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Mexacarbate

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Identification
Molecular formula
C9H11NO2
CAS number
315-18-4
IUPAC name
m-tolyl N-methylcarbamate
State
State

Mexacarbate is a solid at room temperature.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.00
Boiling point (Celsius)
301.00
Boiling point (Kelvin)
574.00
General information
Molecular weight
179.22g/mol
Molar mass
179.2210g/mol
Density
1.1000g/cm3
Appearence

Mexacarbate typically appears as a white crystalline solid.

Comment on solubility

Solubility of m-tolyl N-methylcarbamate

m-tolyl N-methylcarbamate is an intriguing chemical compound with solubility characteristics that are often influenced by its functional groups and hydrophobic properties. While specific solubility data can vary based on conditions, it is generally noted that:

  • Polar solvents: This compound is likely to show improved solubility in polar solvents such as water or alcohols due to hydrogen bonding.
  • Non-polar solvents: Conversely, it may have greater solubility in non-polar solvents like hexane or benzene, given its aromatic characteristics.
  • Temperature dependence: As with many compounds, solubility can increase with temperature. Higher temperatures may break intermolecular forces, enhancing the solubility.

It is important to keep in mind that the solubility can be affected by various factors such as:

  1. The presence of other solutes.
  2. The pH of the solution, which may alter the ionization state of the carbamate.
  3. Individual interactions at the molecular level, particularly among the aromatic ring and the carbamate group.

In summary, understanding the solubility of m-tolyl N-methylcarbamate is vital for its applications in synthesis and formulation. The pronounced influence of solvent choice, temperature, and other interacting substances reinforces the nuanced behavior of this compound in various environments.

Interesting facts

Interesting Facts about m-tolyl N-methylcarbamate

m-tolyl N-methylcarbamate is a unique chemical compound that belongs to the family of carbamate derivatives, which play a significant role in various fields, particularly in agriculture and pharmacology. Here are some noteworthy aspects of this compound:

  • Biological Activity: m-tolyl N-methylcarbamate exhibits interesting biological properties, often utilized for its insecticidal activity. As a derivative of carbamate, it can act on the enzyme acetylcholinesterase, which is vital for nerve function.
  • Pesticide Use: It is widely recognized in agrochemical applications, offering an effective means of pest control. Due to its ability to control a variety of pests, it is frequently studied for its efficiency and selective toxicity.
  • Synthetic Pathways: The synthesis of m-tolyl N-methylcarbamate can be achieved through various methods, including the reaction of m-toluidine with methyl isocyanate. This illustrates the compound's versatility and the fascinating chemistry behind its formation.
  • Environmental Impact: Awareness of the ecological implications of using carbamate compounds is crucial. Researchers are actively investigating the degradation pathways and ecological effects of m-tolyl N-methylcarbamate on non-target organisms.

Quote from a Research Scientist: "Carbamate derivatives like m-tolyl N-methylcarbamate reflect the intricate balance between efficacy and safety in chemical applications." This emphasizes the ongoing need to study such compounds thoroughly to ensure sustainable use in various industries.

As you delve deeper into the field of chemistry, understanding the multifaceted roles of compounds like m-tolyl N-methylcarbamate can provide valuable insights into both their potential applications and environmental stewardship.

Synonyms
METOLCARB
m-Tolyl methylcarbamate
1129-41-5
Metacrate
Tsumacide
m-Cresyl methylcarbamate
3-Tolyl methylcarbamate
3-Methylphenyl N-methylcarbamate
m-Tolyl N-methylcarbamate
3-Methylphenyl methylcarbamate
3-Tolyl N-methylcarbamate
m-Cresyl N-methylcarbamate
Metholcarb
Carbamic acid, methyl-, 3-methylphenyl ester
Tsumaunka
Kumiai
m-Methylphenyl methylcarbamate
Methylcarbamic acid m-tolyl ester
m-Cresyl ester of N-methylcarbamic acid
DRC 3341
Metolcarb [BSI:ISO]
Metholcarb [ISO-French]
Carbamic acid, methyl-, m-tolyl ester
NSC 91193
Tumacide
CHEBI:38537
HSDB 6416
Dicresyl N-methylcarbamate
RCRA waste no. P190
EINECS 214-446-0
m-Tolylester kyseliny methylkarbaminove
S 1065
BRN 2045865
4N7OMZ879V
m-Tolylmethylcarbamate
AI3-27694
METOLCARB [ISO]
METOLCARB [HSDB]
m-Tolylester kyseliny methylkarbaminove [Czech]
NSC-91193
DTXSID8057938
3-methylphenyl-N-methyl carbamate
Carbamic acid, N-methyl-, 3-methylphenyl ester
4-06-00-02050 (Beilstein Handbook Reference)
Carbamic acid, methyl-, 3-tolyl ester
Metholcarb (ISO-French)
m-Tolylester kyseliny methylkarbaminove (Czech)
mTolyl methylcarbamate
3Tolyl methylcarbamate
mCresyl methylcarbamate
mTolyl Nmethylcarbamate
3Tolyl Nmethylcarbamate
mCresyl Nmethylcarbamate
m-Toly-N-methylcarbamate
mMethylphenyl methylcarbamate
3Methylphenyl methylcarbamate
3Methylphenyl Nmethylcarbamate
Methylcarbamic acid mtolyl ester
DTXCID6031706
3-TOLYL-N-METHYLCARBAMATE
mCresyl ester of Nmethylcarbamic acid
mTolylester kyseliny methylkarbaminove
M-METHYLPHENYL N-METHYLCARBAMATE
Carbamic acid, methyl, 3methylphenyl ester
CARBAMIC ACID, METHYL-, M-TOLYL-ESTER
214-446-0
MTMC
(3-methylphenyl) N-methylcarbamate
Metolcarb 10 microg/mL in Cyclohexane
UNII-4N7OMZ879V
MFCD00053076
Maybridge3_000696
WLN: 1MVOR C1
NCIOpen2_001532
Carbamic acid, 3-tolyl ester
SCHEMBL118244
CHEMBL2046816
VOEYXMAFNDNNED-UHFFFAOYSA-
HMS1432P14
NSC91193
BDBM50004687
CCG-52777
AKOS006229276
IDI1_012083
NCGC00160533-01
AS-16081
DB-041141
DB-228722
HY-131126
CS-0129027
NS00005439
Metolcarb, PESTANAL(R), analytical standard
C18747
Q6824213
SR-01000641987-1
InChI=1/C9H11NO2/c1-7-4-3-5-8(6-7)12-9(11)10-2/h3-6H,1-2H3,(H,10,11)