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Fenobucarb

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Identification
Molecular formula
C15H23NO2
CAS number
3766-81-2
IUPAC name
(3,5-ditert-butylphenyl) N-methylcarbamate
State
State

At room temperature, Fenobucarb is in the solid state. It is commonly available as a crystalline solid, which can be easily transported and stored for various uses, particularly in the pesticide industry.

Melting point (Celsius)
44.50
Melting point (Kelvin)
317.65
Boiling point (Celsius)
197.00
Boiling point (Kelvin)
470.15
General information
Molecular weight
265.36g/mol
Molar mass
265.3590g/mol
Density
1.0130g/cm3
Appearence

Fenobucarb appears as a white crystalline solid. It is often manufactured and used in its pure form for agricultural applications. The compound has a slightly aromatic odor due to its phenyl structure.

Comment on solubility

Solubility of (3,5-Ditert-butylphenyl) N-methylcarbamate

The solubility of (3,5-Ditert-butylphenyl) N-methylcarbamate can be influenced by various factors including molecular structure, polarity, and temperature. Understanding its solubility properties is essential for practical applications.

Key Points on Solubility:

  • Polarity: This compound features a bulky tert-butyl group, which can affect its overall polarity, making it more soluble in non-polar solvents.
  • Solvent Compatibility: It tends to dissolve better in organic solvents such as acetone, ethanol, and chloroform compared to water.
  • Temperature Effects: Increased temperatures may enhance solubility in organic solvents, facilitating better interaction.

As a result, it is common to expect limited solubility in polar solvents like water due to its relatively hydrophobic nature influenced by the bulky substituents. In summary, if you are working with (3,5-Ditert-butylphenyl) N-methylcarbamate, consider using organic solvents to maximize solubility and dissolution efficiency.

Interesting facts

Interesting Facts about (3,5-Ditert-butylphenyl) N-methylcarbamate

(3,5-Ditert-butylphenyl) N-methylcarbamate, often referred to in scientific circles as a widely utilized compound in pesticide formulations, offers various intriguing features that any chemistry enthusiast would appreciate.

Key Attributes:

  • Functional Importance: This compound serves as a key ingredient in agricultural chemicals, contributing to insecticide efficacy and resilience.
  • Sustainability Focus: Its usage highlights a growing trend in chemistry aimed at developing safer and more effective chemicals, showcasing the balance between pest control and environmental safety.
  • Research Applications: Studying (3,5-ditert-butylphenyl) N-methylcarbamate contributes to understanding carbamate chemistry and provides insights into related environmental and biological interactions.

Historical Context:

This compound is part of a broader family known as carbamates, which were first synthesized in the early 2000s. The development of these chemicals has often focused on reducing toxicity to non-target species, a critical consideration in agricultural practices today. As the demand for sustainable practices grows, the significance of such compounds only increases.

Environmental Chemistry:

As a pesticide component, this compound is studied for its breakdown products in soil and water systems. Researchers are keenly interested in understanding its biodegradability to predict its long-term environmental impact.

Fun Fact:

Interestingly, the iconic structure of the phenyl ring combined with bulky tert-butyl groups provides unique properties, such as enhanced stability and reduced volatility, making it effective in various applications without posing immediate risks to other organisms.

As we advance in the understanding and utilization of such compounds, the focus on safe, effective pesticide formulations remains paramount in both chemistry and agricultural sciences.

Synonyms
BUTACARB
Butacarbe [French]
Butacarb [ISO]
Butacarbe
Butacarb [ISO:BSI]
Caswell No. 291B
3,5-Di-tert-butylphenyl methylcarbamate
HSDB 2799
3,5-Di-t-butylphenylmethylcarbamate
BTS 14639
EPA Pesticide Chemical Code 291300
UNII-48SLE5Y118
BRN 1914596
RD 14639
3,5-Di-tert-butylphenyl N-methylcarbamate
48SLE5Y118
BUTACARB [HSDB]
3,5-Bis(1,1-dimethylethyl)phenol methylcarbamate
Carbamic acid, methyl-, 3,5-di-tert-butylphenyl ester
Phenol, 3,5-bis(1,1-dimethylethyl)-, methylcarbamate
DTXSID0041690
3,5-BIS(1,1-DIMETHYLETHYL)PHENYL N-METHYLCARBAMATE
3,5Ditbutylphenylmethylcarbamate
DTXCID8021690
3,5Ditertbutylphenyl methylcarbamate
3,5Ditertbutylphenyl Nmethylcarbamate
USEPA/OPP Pesticide Code: 291300
3,5Bis(1,1dimethylethyl)phenol methylcarbamate
Carbamic acid, methyl, 3,5ditertbutylphenyl ester
Phenol, 3,5bis(1,1dimethylethyl), methylcarbamate
Phenol, 3,5-bis(1,1-dimethylethyl)-, methylcarbamate (9CI)
un2757
2655-19-8
(3,5-ditert-butylphenyl) N-methylcarbamate
SCHEMBL77964
CHEBI:82089
NS00125344
C18949
Q27155741