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Thermo Scientific Chemicals
(R)-(-)-2-Aminobutane, 99%
CAS: 13250-12-9 | C4H11N | 73.139 g/mol
化学物質識別子
CAS13250-12-9
IUPAC Namebutan-2-amine
Molecular FormulaC4H11N
InChI KeyBHRZNVHARXXAHW-UHFFFAOYNA-N
SMILESCCC(C)N
さらに表示
仕様
スペックシート
スペックシートFormLiquid
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Appearance (Color)Clear colorless
Optical Rotation-8.0? ? 0.5? (neat)
さらに表示
(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.
(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:
- 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.
- 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.
- 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.