Acetone for Residue Analysis, 99.9%+ Purity 4 Liter, case/4

Acetone Residue Analysis ≥99.9% 4 Liter Case/4

• CAS Number 67-64-1
• Linear Formula CH3COCH3
• Molecular Weight 58.08
• Beilstein/REAXYS Number 635680
• EC Number 200-662-2
• MDL number MFCD00008765
• eCl@ss 39021201
• PubChem Substance ID 329760025
• NACRES NA.02

General description

Acetone is a ketone. Mixtures of TiO₂ (P25) with rare earth oxides (La₂O₃ or Y₂O₃) calcined at 700°C or 650°C has been reported to efficiently photocatalyze oxidation of acetone. Its aldol condensation in vapor-phase has been investigated over MgO promoted with alkali (Li, Na, K and Cs) or alkaline earth (Ca, Sr and Ba) metal ions.It undergoes Aldol condensation in the presence of Mg-Al layered double hydroxides (LDH) as catalysts and Cl^- and/or CO₃^2- as compensating anions to afford diacetone alcohol and mesityl oxide. Enantioselective Aldol condensation of acetone with various isatins in the presence of dipeptides (catalyst) has been described.

Application

Acetone may be used in the following studies:
• NMR spectroscopic evaluation of glucose metabolism in biological samples (blood). 
• Preparation of 13wt% amorphous poly (lactic acid) (PLA) solution, which was required for the preparation of electrospun PLA membranes.
• As a precursor for the synthesis of methyl isobutyl ketone (MIBK) in the presence of sulfonated graphene oxide-Pd/cordierite catalyst.
• Synthesis of (4-hydroxymethyl-2,2-dimethyl-1,3-dioxolane), a solketal from glycerol using supercritical fluids (SCF) technology.
It may be used in the synthesis of the following acetone hydrazones:
• 1-isopropylidene-2-methylhydrazine
• 1-isopropylidene-2-hydroxyethylhydrazine
• 1-isopropylidene-2-formylhydrazine

Acetone′s luminesence intensity is dependent upon the solution components . The absorption of UV light by acetone, results in its photolysis and the production of radials .

Suitable for HPLC, spectrophotometry, environmental testing

GHS02, GHS07

Signal word Danger
Hazard statements H225-H319-H336
Precautionary statements P210-P233-P261-P280-P303 + P361 + P353-P370 + P378
Supplemental Hazard Statements Repeated exposure may cause skin dryness or cracking.
RIDADR UN1090 - class 3 - PG 2 - Acetone
WGK Germany 1
RTECS AL3150000
Flash Point(F) 1.4 °F
Flash Point(C) -17 °C

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WARNING: This product can expose you to chemicals which are known to the State of California to cause cancer and reproductive harm. Prop 65 Warning

Please note: This product is not returnable.

<ul><li>CAS Number 67-64-1</li><li>Linear Formula  CH3COCH3</li><li>Molecular Weight  58.08</li><li>Beilstein/REAXYS Number  635680</li><li>EC Number 200-662-2</li><li>MDL number MFCD00008765</li><li>eCl@ss  39021201</li><li>PubChem Substance ID 329760025</li><li>NACRES  NA.02</li></ul><table><tbody><tr><td>grade</td><td>HPLC Plus</td></tr><tr><td></td><td>for GC</td></tr><tr><td></td><td>for HPLC</td></tr><tr><td></td><td>for residue analysis</td></tr><tr><td>vapor density</td><td>2 (vs air)</td></tr><tr><td>vapor pressure</td><td>184 mmHg ( 20 °C)</td></tr><tr><td>assay</td><td>≥99.9%</td></tr><tr><td>form</td><td>liquid</td></tr><tr><td>expl. lim.</td><td>13.2 %</td></tr><tr><td>impurities</td><td>≤0.5% water</td></tr><tr><td></td><td>≤1.0 ppb Fluorescence (quinine) at 365 nm</td></tr><tr><td>evapn. residue</td><td>≤0.0003%</td></tr><tr><td>halogenated residue</td><td><10 ng/L (as heptachlor epoxide)</td></tr><tr><td>refractive index</td><td>n20/D 1.359 (lit.)</td></tr><tr><td>bp</td><td>56 °C/760 mmHg (lit.)</td></tr><tr><td>mp</td><td>−94 °C (lit.)</td></tr><tr><td>solubility</td><td>water: miscible</td></tr><tr><td>density</td><td>0.791 g/mL at 25 °C (lit.)</td></tr><tr><td>λ</td><td>H2O reference</td></tr><tr><td>UV absorption</td><td>λ: 330 nm Amax: 1.0</td></tr><tr><td></td><td>λ: 340 nm Amax: 0.06</td></tr><tr><td></td><td>λ: 350 nm Amax: 0.01</td></tr><tr><td></td><td>λ: 375-400 nm Amax: 0.005</td></tr><tr><td>Featured Industry</td><td>Food and Beverages</td></tr><tr><td>SMILES string</td><td>CC(C)=O</td></tr><tr><td>InChI</td><td>1S/C3H6O/c1-3(2)4/h1-2H3</td></tr><tr><td>InChI key</td><td>CSCPPACGZOOCGX-UHFFFAOYSA-N</td></tr></tbody></table><p>General description</p><p>Acetone is a ketone. Mixtures of TiO₂ (P25) with rare earth oxides (La₂O₃ or Y₂O₃) calcined at 700&deg;C or 650&deg;C has been reported to efficiently photocatalyze oxidation of acetone.<span id="501484"></span>&nbsp;Its aldol condensation in vapor-phase has been investigated over MgO promoted with alkali (Li, Na, K and Cs) or alkaline earth (Ca, Sr and Ba) metal ions.It undergoes Aldol condensation in the presence of Mg-Al layered double hydroxides (LDH) as catalysts and Cl^- and/or CO₃^2- as compensating anions to afford diacetone alcohol and mesityl oxide.<span id="501488"></span>&nbsp;Enantioselective Aldol condensation of acetone with various isatins in the presence of dipeptides (catalyst) has been described.<span id="501489"></span></p><p>Application</p><p>Acetone may be used in the following studies:<br />&bull;&nbsp;NMR spectroscopic evaluation of glucose metabolism in biological samples (blood).&nbsp;<br />&bull;&nbsp;Preparation of 13wt% amorphous poly (lactic acid) (PLA) solution, which was required for the preparation of electrospun PLA membranes.<span id="519215"></span><br />&bull;&nbsp;As a precursor for the synthesis of methyl isobutyl ketone (MIBK) in the presence of sulfonated graphene oxide-Pd/cordierite catalyst.<span id="602920"></span><br />&bull;&nbsp;Synthesis of (4-hydroxymethyl-2,2-dime<wbr />thyl-1,3-dioxolane), a solketal from glycerol using supercritical fluids (SCF) technology.<span id="602921"></span><br />It may be used in the synthesis of the following acetone hydrazones:<br />&bull;&nbsp;1-isopropylidene-2-meth<wbr />ylhydrazine<span id="602922"></span><br />&bull;&nbsp;1-isopropylidene-2-hydr<wbr />oxyethylhydrazine<span id="602922"></span><br />&bull;&nbsp;1-isopropylidene-2-form<wbr />ylhydrazine<span id="602922"></span></p><p>Acetone&prime;s luminesence intensity is dependent upon the solution components <span id="104954"></span>. The absorption of UV light by acetone, results in its photolysis and the production of radials <span id="104954"></span>.</p><p>Suitable for HPLC, spectrophotometry, environmental testing</p>