1,2-Octanediol CAS#1117-86-8

Diverse chemical applications: It possesses significant potential for use in chemical synthesis and analytical fields, including the preparation of halohydrin palmitates.

Enhancement of chromatographic performance: It is used to improve the HPLC separation of organic acids and bases, facilitating highly efficient analytical processes.

Potential antimicrobial properties: It has shown promise as a pediculicide (lice-killing agent) and has been demonstrated to be effective against lice infestations.

Functional diol structure: It features a unique diol structure, which provides valuable chemical reactivity for applications in pharmaceutical and specialty chemical.

1,2-Octanediol CAS#1117-86-8

1,2-Octanediol is a multifunctional chemical compound with a wide range of applications. It is utilized to enhance the HPLC separation performance of organic acids and bases and serves as a raw material for the synthesis of halohydrin palmitates. Additionally, 1,2-Octanediol has been investigated for its potential use as a pediculicide and has demonstrated effectiveness against louse infestations.

Chemical Properties

Melting point 36-38 °C (lit.)
Boiling point 131-132 °C/10 mmHg (lit.)
density 0.914
vapor density >1 (vs air)
vapor pressure 0.28Pa at 25℃
refractive index 1.4505 (estimate)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
solubility 3 g/L (20°C)
form Low Melting Solid
pka14.60±0.10(Predicted)
color Colorless to white
Water Solubility 3 g/L (20 ºC)
BRN 1719619
Cosmetics Ingredients FunctionsSKIN CONDITIONING - EMOLLIENT
DEODORANT
HAIR CONDITIONING
SKIN CONDITIONING
LogP2.1 at 25℃
CAS DataBase Reference1117-86-8(CAS DataBase Reference)
NIST Chemistry Reference1,2-Octanediol(1117-86-8)
EPA Substance Registry System1,2-Octanediol (1117-86-8)
Hazard Codes Xi
Risk Statements 36
Safety Statements 37/39-26-24/25
WGK Germany 2
TSCA TSCA listed
HazardClass IRRITANT
HS Code 29053990
1,2-Octanediol CAS#1117-86-8

Product Application of 1,2-Octanediol CAS#1117-86-8

Diols generally have high water solubility and strong hygroscopicity. Because of their linear aliphatic carbon chain structures, they are also reactive with various organic compounds. 1,2-Octanediol is a linear diol with two primary hydroxyl groups, so it has bacteriostatic and bactericidal properties. It is a valuable preservative in cosmetic formulas.

It is also widely used in coating materials, slurries, paper manufacturing processes and water circulation systems, and can effectively prevent the fungal growth. In cosmetics and personal care products, 1,2-Octanediol can be used as an emollient, humectant and wetting agent to help improve product performance.

Because alcohol compounds have active hydroxyl groups, they can undergo various chemical reactions, including dehydration, oxidation, nucleophilic substitution and condensation reactions. Under acidic conditions, alcohols may be dehydrated to form alkenes, while primary and secondary alcohols can be oxidized to aldehydes and ketones respectively. Aldehydes are further oxidized to form carboxylic acids.

Alcohols can also participate in condensation reactions to form ethers and esters, such as the esterification reaction between alcohols and carboxylic acids. Alcohol compounds are important solvents and chemical intermediates and are widely used in the production of pharmaceuticals, veterinary medicines, plasticizers, surfactants, lubricants, flotation agents, pesticides, hydraulic fluids and detergents.

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1,2-Octanediol CAS#1117-86-8

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