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3,3'-Iminobis(N,N-dimethylpropylamine)

Catalog Number
ACM6711484-3
Product Name
3,3'-Iminobis(N,N-dimethylpropylamine)
Structure
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CAS
6711-48-4
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Synonyms
DTXSID7044974; 3,3'-Iminobis(N,N-dimethylpropylamine), 97%; (3-{[3-(dimethylamino)propyl]amino}propyl)dimethylamine; Bis-(dimethylaminopropyl)amine; CS-W016846; W-104730; AKOS000120187; 3,3'-Iminobis(N,N-dimethyl-propylamine); CW8R6R660G; NCGC00256130-01;
IUPAC Name
N-[3-(dimethylamino)propyl]-N',N'-dimethylpropane-1,3-diamine;
Molecular Weight
187.331g/mol
Molecular Formula
C10H25N3;
Canonical SMILES
CN(C)CCCNCCCN(C)C;
InChI
InChI=1S/C10H25N3/c1-12(2)9-5-7-11-8-6-10-13(3)4/h11H,5-10H2,1-4H3;
InChI Key
BXYVQNNEFZOBOZ-UHFFFAOYSA-N;
Complexity
90.3
Covalently-Bonded Unit Count
1
EC Number
229-761-9
Exact Mass
187.205g/mol
H-Bond Acceptor
3
H-Bond Donor
1
Heavy Atom Count
13
Monoisotopic Mass
187.205g/mol
NSC Number
129937
Rotatable Bond Count
8
Topological Polar Surface Area
18.5A^2
UNII
CW8R6R660G
Application
3,3'-Iminobis(N,N-dimethylpropylamine) serves multiple roles in various chemical applications, notably as a crucial reagent in the development of an innovative class of anticancer agents known as antracenylisoxazole lexitropsin conjugates. Additionally, it plays an important part in stabilizing polypropylene by preventing its thermo-oxidative degradation as part of the Hindered Amino Stabilizers group. This versatile compound is also utilized in the synthesis of dimeric quaternary alkylammonium conjugates of sterols, acts as a nitrogen-containing tridentate ligand in the formation of [3,3'-iminobis(N,N-dimethylpropylamine)](4'-methoxyflavonolato)zinc(II) perchlorate complex, and is involved in the creation of compounds such as 2-[[[N,N-bis[3-(N,N-dimethylamino)propyl]amino]carbonyl]-1-methyl-4-nitropyrrole and 3-(9-anthracenyl)-N,N-bis[3-(N,N-dimethylamino)propyl]-5-methyl-4-isoxazole carboxamide.
February 20, 2025

Highly Effective Reagent for Synthesis

I've been using 3,3'-Iminobis(N,N-dimethylpropylamine) from Alfa Chemistry in my research on anticancer agents. It performs excellently as a reagent, facilitating synthesis with high efficacy. A reliable choice for advanced scientific applications.

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