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Key Documents

38497

Millipore

Nitrate Reagent A

suitable for microbiology

Sinonimo/i:

1-Naphthylamine solution

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Numero CAS:
Numero MDL:
Codice UNSPSC:
41171621
ID PubChem:
NACRES:
NA.85

Nome Commerciale

BioChemika

Livello qualitativo

Durata

limited shelf life, expiry date on the label

Composizione

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

tecniche

microbe id | metabolite detection: suitable

applicazioni

agriculture
clinical testing
environmental
food and beverages
pharmaceutical

microbiology

Compatibilità

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
RUFPHBVGCFYCNW-UHFFFAOYSA-N

Descrizione generale

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.

Pittogrammi

Corrosion

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Eye Dam. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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


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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)
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)
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
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
Todd M Doran et al.
Proteins, 80(4), 1053-1065 (2012-01-19)
Aromatic amino acids strongly promote cross-β amyloid formation; whether the amyloidogenicity of aromatic residues is due to high hydrophobicity and β-sheet propensity or formation of stabilizing π-π interactions has been debated. To clarify the role of aromatic residues on amyloid

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