Ethylenediamine, 99%, Thermo Scientific Chemicals
Ethylenediamine, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Ethylenediamine, 99%, Thermo Scientific Chemicals

Strongly basic amine useful as a building block in chemical synthesis
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2500 mL
Catalog number A12132.AP
also known as A12132-AP
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Quantity:
500 mL
Request bulk or custom format
Price (USD)/ Each
33.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
39.90 
Save 6.25 (16%)
Add to cart
Ethylenediamine, 99%, Thermo Scientific Chemicals
Catalog numberA12132.AP
Price (USD)/ Each
33.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
39.90 
Save 6.25 (16%)
-
Add to cart
Chemical Identifiers
CAS107-15-3
IUPAC Nameethane-1,2-diamine
Molecular FormulaC2H8N2
InChI KeyPIICEJLVQHRZGT-UHFFFAOYSA-N
SMILESNCCN
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
Identification (FTIR)Conforms
FormLiquid
Water Content≤0.5% (U.S. specification)
Assay (GC)≥98.5%
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Ethylenediamine is a strongly basic amine useful as a building block in chemical synthesis. It is used as a solvent to dissolve proteins such as albumins and casein. It is widely used for color photography developers, binders, adhesives, fabric softeners, curing agents for epoxys and dyes. As a corrosion inhibitor, it plays a vital role in paints and coolants. It is used as an intermediate in the preparation of polyamide resins, fuel additives and lubricants. It acts as a precursor for many polymers like polyurethane fibers and poly(amidoamine), ethylenediamine dihydroiodide (EDDI) as well as the bleaching activator, tetraacetylethylenediamine. It is an important chelating ligand used in the preparation of coordination compounds viz. tris(ethylenediamine)cobalt(III) chloride. It is also involved in the manufacture of many industrial chemicals and forms derivatives with carboxylic acids, nitriles, alcohols, alkylating agents, carbon disulfide, aldehydes and ketones. It is a basic building block to prepare heterocyclic compound such as imidazolidines.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Ethylenediamine is a strongly basic amine useful as a building block in chemical synthesis. It is used as a solvent to dissolve proteins such as albumins and casein. It is widely used for color photography developers, binders, adhesives, fabric softeners, curing agents for epoxys and dyes. As a corrosion inhibitor, it plays a vital role in paints and coolants. It is used as an intermediate in the preparation of polyamide resins, fuel additives and lubricants. It acts as a precursor for many polymers like polyurethane fibers and poly(amidoamine), ethylenediamine dihydroiodide (EDDI) as well as the bleaching activator, tetraacetylethylenediamine. It is an important chelating ligand used in the preparation of coordination compounds viz. tris(ethylenediamine)cobalt(III) chloride. It is also involved in the manufacture of many industrial chemicals and forms derivatives with carboxylic acids, nitriles, alcohols, alkylating agents, carbon disulfide, aldehydes and ketones. It is a basic building block to prepare heterocyclic compound such as imidazolidines.

Notes
Air and moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with oxidizing agents, phosphorus halides, aldehydes and organic halides.
RUO – Research Use Only

General References:

  1. The Li derivative in excess amine is a strong base for the rearrangement of primary allylic alcohols to the isomeric aldehydes in high yield: J. Chem. Soc., Chem. Commun., 812 (1985).
  2. At high temperatures, reduces nitroarenes to azo-compounds. Reaction does not occur for nitro-compounds with o-substituents or p-amino-substituents: J. Org. Chem., 49, 1215 (1984).
  3. The ethylenediamine complex of Cr2+ reduces aryl bromides to the hydrocarbons. For an example, see: Org. Synth. Coll., 6, 821 (1988).
  4. Xue, B.; Zhu, J.; Liu, N.; Li, Y. Facile functionalization of graphene oxide with ethylenediamine as a solid base catalyst for Knoevenagel condensation reaction. Catal. Commun. 2015, 64, 105-109.
  5. Moradpour, A.; Ghaffarinejad, A.; Maleki, A.; Eskandarpour, V.; Motaharian, A. Low loaded palladium nanoparticles on ethylenediamine-functionalized cellulose as an efficient catalyst for electrochemical hydrogen production. RSC Adv. 2015, 5 (86), 70668-70674.