(1R)-(-)-1-Methylpropylamine
Catalogue Number OR59999
Synonym(s): (2R)-(-)-2-Aminobutane, R-(-)-sec-Butylamine
(1R)-(-)-1-methylpropylamine, also known as (2R)-(-)-2-Aminobutane or R-(-)-sec-Butylamine (CAS 13250-12-9) is a primary amine. Apollo Scientific supplies (1R)-(-)-1-methylpropylamine to R&D, Academic institutions, and manufacturers across the UK and USA.
(1R)-(-)-1-methylpropylamine is... Read More
- CAS Number
13250-12-9
- Commodity Code
2921199990
- MDL Number
MFCD00064416
- Formula Weight
- 73.14 g/mol
- Density
- 0.722 g/cm3
- Boiling Point
- 63 °C
- Ref Index
- 1.393
- Flash Point
- -19 °C
- Chemical Hazard
- Highly Flammable/Corrosive/Harmful
- GHS
-
- Hazard Statements
-
Very toxic to aquatic life.|Highly flammable liquid and vapour.|Harmful if inhaled.|Harmful if swallowed.|Causes severe skin burns and eye damage.
- Precautionary Statements
-
Keep away from heat: hazard.Keep away from heat
hot surfaces: hazard. hot surfaces
sparks: hazard. sparks
open flames and other ignition sources. No smoking.|Keep container tightly closed.|Do not breathe mist/vapours/spray.|Wash all exposed external body areas thoroughly after handling.|Use only outdoors or in a well: hazard. open flames and other ignition sources. No smoking.|Keep container tightly closed.|Do not breathe mist/vapours/spray.|Wash all exposed external body areas thoroughly after handling.|Use only outdoors or in a well
- MSDS
- Typical Batch COA
- View
- Request batch specific COA here
Product Description
(1R)-(-)-1-methylpropylamine, also known as (2R)-(-)-2-Aminobutane or R-(-)-sec-Butylamine (CAS 13250-12-9) is a primary amine. Apollo Scientific supplies (1R)-(-)-1-methylpropylamine to R&D, Academic institutions, and manufacturers across the UK and USA.
(1R)-(-)-1-methylpropylamine is used to prepare (R)-(?)-sec-butylbis(2-hydroxyethyl)amine, an intermediate for the synthesis of aminodiphosphine ligands. It can also be used as a model compound in the study or singlet-tripler transitions in cicular dichroism, or as a substrate in the demonstration of the stereochemistry of Mitsunobu reaction to synthesise secondary amines.
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