| Weight | 99.177 g/mol |
|---|---|
| Formula | C6H13N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Hexamethyleneimine (111-49-9)
perhydroazepine · hexahydroazepine hydrochloride · hexahydroazepine
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- The effects of seeding in the synthesis of zeolite MCM-22 in the presence of hexamethyleneimine (Zeolites, 1997)
- Synthesis and protein kinase C inhibitory activities of balanol analogs with replacement of the perhydroazepine moiety (Journal of Medicinal Chemistry, 1997)
- Transition metal ion complexes of thiosemicarbazones derived from 2-acetylpyridine. Part 3. The 3-hexamethyleneimine derivative (Transition Metal Chemistry, 1988)
- The influence of perhydroazepine and piperidine as further ancillary ligands on Ru-PPh3-based catalysts for ROMP of norbornene and norbornadiene (Applied Catalysis A-general, 2010)
- Synthesis and characterization of MCM-49/ZSM-35 composite zeolites in the hexamethyleneimine and cyclohexamine system (Microporous and Mesoporous Materials, 2009)
- Hydrothermal Synthesis of Titanium Silicalite-1 Structurally Directed by Hexamethyleneimine (Industrial & Engineering Chemistry Research, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - perhydroazepine
- hexahydroazepine hydrochloride
- hexahydroazepine
-
SMILESC1CCCNCC1
-
InChIKeyZSIQJIWKELUFRJ-UHFFFAOYSA-N
- Pubchem - Hexamethyleneimine
- Wikipedia - hexahydroazepine
Azepane is a saturated heterocycle, containing one nitrogen atom in seven-membered ring. Analogous to the well-known reaction of other amines, azepane reacts with CO2 and in principle can be used for carbon capture.
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Hexamethyleneimine
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