Skip to Content
Merck
All Photos(3)

Documents

472328

Sigma-Aldrich

1-Octanol

ACS reagent, ≥99%

Synonym(s):

Alcohol C8, Capryl alcohol, Octyl alcohol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)7OH
CAS Number:
Molecular Weight:
130.23
Beilstein:
1697461
EC Number:
MDL number:
UNSPSC Code:
12352104
PubChem Substance ID:

grade

ACS reagent

Quality Level

vapor density

4.5 (vs air)

vapor pressure

0.14 mmHg ( 25 °C)

Assay

≥99%

form

liquid

autoignition temp.

523 °F

expl. lim.

8 %

impurities

≤0.0002 meq/g Titr. acid

evapn. residue

≤0.004%

color

APHA: ≤10
clear

refractive index

n20/D 1.429 (lit.)

bp

196 °C (lit.)

mp

−15 °C (lit.)

solubility

water: partially soluble 107 g/L at 23 °C

density

0.827 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCO

InChI

1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3

InChI key

KBPLFHHGFOOTCA-UHFFFAOYSA-N

Gene Information

mouse ... Chrna1(11435)

Looking for similar products? Visit Product Comparison Guide

General description

1-Octanol (n-octanol) is a monohydroxy alcohol that can be found in essential oils as the butyrate and acetate. It can be synthesized with high selectivity from biomass-derived furfural-acetone (FFA) in the presence of Pd/NbOPO4 (palladium/ niobium oxide phosphate) catalyst. Formation of octyl ether and octyl ester compounds from Chinese fir sawdust by liquefaction in the presence of acidic ionic liquids (AILs) has been reported. The performance of molybdenum carbide/zirconium dioxide (Mo2C/ZrO2) catalyst for the hydrodeoxygenation (HDO) of phenol has been analyzed in 1-octanol. 1-Octanol shows promising combustion properties to be employed as a biofuel for spark-ignition engines.

Application


  • Characterization of Volatile Compounds: This study utilizes 1-Octanol in the analysis of volatile compounds in Valencia orange juice. It highlights its use in the food industry, particularly in quality control and assurance, which is essential for researchers and professionals in the food science sector (Han et al., 2024).

  • Noncontact In Situ Multidiagnostic NMR/Dielectric Spectroscopy: The study discusses the application of 1-Octanol in developing noncontact diagnostic techniques, beneficial for chemists and material scientists involved in analytical and diagnostic methodologies (Morais et al., 2024).

  • Extraction of Bisphenols from Beverages: Highlighting its use in food safety and environmental testing, this study employs 1-Octanol based frameworks for detecting contaminants in consumer products, essential for ensuring public health and safety in the food industry (Cheng et al., 2024).

Biochem/physiol Actions

Blocks T-type Ca2+ channels

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

187.7 °F

Flash Point(C)

86.5 °C


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

Florian Kremer et al.
Frontiers in bioengineering and biotechnology, 3, 112-112 (2015-08-25)
Over the last decade, microbes have been engineered for the manufacture of a variety of biofuels. Saturated linear-chain alcohols have great potential as transport biofuels. Their hydrocarbon backbones, as well as oxygenated content, confer combustive properties that make it suitable
Eagleson M.
Concise Encyclopedia Chemistry, 744-744 (1994)
Activity and stability of Mo2C/ZrO2 as catalyst for hydrodeoxygenation of mixtures of phenol and 1-octanol.
Mortensen PM, et al.
J. Catal., 328, 208-215 (2015)
Liquefaction of sawdust in 1-octanol using acidic ionic liquids as catalyst.
Lu Z, et al.
Bioresource Technology, 142, 579-584 (2013)
Energy-efficient production of 1-octanol from biomass-derived furfural-acetone in water.
Xia Q, et al.
Green Chemistry, 17(8), 4411-4417 (2015)

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