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3,3-DIMETHYL-2-PENTANOL

Base Information
  • Chemical Name:3,3-DIMETHYL-2-PENTANOL
  • CAS No.:19781-24-9
  • Molecular Formula:C7H16 O
  • Molecular Weight:116.203
  • Hs Code.:2905199090
  • Mol file:19781-24-9.mol
3,3-DIMETHYL-2-PENTANOL

Synonyms:3,3-Dimethyl-2-pentanol;Methyl-tert-pentylcarbinol

Suppliers and Price of 3,3-DIMETHYL-2-PENTANOL
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of 3,3-DIMETHYL-2-PENTANOL
Chemical Property:
  • Vapor Pressure:2.83mmHg at 25°C 
  • Melting Point:-30.45°C (estimate) 
  • Refractive Index:1.4280 
  • Boiling Point:138.3°Cat760mmHg 
  • PKA:15.27±0.20(Predicted) 
  • Flash Point:42.3°C 
  • PSA:20.23000 
  • Density:0.818g/cm3 
  • LogP:1.80340 
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 3,3-Dimethyl-2-pentanol is an intermediate in the synthesis of 3,3-Dimethyl-1-pentene (D476815), used to estimate the gas chromatography retention.
Technology Process of 3,3-DIMETHYL-2-PENTANOL

There total 8 articles about 3,3-DIMETHYL-2-PENTANOL which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With lithium aluminium tetrahydride; In diethyl ether; at 0 - 20 ℃; for 4h;
DOI:10.1016/S0040-4020(98)01065-5
Guidance literature:
Multi-step reaction with 3 steps
1.1: 92 percent / H2 / Pd/C / ethyl acetate / 15 h / 20 °C
2.1: trimethyloxonium tetrafluoroborate / CH2Cl2 / 3 h / 0 - 20 °C
2.2: aq. NaOH / CH2Cl2 / 2 h / 0 - 20 °C
3.1: LiAlH4 / diethyl ether / 4 h / 0 - 20 °C
With lithium aluminium tetrahydride; hydrogen; trimethoxonium tetrafluoroborate; palladium on activated charcoal; In diethyl ether; dichloromethane; ethyl acetate; 1.1: Catalytic hydrogenation / 2.1: Methylation / 2.2: Cyclization / 3.1: Reduction;
DOI:10.1016/S0040-4020(98)01065-5
Guidance literature:
Multi-step reaction with 4 steps
1.1: 66 percent / LiAlH4 / tetrahydrofuran / 13 h / 0 °C
2.1: 92 percent / H2 / Pd/C / ethyl acetate / 15 h / 20 °C
3.1: trimethyloxonium tetrafluoroborate / CH2Cl2 / 3 h / 0 - 20 °C
3.2: aq. NaOH / CH2Cl2 / 2 h / 0 - 20 °C
4.1: LiAlH4 / diethyl ether / 4 h / 0 - 20 °C
With lithium aluminium tetrahydride; hydrogen; trimethoxonium tetrafluoroborate; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate; 1.1: Reduction / 2.1: Catalytic hydrogenation / 3.1: Methylation / 3.2: Cyclization / 4.1: Reduction;
DOI:10.1016/S0040-4020(98)01065-5
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