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Merck
CN

33461

N-(1-Naphthyl)ethylenediamine dihydrochloride

ACS reagent, ≥98%

Synonym(s):

2-(1-Naphthylamino)ethylamine dihydrochloride

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About This Item

Linear Formula:
C10H7NHCH2CH2NH2 · 2HCl
CAS Number:
1465-25-4
Molecular Weight:
259.17
UNSPSC Code:
41116105
NACRES:
NA.21
PubChem Substance ID:
329754555
EC Number:
215-981-2
Beilstein/REAXYS Number:
3707471
MDL number:
MFCD00012556

Key Documents

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Product Name

N-(1-Naphthyl)ethylenediamine dihydrochloride, ACS reagent, ≥98%

InChI key

MZNYWPRCVDMOJG-UHFFFAOYSA-N

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

SMILES string

Cl.Cl.NCCNc1cccc2ccccc12

grade

ACS reagent

assay

≥98% (calc with ref. to anhyd. subst.)
≥98%

form

powder

technique(s)

UV/Vis spectroscopy: suitable

impurities

≤5% water (Karl Fischer)

mp

194-198 °C (dec.) (lit.)

suitability

complies for identity

Quality Level

200

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Application

N-(1-Naphthyl)ethylenediamine dihydrochloride dissolved in sulfuric acid-methanol may be used as a reagent for the determination of sugar on thin layer plates. It may also be used for the determination of sub-micromolar concentrations of nitrite ion after diazotisation with sulphanilic acid at low pH, by differential-pulse polarography. It may also be used as the coupling agent for the spectrophotometric determination of aniline by the diazotization-coupling method.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCM7789
BCCM4379
BCCL6973
BCCL1166
BCCM3100

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Spectrophotometric determination of aniline by the diazotization-coupling method with N-(1-naphthyl) ethylenediamine as the coupling agent.
Norwitz G and Keliher PN.
Analytical Chemistry, 53 (8), 1238-1240 (1981)
Determination of nitrite ion by differential-pulse polarography using N-(1-naphthyl) ethylenediamine.
Sabharwal S.
Analyst, 115 (10), 1305-1307 (1990)
N-(1-Naphthyl) ethylenediamine dihydrochloride as a new reagent for nanomole quantification of sugars on thin-layer plates by a mathematical calibration process.
Bounias M.
Analytical Chemistry, 106 (2), 291-295 (1980)
J A Cook et al.
Analytical biochemistry, 238(2), 150-158 (1996-07-01)
S-nitrosothiols have been shown to affect a number of physiological functions. Several techniques have been used to detect these species in biological systems, primarily by methods utilizing chemiluminescence. Since the apparatus required for measurement of chemiluminescence are not readily available
A C Roy et al.
Electrophoresis, 13(6), 396-397 (1992-06-01)
A sensitive staining method for the detection of oxytocinase (EC 3.4.11.3) activity in electrophoresis gels has been described. The method is based on the enzymatic release of p-nitroaniline (PNA) from two specific synthetic oxytocinase substrates, S-benzyl-L-cysteine-p-nitroanilide (BCN) and L-leucine-p-nitroanilide (LN)
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