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(S)-(-)-2-Methylbutylamine, 98+%
(S)-(-)-2-Methylbutylamine, 98+%
(S)-(-)-2-Methylbutylamine, 98+%
Thermo Scientific Chemicals

(S)-(-)-2-Methylbutylamine, 98+%

CAS: 34985-37-0 | C5H13N | 87.166 g/mol
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Quantity:
250 mg
1 g
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Catalog number L14063.03
also known as L14063-03
Price (EUR)
181,00
Each
Quantity:
1 g
Request bulk or custom format
Price (EUR)
181,00
Each
Chemical Identifiers
CAS34985-37-0
IUPAC Name2-methylbutan-1-amine
Molecular FormulaC5H13N
InChI KeyVJROPLWGFCORRM-UHFFFAOYNA-N
SMILESCCC(C)CN
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥94.0%
Optical Rotation-6° ± 0.5° (neat)
Refractive Index1.4080-1.4120 @ 20°C
(S)-(-)-2-Methylbutylamine is used as aintermediate in organic synthesis, as pharmaceutical intermediate.

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
(S)-(-)-2-Methylbutylamine is used as aintermediate in organic synthesis, as pharmaceutical intermediate.

Solubility
Fully miscible in water.

Notes
Air sensitive. Store under inert gas. Store away from oxidizing agents, air, carbondioxide.
RUO – Research Use Only

General References:

  1. Peter G. Gillespie; Susan K. H. Gillespie; John A. Mercer; Kavita Shah and Kevan M. Shokat. Engineering of the Myosin-Iβ Nucleotide-binding Pocket to Create Selective Sensitivity to N6-modified ADP Analogs. The Journal of Biological Chemistry, 1999, 274, 31373-31381.
  2. Robert H. Bradbury; Janet E. Rivett. 1,2,4-Triazolo[4,3-a]pyrazine derivatives with human renin inhibitory activity. 3. Synthesis and biological properties of aminodeoxystatine and difluorostatone derivatives. J. Med. Chem. 1991, 34, (1), 151-157.