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E26266

Sigma-Aldrich

Ethylenediamine

Ethylenediamine

ReagentPlus®, ≥99%

Sinónimos:

1,2-Diaminoethane

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5 ML
$42.70
100 ML
$53.70
1 L
$57.07
2.5 L
$159.00
4 X 100 ML
$138.68

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5 ML
$42.70
100 ML
$53.70
1 L
$57.07
2.5 L
$159.00
4 X 100 ML
$138.68

About This Item

Fórmula lineal:
NH2CH2CH2NH2
Número de CAS:
107-15-3
Peso molecular:
60.10
Beilstein/REAXYS Number:
605263
EC Number:
203-468-6
MDL number:
MFCD00008204
UNSPSC Code:
12352100
eCl@ss:
39030201
PubChem Substance ID:
24894477
NACRES:
NA.21

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agency

suitable for EPA 300

Quality Level

200

vapor density

2.07 (vs air)

vapor pressure

10 mmHg ( 20 °C)

product line

ReagentPlus®

assay

≥99%

form

liquid

autoignition temp.

716 °F

expl. lim.

16 %

refractive index

n20/D 1.4565 (lit.)

bp

118 °C (lit.)

mp

8.5 °C (lit.)

solubility

H2O: soluble at 

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)

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General description

Ethylenediamine (en) is a linear aliphatic diamine that can be synthesized by reacting ethanolamine and ammonia in the presence of zeolite catalyst.[1] Its effect as an allergen has been investigated.[2] It participates in the synthesis of metal chalcogenides[3] and thiogallates.[4]

Application

Ethylenediamine (1,2-Diaminoethane, DAE) can be used as a reagent to prepare various metal ion complexes. For instance, DAE reacts with chromium(II) salts forms a Cr(II)/DAE complex, which is used as an efficient reducing agent for the reduction of primary alkyl halides to alkanes, and aryl bromides or iodides to arenes. This complex is also used to reduce β-substituted alkyl halides and epoxides to alkenes.[5]
DAE can also be used in the following reduction reactions:
  • DAE/Borane (1:1) complex is used as a highly selective reducing agent for the conversion of cinnamaldehyde to cinnamyl alcohol.[5]
  • DAE/Li complex is used as an efficient reagent for the reduction of alkenes, aromatic hydrocarbons, phenols, and alcohols.[5]

Ethylenediamine (en) has been used in the following process:
  • Synthesis of nucleus pulposus (NP)-like collagen-glycosaminoglycans (CG) core.[6]
  • Surface modification of epoxy-activated cryogel.[7]
  • Alteration of the surface of carbon nanoparticles (CNPs) to generate CNPs-ethylene.[8]
It may be used in the following studies:
  • Surface modification of triazolate-bridged metal-organic framework.[9]
  • As a solvent in the synthesis of ZnS (zinc sulfide) and ZnSe (zinc selenium) precursors by solvothermal process.[10]
  • As a reactant in the synthesis of Pd/C-ethylenediamine complex catalyst.[11]
  • As a chelating agent in the synthesis of β-Co(OH)2 nanocrystals.[12]
  • Synthesis of ethylenediamine-templated iron arsenates and fluoroarsenates.[13]
  • As a template agent and coordination agent in the synthesis of CdS (cadmium sulfide) nanocrystals.[14]

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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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_germany

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

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Certificados de análisis (COA)

Lot/Batch Number
SDBB2268
SDBB0409
STBL2397
STBL0978
STBK9716

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1, 2-Diaminoethane
Kostikov RR
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
Aude Demessence et al.
Journal of the American Chemical Society, 131(25), 8784-8786 (2009-06-10)
Reaction of CuCl(2) x 2 H(2)O with 1,3,5-tris(1H-1,2,3-triazol-5-yl)benzene (H(3)BTTri) in DMF at 100 degrees C generates the metal-organic framework H(3)[(Cu(4)Cl)(3)(BTTri)(8)(DMF)(12)] x 7 DMF x 76 H(2)O (1-DMF). The sodalite-type structure of the framework consists of BTTri(3-)-linked [Cu(4)Cl](7+) square clusters in
Synthesis of CdS nanorods by an ethylenediamine assisted hydrothermal method for photocatalytic hydrogen evolution.
Li Y, et al.
The Journal of Physical Chemistry C, 113(21), 9352-9358 (2009)
S Ekambaram et al.
Inorganic chemistry, 39(11), 2405-2410 (2003-01-16)
Four new ethylenediamine-templated iron arsenates and fluoroarsenates have been hydrothermally synthesized from iron metal, hydrofluoric and arsenic acids, and ethylenediamine. Fe(H2AsO4)(HAsO4)2.enH2.H2O (1) is one-dimensional and contains chains, FeIIIFeIIF2(HAsO4)(AsO4).enH2.2H2O (2) is a layered fluoroarsenate, and Fe3(HAsO4)6.enH2.NH3.NH4 (3) and Fe2F2(AsO4)2(H2O).enH2 (4) are
The formation of a novel Pd/C-ethylenediamine complex catalyst: chemoselective hydrogenation without deprotection of the O-benzyl and N-Cbz groups.
Sajiki H, et al.
The Journal of Organic Chemistry, 63(22), 7990-7992 (1998)
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    1. Products may be shipped at a different temperature than the recommended long-term storage temperature. If the product quality is sensitive to short-term exposure to conditions other than the recommended long-term storage, it will be shipped on wet or dry-ice. If the product quality is NOT affected by short-term exposure to conditions other than the recommended long-term storage, it will be shipped at ambient temperature. As shipping routes are configured for minimum transit times, shipping at ambient temperature helps control shipping costs for our customers. For more information, please refer to the Storage and Transport Conditions document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/316/622/storage-transport-conditions-mk.pdf

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    1. If this product has an expiration or retest date, it will be shown on the Certificate of Analysis (COA, CofA). If there is no retest or expiration date listed on the product's COA, we do not have suitable stability data to determine a shelf life. For these products, the only date on the COA will be the release date; a retest, expiration, or use-by-date will not be displayed.
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  3. The concentration of the solution

    1 answer

    1. This product is a neat or pure liquid with a reported density of 0.899 g/mL and a molecular weight of 60.10 g/mol. Assuming a 99.9% purity, the concentration is approximately 14.94 M. The molarity may be determined using the molecular weight, density, and lot specific purity as demonstrated in the calculation below:
      (Density x 1000 x w/w% / Molecular Weight)

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  1. Columbia, MO
    • Reviews 4
    • Votes 0
    5 out of 5 stars.

    Good chemical reagent

    Sigma is known for its high quality of chemical and biochemical reagents, and this is no exception.

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  2. 2 Ratings-Only Reviews

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