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123-12-6

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123-12-6 Usage

Description

N,N,N',N'-Tetraethyldiethylenetriamine (TEDETA) is an N-substituted ethylenediamine ligand characterized by its specific boiling point, density, and refractive index. It is a versatile compound with a wide range of applications across different industries due to its unique chemical properties.

Uses

Used in Chemical Synthesis:
TEDETA is used as a reagent in various chemical synthesis processes for creating complex molecules and compounds. Its ability to act as a ligand allows it to form stable complexes with metal ions, which is crucial in the synthesis of various coordination compounds.
Used in Pharmaceutical Industry:
N,N,N',N'-Tetraethyldiethylenetriamine is used as an N-substituted ethylenediamine ligand for the synthesis of [Ni(Et4dien)(NO2)2] (Et4dien=N,N,N′,N′-tetraethyldiethylenetriamine). N,N,N',N'-TETRAETHYLDIETHYLENETRIAMINE has potential applications in the pharmaceutical industry, particularly in the development of new drugs and therapies.
Used in Material Science:
In the field of material science, TEDETA is used as a reagent in the synthesis of adamantanyl connector, aminated macroligand, and precipiton ligand. These synthesized compounds can be utilized in the development of advanced materials with specific properties, such as improved mechanical strength, thermal stability, or chemical resistance.
Used in Environmental Applications:
TEDETA is used as a multimodal ligand in the synthesis of P(S-DVB)-g-P(S-GMA)-TEDETA beads (poly(styrene-divinylbenzene)-graft-poly(styrene-glycidylmethacrylate)). These beads can be employed in environmental applications, such as water treatment and pollution control, due to their ability to selectively bind and remove contaminants from various sources.
Used in Research and Development:
Due to its unique chemical properties and versatility, TEDETA is also used in research and development for the creation of new compounds and materials. It serves as a valuable tool for scientists and researchers in exploring new avenues and applications in various fields, including pharmaceuticals, material science, and environmental science.

Safety Profile

Poison by intravenous route.When heated to decomposition it emits toxic fumes ofNOx.

Check Digit Verification of cas no

The CAS Registry Mumber 123-12-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123-12:
(5*1)+(4*2)+(3*3)+(2*1)+(1*2)=26
26 % 10 = 6
So 123-12-6 is a valid CAS Registry Number.

123-12-6 Well-known Company Product Price

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  • Aldrich

  • (424072)  N,N,N′,N′-Tetraethyldiethylenetriamine  technical grade, 90%

  • 123-12-6

  • 424072-5ML

  • 819.00CNY

  • Detail
  • Aldrich

  • (424072)  N,N,N′,N′-Tetraethyldiethylenetriamine  technical grade, 90%

  • 123-12-6

  • 424072-25ML

  • 3,006.90CNY

  • Detail

123-12-6SDS

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-[2-(diethylamino)ethyl]-N',N'-diethylethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names 1,1,7,7-tetraethyldiethylene triamine

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:123-12-6 SDS

123-12-6Relevant articles and documents

Evidence for a Strong Labilization Effect by Co-ordinated Sulphite in Amine Complexes of Palladium(II)

Mahal, G.,Eldik, R. van

, p. 328 - 330 (1987)

Acidification of a chelated amine sulphito complex of palladium(II) to pH 8) and reproduces the amine sulphito complex.

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