Direkt zum Inhalt
Merck

E26266

Sigma-Aldrich

Ethylendiamin

ReagentPlus®, ≥99%

Synonym(e):

1,2-Diaminoethan

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise


About This Item

Lineare Formel:
NH2CH2CH2NH2
CAS-Nummer:
Molekulargewicht:
60.10
Beilstein:
605263
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
eCl@ss:
39030201
PubChem Substanz-ID:
NACRES:
NA.21

Agentur

suitable for EPA 300

Qualitätsniveau

Dampfdichte

2.07 (vs air)

Dampfdruck

10 mmHg ( 20 °C)

Produktlinie

ReagentPlus®

Assay

≥99%

Form

liquid

Selbstzündungstemp.

716 °F

Expl.-Gr.

16 %

Brechungsindex

n20/D 1.4565 (lit.)

bp

118 °C (lit.)

mp (Schmelzpunkt)

8.5 °C (lit.)

Löslichkeit

H2O: soluble at 

Dichte

0.899 g/mL at 25 °C (lit.)

Funktionelle Gruppe

amine

SMILES String

NCCN

InChI

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

InChIKey

PIICEJLVQHRZGT-UHFFFAOYSA-N

Angaben zum Gen

human ... FNTA(2339)

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Allgemeine Beschreibung

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

Anwendung

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.
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.
  • DAE/Li complex is used as an efficient reagent for the reduction of alkenes, aromatic hydrocarbons, phenols, and alcohols.

Ethylenediamine (en) has been used in the following process:
  • Synthesis of nucleus pulposus (NP)-like collagen-glycosaminoglycans (CG) core.
  • Surface modification of epoxy-activated cryogel.
  • Alteration of the surface of carbon nanoparticles (CNPs) to generate CNPs-ethylene.
It may be used in the following studies:
  • Surface modification of triazolate-bridged metal-organic framework.
  • As a solvent in the synthesis of ZnS (zinc sulfide) and ZnSe (zinc selenium) precursors by solvothermal process.
  • 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.
  • Synthesis of ethylenediamine-templated iron arsenates and fluoroarsenates.
  • As a template agent and coordination agent in the synthesis of CdS (cadmium sulfide) nanocrystals.

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

100.4 °F - closed cup

Flammpunkt (°C)

38 °C - closed cup

Persönliche Schutzausrüstung

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


Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

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
1, 2-Diaminoethane
Kostikov RR
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
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
S D Prystowsky et al.
Archives of dermatology, 115(8), 959-962 (1979-08-01)
A study population of 1,158 paid adult volunteers was obtained. Prior to patch testing, a history of previous exposure to four allergens also was obtained. Prevalence of positive reactions to patch tests was nickel, 5.8%; neomycin, 1.1%; ethylenediamine, 0.43%; and

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.