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Fenobucarb

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Identification
Molecular formula
C12H17NO2
CAS number
3766-81-2
IUPAC name
(3-sec-butylphenyl) N-methylcarbamate
State
State

At room temperature, Fenobucarb is typically in a liquid state. It remains stable under standard temperature and pressure conditions, making it suitable for use as an agricultural chemical in various environmental settings.

Melting point (Celsius)
12.50
Melting point (Kelvin)
285.65
Boiling point (Celsius)
240.00
Boiling point (Kelvin)
513.15
General information
Molecular weight
193.26g/mol
Molar mass
193.2610g/mol
Density
1.0270g/cm3
Appearence

Fenobucarb is usually a colorless to pale yellow liquid. It may have a mild chemical odor that is typical of carbamate esters. This compound is often used in its liquid form for pesticide and insecticide applications.

Comment on solubility

Solubility of (3-sec-butylphenyl) N-methylcarbamate

(3-sec-butylphenyl) N-methylcarbamate presents unique solubility characteristics that make it a subject of interest in both academic and industrial contexts. The solubility of this compound is influenced by several factors including its chemical structure, polarity, and temperature.

Factors Influencing Solubility

  • Polarity: Due to the presence of the carbamate functional group, the compound can exhibit significant polar characteristics. This may enhance its solubility in polar solvents such as water and alcohols.
  • Alkyl Groups: The sec-butyl group can contribute to hydrophobic interactions, potentially reducing solubility in water while enhancing solubility in organic solvents.
  • Temperature: Generally, an increase in temperature tends to improve the solubility of solid compounds; thus, (3-sec-butylphenyl) N-methylcarbamate may show increased solubility at elevated temperatures.

It is essential to consider that solubility can vary widely based on solvent choice and concentration. For example:

  • In organic solvents such as DMSO or ethanol, the solubility is likely to be higher due to compatible polar and nonpolar interactions.
  • In aqueous solutions, the solubility may be significantly lower owing to the hydrophobic nature of the sec-butyl group.

Overall, the solubility of (3-sec-butylphenyl) N-methylcarbamate exemplifies the delicate balance between its polar and nonpolar characteristics, making it a fascinating compound for further investigation.

Interesting facts

Interesting Facts About (3-sec-butylphenyl) N-methylcarbamate

(3-sec-butylphenyl) N-methylcarbamate is a fascinating compound particularly valued in the field of chemistry for its applications in agriculture and pest control. Here are some key points that highlight its significance:

  • Insecticide Properties: This compound is a member of the carbamate family, which are known for their effectiveness as insecticides. Its ability to inhibit the enzyme acetylcholinesterase makes it a potent agent for controlling insect populations.
  • Mechanism of Action: By blocking the breakdown of acetylcholine in the synapses, (3-sec-butylphenyl) N-methylcarbamate leads to overstimulation of the nervous system in pests, ultimately resulting in their death.
  • Environmental Impact: As a chemical, its environmental footprint is a topic of study. Scientists assess its degradation pathways and effects on non-target organisms to ensure safe application practices in agricultural settings.
  • Diversity of Applications: Beyond its agricultural uses, this compound plays a role in research related to pharmacology and toxicology, making it valuable in various scientific domains.
  • Structural Variability: The presence of the sec-butyl group attached to the phenyl ring allows for variations in reactivity and efficacy, providing chemists with opportunities to modify and enhance its properties for specific applications.
  • Regulatory Status: Due to its insecticidal properties, (3-sec-butylphenyl) N-methylcarbamate is subject to regulation in many countries, and its use is monitored to prevent potential risks associated with chemical residues in the environment.

As a student or scientist, understanding the broader implications of such compounds is crucial. They not only serve immediate practical purposes but also highlight the complex interplay between chemistry, agriculture, and environmental science. “Chemistry is not just about substances; it’s about the relationships and impacts they have on the world.”


In conclusion, (3-sec-butylphenyl) N-methylcarbamate is a compound that represents the intersection of innovation and responsibility in chemical sciences.

Synonyms
673-19-8
Chevron RE5305
Chevron 5305
m-sec-Butylphenyl N-methylcarbamate
Ortho 5305
RE 5305
RE 5305 (California chemical)
3-sec-Butylphenyl N-methylcarbamate
California chemical company RE5305
ENT 27,039
Phenol, m-sec-butyl-, methylcarbamate
m-(1-Methylpropyl)phenylmethylcarbamate
BRN 2214027
3-(1-Methylpropyl)phenol methylcarbamate
AI3-27039
Phenol, 3-(1-methylpropyl)-, methylcarbamate
CARBAMIC ACID, METHYL-, m-sec-BUTYLPHENYL ESTER
CHEMBL2046820
SCHEMBL11509302
DTXSID50986562
3-s-butylphenyl N-methylcarbamate
3-(1-Methylpropyl)phenol 1-(N-methylcarbamate)
3-(Butan-2-yl)phenyl hydrogen methylcarbonimidate