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Metolcarb

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Identification
Molecular formula
C11H15NO2
CAS number
1129-41-5
IUPAC name
(3,4,5-trimethylphenyl) N-methylcarbamate
State
State

At room temperature, Metolcarb is typically in a solid state, presented as a powder or crystalline substance.

Melting point (Celsius)
92.50
Melting point (Kelvin)
365.65
Boiling point (Celsius)
311.40
Boiling point (Kelvin)
584.55
General information
Molecular weight
179.22g/mol
Molar mass
179.2210g/mol
Density
1.0970g/cm3
Appearence

Metolcarb appears as a white crystalline solid or powder. It may also be found in a slightly off-white color.

Comment on solubility

Solubility of (3,4,5-trimethylphenyl) N-methylcarbamate

(3,4,5-trimethylphenyl) N-methylcarbamate, a carbamate derivative, exhibits some interesting solubility characteristics. Generally, the solubility of organic compounds can be influenced by factors such as polarity, molecular structure, and the presence of functional groups.

In the case of (3,4,5-trimethylphenyl) N-methylcarbamate:

  • The presence of the carbamate functional group can enhance solubility in polar solvents.
  • The branching and methyl groups on the phenyl ring may create steric hindrance, potentially affecting solubility.
  • Overall, this compound may show moderate solubility in both water and organic solvents due to the balance of hydrophobic and polar characteristics.

As a rule of thumb, "like dissolves like," meaning that polar solvents tend to dissolve polar compounds well while nonpolar solvents are better for nonpolar compounds. Therefore, an experiment may be beneficial to definitively assess the solubility of (3,4,5-trimethylphenyl) N-methylcarbamate in various solvents.

Interesting facts

Interesting Facts about (3,4,5-trimethylphenyl) N-methylcarbamate

(3,4,5-trimethylphenyl) N-methylcarbamate is a fascinating compound within the realm of synthetic organic chemistry. It belongs to a class of chemicals known as carbamates, which are derived from carbamic acid and have various applications in agriculture and industry.

Key Characteristics

  • Usage: This compound is often employed as an herbicide, making it valuable in the agricultural sector for the control of unwanted plant growth.
  • Mechanism: Carbamates typically work by inhibiting the enzyme acetylcholinesterase, which leads to the buildup of acetylcholine and ultimately disrupts neural function in pests.
  • Synthetic Pathways: The synthesis of (3,4,5-trimethylphenyl) N-methylcarbamate often involves the reaction of a substituted phenol and isocyanates, showcasing the versatility of organic reactions.

Environmental Considerations

While carbamates play an essential role in crop protection, there are also serious considerations regarding their environmental impact:

  • Non-target species: Concern exists over the effects of carbamates on beneficial insects and pollinators.
  • Degradation: Studying the degradation pathways of such compounds provides insight into their longevity in the environment and potential accumulation in ecosystems.

Scientific Intrigue

The study of (3,4,5-trimethylphenyl) N-methylcarbamate exemplifies the balance between efficacy and environmental stewardship. As researchers delve deeper into the compound's behavior and mechanisms, they contribute to the field of sustainable chemistry and the development of safer agricultural practices.

In summary, (3,4,5-trimethylphenyl) N-methylcarbamate is not only crucial for its applications but also serves as a prime example of the complexities involved in chemical safety and environmental health. Understanding compounds like these is vital for a sustainable future.

Synonyms
3,4,5-Trimethacarb
3,4,5-Trimethylphenyl methylcarbamate
2686-99-9
Trimethacarb
Trimethacarb [ANSI]
Phenol, 3,4,5-trimethyl-, methylcarbamate
UNII-JG6XSN0Z2I
JG6XSN0Z2I
EINECS 220-245-9
BRN 2052372
AI3-25843
DTXSID1040322
CHEBI:38894
Trimethacarb (ANSI)
PHENOL, 3,4,5-TRIMETHYL-, 1-(N-METHYLCARBAMATE)
Phenol, 3,4,5-trimethyl-, methylcarbamate (9CI)
DTXCID5012503
Carbamic acid, methyl-, 3,4,5-trimethylphenyl ester (7CI)(8CI)
Phenol, 2,3,5(or 3,4,5)-trimethyl-, methylcarbamate (9CI)
220-245-9
12407-86-2
2,3,5(or 3,4,5)-trimethylphenyl n-methylcarbamate
auqauaiunjiiep-uhfffaoysa-n
carbamic acid, methyl-, 2,3,5(or 3,4,5)-trimethylphenyl ester
carbamic acid, methyl-, 3,4,5-trimethylphenyl ester (7ci)
chebi:38569
dtxsid7032503
epa pesticide chemical code 102400
epa pesticide chemical code 102402
landrin-3,4,5
phenol, 2,3,5(or 3,4,5)-trimethyl-, methylcarbamate
r97fqq0n7w
trimethacarb [iso]
trimethylphenyl methylcarbamate
trimethylphenyl-n-methylcarbamate
uc 27867
unii-r97fqq0n7w
Shell 8530
3,4,5-Trimethylphenyl N-methylcarbamate
Shell SD-8530
SD 8530
OMS-597
Methylcarbamic acid 3,4,5-trimethylphenyl ester
3,4,5-Landrin
3,4,5-Trimethylphenol methylcarbamate
ENT-25,843
Carbamic acid, methyl-, 3,4,5-trimethylphenyl ester
(3,4,5-trimethylphenyl) N-methylcarbamate
3,4,5-Trimethylfenylester kyseliny methylkarbaminove
3,4,5-Trimethacarb 10 microg/mL in Cyclohexane
3,4,5-Trimethylfenylester kyseliny methylkarbaminove [Czech]
SCHEMBL119743
AKOS006274660
1ST20387
NS00010532
Q27118023