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Merck
CN

00568

丙酮

suitable for HPLC, ≥99.8% (GC)

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线性分子式:
CH3COCH3
化学文摘社编号:
分子量:
58.08
EC Number:
200-662-2
UNSPSC Code:
41116105
PubChem Substance ID:
Beilstein/REAXYS Number:
635680
MDL number:
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InChI key

CSCPPACGZOOCGX-UHFFFAOYSA-N

InChI

1S/C3H6O/c1-3(2)4/h1-2H3

SMILES string

CC(C)=O

vapor pressure

184 mmHg ( 20 °C), 184 mmHg

assay

≥99.8% (GC)

shelf life

limited shelf life, expiry date on the label

expl. lim.

13.2 %, 8 % (lit.)

technique(s)

HPLC: suitable

impurities

≤0.2% water

evapn. residue

≤0.001%

mp

-94 °C (lit.), −94 °C (lit.)

density

0.791 g/mL at 25 °C (lit.)

solvent strength ε (Al2O3)

0.56

λ

1 cm path, H2O reference

UV absorption

λ: 330 nm Amax: ≤1.0, λ: 350 nm Amax: ≤0.1, λ: 360 nm Amax: ≤0.01

application(s)

environmental
food and beverages

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Application

丙酮的发光强度取决于溶液组分。丙酮吸收UV光,导致丙酮光分解和放射性产物。

法规信息

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Cell research, 24(12), 1387-1402 (2014-11-22)
T helper (TH)-cell subsets, such as TH1 and TH17, mediate inflammation in both peripheral tissues and central nervous system. Here we show that STAT5 is required for T helper-cell pathogenicity in autoimmune neuroinflammation but not in experimental colitis. Although STAT5
Anna Hultberg et al.
PloS one, 6(4), e17665-e17665 (2011-04-13)
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Journal of molecular biology, 426(1), 256-271 (2013-10-29)
Designed retroaldolases have utilized a nucleophilic lysine to promote carbon-carbon bond cleavage of β-hydroxy-ketones via a covalent Schiff base intermediate. Previous computational designs have incorporated a water molecule to facilitate formation and breakdown of the carbinolamine intermediate to give the

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