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70720

Supelco

N-(1-Naphthyl)ethylenediamine dihydrochloride monomethanolate

for spectrophotometric det. of nitrate and nitrite, ≥99.0%

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About This Item

Linear Formula:
C10H7NHCH2CH2NH2 · 2HCl · MeOH
CAS Number:
Molecular Weight:
291.22
Beilstein:
3707471
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NA.21

Quality Level

Assay

≥99.0% (AT)
≥99.0%

form

crystals

quality

for spectrophotometric det. of nitrate and nitrite

technique(s)

UV/Vis spectroscopy: suitable

ign. residue

≤0.05%

mp

196-199 °C (dec.)

SMILES string

Cl.Cl.CO.NCCNc1cccc2ccccc12

InChI

1S/C12H14N2.CH4O.2ClH/c13-8-9-14-12-7-3-5-10-4-1-2-6-11(10)12;1-2;;/h1-7,14H,8-9,13H2;2H,1H3;2*1H

InChI key

YUMCJWVZLMGNTD-UHFFFAOYSA-N

General description

N-(1-Naphthyl)ethylenediamine dihydrochloride is a hygroscopic analytical reagent generally suitable for determination of drugs, pharmaceuticals with free primary aromatic amino group, sulpha drugs and local anaesthetics. It may decompose on exposure to light.

Application

N-(1-Naphthyl)ethylenediamine dihydrochloride monomethanolate may be used to study antimicrobial effects against bacteria.

Other Notes

Reagent used in the simultaneous spectrophotometric determination of nitrite and nitrate by flow injection analysis

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH Annex XVII (Restriction List)

CAS No.

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L A Ridnour et al.
Analytical biochemistry, 281(2), 223-229 (2000-06-28)
A method for the spectrophotometric determination of nitric oxide, nitrite, and nitrate in tissue culture media is presented. The method is based on the nitric oxide-mediated nitrosative modification of sulfanilic acid that reacts with N-(1-naphthyl)ethylenediamine dihydrochloride forming an orange-colored product
Glen C Ulett et al.
The Journal of infectious diseases, 191(10), 1761-1770 (2005-04-20)
Group B streptococcus (GBS; Streptococcus agalactiae) induces apoptosis of macrophages, and this may be an important mechanism GBS uses to suppress immune responses. The mechanisms whereby GBS induces apoptosis have not been identified. We studied GBS infection in murine macrophage-like
M J Ahmed et al.
Talanta, 43(7), 1009-1018 (1996-07-01)
An automatic direct spectrophotometric method for the simultaneous determination of nitrite and nitrate by flow-injection analysis has been developed. Nitrite reacts with 3-nitroaniline in the presence of hydrochloric acid (0.96-1.8 M HCl or pH 0.5-0.7) to form a diazonium cation
Role of Chemical and Analytical Reagents in Colorimetric Estimation of Pharmaceuticals-A Review.
Somsubhra Ghosh et al.
International Journal of Medicine and Pharmaceutical Research, 1(5), 433-445 (2013)
E E L Lewis et al.
International journal of cosmetic science, 40(2), 148-156 (2018-01-23)
Examination of the skin barrier repair/wound healing process using a living skin equivalent (LSE) model and matrix-assisted laser desorption/ionization-mass spectrometry imaging (MALDI-MSI) to identify lipids directly involved as potential biomarkers. These biomarkers may be used to determine whether an in

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