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TCI

CAS 113158-40-0

Fenoxaprop-P TCI F1196

Fenoxaprop-P TCI F1196

Chemical Identity

Other names
(R)-2-[4-[(6-Chlorobenzo[d]oxazol-2-yl)oxy]phenoxy]propanoic Acid · HOE 088406
CAS No.
113158-40-0
Formula
C16H12ClNO5
Molecular weight
333.72 g/mol
Purity
>95.0%(HPLC)(T)
Storage
0-10°C
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2R)-2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid
SMILES
CC(C(=O)O)OC1=CC=C(C=C1)OC2=NC3=C(O2)C=C(C=C3)Cl
InChIKey
MPPOHAUSNPTFAJ-SECBINFHSA-N
MDL
MDL01311798
PubChem
CID 11949285
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Fenoxaprop-P (TCI F1196) is a chemical compound widely used in laboratory research, particularly in the fields of nutrition and cell biology. It serves as a key reagent for studying the biochemical interactions between plant systems and synthetic compounds. This material is specifically categorized as a herbicide, functioning as an acyltransferase inhibitor, which disrupts the growth of weeds by interfering with essential metabolic processes. Its role in the laboratory is critical for understanding the mechanisms of herbicidal activity and its impact on plant physiology.

Fenoxaprop-P is valued for its chemical stability and solubility in organic solvents, making it easy to prepare and handle in laboratory settings. These properties ensure consistent performance in experiments, reducing variability and enhancing reproducibility. Additionally, its low toxicity to humans and animals makes it a safe choice for research environments where safety is a priority. The solid form of the compound also facilitates secure and efficient storage, supporting long-term use in laboratory operations.

In Indonesian laboratories, Fenoxaprop-P is commonly used in agricultural and biotechnology research. It plays a significant role in studies focused on the efficiency of active ingredients in weed control. These investigations are essential for addressing national agricultural needs and improving crop productivity through scientific innovation.

  • Weed control research benefits from Fenoxaprop-P’s ability to inhibit acyltransferase, offering insights into herbicidal mechanisms.
  • Nutritional studies utilize this compound to examine how synthetic chemicals interact with plant metabolism and nutrient uptake.
  • Cell biology experiments leverage its role as an enzyme inhibitor to study the effects of chemical interference on cellular processes.
  • Agricultural biotechnology applications focus on optimizing herbicide use for sustainable crop management.
  • Environmental impact assessments use Fenoxaprop-P to evaluate the long-term effects of herbicides on soil and plant ecosystems.

Brand TCI
CAS number 113158-40-0
Molecular formula —
Purity —
Category Life Science > Cell Biology > Nutrition Research
Pack sizes —
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight

Fenoxaprop-P should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use sealed containers made of glass or high-density polyethylene to avoid contamination and ensure safety. Due to its low toxicity, it is generally safe to handle, but standard laboratory precautions should still be observed, such as wearing gloves and safety goggles. The solid form allows for easy storage and minimizes the risk of spillage. It is important to keep the substance away from incompatible materials and ensure proper ventilation in the workspace to maintain a safe and controlled environment.

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