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202231

Sigma-Aldrich

Chromium(III) acetylacetonate

97%

Synonym(s):

Chromium(III) 2,4-pentanedionate, Cr(acac)3

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About This Item

Linear Formula:
Cr(C5H7O2)3
CAS Number:
21679-31-2
Molecular Weight:
349.32
Beilstein:
4148971
EC Number:
244-526-0
MDL number:
MFCD00000015
UNSPSC Code:
12352103
PubChem Substance ID:
24852050
NACRES:
NA.23

Assay

97%

form

solid

reaction suitability

core: chromium

bp

340 °C (lit.)

mp

210 °C (lit.)

SMILES string

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

InChI

1S/3C5H8O2.Cr/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3/b3*4-3-;

InChI key

JWORPXLMBPOPPU-LNTINUHCSA-K

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Related Categories

Application

  • Redox-Activity Catalysis: Discusses the ligand field-activated redox activity of Chromium(III) acetylacetonate, highlighting its use in hydrogenation catalysis (Vinum et al., 2020).
  • Diffusion Behavior in Supercritical CO2: A study examining the diffusion behavior of Chromium(III) acetylacetonate in supercritical CO2, aiding in the application of supercritical fluids in materials processing (Cordeiro et al., 2016).

Analysis Note

Used to modify the surface properties of solid polyurethanes formed in its presence.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

>392.0 °F

Flash Point(C)

> 200 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Michael E Ziebel et al.
Chemical science, 11(26), 6690-6700 (2020-09-22)
The incorporation of second-row transition metals into metal-organic frameworks could greatly improve the performance of these materials across a wide variety of applications due to the enhanced covalency, redox activity, and spin-orbit coupling of late-row metals relative to their first-row
Yanfang Li et al.
Dalton transactions (Cambridge, England : 2003), 41(13), 3807-3816 (2012-02-24)
Biscyclometalated iridium(III) complexes with an ancillary acetylacetone ligand, Ir(L)(2)(acac), (L = 2-(benzo[b]thiophen-2-yl)pyridine (btp), 1-phenylisoquinoline (piq), 2-phenylbenzothiazole (bt), 2-phenylpyridine (ppy), acac = deprotonated acetylacetone), demonstrate spectroscopic changes in their UV-Vis absorption and luminescent emission under acidic conditions. Such changes were found
Chih-Chia Huang et al.
Chemical communications (Cambridge, England), (23)(23), 3360-3362 (2009-06-09)
A general approach involving a solvothermal method was developed to synthesize a series of silicate nanoshells (<100 nm) where both Gd silicate and Gd silicate:Eu nanoshells were further demonstrated to exhibit dual-modality MRI and optical imaging functions.
David N Paglia et al.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 30(12), 1971-1978 (2012-06-02)
This study quantified the effects of local intramedullary delivery of an organic vanadium salt, which may act as an insulin-mimetic on fracture healing. Using a BB Wistar rat femoral fracture model, local vanadyl acetylacetonate (VAC) was delivered to the fracture
Gui-Ge Hou et al.
Chemical communications (Cambridge, England), 47(38), 10731-10733 (2011-08-27)
Two NbO-type MOFs based on ditopic pyridyl substituted diketonate ligands were reported. One exhibits a reversible SC-SC water encapsulation, while the other shows an interesting guest-driven luminescent property based on M(III) acetylacetonate (M = Eu and Fe) guest species.
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