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88461

Sigma-Aldrich

2,3-Diaminonaphthalene

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

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C10H10N2
Número CAS:
Peso molecular:
158.20
Beilstein:
2206394
Número CE:
Número MDL:
Código UNSPSC:
12171500
ID de substância PubChem:
NACRES:
NA.32

linha de produto

BioReagent

Nível de qualidade

Ensaio

≥98.0% (HPLC)

Formulário

solid

pf

196-202 °C

fluorescência

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

adequação

suitable for fluorescence

cadeia de caracteres SMILES

Nc1cc2ccccc2cc1N

InChI

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

chave InChI

XTBLDMQMUSHDEN-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Nota de análise

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

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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N R Neng et al.
Journal of chromatography. A, 1169(1-2), 47-52 (2007-09-25)
Stir bar sorptive extraction with in-situ derivatization using 2,3-diaminonaphthalene (DAN) followed by liquid desorption and high performance liquid chromatography with diode array detection (SBSE(DAN)in-situ-LD-HPLC-DAD) was developed for the determination of glyoxal (Gly) and methylglyoxal (MGly) in environmental and biological matrices.
Maria De Lucia et al.
Chemical research in toxicology, 21(12), 2407-2413 (2009-06-24)
With a view to elucidating the structural requisites for effective antinitrosating properties in plant polyphenolics and their metabolites, we have undertaken a comparative investigation of the nitrite scavenging effects of representative catechol derivatives of dietary relevance in the 2,3-diaminonaphthalene (DAN)
A M Serra et al.
Talanta, 81(1-2), 572-577 (2010-03-02)
In the present work, a solid phase extraction (SPE) is hyphenated with an automatic MSFIA system to improve the selenite determination based on the reaction of selenite with aromatic o-diamines (such as 2,3-diaminonaphthalene (DAN)) to form the piazselenol complex. This
Chien-Yuan Kuo et al.
Molecules (Basel, Switzerland), 17(6), 7387-7400 (2012-06-19)
Neutral and acidic monosaccharide components in Ganoderma lucidum polysaccharide are readily labeled with 2,3-naphthalenediamine, and the resulting saccharide-naphthimidazole (NAIM) derivatives are quantified by capillary electrophoresis (CE) in borate buffer. Using sulfated-α-cyclodextrin as the chiral selector, enantiomers of monosaccharide-NAIMs are resolved
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

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