3-Pentanol, 98+%
3-Pentanol, 98+%
3-Pentanol, 98+%
Thermo Scientific Chemicals

3-Pentanol, 98+%

CAS: 584-02-1 | C5H12O | 88.15 g/mol
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Catalog NumberQuantity
ALFL06065.1425 g
Catalog number ALFL06065.14
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Quantity:
25 g
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Specifications
Chemical Name or Material3-Pentanol
CAS584-02-1
Health Hazard 1Warning
Health Hazard 2GHS H Statement
H226-H332-H315-H335
Flammable liquid and vapor.
Harmful if inhaled.
Causes skin irritation.
May cause respiratory irritation.
Health Hazard 3GHS P Statement
P210-P261-P280-P303+P361+P353-P405-P501a
Keep away from heat/sparks/open flames/hot surfaces. - No smoking.
Avoid breathing dust/fume/gas/mist/vapors/spray.
Wear protective gloves/protective clothing/eye protection/face protection.
IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower.
Store locked up.
Dispose of contents/container in accordance with local/regional/national/international regulations.
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3-Pentanol is widely used as a flavoring agent. It is biogenic oxygenated volatile organic compound (BOVOC) and is used as a reagent in the synthesis of pure bromopentanes for infrared standards.

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
3-Pentanol is widely used as a flavoring agent. It is biogenic oxygenated volatile organic compound (BOVOC) and is used as a reagent in the synthesis of pure bromopentanes for infrared standards.

Solubility
Soluble in acetone, benzene, ethanol and diethyl ether.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Leseleuc, M. D.; Collins, S. K. Direct Macrolactonization of Seco Acids via Hafnium(IV) Catalysis. ACS Catal. 2015, 5 (3), 1462-1467.
  2. Tamura, M.; Nakagawa, Y.; Okumura, K.; Tomishige, K. Hydrodeoxygenation of Vicinal OH Groups over Heterogeneous Rhenium Catalyst Promoted by Palladium and Ceria Support. Angew. Chem. 2015, 127 (6), 1917-1920.