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1,3-Propanediamine, 2,2-bis(aminomethyl)-, tetrahydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14302-75-1

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14302-75-1 Usage

Common Uses

Crosslinking agent in epoxy resins and adhesives
Manufacturing of pharmaceuticals
Production of dyes
Textile chemicals

Salt Form

Tetrahydrochloride

Stability

More stable than the free base form

Ease of Handling

Easier to handle due to tetrahydrochloride salt form

Applications

Widely used in various industries and research laboratories

Chemical Structure

A triamine compound with two amine groups connected to a propane chain and an additional amine group on each of the propane's terminal carbons

Solubility

Soluble in water and polar solvents due to its ionic nature

Reactivity

Can react with epoxy resins to form crosslinked polymers

Safety Precautions

Handle with care due to potential irritant and corrosive properties; use appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats.

Check Digit Verification of cas no

The CAS Registry Mumber 14302-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,0 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14302-75:
(7*1)+(6*4)+(5*3)+(4*0)+(3*2)+(2*7)+(1*5)=71
71 % 10 = 1
So 14302-75-1 is a valid CAS Registry Number.

14302-75-1SDS

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 1,1,1,1-tetrakis(2-aminomethyl)methane tetrahydrochloride

1.2 Other means of identification

Product number -
Other names tetrakis(aminomethyl)methane tetrahydrochloride

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:14302-75-1 SDS

14302-75-1Relevant academic research and scientific papers

Multiple metal coordinating behaviour of the tetrapodal ligand 1,1,1,1-tetrakis[(salicylaldimino)methyl]methane

Dutta, Supriya,Biswas, Papu,Fl?rke, Ulrich,Nag, Kamalaksha

, p. 1074 - 1080 (2010)

The tetrapodal ligand 1,1,1,1-tetrakis[(salicylaldimino)methyl]methane (H4tsam) has been introduced for the first time for metal complexation. Two zinc(II) complexes[Zn2(tsam)] (1) and [Zn 3(Htsam)2]?2C7H8 (2) have been obtained by reacting zinc acetylacetonate with the ligand in the presence of triethylamine, while a cobalt(III) complex [Co(Htsam)]?CH 3CN?H2O (3) is obtained when Co(ClO4) 2?6H2O is reacted in air. All the compounds have been characterized by their elemental analyses and ESI-MS, IR, UV-VIS and 1H NMR spectra. The X-ray crystal structures of H4tsam, 2 and 3 have been determined. Compounds 1 and 2 exhibit fluorescence in solution and the lifetimes of their luminescence decay have been measured. Thermal analysis (TGA, DTA) of 2 with regard to loss of encapsulated toluenes and redox behaviour of 3 have been studied.

An efficient synthesis of D-galactose-based multivalent neoglycoconjugates

De Andrade, Saulo F.,Figueiredo, Rute C.,De Souza Filho, Jose? D.,Alves, Ricardo J.

experimental part, p. 1062 - 1069 (2012/09/10)

In this work, the synthesis of dimeric, trimeric and tetrameric D-galactose-based neoglycoconjugates is reported. The monosaccharide ligand was prepared in 5 straightforward steps from D-galactose using the Doebner modification of the Knoevenagel reaction for chain elongation. The ligand was coupled to 1,4-butanediamine, tris-(2-ethylamino)amine, pentaerythrityltetramine and PAMAM dendrimers (1,4-butanodiamine core G0 and 1,12-dodecanediamine core G0). The unprotected glycodendrimers were purified by size-exclusion chromatography (SEC). This was the only step in which a chromatographic method was employed throughout the synthetic route. This is a new and efficient strategy for the preparation of neoglycoconjugates.

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