(+/-)-2-Methyl-1-butanol, 98%
(+/-)-2-Methyl-1-butanol, 98%
(+/-)-2-Methyl-1-butanol, 98%
Thermo Scientific Chemicals

(+/-)-2-Methyl-1-butanol, 98%

CAS: 137-32-6 | C5H12O | 88.15 g/mol
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Catalog number B21825.AE
also known as B21825-AE
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Quantity:
100 mL
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Price (USD)
23.65
Special offer
Online exclusive
Ends: 30-Jun-2026
27.40
Save 3.75 (14%)
Each
Chemical Identifiers
CAS137-32-6
IUPAC Name2-methylbutan-1-ol
Molecular FormulaC5H12O
InChI KeyQPRQEDXDYOZYLA-UHFFFAOYNA-N
SMILESCCC(C)CO
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
Identification (FTIR)Conforms
FormLiquid
Assay (GC)≥97.5%
Refractive Index1.4085-1.4125 @ 20°C

2-Methyl-1-butanol is a volatile metabolite produced by a number of different plant species. Used as a solvent in organic synthesis (introduction of active amyl group), in lubricants, plasticizers, additives for oils & paints. It is also employed as a perfuming agent.

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
2-Methyl-1-butanol is a volatile metabolite produced by a number of different plant species. Used as a solvent in organic synthesis (introduction of active amyl group), in lubricants, plasticizers, additives for oils & paints. It is also employed as a perfuming agent.

Solubility
Soluble in water. [183 g/L (0 C)] and alcohol.

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

General References:

  1. Donald J. Cram.; Janet Allinger. Studies in Stereochemistry. XXIII. The Preparation and Complete Resolution of the 1,2-Diphenyl-2-methyl-1-butanol System. J. Am. Chem. Soc. 1954, 76 (18),4516-4522.
  2. Karin Leontein.; Bengt Lindberg.; Jörgen Lōnngren. Assignment of absolute configuration of sugars by g.l.c. of their acetylated glycosides formed from chiral alcohols. Carbohydr. Res. 1978, 62 (2),359-362.