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| | N-Isopropylmethylamine Basic information |
| | N-Isopropylmethylamine Chemical Properties |
| Melting point | -55.1°C (estimate) | | Boiling point | 50-53 °C (lit.) | | density | 0.702 g/mL at 25 °C (lit.) | | vapor pressure | 4.15 psi ( 20 °C) | | refractive index | n20/D 1.384(lit.) | | Fp | −25 °F | | storage temp. | Refrigerator, Under Inert Atmosphere | | solubility | Soluble in chloroform, DMSO, methanol. | | pka | 10.76±0.10(Predicted) | | form | Liquid | | color | Colorless | | Specific Gravity | 0.702 | | Sensitive | Air Sensitive | | BRN | 1730877 | | Stability: | Volatile | | LogP | 0.52 at 25℃ | | CAS DataBase Reference | 4747-21-1(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Propanamine, N-methyl-(4747-21-1) |
| Hazard Codes | F,C | | Risk Statements | 11-34 | | Safety Statements | 16-26-36/37/39-45 | | RIDADR | UN 2734 8/PG 1 | | WGK Germany | 3 | | F | 9-23 | | HazardClass | 3.1 | | PackingGroup | II | | HS Code | 29211990 |
| | N-Isopropylmethylamine Usage And Synthesis |
| Chemical Properties | Colorless to light yellow liqui | | Uses | N-Isopropylmethylamine is used in the generation of in situ micelles having distinct sizes, by sequential self-assembly of a series of stimuli-responsive amphiphilic block copolymers, prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization. It is suitable for use in the synthesis of novel 5-ethoxy-N,N-dialkyl-[α,α,β,β-H4]-tryptamines and their [α,α,β,β,β-D4]-counterparts following the Speeter and Anthony procedure. | | General Description | N-Isopropylmethylamine is an unsymmetrical amine. Pd/C-catalyzed oxidative cross double carbonylation of N-isopropylmethylamine with alcohols has been reported. | | Flammability and Explosibility | Highlyflammable |
| | N-Isopropylmethylamine Preparation Products And Raw materials |
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