4,4-Dimethoxy-2-butanone

[Description]:

[Related Catalog]:

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
172.1±20.0 °C at 760 mmHg

[ Melting Point ]:
-82 °C

[ Molecular Formula ]:
C₆H₁₂O₃

[ Molecular Weight ]:
132.158

[ Flash Point ]:
49.4±0.0 °C

[ Exact Mass ]:
132.078644

[ PSA ]:
35.53000

[ LogP ]:
0.33

[ Vapour Pressure ]:
1.4±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.399

[ Storage condition ]:
Flammables area

[ Water Solubility ]:
decomposes

Click to get detail MSDS

[ Symbol ]:

GHS02

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H226

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
F

[ Risk Phrases ]:
R10

[ Safety Phrases ]:
S16

[ RIDADR ]:
UN 1989 3/PG 3

[ WGK Germany ]:
2

[ RTECS ]:
EL7592500

[ Packaging Group ]:
III

[ Hazard Class ]:
3

[ HS Code ]:
29145000

Click to get detail synthetic route

Precursor

DownStream

[ HS Code ]: 2914509090

[ Summary ]:
HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Carbonylation as a key reaction in anaerobic acetone activation by Desulfococcus biacutus.

Appl. Environ. Microbiol. 79(20) , 6228-35, (2013)

Acetone is activated by aerobic and nitrate-reducing bacteria via an ATP-dependent carboxylation reaction to form acetoacetate as the first reaction product. In the activation of acetone by sulfate-re...

Yamadazyma Farinosa IFO 10896-mediated reduction of 4, 4-dimethoxy-2-butanone as the key-step for the preparation of 1, 3-diols with unsymmetrical substituents. Yamazaki T, et al.

Synth. Commun. 30(16) , 3061-72, (2000)

β-keto acetals. I. Synthesis of pyrazoles and pyrimidines and the steric inhibition of resonance in 5-alkyl-1-p-nitrophenylpyrazoles. Burness DM.

J. Org. Chem. 21(1) , 97-101., (1956)

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