Skip to Content
Merck
All Photos(3)

Key Documents

More Documents

213705

Sigma-Aldrich

1,2-Octanediol

98%

Synonym(s):

(±)-Octane-1,2-diol, 1,2-Dihydroxyoctane, 1,2-Octylene glycol, 7,8-Dihydroxyoctane, Caprylyl glycol, n-Octane-1,2-diol

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
CH3(CH2)5CH(OH)CH2OH
CAS Number:
1117-86-8
Molecular Weight:
146.23
EC Number:
214-254-7
MDL number:
MFCD00010738
UNSPSC Code:
12352100
PubChem Substance ID:
24852793
NACRES:
NA.22

vapor density

>1 (vs air)

Quality Level

200

Assay

98%

form

solid

bp

131-132 °C/10 mmHg (lit.)

mp

36-38 °C (lit.)

SMILES string

CCCCCCC(O)CO

InChI

1S/C8H18O2/c1-2-3-4-5-6-8(10)7-9/h8-10H,2-7H2,1H3

InChI key

AEIJTFQOBWATKX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

1,2-Octanediol is a potential pediculicide and is useful for treating head louse infestation clinically.

Application

1,2-Octanediol was used as organic modifier to improve the HPLC separation of organic acids and bases. It was also used in preparation of halohydrin palmitates.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ian F Burgess et al.
PloS one, 7(4), e35419-e35419 (2012-04-24)
Interest in developing physically active pediculicides has identified new active substances. The objective was to evaluate a new treatment for clinical efficacy. We describe the selection of 1,2-octanediol as a potential pediculicide. Clinical studies were community based. The main outcome
Shelly Li et al.
Journal of chromatography. A, 964(1-2), 91-98 (2002-08-30)
A straight-chain alcohol or diol additive in the mobile phase was used to modify and improve the HPLC separation of organic acids and bases. Incorporation of 2% 1-butanol, 1% 1,2-hexanediol, or 0.25% 1,2-octanediol into an aqueous mobile phase greatly improved
Mireia Oromí-Farrús et al.
Molecules (Basel, Switzerland), 14(10), 4275-4283 (2009-11-20)
Preparation of (S)-1-chloro-2-octanol and (S)-1-bromo-2-octanol was carried out by the enzymatic hydrolysis of halohydrin palmitates using biocatalysts. Halohydrin palmitates were prepared by various methods from palmitic acid and 1,2-octanediol. A tandem hydrolysis was carried out using lipases from Candida antarctica
Kelli L Hvorecny et al.
Structure (London, England : 1993), 25(5), 697-707 (2017-04-11)
Pseudomonas aeruginosa secretes an epoxide hydrolase with catalytic activity that triggers degradation of the cystic fibrosis transmembrane conductance regulator (CFTR) and perturbs other host defense networks. Targets of this CFTR inhibitory factor (Cif) are largely unknown, but include an epoxy-fatty

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service