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Merck

88461

2,3-Diaminonaphthalene

BioReagent, suitable for fluorescence, ≥98.0% (HPLC)

Synonym(s):

naphthalene-2,3-diamine, 2,3-Naphthalenediamine, DAN

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About This Item

Empirical Formula (Hill Notation):
C10H10N2
CAS Number:
771-97-1
Molecular Weight:
158.20
UNSPSC Code:
12171500
NACRES:
NA.32
PubChem Substance ID:
57653309
EC Number:
212-241-0
Beilstein/REAXYS Number:
2206394
MDL number:
MFCD00004116

Key Documents

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Product Name

2,3-Diaminonaphthalene, BioReagent, suitable for fluorescence, ≥98.0% (HPLC)

InChI key

XTBLDMQMUSHDEN-UHFFFAOYSA-N

InChI

1S/C10H10N2/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6H,11-12H2

SMILES string

Nc1cc2ccccc2cc1N

product line

BioReagent

assay

≥98.0% (HPLC)

form

solid

mp

196-202 °C

fluorescence

λex 364 nm; λem 406 nm in 0.5 M Na carbonate pH 10.0 (after derivatization with NaNO2 in 0.1 M HCl)

suitability

suitable for fluorescence

Quality Level

100

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Analysis Note

In addition to the emission maximum at 406 nm, there are lower maxima at 426, 386 and 450 nm

Application

2,3-Diaminonaphthalene or DAN is suitable for fluorescence-spectroscopic determination of nitrite/ nitrate in milk and soy based food products.

DAN is used in the fluorometric determination of selenium in biological materials.

General description

2,3-Diaminonaphthalene, also known as 2,3 DAN, is an aromatic diamino fluorescent compound designed for carrying out DAN assays. Reacting with nitrite, 2,3 DAN forms the fluorescent product, 3-naphthotriazole (NAT), determined fluorometrically.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN4894
BCCL2092
BCCH9137
BCCD2318
BCBZ6417

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T S Koh et al.
Journal - Association of Official Analytical Chemists, 66(4), 918-926 (1983-07-01)
The reaction of 2,3-diaminonaphthalene (DAN) with Se(IV) to form a fluorescent Se-DAN complex is the basis of a fluorometric method for determination of Se. With the aid of metabolically incorporated 75Se the method was critically re-examined. The study showed that
Raluca Petrican et al.
NeuroImage, 123, 80-88 (2015-08-26)
Current evidence suggests that two spatially distinct neuroanatomical networks, the dorsal attention network (DAN) and the default mode network (DMN), support externally and internally oriented cognition, respectively, and are functionally regulated by a third, frontoparietal control network (FPC). Interactions among
Andreas K Nussler et al.
Nature protocols, 1(5), 2223-2226 (2007-04-05)
We describe a step-by-step protocol for measuring the stable products of the nitric oxide (NO) pathway: nitrite, nitrite plus nitrate and nitrate. This described protocol is easy to apply and is about 50 times more sensitive than the commonly used
Jingqi Tian et al.
The Analyst, 136(11), 2221-2224 (2011-04-01)
In this Communication, we report on the first preparation of conjugation polymer poly(2,3-diaminonaphthalene) (PDAN) microspheres via chemical oxidation polymerization of 2,3-diaminonaphthalene (DAN) monomers by ammonium persulfate (APS) at room temperature. We further demonstrate the use of PDAN microspheres as a
Stavros Selemidis et al.
Cardiovascular research, 75(2), 349-358 (2007-06-15)
Endothelial NADPH oxidase is a major source of superoxide in blood vessels and is implicated in the oxidative stress accompanying vascular diseases, including atherosclerosis. Here we investigate the regulation of NADPH oxidase activity by nitric oxide (NO). Human cultured microvascular
View All Related Papers

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