Crystalline Dmpat-Spermine Chemical Intermediates For Organophosphorus Pesticidescas
2,3-Difluoro-5-Chloropyridine For The Synthesis Of High-Efficiency Pesticide Clodinafop-Propargyl Cas 89402-43-7
DESCRIPTION
DMPAT is an organic compound with the chemical name N, N-dimethyl-3-amino-1-propanol-2-one. It is a kind of amino ketone compound and a pharmaceutical intermediate, which is widely used in the field of pharmaceutical synthesis.It should be noted that DMPAT is a toxic compound that should be strictly operated in organic synthesis laboratories in accordance with operating procedures, wearing appropriate protective equipment, and operating in a well ventilated environment to avoid harm to human health and the environment. At the same time, it should be stored in a dry, ventilated, and dark place to avoid mixing with other chemicals.
Specification
| product Name | DMPAT |
| Synonyms | O,O-dimethylamidothiophosphate; O,O-Dimethyl Phosphoroamido Thioate; N,N-Bis(3-aminopropyl)-1,4-butanediamine; Spermine; N,N-Bis(3-aminopropyl)-1,4-diaminobutane; 4,9-diazadodecamethylenediamine; Spermine dihydrate; N,N-Bis(3-aminopropyl)-1,4-diaminobutane; Gerontine; Musculamine; Neuridine; N,N'-bis(3-aminopropyl)butane-1,4-diamine; O,O-dimethyl phosphoramidothioate; N,N'-bis(3-ammoniopropyl)butane-1,4-diaminium; O,O-Dimethyl thiophosphoramidate |
| Molecular Formula | C10H26N4 |
| Molecular Weight | 202.3698 |
| InChI | InChI=1/C10H26N4/c11-5-3-9-13-7-1-2-8-14-10-4-6-12/h13-14H,1-12H2/p+4 |
| CAS Registry Number | 71-44-3;17321-47-0 |
| EINECS | 200-754-2 |
| Molecular Structure |
71-44-3;17321-47-0 DMPAT |
| Melting point | 26-30℃ |
| Boiling point | 308.4°C at 760 mmHg |
| Flash point | 175.6°C |
| Vapour Pressur | 0.000683mmHg at 25°C |
| Hazard Symbols | C:Corrosive; |
| Risk Codes | R34:; |
| Safety Description | S26:; S36/37/39:; S45:; |
USES
DMPAT can be used as an important intermediate in the synthesis of many drugs, such as β Receptor blockers, calcium antagonists, anticancer drugs, etc. It can be synthesized through a variety of chemical reactions, such as the reaction of p-toluenesulfonic imide with acetylacetone using sodium bisulfite as the reducing agent.
In addition, DMPAT is also a chiral compound that can be used as a chiral inducer in organic synthesis. For example, it can serve as a chiral inducer to catalyze the asymmetric corresponding reaction of aldehydes and imines, forming chiral compounds β- Amino aldehyde. DMPAT can also be used to catalyze other types of asymmetric reactions, such as asymmetric imine addition reaction.


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