Diethylammonium chloride
660-68-4CCNCC.ClHDITUCONWLWUJR-UHFFFAOYSA-NSee also: N-Ethylethan(~15~N)amine--hydrogen chloride (1/1) (annotation moved to).
660-68-4DTXSID9044320CHEMBL3188625Liquid
Off-white hygroscopic solid; [Acros Organics MSDS]
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This chemical does not meet GHS hazard criteria for 1.5% (1 of 67) of reports.
Danger
H315 (92.5%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 67 reports by companies from 14 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Chemical: Ethanamine, N-ethyl-, hydrochloride
Ethanamine, N-ethyl-, hydrochloride (1:1) is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Ethanamine, N-ethyl-, hydrochloride (1:1) are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 25-05-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/23798
Ethanamine, N-ethyl-, hydrochloride: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Causes tremor and respiratory stimulation in intraperitoneal lethal-dose studies of mice; Causes impaired liver function tests and increased urine volume in 26-week intermittent oral studies of rats; [RTECS] An irritant; [Acros Organics MSDS] See Diethylamine.
Synthetic Dye and Pigment Manufacturing
Ethanamine, N-ethyl-, hydrochloride (1:1): ACTIVE
VerwendenDiethylamine hydrochloride acts as a precursor of atrazine and lysergic acid diethylamide. It is also used as a reactant in the production of dyes and pharmaceutical compounds such as ranitidine. Further, it is used in Mannich reaction with paraformaldehyde. In addition to this, it is employed in the synthesis of diethylaminoethyl (DEAE) cottons by reacting with cotton cellulose in the presence of sodium hydroxide.
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