BE384405A - - Google Patents
Info
- Publication number
- BE384405A BE384405A BE384405DA BE384405A BE 384405 A BE384405 A BE 384405A BE 384405D A BE384405D A BE 384405DA BE 384405 A BE384405 A BE 384405A
- Authority
- BE
- Belgium
- Prior art keywords
- hormone
- chloride
- desc
- hormones
- acid
- Prior art date
Links
- 239000005556 hormone Substances 0.000 claims description 20
- 229940088597 hormone Drugs 0.000 claims description 20
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000003163 gonadal steroid hormone Substances 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 210000001550 testis Anatomy 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 210000002700 urine Anatomy 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000010933 acylation Effects 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- PVNIQBQSYATKKL-UHFFFAOYSA-N Glycerol trihexadecanoate Natural products CCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC PVNIQBQSYATKKL-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Landscapes
- Steroid Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE384405A true BE384405A (enrdf_load_stackoverflow) |
Family
ID=53438
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE384405D BE384405A (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE384405A (enrdf_load_stackoverflow) |
-
0
- BE BE384405D patent/BE384405A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4792418A (en) | Method of extraction and purification of polyunsaturated fatty acids from natural sources | |
| EP3294850B2 (en) | Very long chain polyunsaturated fatty acids from natural oils | |
| EP0482344B1 (fr) | Procédé d'obtention de composés insaponifiables | |
| BE384405A (enrdf_load_stackoverflow) | ||
| JPH0320397A (ja) | 魚燐脂質を含有する高鮮度魚油及びその製法 | |
| FR2510558A1 (fr) | Derives nouveaux d'acide chenodesoxycholique | |
| EP0255904B1 (fr) | Procédé pour la préparation de dihydrocyclocitral | |
| EP0069946A1 (fr) | Huile, sa préparation et son utilisation, notamment dans les produits cosmétiques | |
| EP0072293A2 (fr) | Procédé de préparation de l'acide ursodésoxycholique à partir de l'acide 3 alpha, 7 beta, 12 alpha-trihydroxycholanique et produits intermédiaires utilisés | |
| FR2558154A1 (fr) | Acides gras ramifies en c10 a c20 utiles en tant que medicaments, et leur procede de preparation | |
| BE533938A (enrdf_load_stackoverflow) | ||
| Menon et al. | Petroselinic acid: Occurrence in some umbelliferæ seed fats | |
| BE503509A (enrdf_load_stackoverflow) | ||
| KR930000779B1 (ko) | M.s.g. 부산물을 이용한 어유의 탈취 가공방법 | |
| BE424182A (enrdf_load_stackoverflow) | ||
| DE136411C (enrdf_load_stackoverflow) | ||
| CH278133A (fr) | Procédé pour la préparation d'un nouvel ester triphosphorique de l'aneurine. | |
| SU254701A1 (ru) | СПОСОБ ФРАКЦИОНИРОВАНИЯ СМЕСИ ЖИРНЫХ КИСЛОТ, ПОЛУЧЕННЫХ ИЗ ХЛОПКОВОГО СОАПСТаКА | |
| CH351966A (fr) | Procédé de préparation d'esters d'estradiol | |
| CA2014672A1 (fr) | Derives insatures de l'acide 2,6-amino heptanedioique, leur procede de preparation et leur application comme medicaments | |
| BE401185A (enrdf_load_stackoverflow) | ||
| CH293367A (fr) | Procédé de préparation d'une succinimide substituée. | |
| BE422730A (enrdf_load_stackoverflow) | ||
| BE433249A (enrdf_load_stackoverflow) | ||
| FR2532845A1 (fr) | Composition pharmaceutique comprenant a titre de principe actif le docosanol |