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Mecoprop

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Identification
Molecular formula
C10H11ClO3
CAS number
93-65-2
IUPAC name
2-(3-chlorophenoxy)-2-methyl-propanoic acid
State
State

At room temperature, Mecoprop is typically in a solid state, especially in its pure form. However, certain formulations for commercial use, such as in herbicides, may exist as liquids.

Melting point (Celsius)
94.00
Melting point (Kelvin)
367.15
Boiling point (Celsius)
335.80
Boiling point (Kelvin)
608.95
General information
Molecular weight
214.66g/mol
Molar mass
214.6610g/mol
Density
1.2730g/cm3
Appearence

Mecoprop typically appears as a colorless to pale yellow crystalline solid. This compound can occasionally be found in liquid form, and when in a solid state, it bears a crystalline texture and structure.

Comment on solubility

Solubility of 2-(3-chlorophenoxy)-2-methyl-propanoic acid

The solubility of 2-(3-chlorophenoxy)-2-methyl-propanoic acid is a fascinating aspect to explore, particularly due to its unique chemical structure. This compound, often used in various applications, displays interesting characteristics when it comes to solubility in different solvents.

Solubility Characteristics

Generally, the solubility of this acid can be summarized as follows:

  • Polar Solvents: The presence of the carboxylic acid group (-COOH) makes 2-(3-chlorophenoxy)-2-methyl-propanoic acid more soluble in polar solvents, such as water, due to hydrogen bonding.
  • Non-Polar Solvents: Conversely, the aromatic ring and the chlorophenoxy group may impart some degree of hydrophobicity, thus decreasing solubility in non-polar solvents.
  • Temperature Dependency: As is common with acids, solubility can increase with temperature, allowing for better dissolution in warmer conditions.

In practical terms, it is noted that the solubility behavior of compounds like 2-(3-chlorophenoxy)-2-methyl-propanoic acid can be quite informative for their applications in fields such as agriculture and pharmaceuticals. As stated by industry experts, "Understanding the solubility is crucial for effective formulation and application."

In summary, the solubility of 2-(3-chlorophenoxy)-2-methyl-propanoic acid is influenced by several factors including its functional groups, the solvent used, and environmental conditions, making it a compound of great interest in chemical research.

Interesting facts

Exploring 2-(3-chlorophenoxy)-2-methyl-propanoic acid

2-(3-chlorophenoxy)-2-methyl-propanoic acid, often abbreviated as CMPA, is a fascinating compound primarily known for its role as a herbicide. Below are some compelling facts that highlight its significance in agricultural science and beyond:

  • Herbicidal Action: CMPA is utilized for its ability to control a variety of unwanted plants, effectively inhibiting their growth and reproduction. This makes it valuable for maintaining crop yield and managing weeds.
  • Chemical Family: As a member of the aryloxyalkanoic acid family, CMPA shares structural similarities with other important herbicides. This group includes various compounds known for their selective action against certain weed species, making them essential tools for farmers.
  • Mechanism of Action: CMPA acts by disrupting the auxin transport within plants. Auxins are critical growth hormones, and disrupting their normal function can lead to uncontrolled growth or death in susceptible species.
  • Environmental Impact: While effective as a herbicide, scientists study its environmental persistence and potential effects on non-target organisms. Understanding these impacts is crucial to ensuring sustainable agricultural practices.
  • Research Potential: Beyond its use in agriculture, CMPA serves as a model compound for researchers studying plant growth regulators and herbicide resistance mechanisms in weeds.

In summary, 2-(3-chlorophenoxy)-2-methyl-propanoic acid is not merely a chemical formula; it represents a significant advancement in the field of herbicides, showcasing the intricate balance between agricultural efficiency and environmental stewardship. Its study leads to broader insights into plant biology, making it a subject of interest for both chemists and agricultural scientists alike.

Synonyms
2-(3-chlorophenoxy)-2-methylpropanoic acid
808-702-6
17413-73-9
Propanoic acid, 2-(3-chlorophenoxy)-2-methyl-
MFCD01695660
Propionic acid, 2-(m-chlorophenoxy)-2-methyl-
2-(3-Chlorophenoxy)-2-methyl-propanoic acid
BRN 1874066
2-(m-Chlorophenoxy)-2-methylpropionic acid
Acide (m-chlorophenoxy)-2 methyl-2 propionique [French]
Acide (m-chlorophenoxy)-2 methyl-2 propionique
SCHEMBL3374117
DTXSID00169767
ALBB-000883
BBL014136
STK397554
AKOS000102211
AS-37295
DB-064943
CS-0207238
ST50609207
EN300-75658
2-(3-Chlorophenoxy)-2-methylpropanoic acid, AldrichCPR
Z274535144