8-HYDROXYOCTANOIC ACID

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CAS:764-89-6
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  • 8-hydroxyoctanoicacid
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  • 2022-01-15
  • CAS:764-89-6
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  • Purity: 97.5%
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8-HYDROXYOCTANOIC ACID Basic information
Product Name:8-HYDROXYOCTANOIC ACID
Synonyms:8-HYDROXYOCTANOIC ACID;8-HYDROXYCAPRYLIC ACID;8-hydroxyoctanoate;8-HYDROXYOCTANSURE;8-Hydroxyoctanoic acid,90%;Octanoic acid, 8-hydroxy-;8-Hydroxyoctanoic acid 98% (T);8-hydroxyoctanoicaci
CAS:764-89-6
MF:C8H16O3
MW:160.21
EINECS:
Product Categories:Building Blocks;C8;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks
Mol File:764-89-6.mol
8-HYDROXYOCTANOIC ACID Structure
8-HYDROXYOCTANOIC ACID Chemical Properties
Melting point 59-63 °C
Boiling point 130°C/1mm
density 1.0227 (rough estimate)
refractive index 1.4370 (estimate)
storage temp. Inert atmosphere,Room Temperature
pka4.77±0.10(Predicted)
form crystalline powder
color White
BRN 1237092
LogP0.900 (est)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 3261 8/PG 2
WGK Germany 3
10-21
HS Code 2918199890
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
8-HYDROXYOCTANOIC ACID Usage And Synthesis
Chemical Propertieslight yellow powder
Uses8-Hydroxyoctanoic Acid is an intermediate in the synthesis of mono-carboxy-isooctyl-phthalate (M525590). 8-Hydroxyoctanoic Acid is also used as a reagent in the synthesis of histone deacetylases (HDAC) inhibitors with an N-formyl hydroxylamine head group which are promising targets for cancer chemotherapy.
DefinitionChEBI: An omega-hydroxy fatty acid that is caprylic acid in which one of the hydrogens of the terminal methyl group is replaced by a hydroxy group.
General Description8-Hydroxyoctanoic acid is one of the constituents of ‘‘Royal jelly′′ acid found in herbhoneys and genuine honeys.
Synthesis
1,8-Octanediol

629-41-4

8-HYDROXYOCTANOIC ACID

764-89-6

GENERAL PROCEDURE: All catalytic activity testing experiments were carried out in Schlenk tubes (50 mL) equipped with a condenser. 8-Hydroxycaprylic acid (HCA) was prepared by HDO oxidation reaction in alkaline aqueous medium using H2O2 as oxidant. The typical reaction procedure was as follows: first, the aliphatic diol (0.5 mmol) was weighed and dispersed with catalyst (25 mg) in deionized water (3.5 mL) in a Schlenk tube. Subsequently, 30% H2O2 (0.75 mL) and 0.5 M NaOH (0.75 mL) were added to the above mixture. The Schlenk tubes were placed in an oil bath preheated to 353 K and reacted for different time intervals under continuous magnetic stirring (500 rpm). After completion of the reaction, a portion of the reaction solution was taken and diluted 20-fold with 10 mM aqueous H2SO4 and the catalyst was removed by passing it through a 0.20 μm filter (Milex-LG). The resulting filtrate was analyzed by high performance liquid chromatography (HPLC, WATERS 600) on an Aminex HPX-87H column (Bio-Rad Laboratories, Inc.) with a refractive index detector. An aqueous solution of 10 mM H2SO4 was used as the eluent at a flow rate of 0.5 mL/min, and the column temperature was maintained at 323 K. The conversion and yield were determined by the calibration curve method for commercial products.

References[1] Catalysis Today, 2016, vol. 265, p. 231 - 239
8-HYDROXYOCTANOIC ACID Preparation Products And Raw materials
Raw materialsSodium-->oxonan-2-one-->1,8-Octanediol-->Ethanol-->Sodium hydroxide-->Hydrogen peroxide
Preparation Products8-Aminooctanoic acid-->oxonan-2-one
Tag:8-HYDROXYOCTANOIC ACID(764-89-6) Related Product Information
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