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Metolcarb

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Identification
Molecular formula
C10H13NO2
CAS number
1129-41-5
IUPAC name
(3,5-dimethylphenyl) N-methylcarbamate
State
State

At room temperature, Metolcarb is typically found in a solid state as a crystalline powder.

Melting point (Celsius)
98.00
Melting point (Kelvin)
371.15
Boiling point (Celsius)
297.00
Boiling point (Kelvin)
570.15
General information
Molecular weight
179.22g/mol
Molar mass
179.2220g/mol
Density
1.1300g/cm3
Appearence

Metolcarb appears as colorless crystals or as a white crystalline powder. It is often used in its solid form and is known for its crystalline nature.

Comment on solubility

Solubility of (3,5-dimethylphenyl) N-methylcarbamate

(3,5-dimethylphenyl) N-methylcarbamate, a carbamate derivative, exhibits notable solubility characteristics that can be influenced by several factors. Understanding its solubility can provide insights into its behavior in various environments.

Factors Affecting Solubility

  • Polarity: The presence of polar functional groups often increases solubility in polar solvents, such as water.
  • Hydrophobic Interactions: The aromatic ring and methyl groups contribute to hydrophobic interactions, potentially limiting solubility in aqueous environments.
  • Temperature: Increased temperature may enhance solubility, as is typically observed with many organic compounds.

Generally, compounds with significant hydrophobic portions tend to have lower solubility in polar solvents. For (3,5-dimethylphenyl) N-methylcarbamate, one can expect:

  1. A moderate solubility in organic solvents.
  2. Lower solubility in water compared to more polar compounds.

In summary, the solubility of (3,5-dimethylphenyl) N-methylcarbamate can be succinctly expressed as:

"Solubility is a complex interplay of molecular structure, temperature, and solvent characteristics."

Thus, while it may have limited aqueous solubility, it is likely to be more soluble in organic solvents, facilitating its use in various applications.

Interesting facts

Interesting Facts About (3,5-Dimethylphenyl) N-Methylcarbamate

(3,5-dimethylphenyl) N-methylcarbamate is a fascinating chemical compound that falls within the category of carbamates. These compounds are known for their diverse applications, from agricultural pesticides to pharmaceuticals. Here are some intriguing aspects of this specific carbamate:

  • Biological Relevance: Carbamates, such as (3,5-dimethylphenyl) N-methylcarbamate, often exhibit herbicidal or insecticidal properties, making them valuable in crop protection. Their mode of action frequently involves the inhibition of enzyme activity in pests.
  • Environmental Impact: While these compounds can be effective against pests, their use raises important environmental concerns. The breakdown products and potential accumulation in ecosystems are vital considerations for their application.
  • Versatile Structure: The presence of the 3,5-dimethylphenyl group highlights the compound's structural versatility, which can lead to variations in biological activity based on slight modifications. This leads to intense research into structural-activity relationships (SAR) in chemical synthesis and development.
  • Synthetic Pathways: The synthesis of (3,5-dimethylphenyl) N-methylcarbamate showcases multiple reaction mechanisms, requiring an understanding of organic chemistry principles, including nucleophilic substitutions and reactivity of carbamate groups.
  • Research and Development: Ongoing studies into carbamates have led to the development of new derivatives, enhancing efficacy and reducing toxicity. This leads to a continuous evolution of how these compounds are utilized in both industrial and agricultural settings.

As we further explore the potential applications and modifications of (3,5-dimethylphenyl) N-methylcarbamate, we can appreciate how small chemical changes can lead to significant impacts in multiple fields. In the words of chemist Robert H. Grubbs, “Innovation must be rooted in a sound understanding of both theory and practice.” This rings true for the ongoing exploration of carbamate compounds.

Synonyms
3,5-XYLYL METHYLCARBAMATE
2655-14-3
Cosban
Macbal
XMC (pesticide)
3,5-Dimethylphenyl N-methylcarbamate
3,5-Dimethylphenyl Methylcarbamate
Carbaron
Maqbal
3,5-Xylyl N-methylcarbamate
3,5-Xylenyl N-methylcarbamate
3,5-Xylenol, methylcarbamate
DRC 3340
N-Methyl-3,5-xylyl carbamate
Methylcarbamic acid 3,5-xylyl ester
Phenol, 3,5-dimethyl-, methylcarbamate
Carbamic acid, methyl-, 3,5-xylyl ester
3,5-Dimethylphenol methylcarbamate
Phenol, 3,5-dimethyl-, 1-(N-methylcarbamate)
NSC 35375
S 1041
HSDB 6748
3,5-Xylylester kyseliny methylkarbaminove
S0Z6GJ0V0R
BRN 1948121
3,5-Xylyl methylcarbamate (8CI)
XMC, JMAF
NSC-35375
3,5-Xylylester kyseliny methylkarbaminove [Czech]
3,5-Dimethylphenyl methylcarbamate (9CI)
4-06-00-03147 (Beilstein Handbook Reference)
XYLYL METHYLCARBAMATE, 3,5-
3,5-XYLYL METHYLCARBAMATE [HSDB]
Phenol, 3,5-dimethyl-, methylcarbamate (9CI)
3,5Xylyl Nmethylcarbamate
NMethyl3,5xylyl carbamate
3,5-Xylyl-methylcarbamate
3,5Xylenyl Nmethylcarbamate
3,5Xylenol, methylcarbamate
3,5XMC
3,5Dimethylphenol methylcarbamate
3,5Dimethylphenyl methylcarbamate
3,5Dimethylphenyl Nmethylcarbamate
Methylcarbamic acid 3,5xylyl ester
Phenol, 3,5dimethyl, methylcarbamate
3,5-Dimethylphenyl methylcarbamic acid
Carbamic acid, methyl, 3,5xylyl ester
3,5Xylylester kyseliny methylkarbaminove
3,5Dimethylphenyl methylcarbamate (9CI)
Phenol, 3,5dimethyl, methylcarbamate (9CI)
1-3,5-dimethylphenoxy-N-methylmethanimidic acid
Maqbarl
3,5-Xmc
XMC
XMC (VAN)
(3,5-dimethylphenyl) N-methylcarbamate
H-69
CHEBI:38571
XMC (3,5-Xylyl methyl carbamate)
XMC (3,5-xylyl methylcarbamate) 10 microg/mL in Cyclohexane
UNII-S0Z6GJ0V0R
3, methylcarbamate
SCHEMBL338080
WLN: 1MVOR C1 E1
CHEMBL2271132
DTXSID7058042
CVQODEWAPZVVBU-UHFFFAOYSA-
NSC35375
Phenol,5-dimethyl-, methylcarbamate
AKOS006273340
NS00006049
C18771
Q15632708
InChI=1/C10H13NO2/c1-7-4-8(2)6-9(5-7)13-10(12)11-3/h4-6H,1-3H3,(H,11,12)