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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[3-(dimethylaminomethyleneamino)phenyl] N-methylcarbamate
State
State

At room temperature, carbaryl is in a solid state. It is usually presented in crystalline form and can be processed into powders or other forms for application as a pesticide.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
345.00
Boiling point (Kelvin)
618.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2000g/cm3
Appearence

Carbaryl appears as a white crystalline solid. The compound is known for its high solubility in acetone and other organic solvents. It has a distinctive odor and is often formulated in solid or liquid forms as a pesticide.

Comment on solubility

Solubility of [3-(dimethylaminomethyleneamino)phenyl] N-methylcarbamate

[3-(dimethylaminomethyleneamino)phenyl] N-methylcarbamate is an intriguing organic compound that exhibits unique solubility properties. Understanding its solubility is pivotal for both industrial applications and ecological considerations.

General Solubility Characteristics

This compound's solubility can be influenced by various factors, including:

  • Polarity: The presence of the dimethylamino group increases polarity, which may enhance solubility in polar solvents like water.
  • Hydrogen bonding: The carbamate functional group is capable of forming hydrogen bonds, allowing for potential solubility in aqueous environments.
  • Temperature: Solubility typically increases with temperature; therefore, understanding how temperature affects this compound's solubility can be crucial.

Solubility in Common Solvents

Whether [3-(dimethylaminomethyleneamino)phenyl] N-methylcarbamate will dissolve in various solvents can be summarized as follows:

  1. Water: Due to the amphoteric nature introduced by the functional groups, this compound may have moderate solubility.
  2. Alcohols: Generally, organic solvents like methanol or ethanol will likely enhance solubility.
  3. Hydrocarbons: Non-polar solvents (like hexane) are expected to show little to no solubility due to lack of interaction with polar groups.

In conclusion, while [3-(dimethylaminomethyleneamino)phenyl] N-methylcarbamate displays interesting solubility characteristics, its behavior in various solvents can vary significantly, making empirical testing essential for practical applications. Understanding the solubility not only aids in formulating effective solutions but also in predicting environmental interactions.

Interesting facts

Interesting Facts About [3-(Dimethylaminomethyleneamino)phenyl] N-Methylcarbamate

[3-(Dimethylaminomethyleneamino)phenyl] N-methylcarbamate is a remarkable compound with intriguing properties that can capture the attention of both scientists and chemistry students alike.

Chemical Significance

This compound features a backbone that is both versatile and complex. Here are some notable points:

  • Functional Groups: The presence of both a carbamate group and a dimethylamino moiety indicates potential for varied biological activities, impacting both pharmacological and agricultural domains.
  • Reactivity: The dimethylaminomethyleneamine component can be a key player in nucleophilic substitution reactions, making this compound a candidate for various chemical syntheses.
  • Structure-Activity Relationship (SAR): Understanding the interaction of this compound’s structure with biological targets opens pathways for drug design, showcasing the importance of molecular architecture in therapeutic applications.

Potential Applications

This compound may find a range of applications that exemplify its utility:

  • Pest Control: Its design may allow it to function as a pesticide or herbicide, contributing to agricultural chemistry and sustainable practices.
  • Pharmaceutical Research: Its unique structure suggests possibilities in developing new therapeutic agents or enhancing existing ones, thus driving medicinal chemistry forward.

Conclusion

In summary, [3-(Dimethylaminomethyleneamino)phenyl] N-methylcarbamate embodies a unique blend of structural sophistication and functional potential. As we delve into its applications, researchers are excited about the myriad possibilities it presents within the realms of synthetic chemistry and pharmacology. Truly, the world of chemical compounds is vast, and every molecule tells a story!

Synonyms
FORMETANATE
Dicarzol
Formetanat
22259-30-9
Caswell No. 465A
532HEC1KKM
CHEBI:38491
N'-(m-Hydroxyphenyl)-N,N-dimethylformamidine methylcarbamate ester
3-Dimethylaminomethyleneaminophenyl methylcarbamate
N,N-Dimethyl-N'-(3-(((methylamino)carbonyl)oxy)phenyl)methanimidamide
m-(((Dimethylamino)methylene)amino)phenyl methylcarbamate
DTXSID9041990
3-{[(dimethylamino)methylidene]amino}phenyl methylcarbamate
m-[[(Dimethylamino)methylene]amino]phenyl methylcarbamate
3-(((Dimethylamino)methylidene)amino)phenyl methylcarbamate
3-([(Dimethylamino)methylidene]amino)phenyl methylcarbamate
RefChem:141220
DTXCID7021990
3-(((dimethylamino)methylidene)amino)phenyl N-methylcarbamate
244-879-0
Carbamic acid, methyl-, ester with N'-(m-hydroxyphenyl)-N,N-dimethylformamidine
[3-(dimethylaminomethylideneamino)phenyl] N-methylcarbamate
Carbamic acid, methyl-, m-(((dimethylamino)methylene)amino)phenyl ester
Methylcarbamic acid ester with N'-(m-hydroxyphenyl)-N,N-dimethylformamidine
Methanimidamide, N,N-dimethyl-N'-[3-[[(methylamino)carbonyl]oxy]phenyl]-
Formetanate [ISO]
Formetanate [ANSI:BSI:ISO]
EINECS 244-879-0
EP 322
UNII-532HEC1KKM
3-[(Dimethylamino)methylenimino]phenyl N-methylcarbamate
EPA Pesticide Chemical Code 465200
BRN 2807600
formetante
Methanimidamide, N,N-dimethyl-N'-(3-(((methylamino)carbonyl)oxy)phenyl)-
Phenol, m-[[(dimethylamino)methylene]amino]-, methylcarbamate (ester)
SCHEMBL116477
SCHEMBL116478
CHEMBL1907183
CHEMBL3303111
SCHEMBL10975855
SCHEMBL29509381
RMFNNCGOSPBBAD-MDWZMJQESA-N
Methanimidamide, N,N-dimethyl-, N'-(3-(((methylamino)carbonyl)oxy)phenyl)-
NCGC00168315-02
NS00008102
C18668
Q1027605
3-((EZ)-DIMETHYLAMINOMETHYLENEAMINO)PHENYL METHYLCARBAMATE