SE8603846L (sv)	1988-03-13
DE3768743D1 (de)	1991-04-25
CA1320947C (en)	1993-08-03
SE8603846D0 (sv)	1986-09-12
JPS63101396A (ja)	1988-05-06
FI873962A0 (fi)	1987-09-11
NO873817D0 (no)	1987-09-11
ATE61804T1 (de)	1991-04-15
NO167742B (no)	1991-08-26
US4935168A (en)	1990-06-19
NO873817L (no)	1988-03-14
FI85865B (fi)	1992-02-28
ES2021755B3 (es)	1991-11-16
EP0260243A1 (de)	1988-03-16

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