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Merck

C3654

Ammonium cerium(IV) nitrate

≥98% (titration)

Synonym(s):

Ceric ammonium nitrate

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250 G

PLN 741.00

PLN 741.00


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About This Item

Linear Formula:
Ce(NH4)2(NO3)6
CAS Number:
Molecular Weight:
548.22
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.55
Assay:
≥98% (titration)
Form:
powder or crystals

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Assay

≥98% (titration)

form

powder or crystals

reaction suitability

reagent type: oxidant

pH

0.61 (20 °C, 111.11 g/L)

SMILES string

N.N.[Ce+4].O[N+]([O-])=O.O[N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O

InChI

1S/Ce.2HNO3.4NO3.2H3N/c;6*2-1(3)4;;/h;2*(H,2,3,4);;;;;2*1H3/q+4;;;4*-1;;

InChI key

WIBGOERAEYJBOT-UHFFFAOYSA-N

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1 of 4

This Item
2295472154731.02276
form

powder or crystals

form

crystalline

form

powder or crystals

form

crystalline

assay

≥98% (titration)

assay

≥99.99% trace metals basis

assay

≥98.5%

assay

≥99.0% ((NH4)2[Ce(NO3)6] basis, potentiometry)

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

300

pH

0.61 (20 °C, 111.11 g/L)

pH

-

pH

-

pH

0.61 (20 °C, 111.11 g/L in H2O)

reaction suitability

reagent type: oxidant

reaction suitability

reagent type: oxidant

reaction suitability

reagent type: oxidant

reaction suitability

-

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Met. Corr. 1 - Ox. Sol. 2 - Skin Corr. 1B - Skin Sens. 1A

Storage Class Code

5.1B - Oxidizing hazardous materials

WGK

WGK 3


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S Sudha et al.
Ultrasonics sonochemistry, 19(5), 994-998 (2012-03-09)
Tetrahydrobenzo[c]xanthenes-11-ones was synthesized by a three component reaction of α-naphthol, aromatic aldehyde and dimedone. Ceric ammonium nitrate acts as a suitable eco-friendly catalyst for this method. Shorter reaction duration, mild reaction condition and low cost make this protocol more effective.
Vijay Nair et al.
Accounts of chemical research, 37(1), 21-30 (2004-01-21)
Cerium(IV) ammonium nitrate (CAN) has recently emerged as a versatile reagent for oxidative electron transfer; the overwhelming number of reports serve as a testimony to the unparalleled utility of CAN in a variety of transformations of synthetic importance. Our recent
Kuppusamy Sujatha et al.
Bioorganic & medicinal chemistry letters, 19(15), 4501-4503 (2009-06-02)
An efficient and eco-friendly method for the synthesis of 4,4'-(arylmethylene)bis(1H-pyrazol-5-ols) has been accomplished by tandem Knoevenagel-Michael reaction of two equivalents of 5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one with various aromatic aldehydes catalyzed by ceric ammonium nitrate (CAN) in water. All the synthesized compounds 3a-j were
Mazaahir Kidwai et al.
Chemical & pharmaceutical bulletin, 58(10), 1320-1323 (2010-10-12)
An environment friendly method for the synthesis of 2-oxo/thioxooctahydroquinazolin-5-one derivatives has been devised using Ceric ammonium nitrate (CAN) as catalyst and polyethylene glycol (PEG) as solvent. The cytotoxic effect of these compounds was studied on U87 human glioma cells, compounds
Jingliang Jiao et al.
Organic letters, 9(7), 1323-1326 (2007-03-06)
[structure: see text]. The oxidation of selected anions (N3-, SCN-, I-, and Br-) by ceric ammonium nitrate (CAN) in the presence of substituted cyclopropyl alcohols provides a novel approach to beta-functionalized ketones. The protocol has a number of advantages including

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