Skip to Content
Merck

70720

N-(1-Naphthyl)ethylenediamine dihydrochloride monomethanolate

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

Sign In to View Organizational & Contract Pricing.

Select a Size

25 G

HUF 87,800.00

100 G

HUF 284,000.00

HUF 87,800.00


Please contact Customer Service for Availability

Request a Bulk Order

About This Item

Linear Formula:
C10H7NHCH2CH2NH2 · 2HCl · MeOH
CAS Number:
Molecular Weight:
291.22
UNSPSC Code:
23151816
NACRES:
NA.21
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3707471

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

N-(1-Naphthyl)ethylenediamine dihydrochloride monomethanolate, for spectrophotometric det. of nitrate and nitrite, ≥99.0%

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

SMILES string

Cl.Cl.CO.NCCNc1cccc2ccccc12

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.)

Quality Level

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
1.0623787600222488
assay

≥99.0% (AT)

assay

-

assay

-

assay

>98%

form

crystals

form

solid

form

liquid

form

solid

quality

for spectrophotometric det. of nitrate and nitrite

quality

-

quality

-

quality

-

technique(s)

UV/Vis spectroscopy: suitable

technique(s)

-

technique(s)

-

technique(s)

-

ign. residue

≤0.05%

ign. residue

-

ign. residue

-

ign. residue

-

mp

196-199 °C (dec.)

mp

-

mp

-

mp

194-198 °C (dec.) (lit.)

Application

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

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.[2]

Other Notes

Reagent used in the simultaneous spectrophotometric determination of nitrite and nitrate by flow injection analysis[3]

pictograms

Exclamation mark

signalword

Warning

hcodes

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

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Simultaneous spectrophotometric determination of nitrite and nitrate by flow injection analysis
L. Anderson
Analytica Chimica Acta, 110, 123-123 (1979)
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
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
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
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)

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service