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Key Documents

N9125

Sigma-Aldrich

N-(1-Naphthyl)ethylenediamine dihydrochloride

≥98%

Synonym(s):

2-(1-Naphthylamino)ethylamine dihydrochloride

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About This Item

Linear Formula:
C10H7NHCH2CH2NH2 · 2HCl
CAS Number:
Molecular Weight:
259.17
Beilstein:
3707471
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98%

form

powder

mp

194-198 °C (dec.) (lit.)

SMILES string

Cl.Cl.NCCNc1cccc2ccccc12

InChI

1S/C12H14N2.2ClH/c13-8-9-14-12-7-3-5-10-4-1-2-6-11(10)12;;/h1-7,14H,8-9,13H2;2*1H

InChI key

MZNYWPRCVDMOJG-UHFFFAOYSA-N

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Application

N-(1-Naphthyl)ethylenediamine dihydrochloride can be used as a reactant to synthesize:      
  • N


  • -(1-naphthyl)ethylenediamine-substituted cylotriphosphazene derivatives as potential antimicrobial agents.    
  • Fluorescent chemosensor compound with a naphthyl group as fluorophore and cyclen as metal ion chelator for the detection of Zn(II) in an aqueous solution.    
  • (N-1-Naphthyl-ethylenediamine)- dichloroplatinum(II) fluorescence complex (λmax = 405 nm).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Improved dye procedure for determining urea concentration by using o-phthalaldehyde and naphthylethylenediamine.
N T Lequang et al.
Clinical chemistry, 33(1), 192-192 (1987-01-01)
P K Laikind et al.
Analytical biochemistry, 156(1), 81-90 (1986-07-01)
The Bratton-Marshall reaction can be used to identify patients with adenylosuccinate lyase deficiency. These patients excrete in their urine the dephosphorylated derivative of the de novo purine synthesis intermediate 5'-phosphoribosyl-4-(N-succinylcarboxamide)-5-aminoimidazole (SAICAR). The test described here depends on a coupling reaction
C E Davis et al.
Journal - Association of Official Analytical Chemists, 68(3), 485-488 (1985-05-01)
Current methods used for determining residual nitrite concentration in foods involve forming an azo dye that is measured spectrophotometrically. Conventional procedures do not specify control of pH for the final colored solution. Because many indicator dyes are pH-dependent, absorbance of
Shigenori Nakano et al.
Talanta, 81(3), 786-791 (2010-03-20)
A novel flow-injection spectrophotometry has been developed for the determination of molybdenum(VI) at nanograms per milliliter levels. The method is based on the catalytic effect of molybdenum(VI) on the bromate oxidative coupling of p-hydrazinobenzenesulfonic acid with N-(1-naphthyl)ethylenediamine to form an
R K Goldman et al.
Analytical biochemistry, 259(1), 98-103 (1998-05-30)
A high-pressure liquid chromatography (HPLC) assay for measuring picomole quantities of nitrosothiol in biological samples was developed. The assay utilizes the catalytic reduction of nitrosothiol by mercuric cation (Hg2+). Released nitrogen oxide reacts with sulfanilamide (SA) and N-(1-napthyl)ethylenediamine (NNED) to

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