(R)-(-)-2-Aminobutane, 99%, Thermo Scientific Chemicals
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(R)-(-)-2-Aminobutane, 99%, Thermo Scientific Chemicals
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(R)-(-)-2-Aminobutane, 99%, Thermo Scientific Chemicals

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250 mg
1 g
5 g
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Catalog number L03889.MD
also known as L03889-MD
Price (EUR)/ Each
68,70
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Quantity:
250 mg
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Price (EUR)/ Each
68,70
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(R)-(-)-2-Aminobutane, 99%, Thermo Scientific Chemicals
Catalog numberL03889.MD
Price (EUR)/ Each
68,70
-
Add to cart
Chemical Identifiers
CAS13250-12-9
IUPAC Namebutan-2-amine
Molecular FormulaC4H11N
InChI KeyBHRZNVHARXXAHW-UHFFFAOYNA-N
SMILESCCC(C)N
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Appearance (Color)Clear colorless
Optical Rotation-8.0? ? 0.5? (neat)
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(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. 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
(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).

Solubility
Miscible with water.

Notes
Air and light sensitive. Store it in a cool place. Incompatible with acids, acid chloride, acid anhydrides, strong oxidizing agents and carbon dioxide.
RUO – Research Use Only

General References:

  1. Shcherbakova, E. G.; Minami, T.; Brega, V.; James, T. D.; Carvalho, P. O.; Anzenbacher Jr, P. Determination of Enantiomeric Excess in Amine Derivatives with Molecular Self-Assemblies. Angew. Chem. Int. Ed. 2015, 54 (24), 7130-7133.
  2. Pilissao, C.; Carvalho, P. O.; Nascimento, M. G. The influence of conventional heating and microwave irradiation on the resolution of (RS)-sec-butylamine catalyzed by free or immobilized lipases. J. Braz. Chem. Soc. 2012, 23 (9), 1688-1697.
  3. Joubioux, F. L.; Achour, O.; Bridiau, N.; Graber, M.; Maugard, T. Kinetic study of 2-butanol O-acylation and sec-butylamine N-acylation catalyzed by Candida antarctica lipase B. J. Mol. Catal. B: Enzym. 2011, 70 (3-4), 108-113.