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1-methylbutyl carbamate

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Identification
Molecular formula
C6H13NO2
CAS number
1209-20-5
IUPAC name
1-methylbutyl carbamate
State
State

At room temperature, 1-methylbutyl carbamate is mainly found in the liquid state due to its relatively low melting point.

Melting point (Celsius)
-45.90
Melting point (Kelvin)
227.25
Boiling point (Celsius)
222.00
Boiling point (Kelvin)
495.15
General information
Molecular weight
131.17g/mol
Molar mass
131.1730g/mol
Density
0.9353g/cm3
Appearence

1-Methylbutyl carbamate is typically a clear liquid. The exact color and transparency can slightly vary based on purity and storage conditions.

Comment on solubility

Solubility of 1-Methylbutyl Carbamate

1-Methylbutyl carbamate, with its unique structure, displays specific solubility characteristics that are quite engaging for chemists and researchers alike. Understanding its solubility can be approached from several angles:

  • Polar vs. Nonpolar: 1-Methylbutyl carbamate is a polar compound due to the presence of the carbamate functional group. This polarity influences its solubility in various solvents.
  • Solvent Compatibility: It is generally more soluble in polar solvents such as water, methanol, and ethanol, while showing limited solubility in nonpolar solvents. This property makes it particularly useful in reactions and processes requiring polar environments.
  • Temperature Dependence: Solubility may increase with temperature; thus, heating the solvent can improve the dissolution of 1-methylbutyl carbamate, which is often an essential consideration during its preparation and application.

In summary, the solubility of 1-methylbutyl carbamate can be summarized effectively through its interactions with solvents, which strongly depend on its polar character. As always, when working with such compounds, it’s vital to consider the specific conditions and solvent systems involved to maximize efficiency.

Interesting facts

Interesting Facts about 1-Methylbutyl Carbamate

1-Methylbutyl carbamate is a versatile compound that plays an intriguing role in both industrial applications and research settings. Here are some noteworthy aspects:

  • Chemical Structure: The compound features a carbamate functional group, which is characterized by the presence of a carbonyl (C=O) linked to a nitrogen atom (N). This structure contributes to its unique properties and reactivity.
  • Applications: 1-Methylbutyl carbamate is often utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, showcasing its importance in the production of essential compounds.
  • Toxicology and Safety: As with many carbamates, understanding the toxicological profile is crucial. This compound has been studied for its potential effects on human health and the environment, emphasizing the importance of safety measures during handling and application.
  • Research Insights: Ongoing research into 1-methylbutyl carbamate has revealed insights into its behavior as a nucleophile, which can react with electrophilic centers in organic chemistry, thus opening avenues for innovative synthetic pathways.
  • Historical Significance: Carbamic acids were first discovered in the late 18th century, and as derivatives such as 1-methylbutyl carbamate emerged, they led to significant advancements in both organic chemistry and material sciences.
  • Sustainable Chemistry: The development of bio-based carbamates highlights the intersection of green chemistry with traditional industrial practices, as researchers explore renewable sources for producing such compounds, which contributes to a more sustainable chemical industry.

In summary, 1-methylbutyl carbamate serves not only as a significant chemical in various applications but also as a reminder of the intricate relationship between chemistry and societal needs. As we continue to explore the potential of compounds like these, we reveal new layers of innovation and discovery.

Synonyms
1-Methylbutyl carbamate
Hedonal (drug)
CARBAMIC ACID, 1-METHYLBUTYL ESTER
2-Pentanol, carbamate
Hedonal (pharmaceutical)
Methylpropylcarbinol carbamate
NSC 27158
BRN 1751719
1T1KN15LF8
AI3-51975
NSC-27158
UNII-1T1KN15LF8
2-PENTANOL, 2-CARBAMATE
3-03-00-00057 (Beilstein Handbook Reference)
methylpropylcarbinol urethane
hedonal
pentan-2-yl carbamate
541-95-7
WLN: ZVOY3&1
SCHEMBL514364
DTXSID501031558
NSC27158
AKOS006274512