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Ethyl N-butylcarbamate

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Identification
Molecular formula
C7H15NO2
CAS number
13142-03-3
IUPAC name
ethyl N-butylcarbamate
State
State

At room temperature, ethyl N-butylcarbamate is typically encountered as a liquid.

Melting point (Celsius)
-36.00
Melting point (Kelvin)
237.15
Boiling point (Celsius)
213.00
Boiling point (Kelvin)
486.15
General information
Molecular weight
159.22g/mol
Molar mass
159.2210g/mol
Density
0.9705g/cm3
Appearence

Ethyl N-butylcarbamate is a colorless liquid with a faint characteristic odor. It is used as an intermediate in organic synthesis and can appear slightly oily.

Comment on solubility

Solubility of Ethyl N-butylcarbamate

Ethyl N-butylcarbamate, with the chemical formula C7H15N1O2, exhibits distinct solubility characteristics that can be influenced by various factors. Generally, carbamates tend to be soluble in organic solvents, and ethyl N-butylcarbamate is no exception.

Key Points on Solubility:

  • Solvent Compatibility: This compound is typically soluble in organic solvents such as ethanol and acetone due to its relatively hydrophobic nature.
  • Water Solubility: Ethyl N-butylcarbamate has limited solubility in water, which is a characteristic feature of many carbamate derivatives.
  • Temperature Effects: As with many compounds, increased temperature can enhance solubility in organic solvents, leading to higher dissolution rates.
  • pH Influence: The solubility can also be affected by the pH of the solution, with more acidic or basic conditions potentially altering its ionization state.

In summary, the solubility of ethyl N-butylcarbamate can be attributed to its structural features, making it primarily soluble in organic solvents, yet sparingly soluble in water. Understanding these solubility dynamics is crucial for its applications in various chemical processes.

Interesting facts

Interesting Facts about Ethyl N-butylcarbamate

Ethyl N-butylcarbamate, a compound often used in various chemical applications, showcases an intriguing blend of functionality and versatility. Here are some interesting aspects of this compound:

  • Source of Ubiquity: Ethyl N-butylcarbamate can be found in various commercial formulations, including as a solvent and in the synthesis of certain agricultural products.
  • Functional Group Significance: The presence of the carbamate functional group makes this compound particularly interesting, as carbamates are known for their role in pharmacology, being key components in many drugs.
  • Biodegradability: One of the environmental advantages of ethyl N-butylcarbamate is its potential for biocompatibility and biodegradability, which aligns with the growing emphasis on sustainable chemical practices.
  • Application in Research: It is frequently studied in organic synthesis, serving as a building block for various chemical structures sought in pharmaceutical chemistry.
  • Analytical Importance: Ethyl N-butylcarbamate is of interest in analytical chemistry, as it can be used as a standard or a reference material for calibrating instruments.

In the words of renowned chemist Linus Pauling, "The world is in constant change and so is chemistry..." This quote perfectly captures the essence of compounds like ethyl N-butylcarbamate, which embody the dynamic interplay between structure, function, and innovation in the field of chemistry.


Overall, ethyl N-butylcarbamate represents a microcosm of the possibilities inherent in chemical research, drawing attention to both its practical applications and the broader implications for sustainability and innovation!

Synonyms
Ethyl butylcarbamate
N-Butylurethane
Butylurethane
Ethyl N-butylcarbamate
Butyl urethane
1-Butylurethane
1-Butylurethan
Butylcarbamic acid, ethyl ester
591-62-8
Ethyl-N,N-butylcarbamate
CARBAMIC ACID, BUTYL-, ETHYL ESTER
N-Butyl-O-ethylurethane
NSC 454
AI3-16946
NAA2TAQ529
NSC-454
BUR
EINECS 209-724-3
BRN 1751992
n-butyl urethane
starbld0030558
UNII-NAA2TAQ529
WLN: 4MVO2
SCHEMBL593415
NSC454
DTXSID0058435
AKOS003866756
Carbamic acid, N-butyl-, ethyl ester
NS00034100