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120239-63-6

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  • N, N, N', N'-Tetra(3-Aminopropyl)-1, 4-Butanediamine

    Cas No: 120239-63-6

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  • 1 Metric Ton

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120239-63-6 Usage

Description

DAB-AM-4, POLYPROPYLENIMINE TETRAAMINE DENDRIMER, GENERATION 1.0 is a highly branched, synthetic macromolecule with a well-defined structure and a multitude of functional groups. It is a type of dendritic polymer that belongs to the polypropylenimine family and is characterized by its generation 1.0 architecture. This unique structure endows it with a wide range of applications across various industries due to its versatile properties, such as high solubility, excellent biocompatibility, and the ability to form stable complexes with other molecules.

Uses

Used in Coatings Industry:
DAB-AM-4, POLYPROPYLENIMINE TETRAAMINE DENDRIMER, GENERATION 1.0 is used as a coating additive for enhancing the performance and durability of coatings. Its high solubility and ability to form stable complexes with other molecules make it an ideal candidate for improving the adhesion, corrosion resistance, and overall protective properties of coatings.
Used in Adhesives Industry:
In the adhesives industry, DAB-AM-4 is used as a component in the formulation of high-performance adhesives. Its branched structure and multiple functional groups allow for strong interactions with various substrates, resulting in improved bonding strength and durability.
Used in Plastics Industry:
DAB-AM-4, POLYPROPYLENIMINE TETRAAMINE DENDRIMER, GENERATION 1.0 is used as a plastic additive to improve the mechanical, thermal, and chemical properties of plastics. Its incorporation into plastic materials can lead to enhanced toughness, heat resistance, and resistance to environmental degradation.
Used in Cosmetics Industry:
In the cosmetics industry, DAB-AM-4 is used as an ingredient in various cosmetic products due to its biocompatibility and ability to form stable complexes with other molecules. It can be used as a stabilizing agent, emulsifier, or delivery system for active ingredients, enhancing the performance and efficacy of cosmetic formulations.
Used in Catalysts Industry:
DAB-AM-4, POLYPROPYLENIMINE TETRAAMINE DENDRIMER, GENERATION 1.0 is used as a catalyst or catalyst support in various chemical reactions. Its multiple functional groups and high solubility make it an effective catalyst for a wide range of reactions, including polymerization, oxidation, and reduction processes.
Used in Conductive Films Industry:
In the conductive films industry, DAB-AM-4 is used as a component in the development of conductive polymer films. Its ability to form stable complexes with conductive materials, such as metals or conductive polymers, can enhance the electrical conductivity and performance of these films.
Used in Surfactants Industry:
DAB-AM-4 is used as a surfactant or surfactant additive in the formulation of various cleaning and personal care products. Its amphiphilic nature and ability to form micelles make it an effective agent for stabilizing emulsions, reducing surface tension, and enhancing the cleaning properties of these products.
Used in Controlled Release Industry:
In the controlled release industry, DAB-AM-4, POLYPROPYLENIMINE TETRAAMINE DENDRIMER, GENERATION 1.0 is used as a carrier or delivery system for the controlled release of active ingredients, such as drugs, fragrances, or agrochemicals. Its high solubility and ability to form stable complexes with other molecules allow for the precise and sustained release of these active ingredients over time.
Used in Medical Diagnostics Industry:
DAB-AM-4 is used in the medical diagnostics industry as a component in the development of diagnostic tools and assays. Its versatile properties, such as high solubility and biocompatibility, make it an ideal candidate for the development of novel diagnostic platforms, including immunoassays, molecular diagnostics, and biosensors.

Check Digit Verification of cas no

The CAS Registry Mumber 120239-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120239-63:
(8*1)+(7*2)+(6*0)+(5*2)+(4*3)+(3*9)+(2*6)+(1*3)=86
86 % 10 = 6
So 120239-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H40N6/c17-7-3-13-21(14-4-8-18)11-1-2-12-22(15-5-9-19)16-6-10-20/h1-20H2

120239-63-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N,N',N'-tetrakis(3-aminopropyl)butane-1,4-diamine

1.2 Other means of identification

Product number -
Other names DAB-Am-4,Polypropylenimine tetramine dendrimer,generation 1

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120239-63-6 SDS

120239-63-6Upstream product

120239-63-6Relevant articles and documents

Influence of the distance between ionizable groups on the protonation behavior of various hexaamines

Van Duijvenbode, Rene C.,Rajanayagam, Anton,Koper, Ger J.M.,Borkovec, Michal,Paulus, Wolfgang,Steuerle, Ulrich,Haeussling, Lukas

, p. 5649 - 5652 (1999)

A synthesis route for N,N,N',N'-tetraaminoethyl-1,2-ethylenediamine, N,N,N',N'-tetraaminopropyl-1,2-ethylenediamine, N,N,N',N'-tetraaminopropyl- 1,3-propylenediamine and N,N,N',N'-tetraaminopropyl-1,4-butylenediamine is presented. These molecules differ from each other in the number of carbon atoms between the six amino groups. This results in different protonation behavior. Potentiometric titrations are performed in 0.1 M and 1.0 M KCl, and the six macroscopic protonation constants are obtained from these curves. An Ising model with a limited number of microscopic protonation constants and short-ranged pair interactions describes the protonation behavior quantitatively. The results are compared to those of other, similar molecules. The advantage of the Ising model over empirical relations such as the Taft equations is the more systematic approach with which the titration curves of more complex molecules can be described. The values for the Ising model parameters obtained here can be used to predict the protonation behavior of more complex, in particular larger, polyamines.

pyrrole Shalom intermediates

-

Paragraph 0059; 0060; 0061; 0062; 0063; 0064-0072, (2017/07/23)

The invention particularly relates to an amine phosphate binder bixalomer intermediate and a preparation method thereof. The preparation method comprises the following steps: reacting a raw material 3,3'-diamidodipropyl amine under the action of benzyl chloroformate to obtain 3,3'-dibenzyloxyamidodipropyl amine, carrying out substitution reaction on the 3,3'-dibenzyloxyamidodipropyl amine and 1,4-dibromobutane or 1,4-dichlorobutane to obtain N,N,N',N'-tetra(3-dibenzyloxyamido)-1,4-butanediamine, and carrying out deprotection by pressure hydrogenation under the action of Pd-C to obtain N,N,N',N'-tetra(3-aminopropyl)-1,4-butanediamine. The method has the advantages of cheap and accessible raw materials, operable reaction, high yield and fewer three wastes, and thus, has excellent industrial prospects.

Nano polypropylenimine dendrimer (DAB-PPI-G1): As a novel nano basic-polymer catalyst for one-pot synthesis of 2-amino-2-chromene derivatives

Maleki, Behrooz,Sheikh, Safoora

, p. 42997 - 43005 (2015/05/27)

The nano polypropylenimine dendrimer (DAB-PPI-G1) Lewis base catalyst was found to be a highly efficient and recoverable catalyst for the rapid and convenient synthesis of 2-amino-2-chromene derivatives through the three-component condensation of aromatic aldehydes, malononitrile or ethyl cyanoacetate and phenols under solvent-free conditions in excellent yields and short reaction times.

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