Perfluoroheptanesulfonic acid


CAS No. : 375-92-8

(Synonyms: 1-Perfluoroheptanesulfonic acid; Perfluoroheptanesulphonic acid; PFHpS)

375-92-8
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Cat. No. : HY-21200
M.Wt: 450.12
Formula: C7HF15O3S
Purity: >98 %
Solubility: DMSO : 10 mg/mL (ultrasonic;warming)
Introduction of 375-92-8 :

Perfluoroheptanesulfonic acid (1-Perfluoroheptanesulfonic acid; Perfluoroheptanesulphonic acid; PFHpS) is a per- and polyfluoroalkyl substance (PFAS) that penetrates the skin and induces systemic toxicity and immunotoxicity. Perfluoroheptanesulfonic acid reduces the expression of PPARδ in liver tissue; it induces hepatocyte hypertrophy and necrosis in liver tissue and alters serum biochemical markers associated with liver injury. Perfluoroheptanesulfonic acid upregulates genes related to fatty acid metabolism, cell necrosis and inflammation, reduces the relative weights of the spleen and thymus, suppresses humoral immune responses, and alters the composition of immune cell subsets in the spleen and skin. The plasma concentration of Perfluoroheptanesulfonic acid correlates with food intake. Perfluoroheptanesulfonic acid and perfluorooctanesulfonic acid exhibit synchronous pulse events in influent samples from wastewater treatment plants. Perfluoroheptanesulfonic acid can be used in studies related to liver injury and immune system damage[1][2][3]. In Vitro:Perfluoroheptanesulfonic acid (PFHpS) can reach a peak concentration of 18 ng/L during pulse discharge events in influent water of wastewater treatment plants; to reliably detect its concentration fluctuations, at least 9 random hourly grab samples need to be collected per day[2]. In Vivo:Perfluoroheptanesulfonic acid (0.3125-1.25% w/v; topical; daily; 28 days) results in dose-dependent systemic absorption, liver damage (with up to 148% increased relative liver weight), and immunotoxicity in female B6C3F1 mice[1].
Perfluoroheptanesulfonic acid (0.625-2.5% w/v; topical; daily; 10 days) suppresses the spleen humoral immune response to sheep red blood cells (with up to 62.3% reduced total IgM activity) and alters splenic immune cell populations in female B6C3F1 mice[1].

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