CAS 54340-91-9
:Heptanoic acid, 2-hydroxy-, methyl ester
Description:
Heptanoic acid, 2-hydroxy-, methyl ester, also known as methyl 2-hydroxyheptanoate, is an ester derived from heptanoic acid and methanol. This compound features a seven-carbon chain with a hydroxyl group at the second carbon, contributing to its classification as a hydroxy acid. It is a colorless to pale yellow liquid with a characteristic fatty odor. The presence of the hydroxyl group imparts some polar characteristics, making it more soluble in polar solvents compared to its parent heptanoic acid. This compound is often used in the synthesis of various chemicals, as well as in the production of fragrances and flavoring agents due to its pleasant aroma. Additionally, it may have applications in the cosmetic and pharmaceutical industries. Its chemical structure allows for potential reactivity in esterification and transesterification reactions, making it a versatile intermediate in organic synthesis. As with many esters, it is important to handle this compound with care, observing appropriate safety protocols due to potential irritant properties.
Formula:C8H16O3
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
Methyl 2-hydroxyheptanoate
CAS:Methyl 2-hydroxyheptanoate is a fatty acid that is found in soybean lipoxygenase. It has been shown to inhibit prostaglandin synthesis by the enzymatic hydrolysis of methyl 2-hydroxyheptanoate. The hydrolysis products of this reaction are anions, sulfoxide, and carboxylates. Methyl 2-hydroxyheptanoate is also a substrate for the enzyme, soybean lipoxygenase. This enzyme catalyzes the conversion of methyl 2-hydroxyheptanoate to prostaglandin E2 (PGE2). PGE2 is a potent inhibitor of platelet aggregation and vasoconstriction.
Formula:C8H16O3Purity:Min. 95%Molecular weight:160.21 g/mol
