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N,N-Dibutylformamide

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N,N-Dibutylformamide manufacturers

N,N-Dibutylformamide Basic information
Product Name:N,N-Dibutylformamide
Synonyms:n,n-dibutyl-formamid;n,n-di-n-butyl-formamid;N,N-Di(but-1-yl)formamide;N,N-Di(but-1-yl)formamide 99%;N,N-dibutylformamide (DBF);N,N-Dibutylformamide;Dibutylamid kyseliny mravenci;dibutylamidkyselinymravenci
CAS:761-65-9
MF:C9H19NO
MW:157.25
EINECS:212-090-0
Product Categories:Building Blocks;C8 to C20+;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Amides;Carbonyl Compounds;Organic Building Blocks
Mol File:761-65-9.mol
N,N-Dibutylformamide Structure
N,N-Dibutylformamide Chemical Properties
Melting point <-30°C
Boiling point 120 °C15 mm Hg(lit.)
density 0.864 g/mL at 25 °C(lit.)
vapor pressure <1 mm Hg ( 20 °C)
refractive index n20/D 1.44(lit.)
Fp 213 °F
storage temp. 2-8°C
form clear liquid
pka-0.44±0.70(Predicted)
Specific Gravity0.864
color Colorless to Light yellow
Water Solubility Insoluble in water.
BRN 636100
InChI1S/C9H19NO/c1-3-5-7-10(9-11)8-6-4-2/h9H,3-8H2,1-2H3
InChIKeyNZMAJUHVSZBJHL-UHFFFAOYSA-N
SMILES[H]C(=O)N(CCCC)CCCC
LogP2 at 23℃
CAS DataBase Reference761-65-9(CAS DataBase Reference)
NIST Chemistry ReferenceFormamide, N,N-dibutyl-(761-65-9)
EPA Substance Registry SystemN,N-Dibutylformamide (761-65-9)
Safety Information
Hazard Codes Xi
Risk Statements 37-43-36/37/38
Safety Statements 36/37-37/39-26
WGK Germany 1
RTECS LQ1833000
TSCA TSCA listed
HS Code 29241990
Storage Class10 - Combustible liquids
Hazard ClassificationsSkin Sens. 1
MSDS Information
ProviderLanguage
N,N-Dibutylformamide English
ACROS English
SigmaAldrich English
ALFA English
N,N-Dibutylformamide Usage And Synthesis
Chemical PropertiesCLEAR COLOURLESS TO YELLOW LIQUID
UsesN,N-dibutylformamide is a pollutant sourcing from aerosols and or exhaust gases in Los Angeles.
Flammability and ExplosibilityNot classified
Safety ProfilePoison by intraperitoneal route. An experimental teratogen. When heated to decomposition it emits toxic fumes of NOx.
SynthesisIn a glove box, catalyst Rh/I (16.5 mg), N-methylpyrrolidone (1.0 mL), di-n-butylamine (168 L, 1 mmol), and decane (10 L,0.05 mmol) were added to the reaction kettle. Then CO2 was charged to replace the nitrogen in the kettle for three times, and then CO2 (20 atm) and H2 (20 atm) were charged, and the reaction was stirred in an oil bath at 100 for 24 h. After the reaction was completed, the kettle was cooled down to room temperature with an ice-water bath, and then the gas phase was measured after centrifugation of the supernatant, and the yield was 68%.
Purification MethodsPurify the amide by fractional distillation [Mandel & Hill J Am Chem Soc 76 3981 1954]. [Beilstein 4 IV 565.]
N,N-Dibutylformamide Preparation Products And Raw materials
Preparation Productsp-Butoxytoluene
Tag:N,N-Dibutylformamide(761-65-9) Related Product Information
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