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Key Documents

Safety Information

222488

Sigma-Aldrich

N-(1-Naphthyl)ethylenediamine dihydrochloride

ACS reagent, >98%

Synonym(s):

2-(1-Naphthylamino)ethylamine dihydrochloride

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0.2 MG
CN¥2,217.29
0.5 MG
CN¥3,324.19
5 X .2 MG
CN¥6,970.62

CN¥2,217.29


Available to ship onApril 14, 2025Details


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0.2 MG
CN¥2,217.29
0.5 MG
CN¥3,324.19
5 X .2 MG
CN¥6,970.62

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.21

CN¥2,217.29


Available to ship onApril 14, 2025Details


Request a Bulk Order

grade

ACS reagent

Quality Level

Assay

>98%

form

solid

impurities

≤5% water

mp

194-198 °C (dec.) (lit.)

solubility

H2O: passes test

suitability

passes test for sensitivity to sulfanilamide

functional group

amine

SMILES string

Cl.Cl.NCCNc1cccc2ccccc12

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1 of 4

This Item
H1404SRP3027E4127
hEGF EGF, recombinant, expressed in E. coli, lyophilized powder, suitable for cell culture

E9644

hEGF

recombinant

expressed in E. coli

recombinant

expressed in Baculovirus infected High-5 cells

recombinant

expressed in E. coli

recombinant

-

assay

≥97% (SDS-PAGE)

assay

>95% (SDS-PAGE)

assay

≥98% (HPLC), ≥98% (SDS-PAGE)

assay

-

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

Quality Level

300

Quality Level

200

Quality Level

-

Quality Level

200

form

lyophilized powder

form

lyophilized powder

form

lyophilized

form

lyophilized powder

General description

N-(1-Naphthyl)ethylenediamine dihydrochloride (NEDA·2HCl) acts as donor molecule and forms charge transfer (CT) complexes with π-acceptors (quinol and picric acid), σ-acceptors (iodine) and vacant orbital acceptors (tin(IV) tetrachloride and zinc chloride). These complexes were investigated by positron annihilation lifetime spectroscopy (PAL).[1]

Application

N-(1-Naphthyl)ethylenediamine dihydrochloride has been used for the preparation of staining solution for the visualization of the reaction product(s) of starch active enzymes, containing α-1, 4 linked and α-1, 6 linked glucose by thin layer chromatography.[2] It has also been used in modified Saville and Griess assays.[3]
N-(1-Naphthyl)ethylenediamine dihydrochloride may be used in the synthesis of 5-[1,2]dithiolan-3-yl-pentanoic acid [2-(naphthalene-1-ylamino)-ethyl]amide (DPAN) by reacting with (±)-1,2-dithiolane-3-pentanoic acid in the presence of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride and N-hydroxysuccinimide.[4] The solution formed by dissolving N-(1-naphthyl)ethylenediamine dihydrochloride in sulfuric acid-methanol may be used as a reagent for the detection of sugars at nanoscale on thin-layer plates.[5]
Coupling agent for the spectrophotometric determination of aminophenols, phenylenediamines, dinitroanilines, chloroanilines, thiols, and sulfonamides.[6][7][8]
Solution of N-(1-naphthyl)ethylenediamine dihydrochloride in sulfuric acid-methanol may be employed for the quantitation of sugars.[5]

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 Information

危险化学品

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K K Verma et al.
Talanta, 38(3), 283-289 (1991-03-01)
A general assay procedure for a wide variety of thiols is described. The technique has three steps: (1) formation of S-nitrosothiols with nitrous acid, (2) destruction of the excess of nitrous acid, (3) hydrolysis of the S-nitrosothiols with mercuric ions
Analytical Chemistry, 55, 1226-1226 (1983)
Chi-Su Yoon et al.
Molecules (Basel, Switzerland), 23(9) (2018-09-20)
Nardostachys jatamansi contains various types of sesquiterpenoids that may play an important role in the potency of plant's anti-inflammatory effects, depending on their structure. In this study, five new sesquiterpenoids, namely kanshone L (1), kanshone M (2), 7-methoxydesoxo-narchinol (3), kanshone
Product Analysis of Starch Active Enzymes by TLC.
Cockburn D and Koropatkin N.
Bio-protocol, 5(20) (2015)
Analytica Chimica Acta, 204, 271-271 (1988)

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