Skip to main content

Fenobucarb

ADVERTISEMENT
Identification
Molecular formula
C15H21NO2
CAS number
3766-81-2
IUPAC name
(2,6-ditert-butyl-4-methyl-phenyl) N-methylcarbamate
State
State

At room temperature, Fenobucarb is a liquid.

Melting point (Celsius)
22.00
Melting point (Kelvin)
295.15
Boiling point (Celsius)
335.20
Boiling point (Kelvin)
608.35
General information
Molecular weight
265.39g/mol
Molar mass
265.3790g/mol
Density
1.0800g/cm3
Appearence

Fenobucarb (BPMC) is a colorless to pale yellow liquid with a faint aromatic odor. It is typically supplied in liquid form as an insecticide.

Comment on solubility

Solubility of (2,6-ditert-butyl-4-methyl-phenyl) N-methylcarbamate

The solubility of (2,6-ditert-butyl-4-methyl-phenyl) N-methylcarbamate can be considered within the realms of organic chemistry where factors such as molecular structure and functional groups play crucial roles. Here, we delve into some compelling aspects of its solubility:

  • Polarity: The solubility of this compound is significantly influenced by its polarity. The presence of the N-methylcarbamate functional group contributes to its polar character, enhancing its interactions with polar solvents, such as water.
  • Solvent Compatibility: It tends to have better solubility in organic solvents, including ethanol and acetone, which can provide a more favorable environment for its structural features to dissolute.
  • Temperature Effects: Like many organic compounds, its solubility may increase with temperature, making heating a useful technique for dissolving the compound in various solvents.

In conclusion, while solubility data specific to (2,6-ditert-butyl-4-methyl-phenyl) N-methylcarbamate may not be abundantly available, we can infer that its behavior aligns with typical trends observed in organic compounds. Understanding its solubility is essential for applications in chemical synthesis, formulation, and various industrial processes.

Interesting facts

Interesting Facts About (2,6-Ditert-butyl-4-methyl-phenyl) N-methylcarbamate

(2,6-Ditert-butyl-4-methyl-phenyl) N-methylcarbamate, often referred to as a derivative of carbamate, holds a significant position in the realm of chemical compounds. Here are some intriguing aspects about this compound:

  • Uses in Agriculture: This carbamate is primarily utilized as a pesticide and herbicide, showcasing its vital role in protecting crops from pests and weeds.
  • Stability and Reactivity: The presence of tert-butyl groups contributes to its stability, making it less susceptible to degradation compared to other pesticides.
  • Mechanism of Action: It operates by inhibiting certain enzymes, disrupting the normal functioning of pests, which aids in their control.
  • Environmental Considerations: Its use has raised discussions regarding ecological impact, prompting further studies on its bioavailability and residue management during agricultural practices.
  • Synthetic Pathways: The synthesis of this compound often involves multi-step reactions, featuring the creation of carbamate linkages—a functional group celebrated in organic chemistry.

Many agronomists and chemists explore this compound for its potential innovations in sustainable agriculture. As research advances, compounds like (2,6-ditert-butyl-4-methyl-phenyl) N-methylcarbamate continue to be pivotal in balancing productivity and environmental health in farming.


One scientist articulately stated, "The challenge lies not just in efficacy but in ensuring that we safeguard our ecosystems while advancing agricultural technologies." This sentiment resonates deeply in the continuous exploration of such chemical compounds.

Synonyms
Terbucarb
Terbutol
1918-11-2
Mbpmc
Terbucarb [ISO]
Hercules 9573
Caswell No. 294
DTXSID1042441
Phenol, 2,6-bis(1,1-dimethylethyl)-4-methyl-, methylcarbamate
2,6-Di-tert-butyl-p-tolyl methylcarbamate
17B625R8YT
Carbamic acid, methyl-, 2,6-di-tert-butyl-p-tolyl ester
EPA Pesticide Chemical Code 038801
HERCULES-9573
BRN 2056682
UNII-17B625R8YT
DTXCID9022441
2,6-DI-T-BUTYL-P-TOLYL METHYLCARBAMATE
3,5-Di-t-butyl-4-methylphenyl N-methylcarbamate
2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYLPHENYL N-METHYLCARBAMATE
2,6-di-tert-butyl-4-methylphenyl n-methylcarbamate
Phenol, 2,6-bis(1,1-dimethylethyl)-4-methyl-, methylcarbamate (9CI)
pnrazzzisdrwmv-uhfffaoysa-n
azak
AZAR
(2,6-ditert-butyl-4-methylphenyl) N-methylcarbamate
CHEBI:82250
Phenol, 2,6-bis(1,1-dimethylethyl)-4-methyl-, 1-(N-methylcarbamate)
AZAC
2,6-Di-t-butyl-4-methylphenyl-N-methylcarbamate
SCHEMBL132875
CHEMBL3187091
Tox21_302210
AKOS024344754
NCGC00255734-01
CAS-1918-11-2
NS00001387
C19129
2,6-Ditert-butyl-4-methylphenyl methylcarbamate
2,6-Ditert-butyl-4-methylphenyl methylcarbamate #
Q27155838