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1-METHOXY-2-METHYL-2-PROPANOL

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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
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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
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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

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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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