BE433447A - - Google Patents
Info
- Publication number
- BE433447A BE433447A BE433447DA BE433447A BE 433447 A BE433447 A BE 433447A BE 433447D A BE433447D A BE 433447DA BE 433447 A BE433447 A BE 433447A
- Authority
- BE
- Belgium
- Prior art keywords
- magnesium
- hydroxide
- phenolates
- phenol
- weight
- Prior art date
Links
- KRPXAHXWPZLBKL-UHFFFAOYSA-L magnesium;diphenoxide Chemical class [Mg+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 KRPXAHXWPZLBKL-UHFFFAOYSA-L 0.000 claims description 12
- 239000000395 magnesium oxide Substances 0.000 claims description 9
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 9
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000000347 magnesium hydroxide Substances 0.000 claims description 8
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 5
- 230000009466 transformation Effects 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000000227 grinding Methods 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 6
- 229960003742 phenol Drugs 0.000 description 6
- 239000008267 milk Substances 0.000 description 4
- 210000004080 milk Anatomy 0.000 description 4
- 235000013336 milk Nutrition 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000004707 phenolate Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 229960003666 liquefied phenol Drugs 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000003739 xylenols Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/235—Metal derivatives of a hydroxy group bound to a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE433447A true BE433447A (enrdf_load_stackoverflow) |
Family
ID=92813
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE433447D BE433447A (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE433447A (enrdf_load_stackoverflow) |
-
0
- BE BE433447D patent/BE433447A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH02194103A (ja) | アルカリ電池 | |
| BE433447A (enrdf_load_stackoverflow) | ||
| US2062205A (en) | Process of producing the m-alkylethers of protocatechuic aldehyde | |
| Datta et al. | Halogenation. XVI. Iodination by Means of Nitrogen Iodide or by Means of Iodine in the Presence of Ammonia. | |
| US1389862A (en) | Manufacture of potassium sulfate | |
| Chattaway et al. | CCX.—The action of nitrogen iodide on methyl ketones | |
| Black et al. | The Alkaline Cleavage of 4-Nitrobenzil and 3, 3'-Dinitrobenzil | |
| Niederl et al. | The Synthesis of Long Chain Substituted Isocyclics and Similarly Substituted Adipic Acids. 1 The Preparation of γ-t-Octylcyclohexanol, Hexene, Hexanone, Hydroxylamine, Amine, Phenol and β-t-Octyl Adipic Acid | |
| Chattaway et al. | CLXXXI.—The preparation of 4: 4′-dinitrobenzil | |
| US708511A (en) | Paramethyl-amidophenyl-glyoxylic acid and process of making same. | |
| EP0213003B1 (fr) | Procédé discontinu de préparation, en deux étapes de chloration, d'hypochlorite neutre de calcium hydraté | |
| JPS606285B2 (ja) | 立方晶もしくはウルツ鉱型窒化ホウ素の分離法 | |
| BE854097Q (fr) | Procede de preparation industrielle du tri (hydroxymathyl) amino-methane-gluconate-di-hydroxy-aluminate | |
| CH464953A (fr) | Procédé de préparation du sel de lithium de l'acide para-dihydroxy-benzène-sulfonique | |
| DE517539C (de) | Verfahren zur Darstellung aromatischer Oxyaldehyde | |
| Archibald et al. | The Melting-Points of Solid Chloroform, Toluene and Ether. | |
| US730175A (en) | Process of obtaining products from suprarenal glands. | |
| CH501710A (fr) | Procédé de préparation de carbonates de colorants cationiques | |
| BE378389A (enrdf_load_stackoverflow) | ||
| BE500359A (enrdf_load_stackoverflow) | ||
| BE358229A (enrdf_load_stackoverflow) | ||
| BE452466A (enrdf_load_stackoverflow) | ||
| BE726530A (enrdf_load_stackoverflow) | ||
| Moore | The synthesis of some new derivatives of cinnamic acid and o-oxyphenyl | |
| Hilditch et al. | CXXXII.—Aromatic selenonium bases |