Skip to Content
Merck
All Photos(2)

Documents

H13303

Sigma-Aldrich

1-Hexanol

reagent grade, 98%

Synonym(s):

Hexyl alcohol

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CH3(CH2)5OH
CAS Number:
111-27-3
Molecular Weight:
102.17
Beilstein:
969167
EC Number:
203-852-3
MDL number:
MFCD00002982
UNSPSC Code:
12352104
PubChem Substance ID:
329815159
NACRES:
NA.21

grade

reagent grade

Quality Level

200

vapor density

4.5 (vs air)

vapor pressure

1 mmHg ( 25.6 °C)

Assay

98%

form

liquid

autoignition temp.

559 °F

expl. lim.

0.34-6.3 %

refractive index

n20/D 1.418 (lit.)

bp

156-157 °C (lit.)

mp

−52 °C (lit.)

density

0.814 g/mL at 25 °C (lit.)

SMILES string

CCCCCCO

InChI

1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3

InChI key

ZSIAUFGUXNUGDI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

1-Hexanol is a linear primary alcohol, made up of six carbon atoms and is produced by the oligomerization of ethylene. There is a wide range of uses for 1-hexanol, including plasticizers, antiseptics, fragrances, pharmaceuticals, textiles, and leather finishing agents.

Application

1-Hexanol is used:
  • As an oil phase in the preparation of manganese zinc ferrite nanoparticles by precipitation in reverse microemulsion system.
  • As a solvent in the separation of carboxylic acids and tetrahydrofurfuryl alcohol from water.
  • As a solvent in the synthesis of ZnO (zinc oxide) quantum particles from zinc acetate by precipitation method.

Features and Benefits

1-Hexanol or Hexyl alcohol exhibits high reactivity at a lower temperature due to the alkane-like reaction pathways that begin at a secondary carbon site.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H302 + H312,H319

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

140.0 °F - closed cup

Flash Point(C)

60 °C - closed cup

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

Erik Jue et al.
Scientific reports, 10(1), 1940-1940 (2020-02-08)
The success of fundamental and applied nucleic acid (NA) research depends on NA purity, but obtaining pure NAs from raw, unprocessed samples is challenging. Purification using solid-phase NA extractions utilizes sequential additions of lysis and wash buffers followed by elution.
Annie Handler et al.
Cell, 178(1), 60-75 (2019-06-25)
Animals rely on the relative timing of events in their environment to form and update predictive associations, but the molecular and circuit mechanisms for this temporal sensitivity remain incompletely understood. Here, we show that olfactory associations in Drosophila can be
Maria Eugenia Villar et al.
Cell reports, 30(8), 2603-2613 (2020-02-27)
Research on honeybee memory has led to a widely accepted model in which a single pairing of an odor stimulus with sucrose induces memories that are independent of protein synthesis but is unable to form protein-synthesis-dependent long-term memory (LTM). The
Justin T Mohr et al.
Journal of medicinal chemistry, 48(12), 4172-4176 (2005-06-10)
The polyhydroxyalkanes 1,6,11,16-hexadecanetetraol (1) and 2,7,12,17-octadecanetetraol (2) were synthesized utilizing the thiophene ring as a scaffold to affix the hydroxyalkyl chains by lithiation of the acidic alpha-hydrogens and subsequent desulfurization. Both compounds exhibited significant anesthetic potency, individually and in additivity
Abdolhamid Firooz et al.
Journal of colloid and interface science, 370(1), 183-191 (2012-01-27)
The effects of carbon chain length and temperature were investigated on adsorption kinetics and surface tension of a group of slightly volatile, short carbon chain molecules: 1-octanol, 1-hexanol, and 1-butanol. Experiments were performed in a closed chamber where simultaneous adsorption
View All Related Papers

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