2537-36-2C[N+](C)(C)C.[O-][Cl+3]([O-])([O-])[O-]ZCWKIFAQRXNZCH-UHFFFAOYSA-M2537-36-2DTXSID5062502Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
Danger
H272 (98.5%): May intensify fire; oxidizer [Danger Oxidizing liquids; Oxidizing solids]
P210, P220, P260, P261, P262, P264, P264+P265, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P308+P316, P316, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P370+P378, P391, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 67 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Agents that mimic neural transmission by stimulation of the nicotinic receptors on postganglionic autonomic neurons. Drugs that indirectly augment ganglionic transmission by increasing the release or slowing the breakdown of acetylcholine or by non-nicotinic effects on postganglionic neurons are not included here nor are the nonspecific cholinergic agonists.
UsesTetramethylammonium perchlorate acts as an intermediate in organic and chemical synthesis. It is used as a mobile phase in high performance liquid chromatographic analysis and in the quantitation of olanzapine clozapine and N-desmethylclozapine. It acts as a supporting electrolyte in the electrochemical reduction of electrochemical reduction of 1-bromodecanr, 1-iododecane,2-iodooctane and 2-bromooctane at mercury cathodes.
No reaction records under the current filter.
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