4,4-Dimethoxy-2-butanone structure
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Common Name | 4,4-Dimethoxy-2-butanone | ||
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CAS Number | 5436-21-5 | Molecular Weight | 132.158 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 172.1±20.0 °C at 760 mmHg | |
Molecular Formula | C6H12O3 | Melting Point | -82 °C | |
MSDS | Chinese USA | Flash Point | 49.4±0.0 °C | |
Symbol |
GHS02 |
Signal Word | Warning |
Use of 4,4-Dimethoxy-2-butanone4,4-Dimethoxy-2-butanone is an endogenous metabolite. |
Name | Acetylacetaldehyde dimethyl acetal |
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Synonym | More Synonyms |
Description | 4,4-Dimethoxy-2-butanone is an endogenous metabolite. |
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Related Catalog |
Density | 1.0±0.1 g/cm3 |
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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 |
Symbol |
GHS02 |
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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 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2914509090 |
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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... |
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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)
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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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1,1-Dimethoxybutan-3-one |
MFCD00008789 |
4,4-Dimethoxybutan-2-one |
3-Ketobutyraldehyde dimethyl acetal |
EINECS 226-605-1 |
2-Butanone, 4,4-dimethoxy- |
β-Oxobutyraldehyde dimethyl acetal |
1,1-Dimethoxy-3-butanone |
4,4-Dimethoxy-2-butanone |
Acetylacetaldehyde dimethylacetal |
Acetylacetaldehydedimethylacetal |