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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(5-hydroxy-1-naphthyl) N-methylcarbamate
State
State

At room temperature, Carbaryl is a solid. It is used as a pesticide and can be found in formulations as a wettable powder, dust, or granules.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2450g/cm3
Appearence

Carbaryl is a white crystalline solid. It has a faint characteristic odor and appears as a colorless solid when in pure form. As a formulated product, it may appear as a powder or as a liquid in various concentrations.

Comment on solubility

Solubility of (5-hydroxy-1-naphthyl) N-methylcarbamate

The solubility of (5-hydroxy-1-naphthyl) N-methylcarbamate is an important aspect to consider due to its potential applications in various fields, such as pharmaceuticals and agrochemicals. Understanding its solubility can help predict how it will behave in different environments. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is expected to be soluble in organic solvents such as ethanol and methanol, owing to its structure that incorporates naphthalene and carbamate functionalities.
  • Water Solubility: Its solubility in water may be limited due to the hydrophobic nature of the naphthalene ring. Compounds with bulky aromatic systems often exhibit lower solubility in aqueous solutions.
  • Temperature Effects: Like many organic compounds, solubility may increase with an increase in temperature. This phenomenon is critical when considering the dissolution process in various temperature conditions.
  • pH Considerations: The solubility of (5-hydroxy-1-naphthyl) N-methylcarbamate might also be influenced by the pH of the solution, especially because carbamates can undergo hydrolysis or form ionic species in different pH environments.

In summary, while (5-hydroxy-1-naphthyl) N-methylcarbamate exhibits moderate solubility in organic solvents, achieving significant dissolution in water is less likely. As with many chemical compounds, the interaction between structure and solubility is complex, guiding researchers and practitioners to explore optimal conditions for its use.

Interesting facts

Interesting Facts about (5-hydroxy-1-naphthyl) N-methylcarbamate

(5-hydroxy-1-naphthyl) N-methylcarbamate, often referred to in research settings as a derivative of naphthalene, offers intriguing insights into both its structure and applications in chemistry. Here are some engaging facts about this compound:

  • Structural Insights: The presence of a hydroxyl group at the 5-position of the naphthalene ring greatly influences the compound's reactivity and interaction with biological systems. This positioning can enhance its solubility in organic solvents and facilitate various reactions.
  • Biological Relevance: Compounds like this one are of significant interest in the field of agrochemicals. They are researched for their potential use as pesticides or herbicides, and understanding their mechanisms is crucial for developing safer and more effective products.
  • Synthesis: The synthesis of (5-hydroxy-1-naphthyl) N-methylcarbamate often involves a straightforward route of carbamate formation, showcasing the versatility of naphthalene derivatives in synthetic organic chemistry.
  • Research Applications: This compound is often studied for its pharmacological properties, as its structural components could potentially mimic neurotransmitters or enzyme inhibitors, making it valuable in pharmaceutical research.
  • Environmental Impact: As with many carbamate derivatives, gaining an understanding of this compound’s environmental impact is essential. Scientists study its degradation pathways and effects on non-target organisms to ensure ecological safety.

In summary, (5-hydroxy-1-naphthyl) N-methylcarbamate represents a fascinating compound with potential applications in various fields. As researchers delve deeper into its properties, they uncover possibilities that bridge organic chemistry, pharmacology, and environmental science.

Synonyms
5721-72-2
CARBAMIC ACID, METHYL-, 5-HYDROXY-1-NAPHTHYL ESTER
(5-hydroxynaphthalen-1-yl) N-methylcarbamate
5-Hydroxy Carbaryl
5-Hydroxynaphthalen-1-yl methylcarbamate
5-Hydroxycarbaryl
5-Hydroxycarboryl
Carbaryl-5-hydroxy
Methylcarbamic acid 5-hydroxy-1-naphthyl ester
5-Hydroxy-1-naphthyl methylcarbamate
BRN 2333033
1,5-Naphthalenediol, mono(methylcarbamate)
SCHEMBL9125546
DTXSID90205840
5-hydroxynaphthyl N-methylcarbamate
NS00115914
1,5-Naphthalenediol, mono(methylcarbamate) (9CI); Carbamic acid, methyl-, 5-hydroxy-1-naphthyl ester (7CI,8CI); 5-Hydroxy-1-naphthyl N-methylcarbamate; 5-Hydroxy-1-naphthyl methylcarbamate; 5-Hydroxycarbaryl