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Merck
CN

31153

Ammonium metavanadate

puriss. p.a., reag. Ph. Eur., ≥99.5%

Synonym(s):

Ammonium vanadate(V)

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About This Item

Linear Formula:
NH4VO3
CAS Number:
Molecular Weight:
116.98
PubChem Substance ID:
eCl@ss:
38180409
UNSPSC Code:
12352302
EC Number:
232-261-3
MDL number:
Assay:
≥99.5%
Form:
solid
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InChI key

YBVKNHXQSRDWAA-UHFFFAOYSA-M

InChI

1S/H3N.H2O.2O.V/h1H3;1H2;;;/q;;;;+1/p-1

SMILES string

N.O[V](=O)=O

agency

USP/NF, reag. Ph. Eur.

grade

puriss. p.a.

assay

≥99.5%

form

solid

density

2.32 g/cm3 at 25 °C (lit.)

anion traces

chloride (Cl-): ≤20 mg/kg, phosphate (PO43-): ≤50 mg/kg, sulfate (SO42-): ≤100 mg/kg

cation traces

Cd: ≤10 mg/kg, Co: ≤20 mg/kg, Cu: ≤10 mg/kg, Fe: ≤10 mg/kg, Ni: ≤20 mg/kg, Pb: ≤20 mg/kg, Zn: ≤10 mg/kg

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General description

Ammonium metavanadate is an ammonium salt. It participates as an oxidizing agent for condensation reaction of o-phenylenediamine with substituted aryl aldehydes.

Application

Ammonium metavanadate may be employed in the following studies:
  • As catalyst for the synthesis of various 2-substituted aryl benzimidazoles.
  • As oxidizing agent in the determination of chlorpromazine, promethazine, trimeprazine and perphenazine in pharmaceutical samples by flow injection method.
  • Synthesis of dioxidovanadium(V) complex.
  • Preparation of Vanadia modified titania (V2O5/TiO2) photo-catalysts.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 2 - STOT RE 1 Inhalation

target_organs

Respiratory Tract

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Diptipriya Sethi et al.
Journal of photochemistry and photobiology. B, Biology, 144, 68-74 (2015-03-03)
Vanadia modified titania (V₂O₅/TiO₂) photo-catalysts are prepared by incipient wet impregnation method using aqueous ammonium metavanadate and anatase (Aldrich) titania. Titania with various loading concentrations of vanadia from 0 to 10 wt.% have been prepared and characterized by X-ray diffraction
Simona Nica et al.
Journal of inorganic biochemistry, 147, 193-203 (2015-03-10)
The Schiff-base ligand (H2salhyhNH3)Cl (1) derived from salicylaldehyde and 6-aminohexanoic acid hydrazide hydrochloride reacts with ammonium metavanadate in methanol solution to yield the dioxidovanadium(V) complex [VO2(salhyhNH3)] (2). The utilized hydrazone ligand contains a flexible and protonated amino side chain. Crystallization
Flow injection method for the assay of phenothiazine neuroleptics in pharmaceutical preparations using ammonium metavanadate.
Sultan SM.
Analyst, 116(2), 177-181 (1991)
W Ding et al.
Biological trace element research, 80(2), 159-174 (2001-07-05)
The glucose-lowering effect of vanadate, ammonium metavanadate (AMV), on diabetic KK mice was examined. Five-week-old male KK mice were administrated with a solution of AMV via drinking water at concentrations of vanadium (V) with 0.1, 1.0, 10 and 100 microg/mL
Tridib Chakraborty et al.
Biochimica et biophysica acta, 1772(1), 48-59 (2006-12-19)
Carcinogen-induced formation of DNA adducts and other types of DNA lesions are the critical molecular events in the initiation of chemical carcinogenesis and modulation of such events by chemopreventive agents could be an important step in limiting neoplastic transformation in

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