Search
Element Search
Structure Search
Thermo Scientific Chemicals
(+/-)-2-Aminoheptane, 98+%
CAS: 123-82-0 | C7H17N | 115.22 g/mol
Change view
Catalog number B22863.22
also known as B22863-22
Price (JPY)
-
Quantity:
100 g
Chemical Identifiers
CAS123-82-0
IUPAC Nameheptan-2-amine
Molecular FormulaC7H17N
InChI KeyVSRBKQFNFZQRBM-UHFFFAOYNA-N
SMILESCCCCCC(C)N
View more
Specifications
Specification Sheet
Specification SheetRefractive Index1.4170-1.4210 @20?C
Appearance (Color)Clear colorless to yellow
Identification (FTIR)Conforms
Assay (GC)≥98.0%
FormLiquid
(±)-2-Aminoheptane is used as an organic chemical synthesis 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
(+/-)-2-Aminoheptane is used as an organic chemical synthesis intermediate.
Solubility
Soluble in water ( 9 g/L at 20°C).
Notes
Air sensitive. Incompatible with oxidizing agents and carbon dioxide.
(+/-)-2-Aminoheptane is used as an organic chemical synthesis intermediate.
Solubility
Soluble in water ( 9 g/L at 20°C).
Notes
Air sensitive. Incompatible with oxidizing agents and carbon dioxide.
RUO – Research Use Only
General References:
- P.Macaudiere; A.Tambute; M.Caude; R.Rosset; M.A.Alembik; I.W.Wainr. Resolution of enentiomeric amides on a pirklet-type chiral stationary phase : A comparison of subcritical fluid and liquid chromatographic approaches. Journal of Chromatography A. 1986, 371,177-193.
- J.A.Corbin; Lockhart Burgess Rogers. Improved gas chromatographic separations of enantiomeric secondary amine derivatives. Anal. Chem. 1970, 42,(9), 974-979.