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AAPH

Catalog No.
C5140
A free radical initiator used to induce oxidative stress and erythrocyte hemolysis.
Grouped product items
SizePriceStock Qty
5g
$50.00
In stock
10g
$95.00
In stock
50g
$315.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

AAPH (CAS No.: 2997-92-4) is a water-soluble azo compound widely employed in biomedical research as a controlled free radical generator for modeling oxidative stress and evaluating antioxidant activity. Upon thermal decomposition at physiological temperature, AAPH produces alkyl radicals that rapidly react with molecular oxygen to form peroxyl radicals, leading to lipid peroxidation, disruption of membrane integrity, and oxidative damage in biological systems, particularly in erythrocytes where it is commonly used to induce hemolysis. This compound is characterized by a relatively long half-life under neutral aqueous conditions, enabling a steady and sustained generation of radicals, which is advantageous for reproducible in vitro oxidative stress assays. Mechanistically, AAPH-driven radical formation initiates chain reactions affecting membrane lipids and associated biomolecules, thereby serving as a useful tool to investigate redox-dependent signaling pathways and cellular defense mechanisms against oxidative injury. Although it does not act on a specific molecular target, its effects are mediated through the generation of reactive oxygen species and subsequent activation of oxidative stress-responsive pathways. AAPH is extensively applied in cell-based assays, erythrocyte models, and biochemical systems to assess antioxidant efficacy, screen protective compounds, and study the pathophysiology of oxidative stress-related disorders, with experimental concentrations typically adjusted according to assay design and desired levels of oxidative challenge.

Chemical Properties

Physical AppearanceA solid
Storage-20°C
M.Wt271.19
Cas No.2997-92-4
FormulaC8H20Cl2N6
Solubilityinsoluble in EtOH; ≥31 mg/mL in H2O; ≥8.14 mg/mL in DMSO
Chemical Name(E)-2,2'-(diazene-1,2-diyl)bis(2-methylpropanimidamide) dihydrochloride
Canonical SMILESN/C(C(C)(/N=N/C(C)(/C(N)=N/[H])C)C)=N\[H].Cl.Cl
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

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