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M2284

Sigma-Aldrich

Manganese(III) acetylacetonate

technical grade

Synonym(s):

2,4-Pentanedione manganese(III) derivative, Manganic acetylacetonate, Mn(acac)3

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About This Item

Linear Formula:
Mn(C5H7O2)3
CAS Number:
14284-89-0
Molecular Weight:
352.26
EC Number:
238-188-3
MDL number:
MFCD00000023
UNSPSC Code:
12161600
PubChem Substance ID:
24896721
NACRES:
NA.22

grade

technical grade

Quality Level

100

reaction suitability

core: manganese
reagent type: catalyst

mp

159-161 °C (dec.) (lit.)

SMILES string

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

InChI

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

InChI key

HYZQBNDRDQEWAN-LNTINUHCSA-K

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Application

Oxidant used to oxidize phenols, β-dicarbonyl compounds, and thiols.

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Nishino, H. Tategami, S. et al.
Bulletin of the Chemical Society of Japan, 64, 1800-1800 (1991)
Snider, B. B.; Patricia, J. J. et al.
The Journal of Organic Chemistry, 53, 2137-2137 (1988)
The direct writing of plasmonic gold nanostructures by electron-beam-induced deposition.
Katja Höflich et al.
Advanced materials (Deerfield Beach, Fla.), 23(22-23), 2657-2661 (2011-05-04)
S S Arandjelovic et al.
Journal of B.U.ON. : official journal of the Balkan Union of Oncology, 14(2), 271-279 (2009-08-04)
To investigate the antitumor activity of two newly synthesized ruthenium(III) [Ru(III)] compounds carrying bidentate ligands: (acac)-acetylacetonate, [Ru(acac)3), and (tfac)-trifluoroacetylacetonate [Ru(tfac)3]. The activity of ruthenium(III) analogues was evaluated on HeLa, B16, and Femx cell lines for cytotoxicity in vitro using MTT
Gong-Jun Chen et al.
Dalton transactions (Cambridge, England : 2003), 39(44), 10637-10643 (2010-10-06)
Two Eu(III) complexes, [Eu(acac)(3)(dpq)] (1) and [Eu(acac)(3)(dppz)] CH(3)OH (2) {viz. acetylacetonate (acac), dipyrido[3,2-d:20,30-f]quinoxaline (dpq), dipyrido[3,2-a:20,30-c] phenazine (dppz)}, have been synthesized and their DNA binding, photo-induced DNA cleavage activity and cell cytotoxicity are studied. The complexes display significant binding propensity to
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