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471860 Aldrich

(1R)-(+)-(1-Amino-2-methylpropyl)phosphonic acid

98%

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Building Blocks, Organic Building Blocks, Phosphonic/Phosphinic Acids More...
InChI Key   DGSLPJDIFKVSIB-SCSAIBSYSA-N
assay   98%
optical activity   [α]20/D +1.0°, c = 1 in 1 M NaOH
mp   272-277 °C(lit.)

Description

Packaging

250 mg in glass insert

Application

Serves as an attractive substitute for amino carboxylic acids in biological systems. Exhibits interesting and useful properties as peptide analog, antiviral agent, hapten for the generation of catalytic antibodies, enzyme inhibitors, potent antibiotics, herbicides, and pesticides.

General description

The enantiodiscrimination of (1R)-(+)-(1-amino-2-methylpropyl)phosphonic acid from its enantiomer in the gas-phase can be done using ESI-MS-CID technique. [electrospray ionization-mass spectrometric detection-collision induced dissociation]

Price and Availability

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Protocols & Articles
Peer-Reviewed Papers
15

References

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