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Merck
CN

38497

Nitrate Reagent A

suitable for microbiology

Synonym(s):

1-Naphthylamine solution

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About This Item

CAS Number:
134-32-7
UNSPSC Code:
41171621
PubChem Substance ID:
329755769
NACRES:
NA.85
MDL number:
MFCD00004016

Key Documents

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Product Name

Nitrate Reagent A, suitable for microbiology

SMILES string

Nc1c2c(ccc1)cccc2

InChI

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

InChI key

RUFPHBVGCFYCNW-UHFFFAOYSA-N

product line

BioChemika

shelf life

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

suitability

Enterobacter spp.
Neisseria spp.
anaerobic bacteria
bacteria

Quality Level

100

Related Categories

General description

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.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

危险化学品
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Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN6645
BCCL3731
BCCK1475
BCCH7360
BCCJ6787

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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)
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)
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
Elizabeth Rayburn et al.
Cancer chemotherapy and pharmacology, 69(6), 1423-1431 (2012-03-01)
ML-970 (AS-I-145; NSC 716970) is an indolecarboxamide synthesized as a less toxic analog of CC-1065 and duocarmycin, a natural product that binds the A-T-rich DNA minor groove and alkylates DNA. The NCI60 screening showed that ML-970 had potent cytotoxic activity
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