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| Dimedone Basic information |
| Product Name: | Dimedone | | Synonyms: | 5,5-DIMETHYL-1,3-CYCLOHEXANEDIONE;5,5'-DIMETHYLCYCLOHEXANE-1,3-DIONE;5,5-DIMETHYL-CYCLOHEXANE-1,3-DIONE;5,5-DIMETHYLDIHYDRORESORCINOL;1,1-Dimethyl-3,5-cyclohexanedione;1,1-Dimethyl-3,5-diketocyclohexane;1,3-Cyclohexanedione, 5,5-dimethyl-;1,3-Cyclohexanedione,5,5-dimethyl- | | CAS: | 126-81-8 | | MF: | C8H12O2 | | MW: | 140.18 | | EINECS: | 204-804-4 | | Product Categories: | Pyridines ,Halogenated Heterocycles;Building Blocks;C7 to C8;Carbonyl Compounds;Chemical Synthesis;Ketones;Pharmaceutical Intermediates;Aromatic Ketones (substituted);ketone;Materials Science;Organic Building Blocks;bc0001 | | Mol File: | 126-81-8.mol |
| Dimedone Chemical Properties |
| Melting point | 146-148 °C (lit.) | | Boiling point | 216.69°C (rough estimate) | | density | 1.0373 (rough estimate) | | refractive index | 1.4787 (estimate) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | solubility | 4.01g/l | | pka | 4.8(at 25℃) | | form | Liquid | | color | Clear colorless to yellow | | Water Solubility | 0.416 g/100 mL (25 ºC) | | Merck | 14,3242 | | BRN | 471489 | | Stability: | Stable, but may be light sensitive. Incompatible with strong oxidizing agents. | | InChIKey | BADXJIPKFRBFOT-UHFFFAOYSA-N | | LogP | 1.3 at 20℃ | | CAS DataBase Reference | 126-81-8(CAS DataBase Reference) | | NIST Chemistry Reference | Dimedone(126-81-8) | | EPA Substance Registry System | 1,3-Cyclohexanedione, 5,5-dimethyl- (126-81-8) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 24/25-36-26 | | WGK Germany | 2 | | RTECS | GV0345000 | | F | 8-9 | | TSCA | Yes | | HS Code | 29142900 |
| Dimedone Usage And Synthesis |
| Chemical Properties | solid | | Uses | Part of furannulation strategy for the synthesis of naturally occurring fused 3-methylfurans.1 | | Uses | A mentha compound showing antimicrobial properties against common bacteria in the food industry such as E.coli and P.aeruginosa as well as strains of yeast. | | Uses | Used in the synthesis of fused 3-methylfurans via furannulation. | | Uses | Reagent used in synthesis of fused 3-methylfuransDimedone is used in organic chemistry to identify the presence of aldehyde group. It is also used as a catalyst in the formation of transition-metal complexes. Further, it is also employed in colorimetry, crystallography, luminescence and spectrophotometric analysis. In addition to this, it is used in the synthesis of naturally occurring fused 3-methylfurans. | | Synthesis Reference(s) | Journal of the American Chemical Society, 77, p. 6656, 1955 DOI: 10.1021/ja01629a086Organic Syntheses, Coll. Vol. 2, p. 200, 1943 | | General Description | 5,5-dimethyl-1,3-cyclohexanedione (Dimedone) is basically a highly sensitive and very specific reagent used for the determination of aldehydes. It is highly advantageous as it is environment friendly, give high yields and is a simple workup procedure. | | Purification Methods | Crystallise dimedone from acetone (ca 8mL/g), water or aqueous EtOH. Dry it in air. [Schneider & Todd Org Synth Coll Vol II 200 1943, Beilstein 7 H 559, 7 IV 1999.] |
| Dimedone Preparation Products And Raw materials |
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