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Merck
CN

138185

Hydroxyacetone

contains ≤500 ppm sodium carbonate as stabilizer, technical grade, 90%

Synonym(s):

1-Hydroxy-2-propanone, Acetol

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About This Item

Linear Formula:
CH3COCH2OH
CAS Number:
116-09-6
Molecular Weight:
74.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848238
EC Number:
204-124-8
Beilstein/REAXYS Number:
605368
MDL number:
MFCD00004669

Key Documents

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Product Name

Hydroxyacetone, contains ≤500 ppm sodium carbonate as stabilizer, technical grade, 90%

InChI key

XLSMFKSTNGKWQX-UHFFFAOYSA-N

InChI

1S/C3H6O2/c1-3(5)2-4/h4H,2H2,1H3

SMILES string

CC(=O)CO

grade

technical grade

assay

90%

form

liquid

contains

≤500 ppm sodium carbonate as stabilizer

refractive index

n20/D 1.425 (lit.)

bp

145-146 °C (lit.)

mp

−17 °C (lit.)

solubility

water: miscible

density

1.082 g/mL at 25 °C (lit.)

functional group

hydroxyl
ketone

storage temp.

2-8°C

Quality Level

200

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Application

Hydroxyacetone was used to study aerobic oxidation of glycerol and propanediol over metal oxide supported gold nanoparticles in methanol.

General description

Hydroxyacetone (Acetol) is important for the manufacture of polyols, acrolein, dyes and skin tanning agents. It undergoes asymmetric reduction to yield (R)-1,2-propanediol in the presence of microbial cell catalyst.

pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Warning

hcodes

H226,H341

Hazard Classifications

Flam. Liq. 3 - Muta. 2

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

133.7 °F - closed cup

flash_point_c

56.5 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
SDBB5965
STBK7535
STBK0595
STBH8032
STBD6800V

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

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  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. What are the impurities of this Product 138185, Hydroxyacetone?

    The impurities for Product 138185 are not determined.

  6. Is Product 138185, Hydroxyacetone, a liquid or a solid?

    This product is a liquid measured in grams. The density is 1.082 g/mL at 25 °C

  7. Is Product 138185, Hydroxyacetone, on the Toxic Substances Control Act (TSCA) list?

    Yes, Product No. 138185 is currently on the TSCA inventory list.

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Hongliang Zhu et al.
Bioresource technology, 149, 238-243 (2013-10-12)
Escherichia coli Lin43 is a strain which has some mutations in glycerol kinase (GlpK) and the repressor for the glycerol 3-phosphate regulon (GlpR). When exposed to glycerol, it quickly accumulates lethal levels of methylglyoxal, which is a precursor of acetol;
Ganesh Sriram et al.
Metabolic engineering, 9(5-6), 442-451 (2007-09-25)
Biosynthetically directed fractional (13)C labeling, a popular methodology of metabolic flux analysis, involves culture on a mixture of (13)C and (12)C substrates and preparation a 'metabolic flux analyte' (typically protein hydrolysate) from the biomass. Metabolic flux analytes prepared from complex
Terry J Dillon et al.
Physical chemistry chemical physics : PCCP, 8(2), 236-246 (2006-02-17)
Absolute rate coefficients for the title reaction, HO + HOCH(2)C(O)CH(3)--> products (R1) were measured over the temperature range 233-363 K using the technique of pulsed laser photolytic generation of the HO radical coupled to detection by pulsed laser induced fluorescence.
Chen Liu et al.
Organic letters, 13(19), 5248-5251 (2011-09-10)
An efficient direct asymmetric aldol reaction between hydroxyacetone and β,γ-unsaturated α-keto esters has been successfully developed. In the presence of 9-amino-9-deoxy-epi-cinchonine and trifluoroacetic acid, the direct aldol reaction of O-protected hydroxyacetone proceeded in a highly enantioselective manner, affording the desired
Qi-Xiang Guo et al.
The Journal of organic chemistry, 77(7), 3589-3594 (2012-03-02)
The diastereoselectively switchable enantioselective Mannich reaction of isatin imines with hydroxyacetone is reported. The chiral primary amino acid catalyzed this Mannich reaction to afford both anti- and syn-Mannich adducts in high yields, good diastereoselectivities, and enantioselectivities. The reason for the
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