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| 10-Hydroxydecanoic acid Basic information |
| 10-Hydroxydecanoic acid Chemical Properties |
Melting point | 75-77 °C (lit.) | Boiling point | 330.8±15.0 °C(Predicted) | density | 1.013±0.06 g/cm3(Predicted) | storage temp. | Sealed in dry,Room Temperature | solubility | Chloroform (Slightly), Methanol (Slightly) | pka | 4.78±0.10(Predicted) | form | Solid | color | White to Off-White | InChIKey | YJCJVMMDTBEITC-UHFFFAOYSA-N | LogP | 1.847 (est) | CAS DataBase Reference | 1679-53-4(CAS DataBase Reference) | NIST Chemistry Reference | 10-Hydroxydecanoic acid(1679-53-4) |
Hazard Codes | Xi | WGK Germany | 3 | Hazard Note | Irritant | HS Code | 2918199890 |
| 10-Hydroxydecanoic acid Usage And Synthesis |
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 | Uses | 10-Hydroxydecanoic acid is suitable for use in a study on Novozym 435-catalyzed condensation polymerization of cis-9,10-epoxy-18-hydroxyoctadecanoic acid and its comparison with corresponding polymerization of 10-hydroxydecanoic acid. | 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. |
| 10-Hydroxydecanoic acid Preparation Products And Raw materials |
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