DIBUTYL CARBONATE

DIBUTYL CARBONATE
  • CAS No.:542-52-9

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
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DIBUTYL CARBONATE Basic information
Product Name:DIBUTYL CARBONATE
Synonyms:DI-N-BUTYL CARBONATE;DIBUTYL CARBONATE;CARBON DIOXIDEDI-N-BUTYL ESTER;BUTYL CARBONATE;Carbonic acid, dibutyl ester;Carbonic acid, di-n-butyl ester;Carbonicacid,dibutylester;carbonicaciddibutylester
CAS:542-52-9
MF:C9H18O3
MW:174.24
EINECS:208-816-0
Product Categories:Inhibitors;CARBONATES
Mol File:542-52-9.mol
DIBUTYL CARBONATE Chemical Properties
Melting point <25 °C
Boiling point bp 206.6°
density d420 0.9251; d425 0.9388
refractive index nD20 1.4117
storage temp. 2-8°C
form clear liquid
color Colorless to Almost colorless
EPA Substance Registry SystemCarbonic acid, dibutyl ester (542-52-9)
Safety Information
MSDS Information
DIBUTYL CARBONATE Usage And Synthesis
Chemical Propertiesliquid
UsesDibutyl Carbonate is a potential fuel substitute due to the observed decrease in CO2 emissions. Also used in CO2 catalytic activation.
PreparationA 160 mL Parr autoclave was charged with butanol 982 (2.22 g, 0.03 mol), N-cyclohexyl-N',N',N'',N''-tetramethylguanidine (CyTMG; 6.9 g, 0.035 mol), and acetonitrile (30 mL). The autoclave was attached to a pressure head, and 160 psig CO2 was introduced with stirring at room temperature. An exothermic reaction ensued, leading to an increase in temperature to ca. 40℃. In a Fischer–Porter bottle was placed a solution of 1-chlorobutane (8.33 g, 0.09 mol) in acetonitrile (10 mL). This bottle was attached to a pressure head, and 80 psig CO2 was introduced above the solution. After 1 h, the solution of 1-chlorobutane was added in one portion under 80 psig CO2 to the pre-formed carbonate anion solution generated in the autoclave. After the addition, the pressure was increased to 160 psig with CO2, and the reaction mixture was warmed to 85 ℃ for 16 h. Thereafter, the reaction mixture was allowed to cool to room temperature, and then the pressure was released. An aliquot was removed, diluted with diethyl ether, and CyTMGH+Cl- was filtered off; by GC analysis using biphenyl as an internal standard, the yield of dibutyl carbonate was calculated as 73%; oil.
Flammability and ExplosibilityNotclassified
DIBUTYL CARBONATE Preparation Products And Raw materials
Preparation Products1-Butylimidazole-->Butyl chloroformate

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