638-26-6 | 10-Hydroxyoctadecanoic acid

Packsize	Purity	Availability	Price	Discounted Price
50mg	95%	in stock	$116.00	$81.00
100mg	95%	in stock	$189.00	$132.00
250mg	95%	in stock	$376.00	$263.00
1g	95%	in stock	$1,313.00	$919.00

Description

• Catalog Number: AB43220
• Chemical Name: 10-Hydroxyoctadecanoic acid
• CAS Number: 638-26-6
• Molecular Formula: C18H36O3
• Molecular Weight: 300.4766
• MDL Number: MFCD08693364
• SMILES: CCCCCCCCC(CCCCCCCCC(=O)O)O
• NSC Number: 79060

Computed Properties

• Complexity: 229
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 21
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 16
• Undefined Atom Stereocenter Count: 1
• XLogP3: 6.5

Literature

• Production of 10-hydroxystearic acid from oleic acid and olive oil hydrolyzate by an oleate hydratase from Lysinibacillus fusiformis.

  Applied microbiology and biotechnology 20120801

• Production of 10-hydroxystearic acid from oleic acid by whole cells of recombinant Escherichia coli containing oleate hydratase from Stenotrophomonas maltophilia.

  Journal of biotechnology 20120331

• Determination of 10-hydroxystearic, 10-ketostearic, 8-hydroxypalmitic, and 8-ketopalmitic acids in milk fat by solid-phase extraction plus gas chromatography-mass spectrometry.

  Journal of dairy science 20111001

• Post-mortem volatiles of vertebrate tissue.

  Applied microbiology and biotechnology 20110801

• Conversion of oleic acid to 10-hydroxystearic acid by whole cells of Stenotrophomonas nitritireducens.

  Biotechnology letters 20110501

• Myosin-cross-reactive antigen (MCRA) protein from Bifidobacterium breve is a FAD-dependent fatty acid hydratase which has a function in stress protection.

  BMC biochemistry 20110101

• Cloning and characterization of a 9-lipoxygenase gene induced by pathogen attack from Nicotiana benthamiana for biotechnological application.

  BMC biotechnology 20110101

• Production of oxygenated fatty acids from vegetable oils by Flavobacterium sp. strain DS5.

  New biotechnology 20091001

• Adipocere formation via hydrogenation of linoleic acid in a victim kept under dry concealment.

  Forensic science international 20080305

• New bioactive fatty acids.

  Asia Pacific journal of clinical nutrition 20080101

• Chemical constituents of cape aloe and their synergistic growth-inhibiting effect on Ehrlich ascites tumor cells.

  Bioscience, biotechnology, and biochemistry 20070501

• Fluorescein conjugates of 9- and 10-hydroxystearic acids: synthetic strategies, photophysical characterization, and confocal microscopy applications.

  Analytical biochemistry 20041215

• Two distinct pathways for the formation of hydroxy FA from linoleic acid by lactic acid bacteria.

  Lipids 20031201

• Fatty acid composition and preservation of the Tyrolean Iceman and other mummies.

  Journal of lipid research 20021201

• Conversion of fatty acids by Bacillus sphaericus-like organisms.

  Current microbiology 20021001

• Gas chromatography/mass spectrometric assay of endogenous cellular lipid peroxidation products: quantitative analysis of 9- and 10-hydroxystearic acids.

  Rapid communications in mass spectrometry : RCM 20020101