Isobutanol, 99%, Thermo Scientific Chemicals
Isobutanol, 99%, Thermo Scientific Chemicals
Isobutanol, 99%, Thermo Scientific Chemicals
Isobutanol, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Isobutanol, 99%, Thermo Scientific Chemicals

CAS: 78-83-1 | C4H10O | 74.123 g/mol
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2500 mL
500 mL
Catalog number ALFB23091.0F
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2500 mL
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Chemical Identifiers
CAS100587-92-6
IUPAC Nameterbium(3+) triacetate
Molecular FormulaC6H9O6Tb
InChI KeyJQBILSNVGUAPMM-UHFFFAOYSA-K
SMILES[Tb+3].CC([O-])=O.CC([O-])=O.CC([O-])=O
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SpecificationsSpecification SheetSpecification Sheet
Total Rare Earth Oxide Impurities0.1% max.
Isobutanol is a reagent used in organic reactions. It is employed in the synthesis of new fluorinating reagents. It is also used in the lipase-catalyzed production of biodiesel as an energy source. It acts as a catalyst for the liquid-phase esterification of acetic acid by ion-exchange resins. Dehydration of fermented isobutanol is useful in the production of renewable chemicals and fuels.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Isobutanol is a reagent used in organic reactions. It is employed in the synthesis of new fluorinating reagents. It is also used in the lipase-catalyzed production of biodiesel as an energy source. It acts as a catalyst for the liquid-phase esterification of acetic acid by ion-exchange resins. Dehydration of fermented isobutanol is useful in the production of renewable chemicals and fuels.

Solubility
Miscible with alcohol and diethyl ether. Partially miscible with water.

Notes
Avoid all sources of ignition. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only

General References:

  1. Akita, H.; Nakashima, N.; Hoshino. T. Bacterial production of isobutanol without expensive reagents. Appl. Microbiol. Biotechnol. 2015, 99 (2), 991-999.
  2. Dhanala, V.; Maity, S. K.; Shee, D. Oxidative steam reforming of isobutanol over Ni/γ-Al2O3 catalysts: A comparison with thermodynamic equilibrium analysis. J. Ind. Eng. Chem. 2015, 27, 153-163.