Skip to Content
Merck
CN

391085

Ethylenediamine

purified by redistillation, ≥99.5%

Synonym(s):

1,2-Diaminoethane

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
NH2CH2CH2NH2
CAS Number:
Molecular Weight:
60.10
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39030201
UNSPSC Code:
12352100
EC Number:
203-468-6
MDL number:
Beilstein/REAXYS Number:
605263
Assay:
≥99.5%
Bp:
118 °C (lit.)
Vapor pressure:
10 mmHg ( 20 °C)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


vapor density

2.07 (vs air)

Quality Level

vapor pressure

10 mmHg ( 20 °C)

assay

≥99.5%

form

liquid

autoignition temp.

716 °F

purified by

redistillation

expl. lim.

16 %

refractive index

n20/D 1.4565 (lit.)

pH

12.2 (20 °C, 110 g/L)

bp

118 °C (lit.)

mp

8.5 °C (lit.)

solubility

ethanol: soluble(lit.), water: miscible(lit.), water: very soluble(lit.)

density

0.899 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

NCCN

InChI

1S/C2H8N2/c3-1-2-4/h1-4H2

InChI key

PIICEJLVQHRZGT-UHFFFAOYSA-N

Gene Information

human ... FNTA(2339)

General description

Ethylenediamine (en) is a linear aliphatic diamine. The synthesis of ethylenediamine has been reported. Its effect as an allergen has been investigated. It participates in the synthesis of metal chalcogenides and thiogallates.

Application

Ethylenediamine (en) is suitable for use in the synthesis of covalently linked adducts of deoxyribonucleic acid (DNA) oligonucleotides with single-walled carbon nanotubes. It may be used in the following studies:
  • Functionalization of the triazolate-bridged metal-organic framework.
  • As a solvent in the synthesis of ZnS and ZnSe precursors by solvothermal process.
  • As a softening agent for hard wood plant structure.
  • As a reactant in the synthesis of Pd/C-ethylenediamine complex catalyst.
  • As a chelating agent in the synthesis of β-Co(OH)2 nanocrystals.
  • To produce ethylenediamine modified rice hull, used as a sorbent for basic and reactive dyes.
  • Synthesis of ethylenediamine-templated iron arsenates and fluoroarsenates.
  • As a template agent and coordination agent in the synthesis of CdS nanocrystals.
  • As a reagent in the synthesis of imidazolines.


Still not finding the right product?

Explore all of our products under Ethylenediamine


signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Resp. Sens. 1B - Skin Corr. 1B - Skin Sens. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

100.4 °F - closed cup

flash_point_c

38 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

易制爆化学品
危险化学品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



Covalently bonded adducts of deoxyribonucleic acid (DNA) oligonucleotides with single-wall carbon nanotubes: synthesis and hybridization.
Baker SE, et al.
Nano Letters, 2(12), 1413-1417 (2002)
Reactions of some ortho and para halogenated aromatic nitriles with ethylenediamine: selective synthesis of imidazolines.
Crane LJ, et al.
Tetrahedron, 60(25), 5325-5330 (2004)
The use of ethylenediamine in softening hard plant structures for paraffin sectioning.
Carlquist, S.
Biotechnic & Histochemistry, 57(5), 311-317 (1982)



Global Trade Item Number

SKUGTIN
391085-100ML04061831973150
391085-1L04061831973419