EA-4352
![]() | |
![]() | |
| Names | |
|---|---|
| IUPAC name
Isopropyl dimethylphosphoramidocyanidate | |
| Other names
Isopropyl dimethylamidocyanidophosphate | |
| Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
| ChemSpider | |
PubChem CID |
|
CompTox Dashboard (EPA) |
|
SMILES
| |
| Properties | |
Chemical formula |
C6H13N2O2P |
| Molar mass | 176.156 g·mol−1 |
| Appearance | Liquid |
| Odor | Odorless |
| Density | 1.0425 g/mL (77°F) |
| Boiling point | 234 °C; 453 °F; 507 K |
| Vapor pressure | 0.055 mmHg (77°F) |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
Extremely toxic |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
462 μg/kg (mice, intraperitoneal)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
EA-4352 is an organophosphate nerve agent of the G-series. It is the isopropyl analog of tabun.[2]
References
- ↑ "ChemIDplus".
- ↑ Handbook of chemical and biological warfare agents (2nd ed.). CRC Press. ISBN 9780849314346.
| |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Blood agents |
| ||||||||||||||
| Blister agents |
| ||||||||||||||
| Nerve agents |
| ||||||||||||||
| Neurotoxins |
| ||||||||||||||
| Nettle agents |
| ||||||||||||||
| Pulmonary/ choking agents |
| ||||||||||||||
| Vomiting agents |
| ||||||||||||||
| Incapacitating agents |
| ||||||||||||||
| Lachrymatory agents |
| ||||||||||||||
| Malodorant agents |
| ||||||||||||||
| Biological toxins |
| ||||||||||||||
| Other |
| ||||||||||||||
| |||||||||||||||
| Animal toxins |
|
|---|---|
| Bacterial | |
| Cyanotoxins | |
| Plant toxins |
|
| Mycotoxins | |
| Pesticides |
|
| Nerve agents | |
| Bicyclic phosphates |
|
| Other |
|
| Enzyme (modulators) |
| ||||||
|---|---|---|---|---|---|---|---|
| Transporter (modulators) |
| ||||||
| Release (modulators) |
| ||||||
See also: Receptor/signaling modulators • Muscarinic acetylcholine receptor modulators • Nicotinic acetylcholine receptor modulators | |||||||
This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

