| Identification | More | [Name]
10-Hydroxydecanoic acid | [CAS]
1679-53-4 | [Synonyms]
10-HYDROXYDECANOIC ACID
10-Hydroxycapricacid
Decanoic acid, 10-hydroxy-
10-HYDROXY-DECYLIC ACID
10-HYDROXYDECANOIC ACID 95% | [EINECS(EC#)]
216-848-1 | [Molecular Formula]
C10H20O3 | [MDL Number]
MFCD00010510 | [Molecular Weight]
188.26 | [MOL File]
1679-53-4.mol |
| Hazard Information | Back Directory | [Uses]
Reactant involved in: • ;Synthesis of copolymers of acrylamide and sodium acryloyloxydecanoate1• ;Macrolactonization for preparation of Sansalvamide A2• ;Studies of chain length selectivity for cutinase catalyzed polycondensation reactions3• ;Ruthenium-catalyzed esterification followed by macrocyclization4• ;Synthesis of anhydrides and esters5 | [Definition]
ChEBI: A 10-carbon, omega-hydroxy fatty acid, shown to be the preferred hydroxylation product (together with the 9-OH isomer) of capric acid in biosystems, and used as a standard in lipid assays; reported to have cytotoxic effects. | [General Description]
10-Hydroxydecanoic acid (10-HDA) is a saturated fatty acid of hydroxy-trans-2-decenoic acid (10H2DA). Its molecule has two functional groups (-OH and -COOH). It has been reported to prevent the lipopolysaccharide-induced NO production in murine macrophages. 10-HDA has been extracted from royal jelly obtained from honeybees (Apis mellifera) and exhibits estrogenic action. Its polymerization with the polyethylene glycol-modified lipase in a transparent benzene solution has been reported to proceed by the formation of ester linkage. |
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