PHENOXYACETIC ACID

Phenoxyacetic acid is an aromatic carboxylic acid used mainly in chemical synthesis and as a precursor to pharmaceuticals. Direct physiological use is minimal, but exposure may cause irritation, headache, and gastrointestinal discomfort. High exposures can lead to liver or kidney stress, though toxicity is generally low.

SKU: 6075d0968572 Category: Tag:

Product Description


Mechanism of Action

PHENOXYACETIC ACID (ID 27088) demonstrates a broad, multi‑layer biochemical activity profile affecting enzyme‑driven catalytic pathways, receptor‑regulated signalling systems, mitochondrial bioenergetics, redox‑state equilibrium, ion‑channel behaviour, cytoskeletal integrity and transcription‑factor regulatory networks. Its structural features indicate potential interactions with catalytic residues, allosteric protein domains, membrane‑bound receptors and intracellular signalling intermediates, enabling influence over phosphorylation kinetics, Ca²⁺/cAMP/IP₃/DAG‑mediated second‑messenger systems, ATP turnover, ROS buffering and mitochondrial respiratory‑chain performance.

Depending on concentration and biological conditions, PHENOXYACETIC ACID may modulate metabolic flux distribution, alter mitochondrial membrane potential, influence chromatin accessibility, impact vesicular trafficking dynamics and reshape gene‑expression patterns relevant to survival, inflammation, apoptosis, autophagy, metabolic adaptation and redox‑stress response.

Benefits and Advantages

This compound is widely used across advanced biochemical, pharmacological and mechanistic research domains, including:

  • Receptor–ligand interaction studies and affinity‑mapping
  • Enzyme‑kinetic pathway deconstruction and catalytic‑domain profiling
  • Mitochondrial‑function analysis and ATP‑flux/oxidative‑stress modelling
  • Multi‑omics integration (transcriptomics, metabolomics, proteomics, phosphoproteomics)
  • Cytoskeletal‑structure and membrane‑dynamics research
  • Autophagy, apoptosis, necroptosis and ferroptosis signalling investigations
  • SAR (structure–activity relationship) profiling and compound‑optimisation workflows
  • Pharmacodynamic modelling, threshold‑activation mapping and dose–response scaling

Side Effects and Risks

Laboratory‑observed or predicted risks include:

  • Oxidative imbalance and excessive ROS accumulation
  • Mitochondrial overload or respiratory‑chain suppression
  • Dysregulation of Na⁺/K⁺/Ca²⁺ ion‑channel homeostasis
  • Unintended receptor cross‑talk or inhibitory interference
  • Cytoskeletal destabilisation and membrane‑integrity disruption
  • Dose‑dependent cytotoxicity with apoptosis/autophagy activation
  • Transcriptional instability or epigenetic disturbance
  • Inflammatory signalling activation via NF‑κB, MAPK or JNK pathways

Use strictly within controlled laboratory environments under appropriate biosafety protocols.

Datasheet


Molecular Formula

C8H8O3

Molecular Weight

152.15 g/mol

CAS Number

122-59-8

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

1 to 5 mg/mL at 63 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

PHENOXYACETIC ACID; 2-phenoxyacetic acid; 122-59-8; Phenoxyethanoic acid; Glycolic acid phenyl ether

IUPAC/Chemical Name

2-phenoxyacetic acid

InChl Key

LCPDWSOZIOUXRV-UHFFFAOYSA-N

InChl Code

InChI=1S/C8H8O3/c9-8(10)6-11-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)

References

https://pubchem.ncbi.nlm.nih.gov/compound/19188;

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