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Hexadecanediol

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Hexadecanediol is a long-chain aliphatic diol with the chemical formula C16H34O2. It is a white crystalline solid with a high melting point. Hexadecanediol is commonly used as a chemical intermediate in various industrial applications.

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Lab products found in correlation

Dodecylamine, by Merck Group (2 mentions) Poly maleic anhydride alt 1 octadecene, by Merck Group (2 mentions) Lauric acid, by Merck Group (2 mentions) Benzyl ether, by Merck Group (2 mentions) Octadecene, by Merck Group (2 mentions) Iron oxide hydroxide, by Merck Group (2 mentions) Manganese acetylacetonate, by Merck Group (2 mentions) Iron acetylacetonate, by Merck Group (2 mentions) Milli q water, by Merck Group (1 mentions) Hexane, by Merck Group (1 mentions) Ethanol, by Merck Group (1 mentions) Methanol, by Merck Group (1 mentions) Acetonitrile, by Merck Group (1 mentions) Toluene, by Merck Group (1 mentions) Selenium, by Merck Group (1 mentions) Diethylzinc, by Merck Group (1 mentions) Cadmium oxide, by Merck Group (1 mentions) Hexamethyldisilathiane, by Merck Group (1 mentions) N n dimethylethylenediamine, by Merck Group (1 mentions) Tetramethylammonium hydroxide tmaoh, by Merck Group (1 mentions)

Spelling variants of this product

1,2-hexadecanediol (55 citations)

2 protocols using hexadecanediol

1

Synthesis of Functional Nanomaterials

Check if the same lab product or an alternative is used in the 5 most similar protocols
Poly(maleic
anhydride-alt-1-octadecene), Mn 30 000–50 000
g/mol (Aldrich),
Milli-Q water (18.2 MΩ, filtered with filter pore size 0.22
μM) from Millipore, acetonitrile (HPLC grade, J. T. Baker) and
tetrahydrofuran anhydride (Carlo Erba, p.a.), iron oxide hydroxide
(Sigma-Aldrich, #371254), iron acetylacetonate (Sigma-Aldrich, 99%),
manganese acetylacetonate (Sigma-Aldrich, #245763), hexadecanediol
(Sigma-Aldrich, 90%), dodecylamine (Sigma-Aldrich, 98%), lauric acid
(Sigma-Aldrich, 99%), benzyl ether (Sigma-Aldrich, 98%), and octadecene
(Sigma-Aldrich, 90%), YCl3, YbCl3, ErCl3, ammonium fluoride, and sodium oleate, tri-n-octylphosphine oxide (Strem, 99%), tri-n-octylphosphine
(Strem, 97%), n-octadecylphosphonic acid (PolyCarbon
Industries, 99%), cadmium oxide (Sigma-Aldrich, 99.99%), selenium
(Sigma-Aldrich, 99.99%), diethylzinc (Sigma-Aldrich, 1 M in hexane)
and hexamethyldisilathiane (Sigma-Aldrich, synthesis grade), ethanol
(Sigma-Aldrich, 99.8%), methanol (Sigma-Aldrich, 99.9%), toluene (Sigma-Aldrich,
99.5%), and hexane (Sigma-Aldrich, 99%) were used without any further
purification. All reagents for cell cytotoxicity assay were purchased
from Gibco (ThermoFisher Scientific).
Materia M.E., Pernia Leal M., Scotto M., Balakrishnan P.B., Kumar Avugadda S., García-Martín M.L., Cohen B.E., Chan E.M, & Pellegrino T. (2017). Multifunctional Magnetic and Upconverting Nanobeads as Dual Modal Imaging Tools. Bioconjugate Chemistry, 28(11), 2707-2714.
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2

Synthesis of Functionalized Magnetic Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
Poly(maleic anhydride-alt-1-octadecene), Mn 30,000–50,000 (Aldrich), Milli-Q
water
(18.2 MΩ, filtered with filter pore size 0.22 μM) from
Millipore, acetonitrile (HPLC grade, J. T. Baker) and tetrahydrofuran
anhydride (Carlo Erba, p.a.), iron oxide hydroxide (Sigma-Aldrich,
#371254), iron acetylacetonate (Sigma-Aldrich, 99%), manganese acetylacetonate
(Sigma-Aldrich, #245763), hexadecanediol (Sigma-Aldrich, 90%), dodecylamine
(Sigma-Aldrich, 98%), lauric acid (Sigma-Aldrich, 99%), benzyl ether
(Sigma-Aldrich, 98%), and octadecene (Sigma-Aldrich, 90%), as well
as 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide hydrochloride (EDC)
(Aldrich, commercial grade), O-(2-aminoethyl)-O′-methyl polyethylene glycol (“aminoPEG750”,
Aldrich), N,N-dimethylethylenediamine
(for “tertiary amine functionalization”, Aldrich), 2-(2-pyridyl)ethylamine
(for “pyridine functionalization”, Aldrich), and 2,2′-(ethylendedioxy)bis(ethylamine)
(referred to in this article as “diamine” Aldrich),
tetramethylammonium hydroxide (TMAOH, Sigma-Aldrich) were used without
further purification. Acetonitrile (ACN, not anhydrous) was purchased
from J. T. Baker and stored in the glovebox.
Bigall N.C., Rodio M., Avugadda S., Leal M.P., Di Corato R., Conteh J.S., Intartaglia R, & Pellegrino T. (2022). Scaling Up Magnetic Nanobead Synthesis with Improved Stability for Biomedical Applications. The Journal of Physical Chemistry. a, 126(51), 9605-9617.
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