H13303
1-Hexanol
reagent grade, 98%
Synonym(s):
Hexyl alcohol
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About This Item
Linear Formula:
CH3(CH2)5OH
CAS Number:
Molecular Weight:
102.17
UNSPSC Code:
12352104
NACRES:
NA.21
PubChem Substance ID:
EC Number:
203-852-3
Beilstein/REAXYS Number:
969167
MDL number:
Grade:
reagent grade
Assay:
98%
Bp:
156-157 °C (lit.)
Vapor pressure:
1 mmHg ( 25.6 °C)
Product Name
1-Hexanol, reagent grade, 98%
InChI key
ZSIAUFGUXNUGDI-UHFFFAOYSA-N
InChI
1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3
SMILES string
CCCCCCO
grade
reagent grade
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 %
dilution
(for analytical testing)
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.)
Quality Level
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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.
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
140.0 °F - closed cup
flash_point_c
60 °C - closed cup
Regulatory Information
危险化学品
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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
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
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
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