Home Categories Chemical Reagents 3,3'-Iminodipropionitrile
A5092712

3,3'-Iminodipropionitrile , >90.0%(GC) , 111-94-4

Synonym(s):
Bis(2-cyanoethyl)amine

CAS NO.:111-94-4

Empirical Formula: C6H9N3

Molecular Weight: 123.16

MDL number: MFCD00001956

EINECS: 203-922-3

Update time: 2022-07-08

PRODUCT Properties

Melting point: -6 °C
Boiling point: 205 °C25 mm Hg(lit.)
Density  1.02 g/mL at 25 °C(lit.)
refractive index  n20/D 1.47(lit.)
Flash point: >230 °F
storage temp.  2-8°C
pka 6.13±0.19(Predicted)
form  clear liquid
color  Colorless to Light yellow to Light orange
Water Solubility  Soluble in water.
Stability: Stable, but moisture sensitive. Reaction with moisture may lead to a build up of pressure in sealed bottles. Combustible. Incompatible with strong oxidizing agents.

Description and Uses

Bis(2-cyanoethyl)amine is used as pharmaceutical intermediates.

Safety

Symbol(GHS) 
GHS07,GHS05,GHS06
Signal word  Warning
Hazard statements  H315-H319-H301-H318-H335
Precautionary statements  P261-P280a-P301+P310a-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26
RIDADR  UN 3334
WGK Germany  2
RTECS  UG2975000
TSCA  Yes
HS Code  29269095
Toxicity A neurotoxic synthetic nitrile that causes proximal axonopathies in the spinal cord and brain stem. The proximal axonal swellings are due to interruption of slow axonal transport, resulting in a large accumulation of neurofilaments. Secondary to these effects is a progressive atrophy of the distal axon, secondary demyelination, and gliosis. The slow axonal transport defect appears to be selective, as little evidence for perturbations in fast axonal transport have been reported. Behaviorally, IDPN induces hyperactivity, a “waltzing syndrome,” circling and head-rolling in mice and rats. IDPN intoxication has been advanced as a model for certain motor neuron degenerative diseases such as amyotropic lateral sclerosis (ALS) and hereditary canine spinal muscular atrophy (HCSMA).

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