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Butyramide

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Butyramide Basic information

Product Name:
Butyramide
Synonyms:
  • AMIDE C4
  • N-BUTYRAMIDE 99%
  • Butyramide,98%
  • n-Butyramide,98%
  • N-BUTYRAMIDE
  • butanimidicacid
  • butanoicacid,amide
  • Butyricamide
CAS:
541-35-5
MF:
C4H9NO
MW:
87.12
EINECS:
208-776-4
Mol File:
541-35-5.mol
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Butyramide Chemical Properties

Melting point:
114-116 °C
Boiling point:
216 °C
Density 
1.03
refractive index 
1.4560
FEMA 
4252 | BUTYRAMIDE
Flash point:
216°C
storage temp. 
Sealed in dry,Room Temperature
solubility 
alcohol: soluble(lit.)
pka
16.67±0.40(Predicted)
form 
powder to crystal
color 
White to Almost white
Odor
at 100.00?%. nutty
Water Solubility 
soluble
Merck 
14,1592
JECFA Number
1593
BRN 
1361528
LogP
-0.210
CAS DataBase Reference
541-35-5(CAS DataBase Reference)
NIST Chemistry Reference
Butanamide(541-35-5)
EPA Substance Registry System
Butanamide (541-35-5)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
24/25
WGK Germany 
3
TSCA 
Yes
HS Code 
29241900
Hazardous Substances Data
541-35-5(Hazardous Substances Data)

MSDS

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Butyramide Usage And Synthesis

Chemical Properties

Colorless to white crystalline powder or flakes with nutty aroma; soluble in water and alcohol, slightly soluble in ether.

Uses

Butyramide was used in the synthesis of hydroxamic acids, electrorheological fluids and β-amodoorganotin compounds. It was used as substrate of (+)-γ-lactamase to develop a microreactor to study enzyme stability, activity, kinetics and substrate specificity.

Definition

ChEBI: Butanamide is a monocarboxylic acid amide obtained by formal condensation of butanoic acid and ammonia. It is a primary fatty amide and a member of butanamides.

Preparation

Butyramide is prepared by amination of n-butyric acid. n-Butyric acid is heated with ammonia gas bubbled through it, and the reaction mixture reaches 200–215°C after approximately 40 hours. Heating and ammonia flow are then stopped, and the mixture is cooled below 20°C before filtration to yield butyramide.
An alternative method involves reacting n-butyric acid with urea: First, heat a mixture of 8 kg of n-butyric acid and 3 kg of urea under reflux for 10 hours. Allow the mixture to cool to 70–80°C, then add a suitable amount of hot ethanol. Decolorize the hot solution, filter it while hot, and cool. The crude product obtained by filtration is recrystallised from ethanol to yield the final product.

Aroma threshold values

Nutty type odor.

ButyramideSupplier

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