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3,6,9,12,15-Pentaazaheptadecane-1,17-diamine is a complex polyamine compound characterized by its long molecular structure and multiple amine (-NH2) groups. It is known for its unique properties and versatility in creating molecular architectures with specific functions.

4403-32-1

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4403-32-1 Usage

Uses

Used in Chemical and Industrial Applications:
3,6,9,12,15-Pentaazaheptadecane-1,17-diamine is used as a chelating agent for metal ion extraction, leveraging its ability to form stable complexes with metal ions.
3,6,9,12,15-Pentaazaheptadecane-1,17-diamine is also used as a catalyst in organic synthesis, where its amine groups facilitate various chemical reactions, enhancing the efficiency and selectivity of the processes.
Used in Research and Development:
In the field of research and development, 3,6,9,12,15-Pentaazaheptadecane-1,17-diamine serves as a versatile building block for designing new materials and products with tailored properties and functions, thanks to its unique structure and multiple amine groups.

Check Digit Verification of cas no

The CAS Registry Mumber 4403-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4403-32:
(6*4)+(5*4)+(4*0)+(3*3)+(2*3)+(1*2)=61
61 % 10 = 1
So 4403-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H33N7/c13-1-3-15-5-7-17-9-11-19-12-10-18-8-6-16-4-2-14/h15-19H,1-14H2

4403-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-[2-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethylamino]ethyl]ethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names 3,6,9,12,15-Pentaazaheptadecane-1,17-diamine

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:4403-32-1 SDS

4403-32-1Upstream product

4403-32-1Downstream Products

4403-32-1Relevant academic research and scientific papers

Tailored synthetic polyamines for controlled biomimetic silica formation

Bernecker, Anja,Wieneke, Ralph,Riedel, Radostan,Seibt, Michael,Geyer, Armin,Steinem, Claudia

, p. 1023 - 1031 (2010)

Organic compounds isolated from diatoms contain long-chain polyamines with a propylamine backbone and variable methylation levels and chain lengths. These long-chain polyamines are thought to be one of the important classes of molecules that are responsible for the formation of the hierarchically structured silica-based cell walls of diatoms. Here we describe a synthetic route based on solid-phase peptide synthesis from which well-defined long-chain polyamines with different chain lengths, methylation patterns, and subunits can be obtained. Quantitative silica precipitation experiments together with structural information about the precipitated silica structures gained by scanning and transmission electron microscopy revealed a distinct dependence of the amount, size, and form of the silica precipitates on the molecular structure of the polyamine. Moreover, the influence of the phosphate concentration was elucidated, revealing the importance of divalent anions for the precipitation procedure. We were able to derive further insights into the precipitation properties of long-chain polyamines as functions of their hydrophobicity, protonation state, and phosphate concentration, which may pave the way for better control of the formation of nanostructured silica under ambient conditions.

Decolorization of polyalkylene polyamines

-

, (2008/06/13)

A process for decolorizing polyalkylene polyamines, which comprises contacting one or more polyalkylene polyamines having an average molecular weight of greater than about 200 and less than about 1000 with carbon at a temperature greater than or equal to about 100° C. and less than or equal to about 300° C. under conditions effective to reduce the color rating of the one or more polyalkylene polyamines.

Process for the dyeing of leather with anionic dyes and polyaminoamide resin as dyeing auxiliary

-

, (2008/06/13)

To improve the affinity of anionic dyestuffs in the dyeing of leather materials, polycondensation products consisting of at least one amine of the formula STR1 in which the radicals have the meanings mentioned in the description with one dicarboxylic acid and, if desired, ω-aminocarboxylic acid or its lactam are highly suitable.

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