BE369411A - - Google Patents
Info
- Publication number
- BE369411A BE369411A BE369411DA BE369411A BE 369411 A BE369411 A BE 369411A BE 369411D A BE369411D A BE 369411DA BE 369411 A BE369411 A BE 369411A
- Authority
- BE
- Belgium
- Prior art keywords
- alcohol
- water
- desc
- soluble
- formic acid
- Prior art date
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 12
- HSJKGGMUJITCBW-UHFFFAOYSA-N 3-hydroxybutanal Chemical compound CC(O)CC=O HSJKGGMUJITCBW-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000843 powder Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 235000019253 formic acid Nutrition 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical class C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- -1 aliphatic aldehydes Chemical class 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000009965 odorless effect Effects 0.000 description 3
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241000238876 Acari Species 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 1
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE369411A true BE369411A (enrdf_load_stackoverflow) |
Family
ID=41052
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE369411D BE369411A (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE369411A (enrdf_load_stackoverflow) |
-
0
- BE BE369411D patent/BE369411A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2791098B1 (fr) | Procede de purification de la vanilline par extraction liquide-liquide | |
CH679584A5 (enrdf_load_stackoverflow) | ||
Connell | Natural pungent compounds. III. The paradols and associated compounds | |
JPH07500127A (ja) | 抗酸化剤オレオレジン組成物及びその製造方法 | |
US7182973B2 (en) | Low temperature process for extracting principal components from plants or plant materials and plant extracts produced thereby | |
FR2488801A1 (fr) | Extraits a l'eau chaude de l'ecorce du margousier, possedant une activite antineoplastique | |
CH649920A5 (fr) | Derives substitues de l'acide 4-phenyl 4-oxo 2-butenoique, a titre de medicaments. | |
EP1091970B1 (fr) | Procede de preparation d'aloine par extraction | |
BE369411A (enrdf_load_stackoverflow) | ||
CH635810A5 (fr) | Composes alicycliques insatures, procede pour leur preparation et leur utilisation. | |
CA2153646A1 (fr) | Procede de preparation d'extraits contenant des composes polyphenoliques oligomeres de type catechique a partir de sources vegetales et extraits obtenus | |
JPS621396B2 (enrdf_load_stackoverflow) | ||
JP3007417B2 (ja) | マルトール回収 | |
JPH0867874A (ja) | 酸化防止剤の製造方法 | |
JP2022520600A (ja) | オレオカンタールタイプのセコイリドイドを得る方法、及びそれぞれの医薬製剤を製造する方法 | |
JPS61268648A (ja) | オレアノ−ル酸の製造方法 | |
RU2218345C2 (ru) | Способ получения алоина экстракцией | |
EP0081699A1 (fr) | Nouveaux composés alicycliques, leur utilisation à titre d'ingrédients parfumants ou aromatisants, procédé pour leur préparation | |
US2145907A (en) | Therapeutically active principle from ergot and processes for its production | |
BE1000468A7 (fr) | Procede d'extraction de la silymarine. | |
BE841879A (fr) | Produits pharmaceutiques a action hemostatique comprenant des steryl-b -d-glucosides et leurs monopalmitates | |
Phillips et al. | Chemistry of Lignin. VIII. The Oxidation of Alkali Lignin | |
BE519277A (enrdf_load_stackoverflow) | ||
FR2848111A1 (fr) | Extrait de lichen a teneur reduite en acides resiniques, procede de preparation et utilisations | |
Goulding et al. | XXXVI.—Volatile oil from tubers of Kaempferia ethelæ |