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| | 3-Methyl-2-buten-1-ol Basic information |
| Product Name: | 3-Methyl-2-buten-1-ol | | Synonyms: | 3-methyl-2-buten-1-o;3-Methyl-2-butenyl alcohol;3-methyl-but-2-en-1-ol;dimethylallylalcohol;gamma,gamma-Dimethylallyl alcohol;gamma,gamma-dimethylallylalcohol;Methyl-3-but-2-en-1-ol;3-Methyl-2-buten-1-ol,3,3-Dimethylallyl alcohol, Prenol | | CAS: | 556-82-1 | | MF: | C5H10O | | MW: | 86.13 | | EINECS: | 209-141-4 | | Product Categories: | Pesticides intermediate | | Mol File: | 556-82-1.mol |  |
| | 3-Methyl-2-buten-1-ol Chemical Properties |
| Melting point | 43.52°C | | Boiling point | 140 °C(lit.) | | density | 0.848 g/mL at 25 °C(lit.) | | vapor pressure | 1.4 mm Hg ( 20 °C) | | refractive index | n20/D 1.443(lit.) | | FEMA | 3647 | 3-METHYL-2-BUTEN-1-OL | | Fp | 110 °F | | storage temp. | Sealed in dry,2-8°C | | solubility | 64g/l | | pka | 14.83±0.10(Predicted) | | form | Liquid | | color | Clear colorless to very slightly yellow | | Odor | at 100.00 %. fruity green lavender | | Odor Type | fruity | | explosive limit | 2.7-16.3%(V) | | Water Solubility | 170 g/L (20 ºC) | | JECFA Number | 1200 | | BRN | 1633479 | | InChIKey | ASUAYTHWZCLXAN-UHFFFAOYSA-N | | LogP | 1.24 | | CAS DataBase Reference | 556-82-1(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Buten-1-ol, 3-methyl-(556-82-1) | | EPA Substance Registry System | 2-Buten-1-ol, 3-methyl- (556-82-1) |
| | 3-Methyl-2-buten-1-ol Usage And Synthesis |
| Description | 3-Methyl-2-buten-l-ol has a phenolic, metallic odor bearing a
resemblance to iron gallate ink. May be synthesized from isoprene
by hydration via prenyl acetate or by rearrangement of 3-methyll-buten-3-ol. | | Chemical Properties | clear colourless to very slightly yellow liquid | | Chemical Properties | 3-Methyl-2-buten-1-ol has a phenolic, metallic odor bearing a resemblance to iron gallate ink | | Uses | 3-Methyl-2-buten-1-ol is used as a reagent for protection of carboxylic acids as their 3-methyl-2-buten-1-yl (Prenyl) esters. It is also used in perfumery. | | Uses | 3-Methyl-2-buten-1-ol was used as starting reagent during asymmetric total syntheses of (R)-(+)- and (S)-(-)-umbelactone via Sharpless asymmetric epoxidation reaction. | | Definition | ChEBI: Prenol is an alkenyl alcohol and a member of prenols. | | General Description | 3-Methyl-2-buten-1-ol reacts with nitrosocarbonyl benzene to yield 5-hydroxy-isoxazolidines. It is commonly used as fragrance ingredient. | | Flammability and Explosibility | Flammable |
| | 3-Methyl-2-buten-1-ol Preparation Products And Raw materials |
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