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256064

Sigma-Aldrich

Ammonium nitrate

99.999% trace metals basis

Sinónimos:

Nitric acid ammonium salt

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About This Item

Fórmula lineal:
NH4NO3
Número de CAS:
6484-52-2
Peso molecular:
80.04
EC Number:
229-347-8
MDL number:
MFCD00011425
UNSPSC Code:
12352302
PubChem Substance ID:
24855505
NACRES:
NA.23

assay

99.999% trace metals basis

form

crystals and lumps

impurities

≤20.0 ppm Trace Metal Analysis

bp

210 °C (lit.)

mp

169 °C (lit.)

SMILES string

N.O[N+]([O-])=O

InChI

1S/HNO3.H3N/c2-1(3)4;/h(H,2,3,4);1H3

InChI key

PRORZGWHZXZQMV-UHFFFAOYSA-N

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Application

  • Synthesis of 3-Amino-4-substituted Monocyclic ß-Lactams-Important Structural Motifs in Medicinal Chemistry.: This study presents a novel synthesis route for 3-amino-4-substituted monocyclic ß-lactams, which are significant in medicinal chemistry due to their biological activities. The process utilizes ammonium nitrate as a reagent for the synthesis, highlighting its role in advanced organic chemistry applications (Grabrijan et al., 2021).

pictograms

Flame over circleExclamation mark
GHS03,GHS07

signalword

Warning

hcodes

H272,H319

Hazard Classifications

Eye Irrit. 2 - Ox. Sol. 3

Storage Class

5.1C - Ammonium nitrate and ammonium nitrate containing preparations

wgk_germany

WGK 1

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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The nanostructure of the ethanolammonium nitrate (EtAN)-air surface has been investigated using X-ray reflectometry (XRR), vibrational sum frequency spectroscopy (VSFS) and neutral impact collision ion scattering spectroscopy (NICISS). The XRR data decays more rapidly than expected for a perfectly sharp
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The cerium(IV) ammonium nitrate (CAN)-catalyzed sequential multicomponent reaction between tryptamine, α,β-unsaturated aldehydes, and β-dicarbonyl compounds affords highly substituted indolo[2,3-a]quinolizines in a single synthetic operation. Two rings are generated through the creation of two C-C and two C-N bonds by a
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