68054-73-9
Chemical Structure
IPPD-Q
- CAS No.: 68054-73-9
- Formula:C15H16N2O2
- Molecular Weight:256.30
InChIKey: ZQAFKGDWLSVTRI-UHFFFAOYSA-N
SMILES: O=C1C(NC(C)C)=CC(C(NC2=CC=CC=C2)=C1)=O
Biological Activity: IPPD-Q is a p-phenylenediamine quinone and also Environmental pollutant. IPPD-Q can be present in tires, fine particulate matter and urban water bodies. IPPD-Q increases the activities of antioxidant enzymes (SOD, CAT), alters photosynthesis and energy metabolism pathways, and changes gene expression and metabolic profiles. IPPD-Q exhibits phytotoxic effects. IPPD-Q shows acute toxicity to zebrafish embryos and reduces their survival rate[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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IPPD-Q | 97.38% | IPPD-Q is a p-phenylenediamine quinone and also Environmental pollutant. IPPD-Q can be present in tires, fine particulate matter and urban water bodies. IPPD-Q increases the activities of antioxidant enzymes (SOD, CAT), alters photosynthesis and energy metabolism pathways, and changes gene expression and metabolic profiles. IPPD-Q exhibits phytotoxic effects. IPPD-Q shows acute toxicity to zebrafish embryos and reduces their survival rate. | ||||||||||||||||||||
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- [1]. Wang W, et al. Beyond Substituted -Phenylenediamine Antioxidants: Prevalence of Their Quinone Derivatives in PM. Environmental science & technology. 2022 Aug 02;56(15):10629-10637. [Content Brief]
- [2]. Zhao Y, et al. Phytotoxicity of tire-derived IPPD and IPPD-Q in wheat: Integrated physiological response and multi-omics analysis[J]. Journal of Environmental Chemical Engineering, 2026, 14(2): 121842.
- [3]. Chen H, et al. Mechanistic insights into the transformation and toxicity evolution of IPPD-Q during chlorination and chloramination in drinking water. Water research. 2026 Jan 15;289(Pt A):124884. [Content Brief]
Keywords
