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Chemical structure of 3-Oxobutanol | 590-90-9
CAS: 590-90-9
SKU: S2703
3-Oxobutanol | SKU: S2703
Chemical structure of 3-Oxobutanol | 590-90-9
Request Quote — S2703

Specifications

AppearanceN/A
Content of ZincN/A
Boiling Point170°C
Melting PointN/A
Vapor PressureN/A
% Volatile by WeightN/A
Solubility in WaterN/A
DensityN/A
pH of Liquid, Typical (10% soln)N/A
Specific Gravity ApproxN/A
OdorN/A
pHN/A
Flash PointN/A
Ignition temperatureN/A
Lower exposure limitN/A
Upper exposure limitN/A
ColorColorless
Formula Weight88.11
Physical FormClear Liquid at 20°C
Chemical Name or Material4-Hydroxy-2-butanone

Applications

No Application Found

Product Description

111509

Synonym : 4-hydroxy-2-butanone, 2-butanone, 4-hydroxy, methylolacetone, 3-oxo-1-butanol, 3-oxobutanol, 3-ketobutan-1-ol, monomethylolacetone, 4-butanol-2-one, unii-tcm0bj44mf, 2-hydroxyethyl methyl ketone

Safety Information

No Safety Information Found

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FAQs: 3-Oxobutanol

With an aldehyde group at the first carbon atom and a keto group at the third carbon atom, 3-oxobutanal has a four-carbon chain structure. A typical representation that emphasizes its essential functional groups is CH3-CO-CH2-CHO.

Metabolic reactions commonly produce 3-oxobutanal, a chemical molecule with ketone and aldehyde groups. Its reactive carbonyl groups make it an important component of metabolic pathways and an intermediary in many chemical reactions.

The chemical equation for oxobutanol is C4H8O2. The presence of alcohol and a carbonyl group in this molecule gives it its hydroxy ketone structure, making it chemically reactive and essential in biochemistry and organic synthesis.

Because of the aldehyde and ketone functional groups, 3-oxobutanal is very reactive. Its versatility in chemical processes is due to its ability to undertake nucleophilic addition reactions (e.g., with amines or alcohols) and to participate in condensation reactions.

In organic synthesis, 3-oxobutanal is a frequently used intermediate in creating a wide range of chemicals. Its reactive carbonyl groups make it very useful in transformations and reactions such as aldol condensations.