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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(4-methyl-3-sec-butyl-phenyl) N-methylcarbamate
State
State

Carbaryl is typically encountered as a solid at room temperature. It is often utilized in various solid and aqueous formulations depending on its application.

Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is typically seen as a white crystalline solid. It has no distinctive smell and is usually formulated in various forms such as powders, liquid solutions, or granules for agricultural and domestic uses.

Comment on solubility

Solubility of (4-methyl-3-sec-butyl-phenyl) N-methylcarbamate

The solubility of (4-methyl-3-sec-butyl-phenyl) N-methylcarbamate is an important aspect to consider in its applications and interactions. Several factors influence its solubility, including:

  • Polarity: The presence of functional groups such as the carbamate moiety typically increases polarity, which can enhance solubility in polar solvents like water.
  • Molecular Size: As the compound has a relatively large and branched structure, its size can hinder solubility in certain solvents, especially non-polar ones.
  • Temperature: Solubility may be temperature-dependent, often increasing with rising temperatures due to kinetic energy facilitating interactions with solvent molecules.
  • pH Levels: Certain compounds can ionize at different pH levels, potentially increasing solubility in aqueous solutions.

In general, (4-methyl-3-sec-butyl-phenyl) N-methylcarbamate is expected to demonstrate moderate solubility in organic solvents and varying solubility in water depending on the conditions.
"Solubility is key in determining the compound's behavior in biological systems and its efficacy in various formulations."

Interesting facts

Interesting Facts about (4-methyl-3-sec-butyl-phenyl) N-methylcarbamate

(4-methyl-3-sec-butyl-phenyl) N-methylcarbamate is a fascinating compound that mirrors the complexity and creativity found in organic chemistry. Here are some engaging insights into this compound:

  • Structure and Functionality: This compound features a unique molecular structure with both aromatic and aliphatic components, making it an interesting subject for studying substituent effects in organic reactions.
  • Carbamate Classification: As a member of the carbamate family, it exhibits properties that make it of interest in pesticide formulations and the synthesis of pharmaceuticals, showcasing its utility in various fields.
  • Biological Applications: Compounds like N-methylcarbamates are studied as potential insecticides and herbicides. They work effectively due to their inhibition of acetylcholinesterase, an enzyme that plays a critical role in neurotransmission.
  • Versatile Use: The presence of the methyl and sec-butyl groups enhances the compound's lipophilicity, allowing it to easily penetrate biological membranes, which is essential for its efficacy in medicinal and agricultural applications.
  • Environmental Considerations: While useful, it's crucial to study the environmental impact and degradation pathways of carbamate compounds to understand how they interact with ecosystems and to ensure sustainable usage.
  • Research Opportunities: The synthesis and characterization of derivatives of (4-methyl-3-sec-butyl-phenyl) N-methylcarbamate present ample opportunities for research, particularly in improving biological activity and reducing toxicity.

Overall, (4-methyl-3-sec-butyl-phenyl) N-methylcarbamate exemplifies the intricate relationships between chemical structure, reactivity, and application, underscoring the significance of studying such compounds in both academic and practical chemistry.

Synonyms
5-sec-Butyl-4-tolyl methylcarbamate
1020-35-5
BAY 62862
BRN 1968476
AI3-27475
4-Methyl-3-(1-methylpropyl)phenol methylcarbamate
Phenol, 4-methyl-3-(1-methylpropyl)-, methylcarbamate
CARBAMIC ACID, METHYL-, 3-sec-BUTYL-p-TOLYL ESTER
DTXSID50906982
3-(Butan-2-yl)-4-methylphenyl hydrogen methylcarbonimidate