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Hexan

Manufactured by Merck Group
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Sourced in United Kingdom

Hexan is a laboratory equipment used for various applications in scientific research and analysis. It is a colorless, volatile liquid hydrocarbon with the chemical formula C6H14. Hexan serves as a non-polar solvent and can be used for extraction, purification, and other laboratory procedures where a non-polar solvent is required.

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Lab products found in correlation

Acarbose, by Merck Group (1 mentions) Antibacterial antimycotic solution, by Merck Group (1 mentions) Trypsin edta, by Merck Group (1 mentions) Glutamax, by Thermo Fisher Scientific (1 mentions) Ethanol, by Merck Group (1 mentions) Phosphate buffered saline (pbs), by Merck Group (1 mentions) Lactase, by Merck Group (1 mentions)

Spelling variants of this product

Hexan-1-ol (4 citations) N-Hexan (4 citations) Hexanes (HPLC grade) (2 citations) Hexan-2-ol (2 citations)

2 protocols using hexan

1

Enzymatic Carbohydrate Hydrolysis Assay

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All solvents were HPLC grade and were degassed and filtrated before their application, whereas all other chemicals were of analytical reagent grade. Dulbecco’s modified eagle medium (DMEM), GlutaMAX™, was purchased from Life Technologies, Paisley, UK, while antibacterial/antimycotic solution, phosphate-buffered saline, trypsin-EDTA, glucose oxidase/peroxidase and o-dianisidine, baker’s yeast α-glycosidase, p-Nitrophenyl-α-glucopyranoside sucrase, maltase, lactase, and acarbose were obtained from Sigma-Aldrich, Pool, UK, as well as the following reagents: ethanol, hexan, formic acid, and methanol. The multi-well Tecan’s Spark® plate reader was obtained from Tecan Group Ltd., Mannedorf, Switzerland.
Altamimi M.A., Abu-Reidah I.M., Altamimi A, & Jaradat N. (2022). Hydroethanolic Extract of Urtica dioica L. (Stinging Nettle) Leaves as Disaccharidase Inhibitor and Glucose Transport in Caco-2 Hinderer. Molecules, 27(24), 8872.
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2

Optic Nerve Sample Preparation

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Optic nerves were prepared as described in (Dodt et al., 2007 (link)). Briefly optic nerves were post fixed overnight at 4°C in PFA4%, then dehydrated in ethanol (50%, 80% and 95% for 20min each) Optic nerves were incubated for 1h in ethanol 100% and then 2h in Hexan (Sigma). Finally samples were transferred in benzyl benzoate/benzyl alcohol (2:1 in volume-Sigma) clearing solution.
Belin S., Nawabi H., Wang C., Tang S., Latremoliere A., Warren P., Schorle H., Uncu C., Woolf C., He Z, & Steen J. (2015). Injury-induced decline of intrinsic regenerative ability revealed by quantitative proteomics. Neuron, 86(4), 1000-1014.
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