| Weight | 170.083 g/mol |
|---|---|
| Formula | C6H13Cl2N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
Bis(2-chloroethyl)ethylamine (538-07-8)
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- Sigma-Aldrich - Search for Bis(2-chloroethyl)ethylamine
- Fisher Scientific - Search for Bis(2-chloroethyl)ethylamine
- TCI - Search for Bis(2-chloroethyl)ethylamine
- Detection of the chemical warfare agents bis-(2-chloroethyl)ethylamine (HN-1) and tris-(2-chloroethyl)amine (HN-3) in air (Journal of Chromatography A, 1999)
- Characterization of nitrogen mustard formamidopyrimidine adduct formation of bis(2-chloroethyl)ethylamine with calf thymus DNA and a human mammary cancer cell line. (Chemical Research in Toxicology, 2015)
- IR spectra of 2-ethylamine halides III. Stretching vibrations bands of C-Cl bonds in IR spectra of some N-(2-chloroethyl)-aniline and N, N-bis-(2-chloroethyl)-aniline derivatives (Journal of Applied Spectroscopy, 1972)
- Vapor Pressure of Bis-(2-chloroethyl)ethylamine (HN1) (2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCN(CCCl)CCCl
-
InChIKeyUQZPGHOJMQTOHB-UHFFFAOYSA-N
- Pubchem - Bis(2-chloroethyl)ethylamine
- Wikipedia - hn-1
Bis(2-chloroethyl)ethylamine is the organic compound with the formula C2H5N(CH2CH2Cl)2. Often abbreviated HN1, it is a powerful vesicant and a nitrogen mustard gas used for chemical warfare. HN1 was developed in the 1920s and 1930s to remove warts and later as a military agent.
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