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Merck
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Key Documents

38497

Millipore

Nitrate Reagent A

suitable for microbiology

Synonyme(s) :

1-Naphthylamine solution

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About This Item

Numéro CAS:
Numéro MDL:
Code UNSPSC :
41171621
ID de substance PubChem :
Nomenclature NACRES :
NA.85

Gamme de produits

BioChemika

Niveau de qualité

Durée de conservation

limited shelf life, expiry date on the label

Composition

acetic acid 5 N, 1000 mL
α-naphthylamine, 5 g

Technique(s)

microbe id | metabolite detection: suitable

Application(s)

agriculture
clinical testing
environmental
food and beverages
pharmaceutical

microbiology

Adéquation

Enterobacter spp.
Neisseria spp.
anaerobic bacteria
bacteria

InChI

1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2

Clé InChI

RUFPHBVGCFYCNW-UHFFFAOYSA-N

Description générale

α-Naphtylamine and sulfanilic acid are used for detection of nitrate reduction by bacteria. Organisms containing nitrate reductase reduce nitrate to nitrite, which forms a diazonium salt with sulfanilic acid and reacts with α-naphtylamine to form a red azo dye.

Pictogrammes

Corrosion

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Eye Dam. 1 - Skin Corr. 1B

Code de la classe de stockage

8A - Combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Consulter la Bibliothèque de documents

Xiaolin Zhang et al.
Inorganic chemistry, 51(4), 2325-2331 (2012-02-10)
A unique gadolinium complex, Nap-DO3A-Gd, comprising a naphthylamine luminescent moiety, a di-2-picolylamine (DPA) binding chelator, and a 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid (DO3A) moiety has been designed and synthesized as a dual-functional probe for selective magnetic resonance imaging and fluorescent sensing of copper(II)
Zuofu Hu et al.
Optics letters, 37(15), 3072-3074 (2012-08-04)
An ultraviolet photodetector was fabricated based on Mg0.07Zn0.93O heterojunction. N, N'-bis (naphthalen-1-y1)-N, N'-bis(pheny) benzidine was selected as the hole transporting layer. I-V characteristic curves of the device were measured in the dark and under the illumination of 340 nm UV
Arvydas Tamulis et al.
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 43(1), 49-66 (2012-12-18)
The quantum mechanical self-assembly of two separate photoactive supramolecular systems with different photosynthetic centers was investigated by means of density functional theory methods. Quantum entangled energy transitions from one subsystem to the other and the assembly of logically controlled artificial
Time-dependent intensity changes of free fatty acids detected by matrix-assisted laser desorption and ionization time-of-flight mass spectrometry in the presence of 1,8-bis-(dimethylamino)naphthalene--a cautionary note.
Mandy Eibisch et al.
Rapid communications in mass spectrometry : RCM, 26(13), 1573-1576 (2012-05-29)
Yuta Matsuoka et al.
Free radical biology & medicine, 53(11), 2112-2118 (2012-10-03)
Ascorbic acid is a small-molecule reductant with multiple functions in vivo. Reducing ascorbic acid intake leads to a lack of hydroxylation of prolines and lysines, causing a looser triple helix and resulting in scurvy. Ascorbic acid also acts as an

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