5-METHYL-2,3-HEXANEDIONE manufacturers
- 5-METHYL-2,3-HEXANEDIONE
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- $15.00 / 1KG
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2021-07-02
- CAS:13706-86-0
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| | 5-METHYL-2,3-HEXANEDIONE Basic information |
| Product Name: | 5-METHYL-2,3-HEXANEDIONE | | Synonyms: | 5-methyl-3-hexanedione;Methylhexanedione;5-methylhexane-2,3-dione;Isovaleryl acetate;2,3-Hexanedione, 5-methyl-;acetylisopentanoyl;FEMA 3190;5-METHYL-2,3-HEXANEDIONE | | CAS: | 13706-86-0 | | MF: | C7H12O2 | | MW: | 128.17 | | EINECS: | 237-241-8 | | Product Categories: | | | Mol File: | 13706-86-0.mol |  |
| | 5-METHYL-2,3-HEXANEDIONE Chemical Properties |
| Melting point | 26.25°C (estimate) | | Boiling point | 138 °C | | density | 0,92 g/cm3 | | FEMA | 3190 | 5-METHYL-2,3-HEXANEDIONE | | refractive index | 1.4148 (589.3 nm 20℃) | | Fp | 33°C | | form | clear liquid | | color | Light yellow to Brown | | Odor | at 1.00 % in propylene glycol. sweet sharp fruity creamy brown butter | | Odor Type | fruity | | JECFA Number | 414 | | LogP | 0.06 | | EPA Substance Registry System | 2,3-Hexanedione, 5-methyl- (13706-86-0) |
| Risk Statements | 10 | | Safety Statements | 16 | | RIDADR | 1224 | | RTECS | MO3200000 | | TSCA | TSCA listed | | HS Code | 2914.19.0000 | | HazardClass | 3 | | PackingGroup | III |
| | 5-METHYL-2,3-HEXANEDIONE Usage And Synthesis |
| Description | 5-Methyl-2,3-hexanedione has a powerful oily-buttery odor with
a sweet taste in aqueous solution. May be synthesized by bromination of mesityl oxide, followed by treatment of the resulting
dibromide with sulfuric acid. | | Chemical Properties | 5-Methyl-2,3-hexanedione has a powerful, oily-buttery odor and a sweet taste in aqueous solution. | | Occurrence | Reported found in coffee and American potato chips | | Definition | ChEBI: 5-Methyl-2,3-hexanedione is an alpha-diketone. | | Safety Profile | A skin irritant. When
heated to decomposition it emits acrid
smoke and irritating fumes. | | Synthesis | 5-Methyl-2,3-hexanedione is obtained from the starting material 5-methyl-2-hexyne through an oxidation reaction. The synthetic route is as follows:
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| | 5-METHYL-2,3-HEXANEDIONE Preparation Products And Raw materials |
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