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Merck
CN

W446207

羟基丙酮

≥95%, FG

别名:

1-羟基-2-丙酮, 丙酮醇

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关于此项目

线性分子式:
CH3COCH2OH
化学文摘社编号:
分子量:
74.08
PubChem Substance ID:
UNSPSC Code:
12164502
Colour Index Number:
11101
FEMA Number:
4462
Flavis number:
7.169
EC Number:
204-124-8
MDL number:
Beilstein/REAXYS Number:
605368
Organoleptic:
sweet
Grade:
FG, Kosher
Biological source:
synthetic
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InChI

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

InChI key

XLSMFKSTNGKWQX-UHFFFAOYSA-N

SMILES string

CC(=O)CO

biological source

synthetic

grade

FG, Kosher

reg. compliance

EU Regulation 1334/2008 & 178/2002

assay

≥95%

Quality Level

bp

145-146 °C (lit.)

mp

−17 °C (lit.)

density

1.082 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

organoleptic

sweet

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pictograms

FlameHealth hazard

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3 - Muta. 2

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

133.7 °F - closed cup

flash_point_c

56.5 °C - closed cup

法规信息

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I Blank et al.
Advances in experimental medicine and biology, 561, 171-189 (2006-01-28)
The formation of acrylamide (AA) from L-asparagine was studied in Maillard model systems under pyrolysis conditions. While the early Maillard intermediate N-glucosylasparagine generated approximately 2.4 mmol/mol AA, the Amadori compound was a less efficient precursor (0.1 mmol/mol). Reaction with alpha-dicarbonyls
Junsang Ko et al.
Journal of bacteriology, 187(16), 5782-5789 (2005-08-04)
Methylglyoxal (MG) is a toxic metabolite known to accumulate in various cell types. We detected in vivo conversion of MG to acetol in MG-accumulating Escherichia coli cells by use of (1)H nuclear magnetic resonance ((1)H-NMR) spectroscopy. A search for homologs
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
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.

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