3-(4prime-Hydroxy)phenoxybenzoic Acid CAS: 35065-12-4
MF: C13H10O4
MW: 230.22
A metabolite of pyrethroid insecticides.

3-(4′-Hydroxy)phenoxybenzoic Acid (CAS 35065-12-4)

3-(4′-Hydroxy)phenoxybenzoic Acid | CAS 35065-12-4 is rated 5.0 out of 5 by 1.
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Alternate Names: 4'-hydroxy-3-phenoxybenzoic acid
Application: 3-(4′-Hydroxy)phenoxybenzoic Acid is a metabolite of pyrethroid insecticides
CAS Number: 35065-12-4
Purity: ≥98%
Molecular Weight: 230.22
Molecular Formula: C13H10O4
Supplemental Information: This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data (including water content).

3-(4'-Hydroxy)phenoxybenzoic Acid is a metabolite of pyrethroid insecticides such as Permethrin, Deltamethrin, Cypermethrin, Fenvalerate, and Decamethrin.


References

1. Woollen, B H., et al., 1992. The metabolism of cypermethrin in man: differences in urinary metabolite profiles following oral and dermal administration. Xenobiotica; the fate of foreign compounds in biological systems. 22(8): 983-91. PMID: 1413886
2. Saito, K., et al., 2000. Lack of significant estrogenic or antiestrogenic activity of pyrethroid insecticides in three in vitro assays based on classic estrogen receptor alpha-mediated mechanisms. Toxicological sciences : an official journal of the Society of Toxicology. 57(1): 54-60. PMID: 10966511
3. Fang, H., et al., 2001. Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens. Chemical research in toxicology. 14(3): 280-94. PMID: 11258977
4. Andersen, Helle Raun., et al., 2002. Effects of currently used pesticides in assays for estrogenicity, androgenicity, and aromatase activity in vitro. Toxicology and applied pharmacology. 179(1): 1-12. PMID: 11884232

Physical State :
Solid
Storage :
Store at room temperature
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
PubChem CID :
161852
SMILES :
C1=CC(=CC(=C1)OC2=CC=C(C=C2)O)C(=O)O

Download SDS (MSDS)

Certificate of Analysis

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Rated 5 out of 5 by from Akhtar MH; et al Akhtar MH; et al. (PubMed ID: 1355708) determined that 4'-hydroxy-3-phenoxybenzoic acid was transitionary in nature and converted to 3-hydroxybenzoic acid. -SCBT Publication Review
Date published: 2015-01-30
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