3'-Iminobis(N,N-dimethylpropylamine)
[CAS# 6711-48-4]

Identification

• Classification: Organic raw materials >> Amino compound >> Acyclic monoamines, polyamines and their derivatives and salts
• Name: 3'-Iminobis(N,N-dimethylpropylamine)
• Synonyms: 2,10-Dimethyl-2,6,10-triazaundecane; Bis[3-(dimethylamino)propyl]amine; Jeffcat Z 130; N,N,N',N'-Tetramethyliminobispropylamine; N,N,N'',N''-Tetramethyldipropylenetriamine; N,N-Bis[3-(dimethylamino)propyl]amine
• Molecular Formula: C₁₀H₂₅N₃
• Molecular Weight: 187.33
• CAS Registry Number: 6711-48-4
• EC Number: 229-761-9
• SMILES: CN(C)CCCNCCCN(C)C

Properties

• Density: 0.863
• Melting point: -78 ºC
• Boiling point: 239 ºC
• Refractive index: 1.449
• Flash point: 98 ºC

Safety Data

• Hazard Symbols: GHS05;GHS06;GHS07 Danger
• Hazard Statements: H302-H311-H314-H318
• Precautionary Statements: P260-P262-P264-P264+P265-P270-P280-P301+P317-P301+P330+P331-P302+P352-P302+P361+P354-P304+P340-P305+P354+P338-P316-P317-P321-P330-P361+P364-P363-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Acute toxicity	Acute Tox.	4	H302
Acute toxicity	Acute Tox.	3	H311
Serious eye damage	Eye Dam.	1	H318
Skin corrosion	Skin Corr.	1B	H314
Chronic hazardous to the aquatic environment	Aquatic Chronic	3	H412
Skin corrosion	Skin Corr.	1C	H314
Skin corrosion	Skin Corr.	1	H314
Skin sensitization	Skin Sens.	1	H317
Acute toxicity	Acute Tox.	4	H312

Discovory and Applicatios

3'-Iminobis(N,N-dimethylpropylamine) is a notable chemical compound with various applications in chemical synthesis and industrial processes. Known for its unique structural and chemical properties, this compound has found utility in a range of fields, from organic synthesis to material science.

The discovery of 3'-Iminobis(N,N-dimethylpropylamine) dates back to the late 20th century when researchers were exploring novel amine-based compounds for their potential applications. This compound features a distinctive structure where two N,N-dimethylpropylamine groups are connected by an imine linkage, forming a unique bicyclic system. The imine group introduces a reactive site that imparts special properties to the compound, making it useful in various chemical reactions and applications.

One of the primary applications of 3'-Iminobis(N,N-dimethylpropylamine) is as a reagent in organic synthesis. Its structure allows it to act as a nucleophile in various chemical reactions, facilitating the formation of complex organic molecules. The imine functionality is particularly useful in reactions involving electrophiles, where it can form stable adducts or intermediates. This property makes it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.

In addition to its role in organic synthesis, 3'-Iminobis(N,N-dimethylpropylamine) is employed in the development of advanced materials. Its ability to interact with different chemical entities makes it suitable for use in the formulation of specialty polymers and resins. These materials can exhibit enhanced properties, such as improved stability, flexibility, and reactivity, which are desirable in various industrial applications.

The compound also finds applications in catalysis, where its unique structure and reactivity enable it to act as a catalyst in several chemical transformations. For instance, it can be used in the polymerization of monomers or in the synthesis of complex organic frameworks. Its catalytic properties contribute to the efficiency and selectivity of these reactions, making it a useful component in both academic research and industrial processes.

Moreover, 3'-Iminobis(N,N-dimethylpropylamine) has been explored for its potential applications in medicinal chemistry. Its structure and reactivity suggest that it could be used in the development of new drug candidates or as a tool in the study of biological processes. However, further research is needed to fully understand its potential in this area and to explore its biological activity and safety profile.

Overall, 3'-Iminobis(N,N-dimethylpropylamine) is a versatile compound with significant applications in organic synthesis, materials science, and catalysis. Its unique chemical properties and reactivity make it a valuable tool in various fields, contributing to advancements in chemical research and industrial applications.