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About This Item
Linear Formula:
CH3NH(CH2)6NHCH3
CAS Number:
Molecular Weight:
144.26
Beilstein:
1735385
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
form
liquid
refractive index
n20/D 1.447 (lit.)
bp
96 °C/14 mmHg (lit.)
mp
15-18 °C (lit.)
density
0.807 g/mL at 25 °C (lit.)
SMILES string
CNCCCCCCNC
InChI
1S/C8H20N2/c1-9-7-5-3-4-6-8-10-2/h9-10H,3-8H2,1-2H3
InChI key
MDKQJOKKKZNQDG-UHFFFAOYSA-N
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Application
N,N′-Dimethyl-1,6-hexanediamine (DMHDA) can be used as an organic building block to synthesize:
- Hydroxyurethane by reacting with propylene carbonate.
- N,N′-dimethyl, N,N′-di(methacryloxy ethyl)-1,6-hexanediamine (NDMH), a monomer applicable as both a co-initiator and a reactive diluent for dental resins.
- Degradable poly(amino alcohol ester) polymer by nucleophilic addition with diglycidyl adipate for the potential use in gene transfection vectors.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
186.8 °F - closed cup
Flash Point(C)
86 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Reactivity of secondary amines for the synthesis of non-isocyanate polyurethanes
Camara F, et al.
European Polymer Journal, 55, 17-26 (2014)
Synthesis and photopolymerization of N, N?-dimethyl,-N, N?-di (methacryloxy ethyl)-1, 6-hexanediamine as a polymerizable amine coinitiator for dental restorations
Nie J and Bowman CN
Biomaterials, 23(4), 1221-1226 (2002)
Degradable poly (amino alcohol esters) as potential DNA vectors with low cytotoxicity
J Sangyong, et al.
Biomacromolecules, 4(6), 1759-1762 (2003)
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