1-METHOXY-2-METHYL-2-PROPANOL
1-METHOXY-2-METHYL-2-PROPANOL Basic information
- Product Name:
- 1-METHOXY-2-METHYL-2-PROPANOL
- Synonyms:
-
- 1-METHOXY-2-METHYL-2-PROPANOL
- 1-METHOXY-2-METHYLPROPAN-2-OL
- 1,1-Dimethyl-2-methoxyethanol
- 1-METHOXY-2-METHYL-2-PROPANOL, 98+%
- 1-Methoxy-2-methylpropane-2-ol
- 2-(Methoxymethyl)-2-propanol
- 2-(Methoxymethyl)propane-2-ol
- 2-Methoxy-1,1-dimethylethanol
- CAS:
- 3587-64-2
- MF:
- C5H12O2
- MW:
- 104.15
- EINECS:
- 609-188-4
- Product Categories:
-
- Alcohols
- C2 to C6
- Oxygen Compounds
- Aromatic alcohols and diols
- Mol File:
- 3587-64-2.mol
1-METHOXY-2-METHYL-2-PROPANOL Chemical Properties
- Boiling point:
- 115-116 °C (lit.)
- Density
- 0.892 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.4044(lit.)
- Flash point:
- 82 °F
- storage temp.
- 2-8°C
- form
- Liquid
- pka
- 14.56±0.29(Predicted)
- color
- Clear colorless
- LogP
- 0.069 (est)
- CAS DataBase Reference
- 3587-64-2
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 10-36/37/38
- Safety Statements
- 26-36
- RIDADR
- UN 1987 3/PG 3
- WGK Germany
- 3
- HazardClass
- 3
- PackingGroup
- III
- HS Code
- 29094980
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
1-METHOXY-2-METHYL-2-PROPANOL Usage And Synthesis
Synthesis
558-30-5
67-56-1
3587-64-2
1. Catalyst pretreatment: 0.037 mmol of Zr catalyst was added to a 25 mL round-bottomed flask and heated at 150°C under vacuum overnight to remove the absorbed water. 2. Reaction system preparation: 5mL of methanol was added to the flask and sonicated for 15 min. 3. Addition of reactants: 1 mmol of propylene oxide was added. 4. 4. Reaction condition setting: Place the reaction mixture in a bath preheated to 50°C with magnetic stirring. 5. Catalyst activation (if applicable): 2.5 mL of acetone was added as solvent and after sonication of the catalyst, 1.0 mmol of amine and 1.0 mmol of styrene oxide were added sequentially. 6. Reaction termination and product recovery: At the end of the reaction, the catalyst was washed thoroughly with methanol to recover the adsorbed products. 7. Product purification: The product was purified using silica gel. 7. Product purification: The product was purified by rapid column chromatography using silica gel column chromatography with hexane:methylene chloride as eluent. 8. Reaction monitoring: Aliquots of the reaction mixture were withdrawn periodically with a syringe, diluted with methanol and immediately analyzed by GC (Agilent 6890 network GC system), and the product concentration was determined by a calibration curve.
References
[1] Journal of Molecular Catalysis A: Chemical, 2016, vol. 425, p. 332 - 339
[2] Patent: US2886600, 1957,
[3] Journal of Molecular Structure, 1991, vol. 243, p. 111 - 122
[4] Patent: US2886600, 1957,
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