1117-86-8 | 1,2-Octanediol

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$15.00	$10.00
5g	95%	in stock	$16.00	$11.00
10g	95%	in stock	$27.00	$19.00
25g	95%	in stock	$33.00	$23.00
100g	95%	in stock	$73.00	$51.00
400g	95%	in stock	$235.00	$165.00
500g	95%	in stock	$249.00	$175.00

Description

• Catalog Number: AB57171
• Chemical Name: 1,2-Octanediol
• CAS Number: 1117-86-8
• Molecular Formula: C8H18O2
• Molecular Weight: 146.2273
• MDL Number: MFCD00010738
• SMILES: CCCCCCC(CO)O
• NSC Number: 71546

Computed Properties

• Complexity: 64.3
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.8

Upstream Synthesis Route

Octane-1,2-diol, also known as 1,2-octanediol, is a versatile chemical compound commonly used in chemical synthesis processes. This compound is valued for its ability to act as a building block for the synthesis of various other chemicals and materials.In chemical synthesis, octane-1,2-diol serves as a crucial intermediate in the production of a wide range of products. It can be used as a precursor in the synthesis of polymers, resins, surfactants, and pharmaceuticals. Additionally, octane-1,2-diol is utilized in the creation of specialty chemicals, solvents, and additives for various industrial applications.Due to its unique chemical properties, octane-1,2-diol plays a significant role in the development of new compounds and materials. Its ability to function as a versatile building block enables chemists and researchers to explore different pathways for creating innovative products with diverse functionalities.Overall, octane-1,2-diol is a valuable component in chemical synthesis, offering a wide range of applications and contributing to the advancement of various industries.

Literature

• 1,2-Octanediol, a novel surfactant, for treating head louse infestation: identification of activity, formulation, and randomised, controlled trials.

  PloS one 20120101

• Acylation of Chiral Alcohols: A Simple Procedure for Chiral GC Analysis.

  Journal of analytical methods in chemistry 20120101

• Safety assessment of 1,2-glycols as used in cosmetics.

  International journal of toxicology 20120101

• The influence of alkane chain length on the skin irritation potential of 1,2-alkanediols.

  International journal of cosmetic science 20111001

• New insights into silica-based NMR 'chromatography'.

  Journal of magnetic resonance (San Diego, Calif. : 1997) 20110201

• Solvothermal synthesis and characterization of Eu3+ doped Y2O3 nanocrystals.

  Journal of nanoscience and nanotechnology 20100201

• Preparation of (S)-1-Halo-2-octanols Using Ionic Liquids and Biocatalysts.

  Molecules (Basel, Switzerland) 20091023

• Safety of a preservative system containing 1,2-hexanediol and caprylyl glycol.

  Cutaneous and ocular toxicology 20090101

• [BMIM][PF(6)] promotes the synthesis of halohydrin esters from diols using potassium halides.

  Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20081001

• Octanediol treatment of glutaraldehyde fixed bovine pericardium: evidence of anticalcification efficacy in the subcutaneous rat model.

  European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 20080801

• Influence of lipophilia and of the vehicle used in the transdermal absorption of novel benzimidazole compounds with possible anti-HIV activity.

  Pharmaceutical development and technology 20080101

• Purification, characterization, and gene cloning of glycerol dehydrogenase from Hansenula ofunaensis, and its expression for production of optically active diol.

  Journal of bioscience and bioengineering 20061201

• Spreading on and penetration into thin, permeable print media: application to ink-jet printing.

  Advances in colloid and interface science 20061116

• Treatment of bioprosthetic heart valve tissue with long chain alcohol solution to lower calcification potential.

  Journal of biomedical materials research. Part A 20040401

• Organic modifiers for the separation of organic acids and bases by liquid chromatography.

  Journal of chromatography. A 20020726