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94735

Sigma-Aldrich

Vanadyl acetylacetonate

purum, ≥97.0% (RT)

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Synonym(s):
VO(acac)2, Vanadium(IV)-oxy acetylacetonate
Linear Formula:
OV(C5H7O2)2
CAS Number:
3153-26-2
Molecular Weight:
265.16
Beilstein:
4138236
EC Number:
221-590-8
MDL number:
MFCD00000032
UNSPSC Code:
12352300
PubChem Substance ID:
329770380
NACRES:
NA.23

grade

purum

Quality Level

200

Assay

≥97.0% (RT)

form

solid

reaction suitability

reagent type: catalyst

mp

235 °C (dec.) (lit.)

SMILES string

CC(=O)\C=C(\C)O[V](=O)O\C(C)=C/C(C)=O

InChI

1S/2C5H8O2.O.V/c2*1-4(6)3-5(2)7;;/h2*3,6H,1-2H3;;/q;;;+2/p-2/b2*4-3-;;

InChI key

JFHJZWAQYMGNBE-SUKNRPLKSA-L

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Marvin W Makinen et al.
The Journal of biological chemistry, 277(14), 12215-12220 (2002-01-30)
We have investigated the interaction of bis(acetylacetonato)oxovanadium(IV) (VO(acac)(2)) with bovine serum albumin (BSA) by EPR and angle-selected electron nuclear double resonance, correlating results with assays of glucose uptake by 3T3-L1 adipocytes. EPR spectra of VO(acac)(2) showed no broadening in the
[Oxidation of phenothiazine and its N-methyl derivative by the combination of iodobenzene and vanadium acetylacetonate].
F Pautet et al.
Die Pharmazie, 40(3), 202-203 (1985-03-01)
N Farrell et al.
Journal of inorganic biochemistry, 30(4), 309-315 (1987-08-01)
A study of the reactions of purine and pyrimidine bases has been initiated with the V(IV) complex [V(O)(acac)2]. Two distinct modes of reaction have been recognized depending on the nature of the base. Simple adduct formation occurs when the base

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