CAS 24964-76-9
:Triethyl orthobutyrate
Description:
Triethyl orthobutyrate, with the CAS number 24964-76-9, is an organic compound classified as an ester. It is formed from the reaction of butyric acid and ethanol, resulting in a structure characterized by three ethyl groups attached to a butyrate moiety. This compound is typically a colorless liquid with a fruity odor, making it useful in flavoring and fragrance applications. Triethyl orthobutyrate is known for its low toxicity and is often employed as a solvent in various chemical processes. Its boiling point and solubility in organic solvents make it suitable for use in the synthesis of other chemical compounds. Additionally, it can participate in esterification reactions and is sometimes utilized in the production of pharmaceuticals and agrochemicals. As with many esters, it is important to handle triethyl orthobutyrate with care, ensuring proper safety measures are in place to avoid inhalation or skin contact.
Formula:C10H22O3
InChI:InChI=1/C10H22O3/c1-5-9-10(11-6-2,12-7-3)13-8-4/h5-9H2,1-4H3
SMILES:CCCC(OCC)(OCC)OCC
Synonyms:- 1,1,1-Triethoxy-butane
- Teob
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Found 5 products.
Triethyl Orthobutyrate
CAS:Formula:C10H22O3Purity:>90.0%(GC)Color and Shape:Colorless clear liquidMolecular weight:190.28Butane, 1,1,1-triethoxy-
CAS:Formula:C10H22O3Purity:95%Color and Shape:LiquidMolecular weight:190.2799Triethyl Orthobutyrate
CAS:<p>Triethyl Orthobutyrate is a versatile compound with various applications. It is commonly used as a benzylic protecting group in organic synthesis and as an alkaloid precursor. Triethyl Orthobutyrate has been found to exhibit superoxide scavenging activity, making it potentially useful in antioxidant formulations. Additionally, it can serve as a glucuronic acid derivative and has been studied for its potential therapeutic effects on coumarins-induced liver injury. In the medical field, Triethyl Orthobutyrate has shown promise as an additive to atosiban formulations, which are used to inhibit premature labor. It can also be utilized in electrode coatings and antibody immobilization processes due to its ability to form stable complexes with l-lysine. Furthermore, Triethyl Orthobutyrate has been investigated for its role in enhancing the transdermal delivery of drugs like zolmitriptan. Its nuclear magnetic resonance (NMR) properties make it useful for analyzing complex biological extracts, while its magnesium</p>Formula:C10H22O3Purity:Min. 95%Molecular weight:190.28 g/mol




