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Names | |
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Preferred IUPAC name 3,3′-Azanediyldipropanenitrile | |
Other names Bis(2-cyanoethyl)amine | |
Identifiers | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.003.566 |
EC Number |
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PubChem CID | |
UNII | |
UN number | 3334 |
CompTox Dashboard (EPA) | |
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Properties | |
C6H9N3 | |
Molar mass | 123.159 g·mol−1 |
Density | 1.02 |
Melting point | −5.5 °C (22.1 °F; 267.6 K) |
Hazards | |
GHS labelling: | |
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Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
IDPN (3,3'-iminodipropanenitrile) is a neurotoxin with ototoxic and hepatotoxic effects. It causes irreversible movement disorder. [1] [2] [3]
IDPN has been shown to kill vestibular hair cells, disrupting normal vestibular function, in rats, [4] mice, guinea pigs, and frogs. [5] In rodents, the loss of vestibular function results in balance-related deficits, including circling behavior, retropulsion, and head bobbing, as well as weight loss. [5] Type I hair cells are more sensitive to IDPN toxicity than Type II hair cells. [4] No regeneration of vestibular hair cells was observed, thus these effects can be considered to be irreversible. [4]
IDPN has also been shown to kill cochlear hair cells, affecting auditory function. [6] IDPN-induced hearing loss covered a broad range of frequencies.
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: CS1 maint: DOI inactive as of November 2024 (link)