Dibutoxymethane manufacturers
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| | Dibutoxymethane Basic information |
| Product Name: | Dibutoxymethane | | Synonyms: | 1,1'-[methylenebis(oxy)]dibutane;FORMALDEHYDE DI-N-BUTYL ACETAL 98+%;Butane, 1,1-methylenebis(oxy)bis-;5,7-Dioxahendecane;5,7-Dioxaundecane;Bis(butyloxy)methane;Formaldehyde Dibutyl Acetal
5,7-Dioxahendecane;Formaldehyde dibutyl acetal puriss., >=98.5% (GC) | | CAS: | 2568-90-3 | | MF: | C9H20O2 | | MW: | 160.25 | | EINECS: | 219-909-0 | | Product Categories: | | | Mol File: | 2568-90-3.mol |  |
| | Dibutoxymethane Chemical Properties |
| Melting point | -58.1°C | | Boiling point | 180°C | | density | 0,84 g/cm3 | | vapor pressure | 1-1.11hPa at 22.7-25℃ | | refractive index | n20/D1.406 | | Fp | 60°C | | form | clear liquid | | color | Colorless to Almost colorless | | Water Solubility | 222.5-250mg/L at 20℃ | | Cosmetics Ingredients Functions | SURFACTANT - EMULSIFYING
CLEANSING
SOLVENT | | InChI | 1S/C9H20O2/c1-3-5-7-10-9-11-8-6-4-2/h3-9H2,1-2H3 | | InChIKey | QLCJOAMJPCOIDI-UHFFFAOYSA-N | | SMILES | CCCCOCOCCCC | | LogP | 2.77-4.1 at 20-21.5℃ | | EPA Substance Registry System | Butane, 1,1'-[methylenebis(oxy)]bis- (2568-90-3) |
| Risk Statements | 36/37/38 | | Safety Statements | 26-36/37/39 | | RIDADR | 3271 | | WGK Germany | 1 | | TSCA | TSCA listed | | HS Code | 2911.00.5000 | | HazardClass | 3 | | PackingGroup | III | | Storage Class | 10 - Combustible liquids |
| | Dibutoxymethane Usage And Synthesis |
| Uses | Formaldehyde dibutyl acetal is a halogen-free and less toxic solvent that can be used to solubilize commercial low-density polyethylene (LDPE) samples to analyze molecular weight distribution using gel permeation chromatography (GPC). It can also be used as a reactant to prepare butoxymethyltriphenylphosphonium iodide, which is used for carbon homologation and also as a useful key intermediate in organic synthesis. | | Preparation | A flask containing 15 gm (0.5 mole) of paraformaldehyde, 74 gm (1.0 mole) of η-butyl alcohol, and 2.0 gm of anhydrous ferric chloride is refluxed for 10 hr. The lower layer of 3-4 ml of material is discarded and then 50 ml of 10% aqueous sodium carbonate solution is added to remove the ferric chloride as ferric hydroxide. The product is shaken with a mixture of 40 ml of 20% hydrogen peroxide and 5 ml of 10% sodium carbonate solution at 45°C in order to remove any remaining aldehyde. The product is also washed with water, dried, and distilled from excess sodium metal to afford 62 gm (78%).
 | | Synthesis Reference(s) | The Journal of Organic Chemistry, 45, p. 3341, 1980 DOI: 10.1021/jo01304a039 | | General Description | Formaldehyde dibutyl acetal is an acetal used in the manufacture of synthetic resins, antiseptics, deodorants, and fungicides. It is also used as a fuel additive to increase the octane number of gasoline or the n-cetane number of diesel fuels and reduce smoke and particulate emissions. |
| | Dibutoxymethane Preparation Products And Raw materials |
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