7790-62-7O=S(=O)([O-])OS(=O)(=O)[O-].[K+].[K+]KAQHZJVQFBJKCK-UHFFFAOYSA-L7790-62-7DTXSID10889580This chemical does not meet GHS hazard criteria for 1.3% (2 of 149) of reports.
Danger
H314 (97.3%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation];H318 (38.9%): Causes serious eye damage [Danger Serious eye damage/eye irritation];H331 (36.9%): Toxic if inhaled [Danger Acute toxicity, inhalation]
P260, P261, P264, P264+P265, P271, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P363, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 149 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Reported as not meeting GHS hazard criteria per 2 of 149 reports by companies.;There are 7 notifications provided by 147 of 149 reports by companies with hazard statement code(s).;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Chemical: Disulfuric acid, dipotassium salt
Status: Active Update: 04-04-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/11493
Potassium pyrosulphate: Does not have an individual approval but may be used under an appropriate group standard
0.20 [mg/m3]
8.7 [mg/m3]
160 [mg/m3]
Chemical: Disulfuric acid, dipotassium salt
Status: Active Update: 04-04-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/11493
Potassium pyrosulphate: Does not have an individual approval but may be used under an appropriate group standard
UsesPotassium disulfite supported on silica may be used for the synthesis of ethyl pyruvate.
UsesPotassium disulfate (K2S2O7) can be used: As a salt catalyst for the conversion of hemicellulose into reducing sugars such as xylose and galactose by mechanocatalysis . In the preparation of diacylbenzenes via Pd-catalyzed decarboxylative acylation of aromatic ketones with oxocarboxylic acids. As an oxidant for the preparation of monosubstituted triazoles from aryl azides and propargyl alcohol using Ag2O as a catalyst.
UsesAcid flux in analysis, laboratory reagent.
General DescriptionPotassium disulfite (Potassium pyrosulfate) has been synthesized from potassium hydrogen sulfate, via melting.
PreparationPotassium pyrosulphate is obtained by heating potassium hydrogen sulphate to its melting point.
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