Contents

T-1123

T-1123

Names
Preferred IUPAC name N,N-Diethyl-N-methyl-3-[(methylcarbamoyl)oxy]anilinium iodide
Other names AR-16, TL-1217
Identifiers
CAS Number	60398-22-3
3D model (JSmol)	Interactive image
ChemSpider	39424
PubChem CID	43257
CompTox Dashboard (EPA)	DTXSID00975800
InChI InChI=1S/C13H20N2O2.HI/c1-5-15(4,6-2)11-8-7-9-12(10-11)17-13(16)14-3;/h7-10H,5-6H2,1-4H3;1H Key: XYPQGNNSAIEXIS-UHFFFAOYSA-N
SMILES CC[N+](C)(CC)C1=CC(=CC=C1)OC(=O)NC.[I-]
Properties
Chemical formula	C13H21IN2O2
Molar mass	364.227 g·mol−1
Related compounds
Related compounds	Neostigmine Miotine
Hazards
Lethal dose or concentration (LD, LC):
LD50 (median dose)	129 μg/kg (Subcutaneous, mice)[1] 75 μg/kg (Subcutaneous, cats)[1] 75 μg/kg (Subcutaneous, dogs)[1] 150 μg/kg (Subcutaneous, rabbits)[1] 122.5 μg/kg (Intramuscular, rats)[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Chemical compound

T-1123 is a carbamate-based acetylcholinesterase inhibitor. It was investigated as a chemical warfare agent starting in 1940. It does not go through the blood-brain barrier due to the charge on quaternary nitrogen. The antidote is atropine.^[3] T-1123 is a quaternary ammonium ion. A phenyl carbamate ester is bonded in the meta position to the nitrogen on a diethylmethyl amine. The chloride and methylsulfate salt of T-1123 is TL-1299 and TL-1317, respectively.

Synthesis[edit]

T-1123 can be produced from m-diethylaminophenol, methyl isocyanate and methyl iodide. First, m-diethylaminophenol is reacted with methyl isocyanate to produce a methylcarbamate. The resulting methylcarbamate is then reacted with methyl iodide to produce T-1123.^[1]

See also[edit]

• Miotine
• Neostigmine
• TL-1238
• T-1152
• T-1194
• TMTFA

References[edit]

Extra reading[edit]

• Robinson, J. P. (1971). The Problem of Chemical and Biological Warfare: The rise of CB weapons. Almqvist & Wiksell. ISBN 9780391002005.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.