2537-36-2C[N+](C)(C)C.[O-][Cl+3]([O-])([O-])[O-]ZCWKIFAQRXNZCH-UHFFFAOYSA-M2537-36-2DTXSID5062502化学的特性solid
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
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.
使用Tetramethylammonium 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.
純化方法Crystallise it twice from H2O and dry it at 110o in an air oven. It is insoluble in most organic solvents. [Mead et al. J Chem Soc 1210 1933, Coats & Taylor J Chem Soc 1498 1936.]
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