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10916

Sigma-Aldrich

Acetylacetone

produced by Wacker Chemie AG, Burghausen, Germany, ≥99.5% (GC)

Synonym(s):

AcAc, 2,4-Pentanedione

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About This Item

Linear Formula:
CH3COCH2COCH3
CAS Number:
Molecular Weight:
100.12
Beilstein:
741937
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39021208
PubChem Substance ID:
NACRES:
NA.22

grade

produced by Wacker Chemie AG, Burghausen, Germany

vapor density

3.5 (vs air)

vapor pressure

6 mmHg ( 20 °C)

Assay

≥99.5% (GC)

form

liquid

autoignition temp.

662 °F

expl. lim.

11.4 %

refractive index

n20/D 1.452 (lit.)

pH

6 (20 °C, 200 g/L)

bp

140.4 °C (lit.)

mp

−23 °C (lit.)

solubility

H2O: soluble 1 in 8 parts
acetone: miscible
alcohol: miscible
benzene: miscible
chloroform: miscible
diethyl ether: miscible
glacial acetic acid: miscible

density

0.975 g/mL at 25 °C (lit.)

SMILES string

CC(=O)CC(C)=O

InChI

1S/C5H8O2/c1-4(6)3-5(2)7/h3H2,1-2H3

InChI key

YRKCREAYFQTBPV-UHFFFAOYSA-N

Gene Information

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General description

Acetylacetone is a chelating ligand and forms organometallic complexes that are used as gasoline additives, lubricant additives, driers for varnishes and printer′s inks, fungicides, insecticides and colors. It is a selective extraction reagent for determination of molybdenum in ferrous materials.

Application

Acetylacetone was used in preparing Y203, La203 and La2CuO4 thin films and the titanate/anatase dual-phase photocatalyst.

Other Notes

prices for bulk quantities on request

Pictograms

FlameSkull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

95.0 °F - closed cup

Flash Point(C)

35 °C - closed cup

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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Analytical Solvent Extraction of Molybenum Using Acetylacetone.
McKaveney JP and Freiser H.
Analytical Chemistry, 29(2), 290-292 (1957)
Nitrogen- sensitized Dual Phase Titanate/Titania for Visible-light Driven Phenol Degradation.
Hua CY, et al.
Journal of Solid State Chemistry, 1962012, 518-527 null
Growth and characterization of thin films of Y203, La203 and La2CuO4.
Gao YM, et al.
Journal of Solid State Chemistry, 90(2), 228-233 (1991)
Kyoji Tsuchikama et al.
The Journal of organic chemistry, 76(17), 6981-6989 (2011-06-18)
Bacteria have developed a cell-to-cell communication system, termed quorum sensing (QS), which allows for the population-dependent coordination of their behavior via the exchange of chemical signals. Autoinducer-2 (AI-2), a class of QS signals derived from 4,5-dihydroxy-2,3-pentandione (DPD), has been revealed
Rolando R Lozada-García et al.
Physical chemistry chemical physics : PCCP, 14(10), 3450-3459 (2012-02-07)
The photochemistry of the chelated enol form of acetylacetone (AcAc) was investigated by UV excitation of the S(2) state at 266 nm in parahydrogen matrices, complemented by experiments in neon and normal hydrogen matrices. Infrared (IR) spectroscopy, combined with theoretical

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