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| | 3-Hydroxydecanoic acid Basic information |
| Product Name: | 3-Hydroxydecanoic acid | | Synonyms: | 3-Hydroxydecanoic acid, 98 %;Mirmicacin;3-HYDROXY C10:0 ACID;(+/-)-3-HYDROXYDECANOIC ACID;DL-BETA-HYDROXYCAPRIC ACID;Decanoicacid,3-hydroxy-;Endogenous Metabolite,3Hydroxycapric acid,Inhibitor,3 Hydroxycapric acid,3-Hydroxycapric acid,inhibit;3-Hydroxydecanoic acid, 3-Hydroxy C10:0 fatty acid | | CAS: | 14292-26-3 | | MF: | C10H20O3 | | MW: | 188.26 | | EINECS: | | | Product Categories: | | | Mol File: | 14292-26-3.mol |  |
| | 3-Hydroxydecanoic acid Chemical Properties |
| Melting point | 47-48 °C | | Boiling point | 318.2±25.0 °C(Predicted) | | density | 1.011±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Solid | | pka | 4.39±0.10(Predicted) | | color | White to Off-White | | InChI | InChI=1S/C10H20O3/c1-2-3-4-5-6-7-9(11)8-10(12)13/h9,11H,2-8H2,1H3,(H,12,13) | | InChIKey | FYSSBMZUBSBFJL-UHFFFAOYSA-N | | SMILES | OC(=O)CC(O)CCCCCCC | | LogP | 2.293 (est) |
| | 3-Hydroxydecanoic acid Usage And Synthesis |
| Description | 3-hydroxy Decanoic acid is a hydroxy fatty acid and the predominant monomer in methyl-branched poly(3-hydroxyalkanoate) (PHA) polymers produced by P. putida CA-3. It is present in LPS from the H. pylori strain SS1 and in the lipid A component of clinical isolates of P. aeruginosa isolated from patients with cystic fibrosis but not the environment or patients with other conditions. 3-hydroxy Decanoic acid inhibits mitotic progression of O. virens pollens via impairment of plasma membrane function. It also induces a reversible shape change of the membrane crenation in human erythrocytes. [Matreya, LLC. Catalog No. 1727] | | Uses | 3-Hydroxycapric acid is an inhibitor for mitotic progression. | | Definition | ChEBI: A medium-chain fatty acid that is decanoic acid substituted at position 3 by a hydroxy group. | | Synthesis | Preparation of 3-hydroxydecanoic acid: 16.5 g (50 mmol) of ethyl 3-hydroxydecanoate prepared by process (1) was co-dissolved with 10.0 g (250 mmol) of lithium hydroxide in 50 mL of a solvent mixture consisting of tetrahydrofuran and water (1:2, v/v). The reaction mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, the reaction solution was neutralized with dilute hydrochloric acid and subsequently concentrated under reduced pressure. The concentrated residue was extracted with ethyl acetate. The ethyl acetate layer obtained from the extraction was sequentially washed with saturated brine and dried with anhydrous magnesium sulfate, followed by concentration under reduced pressure to remove the solvent. The concentrated residue was purified by silica gel column chromatography (eluent: ethyl acetate/methanol=4/6, v/v) to obtain the target product 3-hydroxydecanoic acid in 90% yield. Yield: 12.2 g (45 mmol). The product was characterized by 1H-NMR (CDCl3,500MHz): δ 0.86 (t, 3H), 1.25 (m, 14H), 1.33 (m, 2H), 2.31 (m, 2H), 3.79 (m, 1H). | | IC 50 | Human Endogenous Metabolite | | References | [1] Iwanami Y. et al. Myrmicacin, a new inhibitor for mitotic progression after metaphase. Protoplasma. 1978;95(3):267-71. DOI:10.1007/BF01294455 |
| | 3-Hydroxydecanoic acid Preparation Products And Raw materials |
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