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Fenobucarb

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Identification
Molecular formula
C12H17NO2
CAS number
3766-81-2
IUPAC name
[3-(1-methylbutyl)phenyl] N-methylcarbamate
State
State
At room temperature, fenobucarb is typically in a liquid state.
Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
142.00
Boiling point (Kelvin)
415.15
General information
Molecular weight
207.27g/mol
Molar mass
207.2720g/mol
Density
1.0864g/cm3
Appearence
Fenobucarb appears as a colorless to light brown liquid. It is used as an insecticide and is known for its efficacy in pest control.
Comment on solubility

Solubility of [3-(1-methylbutyl)phenyl] N-methylcarbamate

[3-(1-methylbutyl)phenyl] N-methylcarbamate, a carbamate derivative, exhibits varying solubility characteristics depending on the solvent used. Understanding its solubility is crucial for applications in fields such as pharmaceuticals and agrochemicals.

Solubility Characteristics:

  • Polar Solvents: Generally, compounds like this one tend to be more soluble in polar solvents such as water and alcohols due to the presence of polar functional groups. However, solubility might still be limited compared to more hydrophilic compounds.
  • Non-Polar Solvents: It typically demonstrates greater solubility in non-polar solvents, including organic solvents like hexane or toluene, owing to its hydrophobic hydrocarbon chain.
  • Temperature Influence: The solubility may increase with temperature, making it essential to consider temperature conditions when dissolving the compound.
  • pH Effect: As a carbamate, changes in pH could potentially affect its solubility and stability, especially in aqueous solutions.

In general, the solubility of [3-(1-methylbutyl)phenyl] N-methylcarbamate is a balance between its polar and non-polar characteristics. This creates a unique profile that can be leveraged in various applications, but careful consideration of solvent choice and environmental conditions is essential for optimal use.

Interesting facts

Interesting Facts About [3-(1-methylbutyl)phenyl] N-methylcarbamate

[3-(1-methylbutyl)phenyl] N-methylcarbamate is an intriguing compound that holds significance in various fields, particularly in environmental science and agriculture. Here are some compelling facts about this compound:

  • Pesticide Application: This compound often finds use as a pesticide, showcasing its potent ability to protect crops from pests and diseases. Its effectiveness makes it a staple in agricultural practices.
  • Mechanism of Action: Like many carbamate derivatives, this compound works by inhibiting the enzyme acetylcholinesterase. This inhibition leads to an accumulation of acetylcholine in the synapses, which disrupts normal nerve function in target organisms.
  • Environmental Impact: Scientists are keenly interested in the environmental fate of [3-(1-methylbutyl)phenyl] N-methylcarbamate. Its degradation products and bioaccumulation potential in ecosystems are important for assessing the ecological risks associated with its usage in agriculture.
  • Structural Variability: The presence of the branched alkyl chain (the 1-methylbutyl group) introduces unique steric and electronic properties, which can influence its reactivity and interactions with biological systems.
  • Research Interests: Ongoing research is focused on enhancing the efficacy and safety profiles of compounds like this one, which includes exploring alternatives to conventional pesticides that are less harmful to non-target organisms and human health.
  • Regulatory Considerations: Due to its biological activity, [3-(1-methylbutyl)phenyl] N-methylcarbamate is subject to rigorous regulatory scrutiny, ensuring its usage aligns with safety standards in agricultural practice.

In summary, [3-(1-methylbutyl)phenyl] N-methylcarbamate exemplifies the complex interplay between agriculture, chemistry, and environmental science. Its significant impacts highlight the importance of responsible chemical use in promoting sustainability while maximizing agricultural yield.


Synonyms
2282-34-0
3-sec-Amylphenyl N-methylcarbamate
M-(1-METHYLBUTYL)PHENYL METHYLCARBAMATE
Chevron RE 5353
Ortho RE-5353
Compound 5353
Ortho 5,353
3-(1-Methylbutyl)phenyl methylcarbamate
m-sec-Amylphenyl N-methyl carbamate
ENT 27,127
Phenol, m-sec-pentyl-, methylcarbamate
RE-5353
OMS 227
Phenol, 3-(1-methylbutyl)-, methylcarbamate
Phenol, m-(1-methylbutyl)-, methylcarbamate
HSDB 2601
Carbamic acid, methyl-, m-(1-methylbutyl)phenyl ester
ZV1MM336WB
EPA Pesticide Chemical Code 059302
BRN 2275572
AI3-27127
OMS-227
ORTHO-5353
DTXSID6042103
ENT-27127
3-SEC-AMYLPHENYL N-METHYLCARBAMATE [HSDB]
PHENOL, 3-(1-METHYLBUTYL)-, 1-(N-METHYLCARBAMATE)
Ortho RE5353
3secAmylphenyl Nmethylcarbamate
msecAmylphenyl Nmethyl carbamate
DTXCID4022103
Carbamic acid, methyl-, m-(1-methylbutyl)phenyl ester (8CI)
Phenol, msecpentyl, methylcarbamate
RE5353
3(1Methylbutyl)phenyl methylcarbamate
Phenol, m(1methylbutyl), methylcarbamate
Phenol, 3(1methylbutyl), methylcarbamate
Carbamic acid, methyl, m(1methylbutyl)phenyl ester
Carbamic acid, methyl, m(1methylbutyl)phenyl ester (8CI)
(3-pentan-2-ylphenyl) N-methylcarbamate
3-(pentan-2-yl)phenyl methylcarbamate
Caswell No. 454C
UNII-ZV1MM336WB
BUX (Salt/Mix)
Bufencarb (Salt/Mix)
starbld0010487
BUX TEN (Salt/Mix)
SCHEMBL1874668
LHTOXQCYXYXXEZ-UHFFFAOYSA-N
3-s-pentylphenyl n -methylcarbamate
AKOS040752886
RE 9659
3-(1-Methylbutyl)phenyl methylcarbamate #
DB-228746
NS00009287
3-(PENTAN-2-YL)PHENYL N-METHYLCARBAMATE
Q27295899