CAS 13250-12-9
:(R)-(-)-2-Aminobutane
- (-)-2-Aminobutane
- (-)-2-Butylamine
- (-)-sec-Butylamine
- (1R)-1-Methylpropylamine
- (2R)-butan-2-amine
- (2S)-butan-2-amine
- (R)-(-)-2-Butylamine
- (R)-1-Methylpropylamine
- (R)-2-Butanamine
- (R)-N-sec-Butylamine
- (R)-sec-butylamine
- 2-Butanamine, (2R)-
- 2-Butanamine, (R)-
- Butan-2-Amine
- sec-Butylamine, (R)-(-)-
- R(-)-SEC-BUTYLAMINE 99+%
- (R)-(-)-2-Aminobutane
- See more synonyms
(R)-(-)-sec-Butylamine
CAS:Formula:C4H11NPurity:>98.0%(GC)(T)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:73.14(R)-(-)-2-Aminobutane, 99%
CAS:(R)-(-)-2-Aminobutane is a chiral amine plays an important role in pharmaceutical chemistry and in organic synthesis as chiral auxiliary, which is used to determine the enantiomeric excess (ee). This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio.
Formula:C4H11NPurity:99%Color and Shape:Liquid, Clear colorlessMolecular weight:73.14(1R)-(-)-1-Methylpropylamine
CAS:(1R)-(-)-1-MethylpropylamineFormula:C4H11NPurity:≥95%Color and Shape: clear. colourless liquidMolecular weight:73.13683g/mol(R)-(-)-2-Aminobutane
CAS:(R)-(-)-2-Aminobutane is an amine with a chloro group. It is used to produce polymers for use in the production of plastics, textiles, and other materials. The amine reacts with the chlorate to form a bifunctional monomer that can be polymerized into a polymer. This reaction is catalyzed by an acid and proceeds through a kinetic process. The rate of this reaction has been shown to be constant over the pH range 2-6. The identity of the monomer can be determined using chromatography or mass spectrometry, and its sequence can be determined using NMR or other methods. (R)-(-)-2-Aminobutane is also used as a reagent in analytical chemistry because it produces asymmetric products when reacted with certain molecules.
Formula:C4H11NPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:73.14 g/mol




