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Key Documents

391085

Sigma-Aldrich

Etilenodiamina

purified by redistillation, ≥99.5%

Sinônimo(s):

1,2-Diaminoetano

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About This Item

Fórmula linear:
NH2CH2CH2NH2
Número CAS:
Peso molecular:
60.10
Beilstein:
605263
Número CE:
Número MDL:
Código UNSPSC:
12352100
eCl@ss:
39030201
ID de substância PubChem:
NACRES:
NA.22

densidade de vapor

2.07 (vs air)

Nível de qualidade

pressão de vapor

10 mmHg ( 20 °C)

Ensaio

≥99.5%

forma

liquid

temperatura de autoignição

716 °F

purificado por

redistillation

Lim. expl.

16 %

índice de refração

n20/D 1.4565 (lit.)

pH

12.2 (20 °C, 110 g/L)

pb

118 °C (lit.)

pf

8.5 °C (lit.)

solubilidade

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

densidade

0.899 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

NCCN

InChI

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

chave InChI

PIICEJLVQHRZGT-UHFFFAOYSA-N

Informações sobre genes

human ... FNTA(2339)

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Descrição geral

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.

Aplicação

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.

Palavra indicadora

Danger

Classificações de perigo

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

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

100.4 °F - closed cup

Ponto de fulgor (°C)

38 °C - closed cup

Equipamento de proteção individual

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


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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)
S T Ong et al.
Bioresource technology, 98(15), 2792-2799 (2007-04-03)
Wastewaters from textile industries may contain a variety of dyes that have to be removed before their discharge into waterways. Rice hull, an agricultural by-product, was modified using ethylenediamine to introduce active sites on its surface to enable it to
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

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