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3724-43-4C[N+](C)=CCl.[Cl-]QQVDYSUDFZZPSU-UHFFFAOYSA-M3724-43-4DTXSID7044423CHEMBL3183181Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Danger
H302: Harmful if swallowed [Warning Acute toxicity, oral]
P203, P260, P264, P270, P280, P301+P317, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P318, P321, P330, P363, P405, and P501 (click each P-code to see the statement)
Danger
H290 (69.3%): May be corrosive to metals [Warning Corrosive to Metals]
P203, P234, P260, P264, P264+P265, P270, P280, P301+P317, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P318, P321, P330, P363, P390, P405, P406, and P501 (click each P-code to see the statement)
Hazard Traits - Reproductive Toxicity
Methanaminium, N-(chloromethylene)-N-methyl-, chloride (1:1) is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Methanaminium, N-(chloromethylene)-N-methyl-, chloride (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: 15-10-2014 https://echa.europa.eu/registration-dossier/-/registered-dossier/15587
Status: No longer Valid Update: 12-11-2010 https://echa.europa.eu/registration-dossier/-/registered-dossier/7015
Methanaminium, N-(chloromethylene)-N-methyl-, chloride: Does not have an individual approval but may be used under an appropriate group standard
Met. Corr. 1 (69.3%)
Met. Corr. 1 (28.6%)
Reproductive toxicity - category 1B
Repr. 1B
Pharmaceutical and Medicine Manufacturing
Methanaminium, N-(chloromethylene)-N-methyl-, chloride (1:1): ACTIVE
Verwenden(Chloromethylene)dimethylammonium chloride is used in the synthesis of beta-lactams, n-vinyl substituted indoles and fused 2-pyridone rings and 2-azetidinones. It is used as a formylating agent and used in the preparation of anti-poxvirus agents. It is used in Staudinger reaction and Hundsdiecker-barton iododecarboxylation reaction. It is widely used for studying organic photosensitizers, which finds application in dye-sensitized solar cells.
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