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13531-52-7

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13531-52-7 Usage

Description

N-(2-Aminoethyl)-1,3-propanediamine, also known as Aminoethylpropylenimine, is an organic compound with the chemical formula C5H15N3. It is a clear liquid and is characterized by its amine functional groups, which contribute to its chemical reactivity and various applications in different industries.

Uses

Used in Chemical Synthesis:
N-(2-Aminoethyl)-1,3-propanediamine is used as a templating agent for the synthesis of new open framework iron(III) phosphite, (C5H18N3)[Fe3(HPO3)6].3H2O. Its role in this application is to guide the formation of the desired crystal structure, which is crucial for the material's properties and potential uses.
Used in Coordination Chemistry:
In coordination chemistry, N-(2-Aminoethyl)-1,3-propanediamine is used in the preparation of dinitrocobalt(III) compound: (11-amino-4-methyl-5,8-diazaundeca-2,4-dien-2-olato-kappa4N(5,8,11),O)-dinitrocobalt(III), [Co(C10H20N3O)(NO2)2]. The compound serves as a ligand, coordinating to the metal center and influencing the compound's stability, reactivity, and potential applications.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, N-(2-Aminoethyl)-1,3-propanediamine, due to its amine functional groups, could potentially be used in the pharmaceutical industry for the synthesis of various drugs, particularly those requiring amine-containing moieties.
Used in Material Science:
Given its ability to act as a templating agent, N-(2-Aminoethyl)-1,3-propanediamine could also find applications in material science, particularly in the development of new materials with specific properties and structures. Its use in the synthesis of metal-organic frameworks (MOFs) or other coordination polymers could lead to advancements in areas such as gas storage, catalysis, and sensing.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 13531-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13531-52:
(7*1)+(6*3)+(5*5)+(4*3)+(3*1)+(2*5)+(1*2)=77
77 % 10 = 7
So 13531-52-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H15N3/c6-2-1-4-8-5-3-7/h8H,1-7H2/p+3

13531-52-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A19108)  3-(2-Aminoethylamino)propylamine, 97%   

  • 13531-52-7

  • 2.5g

  • 421.0CNY

  • Detail
  • Alfa Aesar

  • (A19108)  3-(2-Aminoethylamino)propylamine, 97%   

  • 13531-52-7

  • 10g

  • 1362.0CNY

  • Detail
  • Aldrich

  • (127159)  N-(2-Aminoethyl)-1,3-propanediamine  97%

  • 13531-52-7

  • 127159-25G

  • 460.98CNY

  • Detail

13531-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-AMINOETHYL)-1,3-PROPANEDIAMINE

1.2 Other means of identification

Product number -
Other names 3-azahexane-1,6-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:13531-52-7 SDS

13531-52-7Relevant articles and documents

Synthesis of aminoethyl derivatives of alpha, omega-alkylenediamines and structure-activity relationships for the polyamine-bovine plasma amine oxidase system.

Israel,Modest

, p. 1042 - 1047 (1971)

-

TRANSAMINATION OF NITROGEN-CONTAINING COMPOUNDS TO MAKE CYCLIC AND CYCLIC/ACYCLIC POLYAMINE MIXTURES

-

Page/Page column 18-20, (2012/05/31)

A transamination process is described to prepare polyamine product mixtures from reactants comprising mixed nitrogen-containing compounds with binary carbon spacing between nitrogen-containing groups (a binary component). A second nitrogen-containing component with a second carbon atom spacing between nitrogen-containing groups may also be employed. The molar ratio between the binary and second components can be adjusted to customize the product composition for desired end uses.

First unequivocal synthesis of 1 or 8-N-monosubstituted 1,4,8,12-tetraazacyclopentadecane

Granier, Colin,Guilard, Roger

, p. 1197 - 1208 (2007/10/02)

A novel method derived from Kaden's modification of the Richman and Atkins's cyclization using tosylated synthons allows the unequivocal synthesis of 1 and 8-monofunctionalized 1,4,8,12-tetraazacyclo-pentadecane. Both syntheses are described.

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