1-methoxy-2-propylamine

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Structural formula
Structural formula of 1-methoxy-2-propylamine
( R ) shape (left) and ( S ) shape (right)
General
Surname 1-methoxy-2-propylamine
other names
  • ( RS ) -2-amino-1-methoxypropane
  • (±) -2-amino-1-methoxypropane
  • rac -2-amino-1-methoxypropane
  • 2-methoxyisopropylamine
  • (±) -β-methoxyisopropylamine
  • 1-methoxy-2-aminopropane
Molecular formula C 4 H 11 NO
Brief description

colorless liquid

External identifiers / databases
CAS number 37143-54-7
EC number 422-550-4
ECHA InfoCard 100.102.112
PubChem 123458
Wikidata Q15632831
properties
Molar mass 89.14 g mol −1
Physical state

liquid

density

0.845 g cm −3  (25 ° C)

Melting point

-95 ° C

boiling point

92.5-93.5 ° C

Refractive index

1.4065 (20 ° C)

safety instructions
GHS hazard labeling from  Regulation (EC) No. 1272/2008 (CLP) , expanded if necessary
02 - Highly / extremely flammable 07 - Warning 05 - Corrosive

danger

H and P phrases H: 225-314-302-412
P: 210-273-280-305 + 351 + 338-310
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

1-Methoxy-2-propylamine is a chemical compound that is needed for the synthesis of herbicides. The ( S ) - isomer can be synthesized from isopropylamine and methoxyacetone by stereoselective biocatalysis by a transaminase .

Individual evidence

  1. ↑ a b c d Data sheet 1-Methoxy-2-propylamine, 95% from Sigma-Aldrich , accessed on August 8, 2013 ( PDF ).
  2. ↑ Günter Hommel (Ed.): Handbook of dangerous goods: Leaflets 2072-2502 . Springer, 2004, ISBN 3-540-20370-2 , pp. 2501 ( limited preview in Google Book search).
  3. ↑ a b Entry on 1-methoxy-2-propylamine in the GESTIS substance database of the IFA , accessed on February 1, 2016(JavaScript required) .
  4. ↑ Entry on 1-methoxy-2-propylamine in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .
  5. ↑ Junhua Tao, Romas Joseph Kazlauskas: Biocatalysis for Green Chemistry and Chemical Process Development . Wiley, Hoboken (New Jersey) 2011, ISBN 978-0-470-43778-0 ( limited preview in Google Book Search).