Dimethyldipropylenetriamine

Base Information

• Chemical Name: Dimethyldipropylenetriamine
• CAS No.: 10563-29-8
• Molecular Formula: C8H21N3
• Molecular Weight: 159.275
• Hs Code.: 2921290000
• European Community (EC) Number: 234-148-4
• UNII: B15K0N6194
• DSSTox Substance ID: DTXSID2033445
• Nikkaji Number: J226.992I
• Wikidata: Q27274243
• ChEMBL ID: CHEMBL1462995
• Mol file: 10563-29-8.mol

Synonyms:dimethyldipropylenetriamine;DMDPT

Chemical Property of Dimethyldipropylenetriamine

Chemical Property:

• Vapor Pressure: 3Pa at 20℃
• Refractive Index: n20/D 1.4630(lit.)
• Boiling Point: 231.176 °C at 760 mmHg
• PKA: 10.32±0.19(Predicted)
• Flash Point: 93.612 °C
• PSA: 41.29000
• Density: 0.883 g/cm³
• LogP: 0.96770
• Water Solubility.: 1000g/L at 25℃
• XLogP3: -0.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 159.173547683
• Heavy Atom Count: 11
• Complexity: 73.7

Purity/Quality:

99% ^*data from raw suppliers

N,N-Dimethyldipropylenetriamine 99% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 21/22-34
• Safety Statements: 23-26-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CN(C)CCCNCCCN
• Uses: N,N-Dimethyldipropylenetriamine (DP) may be used to:Prepare poly(ethylene oxide)-b-poly(3-caprolactone-g-DP) [PEO-b-P(CL-g-DP)], a biodegradable amphiphilic polycationic copolymer.Develop a second generation aminoglycoside 6′-N-acetyltransferase (AAC(6′) inhibitor.Prepare a hydrophilic gemcitabine conjugated cationic copolymer, which can be employed in the treatment pancreatic cancer.

Technology Process of Dimethyldipropylenetriamine

There total 3 articles about Dimethyldipropylenetriamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3-[[3-(dimethylamino)propyl]amino]propionitrile (69852-45-5) → N1-(3-dimethylaminopropyl)propane-1,3-diamine (10563-29-8)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether;

Reference yield:

1-amino-3-(dimethylamino)propane (109-55-7) → N1-(3-dimethylaminopropyl)propane-1,3-diamine (10563-29-8)

Guidance literature:

Multi-step reaction with 2 steps

2: LiAlH₄ / diethyl ether

With lithium aluminium tetrahydride; In diethyl ether;

Reference yield:

→ N1-(3-dimethylaminopropyl)propane-1,3-diamine (10563-29-8)

Guidance literature:

3-<3-Dimethylamino-propylamino>-propionitril, H2, aethanol. NH4OH, Raney-Ni;

upstream raw materials:

3-[[3-(dimethylamino)propyl]amino]propionitrile

1-amino-3-(dimethylamino)propane

Downstream raw materials:

N-<3-Dimethylamino-propyl>-N'-<1-methyl-3-(2,6,6-trimethyl-cyclohexen-(1)-yl)-propyl>-1,3-propandiamin

N-<3-Dimethylamino-propyl>-N'-<1-methyl-3-(2,6,6-trimethyl-cyclohexen-(2)-yl)-propyl>-1,3-propandiamin

N'-[3-(dimethylamino)propyl]-N,N,N'-trimethylpropane-1,3-diamine

Refernces