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H13303

Sigma-Aldrich

1-Hexanol

reagent grade, 98%

Synonym(s):

Hexyl alcohol

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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

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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’.

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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
Carolina Aubery et al.
Langmuir : the ACS journal of surfaces and colloids, 29(6), 1779-1789 (2013-01-12)
Phase behavior, dynamics, and structure of W/O microemulsions of the system aqueous solution/Synperonic 13_6.5/1-hexanol/isooctane were studied, with the goal of determining their effect on Mn-Zn ferrite nanoparticle formation, kinetics and characteristics. Microemulsion structure and dynamics were studied systematically by conductivity
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
Mir Ali Farajzadeh et al.
Analytica chimica acta, 713, 70-78 (2011-12-28)
In the present work a new, simple, rapid and environmentally friendly dispersive liquid-liquid microextraction (DLLME) method has been developed for extraction/preconcentration of some triazole pesticides in aqueous samples and in grape juice. The extract was analyzed with gas chromatography-flame ionization
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