CAS 1883-13-2
:Acide (±)-3-hydroxydodécanoïque
- (3Alpha,5Beta,7Beta,12Beta)-3,7,12-Trihydroxycholan-24-Oic Acid
- (RS)-3-Hydroxylauric acid
- 3,16-Dihydroxyandrost-2-En-1-One
- 3-Hydroxy C12:0 Acid
- 3-Hydroxydodecanoic acid, 98 %
- 3-Hydroxylauric acid
- <span class="text-smallcaps">DL</span>-β-Hydroxydodecanoic acid
- Dl-Beta-Hydroxylauric Acid
- Dodecanoic acid, 3-hydroxy-
- β-Hydroxydodecanoic acid
- β-Hydroxylauric acid
- (+/-)-3-HYDROXYDODECANOIC ACID
- Voir plus de synonymes
Dodecanoic acid, 3-hydroxy-
CAS :Formule :C12H24O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :216.31723-Hydroxydodecanoic Acid
CAS :3-Hydroxydodecanoic AcidDegré de pureté :99%Masse moléculaire :216.32g/mol3-Hydroxydodecanoic acid
CAS :Formule :C12H24O3Degré de pureté :>98%Couleur et forme :SolidMasse moléculaire :216.323-Hydroxydodecanoic acid
CAS :3-Hydroxydodecanoic acid is a medium-chain fatty acid commonly linked to fatty acid metabolic disorders.Formule :C12H24O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :216.32Ref: TM-T19120
2mg43,00€5mg63,00€10mg92,00€25mg177,00€50mg264,00€100mg391,00€200mg567,00€1mL*10mM (DMSO)70,00€DL-²-Hydroxylauric acid
CAS :DL-2-Hydroxylauric acid is a metabolic product of L-ascorbic acid and is synthesized from the enzyme esterase. DL-2-Hydroxylauric acid has been shown to have anti-fungal activity in vitro against Candida albicans and Saccharomyces cerevisiae, as well as inhibitory effects on Escherichia coli. The structural analysis of DL-2-hydroxylauric acid revealed that it contains a hydroxyl group at the 2 position and an ester linkage at the 3 position. This compound can be detected by fluorescence detector with a neutral pH and an ethylene diamine.
Formule :C12H24O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :216.32 g/mol3-Hydroxylauric Acid
CAS :Applications 3-Hydroxylauric Acid is used in the study of Lipid A, a major constituent of the lipopolysaccharides, which are responsible for the toxicity of gram negative bacteria. Also used in the synthesis of olefins from β-hydroxy carboxylic acids.
References Ogawa, Y. et al.: Carb. Res., 220, 155 (1991); Hara, S. et al.: Tetrahedron Lett., 1545 (1975);Formule :C12H24O3Couleur et forme :NeatMasse moléculaire :216.3172







